Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
Crosstalk ID
M6ACROT02130
[1], [2]
DNA methylation DNMT3A METTL3 Direct Inhibition m6A modification Linc00662 Linc00662 METTL3 Methylation : m6A sites
m6A Modification:
m6A Regulator Methyltransferase-like 3 (METTL3) WRITER
m6A Target long intergenic non-protein coding RNA 662 (LINC00662)
Epigenetic Regulation that have Cross-talk with This m6A Modification:
Epigenetic Regulation Type DNA methylation (DNAMeth)
Epigenetic Regulator Cysteine methyltransferase DNMT3A (DNMT3A) WRITER View Details
Regulated Target Methyltransferase-like protein 3 (METTL3) View Details
Crosstalk Relationship DNA methylation  →  m6A Inhibition
Crosstalk Mechanism DNA methylation directly impacts m6A modification through modulating the expression level of m6A regulator
Crosstalk Summary Quantitative chromatin immunoprecipitation (ChIP) assays showed that CSC substantially reduced the bindings of DNA methyltransferase 1 (DNMT1) and DNMT3A to the METTL3 promoter. METTL3 was upregulated in PC tissues and cells and was associated with malignant tumor progression and poor progression-free survival in PC.Four m6A motifs were identified in Long intergenic non-protein coding RNA 662 (LINC00662), which maintained the stability of Linc00662 in an IGF2BP3-coupled manner and were closely associated with the pro-tumor properties of Linc00662 in vitro and in vivo.
Responsed Disease Pancreatic cancer ICD-11: 2C10
Pathway Response PI3K-Akt signaling pathway hsa04151
Cell Process Cell proliferation
In-vitro Model
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
BxPC-3 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0186
MIA PaCa-2 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0428
COLO 357 Pancreatic adenosquamous carcinoma Homo sapiens CVCL_0221
CFPAC-1 Cystic fibrosis Homo sapiens CVCL_1119
Human Pancreatic Nestin-Expressing cells (Human Pancreatic Nestin-Expressing cells)
In-vivo Model Female BALB/c nude mice, aged 4-5 weeks, purchased from the Beijing Vital River Laboratory Animal Technology, were allowed to acclimate to local conditions for 1 week and maintained under a 12-h dark/12-h light cycle with food and water provided ad libitum. Mice (five in each group) were injected subcutaneously with 0.1 ml of cell suspension containing 2 × 106 cells in the back flank. When a tumor was palpable, it was measured every other day and the volume was calculated according to the formula volume = length × width2 × 0.5.
Full List of Potential Compound(s) Related to This m6A-centered Crosstalk
Cysteine methyltransferase DNMT3A (DNMT3A) 8 Compound(s) Regulating the Target Click to Show/Hide the Full List
 Compound Name PMID27376512-Compound-Figure3CN Patented [3]
MOA Inhibitor
Activity EC50 = 1100 nM
External Link
 Compound Name PMID27376512-Compound-Figure3CG Patented [3]
MOA Inhibitor
Activity EC50 = 2400 nM
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 Compound Name PMID27376512-Compound-Figure3CM Patented [3]
MOA Inhibitor
Activity EC50 = 1100 nM
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 Compound Name PMID27376512-Compound-Figure2aExample1 Patented [3]
MOA Inhibitor
Activity IC50 = 3000 nM
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 Compound Name PMID27376512-Compound-MTC-424 Patented [3]
MOA Inhibitor
Activity IC50 = 1940 nM
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 Compound Name PMID27376512-Compound-MTC-427 Patented [3]
MOA Inhibitor
Activity IC50 = 295 nM
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 Compound Name PMID27376512-Compound-MTC-422 Patented [3]
MOA Inhibitor
Activity IC50 = 1430 nM
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 Compound Name PMID27376512-Compound-MTC-423 Patented [3]
MOA Inhibitor
Activity IC50 = 363 nM
External Link
2C10: Pancreatic cancer 182 Compound(s) Regulating the Disease Click to Show/Hide the Full List
 Compound Name Atezolizumab Approved [4]
External Link
 Compound Name Trimethadione Approved [5]
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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 Compound Name Motixafortide Approved [4]
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 Compound Name Uridine triacetate Approved [6]
Synonyms
PN401
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 Compound Name Bentiromide Approved [7]
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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 Compound Name Olaparib Approved [4]
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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 Compound Name Streptozocin Approved [8]
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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 Compound Name Plazomicin Phase 3 [9]
Synonyms
ACHN-490; UNII-LYO9XZ250J; 1154757-24-0; LYO9XZ250J; Plazomicin [USAN:INN]; Plazomicin (USAN); ZINC68150640; DB12615; D10151; D-Streptamine,
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 Compound Name Taxol Approved [4]
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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 Compound Name Ibrutinib Phase 3 [4]
Synonyms
PCI-32765; Ibrutinib (BTK inhibitor)
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 Compound Name Erlotinib Approved [10]
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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 Compound Name Ruxolitinib Approved [11]
Synonyms
Ruxolitinib (JAK inhibitor)
