Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
Crosstalk ID
M6ACROT03479
[1], [2]
Histone modification H3K18la EP300 IGF2BP2 Direct Enhancement m6A modification CD274 CD274 IGF2BP2 : m6A sites
m6A Modification:
m6A Regulator Insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) READER
m6A Target Programmed cell death 1 ligand 1 (CD274/PD-L1)
Epigenetic Regulation that have Cross-talk with This m6A Modification:
Epigenetic Regulation Type Histone modification (HistMod)
Epigenetic Regulator Histone acetyltransferase p300 (P300) WRITER View Details
Regulated Target Histone H3 lysine 18 lactylation (H3K18la) View Details
Downstream Gene IGF2BP2 View Details
Crosstalk Relationship Histone modification  →  m6A Enhancement
Crosstalk Mechanism histone modification directly impacts m6A modification through modulating the level of m6A regulator
Crosstalk Summary CTCF interacts with HNRNPU through a FLG-AS1-dependent mechanism, facilitating the recruitment of p300 and activation of the m6A reader IGF2BP2 by Histone H3 lysine 18 lactylation (H3K18la). This activation promotes histone lactylation at the promoter region of IGF2BP2 stimulating the proliferation of PDAC cells. IGF2BP2 enhanced the mRNA stability of CSF1 and MYC. Mechanistically, circMYO1C cyclization was mediated by m6A methyltransferase METTL3. Moreover, methylated RNA immunoprecipitation sequencing (MeRIP-seq) unveiled the remarkable m6A modification on Programmed cell death 1 ligand 1 (CD274/PD-L1) mRNA. Moreover, circMYO1C targeted the m6A site of PD-L1 mRNA to enhance its stability by cooperating with IGF2BP2, thereby accelerating PDAC immune escape.
Responsed Disease Pancreatic cancer ICD-11: 2C10
In-vitro Model
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
Capan-2 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0026
BxPC-3 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0186
CFPAC-1 Cystic fibrosis Homo sapiens CVCL_1119
In-vivo Model Male BALB/c nude mice (5-6 weeks) were obtained from Slac Laboratory Animal Center (Shanghai, China) and maintained under pathogen-free conditions. PANC-1 cells (2 × 106 cells suspended in 100 μ l PBS) transfected with circMYO1C knockdown (sh-circMYO1C) or controls (sh-NC) were subcutaneously injected into the flank of nude mice. One week later, the tumor size was measured every three days.
Full List of Potential Compound(s) Related to This m6A-centered Crosstalk
CD274 molecule (CD274) 55 Compound(s) Regulating the Target Click to Show/Hide the Full List
 Compound Name Avelumab Approved [3]
External Link
 Compound Name Durvalumab Approved [4]
MOA Modulator
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 Compound Name RG-7446 Approved [5]
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 Compound Name Bavencio Approved [6]
MOA Inhibitor
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 Compound Name Atezolizumab Approved [7]
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 Compound Name Sugemalimab Approved in China [8]
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 Compound Name MEDI4736 Phase 3 [9]
MOA Modulator
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 Compound Name MPDL-3280A Phase 3 [10]
MOA Modulator
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 Compound Name CS1001 Phase 3 [11]
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 Compound Name A167 Phase 3 [12]
Synonyms
KL-A167
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 Compound Name KN046 Phase 3 [13]
MOA Inhibitor
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 Compound Name Pidilizumab Phase 2 [14]
Synonyms
CT-011
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 Compound Name KN035 Phase 2 [15]
Synonyms
Envafolimab
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 Compound Name CX-072 Phase 2 [16]
MOA Inhibitor
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 Compound Name INCB86550 Phase 2 [17]
MOA Inhibitor
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 Compound Name Bintrafusp alfa Phase 2 [18]
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 Compound Name M7824 Phase 2 [19]
MOA Inhibitor
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 Compound Name BGB-A333 Phase 1/2 [20]
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 Compound Name GS-4224 Phase 1/2 [21]
Synonyms
Methyl Pyridazine-4-carboxylate; 34231-77-1; PYRIDAZINE-4-CARBOXYLIC ACID METHYL ESTER; 4-PYRIDAZINECARBOXYLIC ACID, METHYL ESTER; MFCD09953488; ACMC-1AJNN; methyl 4-pyridazinecarboxylate; methylpyridazine-4-carboxylate; SCHEMBL1421640; DTXSID30498310; AMY24958; BCP22435; ANW-50355; ZINC12359421; AKOS015854403; Methyl pyridazine-4-carboxylate, 97%; AC-4414; CS-W003697; PB31452; 4-Pyridazinecarboxylic acid methyl ester; AK-48857; SY004472; AB0024323; DB-030309; FT-0717698; W5569; S-2990; J-522632
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MOA Inhibitor
External Link
 Compound Name NM21-1480 Phase 1/2 [22]
MOA Modulator
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 Compound Name LY3300054 Phase 1 [19]
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 Compound Name MSB2311 Phase 1 [15]
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 Compound Name Anti-PD-L1 Phase 1 [23]
Synonyms
BMS-936559
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 Compound Name FAZ053 Phase 1 [16]
MOA Inhibitor
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 Compound Name Anti-PD-L1 CSR T cells Phase 1 [24]
MOA CAR-T-Cell-Therapy
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 Compound Name BMS-986189 Phase 1 [15]
MOA Inhibitor
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 Compound Name Cosibelimab Phase 1 [25]
Synonyms
CK-301/TG-1501
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 Compound Name CA-170 Phase 1 [26]
MOA Inhibitor
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 Compound Name PD-L1 t-haNK Phase 1 [27]
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 Compound Name KD033 Phase 1 [28]
MOA Inhibitor
External Link
 Compound Name C-Met/PD-L1 CAR-T Cell Phase 1 [29]
MOA CAR-T-Cell-Therapy(Dual specific)
External Link
 Compound Name CA-170 Phase 1 [19]
Synonyms
3-Aminopyrrolidine dihydrochloride; 103831-11-4; pyrrolidin-3-amine dihydrochloride; 3-Pyrrolidinamine, dihydrochloride; 3-Aminopyrrolidine 2HCl; 3-Aminopyrrolidine diHCl; SCHEMBL555933; ACMC-2099s1; ACMC-2099s3; ACMC-20989g; 3-pyrrolidinamine dihydrochloride; CTK0H7226; DTXSID00583661; MolPort-002-343-989; NJPNCMOUEXEGBL-UHFFFAOYSA-N; 3-Amino-pyrrolidine dihydrochloride; KS-00000JI6; ACT01710; ANW-14978; SBB003982; ( -3-Aminopyrrolidine dihydrochloride; AKOS015844825; VP60158; AM85320; VP60228; TRA0055207; TRA0000843; TRA0097
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MOA Inhibitor
External Link
 Compound Name FS118 Phase 1 [15]
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 Compound Name PF-07257876 Phase 1 [30]
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 Compound Name MCLA-145 Phase 1 [31]
MOA Agonist
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 Compound Name GEN1046 Phase 1 [32]
MOA Agonist
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 Compound Name ALPN-202 Phase 1 [33]
MOA Inhibitor
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 Compound Name TAK-252 Phase 1 [34]
Synonyms
SL-279252
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MOA Agonist
External Link
 Compound Name INBRX-105 Phase 1 [35]
MOA Inhibitor
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 Compound Name LY3415244 Phase 1 [36]
MOA Inhibitor
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 Compound Name A337 Phase 1 [12]
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 Compound Name IBI318 Phase 1 [37]
MOA Inhibitor
External Link
 Compound Name PMID30107136-Compound-Example2 Patented [38]
MOA Inhibitor
Activity IC50 = 150 nM
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 Compound Name PMID30107136-Compound-Example1 Patented [38]
MOA Inhibitor
Activity IC50 = 18 nM
External Link
 Compound Name PMID30247903-Compound-General structure7 Investigative [15]
Synonyms
PMID30247903Compound7
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MOA Inhibitor
External Link
 Compound Name CA-327 Investigative [15]
MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure8 Investigative [15]
Synonyms
PMID30247903Compound8
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MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure5 Investigative [15]
Synonyms
PMID30247903Compound5
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MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure12 Investigative [15]
Synonyms
PMID30247903Compound12
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MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure9 Investigative [15]
Synonyms
PMID30247903Compound9
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MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure6 Investigative [15]
Synonyms
PMID30247903Compound6
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MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure10 Investigative [15]
Synonyms
PMID30247903Compound10
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MOA Inhibitor
External Link
 Compound Name YH011 Investigative [39]
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 Compound Name YH010 Investigative [40]
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 Compound Name RG6084 Phase 1 [41]
External Link
Histone acetyltransferase p300 (P300) 2 Compound(s) Regulating the Target Click to Show/Hide the Full List
 Compound Name CCS1477 Phase 1/2 [42]
Synonyms
CCS-1477; CBP-IN-1; 2222941-37-7; (S)-1-(3,4-Difluorophenyl)-6-(5-(3,5-dimethylisoxazol-4-yl)-1-((1r,4S)-4-methoxycyclohexyl)-1H-benzo[d]imidazol-2-yl)piperidin-2-one; SCHEMBL20094038; SCHEMBL21515367; SCHEMBL22134021; EX-A3687; NSC818619; NSC-818619; HY-111784; CS-0091862; (S)-1-(3,4-Difluorophenyl)-6-(5-(3,5-dimethylisoxazol-4-yl)-1-(trans-4-methoxycyclohexyl)-1H-benzo[d]imidazol-2-yl)piperidin-2-one
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MOA Inhibitor
External Link
 Compound Name FT-7051 Phase 1 [43]
MOA Inhibitor
External Link
2C10: Pancreatic cancer 182 Compound(s) Regulating the Disease Click to Show/Hide the Full List
 Compound Name Atezolizumab Approved [19]
External Link
 Compound Name Trimethadione Approved [44]
Synonyms
Absentol; Absetil; Convenixa; Convexina; Edion; Epidione; Epidone; Epixal; Etydion; Minoaleuiatin; Minoaleviatin; Petidion; Petidon; Petilep; Petimalin; Pitmal; Ptimal; Tioxanona; Tredione; Tricione; Tridilona; Tridion; Tridione; Tridone; Trilidona; Trimedal; Trimedone; Trimetadiona; Trimetadione; Trimethadion; Trimethadionum; Trimethdione; Trimethin; Trimethinum; Trimetin; Trioksal; Trioxanona; Triozanona; Tromedone; Troxidone; Abbott Brand of Trimethadione; Trimetadione [DCIT]; A 2297; Mino-Aleviatin; Neo-Absentol; Tridione (TN); Trimetadiona [INN-Spanish]; Trimethadione [INN:JAN]; Trimethadionum [INN-Latin]; Trimethadione (JP15/INN); 3,3,5-Trimethyl-2,4-diketooxazolidine; 3,5,5,-Trimethyloxazolidine-2,4-dione; 3,5,5-TRIMETHYL-OXAZOLIDINE-2,4-DIONE; 3,5,5-Trimethyl-1,3-oxazolidine-2,4-dione; 3,5,5-Trimethyl-2,4-oxazolidinedione; 3,5,5-Trojmetylooksazolidyno-2,4-dion; 3,5,5-Trojmetylooksazolidyno-2,4-dion [Polish]
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External Link
 Compound Name Motixafortide Approved [19]
External Link
 Compound Name Uridine triacetate Approved [45]
Synonyms
PN401
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External Link
 Compound Name Bentiromide Approved [46]
Synonyms
