CAS |
19685-09-7 |
Chinese Name |
10-羟基喜树碱 |
English Name |
(S)-10-Hydroxycamptothecin |
Synonyms |
10-羟基喜树碱;伊立替康相关物质A;(S)-10-羟基喜树碱;Hydroxycamptothecine; |
Molecular Formula |
C20H16N2O5 |
Molecular Weight |
364.35 |
Solubility |
Soluble in DMSO ≥10mg/mL |
Purity |
HPLC≥98% |
Appearance |
Light yellow to yellow Solid |
Storage |
Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year |
EC |
EINECS 805-668-4 |
MDL |
MFCD02093100 |
SMILES |
O=C1[C@](O)(CC)C2=C(CO1)C(N3CC4=CC5=CC(O)=CC=C5N=C4C3=C2)=O |
InChIKey |
HAWSQZCWOQZXHI-FQEVSTJZSA-N |
InChI |
InChI=1S/C20H16N2O5/c1-2-20(26)14-7-16-17-11(5-10-6-12(23)3-4-15(10)21-17)8-22(16)18(24)13(14)9-27-19(20)25/h3-7,23,26H,2,8-9H2,1H3/t20-/m0/s1 |
PubChem CID |
97226 |
Target Point |
Topoisomerase |
Passage |
DNA Damage/DNA Repair |
Background |
(S)-10-Hydroxycamptothecin is a DNA topoisomerase I inhibitor. Can significantly induce apoptosis, and can be used for the study of liver cancer, gastric cancer, colon cancer and leukemia. |
Biological Activity |
(S)-10-Hydroxycamptothecin (10-HCPT;10-Hydroxycamptothecin) is a DNA topoisomerase I inhibitor of isolated from the Chinese plant Camptotheca accuminata. (S)-10-Hydroxycamptothecin exhibits a remarkable apoptosis-inducing effect. (S)-10-Hydroxycamptothecin has the potential for hepatoma, gastric carcinoma, colon cancer and leukaemia treatment[1-3]. |
In Vitro |
(S)-10-Hydroxycamptothecin inhibits L1210 leukemia cells with an IC50 of 1.15 μM[1].(S)-10-Hydroxycamptothecin(5-20 μg/L; 6 days; Hep G2 cells)treatment results in the cell cycle arrest at G2/M phase[2].(S)-10-Hydroxycamptothecin induces differentiation,down-regulates nuclear antigen(PCNA)and up-regulates wild-type protein p53 in Hep G2 cells[2]. |
In Vivo |
(S)-10-Hydroxycamptothecin(10-Hydroxycamptothecin)against L1210 leukemia in mice is tested. At the optimal dose(15 mg/kg),(S)-10-Hydroxycamptothecin has a 71% increase in life span(ILS)[1]. |
Data Literature Source |
[1]. Min Liu,et al. Intracellular delivery of 10-hydroxycamptothecin with targeted nanostructured lipid carriers against multidrug resistance . Journal of Drug Targeting. [2]. Min Liu,et al. Intracellular delivery of 10-hydroxycamptothecin with targeted nanostructured lipid carriers against multidrug resistance. J Drug Target,Early Online: 1–8 [3]. Yu P,et al. Synthesis and preliminary anticancer evaluation of 10-hydroxycamptothecin analogs. Biol Pharm Bull. 2012;35(8):1295-9. |
Unit |
Bottle |
Specification |
5mg 10mM*1mL in DMSO 10mg |