U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C18H21N7O4S.ClH
Molecular Weight 467.93
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TIODAZOSIN HYDROCHLORIDE

SMILES

Cl.COC1=CC2=NC(=NC(N)=C2C=C1OC)N3CCN(CC3)C(=O)C4=NN=C(O4)SC

InChI

InChIKey=QASXNJVDTVWTBK-UHFFFAOYSA-N
InChI=1S/C18H21N7O4S.ClH/c1-27-12-8-10-11(9-13(12)28-2)20-17(21-14(10)19)25-6-4-24(5-7-25)16(26)15-22-23-18(29-15)30-3;/h8-9H,4-7H2,1-3H3,(H2,19,20,21);1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C18H21N7O4S
Molecular Weight 431.469
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Tiodazosin is a newly developed antihypertensive agent, structurally related to prazosin. Prazosin and tiodazosin administrated intravenously to anesthetized rats, are equally effective hypotensive agents, but that the hypotensive potency of prazosin is greater than that of tiodazosin. However, chronic administration of equivalent doses of the two compounds for 25 and 52 days via the drinking water indicated approximately equivalent, sustained reductions in blood pressure. Furthermore, at the end of the 52-day chronic dosing period tiodazosin caused appreciably less alpha-adrenergic receptor antagonist activity than prazosin as assessed by the norepinephrine dose-pressor response profiles.

Approval Year

PubMed

PubMed

TitleDatePubMed
Cardiovascular adrenoreceptor function during compensatory and decompensatory hemorrhagic shock.
1984
[New hypotensive drugs].
1984 Dec 17-31
Determination of tiodazosin concentrations in human plasma with a fluorescence high-performance liquid chromatographic method.
1985 Jul 12
Alteration in the pharmacologic activity of alpha 1 adrenergic antagonists by alpha-1-acid glycoprotein.
1989
The effect of alpha 1-acid glycoprotein on the pharmacological activity of alpha 1-adrenergic antagonists in rabbit aortic strips.
1991 Aug
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:19:03 GMT 2023
Edited
by admin
on Fri Dec 15 15:19:03 GMT 2023
Record UNII
8N3U77J896
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TIODAZOSIN HYDROCHLORIDE
Common Name English
PIPERAZINE, 1-(4-AMINO-6,7-DIMETHOXY-2-QUINAZOLINYL)-4-((5-(METHYLTHIO)-1,3,4-OXADIAZOL-2-YL)CARBONYL)-, MONOHYDROCHLORIDE
Common Name English
METHANONE, (4-(4-AMINO-6,7-DIMETHOXY-2-QUINAZOLINYL)-1-PIPERAZINYL)(5-(METHYLTHIO)-1,3,4-OXADIAZOL-2-YL)-, HYDROCHLORIDE (1:1)
Systematic Name English
BL-5111A
Code English
Code System Code Type Description
PUBCHEM
15942777
Created by admin on Fri Dec 15 15:19:03 GMT 2023 , Edited by admin on Fri Dec 15 15:19:03 GMT 2023
PRIMARY
CAS
69873-04-7
Created by admin on Fri Dec 15 15:19:03 GMT 2023 , Edited by admin on Fri Dec 15 15:19:03 GMT 2023
NON-SPECIFIC STOICHIOMETRY
CAS
62412-39-9
Created by admin on Fri Dec 15 15:19:03 GMT 2023 , Edited by admin on Fri Dec 15 15:19:03 GMT 2023
PRIMARY
FDA UNII
8N3U77J896
Created by admin on Fri Dec 15 15:19:03 GMT 2023 , Edited by admin on Fri Dec 15 15:19:03 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY