Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T25175 |
BRD 9757
BRD9757,N-Hydroxy-1-cyclopentene-1-carboxamide,BRD-9757 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
BRD 9757 (N-Hydroxy-1-cyclopentene-1-carboxamide) 是 HDAC6 的选择性抑制剂 (IC50 = 30 nM)。 | |||
T10602L |
BRD 4354
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
BRD 4354 是 HDAC5 和 HDAC9 的抑制剂,对 HDAC5 和 HDAC9 的 IC50 值分别为 0.85 和 1.88 μM。 | |||
T10603 |
BRD-6929
|
HIV Protease; HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome |
BRD-6929 是一种选择性的脑渗透性的HDAC1和HDAC2抑制剂 ,IC50值为 1 和 8 nM。它对 HDAC1 和 HDAC2 有高亲和力,Ki 值为 0.2 和 1.5 nM。它可研究情绪相关行为。 | |||
T26894 |
BRD0209
BRD-0209,BRD 0209 |
GSK-3 | PI3K/Akt/mTOR signaling; Stem Cells |
BRD0209 是一种有效、选择性的 GSK3α/β 抑制剂 | |||
T30577 |
BRD0418
BRD 0418,BRD-0418 |
Others | Others |
BRD0418作为 TRIB1表达的上调因子,导致肝脏脂蛋白代谢从脂肪生成到清除的重新编程。 | |||
T23820 |
BRD32048
BRD-32048,BRD 32048 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
BRD32048 可以与与 ETV1直接结合,KD 为 17.1 μM。BRD32048调节 ETV1 介导的转录活性和 ETV1 驱动的癌细胞侵袭。 BRD32048可以抑制 ETV1 乙酰化并促进其降解。 | |||
T2292 |
FPH2
BRD-9424 |
Others | Others |
FPH2 (BRD-9424) 是促进 iPS 衍生肝细胞分化的小分子。它诱导原代人肝细胞的功能性增殖,有潜质用于研究肝脏疾病的新疗法。 | |||
T6506 |
FPH1
BRD-6125 |
Others | Others |
FPH1 (BRD-6125) 在体外能够提高人肝原代细胞的活性及数量,并促进 iPS 细胞向肝系分化。 | |||
T26901 |
BRD-9526
BRD 9526 |
||
BRD-9526 is a potent and selective inhibitor of Sonic Hedgehog (Shh). | |||
T22279 |
BRD0539
|
CRISPR/Cas9 | DNA Damage/DNA Repair |
BRD0539 是一种具有细胞渗透性的 spCas9 抑制剂,可阻断 spCas9 与 DNA 的结合,抑制化脓性链球菌 Cas9 (SpCas9)。 | |||
T2353 |
BRD7116
BRD7716 |
DNA gyrase; Antibacterial | DNA Damage/DNA Repair; Microbiology/Virology |
BRD7116 与细菌 DNA 促旋酶竞争性结合, 作用于LSCe 细胞,EC50值为200 nM。它具有细胞非自主抗白血病活性。 | |||
T30579 |
BRD4097
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
BRD4097是HDAC1/2/3/8检测中的阴性对照品,是一种选择性组蛋白去乙酰化酶(HDAC3)抑制剂,可用于保护b 细胞和改善胰岛素抵抗,有助于促进认知功能和增强学习和记忆的形成。 | |||
T6793 |
BRD7552
|
Others | Others |
BRD7552 是PDX1转录因子诱导剂,它能够上调人类原代胰岛和导管细胞中 PDX1 的表达,诱导 PDX1 启动子的表观遗传变化与转录激活一致,提高胰岛素表达。其中 PDX1 是参与胰腺发育和β细胞功能的关键转录因子。 | |||
T21715 |
BRD6688
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
BRD6688 为 HDAC2 的选择性抑制剂。本品可使原代小鼠神经元细胞中的 H4K12 和 H3K9 组蛋白的乙酰化作用增强。在 CK-p25 小鼠模型中,它可透过血脑屏障,并改善由p25 引起的神经退行性病变相关的记忆缺陷。 | |||
T26897 |
BRD2492
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
BRD2492 是一种具有选择性和有效的 HDAC1 和 HDAC2 双重抑制剂,具有潜在的抗癌、抗肿瘤和抗增殖活性,抑制 HDAC1/2 、HDAC3 和 HDAC6。BRD2492 对乳腺癌细胞系的生长有抑制作用,诱导细胞凋亡。 | |||
T10602 |
BRD 4354 ditrifluoroacetate
BRD 4354 ditrifluoroacetate (315698-07-8 free base) |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
BRD 4354 (ditrifluoroacetate) is a moderately potent inhibitor of HDAC5 and HDAC9 (IC50s: 0.85 and 1.88 μM). | |||
T2102 |
FH1
BRD-K4477,NSC 12407 |
Others | Others |
FH1 (NSC-12407) 可提高肝细胞功能,促进诱导多能干 (iPS) 衍生的肝细胞向更成熟的表型分化,并促使分化良好的肝细胞样细胞 (iHeps) 培养物的成熟。 | |||
T9329 |
BRD0639
|
Histone Methyltransferase | Chromatin/Epigenetic |
