CAS NO: | 64439-81-2 |
规格: | ≥98% |
包装 | 价格(元) |
50mg | 询价 |
100mg | 询价 |
250mg | 询价 |
500mg | 询价 |
1g | 询价 |
2g | 询价 |
5g | 询价 |
Molecular Weight (MW) | 364.35 |
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Formula | C20H16N2O5 |
CAS No. | 64439-81-2 |
Storage | -20℃ for 3 years in powder form |
-80℃ for 2 years in solvent | |
Solubility (In vitro) | DMSO: 29 mg/mL (79.6 mM) |
Water: <1 mg/mL | |
Ethanol: N/A | |
Solubility (In vivo) | N/A |
Synonyms | Hydroxy Camptothecine, 10-Hydroxycamptothecin, Hydroxycamptothecine, 10-HCPT |
SMILES Code | O=C1C(O)(CC)C2=C(CO1)C(N3CC4=CC5=CC(O)=CC=C5N=C4C3=C2)=O |
In Vitro | In vitro activity: (±)-10-Hydroxycamptothecin (10-OH-camptothecin or 10-HCPT) is an inhibitor of topo I. (±)-10-Hydroxycamptothecin (10-HCPT, 5-20 nM) markedly inhibits the proliferation of Colo 205 cells in a dose-dependent manner. (±)-10-Hydroxycamptothecin (5-20 nM) arrests Colo 205 cells in the G2 phase of the cell cycle and triggers apoptosis through a caspase-3-dependent pathway. (±)-10-Hydroxycamptothecin (HPT, 0.01-10 μg/mL) causes cell shrinage, nuclear fragmentation and condensed chromosomes and induces apoptosis of human urinary bladder cancer cell line (T24). Cell Assay: Colo 205 cells (5×105) (ATCC:CCL-222) are seeded in 25T flasks overnight and then treated without (control) and with 5, 10, 15 or 20 nM of HCPT, respectively. After treatment for 24-120 h, cells are harvested by trypsin-EDTA and then centrifuged at 1,500 rpm for 5 min at 4?C. The cell pellet is resuspended in culture medium containing 0.04% trypan blue and the viable cells are enumerated by a hemocytometer. |
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In Vivo | (±)-10-Hydroxycamptothecin (10-HCPT) can be orally administered safely at a low-dose for long-term treatment. Prolonged elimination of HCPT in vivo may have a significant impact on its therapeutic effects. HCPT is metabolized to its carboxylate form and glucuronides. Dose-dependent toxicity is observed with i.v. administration of HCPT. |
Animal model | BALB/c-nude mice |
Formulation & Dosage | Formulated in propylene glycol; 1, 2.5, 5, 7.5 mg/kg; P.O. |
References | Oncol Rep. 2006 May;15(5):1273-9. |
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