m6A-centered Crosstalk Information
Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
| Crosstalk ID |
M6ACROT06041
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[1] | |||
Histone modification
H3K18la
EP300
IGF2BP2
Direct
Enhancement
m6A modification
CSF1
CSF1
IGF2BP2
: m6A sites
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| m6A Modification: | |||||
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| m6A Regulator | Insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) | READER | |||
| m6A Target | Macrophage colony-stimulating factor 1 (CSF1) | ||||
| 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 Macrophage colony-stimulating factor 1 (CSF1) and MYC. | ||||
| Responsed Disease | Pancreatic cancer | ICD-11: 2C10 | |||
| Responsed Drug | Gemcitabine | ||||
In-vitro Model |
PANC-1 | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0480 | |
| PATU-8988 (Human pancreatic adenocarcinoma cell) | |||||
| In-vivo Model | A total of 5 × 106 PATU-8988 or organoids derived from PDAC patients (PDO) were orthotopically or subcutaneously injected into per BALB/c nude mice. For the mouse model of CSF1Ri application, 5 × 106 PancO2 cells were orthotopically or subcutaneously injected into per C57BL/6 nude mice. | ||||
Full List of Potential Compound(s) Related to This m6A-centered Crosstalk
| Histone acetyltransferase p300 (P300) | 2 Compound(s) Regulating the Target | Click to Show/Hide the Full List | ||
| CCS1477 | Phase 1/2 | [2] | ||
| 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 | |||
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| FT-7051 | Phase 1 | [3] | ||
| MOA | Inhibitor | |||
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| Macrophage colony-stimulating factor 1 (CSF1) | 4 Compound(s) Regulating the Target | Click to Show/Hide the Full List | ||
| RG7155 | Phase 2 | [4] | ||
| MOA | Antagonist | |||
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| Emactuzumab | Phase 1 | [5] | ||
| MOA | Antagonist | |||
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| PLX73086 | Phase 1 | [4] | ||
| MOA | Antagonist | |||
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| MSC110 | Phase 1 | [6] | ||
| Synonyms |
Lacnotuzumab
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| MOA | Inhibitor | |||
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| 2C10: Pancreatic cancer | 182 Compound(s) Regulating the Disease | Click to Show/Hide the Full List | ||
| Atezolizumab | Approved | [4] | ||
| External Link | ||||
| Trimethadione | Approved | [7] | ||
| 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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| Motixafortide | Approved | [4] | ||
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| Uridine triacetate | Approved | [8] | ||
| Synonyms |
PN401
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| Bentiromide | Approved | [9] | ||
| 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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| 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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| Streptozocin | Approved | [10] | ||
| 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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| Plazomicin | Phase 3 | [11] | ||
| Synonyms |
ACHN-490; UNII-LYO9XZ250J; 1154757-24-0; LYO9XZ250J; Plazomicin [USAN:INN]; Plazomicin (USAN); ZINC68150640; DB12615; D10151; D-Streptamine,
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| 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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| Ibrutinib | Phase 3 | [4] | ||
| Synonyms |
PCI-32765; Ibrutinib (BTK inhibitor)
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| Erlotinib | Approved | [12] | ||
| 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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| Ruxolitinib | Approved | [13] | ||
| Synonyms |
Ruxolitinib (JAK inhibitor)
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| Nivolumab | Approved | [4] | ||
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| 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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| Aglatimagene besadenovec | Phase 1/2 | [4] | ||
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| Zolbetuximab | Phase 3 | [14] | ||
| Synonyms |
IMAB362
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| AC-1204 | Phase 3 | [15] | ||
| 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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| Radiosensitizer gene therapy | Phase 3 | [16] | ||
| Synonyms |
Radiosensitizer gene therapy (prostate cancer)
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| Glufosfomide | Phase 3 | [17] | ||
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| Yttrium (90Y) clivatuzumab tetraxetan | Phase 3 | [18] | ||
| 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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| Y-90 Clivatuzumab | Phase 3 | [19] | ||
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| Civacir | Phase 3 | [20] | ||
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| GV1001 | Phase 3 | [21] | ||