Bentiromide sodium; 41748-47-4; N-Benzoyl-L-tyrosyl-4-aminobenzoic acid sodium salt; NCGC00164607-01; EINECS 255-530-7; DSSTox_CID_26476; DSSTox_RID_81647; DSSTox_GSID_46476; DTXSID6046476; CHEMBL3188891; Tox21_112229; AKOS024373587; ACM41748474; Sodium (S)-4-((2-(benzoylamino)-3-(4-hydroxyphenyl)-1-oxopropyl)amino)benzoate; CAS-41748-47-4; FT-0771579; ST51012404; N-Benzoyl-L-tyrosine p-amidobenzoic acid sodium salt; sodium (S)-4-(2-benzamido-3-(4-hydroxyphenyl)propanamido)benzoate; N-Benzoyl-L-tyrosine p-amidobenzoic acid so
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External Link
 Compound Name Olaparib Approved [19]
Synonyms
AZD 2281; AZD2281; AZD-2281; Acylpiperazine analogue, 47; KU-0059436; KU-59436; Olaparib, KU-0059436, AZD2281,KU0059436, AZD2281; 4-[(3-{[4-Cyclopropylcarbonyl)piperazin-4-yl]carbonyl}-4-fluorophenyl)methyl]phtalazin-1(2H)-one; 4-[3-(4-Cyclopropanecarbonyl-piperazine-1-carbonyl)-4-fluoro-benzyl]-2H-phthalazin-1-one
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External Link
 Compound Name Streptozocin Approved [47]
Synonyms
Estreptozocina; STREPTOZOTOCIN; STRZ; Streptozocine; Streptozocinium; Streptozocinum; Streptozosin; Zanosar; Alkylating agent; Binds to DNA; Streptozocinium [Latin]; Streptozocine [INN-French]; Streptozocinum [INN-Latin]; Zanosar (TN); Streptozocin (USAN/INN); Streptozocin, Zanosar, STZ,Streptozotocin;N-(Methylnitrosocarbamoyl)-alpha-D-glucosamine; N-D-Glucosyl-(2)-N'-nitrosomethylharnstoff; N-D-Glucosyl-(2)-N'-nitrosomethylurea; D-Glucose, 2-deoxy-2-(((methylnitrosoamino)carbonyl)amino)-(9CI); 1-methyl-1-nitroso-3-[(2S,3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]urea; 2-Deoxy-2-(((methylnitrosoamino)carbonyl)amino)-D-glucopyranose; 2-Deoxy-2-(3-methyl-3-nitrosoureido)-D-glucopyranose; 2-Deoxy-2[[(methylnitrosoamino)-carbonyl]amino]-D-glucopyranose; 2-deoxy-2-{[methyl(nitroso)carbamoyl]amino}-alpha-D-glucopyranose
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External Link
 Compound Name Plazomicin Phase 3 [48]
Synonyms
ACHN-490; UNII-LYO9XZ250J; 1154757-24-0; LYO9XZ250J; Plazomicin [USAN:INN]; Plazomicin (USAN); ZINC68150640; DB12615; D10151; D-Streptamine,
    Click to Show/Hide
External Link
 Compound Name Taxol Approved [19]
Synonyms
C47H51NO14; weekly paclitaxel; Micellar Paclitaxel; Paclitaxel [USAN:INN:BAN]; SCHEMBL15000506; Benzenepropanoic acid, beta-(benzoylamino)-alpha-hydroxy-, 6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca(3,4)benz(1,2-b)oxet-9-yl ester, (2aR-(2aalpha,4beta,4abeta,6beta,9alpha(alphaR*,betaS*),11alpha,12alpha,12aalpha,12balpha))-
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External Link
 Compound Name Ibrutinib Phase 3 [19]
Synonyms
PCI-32765; Ibrutinib (BTK inhibitor)
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External Link
 Compound Name Erlotinib Approved [49]
Synonyms
Erlotinin; Tarceva; Erlotinib Base; OSI 744; R 1415; CP 358,774; CP-358774; Erlotinib(Tarceva); Tarceva (TN); CP-358,774; Erlotinib, OS-774; N-(3-ethynylphenyl)[6,7-bis(2-methoxyethoxy)quinazolin-4-yl]amine; N-(3-Ethynylphenyl)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine; N-(3-Ethynylphenyl)-6,7-bis(2-methoxyethoxy)quinazolin-4-amine; [6,7-BIS(2-METHOXY-ETHOXY)QUINAZOLINE-4-YL]-(3-ETHYNYLPHENYL)AMINE; [6,7-Bis-(2-methoxy-ethoxy)-quinazolin-4-yl]-(3-ethynyl-phenyl)-amine; 4-[(3-Ethynylphenyl)amino]-6,7-bis(2-methoxyethoxy)quinazoline
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External Link
 Compound Name Ruxolitinib Approved [50]
Synonyms
Ruxolitinib (JAK inhibitor)
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External Link
 Compound Name Nivolumab Approved [19]
External Link
 Compound Name Coenzyme Q10 Phase 2 [19]
Synonyms
CoQ10; Coenzyme Q10 (oral formulation); CoQ10 platform technology, Ryan (Receptagen); Coenzyme Q10 (oral formulation), Receptagen
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External Link
 Compound Name Aglatimagene besadenovec Phase 1/2 [19]
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 Compound Name Zolbetuximab Phase 3 [51]
Synonyms
IMAB362
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External Link
 Compound Name AC-1204 Phase 3 [52]
Synonyms
isoindoline hydrochloride; 32372-82-0; 2,3-Dihydroisoindole hydrochloride; 2,3-dihydro-1H-isoindole hydrochloride; 2,3-Dihydro-1H-isoindole HCl; Isoindoline HCl salt; 1H-Isoindole, 2,3-dihydro-, hydrochloride; Isoindoline hydrochloride, 97%; Isoindolinehydrochloride; Isoindoline, HCl; ISOINDOLINE HCL; AC1Q38WR; dihydroisoindole hydrochloride; KSC491I3F; AMBZ0192; SCHEMBL4702076; CTK3J1432; DTXSID50487241; MolPort-003-986-749; NOVIRODZMIZUPA-UHFFFAOYSA-N; BH168; CS-D1516; ACT08858; ACN-S003258; KS-000001RA
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External Link
 Compound Name Radiosensitizer gene therapy Phase 3 [53]
Synonyms
Radiosensitizer gene therapy (prostate cancer)
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External Link
 Compound Name Glufosfomide Phase 3 [54]
External Link
 Compound Name Yttrium (90Y) clivatuzumab tetraxetan Phase 3 [55]
Synonyms
PAM4 mAb; Yttrium Y 90 clivatuzumab tetraxetan; Anti-MUC1 PAM4 monoclonal antibody; Clivatuzumab tetraxetan-[90Y]; HPAM4-Cide; IMMU-107; PAM-4; PAM4-Y-90; Yttrium-90-hPAM4; 90Y-clivatuzumab tetraxetan; 90Y-hPAM4
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External Link
 Compound Name Y-90 Clivatuzumab Phase 3 [56]
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 Compound Name Civacir Phase 3 [57]
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 Compound Name GV1001 Phase 3 [58]
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 Compound Name Masitinib Phase 3 [19]
Synonyms
790299-79-5; AB1010; Masatinib; Masitinib (AB1010); Masivet; AB-1010; AB 1010; UNII-M59NC4E26P; Masitinib [INN]; M59NC4E26P; 4-[(4-Methyl-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-thiazolyl]amino]phenyl]benzamide; CHEMBL1908391; CHEBI:63450; Masitinib (INN); N-(4-Methyl-3-((4-(pyridin-3-yl)thiazol-2-yl)amino)phenyl)-4-((4-methylpiperazin-1-yl)methyl)benzamide; Q-201339; C28H30N6OS; N-(4-methyl-3-(4-(pyridin-3-yl)thiazol-2-ylamino)phenyl)-4-((4-methylpiperazin-1-yl)methyl)benzamide
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External Link
 Compound Name Glufosfamide Phase 3 [19]
Synonyms
Glucosylifostamide mustard; D 19575; D-19575; Glc-IPM; Glucosyl-ifosfamide mustard; Beta-D-Glucopyranose 1-(N,N'-bis(2-chloroethyl)phosphorodiamidate; Beta-D-Glucopyranose, 1-(N,N'-bis(2-chloroethyl)phosphorodiamidate); (2S,3R,4S,5S,6R)-2-bis(2-chloroethylamino)phosphoryloxy-6-(hydroxymethyl)oxane-3,4,5-triol
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External Link
 Compound Name Sapacitabine Phase 3 [19]
Synonyms
CYC682
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External Link
 Compound Name Pelareorep Phase 2 [16]
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 Compound Name Pamrevlumab Phase 3 [59]
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 Compound Name GRASPA Phase 1 [60]
Synonyms
L-asparaginase (erythrocyte-encapsulated, acute lymphoblastic leukemia/solid tumor), ERYtech
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External Link
 Compound Name Pancreas algenpantucel-L Phase 3 [61]
Synonyms
HyperAcute (TN)
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External Link
 Compound Name CPI-613 Phase 3 [62]
Synonyms
95809-78-2; 6,8-bis(benzylthio)octanoic acid; CPI 613; MLS006010202; SCHEMBL1062218; 6,8-Bis(benzylsulfanyl)octanoic acid; Octanoic acid, 6,8-bis((phenylmethyl)thio)-; Octanoic acid, 6,8-bis[(phenylMethyl)thio]-; 6,8-Bis[(phenylmethyl)thio]octanoic acid; CPI613; CHEMBL3186849; QCR-193; AOB1058; MolPort-023-219-128; HMS3656L06; C22H28O2S2; BCP04663; EX-A2043; s2776; AKOS025142095; BCP9000552; DB12109; RL06062; CS-0961; NCGC00344764-01; SMR004701300; AS-16613; BC261916; AK174899; HY-15453; BCP0726000030; KB-293127; AB0035874
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External Link
 Compound Name Zarnestra Phase 3 [63]
Synonyms
JAN; Tipifarnib; Tipifarnib [USAN]; R 115777; R115777; R-11577; R-115777; Tipifarnib (USAN/INN); Zarnestra, IND 58359, R115777, Tipifarnib; (R)-6-(Amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl)-4-(3-chlorophenyl)-1-methyl-2(1H)-quinolinone; (R)-R115777; 2 (1H))-Quinolinone,6-(amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl)-4-(3-chlorophenyl)-1-methyl-, 2(1H)-quinolinone; 6-[(R)-amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl]-4-(3-chlorophenyl)-1-methylquinolin-2(1H)-one; 6-[(R)-amino-(4-chlorophenyl)-(3-methylimidazol-4-yl)methyl]-4-(3-chlorophenyl)-1-methylquinolin-2-one; 6-[(S)-AMINO(4-CHLOROPHENYL)(1-METHYL-1H-IMIDAZOL-5-YL)METHYL]-4-(3-CHLOROPHENYL)-1-METHYLQUINOLIN-2(1H)-ONE
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 Compound Name MM-398 Phase 3 [64]
External Link
 Compound Name Marimastat Phase 3 [65]
Synonyms
Marimastat [USAN]; BB 2516; BB-2516; Marimastat (USAN/INN); (2R,3S)-N-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-N',3-dihydroxy-2-(2-methylpropyl)butanediamide; (2S,3R)-3-(((1S)-2,2-Dimethyl-1-(methylcarbamoxy)propyl)carboyl)-2-hydroxy-5-methylhexanohydroxamic acid; (2S,3R)-3-(((1S)-2,2-Dimethyl-1-(methylcarbamoyl)propyl)carbamoyl)-2-hydroxy-5-methylhexanohydroxamic acid; (2S,3R)-N(4)-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-N(1),2-dihydroxy-3-(2-methylpropyl)butanediamide
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 Compound Name AM0010 Phase 3 [66]
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 Compound Name ANX-510 Phase 3 [67]
External Link
 Compound Name Napabucasin Phase 3 [19]
Synonyms
83280-65-3; UNII-Z1HHM49K7O; 2-acetylnaphtho[2,3-b]furan-4,9-dione; Z1HHM49K7O; 2-Acetylnaphtho(2,3-b)furan-4,9-dione; 2-Acetyl-4H,9H-naphtho[2,3-b]furan-4,9-dione; Napabucasin [USAN:INN]; Napabucasin (BBI608); 2-Acetylfuranonaphthoquinone; CHEMBL64130; Napabucasin (JAN/USAN/INN); SCHEMBL1883845; Napabucasin - BBI 608/ FNQ; 2-Acetylfuro-1,4-naphthoquinone; DPHUWDIXHNQOSY-UHFFFAOYSA-N; MolPort-039-101-321; EX-A1314; ZINC13306865; s7977; AKOS027470201; DB12155; CS-1747; ACN-053294; HY-13919
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External Link
 Compound Name Algenpantucel-L Phase 3 [68]
Synonyms
HyperAcute pancreas (TN)
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External Link
 Compound Name OT-101 Phase 2/3 [19]
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 Compound Name RP101 Phase 2/3 [69]
Synonyms
SCHEMBL15589316; CHEMBL3703295; BDBM149820; US8975415,
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External Link
 Compound Name NLG8189 Phase 2/3 [19]
Synonyms
1-Methyl-D-tryptophan; Indoximod; 110117-83-4; D-Tryptophan, 1-methyl-; D-1MT; Indoximod (NLG-8189); D-1-methyltryptophan; UNII-TX5CYN1KMZ; D-(+)-1-Methyltryptophan; TX5CYN1KMZ; (R)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic acid; (2R)-2-amino-3-(1-methylindol-3-yl)propanoic acid; NSC-721782; (2R)-2-amino-3-(1-methyl-3-indolyl)propanoic acid; 1-MT; (2R)-2-azanyl-3-(1-methylindol-3-yl)propanoic acid; (2R)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic acid; D-l-Methyltryptophan; Indoximod [USAN:INN]; NLG-8189; NLG 8189
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External Link
 Compound Name LY2157299 Phase 2/3 [19]
Synonyms
Galunisertib; 700874-72-2; LY 2157299; LY-2157299; UNII-3OKH1W5LZE; 4-(2-(6-methylpyridin-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)quinoline-6-carboxamide; 3OKH1W5LZE; Galunisertib (LY2157299); AK-79916; 4-[5,6-Dihydro-2-(6-methyl-2-pyridinyl)-4H-pyrrolo[1,2-b]pyrazol-3-yl]-6-quinolinecarboxamide; 4-(2-(6-Methylpyridin-2-yl)-5,6-dihydro-4H-pyrrolo-[1,2-b]pyrazol-3-yl)quinoline-6-carboxamide; 4-[2-(6-methylpyridin-2-yl)-4H,5H,6H-pyrrolo[1,2-b]pyrazol-3-yl]quinoline-6-carboxamide
    Click to Show/Hide
External Link
 Compound Name SM-88 Phase 2/3 [70]
External Link
 Compound Name SiG12D-LODER Phase 2 [19]
External Link
 Compound Name BNT141 Phase 2 [71]
External Link
 Compound Name BNT321 Phase 2 [72]
Synonyms
MVT-5873
    Click to Show/Hide
External Link
 Compound Name BPM 31510 Phase 2 [73]
External Link
 Compound Name GC4711 Phase 2 [74]
Synonyms
UNII-FW5T90VM32; FW5T90VM32; GC-4419 dipropionate; Bis-propionato(gc4419); Avasopasem manganese dipropionate; GC-4711; 2248030-85-3; Manganese(II), bis-propionato((4aS,13aS,17aS,21aS)-1,2,3,4,4a,5,6,12,13,13a,14,15,16,17,17a,18,19,20,21,21a-eicosahydro-11,7-nitrilo-7H-dibenzo(b,H)(1,4,7,10)tetraaza-cycloheptadecine-kn5,kn13,kn18,kn21,kn22)-,
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External Link
 Compound Name CYTO-401 Phase 2 [75]
External Link
 Compound Name Zenocutuzumab Phase 2 [76]
External Link
 Compound Name Cabiralizumab Phase 2 [19]
External Link
 Compound Name VS-6063 Phase 2 [19]
Synonyms
Defactinib hydrochloride; 1073160-26-5; Defactinib (hydrochloride); UNII-L2S469LM49; Defactinib hydrochloride [USAN]; L2S469LM49; Defactinib hydrochloride (USAN); Benzamide, N-methyl-4-[[4-[[[3-[methyl(methylsulfonyl)amino]-2-pyrazinyl]methyl]amino]-5-(trifluoromethyl)-2-pyrimidinyl]amino]-, hydrochloride; Defactinib HCl; Benzamide, N-methyl-4-((4-(((3-(methyl(methylsulfonyl)amino)-2-pyrazinyl)methyl)amino)-5-(trifluoromethyl)-2-pyrimidinyl)amino)-, hydrochloride (1:1); Benzamide, N-methyl-4-[[4-[[[3-[methyl(methylsu
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External Link
 Compound Name MENK Phase 2 [54]
External Link
 Compound Name CO-101 Phase 2 [77]
Synonyms
methyl 2-(dimethylcarbamoyl)benzoate; 26593-43-1; Phthalamic acid, N,N-dimethyl-, methyl ester; CO 101; BRN 2504723; N,N-Dimethylphthalamic acid methyl ester; N,N-Dimethylphthalamic acid, methyl ester; AC1Q5ZAU; 2-09-00-00601 (Beilstein Handbook Reference); AC1L4V19; CTK4F8203; DTXSID50181156; 2-methoxycarbonyl-N,N-dimethylbenzamide; LS-109082; Benzoic acid,2-[(dimethylamino)carbonyl]-, methyl ester
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External Link
 Compound Name MENK Phase 2 [19]
Synonyms
IRT-101
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External Link
 Compound Name TL-118 Phase 2 [78]
Synonyms
Hamsa 1; TL-111; TL-112; Combination anti-angiogenic therapy (oral suspension, solid tumors), Tiltan Pharma
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External Link
 Compound Name Antroquinonol Phase 2 [19]
Synonyms
Hocena; Fungal extract (cancer), Golden Biotechnology
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External Link
 Compound Name NPC-1C Phase 2 [19]
Synonyms
Ensituximab
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External Link
 Compound Name Necuparanib Phase 2 [79]
External Link
 Compound Name CCX872 Phase 2 [19]
External Link
 Compound Name GC4419 Phase 1/2 [19]
Synonyms
Avasopasem manganese; UNII-EY1WA413UL; EY1WA413UL; Avasopasem manganese [USAN]; SC-72325A; M-40419; 435327-40-5; Manganese, dichloro((4aS,13aS,17aS,21aS)-1,2,3,4,4a,5,6,12,13,13a,14,15,16,17,17a,18,19,20,21,21a-eicosahydro-7,11-nitrilo-7H-dibenzo(b,H)-5,13,18,21-tetraazacycloheptadecine-kappaN5,kappaN13,kappaN18,kappaN21,kappaN22)-, (pb-7-11-2344'3')-
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External Link
 Compound Name Istiratumab Phase 2 [16]
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 Compound Name GI-4000 Phase 2 [80]
External Link
 Compound Name OCV-101 Phase 2 [81]
Synonyms
OTS-11101
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External Link
 Compound Name RX-3117 Phase 2 [19]
Synonyms
Antimetabolite (cancer), Rexahn; Antimetabolite (cancer), Rexahn/ Teva
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External Link
 Compound Name Ensitiximab Phase 2 [54]
External Link
 Compound Name GI-4000 + gemcitabine Phase 2 [82]
External Link
 Compound Name BC-819 Phase 2 [83]
External Link
 Compound Name IRT-102 Phase 2 [84]
External Link
 Compound Name LE-DT Phase 2 [85]
Synonyms
Liposomal docetaxel
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External Link
 Compound Name TH-302 Phase 2 [19]
Synonyms
evofosfamide; 918633-87-1; TH 302; TH302; UNII-8A9RZ3HN8W; Evofosfamide(TH 302); n,n'-bis(2-bromoethyl)phosphorodiamidic acid (1-methyl-2-nitro-1h-imidazol-5-yl)methyl ester; 8A9RZ3HN8W; compound 3b; Evofosfamide;HAP-302; Phosphorodiamidic acid, N,N'-bis(2-bromoethyl)-, (1-methyl-2-nitro-1H-imidazol-5-yl)methyl ester; 2-bromo-N-[(2-bromoethylamino)-[(3-methyl-2-nitroimidazol-4-yl)methoxy]phosphoryl]ethanamine; Evofosfamide [USAN:INN]; Evofosfamide(TH-302); C9H16Br2N5O4P; CHEMBL260046; SCHEMBL2357174
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External Link
 Compound Name Demcizumab Phase 2 [54]
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 Compound Name Anti-PSCA mab Phase 2 [86]
External Link
 Compound Name ALT-803 Phase 2 [16]
Synonyms
IL-15 agonist/ IL-15R alpha-Fc fusion complex (cancer), Altor BioScience
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External Link
 Compound Name ARQ 761 Phase 2 [19]
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 Compound Name Reolysinpelareorep Phase 2 [19]
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 Compound Name PBI-05204 Phase 2 [19]
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 Compound Name PCI-27483 Phase 2 [87]
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 Compound Name RX-0201 Phase 2 [54]
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 Compound Name CP-613 Phase 2 [88]
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 Compound Name CART 19 Preclinical [89]
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 Compound Name VT-122 Phase 1 [54]
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 Compound Name PEGPH20 Phase 2 [90]
External Link
 Compound Name Ficlatuzumab Phase 2 [19]
Synonyms
AV-299
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External Link
 Compound Name Tigatuzumab Phase 2 [91]
