cr-8

(R)-CR8 trihydrochloride (CR8, (R)-Isomer trihydrochloride) 是一种 CDK1 2 5 7 9 抑制剂，可作为分子胶降解剂，具有神经保护活性，可诱导细胞凋亡。

(S)-CR8 is an effective second-generation cyclin-dependent kinase inhibitor.

(R)​-​CR8 ((R)-Isomer) 是 Roscovitine 类似物，是CDK1 2 5 7 9抑制剂。它作为一种分子胶降解剂来消耗细胞周期蛋白 K。它诱导细胞凋亡并具有神经保护作用。

OICR-8268-acrylic acid-amino-PEG9-amine 是一种 E3 泛素酶配体-连接子偶联物 (E3 Ligase Ligand-linker conjugate)，可用于合成 OICR41114。

OICR-8268-acrylic acid 是一种用于 E3 泛素连接酶的配体 (ligand for E3 ubiquitin ligase)，它能够通过 linker 连接靶蛋白配体，形成 OICR41114，该化合物可用于抗癌研究。

OICR-8268是一种可逆DCAF1配体，可与DCAF1 WDR结构域结合，Kd为38 nM，可用于基于DCAF1的PROTAC开发。

CR-8020是一种人源IgG1抗体，专门结合甲型流感病毒H3N2。该抗体与H3N2毒株的血凝素 (HA) 结合，对于A Brisbane 10 2007和A Wyoming 3 2003，其IC50分别为3.36 nM和0.06 nM。CR-8020的同型对照可参考HumanIgG1kappa, Isotype Control。

Ascr#8 is a dauer-inducing ascaroside isolated from Caenorhabditis elegans. It synergizes with ascr#2 and ascr#3, and strongly enhances male attraction.

CCR8 agonist1 (Compound 2) 是CCR8激动剂，用于自身免疫疾病研究。

CCR8 antagonist 2 是一种 CCR8 的有效拮抗剂，能够抑制的 CCR8 活性。CCR8 (C-C Motif 趋化因子受体 8) 主要表达于 Treg 细胞和 Th2 细胞，且不在 Th1 细胞上表达。CCR8 antagonist 2 能够用于由 CCR8 介导的疾病（如癌症和 或神经性疼痛）的治疗。

(2S,4aR,4bS,6aS,7aS,8aS,8bS,8cR,8dR,9aR,9bR)-2,9b-Dihydroxy-4a,6a-dimethylhexadecahydro-1H-cyclopropa[4,5]cyclopenta[1,2-a]cyclopropa[l]phenanthren-7(7aH)-one 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T67508，CAS号为 82543-16-6。

Difelikefalin TFA is a κ-opioid receptor (KOR) agonist. It activates KOR in HEK293 cells expressing the human receptor (EC50 = 0.16 nM in a transactivation assay) and inhibits forskolin-induced cAMP production in R1.G1 mouse thyoma cells (EC50 = 0.048 nM). Difelikefalin TFA is selective for KOR over the μ-opioid receptor (MOR; EC50 = >1 µM in a transactivation assay). It reduces acetic acid-induced writhing, as well as scratching behavior induced by the KOR antagonist GNTI, in mice (ED50s = 0.07 and 0.05 mg kg, respectively).

Difelikefalin HCl is a κ-opioid receptor (KOR) agonist. It activates KOR in HEK293 cells expressing the human receptor (EC50 = 0.16 nM in a transactivation assay) and inhibits forskolin-induced cAMP production in R1.G1 mouse thyoma cells (EC50 = 0.048 nM). Difelikefalin HCl is selective for KOR over the μ-opioid receptor (MOR; EC50 = >1 µM in a transactivation assay). It reduces acetic acid-induced writhing, as well as scratching behavior induced by the KOR antagonist GNTI, in mice (ED50s = 0.07 and 0.05 mg kg, respectively).

SB-649701为一种高效的人源CCR8拮抗剂，具有pIC50值7.7。AZ084则常被用于哮喘研究。

CCR8 antagonist3 (compound 2)是一种CCR8拮抗剂，IC50值为0.062 µM，并显示出人微粒体稳定性。

CCR8 antagonist 1 是 C-C Motif 趋化因子受体 8 (CCR8) 的拮抗剂，Ki 值为 1.6 nM。