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m-PEG9-CH2COOH 是一种属于 PEG 类的 PROTAC linker，可用于 PROTAC 分子的合成。

m-PEG8-CH2CH2-NHS ester is a PEG--based PROTAC linker can be used in the synthesis of PROTACs.

m-PEG9-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

m-PEG9-phosphonic acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG9-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG9-Boc is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG9-C4-SH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG9-Hydrazide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG9-phosphonic acid ethyl ester, a PEG-based PROTAC linker, facilitates the synthesis of PROTACs[1].

m-PEG9-SH 是一种属于 PEG 类的 PROTAC linker，可用于 PROTAC 分子的合成。

N-(m-PEG9)-N'-(PEG5-acid)-Cy5 is a PEG-based PROTAC linker employed for the synthesis of PROTACs[1].

N-(m-PEG9)-N'-(propargyl-PEG8)-Cy5 is a polyethylene glycol (PEG)-based PROTAC linker, specifically designed to aid in the synthesis of PROTACs[1].

m-PEG9-Br is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG9-azide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

EGFRT790M L858R-IN-9 (Compound 8) 是一种EGFR-L858R T790M抑制剂，其对EGFR-L858R T790M突变激酶的磷酸化具有有效的抑制作用，IC50为0.0064 µM。此外，EGFRT790M L858R-IN-9 可抑制非小细胞肺癌 (NSCLC) 细胞的增殖，适用于癌症研究。

BM 957 is an effective Bcl-2 and Bcl-xL inhibitor (Kis: 1.2 and <1 nM; IC50s: 5.4 and 6.0 nM).

CYM 9484 is a selective and potent neuropeptide Y (NPY) Y2 receptor antagonist with IC50 value of 19 nM.

Antibiotic JM 971B 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 T123922，CAS号为 92802-16-9。

YM 9429 is a biochemical.

VULM 993 is a calcium antagonist.

KM 91104 是一种细胞通透性 V-ATPase 抑制剂，选择性作用于 V-ATPase 的 a3-b2 亚单位。

BPR1M97 是一种具有血脑屏障渗透性和有效性的 mu 阿片受体（MOP）和神经肽-啡肽 FQ（NOP）受体激动剂，对 MOP 的 Kis 值为1.8 nM，对 NOP 的Kis 值为 4.2 nM。BPR1M97 具有抗伤害作用和抗痛觉作用。

β-Aminoarteether (SM934 free base) 是一种具有口服活性的青蒿素衍生物。β-Aminoarteether 可用于炎症和自身免疫疾病研究，如狼疮疾病。

HM90822 是一种新型合成凋亡蛋白（IAP）拮抗剂，通过蛋白酶体依赖性降解含有BIR2 3结构域的IAPs诱导人胰腺癌细胞凋亡。HM90822 抑制对 HM822 敏感的 Panc-1 和 BxPC-3 细胞中 XIAP 和 cIAP1 2 蛋白的表达，诱导 IAP 泛素化并促进蛋白酶体依赖性 IAP 降解。