10-Hydroxycamptothecin

Bezeichnung:10-Hydroxycamptothecin

CAS-Nr19685-09-7

Englisch Name:10-Hydroxycamptothecin

CBNumberCB4445430

SummenformelC20H16N2O5

Molgewicht364.35

MOL-Datei19685-09-7.mol

10-Hydroxycamptothecin physikalisch-chemischer Eigenschaften

Schmelzpunkt	265-270°C
Siedepunkt	820.7±65.0 °C(Predicted)
Dichte	1.60
storage temp.	Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
Löslichkeit	≥23.8 mg/mL in DMSO with gentle warming; insoluble in EtOH; insoluble in H2O
Aggregatzustand	powder to crystal
pka	8.93±0.40(Predicted)
Farbe	White to Yellow to Orange
InChIKey	HAWSQZCWOQZXHI-FQEVSTJZSA-N
CAS Datenbank	19685-09-7(CAS DataBase Reference)

Sicherheit

S-Sätze:	24/25
HS Code	29349990

Gefahreninformationscode (GHS)

10-Hydroxycamptothecin Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung
DNA topoisomerases relax supercoiled DNA during replication, transcription, recombination, repair, and chromosome condensation. The relaxation of DNA supercoiling by topoisomerase I at single-strand breaks represents a target for anticancer agents to intercalate between DNA base pairs, leading to the activation of apoptotic and cell cycle arrest pathways. (S)-10-hydroxy-Camptothecin is an inhibitor of topoisomerase I originally isolated from the Chinese tree C. acuminata. It is a member of the camptothecin family that demonstrates less toxicity than its parent compound. (S)-10-hydroxy-Camptothecin has strong anti-tumor activity against a wide range of experimental tumors including L1210 leukemia cells (IC₅₀ = 1.15 μM). In vitro treatment of human HepG2 cells with 5-20 μM (S)-10-hydroxy-camptothecin results in cell cycle arrest at the G₂/M phase.
Chemische Eigenschaften
Yellow Solid
Verwenden
A Camptothecin derivative; a topoisomerase inhibitor for cancer therapy
Definition
ChEBI: 10-Hydroxycamptothecin is a pyranoindolizinoquinoline.
in vitro
10-Hydroxycamptothecin inhibited the growth of BT-20 and MDA-231 cells with IC50 of 34.3nM and 7.27nM, respectively, which was more potent than camptothecin (CPT) with IC50>500nM. 10-Hydroxycamptothecin potently induces the formation of the pBR322 plasmid DNA cleavage complex mediated by human topoisomerase I with an EC50 of 0.35 μM, more than 50-fold more potent than CPT with an EC50 of 18.85 μM. 10-Hydroxycamptothecin treatment caused dose-dependent growth inhibition of human microvascular endothelial cells (HMECs) with IC50 of 0.31 μM and significantly inhibited HMEC migration with IC50 of 0.63 μM. Treatment of HMEC cells with 10-Hydroxycamptothecin also inhibited microtubule formation in a dose-dependent manner with IC50 of 0.96 μM. 10-Hydroxycamptothecin (5-20 nM) significantly inhibits the differentiation of Colo205 cells, arrests the cell cycle in G2 phase, and induces apoptosis through a caspase-3-dependent pathway.
in vivo
In the CAM model, 10-Hydroxycamptothecin treatment inhibited angiogenesis in a concentration-dependent manner, with 95% inhibition at 25 nM, more potent than suramin, which inhibited only 60% of angiogenesis at 125 nM. 10-Hydroxycamptothecin, administered orally at low doses of 2.5-7.5 mg/kg every two days, caused significant growth inhibition in Colo205 xenograft mice, but no acute toxicity. LD50: 104 mg/kg in mice (intraperitoneal injection).
IC 50
0.31 μm
Einzelnachweise
[1] vladu b, woynarowski jm, manikumar g, wani mc, wall me, von hoff dd, wadkins rm. 7- and 10-substituted camptothecins: dependence of topoisomerase i-dna cleavable complex formation and stability on the 7- and 10-substituents. mol pharmacol. 2000 feb;57(2):243-51.
[2] xiao d, tan w, li m, ding j. antiangiogenic potential of 10-hydroxycamptothecin. life sci. 2001 aug 24;69(14):1619-28.
[3] ping yh, lee hc, lee jy, wu ph, ho lk, chi cw, lu mf, wang jj. anticancer effects of low-dose 10-hydroxycamptothecin in human colon cancer. oncol rep. 2006 may;15(5):1273-9.

10-Hydroxycamptothecin Upstream-Materialien And Downstream Produkte

10-Hydroxycamptothecin Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

19685-09-7, 10-Hydroxycamptothecin Verwandte Suche:

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