Drug Information
Drug General Information | Top | |||
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Drug ID |
D0E1QP
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Former ID |
DNC005896
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Drug Name |
2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide
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Synonyms |
2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide; CHEMBL112265; 352549-39-4; CBMicro_001045; Cambridge id 5870454; AC1N6ME3; Oprea1_743470; SCHEMBL251128; CTK1B0687; DTXSID20401358; MolPort-000-735-346; HMS1632P07; SMSF0008851; STL525366; BDBM50178767; carboxamido-1,2,3-tetrahydrocarbazole; AKOS004917884; CB02357; BIM-0000968.P001; SR-01000154363; SR-01000154363-1; 1H-Carbazole-1-carboxamide, 2,3,4,9-tetrahydro-
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C13H14N2O
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Canonical SMILES |
C1CC(C2=C(C1)C3=CC=CC=C3N2)C(=O)N
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InChI |
1S/C13H14N2O/c14-13(16)10-6-3-5-9-8-4-1-2-7-11(8)15-12(9)10/h1-2,4,7,10,15H,3,5-6H2,(H2,14,16)
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InChIKey |
YMLOFDJHJSQCSN-UHFFFAOYSA-N
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CAS Number |
CAS 352549-39-4
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | NAD-dependent deacetylase sirtuin-1 (SIRT1) | Target Info | Inhibitor | [1] |
KEGG Pathway | FoxO signaling pathway | |||
AMPK signaling pathway | ||||
Glucagon signaling pathway | ||||
Amphetamine addiction | ||||
MicroRNAs in cancer | ||||
Panther Pathway | p53 pathway | |||
Pathway Interaction Database | p73 transcription factor network | |||
Signaling events mediated by HDAC Class III | ||||
E2F transcription factor network | ||||
HIF-2-alpha transcription factor network | ||||
Signaling events mediated by HDAC Class I | ||||
FoxO family signaling | ||||
Regulation of Androgen receptor activity | ||||
Regulation of retinoblastoma protein | ||||
Reactome | RORA activates gene expression | |||
Regulation of HSF1-mediated heat shock response | ||||
Circadian Clock | ||||
WikiPathways | Integrated Pancreatic Cancer Pathway | |||
SREBF and miR33 in cholesterol and lipid homeostasis | ||||
Integrated Breast Cancer Pathway | ||||
SREBP signalling | ||||
Androgen receptor signaling pathway |
References | Top | |||
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REF 1 | Discovery of indoles as potent and selective inhibitors of the deacetylase SIRT1. J Med Chem. 2005 Dec 15;48(25):8045-54. |
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