321695-57-2
Chemical Structure
L002
- CAS No.: 321695-57-2
- Formula:C15H15NO5S
- Molecular Weight:321.35
IUPAC Name: 4-((((4-methoxyphenyl)sulfonyl)oxy)imino)-2,6-dimethylcyclohexa-2,5-dien-1-one
InChIKey: VEWFTYOFWIXCIO-UHFFFAOYSA-N
SMILES: O=C1C(C)=C/C(C=C1C)=N\OS(=O)(C2=CC=C(OC)C=C2)=O
Biological Activity: L002 is a potent, cell permeable, reversible and specific acetyltransferase p300 (KAT3B) inhibitor with an IC50 of 1.98 μM[1]. L002 binds the acetyl-CoA pocket and competitively inhibits the FATp300 catalytic domain, blocks histone acetylation and p53 acetylation, and inhibits STAT3 activation[2]. L002 has the potential for hypertension-induced cardiac hypertrophy and fibrogenesis treatment[3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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L002 | 98.94% | L002 is a potent, cell permeable, reversible and specific acetyltransferase p300 (KAT3B) inhibitor with an IC50 of 1.98 μM. L002 binds the acetyl-CoA pocket and competitively inhibits the FATp300 catalytic domain, blocks histone acetylation and p53 acetylation, and inhibits STAT3 activation. L002 has the potential for hypertension-induced cardiac hypertrophy and fibrogenesis treatment. | ||||||||||||||||||||
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L002 (Standard) | ≥98% | L002 (Standard) is the analytical standard of L002 (HY-100671). This product is intended for research and analytical applications. L002 is a potent, cell permeable, reversible and specific acetyltransferase p300 (KAT3B) inhibitor with an IC50 of 1.98 μM. L002 binds the acetyl-CoA pocket and competitively inhibits the FATp300 catalytic domain, blocks histone acetylation and p53 acetylation, and inhibits STAT3 activation. L002 has the potential for hypertension-induced cardiac hypertrophy and fibrogenesis treatment. | ||||||||||||||||||||
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Similarity Score 0.57
HY-121157RChlorfenson (Standard) -
Similarity Score 0.56
HY-W000438N-Boc-O-tosyl hydroxylamine -
Similarity Score 0.56
HY-W011077REthane-1,2-diyl bis4-methylbenzenesulfonate (Standard) -
Similarity Score 0.56
HY-W2493672,6-Naphthalenedisulfonic acid dipotassium -
Similarity Score 0.55
HY-125976ML233 -
Similarity Score 0.55
HY-D0305Tropaeolin O -
Similarity Score 0.54
HY-W110791Sodium diphenylamine-4-sulfonate -
Similarity Score 0.54
HY-W8561604,4'-(Diazene-1,2-diyl)dibenzenesulfonic acid -
Similarity Score 0.54
HY-W0424874-(4-Sulfophenyl)benzenesulfonic acid -
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References
- [1]. Rai R, et al. A novel acetyltransferase p300 inhibitor ameliorates hypertension-associated cardio-renal fibrosis. Epigenetics. 2017;12(11):1004-1013. [Content Brief]
- [2]. Sun XJ, et al. The Role of Histone Acetyltransferases in Normal and Malignant Hematopoiesis. Front Oncol. 2015 May 26;5:108. [Content Brief]
- [3]. Rai R, et al. Acetyltransferase p300 inhibitor reverses hypertension-induced cardiac fibrosis.J Cell Mol Med. 2019 Apr;23(4):3026-3031. [Content Brief]
