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(2S)-1-[3-Ethyl-7-[[(1-oxido-3-pyridinyl)methyl]amino]pyrazolo[1,5-a]pyrimidin-5-yl]-2-piperidineethanol, also known as Dinaciclib, is a small molecule compound that acts as a potent and selective inhibitor of cyclin-dependent kinases (CDKs). It is a chiral molecule with the (2S) configuration and has a complex structure that includes a pyrazolo[1,5-a]pyrimidin-5-yl group, an ethyl group, and a piperidineethanol moiety. Dinaciclib is currently in development as an oncology therapeutic agent.

779353-01-4

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779353-01-4 Usage

Uses

Used in Oncology:
Dinaciclib is used as a CDK inhibitor for the treatment of various types of cancer. It targets CDKs, which are key regulators of cell cycle progression, and inhibits their activity, leading to cell cycle arrest and apoptosis in cancer cells. This makes it a promising therapeutic agent for the treatment of cancer.
Used in Drug Development:
Dinaciclib is currently undergoing development as an oncology therapeutic agent. Its potent and selective inhibition of CDKs makes it a valuable candidate for the treatment of various types of cancer. Researchers are actively investigating its potential efficacy and safety in clinical trials to determine its suitability as a cancer treatment.
Used in Combination Therapy:
Dinaciclib may also be used in combination with other cancer treatments, such as chemotherapy or radiation therapy, to enhance their effectiveness. Its ability to target CDKs and induce cell cycle arrest and apoptosis in cancer cells can potentially synergize with other treatments to improve patient outcomes.

Biological Activity

dinaciclib is a potent cyclin-dependent kinase (cdk) inhibitor with ic50s for cdk2, cdk5, cdk1 and cdk9 at 1 nm, 1 nm, 3 nm, and 4 nm, respectively. [1] it is in phase i or ii

references

[1]parry d., et al. (2010). dinaciclib (sch 727965), a novel and potent cyclin-dependent kinase inhibitor. mol cancer ther (9): 2344- 2353.[2]martin, m. p., et al. (2013). cyclin-dependent kinase inhibitor dinaciclib interacts with the acetyl-lysine recognition site of bromodomains. acs chemical biology 8 (11): 2360–5.[3]payton m., et al. (2006). discovery and evaluation of dual cdk1 and cdk2 inhibitors. cancer res 66: 4299-4308.

Check Digit Verification of cas no

The CAS Registry Mumber 779353-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,9,3,5 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 779353-01:
(8*7)+(7*7)+(6*9)+(5*3)+(4*5)+(3*3)+(2*0)+(1*1)=204
204 % 10 = 4
So 779353-01-4 is a valid CAS Registry Number.

779353-01-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2S)-1-[3-ethyl-7-[(1-oxidopyridin-1-ium-3-yl)methylamino]pyrazolo[1,5-a]pyrimidin-5-yl]piperidin-2-yl]ethanol

1.2 Other means of identification

Product number -
Other names Dinaciclib

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:779353-01-4 SDS

779353-01-4Downstream Products

779353-01-4Relevant academic research and scientific papers

Discovery of dinaciclib (SCH 727965): A potent and selective inhibitor of cyclin-dependent kinases

Paruch, Kamil,Dwyer, Michael P.,Alvarez, Carmen,Brown, Courtney,Chan, Tin-Yau,Doll, Ronald J.,Keertikar, Kerry,Knutson, Chad,McKittrick, Brian,Rivera, Jocelyn,Rossman, Randall,Tucker, Greg,Fischmann, Thierry,Hruza, Alan,Madison, Vincent,Nomeir, Amin A.,Wang, Yaolin,Kirschmeier, Paul,Lees, Emma,Parry, David,Sgambellone, Nicole,Seghezzi, Wolfgang,Schultz, Lesley,Shanahan, Frances,Wiswell, Derek,Xu, Xiaoying,Zhou, Quiao,James, Ray A.,Paradkar, Vidyadhar M.,Park, Haengsoon,Rokosz, Laura R.,Stauffer, Tara M.,Guzi, Timothy J.

scheme or table, p. 204 - 208 (2010/12/20)

Inhibition of cyclin-dependent kinases (CDKs) has emerged as an attractive strategy for the development of novel oncology therapeutics. Herein is described the utilization of an in vivo screening approach with integrated efficacy and tolerability paramete

Process and intermediates for the synthesis of (3-alkyl-5-piperidin-1-yl-3,3a-dihydro-pyrazolo[1,5-a]pyrimidin-7-yl)-amino derivatives and intermediates

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Page/Page column 14-15, (2008/06/13)

This application discloses a novel process to synthesize (3-alkyl-5-piperidin-1-yl-3,3a-dihydro-pyrazolo[1,5-a]pyrimidin-7-yl)-amino derivatives, and intermediates useful in the synthesis thereof. The subject (3-alkyl-5-piperidin-1-yl-3,3a-dihydro-pyrazolo[1,5-a]pyrimidin-7-yl)-amino derivatives are useful as cyclin-dependent kinase inhibitor compounds (CDK inhibitors) in pharmaceutical preparations.

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