JNJ-64619178

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Company Name: Biochempartner
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Products Intro: Product Name:JNJ-64619178
CAS:2086772-26-9
Purity:98% HPLC LCMS Package:10G;20G
Company Name: TargetMol Chemicals Inc.
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Products Intro: Product Name:JNJ-64619178
CAS:2086772-26-9
Purity:98.00% Package:1 mg;10 mg;100 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Finetech Industry Limited
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Products Intro: Product Name:Onametostat
CAS:2086772-26-9
Purity:98% Package:1g,10g,25g,100g,500g,1kg Remarks:N/A
Company Name: InvivoChem
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Products Intro: Product Name:JNJ-64619178
CAS:2086772-26-9
Purity:98% Package:5mg Remarks:V4503
Company Name: Wuhan Topule Biopharmaceutical Co., Ltd
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Products Intro: Product Name:JNJ-64619178
CAS:2086772-26-9
Purity:98%+ Package:500mg;1g;500g;1kg Remarks:Topule Company operates with integrity and has its own laboratory, which supports packaging and customization. Payment will be made after the product has passed third-party testing
JNJ-64619178 Basic information
Product Name:JNJ-64619178
Synonyms:JNJ-64619178;JNJ 64619178;JNJ64619178;CS-2829;1,2-Cyclopentanediol, 3-[2-(2-amino-3-bromo-7-quinolinyl)ethyl]-5-(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-, (1S,2R,3S,5R)-;(1S,2R,3S,5R)-3-(2-(2-Amino-3-bromoquinolin-7-yl)ethyl)-5-(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)cyclopentane-1,2-diol;inhibit,JNJ 64619178,Inhibitor,JNJ64619178,Histone Methyltransferase,Onametostat,JNJ-64619178;(1S,2R,3S,5R)-3-[2-(2-amino-3-bromo-7-quinolinyl)ethyl]-5-(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-1,2-cyclopentanediol;Onametostat (JNJ-64619178)
CAS:2086772-26-9
MF:C22H23BrN6O2
MW:483.36
EINECS:
Product Categories:
Mol File:2086772-26-9.mol
JNJ-64619178 Structure
JNJ-64619178 Chemical Properties
Boiling point 636.2±50.0 °C(Predicted)
density 1.79±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO:111.0(Max Conc. mg/mL);229.64(Max Conc. mM)
form A solid
pka13.37±0.70(Predicted)
color Off-white to light yellow
Safety Information
MSDS Information
JNJ-64619178 Usage And Synthesis
UsesOnametostat (JNJ-64619178) is a selective, orally active and pseudo-irreversible protein arginine methyltransferase 5 (PRMT5) inhibitor with an IC50 of 0.14 nM. Onametostat has potent activity in lung cancer[1][2].
in vivo

Oral administration of Onametostat results in efficient inhibition of dimethylation of SMD1/3 proteins, components of the splicing machinery and direct substrates of the methylosome, in several non-small cell lung cancer and small cell lung cancer? cancer mouse xenograft models[1].

IC 50PRMT5
References[1] Tongfei Wu, et al. Abstract 4859: JNJ-64619178, a selective and pseudo-irreversible PRMT5 inhibitor with potent in vitro and in vivo activity, demonstrated in several lung cancer models.
[2] Tao H, et al. Discovery of Novel PRMT5 Inhibitors by Virtual Screening and Biological Evaluations. Chem Pharm Bull (Tokyo). 2019;67(4):382-388. DOI:10.1248/cpb.c18-00980
JNJ-64619178 Preparation Products And Raw materials
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