General
Preferred name
BMS 753
Synonyms
BMS753 ()
P&D ID
PD040105
CAS
215307-86-1
Tags
drug candidate
available
Drug indication
Discovery agent
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION
BMS 753 is an isotype-selective retinoic acid receptor ¦Á (RAR¦Á) agonist, with a Ki of 2 nM[1].
PRICE
73
DESCRIPTION
BMS 753 is an agonist of isotype-selective retinoic acid receptor ?? (RAR??, Ki= 2 nM).
DESCRIPTION
BMS 753 is a RARα-selective agonist (Ki = 2 nM) that modulates the ATRA-inducible cytochrome P450 26A1 (CYP26A1).
(BOC Sciences Bioactive Compounds)
DESCRIPTION
BMS 753 is an agonist of isotype-selective retinoic acid receptor α (RARα, Ki= 2 nM).
(TargetMol Bioactive Compound Library)
DESCRIPTION
RARalpha agonist; anticancer agent
(Tocris Bioactive Compound Library)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Compound Sets
13
BOC Sciences Bioactive Compounds
Cayman Chemical Bioactives
Concise Guide to Pharmacology 2017/18
Concise Guide to Pharmacology 2019/20
Concise Guide to Pharmacology 2021/22
Concise Guide to Pharmacology 2023/24
CZ-OPENSCREEN Bioactive Library
DrugMAP
EUbOPEN Chemogenomics Library
Guide to Pharmacology
MedChem Express Bioactive Compound Library
TargetMol Bioactive Compound Library
Tocris Bioactive Compound Library
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
15
Molecular Weight
351.15
Hydrogen Bond Acceptors
3
Hydrogen Bond Donors
2
Rotatable Bonds
3
Ring Count
3
Aromatic Ring Count
2
cLogP
3.78
TPSA
83.47
Fraction CSP3
0.29
Chiral centers
0.0
Largest ring
6.0
QED
0.88
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target
RARα
RAR/RXR
Primary Target
Retinoic Acid Receptors
MOA
Agonist
Pathway
Metabolic Enzyme/Protease
Vitamin D Related/Nuclear Receptor
Metabolism
Recommended Cell Concentration
1 uM
Source data

