Comparison

CPTH2

Item no. CS-W013990-100mg
Manufacturer ChemScene
Amount 100mg
Category
Type Molecules
Specific against other
ECLASS 10.1 32169090
ECLASS 11.0 32169090
UNSPSC 12000000
Alias 357649-93-5
Similar products 357649-93-5
Available
CAS
357649-93-5
Purity
>98%
MWt
291.80
Formula
C14H14ClN3S
Solubility
DMSO : 25 mg/mL (85.68 mM; Need ultrasonic); H2O : < 0.1 mg/mL (insoluble); Ethanol : 1 mg/mL (3.43 mM; Need ultrasonic)
Clinical Information
No Development Reported
Pathway
Apoptosis; Epigenetics
Target
Apoptosis; Histone Acetyltransferase
Biological Activity
CPTH2 is a potent histone acetyltransferase (HAT) inhibitor. CPTH2 selectively inhibits the acetylation of histone H3 by Gcn5. CPTH2 induces apoptosis and decreases the invasiveness of a clear cell renal carcinoma (ccRCC) cell line through the inhibition of acetyltransferase p300 (KAT3B)[1][2]. In Vitro: CPTH2 (100 uM; 12, 24, 48 hours) causes a decrease in cell proliferation after as early as 12 h with a further significant reduction after 48 h stimulation[1].
CPTH2 (100 uM; 12 or 48 hours) causes a comparable drop of the activity in both cell lines[1].
CPTH2 (100 uM; 48 hours) produces a drastic increase in apoptotic/dead cell population after 48 h[1].
CPTH2 (100 uM; 12, 24, 48 hours) shows a reduced acetylation of both global AcH3 histone and H3AcK18[1].
CPTH2 (100 uM; 24, 48 hours) is capable to counteract invasion and migration of ccRCC-786-O cells in culture[1].
CPTH2 (0.2, 0.5, 1 mM) inhibits the growth of a GCN5 deleted strain and a single catalytic mutant E173H[2].
CPTH2 (0.6, 0.8 mM; for 24 hours) inhibits histone H3 acetylation in yeast cell cultures[2].
CPTH2 inhibits the Gcn5p dependent functional network[2].
Research Area
Cancer

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Amount: 100mg
Available: In stock
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