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Cat. No. | Product Name | Target | Signaling Pathways |
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T69691 |
Pocenbrodib
FT-7051,P-300 |
Epigenetic Reader Domain | Chromatin/Epigenetic |
Pocenbrodib (FT-7051) 是一种有效的 CBP/p300 家族的溴结构域抑制剂,具有潜在的抗肿瘤活性,可口用于研究癌症。 | |||
T12345 |
CBP/p300-IN-3
P300/CBP-IN-3 |
Histone Acetyltransferase | Chromatin/Epigenetic |
CBP/p300-IN-3 (P300/CBP-IN-3) 是一种组蛋白乙酰转移酶抑制剂。 | |||
T40144 |
CBP/p300 ligand 2
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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. | |||
T12346 |
CBP/p300-IN-5
P300/CBP-IN-5 |
Epigenetic Reader Domain | Chromatin/Epigenetic |
P300/CBP-IN-5 is a potent inhibitor of p300/CBP histone acetyltransferase (IC50 of 18.8 nM). | |||
T40344 |
CBP/p300-IN-14
CBP/p300-IN-14 |
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CBP/p300-IN-14, efficiently inhibits CBP/EP300 (lysine acetyltransferase) with an IC50 value of 3.3 nM. | |||
T39826 |
CBP/p300-IN-8
CBP/p300-IN-8 |
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CBP/p300-IN-8 is a potent inhibitor of the CBP/P300 family of bromodomains . CBP/p300-IN-8 inhibits CBP ( IC 50 =0.01-0.1 μΜ) and BRD4 ( IC 50 =1-1000 μΜ) activity. | |||
T10702 |
CBP/p300-IN-2
CBP/EP300-IN-2 |
Epigenetic Reader Domain; c-Myc | Cell Cycle/Checkpoint; Chromatin/Epigenetic |
CBP/EP300-IN-2 is an inhibitor of CBP/EP300 (IC50s: 1.07 nM and 5.96 nM for CBP/HTRF and Myc). | |||
T40143 |
PROTAC CBP/P300 Degrader-1
PROTAC CBP/P300 Degrader-1 |
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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. | |||
T40142 |
Thalidomide-NH-CBP/p300 ligand 2
Thalidomide-NH-CBP/p300 ligand 2 |
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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). | |||
T14042 |
4-P-PDOT
4-phenyl-2- propionamidotetralin |
Melatonin Receptor; MT Receptor | GPCR/G Protein; Neuroscience |
4-P-PDOT (4-phenyl-2- propionamidotetralin) 是一种选择性和亲和性的褪黑激素受体拮抗剂,可显著抵消褪黑激素介导的抗氧化作用。它对MT2的选择性是 MT1 的 300 倍以上。 | |||
T27389 |
Frequentin
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Frequentin, an antibiotic originally isolated from P. frequentans, is active against bacteria (MICs = 200 and 300 µg/ml for B. subtilis and S. aureus, respectively) and fungi. | |||
T38347 |
Zelkovamycin
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Zelkovamycin is a cyclic peptide antibiotic originally isolated from Streptomyces.1 It inhibits growth of X. oryzae, P. oryzae, S. aureus, and A. laidlawii in a concentration-dependent manner when used at concentrations ranging from 0.01 to 300 μg/ml.References1. Zhang, H., Tomoda, H., Tabata, N., et al. Zelkovamycin, a new cyclic peptide antibiotic from Streptomyces sp. K96-0670. I. Production, isolation and biological properties. J. Antibiot. (Tokyo) 52(1), 29-33 (1999). Zelkovamycin is a cycl... | |||
T78135 |
Nicotelline
Nicotellin |
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Nicotelline(Nicotellin)是一种与尼古丁相关的生物碱,作为人类cDNA表达的细胞色素P-450 2A6(CYP2A6)的弱抑制剂,不显著抑制该酶介导的香豆素7-羟基化反应,在300 μM浓度下效果更是如此。此外,Nicotelline还被用作烟草烟雾中颗粒物(PM)的示踪剂和生物标记物。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T2911 |
Stevioside
甜菊苷,蛇菊苷 |
TLR | Immunology/Inflammation |
Stevioside 是一种天然甜味剂,从甜叶菊叶中提取的获得,具有抗癌作用。 |