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CC-885-CH2-PEG1-NH-CH3 is a neoDegrader compound employed for the production of Antibody neoDegrader Conjugate (AnDC) during synthesis.

CC-885-CH2-PEG1-NH-CH3 TFA 作为一种降解剂，主要应用于AnDC (抗体-降解剂偶联活性分子) 的合成。

Cisplatin（CDDP）是一种具有抗肿瘤活性的化疗药物，是典型的DNA交联剂，能够通过在癌细胞中形成DNA加合物，抑制DNA合成并引起DNA损伤，从而导致细胞死亡。除此之外，Cisplatin 还可激活铁死亡（ferroptosis）并诱导自噬（autophagy）。在动物实验中，Cisplatin 常被用于构建慢性肾损伤和急性肾衰竭模型。

C-176 (STING inhibitor 1) 是一种 STING 抑制剂，具有选择性和血脑屏障渗透性。C-176 可以抑制由 STING 介导的 IFNβ 生成，具有抗炎活性。

NUCC-390 是新型的选择性小分子 CXCR4 receptor 受体激动剂。NUCC-390 可以诱导 CXCR4 受体的内化，作用方式与 AMD3100相反。NUCC-390 在动物模型中，有助于神经退行性变后神经功能恢复。

DCC-3116 是一种具有口服活性、选择性和高效性的 ULK1/2 抑制剂，具有抗癌活性。DCC-3116 抑制自噬，可用于研究癌症。

Vimseltinib (DCC-3014) 是 c-FMS(CSF-IR) 和 c-Kit 抑制剂，IC50值分别为 <0.01 μM 和 0.1-1 μM。

NUCC-390 dihydrochloride is selective agonist of small-molecule CXCR4 receptor.

SNIPER(TACC3)-1 targets TACC3 protein degradation via the ubiquitin-proteasome pathway.It induces cancer cell death.

SNIPER(TACC3)-2 targets TACC3 protein degradation via the ubiquitin-proteasome pathway. It induces cancer cell death.

(S,R,S)-AHPC-C3-NH2 TFA (VH032-C3-NH2 TFA) is a synthesized E3 ligase ligand-linker conjugate that incorporates the VH032 based VHL ligand and a linker used in PROTAC technology. (S,R,S)-AHPC-C3-NH2 can be used in the synthesis of a series of PROTACs, suc

(S,R,S)-AHPC-C3-NH2 (VH032-C3-NH2) is a synthesized conjugate consisting of an E3 ligase ligand-linker and the VH032 based VHL ligand, which is commonly used in PROTAC technology. This compound serves as a key component in the synthesis of various PROTACs, including UNC6852. UNC6852 is a bivalent chemical degrader specifically targeting EED [1].

QCC-374 is a prostanoid agonist. It potentially for the treatment of pulmonary arterial hypertension.

TACC3 inhibitor 2 (Compound 13b) 是一种TACC3抑制剂，其IC50为200 nM。此化合物能够诱导有丝分裂停滞、细胞凋亡 (Apoptosis) 和DNA损伤，并且可用于癌症研究。

Boc-C3-amide-C10-amine 是用于合成 PROTACMS479 的PROTAC连接子。

CC34301, a PqsE inhibitor, binds to the active center of PqsE, inhibiting its thioesterase activity in cell-based and in vitro assays.

CC-3052 is a water-soluble, highly stable thalidomide analogue that is an effective inhibitor of HIV-1 expression and activation-induced TNF-α production. CC-3052 also inhibited PHA-induced and rTNF-α induced TNF-α transcription in PBMC, as well as TNF-α

KHS 101 是一种新型转化酸性卷曲螺旋蛋白 3 (TACC3) 的抑制剂。它是神经元分化的选择性诱导剂。

KHS101 hydrochloride 能够选择性的诱导神经元分化表型，能够与转化酸性含螺旋蛋白发生相互作用。

NUCC-390 dihydrochloride 是新型的选择性小分子CXCR4receptor 受体激动剂。NUCC-390 dihydrochloride 可以诱导CXCR4受体的内化，作用方式与 AMD3100 相反。NUCC-390 dihydrochloride 在动物模型中，有助于神经退行性变后神经功能恢复。

KDI-792 hydrochloride is a thromboxane dual blocker.

Rcc 36 is an active metabolite of temiverine that has inhibitory actions toward the atropine-resistant part of contractions, which may be related to the calcium antagonistic actions of these compounds.

TACC3 inhibitor 1为一种能透过血脑屏障的有效TACC3抑制剂，能诱导Apoptosis及使细胞周期在G2/M期停滞，同时促进细胞内ROS产生，表现出抗增殖与抗肿瘤活性。

SNIPER(TACC3)-11是一种针对FGFR3-TACC3的有效抑制剂，能够降低FGFR3-TACC3蛋白水平，并抑制FGFR3-TACC3阳性癌细胞增殖。