| Field | Specification |
|---|---|
| Mfr No | |
| Activity | |
| Alternative Names | (4S)-4,11-Diethyl-4-hydroxy-3,14-dioxo-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-9-yl 1,4'-bipiperidine-1'-carboxylate, CPT11, Camptothecin 11 |
| Cas No. | |
| Form | Yellow solid |
| Molecular Weight | |
| Product Type | |
| Purity | |
| Shipping | |
| SMILES | |
| Solubility | Soluble to 50 mg/ml in DMSO |
| Source | Synthetic |
| Storage |
Irinotecan is a semisynthetic analogue of camptothecin that inhibits topoisomerase I. It is converted to its active metabolite SN-38, which interferes with DNA replication and transcription. In neurobiology, irinotecan is used to study DNA damage responses and has potential applications in understanding neuronal vulnerability to genotoxic stress.
Classification: Harmful. May be harmful if inhaled, swallowed or absorbed through skin.
Safety Phrases:
- S22 - Do not breathe dust
- S24/25 - Avoid contact with skin and eyes
- S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection
- S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label where possible)
Risk Phrases:
- R20/21/22 - Harmful by inhilation, in contact with skin and if swallowed
- R62 - Possible risk of impaired fertility
- R68 - Possible risk of irreversible effects
Hazard Phrases:
H302
Irinotecan HCl (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-243)
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2. O'Dwyer P.J., and Catalano R.B. (2006) J Clin Oncol. 24(28): 4534-4538.