clazosentan 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
endothelin receptor antagonists 5518 180384-56-9

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • clazosentan
  • clazosentan sodium
  • pivlaz
  • Ro 61-1790
  • AXV-034343
  • VML 588
  • ACT-108475
Clazosentan is an endothelin receptor antagonist indicated for the prevention of cerebrovascular spasm after surgery for subarachnoid hemorrhage caused by cerebral aneurysm, and cerebral infarctions and cerebral ischemic symptoms accompanying the cerebrovascular spasm.
  • Molecular weight: 577.58
  • Formula: C25H23N9O6S
  • CLOGP: 2.11
  • LIPINSKI: 2
  • HAC: 15
  • HDO: 3
  • TPSA: 200.11
  • ALOGS: -4.13
  • ROTB: 10

Drug dosage:

None

ADMET properties:

None

Approvals:

DateAgencyCompanyOrphan
Jan. 20, 2022 PMDA IDORSIA PHARMACEUTICALS JAPAN LTD

FDA Adverse Event Reporting System (Female)

None

FDA Adverse Event Reporting System (Male)

None

FDA Adverse Event Reporting System (Geriatric)

None

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

None

Drug Use | Suggest Off label Use Form| |View source of the data|

DiseaseRelationSNOMED_IDDOID
Prevention of cerebrovascular spasm indication 73173006




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

None

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Endothelin-1 receptor GPCR ANTAGONIST Ki 9.89 CHEMBL SCIENTIFIC LITERATURE
Endothelin B receptor GPCR Ki 6.76 CHEMBL

External reference:

IDSource
CHEMBL109648 ChEMBL_ID
C109641 MESH_SUPPLEMENTAL_RECORD_UI
12286 IUPHAR_LIGAND_ID
503271-02-1 SECONDARY_CAS_RN
DB06677 DRUGBANK_ID
C1721268 UMLSCUI
D11664 KEGG_DRUG
8397 INN_ID
6433095 PUBCHEM_CID
3DRR0X4728 UNII

Pharmaceutical products:

None