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T60072ZL0590non-KAc binding site,ZL0590,ZL-0590,BRD4 BD1,Inhibitor,acute airway inflammation,inhibit,Epige
ZL0590 is an effective and selective inhibitor of BD1-BRD4 (IC50 = 90 nM) with anti-inflammatory activities.
价 格：￥电议型 号：T60072产 地：中国大陆
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T6828ZL0420inhibit,Epigenetic Reader Domain,(E/Z)-ZL0420,BRD4,airway inflammation,immune response genes,Z
ZL0420 is a potent and selective bromodomain-containing protein 4 ( BRD4 ) inhibitor with nanomolar binding affinities to bromodomains (BDs) of BRD4. ZL0420 has IC 50 values of 27 nM against BRD4 BD1 and 32 nM against BRD4 BD2.
价 格：￥电议型 号：T6828产 地：中国大陆
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T61318BRD4 Inhibitor-20
BRD4 Inhibitor-20 is a potent bromodomain protein 4 (BRD4) inhibitor with oral activity. BRD4 Inhibitor-20 has antiproliferative activity in cancer cell lines and is used in studies of various cancers, such as colon cancer.
价 格：￥电议型 号：T61318产 地：中国大陆
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T9629WAY-309060Inhibitor,WAY309060,MCF7,BRD4 Inhibitor-24,antitumor,Epigenetic Reader Domain,inhibit,brea
WAY-309060 is a BRD4 small molecule inhibitor with antitumor activity.
价 格：￥电议型 号：T9629产 地：中国大陆
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T12551PROTAC BRD4 ligand-1PROTAC BRD4 ligand 1,PROTAC BRD4 ligand1,PROTAC BRD-4 ligand-1
PROTAC BRD4 ligand-1 is a ligand for BRD4 for Protac GNE-987 and an inhibitor of BET.
价 格：￥电议型 号：T12551产 地：中国大陆
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T8932GSK046GSK046,Epigenetic Reader Domain,BRDT,BRD2,inhibit,immuno-inflammation,GSK 046,GSK-046,BRD4,Inh
GSK046 is a potent, selective and orally active BD2 bromodomain inhibitor of the BET proteins(IC50s of 264 nM (BRD2 BD2), 98 nM (BRD3 BD2), 49 nM (BRD4 BD2) and 214 nM (BRDT BD2), respectively). It has immunomodulatory activity.
价 格：￥电议型 号：T8932产 地：中国大陆
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T4365FL-411FL411；FL 411；BRD4-IN-1
FL-411 is a potent and selective BRD4 inhibitor with an IC50 of 0.43±0.09 μM for BRD4.
价 格：￥电议型 号：T4365产 地：中国大陆
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T1923BRD4770
BRD4770 is a histone methyltransferase G9a inhibitor and induces cell senescence.
价 格：￥电议型 号：T1923产 地：中国大陆
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T14776BRD4 Inhibitor-10
BRD4 Inhibitor-10 is an inhibitor of BRD4-BD1 (IC50: 8 nM).
价 格：￥电议型 号：T14776产 地：中国大陆
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T12551PROTAC BRD4 ligand-1PROTAC BRD4 ligand-1
PROTAC BRD4 ligand-1 is a potent inhibitor of BET .
价 格：￥电议型 号：T12551产 地：美洲
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T1923BRD4770BRD4770
BRD4770 is a histone methyltransferase G9a inhibitor and induces cell senescence.
价 格：￥电议型 号：T1923产 地：美洲
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T81386PROTAC BRD4 Degrader-22；化合物 PROTAC BRD4 Degrader-22PROTAC BRD4 Degrader-22
PROTAC BRD4 Degrader-22 (Compd 44h) is a PROTAC-based degrader targeting BRD4, exhibiting a pDC50 of 9.2 in MOLT4 cells over 24 hours [1].