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| 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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| 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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| Sapacitabine | Phase 3 | [4] | ||
| Synonyms |
CYC682
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| Pelareorep | Phase 2 | [5] | ||
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| Pamrevlumab | Phase 3 | [22] | ||
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| GRASPA | Phase 1 | [23] | ||
| Synonyms |
L-asparaginase (erythrocyte-encapsulated, acute lymphoblastic leukemia/solid tumor), ERYtech
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| Pancreas algenpantucel-L | Phase 3 | [24] | ||
| Synonyms |
HyperAcute (TN)
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| CPI-613 | Phase 3 | [25] | ||
| 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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| Zarnestra | Phase 3 | [26] | ||
| 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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| MM-398 | Phase 3 | [27] | ||
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| Marimastat | Phase 3 | [28] | ||
| 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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| AM0010 | Phase 3 | [29] | ||
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| ANX-510 | Phase 3 | [30] | ||
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| 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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| Algenpantucel-L | Phase 3 | [31] | ||
| Synonyms |
HyperAcute pancreas (TN)
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| OT-101 | Phase 2/3 | [4] | ||
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| RP101 | Phase 2/3 | [32] | ||
| Synonyms |
SCHEMBL15589316; CHEMBL3703295; BDBM149820; US8975415,
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| 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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| 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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| SM-88 | Phase 2/3 | [33] | ||
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| SiG12D-LODER | Phase 2 | [4] | ||
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| BNT141 | Phase 2 | [34] | ||
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| BNT321 | Phase 2 | [35] | ||
| Synonyms |
MVT-5873
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| BPM 31510 | Phase 2 | [36] | ||
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| GC4711 | Phase 2 | [37] | ||
| 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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| CYTO-401 | Phase 2 | [38] | ||
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| Zenocutuzumab | Phase 2 | [39] | ||
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| Cabiralizumab | Phase 2 | [4] | ||
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| 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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| MENK | Phase 2 | [17] | ||
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| CO-101 | Phase 2 | [40] | ||
| 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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| MENK | Phase 2 | [4] | ||
| Synonyms |
IRT-101
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| TL-118 | Phase 2 | [41] | ||
| Synonyms |
Hamsa 1; TL-111; TL-112; Combination anti-angiogenic therapy (oral suspension, solid tumors), Tiltan Pharma
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| Antroquinonol | Phase 2 | [4] | ||
| Synonyms |
Hocena; Fungal extract (cancer), Golden Biotechnology
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| External Link | ||||
| NPC-1C | Phase 2 | [4] | ||
| Synonyms |
Ensituximab
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| External Link | ||||
| Necuparanib | Phase 2 | [42] | ||
| External Link | ||||
| CCX872 | Phase 2 | [4] | ||
| External Link | ||||
| 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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| External Link | ||||
| Istiratumab | Phase 2 | [5] | ||
| External Link | ||||
| GI-4000 | Phase 2 | [43] | ||
| External Link | ||||
| OCV-101 | Phase 2 | [44] | ||
| Synonyms |
OTS-11101
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| External Link | ||||
| RX-3117 | Phase 2 | [4] | ||
| Synonyms |
Antimetabolite (cancer), Rexahn; Antimetabolite (cancer), Rexahn/ Teva
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| External Link | ||||
| Ensitiximab | Phase 2 | [17] | ||
| External Link | ||||
| GI-4000 + gemcitabine | Phase 2 | [45] | ||
| External Link | ||||
| BC-819 | Phase 2 | [46] | ||
| External Link | ||||
| IRT-102 | Phase 2 | [47] | ||
| External Link | ||||
| LE-DT | Phase 2 | [48] | ||
| Synonyms |
Liposomal docetaxel
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| External Link | ||||
| 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 | ||||
| Demcizumab | Phase 2 | [17] | ||
| External Link | ||||
