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
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.
DBLinks
- CAS Registry Number: 40277-05-2
- PubChem CID: 99735
- ChEBI: 1864
- HMDB: HMDB0013856
- LipidMaps:
- KEGG: C07643
- BioCyc:
- NCBI MeSH: 4-hydroxycyclophosphamide
- Wikipedia: 4-Hydroxycyclophosphamide
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
- WishartLab ClassyFire: [Nitrogen mustard compounds] Nitrogen mustard compounds
- RefMet: [Nitrogen mustard compounds] Nitrogen mustard compounds
- ChEBI: [CHEBI:1864] 4-hydroxycyclophosphamide
| 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 |
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 |