General
Preferred name
SAR-125844
Synonyms
SAR125884 hydrochlorid (1116743-46-4(free base)) ()
SAR125884 ()
SAR125844 ()
SAR 125844 ()
P&D ID
PD101312
CAS
1116743-46-4
Tags
available
drug candidate
Drug indication
Solid tumour/cancer
Drug Status
investigational
Max Phase
2.0
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION SAR125844 is inhibitor of the proto-oncogene c-Met (also known as hepatocyte growth factor receptor [HGFR]) with potential antineoplastic activity. Upon intravenous administration, c-Met inhibitor SAR125844 binds to c-Met, thereby disrupting c-Met-mediated signal transduction pathways. This may result in cell growth inhibition in tumors that overexpress c-Met. c-Met, a receptor tyrosine kinase overexpressed or mutated in a variety of cancers, plays an important role in tumor cell proliferation, survival, invasion, metastasis and tumor angiogenesis. (BOC Sciences Bioactive Compounds)
Cell lines
1
Organisms
0
Compound Sets
9
BOC Sciences Bioactive Compounds
Cayman Chemical Bioactives
ChEMBL Drugs
DrugBank
DrugMAP
MedChem Express Bioactive Compound Library
ReFrame library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
External IDs
18
Properties
(calculated by RDKit )
Molecular Weight
550.14
Hydrogen Bond Acceptors
10
Hydrogen Bond Donors
2
Rotatable Bonds
7
Ring Count
6
Aromatic Ring Count
5
cLogP
4.15
TPSA
109.57
Fraction CSP3
0.24
Chiral centers
0.0
Largest ring
6.0
QED
0.31
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Pathway
Tyrosine Kinase/Adaptors
"Protein Tyrosine Kinase/RTK
Apoptosis
MAPK/ERK Pathway
PI3K/Akt/mTOR
Protein Tyrosine Kinase/RTK
Target
MET RTK
Akt
c-Met/HGFR
MEK
PI3K
c-Met
Solubility
Soluble in DMSO
Source data