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 Compound Name CRS-207 Phase 2 [92]
External Link
 Compound Name CAP1-6D Phase 2 [93]
Synonyms
Modified CEA peptide (pancreatic cancer), University of Chicago
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External Link
 Compound Name SGT-53 Phase 2 [19]
Synonyms
P53 gene stimulator (solid tumor), Synergene Therapeutics
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External Link
 Compound Name Tarextumab Phase 2 [94]
External Link
 Compound Name BVD-523 Phase 2 [19]
External Link
 Compound Name Ocaperidone Phase 2 [16]
Synonyms
Ocaperidona; 129029-23-8; UNII-26HUS7139V; 3-(2-(4-(6-Fluoro-1,2-benzisoxazol-3-yl)piperidino)ethyl)-2,9-dimethyl-4H-pyrido(1,2-a)pyrimidin-4-one; 26HUS7139V; Ocaperidonum; Ocaperidonum [INN-Latin]; Ocaperidona [INN-Spanish]; 4H-Pyrido[1,2-a]pyrimidin-4-one,3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-2,9-dimethyl-; Ocaperidone (USAN); Ocaperidone [USAN:INN:BAN]; 3-[2-[4-(6-Fluorobenzo[d]isoxazol-3-yl)piperidin-1-yl]ethyl]-2,9-dimethyl-4H-pyrido[1,2-a]pyrimidin-4-one; 3-[2-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]ethyl]-2,9-dimethylpyrido[1,2-a]pyrimidin-4-one; 8-[2-[4-(6-fluorobenzo[d]isoxazol-3-yl)-1-piperidyl]ethyl]-2,9-dimethyl-6,10-diazabicyclo[440]deca-2,4,8,10-tetraen-7-one; FG-3019
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External Link
 Compound Name Encapsulated live cells converting ifosfamide Phase 2 [19]
External Link
 Compound Name LY2603618 Phase 2 [95]
Synonyms
Rabusertib; 911222-45-2; LY 2603618; LY-2603618; UNII-3S9L1NU6U7; 3S9L1NU6U7; IC-83; ly2603618 IC-83; (S)-1-(5-bromo-4-methyl-2-(morpholin-2-ylmethoxy)phenyl)-3-(5-methylpyrazin-2-yl)urea; n-(5-bromo-4-methyl-2-((2s)-2-morpholinylmethoxy)phenyl)-n'-(5-methyl-2-pyrazinyl)urea; LY2603618 (IC-83); Rabusertib [USAN:INN]; 3-(5-Bromo-4-methyl-2-[(2s)-morpholin-2-ylmethoxy]phenyl)-1-(5-methylpyrazin-2-yl)urea; N-[5-Bromo-4-methyl-2-[(2S)-2-morpholinylmethoxy)phenyl]-N'-(5-methyl-2-pyrazinyl)urea
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External Link
 Compound Name Salirasib Discontinued in Phase 1/2 [96]
Synonyms
162520-00-5; Farnesylthiosalicylic acid; S-Farnesylthiosalicylic acid; UNII-MZH0OM550M; MZH0OM550M; CHEMBL23293; AK186909; Farnesyl Thiosalicylic Acid; 2-[[(2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-yl]thio]benzoic Acid; 2-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]sulfanylbenzoic acid; 2-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienylthio)benzoic acid; 2-(((2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrienyl)sulfanyl)benzoic acid; Benzoic acid, 2-(((2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrienyl)thio)-; FTS; Farnesylthiosalicyclic acid; FTS, Thyreos; Ras antagonists, Thyreos; S-trans; Th-101; Trans-farnesylthiosalicylicacid; FTS (oral, cancer), Concordia; Farnesylthiosalicyclic acid (oral, cancer), Concordia; Ras-inhibitors (cancer), Concordia; FTS (oral, cancer), Concordia/Ono; KD032
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External Link
 Compound Name MM-141 Phase 2 [19]
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 Compound Name GB1275 Phase 1/2 [97]
External Link
 Compound Name ABTL0812 Phase 1/2 [98]
Synonyms
(9Z,12Z)-2-Hydroxy-9,12-octadecadienoic acid; (9Z,12Z)-2-hydroxyoctadeca-9,12-dienoic acid; (9Z,12Z)-2-hydroxyoctadecadienoic acid; (alpha)-Hydroxylinoleic acid; .ALPHA.-HYDROXYLINOLEIC ACID; 0DE74TJ7EZ; 2-hydroxy-9Z,12Z-Octadecadienoic acid; 2-hydroxylinoleic acid; 57818-44-7; 9,12-Octadecadienoic acid, 2-hydroxy-, (9Z,12Z)-; 9,12-Octadecadienoic acid, 2-hydroxy-, (Z,Z)-; ABTL0812; ABTL-0812; a-Hydroxylinoleic acid; AKOS040740632; alpha-Hydroxylinoleic acid; CHEBI:136927; CS-7178; DTXSID301258077; hydroxylinoleic acid; HY-U00141; LMFA02000290; MS-24253; s9611; SCHEMBL320069; UNII-0DE74TJ7EZ
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 Compound Name GP-2250 Phase 1/2 [99]
External Link
 Compound Name Delolimogene mupadenorepvec Phase 1/2 [100]
Synonyms
LOAd703
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External Link
 Compound Name GSK3145095 Phase 1/2 [101]
Synonyms
1622849-43-7; CHEMBL4452233; (S)-5-benzyl-N-(7,9-difluoro-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-3-yl)-4H-1,2,4-triazole-3-carboxamide; UNII-B4D3WPS7JY; B4D3WPS7JY; SCHEMBL17312826; BCP31015; EX-A3069; BDBM50502339; s8845; GSK-3145095; HY-111946; CS-0094287; GSK 3145095; FC1=CC2=C(NC(=O)[C@H](CC2)NC(=O)C2=NN=C(CC3=CC=CC=C3)N2)C(F)=C1; (S)-5-Benzyl-N-(7,9-difluoro-2-oxo-2,3,4,5-tetrahydro-1hbenzo(b)azepin-3-yl)-1H-1,2,4-triazole-3-carboxamide (7,7-dimethyl-2- oxobicyclo(2.2.1)heptan-1-yl)
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 Compound Name Encapsulated cell therapy Phase 1/2 [102]
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 Compound Name ETBX-011 cancer vaccine Phase 1/2 [80]
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 Compound Name BPX-601 Phase 1/2 [103]
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 Compound Name NANT Phase 1/2 [19]
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 Compound Name BrevaRex Phase 1/2 [104]
Synonyms
BrevaRex MAb; monoclonal antibody
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External Link
 Compound Name DCVax-Pancreas Phase 1/2 [105]
Synonyms
Dendritic cell-based immunotherapy (pancreatic cancer), Northwest Biotherapeutics
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External Link
 Compound Name PEGylated hyaluronidase (human recombinant) Phase 1/2 [106]
Synonyms
PEGylated hyaluronidase; PEGylated hyaluronidase (human recombinant) (intravenous, stroke/cancer), Halozyme
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External Link
 Compound Name CAR-T cells targeting mesothelin Phase 1/2 [107]
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 Compound Name MALP-2S Phase 1/2 [108]
