Comparison

Fotemustine European Partner

Item no. HY-B0733-10mg
Manufacturer MedChem Express
CASRN 92118-27-9
Amount 10 mg
Quantity options 10 mg 5 mg
Category
Type Inhibitors
Specific against other
Purity 91.94
Citations [1]Brakenhoff JP, et al. Molecular mechanisms of toxic effects of fotemustine in rat hepatocytes and subcellular rat liver fractions. Carcinogenesis. 1996 Apr;17(4):715-24.|[2]Merlin JL, et al. Enhancement of fotemustine (Muphoran) cytotoxicity by amifostine in malignant melanoma cell lines. Anticancer Drugs. 2002 Feb;13(2):141-7.
Smiles CC(P(OCC)(OCC)=O)NC(N(CCCl)N=O)=O
ECLASS 10.1 32160490
ECLASS 11.0 32160490
UNSPSC 12000000
Alias S10036
Shipping Condition Room temperature
Available
Manufacturer - Type
Reference compound
Manufacturer - Applications
Cancer-programmed cell death
Manufacturer - Targets
DNA Alkylator/Crosslinker
Shipping Temperature
Room Temperature
Storage Conditions
4°C (Powder, protect from light)
Molecular Weight
315.69
Product Description
Fotemustine is a DNA-alkylating agent, with antitumor activity.
Manufacturer - Research Area
Cancer
Solubility
DMSO: ≥ 3.2 mg/mL
Manufacturer - Pathway
Cell Cycle/DNA Damage
Clinical information
Launched

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 10 mg
Available: In stock
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