Drug Information
Drug General Information | Top | |||
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Drug ID |
D09NTC
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Former ID |
DNCL003453
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Drug Name |
CC-486
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Synonyms |
AG-14361; AG14361; 328543-09-5; UNII-48N0U0K50I; AG 14361; CHEMBL65892; 48N0U0K50I; Imidazo[4,5,1-jk][1,4]benzodiazepin-7(4H)-one, 2-[4-[(dimethylamino)methyl]phenyl]-5,6-dihydro-; AG-014361; 1-(4-((dimethylamino)methyl)phenyl)-8,9-dihydro-2,7,9a-triazabenzo[cd]azulen-6(7H)-one; Imidazo(4,5,1-jk)(1,4)benzodiazepin-7(4H)-one, 2-(4-((dimethylamino)methyl)phenyl)-5,6-dihydro-; 2-[4-[(Dimethylamino)methyl]phenyl]-5,6-dihydroimidazo[4,5,1-jk][1,4]benzodiazepin-7(4H)-one; SMR000486393; MLS006011157; MLS001065917; Nucleoside analogue
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Drug Type |
Small molecular drug
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Indication | Acute myeloid leukaemia [ICD-11: 2A60] | Phase 3 | [1] | |
Myelodysplastic syndrome [ICD-11: 2A37; ICD-9: 238.7] | Phase 3 | [2] | ||
Diffuse large B-cell lymphoma [ICD-11: 2A81; ICD-10: C83.3; ICD-9: 200] | Phase 1 | [1] | ||
Company |
Celgene
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Structure |
Download2D MOL |
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Formula |
C19H20N4O
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Canonical SMILES |
CN(C)CC1=CC=C(C=C1)C2=NC3=CC=CC4=C3N2CCNC4=O
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InChI |
1S/C19H20N4O/c1-22(2)12-13-6-8-14(9-7-13)18-21-16-5-3-4-15-17(16)23(18)11-10-20-19(15)24/h3-9H,10-12H2,1-2H3,(H,20,24)
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InChIKey |
SEKJSSBJKFLZIT-UHFFFAOYSA-N
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CAS Number |
CAS 328543-09-5
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PubChem Compound ID | ||||
PubChem Substance ID |
14801398, 24138480, 44938160, 49645682, 75980483, 99431558, 99460875, 103261452, 104015396, 104253502, 124757624, 124792817, 125164428, 136340148, 136920261, 137275824, 140105717, 152258354, 160647192, 162011827, 162037796, 162202721, 163908012, 164194027, 165247593, 172649965, 174528919, 178118772, 179551797, 185990463, 198960971, 223396135, 223704418, 231943732, 247394852, 249565774, 251962950, 252109983, 252214684, 252436436
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ChEBI ID |
CHEBI:92015
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Target and Pathway | Top | |||
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Target(s) | DNA [cytosine-5]-methyltransferase 1 (DNMT1) | Target Info | Inhibitor | [3] |
Poly [ADP-ribose] polymerase 1 (PARP1) | Target Info | Inhibitor | [4] | |
KEGG Pathway | Base excision repair | |||
NF-kappa B signaling pathway | ||||
Cysteine and methionine metabolism | ||||
Metabolic pathways | ||||
MicroRNAs in cancer | ||||
Panther Pathway | FAS signaling pathway | |||
Pathwhiz Pathway | Methionine Metabolism | |||
Pathway Interaction Database | Integrin-linked kinase signaling | |||
Caspase Cascade in Apoptosis | ||||
Notch-mediated HES/HEY network | ||||
Regulation of retinoblastoma protein | ||||
Reactome | Dual Incision in GG-NER | |||
PRC2 methylates histones and DNA | ||||
NoRC negatively regulates rRNA expression | ||||
DNA methylation | ||||
WikiPathways | FAS pathway and Stress induction of HSP regulation | |||
Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | ||||
Nanoparticle triggered regulated necrosis | ||||
Corticotropin-releasing hormone | ||||
Trans-sulfuration and one carbon metabolism | ||||
Retinoblastoma (RB) in Cancer | ||||
One Carbon Metabolism | ||||
Trans-sulfuration pathway |
References | Top | |||
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REF 1 | Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA) | |||
REF 2 | J Clin Oncol 33, 2015 (suppl, abstr TPS7097). | |||
REF 3 | Efficacy and safety of extended dosing schedules of CC-486 (oral azacitidine) in patients with lower-risk myelodysplastic syndromes. Leukemia. 2016 Apr;30(4):889-96. | |||
REF 4 | Tricyclic benzimidazoles as potent poly(ADP-ribose) polymerase-1 inhibitors. J Med Chem. 2003 Jan 16;46(2):210-3. |
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