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Details

Stereochemistry ACHIRAL
Molecular Formula C25H26N6O
Molecular Weight 426.5135
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PRATOSARTAN

SMILES

CCCC1=NC2=C(N1CC3=CC=C(C=C3)C4=CC=CC=C4C5=NN=NN5)C(=O)CCCC2

InChI

InChIKey=KCTFTBCZZUBAKN-UHFFFAOYSA-N
InChI=1S/C25H26N6O/c1-2-7-23-26-21-10-5-6-11-22(32)24(21)31(23)16-17-12-14-18(15-13-17)19-8-3-4-9-20(19)25-27-29-30-28-25/h3-4,8-9,12-15H,2,5-7,10-11,16H2,1H3,(H,27,28,29,30)

HIDE SMILES / InChI

Molecular Formula C25H26N6O
Molecular Weight 426.5135
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Pratosartan is an orally active angiotensin II type 1 receptor blocker. It is being developed for the treatment of hypertension. Pratosartan was efficacious throughout the long-term study, without serious adverse effects. Pratosartan significantly decreased serum total cholesterol in patients with hypercholesterolemia and uric acid in patients with hyperuricemia. It may have beneficial effects on hypertensive patients with some metabolic disorders. Pratosartan is still in phase III development in South Korea and phase II in Japan for hypertension.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:48:41 GMT 2023
Edited
by admin
on Fri Dec 15 15:48:41 GMT 2023
Record UNII
66VLQ6E6DL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PRATOSARTAN
INN   JAN   WHO-DD  
INN  
Official Name English
KT3-671
Code English
Pratosartan [WHO-DD]
Common Name English
pratosartan [INN]
Common Name English
PRATOSARTAN [JAN]
Common Name English
DA-727
Code English
Classification Tree Code System Code
NCI_THESAURUS C66930
Created by admin on Fri Dec 15 15:48:42 GMT 2023 , Edited by admin on Fri Dec 15 15:48:42 GMT 2023
Code System Code Type Description
CHEBI
32041
Created by admin on Fri Dec 15 15:48:42 GMT 2023 , Edited by admin on Fri Dec 15 15:48:42 GMT 2023
PRIMARY
CAS
153804-05-8
Created by admin on Fri Dec 15 15:48:42 GMT 2023 , Edited by admin on Fri Dec 15 15:48:42 GMT 2023
PRIMARY
MESH
C528642
Created by admin on Fri Dec 15 15:48:42 GMT 2023 , Edited by admin on Fri Dec 15 15:48:42 GMT 2023
PRIMARY
FDA UNII
66VLQ6E6DL
Created by admin on Fri Dec 15 15:48:42 GMT 2023 , Edited by admin on Fri Dec 15 15:48:42 GMT 2023
PRIMARY
SMS_ID
300000034285
Created by admin on Fri Dec 15 15:48:42 GMT 2023 , Edited by admin on Fri Dec 15 15:48:42 GMT 2023
PRIMARY
ChEMBL
CHEMBL41194
Created by admin on Fri Dec 15 15:48:42 GMT 2023 , Edited by admin on Fri Dec 15 15:48:42 GMT 2023
PRIMARY
INN
8100
Created by admin on Fri Dec 15 15:48:42 GMT 2023 , Edited by admin on Fri Dec 15 15:48:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID90934820
Created by admin on Fri Dec 15 15:48:42 GMT 2023 , Edited by admin on Fri Dec 15 15:48:42 GMT 2023
PRIMARY
PUBCHEM
9802561
Created by admin on Fri Dec 15 15:48:42 GMT 2023 , Edited by admin on Fri Dec 15 15:48:42 GMT 2023
PRIMARY
NCI_THESAURUS
C72935
Created by admin on Fri Dec 15 15:48:42 GMT 2023 , Edited by admin on Fri Dec 15 15:48:42 GMT 2023
PRIMARY
Related Record Type Details
TRANSPORTER -> INHIBITOR
TRANSPORTER -> INHIBITOR
TRANSPORTER -> INHIBITOR
TRANSPORTER -> INHIBITOR
TARGET -> INHIBITOR
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ACTIVE MOIETY