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BS-181 hydrochloride

Catalog No. T6162Cas No. 1397219-81-6
Alias BS-181 HCl

BS-181 hydrochloride (BS-181 HCl) is a highly selective CDK7 inhibitor with IC50 of 21 nM. It is more than 40-fold selective for CDK7 than CDK1, 2, 4, 5, 6, or 9.

BS-181 hydrochloride

BS-181 hydrochloride

Purity: 99.97%
Catalog No. T6162Alias BS-181 HClCas No. 1397219-81-6
BS-181 hydrochloride (BS-181 HCl) is a highly selective CDK7 inhibitor with IC50 of 21 nM. It is more than 40-fold selective for CDK7 than CDK1, 2, 4, 5, 6, or 9.
Pack SizePriceAvailabilityQuantity
1 mg$31In Stock
2 mg$44In Stock
5 mg$72In Stock
10 mg$128In Stock
25 mg$288In Stock
50 mg$478In Stock
100 mg$689In Stock
1 mL x 10 mM (in DMSO)$79In Stock
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Purity:99.97%
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Product Introduction

Bioactivity
Description
BS-181 hydrochloride (BS-181 HCl) is a highly selective CDK7 inhibitor with IC50 of 21 nM. It is more than 40-fold selective for CDK7 than CDK1, 2, 4, 5, 6, or 9.
Targets&IC50
CDK7:21 nM
In vitro
BS-181 is a small molecule inhibitor of CDK7 in a cell-free environment, which displays more potential activity than roscovitine with IC 50 of 510 nM. Among the CDKs and other 69 kinases from many different classes, BS-181 shows high inhibitory selectivity for CDK7, inhibits CDK2 at concentrations lower than 1 μM which being inhibited 35-fold less potently (IC50 with 880 nM) than CDK7, shows slight inhibition for CDK1, CDK4, CDK5, CDK6 and CDK9 with IC50 values higher than 3.0 μM, and only shows inhibition for several kinases from other classes at high concentrations (>10 μM). BS-181 promotes cell cycle arrest and inhibits the cancer cell growth of a range of tumor types, including breast, lung, prostate and colorectal cancer with IC50 in the range of 11.5-37 μM. In MCF-7 cells, BS-181 inhibits the phosphorylation of the CDK7 substrate RNA polymerase II COOH-terminal domain (CTD), and promotes cell cycle arrest and apoptosis to inhibit the growth of cancer cell lines. [1]
In vivo
BS-181 is stable in vivo with a plasma elimination half-life in mice of 405 minutes after i.p. administration of 10 mg/kg. BS-181 inhibits the growth of MCF-7 xenografts in the nude mice model in a dose-dependent manner, with 25% and 50% reduction in tumor growth after 2 weeks of treatment at 10 mg/kg/day and 20 mg/kg/day, respectively without apparent toxicity. [1]
Kinase Assay
In vitro kinase inhibition.: Inhibition of CDK7 activity is measured by incubation of increasing amounts of BS-181 with purified recombinant CDK7/CycH/MAT1 complex, followed by measurement of free ATP remaining in the reaction using a luciferase assay, luciferase activity therefore providing a measure of inhibition of CDK7 activity for the determination of IC50.
Cell Research
MCF-7 cells are exposed to BS-181 for 24 hours. For the determination of cell cycle and apoptosis, cells are stained with propidium iodide or labeled with Annexin V-FITC, then labeled cells are acquired within 1 hour, by using the RXP cytomics software on a Beckman Coulter Elite ESP, and the data are analyzed using Flow Jo v7.2.5. For the assessment of CDKs, cells are lysed and analyzed by western blotting.(Only for Reference)
AliasBS-181 HCl
Chemical Properties
Molecular Weight416.99
FormulaC22H32N6·HCl
Cas No.1397219-81-6
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
Ethanol: 22 mg/mL (52.75 mM), Heating is recommended.
H2O: 50 mg/mL (119.9 mM), Sonication is recommended.
DMSO: 100 mg/mL (239.8 mM), Sonication is recommended.
Solution Preparation Table
Ethanol/H2O/DMSO
1mg5mg10mg50mg
1 mM2.3981 mL11.9907 mL23.9814 mL119.9070 mL
5 mM0.4796 mL2.3981 mL4.7963 mL23.9814 mL
10 mM0.2398 mL1.1991 mL2.3981 mL11.9907 mL
20 mM0.1199 mL0.5995 mL1.1991 mL5.9953 mL
50 mM0.0480 mL0.2398 mL0.4796 mL2.3981 mL
H2O/DMSO
1mg5mg10mg50mg
100 mM0.0240 mL0.1199 mL0.2398 mL1.1991 mL

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