Cyclophosphamide
A nitrogen mustard alkylating agent that cross-links DNA strands to kill rapidly dividing cells, used to treat various cancers including lymphoma, leukemia, and breast cancer, as well as severe autoimmune diseases. It requires activation by liver enzymes and can cause serious side effects including hemorrhagic cystitis.
Молекулярная масса
261,0800 g/mol
LogP
0,60
TPSA
41,60 Ų
Правило пяти Липинского
Соответствует
Терапевтические области
Механизм действия
Forms covalent bonds with DNA bases, creating cross-links and strand breaks that prevent DNA replication and transcription. This triggers apoptosis in rapidly dividing cells, particularly cancer cells.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Forms covalent bonds with DNA bases, creating cross-links and strand breaks that prevent DNA replication and transcription. This triggers apoptosis in rapidly dividing cells, particularly cancer cells.
2D Структура
Cite this structure
Embed this structure
SMILES
O.O=P1(N(CCCl)CCCl)NCCCO1
InChI
InChI=1S/C7H15Cl2N2O2P.H2O/c8-2-5-11(6-3-9)14(12)10-4-1-7-13-14;/h1-7H2,(H,10,12);1H2
Molecular Formula
C7H15Cl2N2O2P
HBD / HBA
1 / 4
Вращаемые Связи
5
Тяжёлые Атомы
14
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Часто задаваемые вопросы
A nitrogen mustard alkylating agent that cross-links DNA strands to kill rapidly dividing cells, used to treat various cancers including lymphoma, leukemia, and breast cancer, as well as severe autoimmune diseases. It requires activation by liver enzymes and can cause serious side effects including hemorrhagic cystitis.
Forms covalent bonds with DNA bases, creating cross-links and strand breaks that prevent DNA replication and transcription. This triggers apoptosis in rapidly dividing cells, particularly cancer cells.
Yes, Cyclophosphamide is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200796. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 2907. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
Медицинский отказ от ответственности
This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.
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