CH-0793076

Modify Date: 2025-08-28 22:32:16

CH-0793076 Structure
CH-0793076 structure
Common Name CH-0793076
CAS Number 534605-78-2 Molecular Weight 458.51
Density N/A Boiling Point N/A
Molecular Formula C26H26N4O4 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of CH-0793076


CH-0793076 (TP3076), a hexacyclic camptothecin analog, is active drug and major metabolite of TP300. CH-0793076 inhibits DNA topoisomerase I with an IC50 of 2.3 μM. CH-0793076 is efficacious against cells expressing BCRP (breast cancer resistance protein)[1].

 Names

Name CH-0793076

 CH-0793076 Biological Activity

Description CH-0793076 (TP3076), a hexacyclic camptothecin analog, is active drug and major metabolite of TP300. CH-0793076 inhibits DNA topoisomerase I with an IC50 of 2.3 μM. CH-0793076 is efficacious against cells expressing BCRP (breast cancer resistance protein)[1].
Related Catalog
Target

Topoisomerase I:2.3 μM (IC50)

In Vitro CH0793076 (TP3076) (6 days at 37°C) shows antiproliferative activity against PC-6/BCRP and PC-6/pRC cells, with IC50 of 0.35 and 0.18 nM[1].
In Vivo TP300 (1-100 mg/kg; bolus intravenous injection once per week for 3 weeks, for a total of three doses) shows more than 50% of tumor growth inhibition in all nine models, regardless of the expression of BCRP (WiDr, HT-29, NCI-H460 and AsPC-1, HCT116, COLO 201, HCT-15, Calu-6 and NCI-N87)[1].
References

[1]. Endo M, et al. A water soluble prodrug of a novel camptothecin analog is efficacious against breast cancer resistance protein-expressing tumor xenografts. Cancer Chemother Pharmacol. 2010 Jan;65(2):363-71.

 Chemical & Physical Properties

Molecular Formula C26H26N4O4
Molecular Weight 458.51
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