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首页-小分子抑制剂&激动剂-Epigenetics-Histone Acetyltransferase (HAT)

Request The Product List ofHistone Acetyltransferase (HAT) Histone Acetyltransferase (HAT)

Cat. No. Product Name Information
PC-61685

PU-141

p300/CBP inhibitor

PU-141 is a potent, selective CBP/p300 inhibitor that inhibits SK-N-SH cell growth with GI50 of 0.48 uM.
PC-60499

TH1834 dihydrochloride

Tip60 inhibitor

TH1834 dihydrochloride (TH-1834, TH 1834) is a novel potent specific histone acetyltransferase Tip60 inhibitor.
PC-60498

TH1834

Tip60 inhibitor

TH1834 (TH-1834, TH 1834) is a novel potent specific histone acetyltransferase Tip60 inhibitor.
PC-70121

Windorphen

p300 inhibitor

Windorphen is a potent, selective inhibitor of p300 histone acetyltransferase (IC50=4.2 uM).
PC-60028

A-485

p300/CBP inhibitor

A-485 (A485) is a potent, selective and, cell and in vivo active p300/CBP catalytic inhibitor with IC50 of 9.8/2.6 nM.
PC-45646

I-CBP112

CBP/p300 inhibitor

I-CBP112 is a specific and potent inhibitor of CBP/p300 bromodomain with Kd of 150-170 nM.
PC-45052

Remodelin hydrobromide

NAT10 inhibitor

Remodelin hydrobromide is a potent inhibitor of the acetyl-transferase protein NAT10 that acetylates both histones and microtubules.
PC-45051

Remodelin

NAT10 inhibitor

Remodelin is a potent inhibitor of the acetyl-transferase protein NAT10 that acetylates both histones and microtubules.
PC-27595

CBP/p300 ligand 2

CBP/p300 ligand

CBP/p300 ligand 2 is a high affinity ligand of CBP/p300 for PROTAC design.
PC-27555

CTX-0124143

KAT6A inhibitor

CTX-0124143 is a small molecule inhibitor of Monocytic leukemia zinc finger protein (MOZ/KAT6A) with IC50 of 1.0 uM.
PC-27554

MOZ-IN-3

KAT6A inhibitor

MOZ-IN-3 (KAT6A inhibitor 6j) is a potent, selective inhibitor of KAT6A (MOZ, Monocytic leukemia zinc finger protein) with IC50 of 0.03 uM, shows 25-333 fold selectivity against KAT7, KAT5, KAT8 and KAT6B, exhibitsstrong antitumor activity on leukemia cell line K562 (IC50=82 nM).
PC-25583

Anacardic acid

HAT inhibitor

Anacardic acid is a small molecule inhibitor of histone acetyltransferase (HAT) with IC50 of 8.5 and 5.0 uM for p300 and PCAF respectively.

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