Drug General Information
Drug ID
D02TSN
Former ID
DIB018925
Drug Name
AZ20
Synonyms
AZ-20; AZ 20; compound 6 [PMID: 46244454]
Drug Type
Small molecular drug
Indication Discovery agent Investigative [532224]
Structure
Download
2D MOL
Formula
C21H24N4O3S
InChI
InChI=1S/C21H24N4O3S/c1-14-13-28-11-10-25(14)19-12-18(21(7-8-21)29(2,26)27)23-20(24-19)16-4-3-5-17-15(16)6-9-22-17/h3-6,9,12,14,22H,7-8,10-11,13H2,1-2H3/t14-/m1/s1
InChIKey
SCGCBAAYLFTIJU-CQSZACIVSA-N
PubChem Compound ID
PubChem Substance ID
Target and Pathway
Target(s) Serine threonine protein kinase ATR Target Info Inhibitor [532224]
KEGG Pathway Fanconi anemia pathway
Cell cycle
p53 signaling pathway
HTLV-I infection
PANTHER Pathway p53 pathway
p53 pathway feedback loops 2
Pathway Interaction Database Fanconi anemia pathway
ATR signaling pathway
Signaling events mediated by TCPTP
Circadian rhythm pathway
BARD1 signaling events
p53 pathway
Reactome Meiotic synapsis
Activation of ATR in response to replication stress
Regulation of HSF1-mediated heat shock response
HDR through Single Strand Annealing (SSA)
Processing of DNA double-strand break ends
Presynaptic phase of homologous DNA pairing and strand exchange
G2/M DNA damage checkpoint
WikiPathways DNA Damage Response
Meiotic Synapsis
Prostate Cancer
Integrated Breast Cancer Pathway
Integrated Cancer pathway
Cell Cycle
Cell Cycle Checkpoints
miRNA Regulation of DNA Damage Response
References
Ref 532224Discovery of 4-{4-[(3R)-3-Methylmorpholin-4-yl]-6-[1-(methylsulfonyl)cyclopropyl]pyrimidin-2-yl}-1H-indole (AZ20): a potent and selective inhibitor of ATR protein kinase with monotherapy in vivo antitumor activity. J Med Chem. 2013 Mar 14;56(5):2125-38.
Ref 532224Discovery of 4-{4-[(3R)-3-Methylmorpholin-4-yl]-6-[1-(methylsulfonyl)cyclopropyl]pyrimidin-2-yl}-1H-indole (AZ20): a potent and selective inhibitor of ATR protein kinase with monotherapy in vivo antitumor activity. J Med Chem. 2013 Mar 14;56(5):2125-38.

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