Drug General Information |
Drug ID |
D0U3WQ
|
Former ID |
DIB018776
|
Drug Name |
AGL 2043
|
Synonyms |
AGL-2043; HMS3229A05; AGL2043
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
Download
2D MOL
|
Formula |
C15H12N4S
|
InChI |
InChI=1S/C15H12N4S/c1-9-17-12-6-11-10(7-14(12)19(9)2)16-8-13(18-11)15-4-3-5-20-15/h3-8H,1-2H3
|
InChIKey |
ZGDACLBJJXLKJY-UHFFFAOYSA-N
|
PubChem Compound ID |
|
PubChem Substance ID |
14775296, 24121527, 26758177, 44853130, 47943735, 77674142, 99302611, 121380097, 141995359, 163132525, 163315706, 163688651, 172649782, 175607386, 178102541, 198983575, 227116437, 244346939, 249776632
|
Target and Pathway |
Target(s) |
Beta platelet-derived growth factor receptor |
Target Info |
Inhibitor |
[1]
|
KEGG Pathway
|
MAPK signaling pathway
|
Ras signaling pathway
|
Rap1 signaling pathway
|
Calcium signaling pathway
|
Cytokine-cytokine receptor interaction
|
PI3K-Akt signaling pathway
|
Focal adhesion
|
Gap junction
|
Regulation of actin cytoskeleton
|
HTLV-I infection
|
Pathways in cancer
|
MicroRNAs in cancer
|
Glioma
|
Prostate cancer
|
Melanoma
|
Central carbon metabolism in cancer
|
Choline metabolism in cancer
|
PANTHER Pathway
|
Angiogenesis
|
PDGF signaling pathway
|
Pathway Interaction Database
|
Signaling events mediated by PTP1B
|
Beta3 integrin cell surface interactions
|
S1P3 pathway
|
Nectin adhesion pathway
|
Signaling events mediated by TCPTP
|
SHP2 signaling
|
S1P1 pathway
|
Urokinase-type plasminogen activator (uPA) and uPAR-mediated signaling
|
PDGFR-beta signaling pathway
|
Validated targets of C-MYC transcriptional repression
|
PDGF receptor signaling network
|
Reactome
|
PIP3 activates AKT signaling
|
Constitutive Signaling by Aberrant PI3K in Cancer
|
RAF/MAP kinase cascade
|
WikiPathways
|
Regulation of Actin Cytoskeleton
|
MAPK Signaling Pathway
|
Osteoblast Signaling
|
Focal Adhesion
|
PIP3 activates AKT signaling
|
PDGF Pathway
|
Signaling Pathways in Glioblastoma
|
Signaling by PDGF
|
References |
REF 1 | Tricyclic quinoxalines as potent kinase inhibitors of PDGFR kinase, Flt3 and Kit. Bioorg Med Chem. 2003 May 1;11(9):2007-18. |