价 格：￥电议型 号：T81386产 地：中国大陆
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T79818PROTAC BRD4 Degrader-21；化合物 PROTAC BRD4 Degrader-21PROTAC BRD4 Degrader-21
PROTAC BRD4 Degrader-21 (Comp 74), a potent degrader of BRD4, has demonstrated substantial inhibition of tumor growth in mouse xenograft models, showing its potential for use in anticancer research [1].
价 格：￥电议型 号：T79818产 地：中国大陆
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T79768HDAC/JAK/BRD4-IN-1；化合物 HDAC/JAK/BRD4-IN-1HDAC/JAK/BRD4-IN-1
HDAC/JAK/BRD4-IN-1 (compound 25ap) is a potent triple inhibitor targeting HDAC, JAK, and BRD4. This compound not only inhibits cell proliferation but also induces apoptosis in MDA-MB-231 cells and demonstrates in vivo anticancer efficacy [1].
价 格：￥电议型 号：T79768产 地：中国大陆
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T78956PROTAC BRD3/BRD4-L degrader-2；化合物 PROTAC BRD3/BRD4-L degrader-2PROTAC BRD3/BRD4-L degrader-2
PROTAC BRD3/BRD4-L degrader-2, a PROTAC molecule, selectively degrades cellular BRD3 and BRD4-L with K i values of 16.91 and 2.8 nM, respectively, and exhibits robust antitumor activity in mouse xenograft models, serving as a research tool for cancer [1].
价 格：￥电议型 号：T78956产 地：中国大陆
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T78851BRD4 Inhibitor-28；化合物 BRD4 Inhibitor-28BRD4 Inhibitor-28
BRD4 Inhibitor-28 (Compound 18), an orally active molecule, selectively inhibits the bromodomains of BRD4 (BRD4-BD1 and BRD4-BD2) with IC50 values of 15 and 55 nM, respectively. It also demonstrates inhibition of BRD2-BD1, BRD3-BD1, and BRDT-BD1 with IC50 values of 19, 25, and 68 nM, respectively. Furthermore, this compound exhibits anti-melanoma activity [1].
价 格：￥电议型 号：T78851产 地：中国大陆
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T78647PROTAC BRD4 Degrader-16；化合物 PROTAC BRD4 Degrader-16PROTAC BRD4 Degrader-16
PROTAC BRD4 Degrader-16 is a potent degrader of BRD4, exhibiting IC50 values of 34.58 nM for BRD4 (BD1) and 40.23 nM for BRD4 (BD2). It significantly reduces Cyclin B1 expression, thereby impeding G2/M phase progression, and induces apoptosis in MV-4-11 cells [1].
价 格：￥电议型 号：T78647产 地：中国大陆
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T78555BRD4u00A0Inhibitor-27；BRD4抑制剂27BRD4u00A0Inhibitor-27
BRD4?Inhibitor-27 is a potent BRD4 inhibitor that inhibits BRD4 BD1 and BRD4 BD2 with IC50s of 9.6 and 11.3 μM, respectively.BRD4?Inhibitor-27 has anticancer activity and can be used for breast cancer research.
价 格：￥电议型 号：T78555产 地：中国大陆
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T77921PROTAC BRD4 ligand-2 hydrochloride；化合物 PROTAC BRD4 ligand-2 hydrochloridePROTAC BRD4 ligand-2 hydroc
PROTAC BRD4 Ligand-2 Hydrochloride serves as a ligand targeting the BRD4 protein, specifically designed for use with PROTAC CFT-2718.
价 格：￥电议型 号：T77921产 地：中国大陆
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T77339BRD4-IN-4；化合物BRD4-IN-4BRD4-IN-4
BRD4-IN-4 is a selective BRD4 inhibitor with an IC50 value of 6.83 μM for BRD4.BRD4-IN-4 selectively inhibits the proliferation of the MV4-11 cell line and arrests the cells in G1 phase.BRD4-IN-4 can be used to study MLL leukemias.
价 格：￥电议型 号：T77339产 地：中国大陆
