CEFOPERAZONE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C25H27N9O8S2
Molecular Weight	645.667
Optical Activity	UNSPECIFIED
Defined Stereocenters	3 / 3
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CEFOPERAZONE

Structure Search

SMILES

[H][C@]12SCC(CSC3=NN=NN3C)=C(N1C(=O)[C@H]2NC(=O)[C@H](NC(=O)N4CCN(CC)C(=O)C4=O)C5=CC=C(O)C=C5)C(O)=O

InChI

InChIKey=GCFBRXLSHGKWDP-XCGNWRKASA-N

InChI=1S/C25H27N9O8S2/c1-3-32-8-9-33(21(39)20(32)38)24(42)27-15(12-4-6-14(35)7-5-12)18(36)26-16-19(37)34-17(23(40)41)13(10-43-22(16)34)11-44-25-28-29-30-31(25)2/h4-7,15-16,22,35H,3,8-11H2,1-2H3,(H,26,36)(H,27,42)(H,40,41)/t15-,16-,22-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C25H27N9O8S2
Molecular Weight	645.667
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 16:34:23 UTC 2023` Edited by `admin` on `Fri Dec 15 16:34:23 UTC 2023`
Record UNII	7U75I1278D
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

CEFOPERAZONE

Official Name

English

CEFOPERAZONE [MI]

Common Name

English

CEFOPERAZONE [VANDF]

Common Name

English

cefoperazone [INN]

Common Name

English

PERACEF

Brand Name

English

5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-(((((4-ETHYL-2,3-DIOXO-1-PIPERAZINYL)CARBONYL)AMINO)(4-HYDROXYPHENYL)ACETYL)AMINO)-3-(((1-METHYL-1H-TETRAZOL-5-YL)THIO)METHYL)-8-OXO, (6R-(6.ALPHA.,7.BETA.(R*)))-

Common Name

English

Cefoperazone [WHO-DD]

Common Name

English

(6R,7R)-7-((R)-2-(4-ETHYL-2,3-DIOXO-1-PIPERAZINECARBOXAMIDO)-2-(P-HYDROXYPHENYL)ACETAMIDO-3-(((1-METHYL-1H-TETRAZOL-5-YL)THIO)METHYL)-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID

Common Name

English

Classification Tree Code System Code

NDF-RT

N0000011161

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

NDF-RT

N0000011161

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

WHO-VATC

QJ01DD62

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

NDF-RT

N0000011161

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

WHO-ATC

J01DD62

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

LIVERTOX

NBK547862

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

NDF-RT

N0000011161

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

NDF-RT

N0000011161

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

NDF-RT

N0000011161

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

NDF-RT

N0000011161

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

NDF-RT

N0000011161

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

LIVERTOX

NBK548666

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

NDF-RT

N0000011161

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

WHO-VATC

QJ51DD12

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

NCI_THESAURUS

C357

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

WHO-ATC

J01DD12

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

WHO-VATC

QJ01DD12

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

NDF-RT

N0000175488

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

NDF-RT

N0000011161

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

NDF-RT

N0000011161

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

NDF-RT

N0000011161

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

Code System Code Type Description

FDA UNII

7U75I1278D

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

ECHA (EC/EINECS)

263-749-4

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

CHEBI

3493

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

DRUG CENTRAL

543

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

PUBCHEM

44187

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

EVMPD

SUB07402MIG

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

WIKIPEDIA

CEFOPERAZONE

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

ChEMBL

CHEMBL507674

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

NCI_THESAURUS

C61663

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

MERCK INDEX

m3201

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

Merck Index

CAS

62893-19-0

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

SMS_ID

100000081804

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

LACTMED

Cefoperazone

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

MESH

D002438

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

RXCUI

2184

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

RxNorm

EPA CompTox

DTXSID2022759

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

DRUG BANK

DB01329

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

INN

4742

Created by admin on Fri Dec 15 16:34:23 UTC 2023 , Edited by admin on Fri Dec 15 16:34:23 UTC 2023

PRIMARY

Related Record Type Details


					ZWJ2Y6JZWY

OAT-3

TRANSPORTER -> INHIBITOR


					P4ABU378WM

Cefoperazone Dihydrate

SOLVATE->ANHYDROUS

Amount:


					4HZ67LW8L7

OAT-4

TRANSPORTER -> INHIBITOR


					I81U7H57XI

OAT-1

TRANSPORTER -> INHIBITOR


					P4ABU378WM

Cefoperazone Dihydrate

SALT/SOLVATE -> PARENT

Amount:


					5840721PJZ

OAT-2

TRANSPORTER -> INHIBITOR

Amount:


					5FQG9774WD

CEFOPERAZONE SODIUM

SALT/SOLVATE -> PARENT

Amount:

Related Record Type Details


					ZRB9LL6WTB

1-METHYL-5-MERCAPTOTETRAZOLE

METABOLITE TOXIC -> PARENT

Amount:

Related Record Type Details


					7U75I1278D

ACTIVE MOIETY

Amount:

Name	Property Type	Amount	Referenced Substance	Defining	Parameters	References
Biological Half-life	PHARMACOKINETIC