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Details

Stereochemistry ACHIRAL
Molecular Formula C7H15Cl2N2O2P
Molecular Weight 261.086
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CYCLOPHOSPHAMIDE ANHYDROUS

SMILES

ClCCN(CCCl)P1(=O)NCCCO1

InChI

InChIKey=CMSMOCZEIVJLDB-UHFFFAOYSA-N
InChI=1S/C7H15Cl2N2O2P/c8-2-5-11(6-3-9)14(12)10-4-1-7-13-14/h1-7H2,(H,10,12)

HIDE SMILES / InChI

Molecular Formula C7H15Cl2N2O2P
Molecular Weight 261.086
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:13:25 UTC 2023
Edited
by admin
on Fri Dec 15 15:13:25 UTC 2023
Record UNII
6UXW23996M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CYCLOPHOSPHAMIDE ANHYDROUS
Common Name English
NSC-26271
Code English
ANHYDROUS CYCLOPHOSPHAMIDE
Common Name English
(±)-2-(BIS(2-CHLOROETHYL)AMINO)TETRAHYDRO-2H-1,3,2-OXAZAPHOSPHORINE 2-OXIDE
Systematic Name English
2H-1,3,2-OXAZAPHOSPHORIN-2-AMINE, N,N-BIS(2-CHLOROETHYL)TETRAHYDRO-, 2-OXIDE
Systematic Name English
CYCLOPHOSPHAMIDE [HSDB]
Common Name English
Cyclophosphamide [WHO-DD]
Common Name English
CYCLOPHOSPHAMIDE LYOPHILIZED
Common Name English
CYCLOPHOSPHAMIDE ANHYDROUS [MI]
Common Name English
cyclophosphamide [INN]
Common Name English
CYCLOPHOSPHAMIDE, ANHYDROUS
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C697
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
NDF-RT N0000000236
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
EPA PESTICIDE CODE 624870
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
NDF-RT N0000175558
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
WHO-ATC L01AA01
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
NCI_THESAURUS C574
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
Code System Code Type Description
HSDB
3047
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
CAS
50-18-0
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
DAILYMED
6UXW23996M
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
FDA UNII
6UXW23996M
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
EVMPD
SUB121739
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
PUBCHEM
2907
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
RXCUI
221085
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
ALTERNATIVE
EVMPD
SUB06859MIG
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
INN
878
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
DRUG BANK
DB00531
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
NSC
26271
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
MERCK INDEX
m4013
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID5020364
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-015-4
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
RXCUI
1545988
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
NCI_THESAURUS
C61694
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
CHEBI
4027
Created by admin on Fri Dec 15 15:13:25 UTC 2023 , Edited by admin on Fri Dec 15 15:13:25 UTC 2023
PRIMARY
Related Record Type Details
METABOLIC ENZYME -> SUBSTRATE
SALT/SOLVATE -> PARENT
EXCRETED UNCHANGED
URINE
BINDER->LIGAND
BINDING
SOLVATE->ANHYDROUS
METABOLIC ENZYME -> SUBSTRATE
METABOLIC ENZYME -> SUBSTRATE
METABOLIC ENZYME -> SUBSTRATE
METABOLIC ENZYME -> SUBSTRATE
METABOLIC ENZYME -> SUBSTRATE
DEGRADENT -> PARENT
METABOLIC ENZYME -> SUBSTRATE
Related Record Type Details
METABOLITE ACTIVE -> PRODRUG
METABOLITE -> PARENT
METABOLITE -> PARENT
METABOLITE -> PARENT
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ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC INTRAVENOUS ADMINISTRATION

Volume of Distribution PHARMACOKINETIC
Tmax PHARMACOKINETIC ORAL ADMINISTRATION