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Details

Stereochemistry ACHIRAL
Molecular Formula C6H6N2O
Molecular Weight 122.1246
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NIACINAMIDE

SMILES

NC(=O)C1=CN=CC=C1

InChI

InChIKey=DFPAKSUCGFBDDF-UHFFFAOYSA-N
InChI=1S/C6H6N2O/c7-6(9)5-2-1-3-8-4-5/h1-4H,(H2,7,9)

HIDE SMILES / InChI

Molecular Formula C6H6N2O
Molecular Weight 122.1246
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:23:22 UTC 2023
Edited
by admin
on Fri Dec 15 15:23:22 UTC 2023
Record UNII
25X51I8RD4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NIACINAMIDE
FCC   HSDB   II   INCI   ORANGE BOOK   USP   USP-RS   VANDF  
INCI  
Official Name English
TPN COMPONENT NIACINAMIDE
Common Name English
NIACINAMIDE [HSDB]
Common Name English
NIACIN (AS NIACINAMIDE) [VANDF]
Common Name English
NICOTINAMIDE [JAN]
Common Name English
Nicotinamide [WHO-DD]
Common Name English
Nicotinamide
EP   INN   MART.   MI   WHO-DD   WHO-IP  
INN  
Official Name English
NSC-13128
Code English
NICOTINAMIDUM
HPUS   WHO-IP LATIN  
Common Name English
nicotinamide [INN]
Common Name English
NIACINAMIDE [USP MONOGRAPH]
Common Name English
NICOTINAMIDE [EP MONOGRAPH]
Common Name English
NICOTINAMIDE [WHO-IP]
Common Name English
NIACINAMID
Common Name English
NICOTINAMIDE [MART.]
Common Name English
NIACINAMIDE COMPONENT OF TPN
Common Name English
NICOTINAMIDE [EP IMPURITY]
Common Name English
NIACINAMIDE [INCI]
Common Name English
NSC-27452
Code English
NICOTINAMIDE [MI]
Common Name English
NIACINAMIDE [VANDF]
Common Name English
NIACINAMIDE [II]
Common Name English
NIACINAMIDE [USP-RS]
Common Name English
NIACINAMIDE [FCC]
Common Name English
NICOTINAMIDUM [WHO-IP LATIN]
Common Name English
NICOTINAMIDUM [HPUS]
Common Name English
NIACINAMIDE [ORANGE BOOK]
Common Name English
Classification Tree Code System Code
WHO-ATC A11HA01
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
DSLD 2664 (Number of products:4764)
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
NCI_THESAURUS C26017
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
LIVERTOX 681
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
WHO-ESSENTIAL MEDICINES LIST 27
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
NCI_THESAURUS C275
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
DSLD 1097 (Number of products:12)
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
CFR 21 CFR 184.1535
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
DSLD 204 (Number of products:661)
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
WHO-VATC QA11HA01
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
Code System Code Type Description
ECHA (EC/EINECS)
202-713-4
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
NSC
13128
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
RXCUI
7405
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY RxNorm
HSDB
1237
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
DAILYMED
25X51I8RD4
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
MESH
D009536
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
INN
404
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
NSC
27452
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
PUBCHEM
936
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
NCI_THESAURUS
C2327
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
WIKIPEDIA
NICOTINAMIDE
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
CAS
98-92-0
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
EPA CompTox
DTXSID2020929
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
DRUG BANK
DB02701
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
DRUG CENTRAL
1906
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
SMS_ID
100000092193
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
NIACINAMIDE
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY Description: Colourless crystals or a white, crystalline powder; odourless or almost odourless. Solubility: Soluble in 1 part of water and 2 parts of ethanol (~750 g/l) TS; slightly soluble in ether R. Category: Vitamin. Storage: Nicotinamide should be kept in a well-closed container. Definition: Nicotinamide contains not less than 99.0% and not more than 101.0% of C6H6N2O, calculated with reference to thedried substance.
MERCK INDEX
m7878
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY Merck Index
RS_ITEM_NUM
1462006
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
FDA UNII
25X51I8RD4
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
EVMPD
SUB09246MIG
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
CHEBI
17154
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
ChEMBL
CHEMBL1140
Created by admin on Fri Dec 15 15:23:22 UTC 2023 , Edited by admin on Fri Dec 15 15:23:22 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
NAD-dependent lysine desuccinylase activity is inhibited by physiological nicotinamide concentrations, while deacetylase activity is not.
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METABOLITE ACTIVE -> PARENT
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ACTIVE MOIETY