CADAZOLID

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C29H29F2N3O8
Molecular Weight	585.5527
Optical Activity	UNSPECIFIED
Defined Stereocenters	1 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CADAZOLID

Structure Search

SMILES

OC[C@H]1CN(C(=O)O1)C2=CC=C(OCC3(O)CCN(CC3)C4=CC5=C(C=C4F)C(=O)C(=CN5C6CC6)C(O)=O)C(F)=C2

InChI

InChIKey=XWFCFMXQTBGXQW-GOSISDBHSA-N

InChI=1S/C29H29F2N3O8/c30-21-10-19-23(33(16-1-2-16)13-20(26(19)36)27(37)38)11-24(21)32-7-5-29(40,6-8-32)15-41-25-4-3-17(9-22(25)31)34-12-18(14-35)42-28(34)39/h3-4,9-11,13,16,18,35,40H,1-2,5-8,12,14-15H2,(H,37,38)/t18-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C29H29F2N3O8
Molecular Weight	585.5527
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	1 / 1
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:17:40 UTC 2023` Edited by `admin` on `Fri Dec 15 15:17:40 UTC 2023`
Record UNII	2OEA2UN10Y
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

CADAZOLID

Official Name

English

cadazolid [INN]

Common Name

English

Cadazolid [WHO-DD]

Common Name

English

ACT-179811

Code

English

3-QUINOLINECARBOXYLIC ACID, 1-CYCLOPROPYL-6-FLUORO-7-(4-((2-FLUORO-4-((5R)-5-(HYDROXYMETHYL)-2-OXO-3-OXAZOLIDINYL)PHENOXY)METHYL)-4-HYDROXY-1-PIPERIDINYL)-1,4-DIHYDRO-4-OXO-

Common Name

English

CADAZOLID [USAN]

Common Name

English

1-CYCLOPROPYL-6-FLUORO-7-(4-((2-FLUORO-4-((R)-5-HYDROXYMETHYL-2-OXOOXAZOLIDIN-3-YL)PHENOXY)METHYL)-4-HYDROXYPIPERIDIN-1-YL)-4-OXO-1,4-DIHYDROQUINOLINE-3-CARBOXYLIC ACID

Systematic Name

English

Classification Tree Code System Code

FDA ORPHAN DRUG

592917

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

NCI_THESAURUS

C258

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

Code System Code Type Description

DRUG BANK

DB11847

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

PRIMARY

PUBCHEM

44242317

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

PRIMARY

ChEMBL

CHEMBL3707376

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

PRIMARY

USAN

CD-147

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

PRIMARY

EVMPD

SUB184432

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

PRIMARY

INN

9377

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

PRIMARY

EPA CompTox

DTXSID10145234

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

PRIMARY

WIKIPEDIA

Cadazolid

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

PRIMARY

NCI_THESAURUS

C118642

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

PRIMARY

CAS

1025097-10-2

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

PRIMARY

FDA UNII

2OEA2UN10Y

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

PRIMARY

SMS_ID

100000170453

Created by admin on Fri Dec 15 15:17:40 UTC 2023 , Edited by admin on Fri Dec 15 15:17:40 UTC 2023

PRIMARY

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					PJX89V9R6N

CLOSTRIDIUM DIFFICILE

TARGET ORGANISM->INHIBITOR

Amount:

Related Record Type Details


					2OEA2UN10Y

CADAZOLID

ACTIVE MOIETY

Amount: