4-Hydroxycyclophosphamide (BioCAD00000004382)

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Metabolite Card

Formula: C7H15Cl2N2O3P (276.0197)
SMILES: OC1CCOP(=O)(N1)N(CCCl)CCCl

Synonyms [en]

4-Hydroxycyclophosphamide; Tetrahydro-2-(bis(2-chloroethyl)amino)-2H-1,3,2-oxazaphosphorin-4-ol 2-oxide; 2-[bis(2-chloroethyl)amino]-1,3,2-oxazaphosphinan-4-ol 2-oxide; 4-hydroxycyclophosphamide, (cis)-isomer; 4-hydroxycyclophosphamide, (trans)-isomer; 2-(Bis(2-chloroethyl)amino)-4-hydroxy-1,3,2-oxazaphosphinane 2-oxide

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

4-Hydroxycyclophosphamide. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China. https://biocad_registry.innovation.ac.cn/s/(-)-arctiin (retrieved 2026-01-03) (CAD Registry RN: BioCAD00000004382). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

4-Hydroxycyclophosphamide is a primary activation metabolite of cyclophosphamide and of mafosfamide (an experimental drug) after they partially metabolized by cytochrome P450 (PMID: 12021633). Cyclophosphamide is a chemotherapeutic used to suppress the immune system and to treat several cancers including lymphoma, multiple myeloma, leukemia, ovarian cancer, breast cancer and small cell lung cancer. After cyclphosphamide is converted to 4-hydroxycyclophosphamide it is then partially tautomerized into aldophosphamide, which easily enters live cells whereupon it is partially detoxified into inactive carboxycyclophosphamide by the enzyme ALDH. 4-Hydroxycyclophosphamide is also an intermediate metabolite in the formation of phosphoramide mustard, the active metabolite, and acrolein, the metabolite responsible for much of the toxicity associated with cyclophosphamides (PMID: 7059981). 4-Hydroxycyclophosphamide is not cytotoxic at physiologic pH, readily diffuses into cells and spontaneously decomposes into the active phosphoramide mustard. In human liver microsomes, 4-Hydroxycyclophosphamide formation correlates with known phenotypic markers of CYP2B6 activity, specifically formation of (S)-2-ethyl-1,5-dimethyl-3,3-diphenyl pyrrolidine and hydroxybupropion. In addition, it is reported that the CYP2B6 genotype is not consistently related to 4-Hydroxycyclophosphamide formation in vitro or in vivo (PMID: 21976622). 4-Hydroxycyclophosphamide is only found in individuals who have consumed the drug cyclophosphamide.

Entity Information

DBLinks

Other DBLinks
  • CAS Registry Number: 40277-05-2
  • PubChem: 99735
  • ChEBI: ChEBI:1864
  • HMDB: HMDB0013856
  • KEGG: C07643
  • NCBI MeSH: 4-hydroxycyclophosphamide
  • Wikipedia: 4-Hydroxycyclophosphamide
  • RefMet: RM0118231
  • Metlin: METLIN_630

Class / Ontology

Metabolic Network
ID EC Number Name
KEGG:R08275 1.14.14.- C07888 + C00005 + C00080 + C00007<=>C07643 + C00006 + C00001
KEGG:R08277 1.14.14.- C07643<=>C07644
KEGG:R08278 C07643<=>C07645
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Organism Source

Taxonomy Source

Pathway Synthetic

pathway id name
Reactome:R-BTA-1430728 Metabolism
Reactome:R-BTA-211945 Phase I - Functionalization of compounds
Reactome:R-BTA-211981 Xenobiotics
Reactome:R-CEL-211859 Biological oxidations
Reactome:R-CEL-211981 Xenobiotics
Reactome:R-CFA-1430728 Metabolism
Reactome:R-DRE-211897 Cytochrome P450 - arranged by substrate type
Reactome:R-DDI-211859 Biological oxidations
Reactome:R-DDI-211981 Xenobiotics
Reactome:R-HSA-211859 Biological oxidations
Reactome:R-MMU-1430728 Metabolism
Reactome:R-MMU-211859 Biological oxidations
Reactome:R-RNO-211945 Phase I - Functionalization of compounds
Reactome:R-RNO-211981 Xenobiotics
Reactome:R-SSC-211945 Phase I - Functionalization of compounds
Reactome:R-SSC-211981 Xenobiotics
Reactome:R-XTR-211897 Cytochrome P450 - arranged by substrate type
Reactome:R-BTA-211859 Biological oxidations
Reactome:R-CFA-211897 Cytochrome P450 - arranged by substrate type
Reactome:R-DRE-211945 Phase I - Functionalization of compounds
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