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 Compound Name Nivolumab Approved [4]
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 Compound Name Coenzyme Q10 Phase 2 [4]
Synonyms
CoQ10; Coenzyme Q10 (oral formulation); CoQ10 platform technology, Ryan (Receptagen); Coenzyme Q10 (oral formulation), Receptagen
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 Compound Name Aglatimagene besadenovec Phase 1/2 [4]
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 Compound Name Zolbetuximab Phase 3 [12]
Synonyms
IMAB362
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 Compound Name AC-1204 Phase 3 [13]
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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 Compound Name Radiosensitizer gene therapy Phase 3 [14]
Synonyms
Radiosensitizer gene therapy (prostate cancer)
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 Compound Name Glufosfomide Phase 3 [15]
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 Compound Name Yttrium (90Y) clivatuzumab tetraxetan Phase 3 [16]
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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 Compound Name Y-90 Clivatuzumab Phase 3 [17]
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 Compound Name Civacir Phase 3 [18]
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 Compound Name GV1001 Phase 3 [19]
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 Compound Name Masitinib Phase 3 [4]
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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 Compound Name Glufosfamide Phase 3 [4]
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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 Compound Name Sapacitabine Phase 3 [4]
Synonyms
CYC682
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 Compound Name Pelareorep Phase 2 [20]
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 Compound Name Pamrevlumab Phase 3 [21]
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 Compound Name GRASPA Phase 1 [22]
Synonyms
L-asparaginase (erythrocyte-encapsulated, acute lymphoblastic leukemia/solid tumor), ERYtech
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 Compound Name Pancreas algenpantucel-L Phase 3 [23]
Synonyms
HyperAcute (TN)
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 Compound Name CPI-613 Phase 3 [24]
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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 Compound Name Zarnestra Phase 3 [25]
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 [26]
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 Compound Name Marimastat Phase 3 [27]
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 [28]
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 Compound Name ANX-510 Phase 3 [29]
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 Compound Name Napabucasin Phase 3 [4]
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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 Compound Name Algenpantucel-L Phase 3 [30]
Synonyms
HyperAcute pancreas (TN)
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 Compound Name OT-101 Phase 2/3 [4]
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 Compound Name RP101 Phase 2/3 [31]
Synonyms
SCHEMBL15589316; CHEMBL3703295; BDBM149820; US8975415,
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 Compound Name NLG8189 Phase 2/3 [4]
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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 Compound Name LY2157299 Phase 2/3 [4]
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
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 Compound Name SM-88 Phase 2/3 [32]
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 Compound Name SiG12D-LODER Phase 2 [4]
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 Compound Name BNT141 Phase 2 [33]
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 Compound Name BNT321 Phase 2 [34]
Synonyms
MVT-5873
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 Compound Name BPM 31510 Phase 2 [35]
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 Compound Name GC4711 Phase 2 [36]
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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 Compound Name CYTO-401 Phase 2 [37]
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 Compound Name Zenocutuzumab Phase 2 [38]
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 Compound Name Cabiralizumab Phase 2 [4]
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 Compound Name VS-6063 Phase 2 [4]
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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 Compound Name MENK Phase 2 [15]
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 Compound Name CO-101 Phase 2 [39]
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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 Compound Name MENK Phase 2 [4]
Synonyms
IRT-101
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 Compound Name TL-118 Phase 2 [40]
Synonyms
Hamsa 1; TL-111; TL-112; Combination anti-angiogenic therapy (oral suspension, solid tumors), Tiltan Pharma
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 Compound Name Antroquinonol Phase 2 [4]
Synonyms
Hocena; Fungal extract (cancer), Golden Biotechnology
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 Compound Name NPC-1C Phase 2 [4]
Synonyms
Ensituximab
