Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
Crosstalk ID
M6ACROT05923
[1]
Non-coding RNA circRHBDD1 IGF2BP2  lncRNA       miRNA   circRNA 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 Non-coding RNA (ncRNA)
Epigenetic Regulator hsa_circ_0058493 (Circ_RHBDD1) circRNA View Details
Regulated Target Insulin like growth factor 2 mRNA binding protein 2 (IGF2BP2) View Details
Crosstalk Relationship ncRNA  →  m6A Enhancement
Crosstalk Mechanism ncRNAs directly impacts m6A modification through recruiting m6A regulator
Crosstalk Summary Circ_RHBDD1 binds to IGF2BP2, disrupting the interaction between E3 ligase TRIM25 and IGF2BP2, and ultimately inhibiting IGF2BP2 ubiquitination and degradation. Intriguingly, IGF2BP2 enhances Programmed cell death 1 ligand 1 (CD274/PD-L1) mRNA stability through m6A modification.
Responsed Disease Gastric cancer ICD-11: 2B72
Cell Process Immune Evasion
In-vitro Model
MKN28 Gastric tubular adenocarcinoma Homo sapiens CVCL_1416
In-vivo Model C57BL/6 mice (6-8 weeks old, female) were used to create tumor models by subcutaneous injection of GC cells. When tumors reached ~ 100 mm3, mice were injected with PLGA-PEG(si-circRHBDD1) NPs or PLGA-PEG(siRNA control) NPs (200 mg/kg) via tail vein.
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 [2]
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 Compound Name Durvalumab Approved [3]
MOA Modulator
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 Compound Name RG-7446 Approved [4]
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 Compound Name Bavencio Approved [5]
MOA Inhibitor
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 Compound Name Atezolizumab Approved [6]
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 Compound Name Sugemalimab Approved in China [7]
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 Compound Name MEDI4736 Phase 3 [8]
MOA Modulator
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 Compound Name MPDL-3280A Phase 3 [9]
MOA Modulator
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 Compound Name CS1001 Phase 3 [10]
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 Compound Name A167 Phase 3 [11]
Synonyms
KL-A167
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 Compound Name KN046 Phase 3 [12]
MOA Inhibitor
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 Compound Name Pidilizumab Phase 2 [13]
Synonyms
CT-011
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 Compound Name KN035 Phase 2 [14]
Synonyms
Envafolimab
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 Compound Name CX-072 Phase 2 [15]
MOA Inhibitor
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 Compound Name INCB86550 Phase 2 [16]
MOA Inhibitor
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 Compound Name Bintrafusp alfa Phase 2 [17]
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 Compound Name M7824 Phase 2 [18]
MOA Inhibitor
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 Compound Name BGB-A333 Phase 1/2 [19]
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 Compound Name GS-4224 Phase 1/2 [20]
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
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 Compound Name NM21-1480 Phase 1/2 [21]
MOA Modulator
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 Compound Name LY3300054 Phase 1 [18]
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 Compound Name MSB2311 Phase 1 [14]
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 Compound Name Anti-PD-L1 Phase 1 [22]
Synonyms
BMS-936559
