L1000FWD
Large Scale Visualization of Drug
Induced Transcriptomic Signatures
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Drugs
Signatures
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Signature Report
Signature ID
CPC014_MCF7_6H:BRD-K52751261-001-01-2:10
Cell Line
MCF7
Dose
10.0 μM
Time
6 hours
p-value
0.0007
Drug Name
TAK-715
External Links and Downloads
Up (210)
Down (206)
Combined (416)
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TAK-715 (BRD-K52751261)
Overview
pert_id
BRD-K52751261
Name
TAK-715
Synonyms
S2928
Collection
BIOA
Summary
TAK 715 is a p38 MAPK inhibitor for p38α with IC50 of 7.1 nM.
MOA
p38 MAPK inhibitor
Target(s)
MAPK14
Indication(s)
Unknown
Phase
Phase 2
Canonical SMILES
CCc1nc(c(s1)-c1ccnc(NC(=O)c2ccccc2)c1)-c1cccc(C)c1
InChI key
InChIKey=HEKAIDKUDLCBRU-UHFFFAOYSA-N
InChI string
InChI=1S/C24H21N3OS/c1-3-21-27-22(18-11-7-8-16(2)14-18)23(29-21)19-12-13-25-20(15-19)26-24(28)17-9-5-4-6-10-17/h4-15H,3H2,1-2H3,(H,25,26,28)
Molecular formula
C24H21N3OS
Molecular weight
399.508
External links
PubChem
9952773
Wikipedia
http://www.selleckchem.com/products/tak-715.html
SEP-L1000
BRD-K52751261
Predicted MOAs
MOA
Probability
cyclooxygenase inhibitor
0.3741
PI3K inhibitor
0.1936
PARP inhibitor
0.1252
dopamine receptor antagonist
0.0445
PLK inhibitor
0.0395
histamine receptor antagonist
0.0356
EGFR inhibitor
0.0237
HDAC inhibitor
0.0184
MEK inhibitor
0.0180
Aurora kinase inhibitor
0.0173
Chemical structure