General
Preferred name
SU5614
Synonyms
SU-5614 ()
(Z)-SU5614 ()
Chloro-SU5416, Chloro-Semaxanib ()
AC1NS4RE ()
SU 5614 ()
P&D ID
PD017779
CAS
1055412-47-9
Tags
available
drug candidate
Drug indication
Airway inflammation
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 (Z)-SU5614 is a potent FLT3 inhibitor and selectively induces growth arrest, apoptosis, and cell cycle arrest in Ba/F3 and AML cell lines expressing a constitutively activated FLT3[1].
PRICE 56
DESCRIPTION (Z)-SU5614 is a FLT3 inhibitor and selectively induces growth arrest, apoptosis, and cell cycle arrest in Ba/F3 and AML cell lines expressing a constitutively activated FLT3. (Enamine Bioactive Compounds)
DESCRIPTION It is a tyrosine kinase inhibitor. (TargetMol Bioactive Compound Library)
Compound Sets
8
AdooQ Bioactive Compound Library
Cayman Chemical Bioactives
DrugMAP
Enamine Bioactive Compounds
MedChem Express Bioactive Compound Library
ReFrame library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
External IDs
15
Properties
(calculated by RDKit )
Molecular Weight
272.07
Hydrogen Bond Acceptors
1
Hydrogen Bond Donors
2
Rotatable Bonds
1
Ring Count
3
Aromatic Ring Count
2
cLogP
3.78
TPSA
44.89
Fraction CSP3
0.13
Chiral centers
0.0
Largest ring
6.0
QED
0.76
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target
tyrosine kinase
Apoptosis
FLT3
Apoptosis related,c-Kit,FLT3,VEGFR
Pathway
Protein Tyrosine Kinase/RTK
Proteases/Proteasome
Source data