| Anti-PSCA mab | Phase 2 | [49] | ||
| External Link | ||||
| ALT-803 | Phase 2 | [5] | ||
| Synonyms |
IL-15 agonist/ IL-15R alpha-Fc fusion complex (cancer), Altor BioScience
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| External Link | ||||
| ARQ 761 | Phase 2 | [4] | ||
| External Link | ||||
| Reolysinpelareorep | Phase 2 | [4] | ||
| External Link | ||||
| PBI-05204 | Phase 2 | [4] | ||
| External Link | ||||
| PCI-27483 | Phase 2 | [50] | ||
| External Link | ||||
| RX-0201 | Phase 2 | [17] | ||
| External Link | ||||
| CP-613 | Phase 2 | [51] | ||
| External Link | ||||
| CART 19 | Preclinical | [52] | ||
| External Link | ||||
| VT-122 | Phase 1 | [17] | ||
| External Link | ||||
| PEGPH20 | Phase 2 | [53] | ||
| External Link | ||||
| Ficlatuzumab | Phase 2 | [4] | ||
| Synonyms |
AV-299
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| External Link | ||||
| Tigatuzumab | Phase 2 | [54] | ||
| External Link | ||||
| CRS-207 | Phase 2 | [55] | ||
| External Link | ||||
| CAP1-6D | Phase 2 | [56] | ||
| Synonyms |
Modified CEA peptide (pancreatic cancer), University of Chicago
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| External Link | ||||
| SGT-53 | Phase 2 | [4] | ||
| Synonyms |
P53 gene stimulator (solid tumor), Synergene Therapeutics
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| External Link | ||||
| Tarextumab | Phase 2 | [57] | ||
| External Link | ||||
| BVD-523 | Phase 2 | [4] | ||
| External Link | ||||
| Ocaperidone | Phase 2 | [5] | ||
| 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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|
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| External Link | ||||
| Encapsulated live cells converting ifosfamide | Phase 2 | [4] | ||
| External Link | ||||
| LY2603618 | Phase 2 | [58] | ||
| 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 | ||||
| Salirasib | Discontinued in Phase 1/2 | [59] | ||
| 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 | ||||
| MM-141 | Phase 2 | [4] | ||
| External Link | ||||
| GB1275 | Phase 1/2 | [60] | ||
| External Link | ||||
| ABTL0812 | Phase 1/2 | [61] | ||
| 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 | ||||
| GP-2250 | Phase 1/2 | [62] | ||
| External Link | ||||
| Delolimogene mupadenorepvec | Phase 1/2 | [63] | ||
| Synonyms |
LOAd703
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| External Link | ||||
| GSK3145095 | Phase 1/2 | [64] | ||
| 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 | ||||
| Encapsulated cell therapy | Phase 1/2 | [65] | ||
| External Link | ||||
| ETBX-011 cancer vaccine | Phase 1/2 | [43] | ||
| External Link | ||||
| BPX-601 | Phase 1/2 | [66] | ||
| External Link | ||||
| NANT | Phase 1/2 | [4] | ||
| External Link | ||||
| BrevaRex | Phase 1/2 | [67] | ||
| Synonyms |
BrevaRex MAb; monoclonal antibody
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| External Link | ||||
| DCVax-Pancreas | Phase 1/2 | [68] | ||
| Synonyms |
Dendritic cell-based immunotherapy (pancreatic cancer), Northwest Biotherapeutics
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| External Link | ||||
| PEGylated hyaluronidase (human recombinant) | Phase 1/2 | [69] | ||
| Synonyms |
PEGylated hyaluronidase; PEGylated hyaluronidase (human recombinant) (intravenous, stroke/cancer), Halozyme
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| External Link | ||||
| CAR-T cells targeting mesothelin | Phase 1/2 | [70] | ||
| External Link | ||||
| MALP-2S | Phase 1/2 | [71] | ||
| External Link | ||||
| Anti-Mesothelin CAR-T cells | Phase 1/2 | [72] | ||
| External Link | ||||
| Anti-MUC1 CAR T Cells | Phase 1/2 | [73] | ||
| External Link | ||||
| Anti-HER2 CAR-T | Phase 1/2 | [74] | ||
| External Link | ||||
| CAR-T Cells targeting EpCAM | Phase 1/2 | [75] | ||
| External Link | ||||
| Anti-MUC1 AR20.5 | Phase 1/2 | [5] | ||
| External Link | ||||
| AR20.5 | Phase 1/2 | [4] | ||
| External Link | ||||
| G0-203-2c | Phase 1/2 | [76] | ||
| External Link | ||||
| LOAd703 | Phase 1/2 | [4] | ||
| External Link | ||||
| Anti-mesothelin CAR transduced PBL | Phase 1/2 | [77] | ||
| External Link | ||||
| M9241 | Phase 1 | [78] | ||
| Synonyms |
NHS-IL12
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| External Link | ||||
| NBF-006 | Phase 1 | [79] | ||
| External Link | ||||
| AB680 | Phase 1 | [80] | ||
| 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 | ||||
| STAT400 | Phase 1 | [81] | ||
| External Link | ||||
| CEND-1 | Phase 1 | [82] | ||
| 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 | ||||
| CAR-T Cells targeting EGFRvIII | Phase 1 | [83] | ||
| External Link | ||||
| HuCART-meso cells | Phase 1 | [84] | ||
| External Link | ||||
| OCV-105 | Phase 1 | [85] | ||
| Synonyms |
Cancer vaccine (pancreas), Otsuka/OncoTherapy
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| External Link | ||||
| SBP-101 | Phase 1 | [17] | ||
| Synonyms |
diethyl dihydroxyhomospermine
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| External Link | ||||
| RG7882 | Phase 1 | [5] | ||
| External Link | ||||
| CART-meso-19 T cells | Phase 1 | [86] | ||
| External Link | ||||
| MOv19-BBz CAR T cells | Phase 1 | [87] | ||
| External Link | ||||
