CEPHALOTHIN

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C16H16N2O6S2
Molecular Weight	396.438
Optical Activity	UNSPECIFIED
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CEPHALOTHIN

Structure Search

SMILES

[H][C@]12SCC(COC(C)=O)=C(N1C(=O)[C@H]2NC(=O)CC3=CC=CS3)C(O)=O

InChI

InChIKey=XIURVHNZVLADCM-IUODEOHRSA-N

InChI=1S/C16H16N2O6S2/c1-8(19)24-6-9-7-26-15-12(14(21)18(15)13(9)16(22)23)17-11(20)5-10-3-2-4-25-10/h2-4,12,15H,5-7H2,1H3,(H,17,20)(H,22,23)/t12-,15-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C16H16N2O6S2
Molecular Weight	396.438
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:02:14 UTC 2023` Edited by `admin` on `Fri Dec 15 15:02:14 UTC 2023`
Record UNII	R72LW146E6
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

CEPHALOTHIN

Common Name

English

CEPHALOTHIN [HSDB]

Common Name

English

CEFALOTIN

Official Name

English

5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 3-((ACETYLOXY)METHYL)-8-OXO-7-((2-THIENYLACETYL)AMINO)-, (6R-TRANS)-

Common Name

English

Cefalotin [WHO-DD]

Common Name

English

cefalotin [INN]

Common Name

English

CEPHALOTHIN [MI]

Common Name

English

CEPHALOTHIN [VANDF]

Common Name

English

CEPHALOTHIN [GREEN BOOK]

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C357

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

WHO-ATC

J01DB03

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

WHO-VATC

QJ01DB03

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

Code System Code Type Description

PUBCHEM

6024

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

PRIMARY

SMS_ID

100000081576

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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EVMPD

SUB06170MIG

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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INN

1477

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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MERCK INDEX

m3251

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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Merck Index

EPA CompTox

DTXSID4022783

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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NCI_THESAURUS

C62021

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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ECHA (EC/EINECS)

205-815-7

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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WIKIPEDIA

CEFALOTIN

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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DRUG CENTRAL

574

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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ChEMBL

CHEMBL617

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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IUPHAR

8798

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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DRUG BANK

DB00456

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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MESH

D002512

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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RXCUI

2236

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

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RxNorm

HSDB

3024

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

PRIMARY

CHEBI

124991

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

PRIMARY

FDA UNII

R72LW146E6

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

PRIMARY

CAS

153-61-7

Created by admin on Fri Dec 15 15:02:15 UTC 2023 , Edited by admin on Fri Dec 15 15:02:15 UTC 2023

PRIMARY

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TRANSPORTER -> INHIBITOR

Related Record Type Details


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ACTIVE MOIETY