CANFOSFAMIDE

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C26H40Cl4N5O10PS
Molecular Weight	787.474
Optical Activity	UNSPECIFIED
Defined Stereocenters	3 / 3
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CANFOSFAMIDE

Structure Search

SMILES

N[C@@H](CCC(=O)N[C@@H](CS(=O)(=O)CCOP(=O)(N(CCCl)CCCl)N(CCCl)CCCl)C(=O)N[C@@H](C(O)=O)C1=CC=CC=C1)C(O)=O

InChI

InChIKey=OJLHWPALWODJPQ-QNWVGRARSA-N

InChI=1S/C26H40Cl4N5O10PS/c27-8-12-34(13-9-28)46(42,35(14-10-29)15-11-30)45-16-17-47(43,44)18-21(32-22(36)7-6-20(31)25(38)39)24(37)33-23(26(40)41)19-4-2-1-3-5-19/h1-5,20-21,23H,6-18,31H2,(H,32,36)(H,33,37)(H,38,39)(H,40,41)/t20-,21-,23+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C26H40Cl4N5O10PS
Molecular Weight	787.474
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 16:03:15 UTC 2023` Edited by `admin` on `Fri Dec 15 16:03:15 UTC 2023`
Record UNII	1RS284BFUI
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

CANFOSFAMIDE

Official Name

English

Canfosfamide [WHO-DD]

Common Name

English

(2S)-2-AMINO-5-(((1R)-1-(((2-((BIS(BIS(2-CHLOROETHYL)AMINO)PHOSPHINYL)OXY)ETHYL)SULFONYL)METHYL)-2-(((R)-CARBOXYPHENYLMETHYL)AMINO)-2-OXOETHYL)AMINO)-5-OXOPENTANOIC ACID

Common Name

English

GLYCINE, L-.GAMMA.-GLUTAMYL-S-(2-((BIS(BIS(2-CHLOROETHYL)AMINO)PHOSPHINYL)OXY)ETHYL)-S,S-DIOXIDO-L-CYSTEINYL-2-PHENYL-, (2R)-

Common Name

English

CANFOSFAMIDE [MI]

Common Name

English

GLYCINE, L-.GAMMA.-GLUTAMYL-3-((2-((BIS(BIS(2-CHLOROETHYL)AMINO)PHOSPHINYL)OXY)ETHYL)SULFONYL)-L-ALANYL-2-PHENYL, (2R)-

Common Name

English

canfosfamide [INN]

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C2129

Created by admin on Fri Dec 15 16:03:15 UTC 2023 , Edited by admin on Fri Dec 15 16:03:15 UTC 2023

Code System Code Type Description

DRUG CENTRAL

3062

Created by admin on Fri Dec 15 16:03:15 UTC 2023 , Edited by admin on Fri Dec 15 16:03:15 UTC 2023

PRIMARY

CAS

158382-37-7

Created by admin on Fri Dec 15 16:03:15 UTC 2023 , Edited by admin on Fri Dec 15 16:03:15 UTC 2023

PRIMARY

FDA UNII

1RS284BFUI

Created by admin on Fri Dec 15 16:03:15 UTC 2023 , Edited by admin on Fri Dec 15 16:03:15 UTC 2023

PRIMARY

EPA CompTox

DTXSID40166412

Created by admin on Fri Dec 15 16:03:15 UTC 2023 , Edited by admin on Fri Dec 15 16:03:15 UTC 2023

PRIMARY

SMS_ID

100000163090

Created by admin on Fri Dec 15 16:03:15 UTC 2023 , Edited by admin on Fri Dec 15 16:03:15 UTC 2023

PRIMARY

NCI_THESAURUS

C83581

Created by admin on Fri Dec 15 16:03:15 UTC 2023 , Edited by admin on Fri Dec 15 16:03:15 UTC 2023

PRIMARY

PUBCHEM

5312109

Created by admin on Fri Dec 15 16:03:15 UTC 2023 , Edited by admin on Fri Dec 15 16:03:15 UTC 2023

PRIMARY

DRUG BANK

DB04972

Created by admin on Fri Dec 15 16:03:15 UTC 2023 , Edited by admin on Fri Dec 15 16:03:15 UTC 2023

PRIMARY

ChEMBL

CHEMBL2111086

Created by admin on Fri Dec 15 16:03:15 UTC 2023 , Edited by admin on Fri Dec 15 16:03:15 UTC 2023

PRIMARY

EVMPD

SUB177216

Created by admin on Fri Dec 15 16:03:15 UTC 2023 , Edited by admin on Fri Dec 15 16:03:15 UTC 2023

PRIMARY

INN

8455

Created by admin on Fri Dec 15 16:03:15 UTC 2023 , Edited by admin on Fri Dec 15 16:03:15 UTC 2023

PRIMARY

MERCK INDEX

m3018

Created by admin on Fri Dec 15 16:03:15 UTC 2023 , Edited by admin on Fri Dec 15 16:03:15 UTC 2023

PRIMARY

Merck Index

Related Record Type Details


					1LI341K7NQ

CANFOSFAMIDE HYDROCHLORIDE

SALT/SOLVATE -> PARENT

Amount:

Related Record Type Details


					WNG97RSQ4S

L-γ-glutamyl-3-(ethenylsulfonyl)-L-alanyl-2-phenylGlycine, (2R)-

METABOLITE -> PARENT

Amount:


					87MF79KUY8

1,1′-Phosphinicobis[1-(2-chloroethyl)aziridinium]

METABOLITE ACTIVE -> PRODRUG

Amount:

Related Record Type Details


					87MF79KUY8

1,1′-Phosphinicobis[1-(2-chloroethyl)aziridinium]

ACTIVE MOIETY

Amount: