ala

(-)-Menthyl acetate具有广谱抗菌活性，对白色念珠菌和黑曲霉等致病真菌的最小抑菌浓度(MIC)范围为0.12至8.0 μL/mL。(-)-Menthyl acetate还能抑制真菌生物膜的形成。(-)-Menthyl acetate可增强5-氨基乙酰丙酸的皮肤渗透性，使其成为研究经皮药物吸收的潜在工具。

5-ALA benzyl ester hydrochloride (Benzyl-ALA hydrochloride) 是一种原卟啉前体，可用作光检测器。5-ALA benzyl ester hydrochloride 在结肠癌细胞系中可以诱导原卟啉 IX (PPIX) 的积聚。

Fmoc-Ala-Ala-Asn(Trt)-OH 是一种可切割的 ADC 接头，用于抗体-药物偶联物。

Fmoc-Val-Ala-PAB-OH (Fmoc-Val-Ala-PAB) 是一种有用的接头，可用于制备用于靶向药物递送的抗体-药物偶联物。它还用于合成带有溶酶体可切割接头的 RGD 拟肽-紫杉醇缀合物。

Mc-​Val-​Ala-​PAB 是一种可降解的 ADC 接头，用于抗体-药物偶联物。

N-Me-L-Ala-maytansinol used for making antibody-drug conjugate (ADC),is a hydrophobic, cell permeable payload.

Azide-PEG3-C1-Ala 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.

Azido-PEG3-Ala-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.

Azido-PEG5-Ala-Ala-Asn-PAB is a cleavable 5-unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].

Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB is a cleavable three-unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].

Fmoc-PEG4-Ala-Ala-Asn-PAB is a four-unit polyethylene glycol (PEG) linker, cleavable in nature. It is specifically employed for the synthesis of antibody-drug conjugates (ADCs)[1].

Aloc-D-Ala-Phe-Lys(Aloc)-PAB-PNP is a cleavable linker utilized in the synthesis of antibody-drug conjugates (ADCs), which are innovative therapeutic agents that combine the targeting ability of antibodies with potent cytotoxic drugs.

Boc-Val-Ala-PAB-PNP is an ADC linker employed for the synthesis of antibody-drug conjugates (ADCs)[1]. This cleavable compound efficiently facilitates the attachment of drugs to antibodies, allowing for targeted delivery and release of therapeutic agents within the body, making it an important component in ADC development.

Fmoc-Ala-Ala-Asn-PABC-PNP is a cleavable peptide ADC linker [1].

MC-Val-Ala-PAB-PNP 是一种用于合成抗体偶联药物的 linker，可降解。

D-Ala-Lys-AMCA hydrochloride 是发射蓝色荧光的质子偶联寡肽转运蛋白 1 (PEPT1) 的已知底物。 D-Ala-Lys-AMCA 可能被转运到 Caco-2 细胞和肝癌细胞中。

(S,R,S)-AHPC-Ala 为E3 泛素酶配体，常用于合成 PROTAC SMARCA2/4-degrader-23。

(S,R,S)-AHPC-Ala-CO-cyclohexene-Bpin 属于 E3 泛素酶配体+连接子偶联物 (E3 Ligase Ligand-Linker Conjugates) 类型。此化合物主要应用于制备 PROTAC SMARCA2/4-degrader-23。

Val-Ala-PABC-N(Mesylpropane)-Exatecan 是一种结合了可裂解的 Val-Ala-PABC-N(Mesylpropane) linker 以及 Exatecan（topoisomerase I 抑制剂）的药物-linker 偶联物（Drug-Linker Conjugates for ADC）。

Alanine glutamate is an agent of the dipeptide.

FA-Leu-Gly-Pro-Ala-OH是一种合成肽和特异性的胶原酶底物，广泛应用于生物化学实验和药物合成研究。

Val-Ala-PAB-SN38 是一种ADC的药物连接物缀合物，由ADC linker Val-Ala-PAB和SN38组成，SN38是伊立替康的活性代谢产物，作用为拓扑异构酶I (Topoisomerase I) 抑制剂。

Mal-Val-Ala-PAB(C2-glucuronic acid)-DMEA-PNU-159682 是一种用于ADC的活性分子-偶联物，其结构包括可裂解的Val-Ala linker和高效的ADC细胞毒素PNU-159682。

MeO-Suc-Ala-Ala-Pro-Ala-CMK (MSACK) 是一种抑制人中性粒细胞弹性蛋白酶 (HNE) 的化合物，IC50为 20.3 μM。该化合物能够抑制HNE对肺组织弹性蛋白等底物的水解作用，并可用于与慢性阻塞性肺疾病 (COPD) 等相关疾病的研究。