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 Compound Name Necuparanib Phase 2 [41]
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 Compound Name CCX872 Phase 2 [4]
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 Compound Name GC4419 Phase 1/2 [4]
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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 Compound Name Istiratumab Phase 2 [20]
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 Compound Name GI-4000 Phase 2 [42]
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 Compound Name OCV-101 Phase 2 [43]
Synonyms
OTS-11101
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 Compound Name RX-3117 Phase 2 [4]
Synonyms
Antimetabolite (cancer), Rexahn; Antimetabolite (cancer), Rexahn/ Teva
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 Compound Name Ensitiximab Phase 2 [15]
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 Compound Name GI-4000 + gemcitabine Phase 2 [44]
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 Compound Name BC-819 Phase 2 [45]
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 Compound Name IRT-102 Phase 2 [46]
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 Compound Name LE-DT Phase 2 [47]
Synonyms
Liposomal docetaxel
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 Compound Name TH-302 Phase 2 [4]
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 [15]
External Link
 Compound Name Anti-PSCA mab Phase 2 [48]
External Link
 Compound Name ALT-803 Phase 2 [20]
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 [4]
External Link
 Compound Name Reolysinpelareorep Phase 2 [4]
External Link
 Compound Name PBI-05204 Phase 2 [4]
External Link
 Compound Name PCI-27483 Phase 2 [49]
External Link
 Compound Name RX-0201 Phase 2 [15]
External Link
 Compound Name CP-613 Phase 2 [50]
External Link
 Compound Name CART 19 Preclinical [51]
External Link
 Compound Name VT-122 Phase 1 [15]
External Link
 Compound Name PEGPH20 Phase 2 [52]
External Link
 Compound Name Ficlatuzumab Phase 2 [4]
Synonyms
AV-299
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External Link
 Compound Name Tigatuzumab Phase 2 [53]
External Link
 Compound Name CRS-207 Phase 2 [54]
External Link
 Compound Name CAP1-6D Phase 2 [55]
Synonyms
Modified CEA peptide (pancreatic cancer), University of Chicago
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External Link
 Compound Name SGT-53 Phase 2 [4]
Synonyms
P53 gene stimulator (solid tumor), Synergene Therapeutics
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External Link
 Compound Name Tarextumab Phase 2 [56]
External Link
 Compound Name BVD-523 Phase 2 [4]
External Link
 Compound Name Ocaperidone Phase 2 [20]
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 [4]
External Link
 Compound Name LY2603618 Phase 2 [57]
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 [58]
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 [4]
External Link
 Compound Name GB1275 Phase 1/2 [59]
External Link
 Compound Name ABTL0812 Phase 1/2 [60]
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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External Link
 Compound Name GP-2250 Phase 1/2 [61]
External Link
 Compound Name Delolimogene mupadenorepvec Phase 1/2 [62]
Synonyms
LOAd703
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External Link
 Compound Name GSK3145095 Phase 1/2 [63]
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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External Link
 Compound Name Encapsulated cell therapy Phase 1/2 [64]
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 Compound Name ETBX-011 cancer vaccine Phase 1/2 [42]
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 Compound Name BPX-601 Phase 1/2 [65]
External Link
 Compound Name NANT Phase 1/2 [4]
External Link
 Compound Name BrevaRex Phase 1/2 [66]
Synonyms
BrevaRex MAb; monoclonal antibody
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External Link
 Compound Name DCVax-Pancreas Phase 1/2 [67]
Synonyms
Dendritic cell-based immunotherapy (pancreatic cancer), Northwest Biotherapeutics
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External Link
 Compound Name PEGylated hyaluronidase (human recombinant) Phase 1/2 [68]
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 [69]
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 Compound Name MALP-2S Phase 1/2 [70]
External Link
 Compound Name Anti-Mesothelin CAR-T cells Phase 1/2 [71]
External Link
 Compound Name Anti-MUC1 CAR T Cells Phase 1/2 [72]
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 Compound Name Anti-HER2 CAR-T Phase 1/2 [73]
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 Compound Name CAR-T Cells targeting EpCAM Phase 1/2 [74]
External Link
 Compound Name Anti-MUC1 AR20.5 Phase 1/2 [20]
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 Compound Name AR20.5 Phase 1/2 [4]
External Link
 Compound Name G0-203-2c Phase 1/2 [75]
External Link
 Compound Name LOAd703 Phase 1/2 [4]
External Link
 Compound Name Anti-mesothelin CAR transduced PBL Phase 1/2 [76]
External Link
 Compound Name M9241 Phase 1 [77]
Synonyms
NHS-IL12
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External Link
 Compound Name NBF-006 Phase 1 [78]
External Link
 Compound Name AB680 Phase 1 [79]
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 [80]
External Link
 Compound Name CEND-1 Phase 1 [81]
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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External Link
