bim

ABT-737 是 BH3 模拟物，是一种 Bcl-2、Bcl-xL 和 Bcl-w 的抑制剂 (EC50=30.3 nM 78.7 nM 197.8 nM)。ABT-737 具有抗肿瘤活性和抗衰老活性。

BIM-46174 是一种5,6,7,8-四氢咪唑[1,2-a]吡嗪衍生物，抑制异源三聚体 Galpha Gbetagamma 蛋白复合物，具有抗癌活性，可抑制大量人类癌细胞系的生长，诱导 caspase-3 依赖性癌细胞凋亡，诱导聚 （ADP-核糖） 聚合酶裂解。

BIM-46174 HCl 是选择性 G 蛋白抑制剂，具有抗癌活性，抑制大量人类癌细胞系的生长，可诱导半胱天冬酶 3 依赖性细胞凋亡。

BIM 23056 Acetate 是一种有效且可克服的人类重组 sst5 受体拮抗剂。

Bim 21009 is an inhibitor of gonadorelin.

Bim-BLK-A efficiently blocks Bim-induced apoptosis after Bax is activated on the mitochondria. The cellular target of Bim-BLK-A was identified to be the succinate dehydrogenase subunit B (SDHB) protein of complex II of the mitochondrial electron transfer

BIM-23190 hydrochloride, a selective agonist for somatostatin receptors SSTR2 and SSTR5 with Ki values of 0.34 nM and 11.1 nM respectively, is a somatostatin analog utilized in research on cancer and acromegaly[1][3].

BIM-23190 is a somatostatin analog that acts as a selective agonist for SSTR2 and SSTR5 receptors. It displays potency with K i values of 0.34 nM and 11.1 nM for SSTR2 and SSTR5, respectively. BIM-23190 finds utility in cancer and acromegaly research.

BIM-23190 aceate 是一种生长抑素类似物，一种 SSTR2 和 SSTR5 的选择性激动剂。 BIM-23190 可用于癌症和肢端肥大症研究。

Bim-IN-1 是一种 Bim 表达的有效抑制剂，毒性较低。Bim-IN-1 可以减少 Bim 的表达水平，且几乎不会抑制蛋白激酶 A。

BIM-46068 is a potent and specific inhibitor of human farnesyltransferase. In regard to a panel of cell lines, using the Compare analysis to determine the Pearson coefficient correlation, the anti-proliferative spectrum of BIM-46068 has been shown to be distinct from the profile of typical chemotherapeutic agents.

BIM-46050 is a potent and specific inhibitor of human farnesyltransferase. BIM-46050 is free acidic form of BIM-46068. The IC50 values for in vitro inhibition of human brain FTase indicate that BIM-46050 and the ester form BIM-46068 are potent inhibitors of farnesyltransferase. Their potencies are in the nanomolar range and compare favorably with the compounds B581, FTI-277 and L745,631. B581 is an analog of the tetrapeptide Cys-Val-Phe-Met obtained by replacement of the amino-terminal amide bonds inhibiting processing of farnesylated proteins specifically. FTI-277 is a methyl ester of FTI-276, reported as a preferential inhibitor of FTase over GGTase I (100-fold). L745,631 is a 2-substituted piperazine reported to be a highly selective inhibitor of FTase over GGTase (2,000-fold). The selectivity of BIM-46050 and BIM-46068 for FTase over GGTase is very similar for both compounds (3,000-fold).

BIM-26226 是一种胃泌素释放肽，是一种强效选择性的bombesin receptor 拮抗剂。 BIM-26226 抑制 BN 或 GRP 刺激的淀粉酶释放，IC50值在纳摩尔范围内。BIM-26226 可用于癌症研究。

BIM23056 TFA为线性八肽类化合物，作为sst3与sst5生长抑素受体的有效拮抗剂，其Ki值分别为10.8和5.7。

BimBH3，一种具有生物活性的肽，属于促凋亡Bcl-2蛋白家族。

BIM-23027为高选择性sst2受体激动剂（EC50=0.32 nM），其功能效果类似生长抑素（SRIF，环状十四肽）。该化合物可促进多巴胺的释放，此过程通过Glu依赖的机制进行调控。

Angiopep-Bim BH3 hydrochloride，一种可穿透血脑屏障的多肽，用于探究中枢神经系统通透性的研究。

This Bim peptide belongs to the pro-apoptotic group of the Bcl-2 family of proteins.

Bim BH3, Peptide IV TFA is a 26-site residue of BH3 protein Bim, belonging to the pro-apoptotic group of bcl-2 protein family.

BIM-46187 4HCl (PH-064 4HCl) 是一种异源三聚体 G 蛋白复合物抑制剂。

BIM 23042 Acetate 是一种选择性的神经调节素 B 拮抗剂。

BIM, Biotinylated is a Bim peptide fragment (residues 81-106) with a biotin moiety attached.

MJN68390 对 CASP8 的表观 IC50值为 15 μM，对 CASP10 不显示活性。

BTSA1 是一种有口服活性的 BAX 激活剂，IC50为 250 nM，EC50为 144 nM。它以高亲和力和特异性与 N 末端激活位点结合，并诱导 BAX 发生构象变化，从而导致BAX 介导的细胞凋亡。