BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetGTPase KRas [G12C]
LigandBDBM608984
Substrate/Competitorn/a
Meas. Tech.Scintillation Proximity Assay (SPA)
IC50 46.0±n/a nM
Citation Cotesta, SGerspacher, MLeblanc, CLorthiois, ELLiu, BMachauer, RMah, RMura, CRigollier, PSchneider, NStutz, SVaupel, AWarin, NWilcken, R Pyrazolyl derivatives useful as anti-cancer agents US Patent US11702409 Publication Date 7/18/2023
More Info.:Get all data from this article,  Assay Method
 
GTPase KRas [G12C]
Name:GTPase KRas [G12C]
Synonyms:GTPase KRas (G12C) | KRAS | KRAS2 | RASK2 | RASK_HUMAN
Type:Enzyme Catalytic Domain
Mol. Mass.:21702.19
Organism:Homo sapiens (Human)
Description:P01116[G12C]
Residue:189
Sequence:
MTEYKLVVVGACGVGKSALTIQLIQNHFVDEYDPTIEDSYRKQVVIDGETCLLDILDTAG
QEEYSAMRDQYMRTGEGFLCVFAINNTKSFEDIHHYREQIKRVKDSEDVPMVLVGNKCDL
PSRTVDTKQAQDLARSYGIPFIETSAKTRQRVEDAFYTLVREIRQYRLKKISKEEKTPGC
VKIKKCIIM
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM608984
n/a
NameBDBM608984
Synonyms:US11702409, Example 65a | US11702409, Example 65b
TypeSmall organic molecule
Emp. Form.C32H36ClN7O2
Mol. Mass.586.127
SMILESCN(C)CCNC(=O)c1ccc(cc1)-c1nn(C2CC3(C2)CN(C3)C(=O)C=C)c(C)c1-c1c(Cl)c(C)cc2[nH]ncc12 |(9.33,-6.4,;8.93,-4.91,;10.02,-3.82,;7.44,-4.51,;7.04,-3.02,;5.56,-2.63,;4.47,-3.71,;4.79,-5.22,;3,-3.24,;1.86,-4.27,;.39,-3.79,;.07,-2.29,;1.22,-1.26,;2.68,-1.73,;-1.39,-1.81,;-1.87,-.35,;-3.41,-.35,;-4.18,.99,;-5.66,1.39,;-5.27,2.87,;-3.78,2.48,;-6.75,3.27,;-6.35,4.76,;-4.87,4.36,;-7.44,5.85,;-7.04,7.34,;-8.93,5.45,;-10.02,6.54,;-3.88,-1.81,;-5.35,-2.29,;-2.64,-2.72,;-2.64,-4.26,;-3.97,-5.03,;-5.3,-4.26,;-3.97,-6.57,;-5.3,-7.34,;-2.64,-7.34,;-1.3,-6.57,;.16,-7.04,;1.07,-5.8,;.16,-4.55,;-1.3,-5.03,)|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: