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/ p300/CBP
货号 产品名 纯度
A122218 现货 C646

C646 is a selective inhibitor of histone acetyltransferase p300 with Ki of 400 nM.

99%+
A147405 现货 Curcumin/姜黄素

Curcumin is a natural phenolic compound with impressive antioxidant properties.

98%
A636668 现货 SGC-CBP30

SGC-CBP30 is a potent CREBBP/EP300 bromodomain inhibitor with IC50 of 21-69 and 38 nM for CREBBP and EP300 bromodomains, respectively.

99%+
A1176639 现货 GNE-781

99%
A479140 现货 Histone Acetyltransferase Inhibitor II/组蛋白乙酰转移酶抑制剂II

Histone Acetyltransferase inhibitor II, insulin producing cells capable of secreting blood glucose regulating hormones, specially insulin, in response to physiological signals, method of production of said cells and uses thereof.

98%
A1359463 现货 NEO2734

NEO2734 is an orally dual p300/CBP and BET bromodomain inhibitor with IC50 values of <30 nM for both p300/CBP and BET bromodomains.

99%+
A594660 现货 I-CBP112

I-CBP112 is a specific and potent acetyl-lysine competitive protein-protein interaction inhibitor, that targets the CBP/p300 bromodomains.

98+%
A732746 现货 A-485

A 485 is a potent and selective p300/CREB-binding protein (CBP) HAT domain inhibitor with IC50 of 2.6 and 9.8 nM for the CBP-bromodomain HAT-C/H3 (BHC) and p300-BHC domains, respectively.

99%+
A788310 现货 CPI-637

CPI-637 is an efficient inhibitor of CBP/EP300 bromodomain with IC50 of 0.03 ± 0.01μM.

99%+
A441088 现货 PF-CBP1 HCl

PF-CBP1 HCl is a highly selective inhibitor of the bromodomain of CREB-binding protein (CREBBP).It inhibits CREBBP and p300 bromodomains with IC50 of 125 and 363 nM respectively.

97%
A190197 现货 Anacardic Acid/漆树酸

Anacardic acid is a potent inhibitor of p300 and p300/CBP-associated factor histone acetyltranferases, which also has antibacterial activity, antimicrobial activity,prostaglandin synthase inhibition, and tyrosinase and lipoxygenase inhibition.

99%+
A650610 现货 Foscenvivint

PRI-724 is a selective inhibitor of the CBP/β-catenin interaction.

99%+
A867405 Nordihydroguaiaretic acid/去甲二氢愈创木酸

Nordihydroguaiaretic Acid is a naturally occuring mTORC1 inhibitor.

99%+
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