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Details

Stereochemistry RACEMIC
Molecular Formula C19H25N5O4.ClH
Molecular Weight 423.894
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TERAZOSIN HYDROCHLORIDE ANHYDROUS

SMILES

Cl.COC1=CC2=NC(=NC(N)=C2C=C1OC)N3CCN(CC3)C(=O)C4CCCO4

InChI

InChIKey=IWSWDOUXSCRCKW-UHFFFAOYSA-N
InChI=1S/C19H25N5O4.ClH/c1-26-15-10-12-13(11-16(15)27-2)21-19(22-17(12)20)24-7-5-23(6-8-24)18(25)14-4-3-9-28-14;/h10-11,14H,3-9H2,1-2H3,(H2,20,21,22);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 C19H25N5O4
Molecular Weight 387.4329
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 05:00:55 UTC 2023
Edited
by admin
on Sat Dec 16 05:00:55 UTC 2023
Record UNII
8QOP8Z9955
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TERAZOSIN HYDROCHLORIDE ANHYDROUS
WHO-DD  
Common Name English
ABBOTT-45975 ANHYDROUS
Code English
Terazosin hydrochloride anhydrous [WHO-DD]
Common Name English
TERAZOSIN HYDROCHLORIDE, ANHYDROUS
Common Name English
TERAZOSIN HCL
Common Name English
TERAZOSIN HYDROCHLORIDE [MI]
Common Name English
METHANONE, (4-(4-AMINO-6,7-DIMETHOXY-2-QUINAZOLINYL)-1-PIPERAZINYL)(TETRAHYDRO-2-FURANYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
PIPERAZINE, 1-(4-AMINO-6,7-DIMETHOXY-2-QUINAZOLINYL)-4-((TETRAHYDRO-2-FURANYL)CARBONYL)-, MONOHYDROCHLORIDE
Common Name English
6,7-DIMETHOXY-2-(4-(TETRAHYDROFURAN-2-YLCARBONYL)PIPERAZIN-1-YL)QUINAZOLIN-4-AMINE HYDROCHLORIDE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29713
Created by admin on Sat Dec 16 05:00:56 UTC 2023 , Edited by admin on Sat Dec 16 05:00:56 UTC 2023
Code System Code Type Description
ChEMBL
CHEMBL611
Created by admin on Sat Dec 16 05:00:56 UTC 2023 , Edited by admin on Sat Dec 16 05:00:56 UTC 2023
PRIMARY
FDA UNII
8QOP8Z9955
Created by admin on Sat Dec 16 05:00:56 UTC 2023 , Edited by admin on Sat Dec 16 05:00:56 UTC 2023
PRIMARY
NCI_THESAURUS
C75056
Created by admin on Sat Dec 16 05:00:56 UTC 2023 , Edited by admin on Sat Dec 16 05:00:56 UTC 2023
PRIMARY
EPA CompTox
DTXSID7045493
Created by admin on Sat Dec 16 05:00:56 UTC 2023 , Edited by admin on Sat Dec 16 05:00:56 UTC 2023
PRIMARY
EVMPD
SUB04722MIG
Created by admin on Sat Dec 16 05:00:56 UTC 2023 , Edited by admin on Sat Dec 16 05:00:56 UTC 2023
PRIMARY
RXCUI
1299927
Created by admin on Sat Dec 16 05:00:56 UTC 2023 , Edited by admin on Sat Dec 16 05:00:56 UTC 2023
PRIMARY RxNorm
PUBCHEM
44383
Created by admin on Sat Dec 16 05:00:56 UTC 2023 , Edited by admin on Sat Dec 16 05:00:56 UTC 2023
PRIMARY
SMS_ID
100000092660
Created by admin on Sat Dec 16 05:00:56 UTC 2023 , Edited by admin on Sat Dec 16 05:00:56 UTC 2023
PRIMARY
CAS
63074-08-8
Created by admin on Sat Dec 16 05:00:56 UTC 2023 , Edited by admin on Sat Dec 16 05:00:56 UTC 2023
PRIMARY
MERCK INDEX
m10567
Created by admin on Sat Dec 16 05:00:56 UTC 2023 , Edited by admin on Sat Dec 16 05:00:56 UTC 2023
PRIMARY Merck Index
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
SOLVATE->ANHYDROUS
SUBSTANCE->BASIS OF STRENGTH
SALT/SOLVATE -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY