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

Details

Stereochemistry ABSOLUTE
Molecular Formula C19H19N3O5S
Molecular Weight 401.436
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXACILLIN

SMILES

[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)C3=C(C)ON=C3C4=CC=CC=C4)C(O)=O

InChI

InChIKey=UWYHMGVUTGAWSP-JKIFEVAISA-N
InChI=1S/C19H19N3O5S/c1-9-11(12(21-27-9)10-7-5-4-6-8-10)15(23)20-13-16(24)22-14(18(25)26)19(2,3)28-17(13)22/h4-8,13-14,17H,1-3H3,(H,20,23)(H,25,26)/t13-,14+,17-/m1/s1

HIDE SMILES / InChI

Molecular Formula C19H19N3O5S
Molecular Weight 401.436
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 18:03:27 UTC 2023
Edited
by admin
on Sat Dec 16 18:03:27 UTC 2023
Record UNII
UH95VD7V76
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OXACILLIN
INN   MART.   MI   VANDF   WHO-DD  
INN  
Official Name English
OXACILINA
Brand Name English
OXACILLIN [MI]
Common Name English
Oxacillin [WHO-DD]
Common Name English
OXACILLIN [MART.]
Common Name English
OXACILLIN [VANDF]
Common Name English
4-THIA-1-AZABICYCLO(3.2.0)HEPTANE-2-CARBOXYLIC ACID, 3,3-DIMETHYL-6-(((5-METHYL-3-PHENYL-4-ISOXAZOLYL)CARBONYL)AMINO)-7-OXO-,(2S,5R,6R)-
Common Name English
OXAZOCILLINE
Common Name English
oxacillin [INN]
Common Name English
Classification Tree Code System Code
WHO-VATC QJ01CF04
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
NDF-RT N0000011281
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
NDF-RT N0000011281
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
WHO-VATC QG51AG04
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
NDF-RT N0000175497
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
WHO-ATC J01CF04
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
NDF-RT N0000011281
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
NDF-RT N0000011281
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
NDF-RT N0000011281
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
LIVERTOX NBK548078
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
NCI_THESAURUS C1500
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
NDF-RT N0000011281
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
NDF-RT N0000011281
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
NDF-RT N0000011281
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
WHO-VATC QJ51CF04
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
NDF-RT N0000011281
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
Code System Code Type Description
RXCUI
7773
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY RxNorm
NCI_THESAURUS
C62063
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
EPA CompTox
DTXSID8023397
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
CHEBI
7809
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
MESH
D010068
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
EVMPD
SUB09484MIG
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
DAILYMED
UH95VD7V76
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
ChEMBL
CHEMBL819
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
DRUG CENTRAL
2006
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
FDA UNII
UH95VD7V76
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
SMS_ID
100000083558
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
WIKIPEDIA
OXACILLIN
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
DRUG BANK
DB00713
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
PUBCHEM
6196
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
INN
1372
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-635-5
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
CAS
66-79-5
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
MERCK INDEX
m8273
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY Merck Index
LACTMED
Oxacillin
Created by admin on Sat Dec 16 18:03:28 UTC 2023 , Edited by admin on Sat Dec 16 18:03:28 UTC 2023
PRIMARY
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BINDING
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ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC