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Details

Stereochemistry ACHIRAL
Molecular Formula C27H30N7OS.K.3H2O
Molecular Weight 593.783
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FIMASARTAN POTASSIUM TRIHYDRATE

SMILES

O.O.O.[K+].CCCCC1=NC(C)=C(CC(=S)N(C)C)C(=O)N1CC2=CC=C(C=C2)C3=CC=CC=C3C4=NN=N[N-]4

InChI

InChIKey=IJEKJHQBGZFMMI-UHFFFAOYSA-N
InChI=1S/C27H30N7OS.K.3H2O/c1-5-6-11-24-28-18(2)23(16-25(36)33(3)4)27(35)34(24)17-19-12-14-20(15-13-19)21-9-7-8-10-22(21)26-29-31-32-30-26;;;;/h7-10,12-15H,5-6,11,16-17H2,1-4H3;;3*1H2/q-1;+1;;;

HIDE SMILES / InChI

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C27H31N7OS
Molecular Weight 501.646
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula K
Molecular Weight 39.0983
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/23811571, http://www.boryung.co.kr/eng/product/mainProduct.do

Fimasartan is a angiotensin II receptor antagonist which was developed in Korea for the treatment of hypertension. The drug is available in different forms: Kanarb, Dukarb (in combination with Amlodipine), Tuvero (in combination with Rosuvastatin). Fimasartan was tested to be effective in Mexican and Russian population and now is being tested in the USA.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.13 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
KANARB

Approved Use

For the treatment of essential hypertension.

Launch Date

1.28329921E12
PubMed

PubMed

TitleDatePubMed
Fimasartan, anti-hypertension drug, suppressed inducible nitric oxide synthase expressions via nuclear factor-kappa B and activator protein-1 inactivation.
2013
Influence of Fimasartan (a Novel AT(1) Receptor Blocker) on Catecholamine Release in the Adrenal Medulla of Spontaneously Hypertensive Rats.
2013 Feb
Effect of renal function on the pharmacokinetics of fimasartan: a single-dose, open-label, Phase I study.
2014
Patents

Sample Use Guides

Fimasartan is taken as a single oral dose of 60-mg tablet or a single 30-mg intravenous (IV) infusion.
Route of Administration: Other
Rabbit thoracic aorta cells were incubated with different concentrations of fimasartan ((0.1, 1, 10 nM). At those concentrations fimasartan caused nonparallel rightward shifts in the concentration–contractile response curve to Ang II with a significant reduction in the maximal contractile response to 96.6, 47 and 18%, respectively.
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:10:40 UTC 2023
Edited
by admin
on Sat Dec 16 08:10:40 UTC 2023
Record UNII
4516BN0T4B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FIMASARTAN POTASSIUM TRIHYDRATE
WHO-DD  
Common Name English
5-PYRIMIDINEETHANETHIOAMIDE, 2-BUTYL-1,6-DIHYDRO-N,N,4-TRIMETHYL-6-OXO-1-((2'-(2H-TETRAZOL-5-YL)(1,1'-BIPHENYL)-4-YL)METHYL)-, POTASSIUM SALT, HYDRATE (1:1:3)
Systematic Name English
BR-A-657
Code English
Fimasartan potassium trihydrate [WHO-DD]
Common Name English
Code System Code Type Description
DRUG BANK
DBSALT001281
Created by admin on Sat Dec 16 08:10:40 UTC 2023 , Edited by admin on Sat Dec 16 08:10:40 UTC 2023
PRIMARY
PUBCHEM
46929800
Created by admin on Sat Dec 16 08:10:40 UTC 2023 , Edited by admin on Sat Dec 16 08:10:40 UTC 2023
PRIMARY
CAS
1020110-23-9
Created by admin on Sat Dec 16 08:10:40 UTC 2023 , Edited by admin on Sat Dec 16 08:10:40 UTC 2023
PRIMARY
SMS_ID
100000165808
Created by admin on Sat Dec 16 08:10:40 UTC 2023 , Edited by admin on Sat Dec 16 08:10:40 UTC 2023
PRIMARY
FDA UNII
4516BN0T4B
Created by admin on Sat Dec 16 08:10:40 UTC 2023 , Edited by admin on Sat Dec 16 08:10:40 UTC 2023
PRIMARY
EVMPD
SUB179690
Created by admin on Sat Dec 16 08:10:40 UTC 2023 , Edited by admin on Sat Dec 16 08:10:40 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
ANHYDROUS->SOLVATE
Related Record Type Details
ACTIVE MOIETY