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)。

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

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。

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。

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) 。

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。

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

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

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

Fmoc-Gly-Gly-D-Phe-OtBu, an ADC cleavable linker, is utilized in the synthesis of antibody-drug conjugates. It is the R-isomer of Fmoc-Gly-Gly-Phe-OtBu [1].

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

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

The chemical compound Mal-Phe-C4-Val-Cit-PAB-DMEA is a cleavable antibody-drug conjugate (ADC) linker that incorporates a Maleimide group. It is commonly employed in the synthesis of ADCs.

Mal-Phe-C4-Val-Cit-PAB is a cleavable antibody-drug conjugate (ADC) linker featuring a Maleimide functional group. It is employed in the synthesis of ADCs.

Mal-Phe-C4-VC-PAB-DMEA-PNU-159682 is a drug-linker conjugate utilized in antibody-drug conjugate (ADC) therapy. It comprises the ADC linker Mal-Phe-C4-VC-PAB and the potent ADC cytotoxin DMEA-PNU-159682. DMEA-PNU-159682 encompasses metabolites of nemorubicin (MMDX) derived from liver microsomes, as well as the ADC cytotoxin PNU-159682[1].

Mal-Phe-C4-VC-PAB-MMAE is a chemical compound resulting from the conjugation of monomethyl auristatin E (MMAE), a potent tubulin inhibitor serving as a toxin payload in antibody-drug conjugates, with a Mal-Phe-C4-VC-PAB linker.

MC-Gly-Gly-Phe 是一种用于抗体-药物偶联物的可切割接头。

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。

'(Ac)Phe-Lys(Alloc)-PABC-PNP serves as a valuable cleavable linker in the development of antibody-drug conjugates.'

Mal-C5-Gly-Gly-Phe-MMAE（Compound S5）是一种用于ADC的drug-linker conjugate。该化合物由MMAE和一种linker构成，主要应用于ADC的合成及癌症研究领域。

EMCC-Peg8-Phe-Lys-PNP 是一种可裂解的连接子，可用于ADC 的合成。

(S)-Phe-A110/B319 是一种选择性化合物，其对 p110α/p85αPI3K 复合物中 p110α 的 H1047R 突变体具有更高的亲和力，达 20 倍。