170364-57-5 Usage
Description
Enzastaurin (LY317615) is a potent and selective protein kinase C beta (PKCβ) inhibitor with the chemical formula 170364-57-5. It exhibits a range of biological activities, including the induction of apoptosis in multiple myeloma cell lines, mitotic missegregation in colorectal cancer cells, attenuation of amphetamine-stimulated dopamine efflux, and inhibition of blood-brain barrier leakiness. Enzastaurin has also been utilized in splicing analysis to study its effects on the splicing of a mutated exon.
Uses
Used in Pharmaceutical Industry:
Enzastaurin (LY317615) is used as a PKCβ-selective inhibitor for suppressing angiogenesis, which is a critical process in the growth and metastasis of various types of cancer. Its ability to inhibit the AKT signaling pathway makes it a promising candidate for the treatment of multiple myeloma and other cancers.
Used in Cancer Research:
In cancer research, Enzastaurin (LY317615) is employed as a tool to study the effects of PKCβ inhibition on tumor growth and progression. Its use in splicing analysis helps researchers understand the molecular mechanisms underlying cancer development and identify potential therapeutic targets.
Used in Drug Development:
Enzastaurin (LY317615) serves as a lead compound in the development of novel therapeutic agents targeting PKCβ. Its potent and selective inhibition of PKCβ makes it a valuable starting point for the design and synthesis of new drugs with improved efficacy and reduced side effects.
Used in Preclinical Studies:
Enzastaurin (LY317615) is used in preclinical studies to evaluate its potential as a therapeutic agent for various types of cancer. These studies involve testing the compound in cell culture and animal models to assess its efficacy, safety, and pharmacokinetic properties.
Used in Neurological Research:
In neurological research, Enzastaurin (LY317615) is used to investigate its effects on amphetamine-stimulated dopamine efflux and blood-brain barrier leakiness. These studies contribute to a better understanding of the role of PKCβ in neurological disorders and the potential of Enzastaurin as a therapeutic agent for conditions such as Parkinson's disease and multiple sclerosis.
Biochem/physiol Actions
Enzastaurin is a potent and PKCβ preferring inhibitor. Also, Enzastaurin inhibits AKT and GSK3β. Enzastaurin acts as anti-angiogenic and antineoplastic agent.
References
1) Graff et al. (2005), The protein kinase Cbeta-selective inhibitor, Enzastaurin (LY317615.HCl), suppresses signaling through the AKT pathway, induces apoptosis, and suppresses growth of human colon cancer and glioblastoma xenografts; Cancer Res. 65 7462
2) Rizvi et al. (2006) Enzastaurin (LY317615), a protein kinase Cβ inhibitor, inhibits the AKT pathway and induces apoptosis in multiple myeloma cell lines; Mol.Cancer Ther. 5 1783
3) Ouaret and Larsen (2014), Protein kinase Cβ inhibition by enzastaurin leads to mitotic missegregation and preferential cytotoxicity toward colorectal cancer cells with chromosomal instability (CIN); Cell Cycle 13 2697
4) Zestos et al. (2016), PKCβ Inhibitors Attenuate Amphetamine-Stimulated Dopamine Efflux; ACS Chem.Neurosci. 7 757
5) Stranahan et al. (2016), Blood-brain barrier breakdown promotes macrophage infiltration and cognitive impairment in leptin receptor-deficient mice; J.Cereb.Blood Flow Metab. 36 2108
Check Digit Verification of cas no
The CAS Registry Mumber 170364-57-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,3,6 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 170364-57:
(8*1)+(7*7)+(6*0)+(5*3)+(4*6)+(3*4)+(2*5)+(1*7)=125
125 % 10 = 5
So 170364-57-5 is a valid CAS Registry Number.
InChI:InChI=1/C32H29N5O2/c1-35-19-25(23-9-2-4-11-27(23)35)29-30(32(39)34-31(29)38)26-20-37(28-12-5-3-10-24(26)28)22-13-16-36(17-14-22)18-21-8-6-7-15-33-21/h2-12,15,19-20,22H,13-14,16-18H2,1H3,(H,34,38,39)
170364-57-5Relevant articles and documents
Acyclic N-(azacycloalkyl)bisindolylmaleimides: Isozyme selective inhibitors of PKCβ
Faul, Margaret M.,Gillig, James R.,Jirousek, Michael R.,Ballas, Lawrence M.,Schotten, Theo,Kahl, Astrid,Mohr, Michael
, p. 1857 - 1859 (2003)
The synthesis and structure-activity relationship (SAR) trends of a new class of N-(azacycloalkyl)bisindolylmaleimides 1, acyclic derivatives of staurosporine, is described. The representative compound for this series (1e) exhibits an IC50 of 40-50 nM against the human PKCβ1 and PKCβ2 isozymes and selectively inhibits the PKCβ isozymes in comparison to other PKC isozymes (α, γ, δ, ε, λ, and η). The series is also kinase selective for PKC in comparison to other ATP-dependent kinases. A comparison of the PKC isozyme and kinase activity of the series is made to the kinase inhibitor staurosporine.
[11C]Enzastaurin, the first design and radiosynthesis of a new potential PET agent for imaging of protein kinase C
Wang, Min,Xu, Lu,Gao, Mingzhang,Miller, Kathy D.,Sledge, George W.,Zheng, Qi-Huang
, p. 1649 - 1653 (2011/05/11)
Enzastaurin (LY317615) is a potent and selective protein kinase C (PKC) inhibitor with an IC50 value of ~6 nM. [11C] Enzastaurin (3-(1-[11C]methyl-1H-indol-3-yl)-4-[1-[1-(2- pyridinylmethyl)-4-piperidinyl]-1H-indol-3-yl]-1H-pyrrole-2,5-dione), a new potential PET agent for imaging of PKC, was first designed and synthesized in 20-25% decay corrected radiochemical yield and 370-555 GBq/μmol specific activity at end of bombardment (EOB). The synthetic strategy was to prepare a carbon-11-labeled maleic anhydride intermediate followed by the conversion to maleimide.
Strategies for the synthesis of N-(azacycloalkyl)bisindolylmaleimides: Selective inhibitors of PKCβ
Faul, Margaret M.,Grutsch, John L.,Kobierski, Michael E.,Kopach, Michael E.,Krumrich, Christine A.,Staszak, Michael A.,Udodong, Uko,Vicenzi, Jeffrey T.,Sullivan, Kevin A.
, p. 7215 - 7229 (2007/10/03)
N-(Azacycloalkyl)bisindolylmaleimides 1 have been identified to be selective inhibitors of PKCβ. This manuscript will describe the synthetic approaches employed to prepare this class of compounds that resulted in development of efficient methods for prepa