 Compound Name CAR-T Cells targeting EGFRvIII Phase 1 [82]
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 Compound Name HuCART-meso cells Phase 1 [83]
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 Compound Name OCV-105 Phase 1 [84]
Synonyms
Cancer vaccine (pancreas), Otsuka/OncoTherapy
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External Link
 Compound Name SBP-101 Phase 1 [15]
Synonyms
diethyl dihydroxyhomospermine
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External Link
 Compound Name RG7882 Phase 1 [20]
External Link
 Compound Name CART-meso-19 T cells Phase 1 [85]
External Link
 Compound Name MOv19-BBz CAR T cells Phase 1 [86]
External Link
 Compound Name Anti-MUC1 AR20.5 mab Phase 1 [87]
External Link
 Compound Name Anti-CEA-CAR T Phase 1 [88]
External Link
 Compound Name MVT-5873 Phase 1 [20]
External Link
 Compound Name CART-meso cells Phase 1 [89]
External Link
 Compound Name CAR-20/19-T Cells Phase 1 [90]
External Link
 Compound Name CARTmeso/19 Phase 1 [91]
External Link
 Compound Name CAR-T Cells targeting Mesothelin Phase 1 [82]
External Link
 Compound Name CAR-T Cells targeting CEA Phase 1 [82]
External Link
 Compound Name HLA-A*2402-restricted KIF20A and VEGFR-1 epitope peptide vaccine Phase 1 [92]
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 [93]
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 Compound Name MORAb-066 Phase 1 [94]
Synonyms
Anti-tissue factor monoclonal antibody (pancreatic tumor), Morphotek
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External Link
 Compound Name Anti-MUC1 mab Phase 1 [95]
External Link
 Compound Name Anti-meso-CAR vector transduced T cells Phase 1 [96]
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 Compound Name CRS-207 + GVAX Phase 2 [15]
External Link
 Compound Name Autologous T cells transfected with chimeric anti-mesothelin immunoreceptor SS1 Phase 1 [97]
External Link
 Compound Name Meso-CART Phase 1 [98]
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 Compound Name ASG-5ME Phase 1 [99]
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 Compound Name Anti-CD133-CAR vector-transduced T cells Phase 1 [100]
External Link
 Compound Name IRX4204 Phase 1 [4]
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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External Link
 Compound Name AbGn-107 Phase 1 [4]
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 Compound Name LMB-100 Phase 1/2 [4]
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 Compound Name PLX7486 Phase 1 [101]
External Link
 Compound Name CAR-T Cells targeting HER2 Phase 1 [82]
External Link
 Compound Name CAR-T Cells targeting MUCI Phase 1 [82]
External Link
 Compound Name SEL-403 Phase 1 [4]
External Link
 Compound Name CAR-T Cells targeting PSCA Phase 1 [82]
External Link
 Compound Name Anti-CEA CAR-T cells Phase 1 [102]
External Link
 Compound Name MVT-1075 Phase 1 [4]
External Link
 Compound Name CAR-CLD18 T cell Clinical trial [103]
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 Compound Name CART-meso cells Clinical trial [104]
External Link
 Compound Name PMID28460551-Compound-1 Patented [105]
External Link
 Compound Name Tanomastat Discontinued in Phase 3 [106]
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 [107]
Synonyms
Benzenepropanoic acid; PNU 100940; XRP 9881; XRP9881
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External Link
 Compound Name Apricoxib Discontinued in Phase 2 [108]
Synonyms
TG01
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External Link
 Compound Name Lintitript Discontinued in Phase 2 [109]
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 [110]
Synonyms
NSC-336628
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External Link
 Compound Name LY293111 Discontinued in Phase 2 [111]
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 [112]
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 [113]
External Link
 Compound Name IC261 Preclinical [114]
Synonyms
IC-261; IC 261
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External Link
 Compound Name ANAVEX 1007 Preclinical [115]
External Link
 Compound Name IPH-4201 Terminated [116]
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 [117]
External Link
 Compound Name PAT-PM-1 Investigative [117]
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 [117]
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 [118]
Synonyms
AKT inhibitor (pancreatic cancer), NovaLead Pharma
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External Link
 Compound Name GS-326 Investigative [117]
Synonyms
GS-326C
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External Link
 Compound Name PX-12 Phase 2 [119]
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 Compound Name Prodigiosin Investigative [117]
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 Compound Name Pbi-shPDX-1 LP Investigative [117]
External Link
 Compound Name Gastrin 17C diphtheria toxoid conjugate Investigative [117]
Synonyms
Gastrin 17C diphtheria toxoid conjugate (pancreatic cancer)
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 Compound Name HS-P1 Investigative [117]
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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External Link
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Ref 115 2011 Pipeline of Anavex.
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Ref 119 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.