Belotecan hydrochloride(CKD-602)

Modify Date: 2024-01-03 18:51:03

Belotecan hydrochloride(CKD-602) Structure
Belotecan hydrochloride(CKD-602) structure
Common Name Belotecan hydrochloride(CKD-602)
CAS Number 213819-48-8 Molecular Weight 469.96100
Density N/A Boiling Point 772.4ºC at 760mmHg
Molecular Formula C25H28ClN3O4 Melting Point N/A
MSDS N/A Flash Point 420.9ºC

 Use of Belotecan hydrochloride(CKD-602)


Belotecan hydrochloride (CKD-602 hydrochloride), a Topoisomerase I inhibitor, is a synthetic and water-soluble camptothecin derivative.

 Names

Name Belotecan hydrochloride
Synonym More Synonyms

 Belotecan hydrochloride(CKD-602) Biological Activity

Description Belotecan hydrochloride (CKD-602 hydrochloride), a Topoisomerase I inhibitor, is a synthetic and water-soluble camptothecin derivative.
Related Catalog
Target

Top1

In Vitro Belotecan exerts a significant cytotoxic effect on YD-8, YD-9 and YD-38 cells in a time- and dose-dependent manner with IC50 values of 2.4, 0.18 and 0.05 μg/mL at 72 h following treatment. Belotecan induces apoptosis in these cell lines. Belotecan induces G2/M phase arrest in oral squamous cell cancer cells[1]. Belotecan shows a significant anticancer effect on glioma cells, with IC50 values of 9.07 nM for LN229, 14.57 nM for U251 MG, 29.13 nM for U343 MG, and 84.66 nM for U87 MG[2].
In Vivo Belotecan has a significant effect on intracerebral glioma growth, with animals having significantly smaller tumors than those in the control group[3].
Cell Assay The cells are treated with different concentrations (0.01, 0.1, 0.5, 1, 5 and 10 μg/mL) of belotecan for 24, 48 and 72 h. Control samples of each cell line are treated with medium only. Cell viability is measured using the MTS assay[1].
Animal Admin Mice: Nude mice with established U87MG glioma are treated with a dose of belotecan of 0 mg/kg (control group, injection with saline), 40 mg/kg (group A) or 60 mg/kg (group B). Thereafter, the dose is repeated once every 4 days for a total of four doses. Tumor volume is measured histologically and apoptosis is detected[1].
References

[1]. Kim YK, et al. Anticancer effects of CKD-602 (Camtobell®) via G2/M phase arrest in oral squamous cell carcinoma cell lines. Oncol Lett. 2015 Jan;9(1):136-142.

[2]. Kim YY, et al. CKD-602, a camptothecin derivative, inhibits proliferation and induces apoptosis in glioma cell lines. Oncol Rep. 2009 Jun;21(6):1413-9.

[3]. Kim CY, et al. Antitumor activity of CKD-602, a camptothecin derivative, in a mouse glioma model. J Clin Neurosci. 2012 Feb;19(2):301-5.

 Chemical & Physical Properties

Boiling Point 772.4ºC at 760mmHg
Molecular Formula C25H28ClN3O4
Molecular Weight 469.96100
Flash Point 420.9ºC
Exact Mass 469.17700
PSA 93.45000
LogP 3.81300
Vapour Pressure 4.21E-25mmHg at 25°C
Storage condition 2-8℃

 Synthetic Route

~46%

Belotecan hydrochloride(CKD-602) Structure

Belotecan hydro...

CAS#:213819-48-8

Literature: Ahn, Soon Kil; Choi, Nam Song; Jeong, Byeong Seon; Kim, Kye Kwang; Journ, Duck Jin; Kim, Joon Kyum; Lee, Sang Joon; Kim, Jung Woo; Hong, Chung Il; Jew, Sang-sup Journal of Heterocyclic Chemistry, 2000 , vol. 37, # 5 p. 1141 - 1144

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Belotecan hydrochloride(CKD-602) Structure

Belotecan hydro...

CAS#:213819-48-8

Literature: Journal of Heterocyclic Chemistry, , vol. 37, # 5 p. 1141 - 1144

 Synonyms

Belotecan HCl
Camtobell hydrochloride
CKD 602
Belotecan (hydrochloride)
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