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Details

Stereochemistry ACHIRAL
Molecular Formula C8H10ClN3S
Molecular Weight 215.703
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TIAMENIDINE

SMILES

CC1=CSC(Cl)=C1NC2=NCCN2

InChI

InChIKey=CVWILQHZFWRYPB-UHFFFAOYSA-N
InChI=1S/C8H10ClN3S/c1-5-4-13-7(9)6(5)12-8-10-2-3-11-8/h4H,2-3H2,1H3,(H2,10,11,12)

HIDE SMILES / InChI

Molecular Formula C8H10ClN3S
Molecular Weight 215.703
Charge 0
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description

Tiamenidine (also known as HOE 440) is a diazacycloalkene derivative patented by Farbwerke Hoechst A.-G. as 2 alpha-sympathomimetic antihypertensive agents. In preclinical models, tiamenidine induces hypotension and bradycardia in renal hypertensive cats and rats and in normal rats and dogs. Furthermore, Tiamenidine inhibits the liberation of norepinephrine from nerves leading to the heart and suppress sympathetic circulatory reflexes in dogs. In clinical trials, Tiamenidine exerts favor influences on systolic and diastolic blood pressure, and reduces plasma noradrenaline and adrenaline levels and suppresses plasma renin activity. Unfortunately, during the withdrawal of Tiamenidine, there is a rebound of blood pressure and plasma noradrenaline and adrenaline, overshooting baseline levels.

Originator

Approval Year

PubMed

Patents

Sample Use Guides

In Vivo Use Guide
1-3mg for 1 year
Route of Administration: Oral
Substance Class Chemical
Record UNII
195V08O55G
Record Status Validated (UNII)
Record Version