U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C22H29N3O6S
Molecular Weight 463.547
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIVAMPICILLIN

SMILES

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

InChI

InChIKey=ZEMIJUDPLILVNQ-ZXFNITATSA-N
InChI=1S/C22H29N3O6S/c1-21(2,3)20(29)31-11-30-19(28)15-22(4,5)32-18-14(17(27)25(15)18)24-16(26)13(23)12-9-7-6-8-10-12/h6-10,13-15,18H,11,23H2,1-5H3,(H,24,26)/t13-,14-,15+,18-/m1/s1

HIDE SMILES / InChI

Molecular Formula C22H29N3O6S
Molecular Weight 463.547
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:19:13 UTC 2023
Edited
by admin
on Fri Dec 15 16:19:13 UTC 2023
Record UNII
0HLM346LL7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PIVAMPICILLIN
EP   INN   MART.   MI   WHO-DD  
INN  
Official Name English
PIVAMPICILLIN [MART.]
Common Name English
HYDROXYMETHYL D-(-)-6-(2-AMINO-2-PHENYLACETAMIDO)-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO(3.2.0)HEPTANE-2-CARBOXYLATE PIVALATE (ESTER)
Common Name English
PIVAMPICILLIN [MI]
Common Name English
pivampicillin [INN]
Common Name English
Pivampicillin [WHO-DD]
Common Name English
4-THIA-1-AZABICYCLO(3.2.0)HEPTANE-2-CARBOXYLIC ACID, 6-((AMINOPHENYLACETYL)AMINO)-3,3-DIMETHYL-7-OXO-, (2,2-DIMETHYL-1-OXOPROPOXY)METHYL ESTER (2S-(2.ALPHA.,5.ALPHA.,6.BETA.(S*)))-
Common Name English
PIVAMPICILLIN [EP MONOGRAPH]
Common Name English
MK-191
Code English
Classification Tree Code System Code
WHO-VATC QJ51RC21
Created by admin on Fri Dec 15 16:19:14 UTC 2023 , Edited by admin on Fri Dec 15 16:19:14 UTC 2023
WHO-ATC J01CA02
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
NCI_THESAURUS C1500
Created by admin on Fri Dec 15 16:19:14 UTC 2023 , Edited by admin on Fri Dec 15 16:19:14 UTC 2023
WHO-VATC QJ01CA02
Created by admin on Fri Dec 15 16:19:14 UTC 2023 , Edited by admin on Fri Dec 15 16:19:14 UTC 2023
LIVERTOX 784
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
Code System Code Type Description
MERCK INDEX
m8896
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
PRIMARY Merck Index
WIKIPEDIA
PIVAMPICILLIN
Created by admin on Fri Dec 15 16:19:14 UTC 2023 , Edited by admin on Fri Dec 15 16:19:14 UTC 2023
PRIMARY
DRUG BANK
DB01604
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
PRIMARY
EPA CompTox
DTXSID1045459
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
PRIMARY
EVMPD
SUB09949MIG
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
PRIMARY
SMS_ID
100000081685
Created by admin on Fri Dec 15 16:19:14 UTC 2023 , Edited by admin on Fri Dec 15 16:19:14 UTC 2023
PRIMARY
ChEMBL
CHEMBL323354
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
PRIMARY
RXCUI
8372
Created by admin on Fri Dec 15 16:19:14 UTC 2023 , Edited by admin on Fri Dec 15 16:19:14 UTC 2023
PRIMARY RxNorm
INN
2864
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
PRIMARY
PUBCHEM
33478
Created by admin on Fri Dec 15 16:19:14 UTC 2023 , Edited by admin on Fri Dec 15 16:19:14 UTC 2023
PRIMARY
CAS
33817-20-8
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
PRIMARY
FDA UNII
0HLM346LL7
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
PRIMARY
NCI_THESAURUS
C84068
Created by admin on Fri Dec 15 16:19:14 UTC 2023 , Edited by admin on Fri Dec 15 16:19:14 UTC 2023
PRIMARY
DRUG CENTRAL
2218
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
PRIMARY
CHEBI
8255
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
PRIMARY
MESH
D010917
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
PRIMARY
ECHA (EC/EINECS)
251-688-6
Created by admin on Fri Dec 15 16:19:13 UTC 2023 , Edited by admin on Fri Dec 15 16:19:13 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
METABOLITE -> PARENT
Does not undergo extensive metabolism. Excretion in urine. Can lead to depletion of carnitine.
Related Record Type Details
ACTIVE MOIETY