lss

Oxiconazole nitrate (Ro 13-8996) 是广谱抗真菌药物，抑制T. tonsurans 和T.rubrum 的生长，MIC90值分别为 0.25 和 0.5 μg mL。

MM0299 具有脑渗透性，具有抗胶质母细胞瘤活性，抑制羊毛甾醇合酶 （LSS），诱导原位GBM肿瘤中EPC的产生。

DSTYSLSSTLTLSK TFA 是用于 Infliximab (Avakine) 定量检测的通用肽。Infliximab (Avakine) 是一种嵌合单克隆IgG1抗体，能特异性地结合到 TNF-α。

DSTYSLSSTLTLSK acetate 是可以用于英夫利昔单抗定量检测的人通用肽。

SNNF(N-Me)GA(N-Me)ILSS 为一种具有生物活性的肽类化合物，为淀粉样蛋白生成和细胞毒性部分 IAPP 序列的双N-甲基化衍生物。

DSTYSLSSTLTLSK is a generic human peptide and can be used for infliximab quantitative detection. Infliximab (Avakine) is a chimeric monoclonal IgG1 antibody that specifically binds to TNF-α.

2-Bromohexadecanoic acid (2-BP) 是一种不可代谢的棕榈酸酯类似物，一种 PPARδ 的激动剂，可用作棕榈酰化抑制剂，抑制 DHHC 介导的棕榈酰化。

Azidoethyl-SS-propionic acid is an ADC linker, specifically designed for the synthesis of antibody-drug conjugates (ADCs)[1]. It possesses cleavable properties, allowing for the controlled release of drug payloads.

Fmoc-NH-ethyl-SS-propionic acid is a cleavable linker compound utilized for the synthesis of antibody-drug conjugates (ADCs)[1].

Boc-aminooxy-ethyl-SS-propanol is a cleavable linker employed for the synthesis of antibody-drug conjugates (ADCs)[1].

Boc-NH-ethyl-SS-propionic acid is an ADC linker compound employed for the synthesis of antibody-drug conjugates (ADCs)[1].

Azidoethyl-SS-ethylalcohol is a cleavable PEG Linker that may be useful in the development of antibody drug conjugates.

NLS-StAx-h TFA 是选择性的、细胞可渗透的Wnt 信号传导的固定肽抑制剂，IC50为 1.4 μM。NLS-StAx-h TFA 可有效抑制 β-catenin-转录因子的相互作用，具有对癌细胞的抗增殖活性。

Azidoethyl-SS-PEG2-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.

Aminoethyl-SS-ethylalcohol (Compound 3) is an Alkyl-Chain-based PROTAC linker can be used in the synthesis of PROTACs[1]. Aminoethyl-SS-ethylalcohol is also a glutathione cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[2].

Mal-NH-ethyl-SS-propionic acid, a cleavable linker employed for the synthesis of antibody-drug conjugates (ADCs)[1], plays a crucial role in the modulation of drug release from the conjugate.

Azidoethyl-SS-ethylazide is a cleavable linker employed for the synthesis of antibody-drug conjugates (ADCs)[1].

HS-243 是 IRAK-4 和 IRAK-1 的抑制剂，IC50 分别为 20 和 24 nM。 HS-243 显示出抗炎和抗癌活性。

Azidoethyl-SS-propionic NHS ester is a cleavable linker frequently employed in the synthesis of antibody-drug conjugates (ADCs) [1].

Wnt inhibitor (IC50 = 1.4 μM). Stapled peptide inhibitor of oncogenic Wnt signaling. Inhibits β-catenin-transcription factor interactions. Inhibits proliferation and migration of colorectal cancer cells. Cell permeable.

Azidoethyl-SS-ethylamine is a cleavable linker compound employed for the synthesis of antibody-drug conjugates (ADCs)[1].

Amino-ethyl-SS-PEG3-NHBoc is a cleavable 3-unit PEG ADC linker employed for the synthesis of antibody-drug conjugates (ADCs)[1].

Aminoethyl-SS-propionic acid is an ADC linker compound employed in ADC synthesis [1]. It functions as a cleavable linker in the conjugation of antibodies with drugs, allowing for targeted drug delivery.

Fmoc-NH-ethyl-SS-propionic NHS ester is a cleavable linker for antibody-drug conjugates (ADCs)[1]. It is employed in the synthesis of ADCs, facilitating the covalent attachment of drugs to antibodies through the formation of stable amide bonds.