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Details

Stereochemistry RACEMIC
Molecular Formula C10H15N3O5.ClH
Molecular Weight 293.704
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENSERAZIDE HYDROCHLORIDE

SMILES

Cl.NC(CO)C(=O)NNCC1=CC=C(O)C(O)=C1O

InChI

InChIKey=ULFCBIUXQQYDEI-UHFFFAOYSA-N
InChI=1S/C10H15N3O5.ClH/c11-6(4-14)10(18)13-12-3-5-1-2-7(15)9(17)8(5)16;/h1-2,6,12,14-17H,3-4,11H2,(H,13,18);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 C10H15N3O5
Molecular Weight 257.2432
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 Fri Dec 15 15:24:39 UTC 2023
Edited
by admin
on Fri Dec 15 15:24:39 UTC 2023
Record UNII
B66E5RK36Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BENSERAZIDE HYDROCHLORIDE
EP   MART.   MI   WHO-DD  
Common Name English
Benserazide hydrochloride [WHO-DD]
Common Name English
BENSERAZIDE (AS HYDROCHLORIDE)
Common Name English
NSC-755907
Code English
BENSERAZIDE HYDROCHLORIDE [JAN]
Common Name English
BENSERAZIDE HYDROCHLORIDE [MI]
Common Name English
BENSERAZIDE HYDROCHLORIDE [MART.]
Common Name English
BENSERAZIDE HCL
Common Name English
BENSERAZIDE HYDROCHLORIDE [EP MONOGRAPH]
Common Name English
Classification Tree Code System Code
EU-Orphan Drug EU/3/18/2125
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
NCI_THESAURUS C471
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
NCI_THESAURUS C38149
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
Code System Code Type Description
ECHA (EC/EINECS)
238-991-9
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY
NSC
755907
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY
SMS_ID
100000091558
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY
PUBCHEM
26964
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY
EVMPD
SUB00706MIG
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY
EPA CompTox
DTXSID0045412
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY
MERCK INDEX
m2322
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY Merck Index
FDA UNII
B66E5RK36Q
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY
CAS
14919-77-8
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY
RXCUI
235765
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY RxNorm
ChEMBL
CHEMBL1096979
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY
NCI_THESAURUS
C81110
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY
CHEBI
31262
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY
DRUG BANK
DBSALT002687
Created by admin on Fri Dec 15 15:24:40 UTC 2023 , Edited by admin on Fri Dec 15 15:24:40 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
Related Record Type Details
IMPURITY -> PARENT
IMPURITY -> PARENT
IMPURITY -> PARENT
Related Record Type Details
ACTIVE MOIETY