[CAS NO. 192441-08-0]  Lomeguatrib

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PRODUCTS SPECIFICATIONS [192441-08-0]

Catalog
SLK-S8056
Brand
Selleck
CAS
192441-08-0

DESCRIPTION [192441-08-0]

Overview

MDLMFCD23703756
Molecular Weight326.17
Molecular FormulaC10H8BrN5OS
SMILESO(CC1=CC(Br)=CS1)C2=C3C(=NC(N)=N2)N=CN3

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM3.0659 mL15.3294 mL30.6589 mL
5 mM0.6132 mL3.0659 mL6.1318 mL
10 mM0.3066 mL1.5329 mL3.0659 mL
50 mM0.0613 mL0.3066 mL0.6132 mL

Description

Lomeguatrib (PaTrin-2) is a potent inhibitor of with of 5 nM.

Targets

O6-alkylguanine-DNA-alkyltransferas [1]
5 nM

In vitro

Lomeguatrib inactivates O-alkylguanine-DNA-alkyltransferase (ATase) with a IC50 10-fold lower than O-Benzylguanine. Lomeguatrib inhibits the activity of ATase in Raji cells with IC50 of 10 nM. Lomeguatrib effectively inactivates MGMT in MCF-7 cells with IC50 of ~6nM ). Lomeguatrib (10 μM ) substantially increases the growth inhibitory effects of temozolomide in MCF-7 cells (D60= 10 μM with Lomeguatrib vs 400 μM without).

In vivo

Lomeguatrib (20 mg/kg/day for 5 days) combined with temozolomide (100 mg/kg/day for 5 days) produces a substantial tumour growth delay: median tumour quintupling time is increased by 22 days without any significant increase in toxicity, while neither of the two drugs administrated along show any antitumor activity. Lomeguatrib inactivates ATase and enhances the anti-tumour effect of temozolomide in A375M human melanoma xenografts model. Lomeguatrib, at a single dose of 20 mg/kg i.p., produces complete ATase depletion in tumor within 2 hr. Temozolomide (100 g/kg/day) significantly delays growth of the A375M tumour xenograft with an estimated delay in the time for tumour to quintuple in size of 9.6 days. Addition of Lomeguatrib to temozolomide significantly enhances the latter’s effect, delaying the quintupling time a further 8.7 days. Moreover, the Lomeguatrib combination results in considerably less toxicity (0/9 vs. 2/9 deaths; 6.84% weight loss vs. 9.48%). Lomeguatrib alone has no significant effect on tumour growth.


Synonyms

9H-Purin-2-amine, 6-[(4-bromo-2-thienyl)methoxy]-
1H-Purin-2-amine, 6-[(4-bromo-2-thienyl)methoxy]-
6-[(4-Bromo-2-thienyl)methoxy]-9H-purin-2-amine
Lomeguatrib
2-Amino-6-(4-bromothiophen-2-ylmethoxy)-9H-purine
PaTrin 2