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Ifosfamide

A nitrogen mustard alkylating agent used in the treatment of cancer.Chemotherapeutic Agents Approved (In Vitro) :Ifosfamide is an alkylating chemotherapeutic agent with activity against a wide range of tumors. Ifosfamide is activated by the cytochrome P450 family. Ifosfamide (0-5 mM) suppresses the viability of CYP2B1-expressing C8III-1 cells, while it is cytotoxic to the non-CYP2B1-expressing CrFK cells only at high concentration (5 mM) . CYP BM3 mutants activates Ifosfamide, and Ifosfamide shows inhibitory activity against human U2OS cells. (In Vivo) :Ifosfamide (50 mg/kg, i.p.) treatment before mating increases percentage of post-implantation loss and resorbs fetuses in pregnant rats. Ifosfamide also (50 mg/kg, i.p.) decreases the progesterone in the serum of pregnant rats. However, Ifosfamide causes no obvious difference with the control rats at 25 mg/kg. Ifosfamide (25, 50 mg/kg, i.p.) induces apoptosis and histological changes in the placentas and prenatal rats, most sensitive fetal organs are the brain, liver and kidney.

Product Specifications

CAS Number

3778-73-2

Product Name Alternative

Isophosphamide | NSC 109724

Field of Research

Pharmacology & Drug Discovery

Purity

>98% (HPLC)

Solubility

10 mM in DMSO

Smiles

ClCCNP1 (OCCCN1CCCl) =O

Molecular Formula

C7H15Cl2N2O2P

Molecular Weight

261.086

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

2H-1,3,2-Oxazaphosphorin-2-amine, N,3-bis (2-chloroethyl) tetrahydro-, 2-oxide

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