2669785-84-4
Chemical Structure
JPS035
- CAS No.: 2669785-84-4
- Formula:C49H65N7O7S
- Molecular Weight:896.15
IUPAC Name: (2S,4R)-N-(2-((12-((4-((2-aminophenyl)carbamoyl)phenyl)amino)-12-oxododecyl)oxy)-4-(4-methylthiazol-5-yl)benzyl)-1-((S)-2-(1-fluorocyclopropane-1-carboxamido)-3,3-dimethylbutanoyl)-4-hydroxypyrrolidine-2-carboxamide
InChIKey: XPJGKIYHVFVWKJ-XVYMMXEDSA-N
SMILES: CC(N[C@@H](C(C)(C)C)C(N1[C@@H](C[C@H](C1)O)C(NCC2=C(C=C(C3=C(C)N=CS3)C=C2)OCCCCCCCCCCCC(NC4=CC=C(C=C4)C(NC5=C(C=CC=C5)N)=O)=O)=O)=O)=O
Biological Activity: JPS035 is a HDAC1, HDAC2 and HDAC3 PROTAC degrader, with a DC50 value of 3.58 μM against HDAC1 and 1.38 μM against HDAC3. JPS035 recruits the VHL E3 ligase to mediate the ubiquitination and degradation of HDAC1, HDAC2 and HDAC3. JPS035 increases the acetylation level of histone H3 lysine 56 and regulates global gene expression. JPS035 can be used in colon cancer-related research[1].
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JPS035 | JPS035 is a HDAC1, HDAC2 and HDAC3 PROTAC degrader, with a DC50 value of 3.58 μM against HDAC1 and 1.38 μM against HDAC3. JPS035 recruits the VHL E3 ligase to mediate the ubiquitination and degradation of HDAC1, HDAC2 and HDAC3. JPS035 increases the acetylation level of histone H3 lysine 56 and regulates global gene expression. JPS035 can be used in colon cancer-related research. | |||||||||||||||||||||
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Keywords