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 Compound Name FAZ053 Phase 1 [15]
MOA Inhibitor
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 Compound Name Anti-PD-L1 CSR T cells Phase 1 [23]
MOA CAR-T-Cell-Therapy
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 Compound Name BMS-986189 Phase 1 [14]
MOA Inhibitor
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 Compound Name Cosibelimab Phase 1 [24]
Synonyms
CK-301/TG-1501
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 Compound Name CA-170 Phase 1 [25]
MOA Inhibitor
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 Compound Name PD-L1 t-haNK Phase 1 [26]
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 Compound Name KD033 Phase 1 [27]
MOA Inhibitor
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 Compound Name C-Met/PD-L1 CAR-T Cell Phase 1 [28]
MOA CAR-T-Cell-Therapy(Dual specific)
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 Compound Name CA-170 Phase 1 [18]
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
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 Compound Name FS118 Phase 1 [14]
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 Compound Name PF-07257876 Phase 1 [29]
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 Compound Name MCLA-145 Phase 1 [30]
MOA Agonist
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 Compound Name GEN1046 Phase 1 [31]
MOA Agonist
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 Compound Name ALPN-202 Phase 1 [32]
MOA Inhibitor
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 Compound Name TAK-252 Phase 1 [33]
Synonyms
SL-279252
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MOA Agonist
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 Compound Name INBRX-105 Phase 1 [34]
MOA Inhibitor
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 Compound Name LY3415244 Phase 1 [35]
MOA Inhibitor
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 Compound Name A337 Phase 1 [11]
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 Compound Name IBI318 Phase 1 [36]
MOA Inhibitor
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 Compound Name PMID30107136-Compound-Example2 Patented [37]
MOA Inhibitor
Activity IC50 = 150 nM
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 Compound Name PMID30107136-Compound-Example1 Patented [37]
MOA Inhibitor
Activity IC50 = 18 nM
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 Compound Name PMID30247903-Compound-General structure7 Investigative [14]
Synonyms
PMID30247903Compound7
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MOA Inhibitor
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 Compound Name CA-327 Investigative [14]
MOA Inhibitor
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 Compound Name PMID30247903-Compound-General structure8 Investigative [14]
Synonyms
PMID30247903Compound8
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MOA Inhibitor
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 Compound Name PMID30247903-Compound-General structure5 Investigative [14]
Synonyms
PMID30247903Compound5
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MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure12 Investigative [14]
Synonyms
PMID30247903Compound12
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MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure9 Investigative [14]
Synonyms
PMID30247903Compound9
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MOA Inhibitor
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 Compound Name PMID30247903-Compound-General structure6 Investigative [14]
Synonyms
PMID30247903Compound6
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MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure10 Investigative [14]
Synonyms
PMID30247903Compound10
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MOA Inhibitor
External Link
 Compound Name YH011 Investigative [38]
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 Compound Name YH010 Investigative [39]
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 Compound Name RG6084 Phase 1 [40]
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2B72: Gastric cancer 81 Compound(s) Regulating the Disease Click to Show/Hide the Full List
 Compound Name Leniolisib Approved [41]
Synonyms
1354690-24-6; Leniolisib free base; UNII-L22772Z9CP; (S)-1-(3-((6-(6-methoxy-5-(trifluoromethyl)pyridin-3-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-yl)amino)pyrrolidin-1-yl)propan-1-one; L22772Z9CP; 1354690-24-6 (free base); leniolisib(CDZ 173); CDZ173; CDZ-173; 1-[(3S)-3-[[6-[6-methoxy-5-(trifluoromethyl)pyridin-3-yl]-7,8-dihydro-5H-pyrido[4,3-d]pyrimidin-4-yl]amino]pyrrolidin-1-yl]propan-1-one; Leniolisib [INN]; Leniolisib (CDZ173); Leniolisib (USAN/INN); CDZ173-NX; SCHEMBL323054; GTPL9424; CHEMBL3643413; BDBM118299; EX-A2854; MFCD30470232; s8752; ZB1510; CS-7524; DC22326; SB18839; Example 67 [WO2012004299]; 1-{(S)-3-[6-(6-methoxy-5-trifluoromethyl-pyridin-3-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-y; 1-{(S)-3-[6-(6-methoxy-5-trifluoromethyl-pyridin-3-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-ylamino]-pyrrolidin-1-yl}-propan-1-one; AS-56217; HY-17635; A16796; D11158; US8653092, 67; Q27282602; 1-Propanone, 1-((3S)-3-((5,6,7,8-tetrahydro-6-(6-methoxy-5-(trifluoromethyl)-3-pyridinyl)pyrido(4,3-d)pyrimidin-4-yl)amino)-1-pyrrolidinyl)-; 9NQ
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 Compound Name Atezolizumab Approved [18]
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 Compound Name Bavencio Approved [18]
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 Compound Name Tebentafusp Approved [42]
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 Compound Name Merimepodib Approved [43]
Synonyms
Merimebodib; Merimepodib [USAN:INN]; Tyverb/Tykerb; MMPD; 198821-22-6; 2ZL2BA06FU; C23H24N4O6; CHEMBL304087; MERIMEPODIB, VI-21497, VX-497; UNII-2ZL2BA06FU; VI-21497; VX-497; VX497; Vx 497; carbamic acid
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External Link
 Compound Name Taxol Approved [44]
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 Ramucirumab Approved [45]
Synonyms
LY3009806
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 Compound Name Tucatinib Approved [46]
Synonyms
Irbinitinib; 937263-43-9; ONT-380; UNII-234248D0HH; 234248D0HH; N6-(4,4-Dimethyl-4,5-dihydrooxazol-2-yl)-N4-(3-methyl-4-((1,2,4)triazolo(1,5-a)pyridin-7-yloxy)phenyl)quinazoline-4,6-diamine; 4,6-Quinazolinediamine, N6-(4,5-dihydro-4,4-dimethyl-2-oxazolyl)-N4-(3-methyl-4-((1,2,4)triazolo(1,5-a)pyridin-7-yloxy)phenyl)-; ONT 380; 4,6-QuinazolinediaMine, N6-(4,5-dihydro-4,4-diMethyl-2-oxazolyl)-N4-[3-Methyl-4-([1,2,4]triazolo[1,5-a]pyridin-7-yloxy)phenyl]-; Tucatinib [USAN:INN]; 6-DIAMINE
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External Link
 Compound Name Antacids Approved [47]
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 Compound Name Trastuzumab Approved [18]
Synonyms
Herceptin; Herceptin (TN); Trastuzumab (INN); Trastuzumab (genetical recombination); Trastuzumab (genetical recombination) (JAN); Trastuzumab (ERBB2 mAb inhibitor)
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External Link
 Compound Name Carbamazepine Phase 3 [48]
Synonyms
Carbamazepine (iv, epilepsy); Carbamazepine (iv, epilepsy), Lundbeck; Carbamazepine (iv, epilepsy), Ovation Pharmaceuticals
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External Link
 Compound Name Margetuximab Approved [18]
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 Compound Name Nivolumab Approved [18]
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 Compound Name GRANITE Phase 3 [49]
Synonyms
Penoxsulam; 219714-96-2; 2-(2,2-difluoroethoxy)-N-(5,8-dimethoxy-[1,2,4]triazolo[1,5-c]pyrimidin-2-yl)-6-(trifluoromethyl)benzenesulfonamide; UNII-784ELC1SCZ; 784ELC1SCZ; CHEBI:81776; 2-(2,2-difluoroethoxy)-n-(5,8-dimethoxy[1,2,4]triazolo[1,5-c]pyrimidin-2-yl)-6-(trifluoromethyl)benzenesulfonamide; Penoxsulam [ISO]; PXD; DSSTox_CID_14803; DSSTox_RID_79204; DSSTox_GSID_34803; SCHEMBL116968; CHEMBL1895913; DTXSID0034803; HSDB 7887; AMY12535; BCP18718; EBD18529; Tox21_301010; MFCD07363876; ZINC13827750; AKOS025401685; NCGC00163715-01; NCGC00163715-02; NCGC00163715-03; NCGC00254912-01; AC-24494; Penoxsulam 100 microg/mL in Acetonitrile; CAS-219714-96-2; FT-0696708; Penoxsulam, PESTANAL(R), analytical standard; C18481; Q22808507; 2-(2,2-Difluoroethoxy)-6-trifluoromethyl-N-(5, 8-dimethoxy[1,2,4]triazolo[1,5-c]pyrimidin-2-yl)benzenesulfonamide; 2-(2,2-Difluoroethoxy)-N-(5,8-dimethoxy[1,2,4]-triazolo[1,5-c]pyrimidin-2-yl)-6-(trifluoromethyl)benzenesulfonamide; 2-(2,2-difluoroethoxy)-N-{5,8-dimethoxy-[1,2,4]triazolo[1,5-c]pyrimidin-2-yl}-6-(trifluoromethyl)benzene-1-sulfonamide; 2-(2,2-difluoroethyl)-N-(5,8-dimethoxy[1,2,4]triazolo[1,5-c]pyrimidin-2-yl)-6-(trifluoromethyl)benzenesulfonamide; Benzenesulfonamide, 2-(2,2-difluoroethoxy)-N-(5,8-dimethoxy(1,2,4)triazolo(1,5-c)pyrimidin-2-yl)-6-(trifluoromethyl)-
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External Link
 Compound Name Zolbetuximab Phase 3 [50]
Synonyms
IMAB362
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 Compound Name Tusamitamab ravtansine Phase 3 [51]
Synonyms
SAR408701
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 Compound Name Andecaliximab Phase 3 [52]
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 Compound Name ABP 980 Phase 3 [15]
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 Compound Name GS-5745 Phase 3 [44]
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 Compound Name S-1 Phase 3 [53]
Synonyms
Ciprofibrate-coa; Ciprofibrate-coenzyme A; Coenzyme A, ciprofibrate-; AC1L4TRG; AC1Q3T4H; 111900-25-5; s-{1-[(2r,3s,4r,5r)-5-(6-amino-9h-purin-9-yl)-4-hydroxy-3-(phosphonooxy)tetrahydrofuran-2-yl]-3,5,9-trihydroxy-8,8-dimethyl-3,5-dioxido-10,14-dioxo-2,4,6-trioxa-11,15-diaza-3; E5,5; E5-diphosphaheptadecan-17-yl} 2-[4-(2,2-dichlorocyclopropyl)phenoxy]-2-methylpropanethioate(non-preferred name); Coenzyme A, S-(2-(4-(2,2-dichlorocyclopropyl)phenoxy)-2-methylpropanoate)
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 Compound Name Lonsurf Phase 3 [18]
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 Compound Name GDC-0068 Phase 3 [44]
Synonyms
RG7440
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External Link
 Compound Name Edotecarin Phase 3 [54]
Synonyms
ED-749; Edotecarin < Prop INN; J-107088; PF-804950; 12-(beta-D-Glucopyranosyl)-2,10-dihydroxy-6-[2-hydroxy-1-(hydroxymethyl)ethylamino]-6,7,12,13-tetrahydro-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7-dione
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 Compound Name RG3638 Phase 3 [55]
Synonyms
Onartuzumab