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 Compound Name Anti-Mesothelin CAR-T cells Phase 1/2 [109]
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 Compound Name Anti-MUC1 CAR T Cells Phase 1/2 [110]
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 Compound Name Anti-HER2 CAR-T Phase 1/2 [111]
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 Compound Name CAR-T Cells targeting EpCAM Phase 1/2 [112]
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 Compound Name Anti-MUC1 AR20.5 Phase 1/2 [16]
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 Compound Name AR20.5 Phase 1/2 [19]
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 Compound Name G0-203-2c Phase 1/2 [113]
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 Compound Name LOAd703 Phase 1/2 [19]
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 Compound Name Anti-mesothelin CAR transduced PBL Phase 1/2 [114]
External Link
 Compound Name M9241 Phase 1 [115]
Synonyms
NHS-IL12
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External Link
 Compound Name NBF-006 Phase 1 [116]
External Link
 Compound Name AB680 Phase 1 [117]
Synonyms
AB-680; UNII-J6K8WSV73A; J6K8WSV73A; CHEMBL4471306; 2105904-82-1; (((((2R,3S,4R,5R)-5-(6-chloro-4-(((S)-1-(2-fluorophenyl)ethyl)amino)-1H-pyrazolo[3,4-b]pyridin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(hydroxy)phosphoryl)methyl)phosphonic acid; [[(2~{R},3~{S},4~{R},5~{R})-5-[6-chloranyl-4-[[(1~{S})-1-(2-fluorophenyl)ethyl]amino]pyrazolo[3,4-b]pyridin-1-yl]-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl]methylphosphonic acid; SCHEMBL19100484; GTPL10707; BDBM50527134; HY-125286; CS-0090231; [[(2R,3S,4R,5R)-5-[6-chloro-4-[[(1S)-1-(2-fluorophenyl)ethyl]amino]pyrazolo[3,4-b]pyridin-1-yl]-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]methylphosphonic acid; QDH
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External Link
 Compound Name STAT400 Phase 1 [118]
External Link
 Compound Name CEND-1 Phase 1 [119]
Synonyms
iRGD; UNII-Z8MXU5GH4Q; Z8MXU5GH4Q; iRGD-peptide; 1392278-76-0; Internalized-arginylglycylaspartic acid cyclic peptide; Q48988348; L-Cysteine, L-cysteinyl-L-arginylglycyl-L-alpha-aspartyl-L-lysylglycyl-L-prolyl-L-alpha-aspartyl-, cyclic (1->9)-disulfide
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 Compound Name CAR-T Cells targeting EGFRvIII Phase 1 [120]
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 Compound Name HuCART-meso cells Phase 1 [121]
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 Compound Name OCV-105 Phase 1 [122]
Synonyms
Cancer vaccine (pancreas), Otsuka/OncoTherapy
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External Link
 Compound Name SBP-101 Phase 1 [54]
Synonyms
diethyl dihydroxyhomospermine
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External Link
 Compound Name RG7882 Phase 1 [16]
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 Compound Name CART-meso-19 T cells Phase 1 [123]
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 Compound Name MOv19-BBz CAR T cells Phase 1 [124]
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 Compound Name Anti-MUC1 AR20.5 mab Phase 1 [125]
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 Compound Name Anti-CEA-CAR T Phase 1 [126]
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 Compound Name MVT-5873 Phase 1 [16]
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 Compound Name CART-meso cells Phase 1 [127]
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 Compound Name CAR-20/19-T Cells Phase 1 [128]
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 Compound Name CARTmeso/19 Phase 1 [129]
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 Compound Name CAR-T Cells targeting Mesothelin Phase 1 [120]
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 Compound Name CAR-T Cells targeting CEA Phase 1 [120]
External Link
 Compound Name HLA-A*2402-restricted KIF20A and VEGFR-1 epitope peptide vaccine Phase 1 [130]
Synonyms
HLA-A*2402-restricted KIF20A and VEGFR-1 epitope peptide vaccine (pancreatic cancer, subcutaneous)
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External Link
 Compound Name Anti-hCD70 CAR transduced PBL Phase 1 [131]
External Link
 Compound Name MORAb-066 Phase 1 [132]
Synonyms
Anti-tissue factor monoclonal antibody (pancreatic tumor), Morphotek
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External Link
 Compound Name Anti-MUC1 mab Phase 1 [133]
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 Compound Name Anti-meso-CAR vector transduced T cells Phase 1 [134]
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 Compound Name CRS-207 + GVAX Phase 2 [54]
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 Compound Name Autologous T cells transfected with chimeric anti-mesothelin immunoreceptor SS1 Phase 1 [135]
External Link
 Compound Name Meso-CART Phase 1 [136]
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 Compound Name ASG-5ME Phase 1 [137]
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 Compound Name Anti-CD133-CAR vector-transduced T cells Phase 1 [138]
External Link
 Compound Name IRX4204 Phase 1 [19]
Synonyms
220619-73-8; CHEMBL75133; UNII-877M97Z38Y; VTP-194204; 877M97Z38Y; KB-145960; SCHEMBL3437269; MolPort-042-665-869; ZINC1550770; IRX-4204; 3-Methyl-5-[2-methyl-2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-cyclopropyl]-penta-2,4-dienoic acid; BDBM50101445; DB11806; VTP 194204; (+)-VTP-194204; AGN 4204; (2E,4E)-3-Methyl-5-[(1S,2S)-2-methyl-2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-cyclopropyl]-penta-2,4-dienoic acid
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 Compound Name AbGn-107 Phase 1 [19]
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 Compound Name LMB-100 Phase 1/2 [19]
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 Compound Name PLX7486 Phase 1 [139]
