phe

H-Phe-Trp-OH (Phenylalanyltryptophan) 是一种小分子二肽化合物，参与机体蛋白质的合成。

[D-p-Cl-Phe6,Leu17]-VIP acetate 是一种竞争性和选择性的血管活性肠肽 (VIP) 受体拮抗剂 (IC50 = 125.8 nM)。

Gly-Phe β-naphthylamide acetate 是 Cathepsin C 的底物，可用于研究组织蛋白酶 C 的功能、溶酶体内水解和溶酶体膜通透性。

N-Formyl-Met-Leu-Phe-Lys (fMLFK) 是一种多肽，是选择性FPR1激动剂，作用于 FPR1(IC50:3.5 nM)，FPR2(IC50:6.7 nM) 和 FPR2-D2817.32G(IC50:0.88 nM) 。

Phe-Lys(Trt)-PAB 是一种组织蛋白酶可裂解的 ADC 接头，用于合成抗体-药物偶联物。

Gly-Phe-Arg acetate(121822-47-7 free base) 是一种模拟泥蟹抽吸信息素的超强合成三肽。

Boc-Gly-Gly-Phe-Gly-OH acetate (GGFG acetate)(187794-49-6 free base) 是 N 和 C 保护的四肽的自组装体。

Fmoc-Gly-Gly-Phe-OtBu 是一种用于合成抗体偶联药物的 linker，可降解。

γ-Glu-Phe TFA(7432-24-8 free base) 是由γ-谷氨酸和苯丙氨酸组成的二肽，是较大蛋白质的蛋白水解分解产物。它可能是由谷胱甘肽与相应氨基酸之间的转肽作用形成的，由γ-谷氨酰转肽酶催化。

MC-Gly-Gly-Phe-Boc 参与抗体-活性分子偶联物的合成，并连接曲妥珠单抗 (Trastuzumab)，用于肿瘤研究。

Gly-Gly-Phe-Gly-NH-O-CO-Exatecan 属于 ADC 毒素类化合物.

MC-Gly-Gly-Phe-Gly-GABA-Exatecan ADC 是一种药物连接子偶联物，其包含的拓扑异构酶Exatecan具有22 μM 的IC50值。该化合物在体外和体内对多种抗体显示出细胞毒性及抗肿瘤效果。

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.

Cyclo(L-Phe-L-Val) is a metabolite of the sponge bacterium Pseudoalteromonas sp. NJ6-3-1 that can autoinduce production of antibacterial substances active against S. aureus when co-cultured at a low cell density. It induces neurite outgrowth and branching of chick cortical neurons in vitro when used at concentrations of 16 and 32 μM. It increases phosphorylation of the PI3K substrate Akt, and neurite outgrowth induced by cyclo(L-Phe-L-Val) can be blocked by the PI3K inhibitor LY294002 . Cyclo(L-Phe-L-Val) enhances axon sprouting of calcitonin gene-related protein positive (CGRP+) primary afferents in the spinal cord following crush injury and of serotonin neurons in uninjured spinal cord. Cyclo(L-Phe-L-Val) is also a bitter taste component of cocoa and roasted coffee.

Potent and selective bradykinin B1 receptor agonist (EC50 = 9.02 nM in rabbit aorta) that is resistant to aminopeptidase, kininase I and II (ACE) and neutral endopeptidase cleavage. Exhibits hypotensive and angiogenic activity in vivo.

MC-Gly-Gly-{D-Phe}-Gly-NH-CH2-O-CH2COOH是一种可降解的ADC linker，用于抗体偶联活性分子(ADC)的合成。

Cbz-Phe-(Alloc)Lys-PAB-PNP serves as a cleavable linker in the design of antibody-drug conjugates (ADC).

Selective bradykinin B2 receptor agonist that is resistant to carboxypeptidase cleavage. 5-fold more potent and exhibits a more prolonged duration of action than bradykinin in vivo.

Gly-Phe-Arg is a highly potent synthetic tripeptide that mimics the pumping pheromone of the mud-crab.

Arg-Gly-Asp-D-Phe-Val (TFA) has anti-tumor activity and is an inhibitor of integrin αvβ3.

Mc-Gly-Gly-Phe-Gly-PAB-OH, also known as Mc-GGFG-PAB-OH, serves as a cleavable ADC linker exclusively employed in the synthesis of antibody-drug conjugates (ADCs).

Fmoc-Phe-Lys(Boc)-PAB-PNP is a cleavable antibody-drug conjugate (ADC) linker employed in the synthesis of ADCs.

Hyp-Phe-Phe is a tripeptide known for its strong aromatic interactions between the Phe rings, resulting in the formation of helical-like sheets and a cross helical architecture. Notably, Hyp-Phe-Phe exhibits excellent shear piezoelectricity properties, making it a valuable candidate for piezoelectric materials.

Fmoc-Phe-Lys(Trt)-PAB-PNP is a cleavable linker for antibody-drug conjugate (ADC) synthesis, specifically designed for use in ADC synthesis.