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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H17N3O5S
Molecular Weight 363.388
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CEFADROXIL ANHYDROUS

SMILES

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

InChI

InChIKey=BOEGTKLJZSQCCD-UEKVPHQBSA-N
InChI=1S/C16H17N3O5S/c1-7-6-25-15-11(14(22)19(15)12(7)16(23)24)18-13(21)10(17)8-2-4-9(20)5-3-8/h2-5,10-11,15,20H,6,17H2,1H3,(H,18,21)(H,23,24)/t10-,11-,15-/m1/s1

HIDE SMILES / InChI

Molecular Formula C16H17N3O5S
Molecular Weight 363.388
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 Fri Dec 15 15:56:15 UTC 2023
Edited
by admin
on Fri Dec 15 15:56:15 UTC 2023
Record UNII
Q525PA8JJB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CEFADROXIL ANHYDROUS
Common Name English
CEFADROXIL [JAN]
Common Name English
cefadroxil [INN]
Common Name English
(6R,7R)-7-(((2R)-2-AMINO-2-(4-HYDROXYPHENYL)ACETYL)AMINO)-3-METHYL-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID
Systematic Name English
CEFADROXIL [MI]
Common Name English
ANHYDROUS CEFADROXIL
Common Name English
CEFPROZIL E IMPURITY B [EP IMPURITY]
Common Name English
5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-(((2R)-2-AMINO-2-(4-HYDROXYPHENYL)ACETYL)AMINO)-3-METHYL-8-OXO-, (6R,7R)-
Common Name English
CEFPROZIL MONOHYDRATE IMPURITY B [EP IMPURITY]
Common Name English
Cefadroxil [WHO-DD]
Common Name English
CEFPROZIL IMPURITY B [EP IMPURITY]
Common Name English
Classification Tree Code System Code
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
LIVERTOX NBK548358
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
LIVERTOX NBK548666
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
WHO-ATC J01DB05
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
NDF-RT N0000175488
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
NCI_THESAURUS C357
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
Code System Code Type Description
INN
3719
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY
MERCK INDEX
m3185
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY Merck Index
EVMPD
SUB121209
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY
CHEBI
3479
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY
RXCUI
1545975
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY RxNorm
EVMPD
SUB06164MIG
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY
FDA UNII
Q525PA8JJB
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY
EPA CompTox
DTXSID8022749
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY
CAS
50370-12-2
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY
SMS_ID
100000081356
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY
NCI_THESAURUS
C79562
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY
DAILYMED
Q525PA8JJB
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY
ECHA (EC/EINECS)
256-555-6
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY
PUBCHEM
47965
Created by admin on Fri Dec 15 15:56:15 UTC 2023 , Edited by admin on Fri Dec 15 15:56:15 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SOLVATE->ANHYDROUS
SUBSTANCE->BASIS OF STRENGTH
SOLVATE->ANHYDROUS
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Related Record Type Details
ACTIVE MOIETY