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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H21N6O7S2.H
Molecular Weight 546.576
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CEFTAZIDIME ANHYDROUS

SMILES

[H+].[H][C@]12SCC(C[N+]3=CC=CC=C3)=C(N1C(=O)[C@H]2NC(=O)C(=N/OC(C)(C)C([O-])=O)\C4=CSC(N)=N4)C([O-])=O

InChI

InChIKey=ORFOPKXBNMVMKC-DWVKKRMSSA-N
InChI=1S/C22H22N6O7S2/c1-22(2,20(33)34)35-26-13(12-10-37-21(23)24-12)16(29)25-14-17(30)28-15(19(31)32)11(9-36-18(14)28)8-27-6-4-3-5-7-27/h3-7,10,14,18H,8-9H2,1-2H3,(H4-,23,24,25,29,31,32,33,34)/b26-13-/t14-,18-/m1/s1

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
CEFTAZIDIME ANHYDROUS
Common Name English
NSC-759260
Code English
1-(((6R,7R)-7-(2-(2-AMINO-4-THIAZOLYL)GLYOXYLAMIDO)-2-CARBOXY-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-EN-3-YL)METHYL)PYRIDINIUM HYDROXIDE INNER SALT 7(SUP 2)-(Z)-(O-(1-CARBOXY-1-METHYLETHYL)OXIME)
Common Name English
1-(((6R,7R)-7-(((2Z)-(2-AMINO-4-THIAZOLYL)((1-CARBOXY-1-METHYLETHOXY)IMINO)ACETYL)AMINO)-2-CARBOXY-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-EN-3-YL)METHYL)PYRIDINIUM INNER SALT
Common Name English
PYRIDINIUM, 1-(((6R,7R)-7-(((2Z)-(2-AMINO-4-THIAZOLYL)((1-CARBOXY-1-METHYLETHOXY)IMINO)ACETYL)AMINO)-2-CARBOXY-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-EN-3-YL)METHYL)-, INNER SALT
Common Name English
PYRIDINIUM, 1-((7-(((2-AMINO-4-THIAZOLYL)((1-CARBOXY-1-METHYLETHOXY)IMINO)ACETYL)AMINO)-2-CARBOXY-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-EN-3-YL)METHYL)-, HYDROXIDE, INNER SALT, (6R-(6.ALPHA.,7.BETA.(Z)))-
Common Name English
ceftazidime [INN]
Common Name English
CEFTAZIDIME [MI]
Common Name English
Ceftazidime [WHO-DD]
Common Name English
Classification Tree Code System Code
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
NCI_THESAURUS C357
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
WHO-ATC J01DD02
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
NDF-RT N0000175488
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
LIVERTOX NBK548666
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
LIVERTOX NBK547862
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
NDF-RT N0000011161
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
Code System Code Type Description
CHEBI
3508
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY
INN
4886
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY
NSC
759260
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY
DAILYMED
DZR1ENT301
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY
PUBCHEM
5481173
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY
CAS
72558-82-8
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY
FDA UNII
DZR1ENT301
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY
SMS_ID
100000092630
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY
EVMPD
SUB07422MIG
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY
MERCK INDEX
m3218
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY Merck Index
RXCUI
1545984
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
276-715-9
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY
NCI_THESAURUS
C90827
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY
EVMPD
SUB115175
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY
EPA CompTox
DTXSID5022770
Created by admin on Fri Dec 15 15:53:49 UTC 2023 , Edited by admin on Fri Dec 15 15:53:49 UTC 2023
PRIMARY
SALT/SOLVATE (PARENT)
Structure of CEFTAZIDIME
NIH
NCATS
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DISCLAIMER
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