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T12345CBP/p300-IN-3P300/CBP-IN-3
P300/CBP-IN-3 is an inhibitor of p300/CBP histone acetyltransferase.
价 格：￥电议型 号：T12345产 地：中国大陆
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T79395CBP/p300-IN-21；化合物 CBP/p300-IN-21CBP/p300-IN-21
CBP/p300-IN-21 (Compound 5d), a selective inhibitor of CBP/p300 with IC50 values of 0.07 μM for p300 and 1.755 μM for CBP, reduces H3K18Ac levels and inhibits the growth of 4T1 tumors in mice [1].
价 格：￥电议型 号：T79395产 地：中国大陆
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T72815CBP/p300-IN-10；化合物 CBP/p300-IN-10CBP/p300-IN-10
CBP/p300-IN-10, a potent inhibitor targeting histone acetyltransferase enzymes EP300 and CREBBP, exhibits IC50 values of 26 nM and 39 nM, respectively. This compound shows potential for anticancer research applications.
价 格：￥电议型 号：T72815产 地：中国大陆
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T63565CBP/p300-IN-19 hydrochloride；化合物 CBP/p300-IN-19 hydrochlorideCBP/p300-IN-19 hydrochloride
CBP/p300-IN-19 hydrochloride is a selective and potent inhibitor of p300/CBP HAT, capable of acting on p300-HAT (IC50: 1.4 μM), CBP-HAT (IC50: 2.2 μM), PCAF (IC50>100 μM), Myst3 (IC50>100 μM). CBP/p300-IN-19 hydrochloride has antitumor effects.
价 格：￥电议型 号：T63565产 地：中国大陆
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T63122CBP/p300-IN-19；化合物 CBP/p300-IN-19CBP/p300-IN-19
CBP/p300-IN-19 is a potent inhibitor of p300/CBP HAT, which can act on P300-HAT (IC50: 1.4 μM), CBP-HAT (IC50: 1.4 μm), 2.2 μM), PCAF (IC50>100 μM), and Myst3 (IC50>100 μM). CBP/p300-IN-19 has anti-tumor activity.
价 格：￥电议型 号：T63122产 地：中国大陆
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T63110CBP/p300-IN-15；化合物 CBP/p300-IN-15CBP/p300-IN-15
CBP/p300-IN-15 (compound 13a) is a potent inhibitor of p300 (IC50: 2.5 nM) and CBP (IC50: 28.0 nM). p300-IN-15 inhibits OVCAR-3 cells (EC50: 0.865 μM) and A2780 cells (EC50. 2.71 μM). 2.71 μM). CBP/p300-IN-15 can be used to study ovarian cancer.
价 格：￥电议型 号：T63110产 地：中国大陆
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T62720CBP/p300-IN-18；化合物 CBP/p300-IN-18CBP/p300-IN-18
CBP/p300-IN-18 (compound 8) is a potent inhibitor of EP300/CBP HAT, acting on HAT EP300 (IC50: 0.056 μM) and LK2 H3K27 (IC50: 0.46 μM).
价 格：￥电议型 号：T62720产 地：中国大陆
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T62700CBP/p300-IN-16；化合物 CBP/p300-IN-16CBP/p300-IN-16
CBP/p300-IN-16 (compound 1) is a potent inhibitor of EP300/CBP HAT, acting on HAT EP300 (IC50: 0.61 μM) and LK2 H3K27 (IC50: 2.24 μM).
价 格：￥电议型 号：T62700产 地：中国大陆
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T62415CBP/p300-IN-17；化合物 CBP/p300-IN-17CBP/p300-IN-17
CBP/p300-IN-17 (compound 7) is a potent inhibitor of EP300/CBP HAT, acting on HAT EP300 (IC50: 0.18 μM) and LK2 H3K27 (IC50: 0.69 μM).
价 格：￥电议型 号：T62415产 地：中国大陆
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T40344CBP/p300-IN-14CBP/p300-IN-14CBP/p300-IN-14
CBP/p300-IN-14, efficiently inhibits CBP/EP300 (lysine acetyltransferase) with an IC50 value of 3.3 nM.
价 格：￥电议型 号：T40344产 地：中国大陆
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T40144CBP/p300 ligand 2；CBP/p300 ligand 2CBP/p300 ligand 2
CBP/p300 ligand 2 is a selective ligand that binds to the target protein for PROTAC of dCBP-1, a potent and selective heterobifunctional degrader of p300/CBP.
价 格：￥电议型 号：T40144产 地：中国大陆
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T40143PROTAC CBP/P300 Degrader-1；PROTAC CBP/P300 Degrader-1PROTAC CBP/P300 Degrader-1；PROTAC CBP/P300 Degr
PROTAC CBP/P300 Degrader-1 is an effective compound that degrades CBP/P300 in a potent manner. It significantly reduces cell viability in various cancer cell lines.
价 格：￥电议型 号：T40143产 地：中国大陆
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T40142Thalidomide-NH-CBP/p300 ligand 2；Thalidomide-NH-CBP/p300 ligand 2Thalidomide-NH-CBP/p300 ligand 2；Th
Thalidomide-NH-CBP/p300 ligand 2 (P-007) is a PROTAC-based compound designed to degrade CBP and p300, acting as a functional antagonist (WO2020173440).
价 格：￥电议型 号：T40142产 地：中国大陆
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T12346CBP/p300-IN-5；化合物 T12346P300/CBP-IN-5；P300/CBP-IN-5
P300/CBP-IN-5 is a potent inhibitor of p300/CBP histone acetyltransferase (IC50 of 18.8 nM).
价 格：￥电议型 号：T12346产 地：中国大陆
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T12345CBP/p300-IN-3；化合物P300/CBP-IN-3P300/CBP-IN-3；P300/CBP-IN-3
CBP/p300-IN-3 (P300/CBP-IN-3) is an inhibitor of p300/CBP histone acetyltransferase.
价 格：￥电议型 号：T12345产 地：中国大陆
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T10702CBP/p300-IN-2；化合物 T10702CBP/EP300-IN-2；CBP/EP300-IN-2
CBP/EP300-IN-2 is an inhibitor of CBP/EP300 (IC50s: 1.07 nM and 5.96 nM for CBP/HTRF and Myc).
价 格：￥电议型 号：T10702产 地：中国大陆
