e-selectin

Carvedilol phosphate hemihydrate (BM 14190 phosphate hemihydrate) 是一种外消旋混合物，是一种非选择性β α-1受体阻断剂，具有抗高血压活性且缺乏内在拟交感神经活性。

Bimosiamose disodium has anti-inflammatory effects[1]. Bimosiamose disodium (TBC-1269Z) is a nonoligosaccharide pan-selectin inhibitor with IC50s of 88 μM, 20 μM, and 86 μM for E-selectin, P-selectin, and L-selectin, respectively.

Bimosiamose has anti-inflammatory effects[1]. Bimosiamose (TBC-1269) is a nonoligosaccharide pan-selectin antagonist with IC50s of 88 μM, 20 μM, and 86 μM for E-selectin, L-selectin, and P-selectin respectively.

ICAM-1-IN-1 是选择性的 ICAM-1和 E-selectin 抑制剂，IC50值分别为5和7 nM。

A-205804 是一种选择性口服有效的先导抑制剂，抑制 E-selectin 和 ICAM-1表达，IC50分别为 20 nM 和 25 nM，可用于慢性炎症疾病的研究。

2'-Hydroxychalcone 是一种药物合成中间体，可用于合成黄酮类化合物。负载在纳米乳液中的2'-Hydroxychalcone 在Danio rerio 模型对副球孢子菌显示出杀真菌活性。2'-Hydroxychalcone 通过负载脂质的Hepg2细胞中的氧化应激诱导细胞毒性。2'-Hydroxychalcone 抑制通过逆转录聚合酶链反应确定的肿瘤坏死因子-α诱导ICAM-1，VCAM-1和E-选择素的稳态转录水平，因此可能会干扰其基因的转录。

Anti-E-Selectin Antibody (CL2)为小鼠IgG2a, κ 嵌合抗体，专一性靶向人源E-Selectin。其同型对照为Mouse IgG2a kappa, Isotype Control。

Sialyl-Lewis X (sLeX), a sialylated fucosylated tetrasaccharide and endogenous antigen, serves as a high-affinity ligand for selectins (E-, P-, and L-selectin)[1]. It interacts with ELAM-1 and CD62, consequently inhibiting CD62-mediated neutrophil recruitment to inflammation sites[2].

15(S)-HpETE 是在 15-脂氧合酶途径中形成的花生四烯酸的产物，抑制血管生成。15(S)-HpETE 可在细胞中上调 CD31、E-选择素和基因选择素的表达。

2-chloro Palmitic acid is a monochlorinated form of palmitic acid . It is produced in a myeloperoxidase (MPO) and time-dependent manner in neutrophils stimulated by phorbol 12-myristate 13-acetate . 2-chloro Palmitic acid (10 μM) induces neutrophil extracellular trap (NET) formation (NETosis) in human neutrophils, increasing DNA release from neutrophils, colocalization of MPO with extracellular DNA (ecDNA), and trapping of E. coli. It increases COX-2 protein levels in human coronary artery endothelial cells (HCAECs) when used at a concentration of 50 μM and increases production of P-selectin, von Willebrand factor, and angiopoietin-2 in HCAECs, as well as neutrophil and platelet adherence, when used at a concentration of 10 μM. 2-chloro Palmitic acid (10-50 μM) also induces apoptosis in THP-1 cells and primary human monocytes and increases caspase-3 activity in THP-1 cells.

Trofinetide是一种衍生自具有神经保护作用的三肽Gly-Pro-Glu的化合物，后者是胰岛素样生长因子-1（IGF-1）的N-端序列。在10 nM的浓度下使用时，它能减少由蛋白磷酸酶抑制剂奥卡达酸在原代大鼠胚胎纹状体神经元中引起的细胞死亡。Trofinetide在一种由穿透性弹道样脑损伤引起的大鼠神经炎症模型中减少了编码IL-1β、TNF-α、IL-6和E-selectin的mRNA的脑表达。在通过中脑动脉闭塞（MCAO）引起的大鼠脑损伤模型中，以30和60 mg kg的剂量给药时，它减少了皮层和纹状体梗塞区域。Trofinetide（每天100 mg kg）减少了树突棘的数量，并逆转了在fmr1- -敲除小鼠脆性X综合征模型中的社交识别和情景恐惧条件反射的缺陷，同时也减少了睾丸重量的增加。含有Trofinetide的制剂已被用于治疗Rett综合征。

P-selectin antagonist 1 (Compound 11b) 是一种对pan-selectin (IC50 82 μM) 和E-selectin (KD 0.91 μM) 有效的拮抗剂。

HUN-7293 是一种细胞粘附分子抑制剂，能选择性地抑制VCAM-1、ICAM-1和E-selectin的表达 (IC50=1-24 nM)。HUN-7293 可用于以细胞粘附分子过度表达为特征的炎症性和自身免疫性疾病的研究。

P-ESBP-DOX 是由 E-selectin 结合肽和 Doxorubicin 组成的 HPMA 共聚物-药物偶联物。此化合物在 TNFα 激活的人类血管内皮细胞 IVEC 中显示出细胞毒性，其 IC50 为 0.28 μM。P-ESBP-DOX 可应用于肿瘤血管研究。