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Details

Stereochemistry EPIMERIC
Molecular Formula C21H27N3O7S
Molecular Weight 465.52
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BACAMPICILLIN

SMILES

[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)[C@H](N)C3=CC=CC=C3)C(=O)OC(C)OC(=O)OCC

InChI

InChIKey=PFOLLRNADZZWEX-FFGRCDKISA-N
InChI=1S/C21H27N3O7S/c1-5-29-20(28)31-11(2)30-19(27)15-21(3,4)32-18-14(17(26)24(15)18)23-16(25)13(22)12-9-7-6-8-10-12/h6-11,13-15,18H,5,22H2,1-4H3,(H,23,25)/t11?,13-,14-,15+,18-/m1/s1

HIDE SMILES / InChI
Molecular Formula C21H27N3O7S
Molecular Weight 465.52
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 4 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Sat Dec 16 15:49:49 UTC 2023
Edited
by admin
on Sat Dec 16 15:49:49 UTC 2023
Record UNII
8GM2J22278
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BACAMPICILLIN
INN   MI   VANDF   WHO-DD  
INN  
Official Name English
BACAMPICILLIN [MI]
Common Name English
BACAMPICILLIN [VANDF]
Common Name English
4-THIA-1-AZABICYCLO(3.2.0)HEPTANE-2-CARBOXYLIC ACID, 6-((AMINOPHENYLACETYL)AMINO)-3,3-DIMETHYL-7-OXO-, 1-((ETHOXYCARBONYL)OXY)ETHYL ESTER, (2S-(2.ALPHA.,5.ALPHA.,6.BETA.(S*)))-
Common Name English
Bacampicillin [WHO-DD]
Common Name English
PENGLOBE
Brand Name English
bacampicillin [INN]
Common Name English
Classification Tree Code System Code
WHO-ATC J01CA06
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
WHO-VATC QJ01CA06
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
LIVERTOX 86
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
NCI_THESAURUS C1500
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
Code System Code Type Description
WIKIPEDIA
BACAMPICILLIN
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
ChEMBL
CHEMBL1583
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
CAS
50972-17-3
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
INN
3630
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
SMS_ID
100000090507
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
FDA UNII
8GM2J22278
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
DRUG BANK
DB01602
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
EPA CompTox
DTXSID2048030
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
CHEBI
2968
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
DRUG CENTRAL
280
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
LACTMED
Bacampicillin
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
PUBCHEM
441397
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
RXCUI
18687
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY RxNorm
EVMPD
SUB05666MIG
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
NCI_THESAURUS
C65245
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY
MERCK INDEX
m2194
Created by admin on Sat Dec 16 15:49:50 UTC 2023 , Edited by admin on Sat Dec 16 15:49:50 UTC 2023
PRIMARY Merck Index
Related Record Type Details
Structure of BACAMPICILLIN HYDROCHLORIDE
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of AMPICILLIN
METABOLITE ACTIVE -> PRODRUG
NIH
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