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Details

Stereochemistry ACHIRAL
Molecular Formula C7H4O3.Bi.HO
Molecular Weight 362.0926
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BISMUTH SUBSALICYLATE

SMILES

[OH-].[Bi+3].[O-]C(=O)C1=C([O-])C=CC=C1

InChI

InChIKey=ZREIPSZUJIFJNP-UHFFFAOYSA-K
InChI=1S/C7H6O3.Bi.H2O/c8-6-4-2-1-3-5(6)7(9)10;;/h1-4,8H,(H,9,10);;1H2/q;+3;/p-3

HIDE SMILES / InChI
Molecular Formula HO
Molecular Weight 17.0073
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE
Molecular Formula C7H4O3
Molecular Weight 136.1049
Charge -2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE
Molecular Formula Bi
Molecular Weight 208.9804
Charge 3
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:03:59 UTC 2023
Edited
by admin
on Fri Dec 15 15:03:59 UTC 2023
Record UNII
62TEY51RR1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BISMUTH SUBSALICYLATE
EP   GREEN BOOK   HSDB   JAN   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN  
Official Name English
BISMUTH SALICYLATE [MART.]
Common Name English
(2-HYDROXYBENZOATO-O(SUP 1))-OXOBISMUTH
Common Name English
Bismuth subsalicylate [WHO-DD]
Common Name English
2-HYDROXYBENZOIC ACID BISMUTH (3+) SALT
Common Name English
BISMUTH SUBSALICYLATE [VANDF]
Common Name English
BISMUTH SUBSALICYLATE [JAN]
Common Name English
BISMUTH SUBSALICYLATE [USP MONOGRAPH]
Common Name English
BISMUTH SUBSALICYLATE [HSDB]
Common Name English
BISMUTH SUBSALICYLATE [USAN]
Common Name English
BISMUTH SUBSALICYLATE [EP IMPURITY]
Common Name English
BISMUTH SUBSALICYLATE [EP MONOGRAPH]
Common Name English
BISMUTH SUBSALICYLATE [GREEN BOOK]
Common Name English
4H-1,3,2-BENZODIOXABISMIN-4-ONE, 2-HYDROXY-
Systematic Name English
BISMUTH SUBSALICYLATE [USP-RS]
Common Name English
BISMUTH SUBSALICYLATE COMPONENT OF HELIDAC
Common Name English
NSC-759117
Code English
BISMUTH SUBSALICYLATE [ORANGE BOOK]
Common Name English
BISMUTH SUBSALICYLATE [MI]
Common Name English
BISMUTH OXIDE SALICYLATE
Systematic Name English
HELIDAC COMPONENT BISMUTH SUBSALICYLATE
Common Name English
Classification Tree Code System Code
CFR 21 CFR 335.10
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
NCI_THESAURUS C266
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
NDF-RT N0000007888
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
NDF-RT N0000180183
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
NDF-RT N0000007888
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
CFR 21 CFR 335.50
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
NCI_THESAURUS C2080
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
Code System Code Type Description
NSC
759117
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
FDA UNII
62TEY51RR1
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
ChEMBL
CHEMBL1120
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
DRUG BANK
DB01294
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
ECHA (EC/EINECS)
238-953-1
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
WIKIPEDIA
BISMUTH SUBSALICYLATE
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
EVMPD
SUB13093MIG
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
RS_ITEM_NUM
1075553
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
DAILYMED
62TEY51RR1
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
CAS
14882-18-9
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
DRUG CENTRAL
4257
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
HSDB
332
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
RXCUI
19478
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY RxNorm
MERCK INDEX
m2555
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY Merck Index
PUBCHEM
53629521
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
NCI_THESAURUS
C1020
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
LACTMED
Bismuth Subsalicylate
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
CHEBI
261649
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
EPA CompTox
DTXSID6024622
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
MESH
C015715
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
SMS_ID
100000076869
Created by admin on Fri Dec 15 15:03:59 UTC 2023 , Edited by admin on Fri Dec 15 15:03:59 UTC 2023
PRIMARY
Related Record Type Details
Structure of Salicylic acid
PARENT -> SALT/SOLVATE
PLASMA PROTEIN FRACTION (HUMAN)
BINDER->LIGAND
BINDING
Related Record Type Details
Structure of Salicylic acid
ACTIVE MOIETY
Structure of BISMUTH CATION
ACTIVE MOIETY
NIH
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