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Details

Stereochemistry ACHIRAL
Molecular Formula C23H28N8
Molecular Weight 416.522
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FORASARTAN

SMILES

CCCCC1=NN(CC2=CN=C(C=C2)C3=CC=CC=C3C4=NN=NN4)C(CCCC)=N1

InChI

InChIKey=YONOBYIBNBCDSJ-UHFFFAOYSA-N
InChI=1S/C23H28N8/c1-3-5-11-21-25-22(12-6-4-2)31(28-21)16-17-13-14-20(24-15-17)18-9-7-8-10-19(18)23-26-29-30-27-23/h7-10,13-15H,3-6,11-12,16H2,1-2H3,(H,26,27,29,30)

HIDE SMILES / InChI

Molecular Formula C23H28N8
Molecular Weight 416.522
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Forasartan (also known as SC-52458) was developed as an orally active, competitive angiotensin (Ang) II subtype 1 (AT1)-receptor antagonist for the treatment of hypertension. Forasartan competes with angiotensin II for binding at the AT1 receptor subtype. It is known that angiotensin II is a vasoconstrictor and stimulates the synthesis and release of aldosterone, and blockage of its effects results in a decrease in systemic vascular resistance. Information about the further development of forasartan is not available.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P30556
Gene ID: 185.0
Gene Symbol: AGTR1
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
Non-peptide angiotensin II receptor antagonists: chemical feature based pharmacophore identification.
2003 Feb 27

Sample Use Guides

two groups of eight healthy men ingested placebo or increasing single oral doses (10, 25, and 50 mg or 100, 150, and 200 mg) of SC-52458 (FORASARTAN).
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:47:30 GMT 2023
Edited
by admin
on Fri Dec 15 15:47:30 GMT 2023
Record UNII
065F7WPT0B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FORASARTAN
INN   USAN  
USAN   INN  
Official Name English
forasartan [INN]
Common Name English
FORASARTAN [USAN]
Common Name English
5-[(3,5-Dibutyl-1H-1,2,4-triazol-1-yl)methyl]-2-(O-1H-tetrazol-5-ylphenyl)pyridine
Common Name English
PYRIDINE, 5-((3,5-DIBUTYL-1H-1,2,4-TRIAZOL-1-YL)METHYL)-2-(2-(1H-TETRAZOL-5-YL)PHENYL)-
Systematic Name English
SC-52458
Code English
Classification Tree Code System Code
NCI_THESAURUS C66930
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
Code System Code Type Description
CAS
145216-43-9
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
PUBCHEM
132706
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
DRUG BANK
DB01342
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
CHEBI
141552
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
SMS_ID
100000080432
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
INN
7415
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
ChEMBL
CHEMBL315021
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
IUPHAR
6896
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
WIKIPEDIA
Forasartan
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
EVMPD
SUB07781MIG
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
NCI_THESAURUS
C65749
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
MESH
C084927
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
FDA UNII
065F7WPT0B
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
USAN
GG-68
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID70162942
Created by admin on Fri Dec 15 15:47:30 GMT 2023 , Edited by admin on Fri Dec 15 15:47:30 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY