2b1

1-Ethynylpyrene 是有效的细胞色素P450 1A1, 1A2和2B1抑制剂，抑制的IC50分别为 0.18，0.32 和 0.04 μM。

Rutin (Quercetin 3-O-rutinoside) 属于黄酮类天然产物，具有血脑屏障渗透性。Rutin 具有广泛的生物活性，包括抗氧化、抗炎、抗肿瘤、降血糖、神经保护、抗菌、抗衰老等等。

Inh2-B1是一种针对STK1（即Ser Thr蛋白激酶）的抑制剂，通过直接结合到STK1的ATP结合催化区域发挥作用。STK1是金黄色葡萄球菌细胞壁生物合成的重要组成部分，且是导致MRSA耐药性的关键因素。因此，Inh2-B1被视为一种“抗生素耐药性破解剂”，具有阻止生物膜形成的功能。

Histone H2B (108-125) is a peptide fragment of histone H2B that corresponds to amino acid residues 109-126 of the human histone H2B sequence. It contains an N-terminal biotinylated lysine followed by a tryptophan linker. Histone H2B can be modified by addition of an O-linked N-acetylglucosamine (GlcNAc) moiety to the serine residue at position 112, which promotes monoubiquitination of the lysine at position 120.1 Both of these modifications are associated with active transcription. Histone H2B also has lysine residues at positions 108, 116, and 120 that are subject to acetylation.2References1. Fujiki, R., Hashiba, W., Sekine, H., et al. GlcNAcylation of histone H2B facilitates its monoubiquitination. Nature 480(7378), 557-560 (2011).2. Portela, A., and Esteller, M. Epigenetic modifications and human disease. Nat. Biotechnol. 28(10), 1057-1068 (2010). Histone H2B (108-125) is a peptide fragment of histone H2B that corresponds to amino acid residues 109-126 of the human histone H2B sequence. It contains an N-terminal biotinylated lysine followed by a tryptophan linker. Histone H2B can be modified by addition of an O-linked N-acetylglucosamine (GlcNAc) moiety to the serine residue at position 112, which promotes monoubiquitination of the lysine at position 120.1 Both of these modifications are associated with active transcription. Histone H2B also has lysine residues at positions 108, 116, and 120 that are subject to acetylation.2 References1. Fujiki, R., Hashiba, W., Sekine, H., et al. GlcNAcylation of histone H2B facilitates its monoubiquitination. Nature 480(7378), 557-560 (2011).2. Portela, A., and Esteller, M. Epigenetic modifications and human disease. Nat. Biotechnol. 28(10), 1057-1068 (2010).

LM22B-10 是TrkB TrkC 神经营养因子受体激活剂，诱导体内外TrkB、TrkC、AKT 和ERK 的活化。

Bergamottin (5-Geranoxypsoralen) 是竞争性CYP1A1抑制剂(Ki:10.703 nM)。

NOX-6-18 (GPR132-B-160) 是一种具有高效性和选择性的 GPR132 拮抗剂，具有促进胰岛素分泌活性，可以调节胰岛内的巨噬细胞重编程，减少体重增加。

2-Pentyl-1H-benzo[d]imidazole是Cytochrome P450 1A1和2B1的微摩尔级别抑制剂，并且对Fusarium verticillioides有抗菌活性。

7ETMC is a selective Human Cytochrome P450s 1A1 and 1A2 inhibitor. 7ETMC showed IC50s of 0.46 μM and 0.50 μM for P450s 1A1 and 1A2 in the first six minutes, respectively, and did not show any inhibition activity for P450s 2A6 and 2B1 even at the dose of 5

Mulberrin (Kuwanon C) 能够抑制有机阴离子转运多肽 2B1 介导的雌酮-3-硫酸盐摄取(IC50:1.8±1.5 μM)。