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RP106 is a cell-permeable pyrrolo-pyrazine compound that functions as a potent, selective, reversible, and ATP-competitive inhibitor of Cdk1/cyclin B, Cdk5/p35, and GSK-3, with respective IC50 values of 700nM, 1.5 μM, and 920 nM. It is characterized by its off-white solid chemical properties.

496864-15-4

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496864-15-4 Usage

Uses

Used in Pharmaceutical Industry:
RP106 is used as a pharmaceutical agent for its potent inhibitory effects on various cyclin-dependent kinases (CDKs) and glycogen synthase kinase-3 (GSK-3). Its ability to selectively target these proteins makes it a valuable compound in the development of therapies for conditions related to the dysregulation of these proteins.
Used in Cancer Research:
RP106 is used as a research tool in cancer biology for its inhibitory effects on Cdk1/cyclin B, which plays a crucial role in cell cycle regulation and has been implicated in the development and progression of various cancers. By targeting this protein complex, RP106 can provide insights into the mechanisms underlying cancer cell proliferation and contribute to the development of novel cancer treatments.
Used in Neurodegenerative Disease Research:
RP106 is used as a research compound in the study of neurodegenerative diseases due to its inhibitory effects on Cdk5/p35. Dysregulation of this protein complex has been associated with several neurodegenerative conditions, including Alzheimer's disease and Parkinson's disease. RP106 can help researchers understand the role of Cdk5/p35 in these diseases and potentially lead to the development of new therapeutic strategies.
Used in Cell Biology Research:
RP106 is used as a research tool in cell biology to investigate the role of GSK-3 in cellular processes. GSK-3 is a multifunctional kinase involved in various cellular pathways, including apoptosis, inflammation, and metabolism. By inhibiting GSK-3, RP106 can provide valuable information on the role of this kinase in cellular function and contribute to the development of targeted therapies for conditions involving GSK-3 dysregulation.

Check Digit Verification of cas no

The CAS Registry Mumber 496864-15-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,6,8,6 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 496864-15:
(8*4)+(7*9)+(6*6)+(5*8)+(4*6)+(3*4)+(2*1)+(1*5)=214
214 % 10 = 4
So 496864-15-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H19N3O/c1-3-4-5-14-15(12-6-8-13(21-2)9-7-12)20-17-16(14)18-10-11-19-17/h6-11H,3-5H2,1-2H3,(H,19,20)

496864-15-4 Well-known Company Product Price

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  • Sigma

  • (R3405)  RP-107  ≥98% (HPLC), solid

  • 496864-15-4

  • R3405-5MG

  • 1,749.15CNY

  • Detail
  • Sigma

  • (R3405)  RP-107  ≥98% (HPLC), solid

  • 496864-15-4

  • R3405-25MG

  • 7,043.40CNY

  • Detail

496864-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Aloisine RP106

1.2 Other means of identification

Product number -
Other names 7-butyl-6-(4-methoxyphenyl)-5H-pyrrolo[2,3-b]pyrazine

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:496864-15-4 SDS

496864-15-4Downstream Products

496864-15-4Relevant academic research and scientific papers

Pyrrolopyrazines as kinase inhibitors

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Page 8, (2010/02/05)

The invention relates to pyrrolo [2,3b]-pyrazine derivatives having the general formula (I) : ???wherein :R2 and R3 are identical or different and represent H, C1-C6 alkyl, said alkyl being a straight or branched-chain alkyl, which can be substituted,R6 i

Aloisines, a new family of CDK/GSK-3 inhibitors. SAR study, crystal structure in complex with CDK2, enzyme selectivity, and cellular effects

Mettey, Yvette,Gompel, Marie,Thomas, Virginie,Garnier, Matthieu,Leost, Maryse,Ceballos-Picot, Irène,Noble, Martin,Endicott, Jane,Vierfond, Jean-Michel,Meijer, Laurent

, p. 222 - 236 (2007/10/03)

Cyclin-dependent kinases (CDKs) regulate the cell cycle, apoptosis, neuronal functions, transcription, and exocytosis. The observation of CDK deregulations in various pathological situations suggests that CDK inhibitors may have a therapeutic value. In th

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