BRD0639 是首创的PRMT5-substrate adaptor interaction 的抑制剂。BRD0639 是一种 PRMT5 结合基序 (PBM) 竞争性抑制剂,可以支持 PBM 依赖的 PRMT5 活性的研究。 | |||
T7378 |
BRD9539
|
Histone Methyltransferase | Chromatin/Epigenetic |
BRD9539 是一种组蛋白甲基转移酶G9a 抑制剂,IC50为 6.3 μM,还抑制PRC2活性。 | |||
T35872 | BRD-8000.3 | ||
BRD-8000.3 is a narrow-spectrum, bactericidal antimycobacterial agent known for its specific inhibition of EfpA. It exhibits potent activity against wild-type strains and proves to be a valuable tool in tuberculosis research[1]. | |||
T6421 |
BRD73954
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
BRD73954 是一种有效且特异性的 HDAC 抑制剂,对 HDAC6 和 HDAC8 的 IC50 分别为 36 nM 和 120 nM。 | |||
T14779 |
BRD7389
|
SGK; FLT; Pim; CDK; S6 Kinase; DAPK | Angiogenesis; Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; JAK/STAT signaling; MAPK; Metabolism; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors |
BRD7389 是一种 RSK 家族激酶抑制剂,对 RSK1、RSK2 和 RSK3 的 IC50 分别为 1.5 μM、2.4 μM 和 1.2 μM。 | |||
T1923 |
BRD4770
|
Histone Methyltransferase | Chromatin/Epigenetic |
BRD4770 是组蛋白甲基转移酶G9a 抑制剂,可激活共济失调毛细血管扩张突变途径并诱导细胞衰老。它可抑制H3K9的二甲基和三甲基化,EC50为 5 µM。 | |||
T14778 |
BRD6989
|
IL Receptor; CDK; Interleukin | Cell Cycle/Checkpoint; Immunology/Inflammation |
BRD6989 是天然产物皮质抑素 A 的类似物,可抑制CDK8并上调IL-10,抑制重组 CDK8 或 CDK19 复合物的激酶活性。它选择性结合 CDK8 复合物,IC50约为 200 nM。 | |||
T10608 |
BRD5648
(R)-BRD0705 |
GSK-3 | PI3K/Akt/mTOR signaling; Stem Cells |
BRD5648 ((R)-BRD0705) 是 BRD0705 的 阴性对照,BRD0705 是旁系选择性和口服有效的 GSK3α 抑制剂,Kd 为 4.8 μM,IC50为 66 nM。与 GSK3β (IC50为 515 nM) 相比,BRD0705 对 GSK3α 的选择性更高 (8 倍)。BRD0705 可用于急性髓细胞性白血病。 | |||
T8233 |
BRD3308
|
Apoptosis; HIV Protease; HDAC | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome |
BRD3308 是一种高选择性的HDAC3抑制剂,IC50为 54 nM。它可激活HIV-1转录并破坏HIV-1潜伏期。它抑制由炎性细胞因子或糖脂毒性应激诱导的胰腺 β 细胞凋亡,并增加功能性胰岛素释放。 | |||
T10606 |
BRD0705
|
GSK-3 | PI3K/Akt/mTOR signaling; Stem Cells |
BRD0705 是一种具有旁系选择性的、口服具有活性的GSK3α抑制剂,其 IC50=66 nM,Kd=4.8 μM。 它与 GSK3β (其 IC50=515 nM) 相比,对GSK3α的选择性更高 (8 倍)。它可用于研究急性髓细胞性白血病。 | |||
T70600 | BRD-7880 | ||
BRD-7880 is a potent and highly specific inhibitor of aurora kinases B and C. | |||
T10605 | BRD-K98645985 | Others | Others |
BRD-K98645985 is a BAF transcriptional repression inhibitor (EC50: ~2.37 µM). It binds ARID1A-specific BAF complexes, potently reverses HIV-1 latency and prevents nucleosomal positioning. | |||
T12664 |
(Rac)-BRD0705
|
Others | Others |
(Rac)-BRD0705 是 BRD0705 的活性较低的外消旋体。 BRD0705 是一种有效的特异性 GSK3α 抑制剂。 | |||
T16905 |
SNIPER(BRD)-1
|
Others | Others |
SNIPER(BRD)-1 is a chemical compound composed of a derivative of the IAP antagonist LCL-161 and the BET inhibitor (+)-JQ-1, linked together. It promotes the degradation of BRD4 through the ubiquitin-proteasome pathway and effectively degrades cIAP1, cIAP2, and XIAP with IC50 values of 6.8 nM, 17 nM, and 49nM, respectively[1]. | |||
T69692 |
BRD-K25923209
|
||
BRD-K25923209 is a novel inhibitor of BAF transcriptional repression. | |||
T41198 |
