Enzastaurin (LY317615)

Enzastaurin (LY317615) Basic information
Product Name:Enzastaurin (LY317615)
Synonyms:Enzastaurin;1H-Pyrrole-2,5-dione, 3-(1-methyl-1H-indol-3-yl)-4-(1-(1-(2-pyridinylmethyl)-4-piperidinyl)-1H-indol-3-yl)-;Ly317615;Unii-uc96G28eqf;Enzastaurin,Enzstataurin,LY317615,170364-57-5,1H-Pyrrole-2,5-dione, 3-;3-(1-Methyl-1H-indol-3-yl)-4-(1-(1-(2-pyridinylmethyl)-4-piperidinyl)-1H-indol-3-yl)-1H-pyrrole-2,5-dione;Enzastaurin ( LY317615 );Enzastaurine
CAS:170364-57-5
MF:C32H29N5O2
MW:515.6
EINECS:
Product Categories:Inhibitors;Smad;Intermediates & Fine Chemicals;Pharmaceuticals;TGF-beta/Smad;TGF-beta
Mol File:170364-57-5.mol
Enzastaurin (LY317615) Structure
Enzastaurin (LY317615) Chemical Properties
Melting point 249-261℃
Boiling point 767.2±60.0 °C(Predicted)
density 1.34
RTECS UX9626850
Fp 417.8℃
storage temp. -20°C
solubility DMSO: soluble10mg/mL, clear (warmed)
pka7.88±0.60(Predicted)
form powder
color , light orange to dark orange-red
Stability:Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
HS Code 29339900
MSDS Information
Enzastaurin (LY317615) Usage And Synthesis
DescriptionEnzastaurin (170364-57-5) is a potent and selective PKCβ inhibitor.? IC50 = 6, 39, 83 and 110 nM, for PKCβ, PKCα, PKCγ and PKCε respectively.1 Induces apoptosis in multiple myeloma cell lines via inhibition of the AKT signaling pathway.2 Induces mitotic missegregation and preferential cytotoxicity in colorectal cancer cells with chromosomal instability.3 Attenuates amphetamine-stimulated dopamine efflux.4 Inhibits blood-brain barrier leakiness in a mouse model.5
UsesPKCβ-selective inhibitor, suppresses angiogenesis.
UsesEnzastaurin has been used in splicing analysis to study its effects on splicing of a mutated exon.
DefinitionChEBI: 3-(1-methyl-3-indolyl)-4-[1-[1-(2-pyridinylmethyl)-4-piperidinyl]-3-indolyl]pyrrole-2,5-dione is a member of indoles and a member of maleimides.
Biochem/physiol ActionsEnzastaurin is a potent and PKCβ preferring inhibitor. Also, Enzastaurin inhibits AKT and GSK3β. Enzastaurin acts as anti-angiogenic and antineoplastic agent.
References1) 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
Enzastaurin (LY317615) Preparation Products And Raw materials
JX401 AICAR Methylparaben Methyl Indometacin Bensulfuron methyl Diphenoxylate Parathion-methyl Polyvinylpyrrolidone Kresoxim-methyl Thiophanate-methyl Haloperidol Methyl salicylate Indole-3-acetic acid Methyl acetate Methyl bromide Enzastaurin (LY317615) METSULFURON METHYL

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