| Anti-MUC1 AR20.5 mab | Phase 1 | [88] | ||
| External Link | ||||
| Anti-CEA-CAR T | Phase 1 | [89] | ||
| External Link | ||||
| MVT-5873 | Phase 1 | [5] | ||
| External Link | ||||
| CART-meso cells | Phase 1 | [90] | ||
| External Link | ||||
| CAR-20/19-T Cells | Phase 1 | [91] | ||
| External Link | ||||
| CARTmeso/19 | Phase 1 | [92] | ||
| External Link | ||||
| CAR-T Cells targeting Mesothelin | Phase 1 | [83] | ||
| External Link | ||||
| CAR-T Cells targeting CEA | Phase 1 | [83] | ||
| External Link | ||||
| HLA-A*2402-restricted KIF20A and VEGFR-1 epitope peptide vaccine | Phase 1 | [93] | ||
| Synonyms |
HLA-A*2402-restricted KIF20A and VEGFR-1 epitope peptide vaccine (pancreatic cancer, subcutaneous)
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| External Link | ||||
| Anti-hCD70 CAR transduced PBL | Phase 1 | [94] | ||
| External Link | ||||
| MORAb-066 | Phase 1 | [95] | ||
| Synonyms |
Anti-tissue factor monoclonal antibody (pancreatic tumor), Morphotek
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| External Link | ||||
| Anti-MUC1 mab | Phase 1 | [96] | ||
| External Link | ||||
| Anti-meso-CAR vector transduced T cells | Phase 1 | [97] | ||
| External Link | ||||
| CRS-207 + GVAX | Phase 2 | [17] | ||
| External Link | ||||
| Autologous T cells transfected with chimeric anti-mesothelin immunoreceptor SS1 | Phase 1 | [98] | ||
| External Link | ||||
| Meso-CART | Phase 1 | [99] | ||
| External Link | ||||
| ASG-5ME | Phase 1 | [100] | ||
| External Link | ||||
| Anti-CD133-CAR vector-transduced T cells | Phase 1 | [101] | ||
| External Link | ||||
| 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 | ||||
| AbGn-107 | Phase 1 | [4] | ||
| External Link | ||||
| LMB-100 | Phase 1/2 | [4] | ||
| External Link | ||||
| PLX7486 | Phase 1 | [102] | ||
| External Link | ||||
| CAR-T Cells targeting HER2 | Phase 1 | [83] | ||
| External Link | ||||
| CAR-T Cells targeting MUCI | Phase 1 | [83] | ||
| External Link | ||||
| SEL-403 | Phase 1 | [4] | ||
| External Link | ||||
| CAR-T Cells targeting PSCA | Phase 1 | [83] | ||
| External Link | ||||
| Anti-CEA CAR-T cells | Phase 1 | [103] | ||
| External Link | ||||
| MVT-1075 | Phase 1 | [4] | ||
| External Link | ||||
| CAR-CLD18 T cell | Clinical trial | [104] | ||
| External Link | ||||
| CART-meso cells | Clinical trial | [105] | ||
| External Link | ||||
| PMID28460551-Compound-1 | Patented | [106] | ||
| External Link | ||||
| Tanomastat | Discontinued in Phase 3 | [107] | ||
| Synonyms |
Tanomastat (USAN/INN); (2S)-4-[4-(4-chlorophenyl)phenyl]-4-oxo-2-(phenylsulfanylmethyl)butanoic acid
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| Larotaxel | Discontinued in Phase 3 | [108] | ||
| Synonyms |
Benzenepropanoic acid; PNU 100940; XRP 9881; XRP9881
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| Apricoxib | Discontinued in Phase 2 | [109] | ||
| Synonyms |
TG01
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| Lintitript | Discontinued in Phase 2 | [110] | ||
| 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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| Merbarone | Discontinued in Phase 2 | [111] | ||
| Synonyms |
NSC-336628
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| LY293111 | Discontinued in Phase 2 | [112] | ||
| 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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| HMN-214 | Discontinued in Phase 1 | [113] | ||
| 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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| RG7600 | Discontinued in Phase 1 | [114] | ||
| External Link | ||||
| IC261 | Preclinical | [115] | ||
| Synonyms |
IC-261; IC 261
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| ANAVEX 1007 | Preclinical | [116] | ||
| External Link | ||||
| IPH-4201 | Terminated | [117] | ||
| 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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| MesoTarg | Investigative | [118] | ||
| External Link | ||||
| PAT-PM-1 | Investigative | [118] | ||
| 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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| OP-04 | Investigative | [118] | ||
| Synonyms |
OP-04 program (prodrug, pancreatic cancer); OP-04 program (prodrug, pancreatic cancer), Onco-Pharmakon
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| VLI-27 | Investigative | [119] | ||
| Synonyms |
AKT inhibitor (pancreatic cancer), NovaLead Pharma
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| GS-326 | Investigative | [118] | ||
| Synonyms |
GS-326C
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| PX-12 | Phase 2 | [120] | ||
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| Prodigiosin | Investigative | [118] | ||
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| Pbi-shPDX-1 LP | Investigative | [118] | ||
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| Gastrin 17C diphtheria toxoid conjugate | Investigative | [118] | ||
| Synonyms |
Gastrin 17C diphtheria toxoid conjugate (pancreatic cancer)
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| HS-P1 | Investigative | [118] | ||
| 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
: m6A sites