BRD PHOTAC-I-3
|
||
BRD PHOTAC-I-3 is a photoswitchable BET bromodomain degrader (PHOTAC, PHOtochemically TArgeting Chimera). BRD PHOTAC-I-3 comprises a ligand for an E3 ligase, a photoswitch, and the BET bromodomain targeting ligand (+)-JQ1. Exhibits cytotoxicity and degrades BRD4, BRD3 and to a lesser extent BRD2 in lymphoblast cells upon irradiation with 390 nm light, but not in the dark. | |||
T10604 | BRD-IN-3 | Others | Others |
BRD-IN-3 is a highly potent PCAF bromodomain (BRD) inhibitor (IC50: 7 nM). It also exhibits activity against GCN5 and FALZ. | |||
T17697 |
BRD7-IN-1
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
BRD7-IN-1 是一种修饰的 BI7273 衍生物 (BRD7/9 抑制剂)。BRD7-IN-1 通过与 VHL 配体连接形成 PROTAC VZ185。VZ185 抑制 BRD7/9 的 DC50分别是 4.5 nM 和1.8 nM。 | |||
T12551 |
PROTAC BRD4 ligand-1
|
Epigenetic Reader Domain; Ligands for Target Protein for PROTAC | Chromatin/Epigenetic; PROTAC |
PROTAC BRD4 ligand-1 是 PROTAC GNE-987 靶向 BRD4 蛋白的配体,也是一种 BET 的抑制剂。 | |||
T14776 |
BRD4 Inhibitor-10
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
BRD4 Inhibitor-10 是一种BRD4-BD1抑制剂,IC50为 8 nM。 | |||
T61361 |
BRD-8899
|
||
BRD-8899是STK33的抑制剂,其IC50值为 11 nM。 | |||
T30584 |
BRD9092
BRD 9092,BRD-9092 |
||
BRD9092 is an enhancer of reactive oxygen species that are nontoxic or cause genotype-selective cell death. | |||
T26900 |
BRD7539
BRD-7539,BRD 7539 |
||
BRD7539B is a Dihydroorotate dehydrogenase (DHODH) inhibitor . RD7539 shows to target PfDHODH (IC50 = 0.033 μM) selectively over human (Hs) DHODH (IC50 > 50 μM). | |||
T30578 |
BRD3067
BRD-3067,BRD 3067 |
||
BRD3067 is a negative control for tubastatin A. | |||
T23821 |
BRD4884
BRD-4884,BRD 4884 |
||
BRD4884 is a selective inhibitor of HDAC2 that acts by enhancing the learning and memory processes. | |||
T30582 |
BRD56491
BRD-56491,BRD 56491 |
||
BRD56491 is a non-toxic reactive oxygen species (ROS) enhancer that strongly elevates markers of oxidative stress without causing cell death. | |||
T25176 |
BRD2577
BRD-2577,BRD 2577 |
||
BRD2577 is an HDAC inhibitor, by suppressing multiple HDAC enzymes and modulating acetylation levels in cells. | |||
T26898 |
BRD2879
BRD 2879,BRD-2879 |
||
BRD2879 is a potent and cell-active inhibitor of IDH1-R132H (IC50 = 50 nM). | |||
T26896 |
BRD1652
BRD-1652,BRD 1652 |
||
BRD1652 is a highly selective and potent GSK3 inhibitor. | |||
T30581 |
BRD5459
BRD-5459,BRD 5459 |
||
BRD5459 is a kind of reactive oxygen species enhancer that is non-toxic or leads to genotype selective cell death. Brd5459 can selectively kill cancer cells in various in vitro and in vivo models. | |||
T30583 |
BRD6897
BRD-6897,BRD 6897 |
||
BRD6897 is a mitochondrial content inducer. | |||
T26899 |
BRD50837
BRD-50837,BRD 50837 |
||
BRD50837 is a potent and selective inhibitor of Sonic Hedgehog (Shh). | |||
T6859 |
I-BRD9
GSK602 |
Epigenetic Reader Domain | Chromatin/Epigenetic |
I-BRD9 (GSK602) 是一种选择性的 BRD9 细胞抑制剂,pIC50 为 7.3。 |