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External Link
 Compound Name G17DT Phase 3 [56]
Synonyms
Gastrimmune; Insegia
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External Link
 Compound Name DE-766 Phase 3 [57]
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 Compound Name Tesetaxel Phase 2 [58]
Synonyms
DJ-927; 333754-36-2; UNII-UG97LO5M8Y; UG97LO5M8Y; Tesetaxel [INN]; DJ927; DJ 927; CHEMBL2107787; SCHEMBL12060837; DB12019; Z-3104; (2AS,2BR,3S,4S,6S,8AR,10R,11AS,11BR,13AR)-2A-ACETOXY-6-(((2R,3S)-3-((TERT-BUTOXYCARBONYL)AMINO)-3-(3-FLUOROPYRIDIN-2-YL)-2-HYDROXYPROPANOYL)OXY)-10-((DIMETHYLAMINO)METHYL)-4-HYDROXY-7,11B,14,14-TETRAMETHYL-2A,2B,3,4,5,6,8A,11A,11B,12,13,13A-DODECAHYDRO-2H-4,8-METHANOOXETO[3'',2'':3',4']BENZO[1',2':3,4]CYCLODECA[1,2-D][1,3]DIOXOL-3-YL BENZOATE
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 Compound Name Nelipepimut S Phase 3 [59]
Synonyms
E75
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External Link
 Compound Name BMS-986205 Phase 3 [18]
Synonyms
KRTIYQIPSAGSBP-KLAILNCOSA-N; 1923833-60-6; BMS986205; UNII-0A7729F42K; 0A7729F42K; GTPL9707; SCHEMBL18826792; SCHEMBL17740982; SCHEMBL19105151; EX-A2606; AKOS032954040; HY-101560; CS-0021719; Q29213697; (R)-N-(4-chlorophenyl)-2-((1s,4S)-4-(6-fluoroquinolin-4-yl)cyclohexyl)propanamide; (2R)-N-(4-chlorophenyl)-2-[4-(6-fluoroquinolin-4-yl)cyclohexyl]propanamide; (2R)-N-(4-Chlorophenyl)-2-(4-(6-fluoro-4-quinolyl)cyclohexyl)propanamide, cis; Cyclohexaneacetamide, N-(4-chlorophenyl)-4-(6-fluoro-4-quinolinyl)-alpha-methyl-, cis-(alphaR)-
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 Compound Name Rivoceranib Phase 3 [18]
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 Compound Name Claudiximab Phase 3 [18]
Synonyms
IMAB-362; Anti-GC182 mAbs (cancer), Ganymed; Anti-GC182 monoclonal antibodies (cancer), Ganymed; Anti-CLDN18-2 mAbs (cancer), Ganymed; Anti-CLDN18-2 monoclonal antibodies (cancer), Ganymed
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 Compound Name OS-440 Phase 3 [60]
Synonyms
CNS modulator (spasticity), Osmotica
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 Compound Name Oraxol Phase 3 [18]
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 Compound Name ICI 118,551 Phase 3 [44]
Synonyms
Ici 118551; (2R,3S)-1-[(7-methyl-2,3-dihydro-1H-inden-4-yl)oxy]-3-(propan-2-ylamino)butan-2-ol; CHEMBL198059; CHEBI:73289; ICI-118551; ICI118551; erythro-DL-1-(7-Methylindan-4-yloxy)-3-isopropylaminobutan-2-ol; (2R,3S)-3-(isopropylamino)-1-[(7-methyl-2,3-dihydro-1H-inden-4-yl)oxy]butan-2-ol; 2-Butanol, 1-((2,3-dihydro-7-methyl-1H-inden-4-yl)oxy)-3-((1-methylethyl)amino)-, (2R,3S)-rel-; 2-Butanol, 1-((2,3-dihydro-7-methyl-1H-inden-4-yl)oxy)-3-((1-methylethyl)amino)-, (R*,S*)-(+-)-; ICI-118,551; Ici 111,581; AC1NUNSO
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 Compound Name Evorpacept Phase 2/3 [61]
Synonyms
ALX148
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 Compound Name BNT141 Phase 2 [62]
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 Compound Name Anti-LAG3 Phase 2 [15]
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 Compound Name GSK1292263 Phase 2 [63]
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 Compound Name MM-111 Phase 2 [64]
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 Compound Name Plevitrexed Phase 2 [65]
Synonyms
