General
Preferred name
MACITENTAN
Synonyms
ACT-064992 ()
Macitentan?(ACT 064992) ()
ACT 064992 ()
Opsumit ()
Macitentan-d4 ()
P&D ID
PD009165
CAS
441798-33-0
1258428-05-5
Tags
available
drug
Approved by
EMA
FDA
First approval
2013
2010
Drug Status
approved
Drug indication
Cardiovascular disease
Max Phase
Phase 4
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
TOXICITY Macitentan has a black box warning of embryo-fetal toxicity. Special precautions must be taken for all females of child-bearing age, and women who are pregnant must not be given macitentan. ;
DESCRIPTION Macitentan is an endothelin receptor antagonist (ERA). It exhibits approximately 50-fold selectivity for the ETA receptor over the ETB receptor . (GtoPdb)
Compound Sets
23
AdooQ Bioactive Compound Library
Cayman Chemical Bioactives
ChEMBL Approved Drugs
ChEMBL Drugs
Concise Guide to Pharmacology 2017/18
Concise Guide to Pharmacology 2019/20
Concise Guide to Pharmacology 2021/22
Concise Guide to Pharmacology 2023/24
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
EU-OPENSCREEN Bioactive Compound Library
Guide to Pharmacology
LSP-MoA library (Laboratory of Systems Pharmacology)
MedChem Express Bioactive Compound Library
NCATS Inxight Approved Drugs
ReFrame library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
External IDs
32
Properties
(calculated by RDKit )
Molecular Weight
585.96
Hydrogen Bond Acceptors
8
Hydrogen Bond Donors
2
Rotatable Bonds
11
Ring Count
3
Aromatic Ring Count
3
cLogP
3.57
TPSA
128.22
Fraction CSP3
0.26
Chiral centers
0.0
Largest ring
6.0
QED
0.33
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Pathway
GPCR/G protein
Apoptosis
Target
ET-A
ET-B
EDNRA, EDNRB
Endothelin Receptor
Indication
contraceptive
MOA
Endothelin Receptor antagonist
Source data