JNJ26481585

Modify Date: 2024-02-04 19:13:30

JNJ26481585 Structure
JNJ26481585 structure
Common Name JNJ26481585
CAS Number 1083078-98-1 Molecular Weight 430.93100
Density N/A Boiling Point N/A
Molecular Formula C21H27ClN6O2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of JNJ26481585


Quisinostat, also known as JNJ-26481585, is an orally bioavailable, second-generation, hydroxamic acid-based inhibitor of histone deacetylase (HDAC) with potential antineoplastic activity. HDAC inhibitor JNJ-26481585 inhibits HDAC leading to an accumulation of highly acetylated histones, which may result in an induction of chromatin remodeling; inhibition of the transcription of tumor suppressor genes; inhibition of tumor cell division; and the induction of tumor cell apoptosis. HDAC, an enzyme upregulated in many tumor types, deacetylates chromatin histone proteins. Compared to some first generation HDAC inhibitors, JNJ-26481585 may induce superior HSP70 upregulation and bcl-2 downregulation.

 Names

Name N-hydroxy-2-[4-[[(1-methylindol-3-yl)methylamino]methyl]piperidin-1-yl]pyrimidine-5-carboxamide,hydrochloride
Synonym More Synonyms

 Chemical & Physical Properties

Molecular Formula C21H27ClN6O2
Molecular Weight 430.93100
Exact Mass 430.18800
PSA 98.80000
LogP 3.92620

 Synonyms

Quisinostat HCl
UNII-WUV1QHM1CS
Quisinostat hydrochloride
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