ZD 9331; ZD9331; 153537-73-6; Plevitrexed [INN]; ZD-9331; NSC 696259; UNII-L9P2881C3H; CHEMBL126648; (2s)-2-[(2-fluoro-4-{[(4-hydroxy-2,7-dimethylquinazolin-6-yl)methyl](prop-2-yn-1-yl)amino}benzoyl)amino]-4-(2h-tetrazol-5-yl)butanoic acid; L9P2881C3H; Plevitrexed (INN); 172521-94-7; (2S)-2-[[4-[(2,7-dimethyl-4-oxo-1H-quinazolin-6-yl)methyl-prop-2-ynylamino]-2-fluorobenzoyl]amino]-4-(2H-tetrazol-5-yl)butanoic acid; 1H-Tetrazole-5-butanoic acid,
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External Link
 Compound Name DS-8201 Phase 1 [15]
Synonyms
9-Aminofluorene; 9H-Fluoren-9-amine; 525-03-1; FLUOREN-9-AMINE; Fluoren-9-ylamine; UNII-4NHO2K4K5B; CCRIS 7000; BRN 2209545; 4NHO2K4K5B; OUGMRQJTULXVDC-UHFFFAOYSA-N; fluorene-9-ylamine; 9-Amino-fluoren; 9-amino-fluorene; 9H-9-fluorenamine; 9H-fluoren-9-yl-amine; AC1L1VP5; 4-12-00-03390 (Beilstein Handbook Reference); SCHEMBL353865; AC1Q53A2; AC1Q53A1; KS-00000JGC; CTK1H0380; DTXSID90200496; MolPort-001-794-448; HMS1780P20; 9H-fluoren-9-ylamine hydrochloride; ZINC1724407; ALBB-023296; CA-733; SBB005783; AKOS000264388; MCULE-8757055914; DS-
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External Link
 Compound Name XL880 Phase 2 [66]
Synonyms
GSK 089; GSK 1363089; GSK1363089; XL 880; GSK1363089, GSK089, foretinib, EXEL-2880, XL880; 88Z; MET inhibitors
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 Compound Name Matuzumab Phase 2 [67]
Synonyms
EMD-62000; EMD-72000; Anti-EGF receptor humanized antibody (iv, cancer), Merck KGaA/ Takeda Pharmaceuticals; Anti-EGFR humanized mAb (iv, cancer), Merck KGaA/ Takeda Pharmaceuticals; Anti-epidermal growth factor receptor humanized antibody (iv, cancer), Merck KGaA/ Takeda Pharmaceuticals
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 Compound Name BAY-57-9352 Phase 2 [44]
Synonyms
Telatinib; Bay 57-9352
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 Compound Name Bemarituzumab Phase 2 [68]
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 Compound Name PEGPH20 Phase 2 [18]
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 Compound Name Plevitrexed (R)-isomer Phase 2 [69]
Synonyms
YW3548
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 Compound Name APR-246 Phase 2 [70]
Synonyms
Eprenetapopt
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 Compound Name CRS-207 Phase 2 [59]
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 Compound Name Opdivo + Yervoy Phase 3 [18]
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 Compound Name CT-041 Phase 1/2 [71]
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 Compound Name BPX-601 Phase 1/2 [72]
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 Compound Name Anti-MUC1 CAR-T cells Phase 1/2 [73]
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 Compound Name Anti-Mesothelin CAR-T cells Phase 1/2 [74]
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 Compound Name Anti-HER2 CAR-T Phase 1/2 [75]
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 Compound Name CAR-T Cells targeting EpCAM Phase 1/2 [76]
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 Compound Name PAT-SC1 Phase 1/2 [77]
Synonyms
SC-1; Adjuvant therapy (gastric cancer), University of Wurzburg; SC-1 (gastric cancer), CAT; SC-1 (gastric cancer), Debiopharm; SC-1 (gastric cancer), Patrys; SC-1 (stomach cancer), OncoMab
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 Compound Name ASP2138 Phase 1 [78]
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 Compound Name SAR443216 Phase 1 [79]
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 Compound Name AMG 199 Phase 1 [80]
External Link
 Compound Name AMG 910 Phase 1 [81]
External Link
 Compound Name Alofanib Phase 1 [82]
Synonyms