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 Compound Name CAR-T Cells targeting HER2 Phase 1 [120]
External Link
 Compound Name CAR-T Cells targeting MUCI Phase 1 [120]
External Link
 Compound Name SEL-403 Phase 1 [19]
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 Compound Name CAR-T Cells targeting PSCA Phase 1 [120]
External Link
 Compound Name Anti-CEA CAR-T cells Phase 1 [140]
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 Compound Name MVT-1075 Phase 1 [19]
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 Compound Name CAR-CLD18 T cell Clinical trial [141]
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 Compound Name CART-meso cells Clinical trial [142]
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 Compound Name PMID28460551-Compound-1 Patented [143]
External Link
 Compound Name Tanomastat Discontinued in Phase 3 [144]
Synonyms
Tanomastat (USAN/INN); (2S)-4-[4-(4-chlorophenyl)phenyl]-4-oxo-2-(phenylsulfanylmethyl)butanoic acid
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External Link
 Compound Name Larotaxel Discontinued in Phase 3 [145]
Synonyms
Benzenepropanoic acid; PNU 100940; XRP 9881; XRP9881
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External Link
 Compound Name Apricoxib Discontinued in Phase 2 [146]
Synonyms
TG01
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External Link
 Compound Name Lintitript Discontinued in Phase 2 [147]
Synonyms
SR 27897; SR 27897B; SR27897; SR-27897; SR-27897B; 1-((2-(4-(2-Chlorophenyl)thiazol-2-yl)aminocarbonyl)indolyl)acetic acid; 2-((4-(o-Chlorophenyl)-2-thiazolyl)carbamoyl)indole-1-acetic acid; 2-[2-[[4-(2-chlorophenyl)-1,3-thiazol-2-yl]carbamoyl]indol-1-yl]acetic acid
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External Link
 Compound Name Merbarone Discontinued in Phase 2 [148]
Synonyms
NSC-336628
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External Link
 Compound Name LY293111 Discontinued in Phase 2 [149]
Synonyms
Etalocib; 161172-51-6; UNII-THY6RIW44R; LY 293111; THY6RIW44R; CHEMBL329123; LY-193111; 2-[3-[3-[2-ethyl-4-(4-fluorophenyl)-5-hydroxyphenoxy]propoxy]-2-propylphenoxy]benzoic acid; VML295; Etalocib [USAN:INN]; Etalocib (USAN); GTPL2948; SCHEMBL1649516; CTK8E7596; C33H33FO6; VML 295; DTXSID70167073; YFIZRWPXUYFCSN-UHFFFAOYSA-N; MolPort-009-019-411; ZINC3930629; AC1L4328; PDSP2_001221; BDBM50029450; PDSP1_001237; 1758AH; DB12850; RT-013626; D04074; L001468; J-009797; Benzoic acid, 2-(3-(3-((5-ethyl-4'-fluoro-2-hydroxy(1,1'-bipheny
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External Link
 Compound Name HMN-214 Discontinued in Phase 1 [150]
Synonyms
N-(4-methoxyphenyl)sulfonyl-N-[2-[(E)-2-(1-oxidopyridin-4-yl)ethenyl]phenyl]acetamide; (E)-4-(2-(2-(N-Acetyl-N-((p-methoxyphenyl)sulfonyl)amino)phenyl)ethenyl)pyridine 1-oxide
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External Link
 Compound Name RG7600 Discontinued in Phase 1 [151]
External Link
 Compound Name IC261 Preclinical [152]
Synonyms
IC-261; IC 261
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External Link
 Compound Name ANAVEX 1007 Preclinical [153]
External Link
 Compound Name IPH-4201 Terminated [154]
Synonyms
MAb-16D10; MAb-J28; FAPP-targeting mAb (pancreatic cancer), Innate Pharma; FAPP-targeting mAb (pancreatic cancer), Universite de la Mediterranee/ INSERM; Feto-acinar pancreatic protein-targeting monoclonal antibodies (pancreatic cancer), Innate Pharma; Feto-acinar pancreatic protein-targeting monoclonal antibodies (pancreatic cancer), Universite de la Mediterranee/ INSERM
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 Compound Name MesoTarg Investigative [155]
External Link
 Compound Name PAT-PM-1 Investigative [155]
Synonyms
PM-1; Human monoclonal antibody (pancreatic cancer), Patrys; Human MAb (pancreas cancer), OncoMab/ Acceptys; Human monoclonal antibody (pancreatic cancer), OncoMab/ Acceptys; PM-1 antibody, OncoMab/ Acceptys
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 Compound Name OP-04 Investigative [155]
Synonyms
OP-04 program (prodrug, pancreatic cancer); OP-04 program (prodrug, pancreatic cancer), Onco-Pharmakon
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External Link
 Compound Name VLI-27 Investigative [156]
Synonyms
AKT inhibitor (pancreatic cancer), NovaLead Pharma
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External Link
 Compound Name GS-326 Investigative [155]
Synonyms
GS-326C
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External Link
 Compound Name PX-12 Phase 2 [157]
External Link
 Compound Name Prodigiosin Investigative [155]
External Link
 Compound Name Pbi-shPDX-1 LP Investigative [155]
External Link
 Compound Name Gastrin 17C diphtheria toxoid conjugate Investigative [155]
Synonyms
Gastrin 17C diphtheria toxoid conjugate (pancreatic cancer)
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External Link
 Compound Name HS-P1 Investigative [155]
Synonyms
HS-310; Endoplasmin modulator (pancreas tumor, HeatShock/fusion protein/antigen), Heat Biologics; Gp-96-Ig + unspecified tumor antigen secreting live cell vaccine (pancreas tumor, HeatShock), Heat Biologics
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References
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Ref 151 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800035599)
Ref 152 Circadian rhythm as a therapeutic target. Nat Rev Drug Discov. 2021 Apr;20(4):287-307.
Ref 153 2011 Pipeline of Anavex.
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Ref 155 The ChEMBL database in 2017. Nucleic Acids Res. 2017 Jan 4;45(D1):D945-D954.
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Ref 157 A Randomized Phase II Study of PX-12, an Inhibitor of Thioredoxin in Patients With Advanced Cancer of the Pancreas Following Progression After a Gemcitabine-Containing Combination. Cancer Chemother Pharmacol. 2011 Mar;67(3):503-9.