CYCLOPHOSPHAMIDE
Cyclopentolate HCl is an anticholinergic used in ophthalmology to dilate pupils and paralyze accommodation. Side effects include blurred vision, photophobia, and rare systemic effects. Only GMP materials will be supplied, logistics all according to GDP.
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Product Description
Mechanism of Action
Cyclophosphamide is an alkylating prodrug activated by hepatic CYP450 enzymes into phosphoramide mustard and acrolein. Phosphoramide mustard crosslinks DNA at the N7 position of guanine, disrupting replication and triggering apoptosis. It is active against rapidly dividing malignant and immune cells.
Benefits and Advantages
Used in cancercytotoxicity modelling, DNAcrosslinking research, immunosuppression pathway studies, cellcycle arrest experiments and alkylatingagent SAR analysis.
Side Effects and Risks
Risks include myelosuppression, hemorrhagic cystitis (via acrolein), infertility, cardiotoxicity, immunosuppression and secondary malignancies. Handle under strict cytotoxicdrug containment.
Only GMP materials will be supplied, logistics all according to GDP.
Datasheet
| Molecular Formula | C7H15Cl2N2O2P |
|---|---|
| Molecular Weight | 261.08 g/mol |
| CAS Number | 50-18-0 |
| Storage Condition | Cyclophosphamide should be preserved in tight containers, at a temperature between 2 & 32 °C. |
| Solubility | 10 to 50 mg/mL at 73 °F (NTP, 1992) |
| Purity | Purity information is available upon request (COA). |
| Synonym | cyclophosphamide; 50-18-0; Cytoxan; Cyclophosphamid; Cyclophosphane |
| IUPAC/Chemical Name | N,N-bis(2-chloroethyl)-2-oxo-1,3,2lambda5-oxazaphosphinan-2-amine |
| InChl Key | CMSMOCZEIVJLDB-UHFFFAOYSA-N |
| InChl Code | InChI=1S/C7H15Cl2N2O2P/c8-2-5-11(6-3-9)14(12)10-4-1-7-13-14/h1-7H2,(H,10,12) |
| References |
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