1612888-66-0; 3-(N-(4-methyl-2-nitro-5-(pyridin-3-yl)phenyl)sulfamoyl)benzoic acid; RPT-835(alofanib); UNII-LQX7RFK8MZ; RPT-835; RPT835; LQX7RFK8MZ; ES000835; Alofanib [INN]; Alofanib(RPT835); Syn007154; CHEMBL4594436; SCHEMBL18660613; AMY16650; BCP31905; EX-A2731; MFCD30533418; NSC790182; s8754; Benzoic acid, 3-(((4-methyl-2-nitro-5-(3-pyridinyl)phenyl)amino)sulfonyl)-; NSC-790182; SB19665; AC-31695; AK668992; AS-56846; HY-17601; CS-0014684; RPT 835; Q27283135; 3-{[4-methyl-2-nitro-5-(pyridin-3-yl)phenyl]sulfamoyl}benzoic acid
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 Compound Name HER2-specific CAR T cell Phase 1 [83]
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 Compound Name Anti-CEA-CAR T Phase 1 [84]
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 Compound Name XR-5944 Phase 1 [85]
Synonyms
MLN-944; XR-11576 analogs; XR-5000 analogs; XR-5942
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 Compound Name A168 Phase 1 [11]
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 Compound Name EGFR806-specific CAR T cell Phase 1 [86]
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 Compound Name AbGn-107 Phase 1 [18]
External Link
 Compound Name FPA144 Phase 1 [15]
External Link
 Compound Name Minnelide 001 Phase 1 [44]
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 Compound Name CAR-T cells targeting EpCAM Phase 1 [87]
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 Compound Name Anti-CEA CAR-T cells Phase 1 [88]
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 Compound Name EPCAM-targeted CAR-T cells Clinical trial [89]
External Link
 Compound Name PMID28460551-Compound-1 Patented [90]
External Link
 Compound Name Conjugated 3-(indolyl)-and 3-(azaindolyl)-4-arylmaleimide compound 1 Patented [91]
Synonyms
PMID28621580-Compound-WO2012084683c62
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 Compound Name TOPIXANTRONE HYDROCHLORIDE Discontinued in Phase 2 [92]
Synonyms
SCHEMBL1418986; Topixantrone hydrochloride < Prop INNM; BBR-3409 (dimaleate); 5-[2-(Dimethylamino)ethylamino]-2-[2-(2-hydroxyethylamino)ethyl]indazolo[4,3-gh]isoquinolin-6(2H)-one dihydrochloride
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 Compound Name MDL 101,731 Discontinued in Phase 2 [93]
Synonyms
Tezacitabine; Fmdc cpd; 130306-02-4; UNII-7607Y95N9S; Mdl 101731; (E)-2'-Deoxy-2'-(fluoromethylene) cytidine; MDL-101731; 2'-Deoxy-2'-(fluoromethylene)cytidine; 7607Y95N9S; Cytidine, 2'-deoxy-2'-(fluoromethylene)-, (2E)-; (E)-2'-Deoxy-2'-(fluoromethylene)cytidine; Tezacitabine [INN]; tezaciabine; Tezacitabine, anhydrous; AC1O5KIG; SCHEMBL18724; SCHEMBL18725; Tezacitabine, anhydrous [INN]; CHEMBL2105467; C10H12FN3O4; DTXSID10156446; GFFXZLZWLOBBLO-ASKVSEFXSA-N; ZINC3777826; KW-2331
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 Compound Name BBR-3438 Discontinued in Phase 2 [94]
Synonyms
Nortopixantrone; UNII-PH2639TAB4; PH2639TAB4; Nortopixantrone [INN:BAN]; AC1MI4ZO; CHEMBL150303; SCHEMBL7804438
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 Compound Name IPI-493 Discontinued in Phase 1 [95]
Synonyms
[(3R,5R,6S,7R,8E,10R,11R,12Z,14E)-21-amino-6-hydroxy-5,11-dimethoxy-3,7,9,15-tetramethyl-16,20,22-trioxo-17-azabicyclo[16.3.1]docosa-1(21),8,12,14,18-pentaen-10-yl] carbamate; AC1NS08X; SCHEMBL16226496; SCHEMBL16225851
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 Compound Name Kanjinti Application submitted [18]
External Link
 Compound Name Anti-CD9 mab Investigative [96]
Synonyms
ALB-6; Anti-CD9 mAb (gastric cancer); Anti-CD9 mAb (gastric cancer), Osaka University
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