Phe-leu

Cyclo(Phe-Leu) is a new cell cycle inhibitor.

L-Phenylalanyl-L-leucine是一种亮氨酸衍生物，可用于生物化学实验和药物合成研究。

{Boc}-Phe-Leu-Phe-Leu-Phe ({Boc}-FLFLF) is a selective antagonist of the formyl peptide receptor (FPR) family, effectively inhibiting receptor activity in response to formyl peptides.

Z-Phe-Leu-OH 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 T65512，CAS号为 4313-73-9。

{Boc}-Phe-Leu-Phe-Leu-Phe TFA 是一种抑制FPR (甲酰肽受体) 家族的优先级拮抗剂，专门针对通过该受体家族触发的活性进行抑制。

Z-Gly-Pro-Phe-Leu-CHO（Z-GPFL-CHO）是一种具有高选择性和高效率的四肽醛类蛋白酶体抑制剂，优先抑制支链氨基酸（Ki为1.5 µM），对小中性氨基酸的Ki值为2.3 µM，胰凝乳蛋白酶样活性的Ki值为40.5 µM，对肽基-谷氨酰肽水解活性的IC50为3.1 µM。

N-Boc-Phe-Leu-Phe-Leu-Phe (Boc-FLFLF) 是甲酰肽受体 1(FPR1)拮抗剂，能够增加疼痛作用，抑制膜联蛋白的抗疼痛活性。

Boc-Phe-Leu-Phe-Leu-Phe 作为一种化学趋化肽拮抗剂，具有抑制FMLP引发的肽白三烯释放的功能。

Pheleuin is a pyrazinone derivative synthesized from a dipeptide aldehyde. Although the biological activity of this compound has not been reported, similar diketopiperazines are known to inhibit calpain and/or regulate S. aureus virulence factor expression.

Acetyl Angiotensinogen (1-14), porcine Acetate 是一种肽，序列为 AC-ASP-ARG-VAL-TYR-ILE-HIS-PRO-PHE-HIS-LEU-LEU-VAL-TYR-SER-OH。由血管紧张素原基因编码的蛋白质被称为前血管紧张素原或血管紧张素原前体。

ST271 是蛋白质酪氨酸激酶 (PTK) 抑制剂，抑制 fMet-Leu-Phe 和 PAF 引起的 phospholipase D 活化的IC50值分别为 6.7 和 9 μM。

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) 。

Boc-MLF (TFA) is a specific antagonist of formyl peptide receptor (FPR) and also inhibits signaling through FPRL1 at higher concentrations.

Leucyl-phenylalanine (H-LEU-PHE-OH) 是一种二肽化合物，可用于蛋白质合成。

Antagonist G is an anticancer peptide and is also a broad spectrum neuropeptide growth factor antagonist.

Glycoprotein B is a peptide with the sequence H2N-Ser-Ser-Ile-Glu-Phe-Ala-Arg-Leu-OH, MW= 922.04. glycoprotein B is a viral glycoprotein that is involved in the viral cell entry of Herpes simplex virus. The herpesvirus glycoprotein B is the most highly c

Immunoglobulin light chain variable region fragment [Homo sapiens] is a fragment (Phe-Thr-Leu-Lys-Ile-Ser-Arg) on the variable region of the human immunoglobulin light chain.

Influenza A virus fragment has the RNA sequence of Leu-Lys-Phe-Ala-Phe-Ser-Met-Met.

Troponin I is a cardiac and skeletal muscle protein useful in the laboratory diagnosis of a heart attack. Troponin I is a part of the troponin protein complex, where it binds to actin in thin myofilaments to hold the actin-tropomyosin complex in place.

Antho-rpamide II is a biologically active neuropeptide isolated from the sea anemone Anthopleura elegantissima.

Boc-ypgflt(O-tbu) is a delta-receptor-selective opioid antagonist.

CH 66 is an inhibitor of renin.

Leucomyosuppressin, isolated from head extracts of the cockroach Leucophaea maderae, inhibits evoked transmitter release at the mealworm neuromuscular junction.

Leucyl-phenylalanine amide is an intermediate in the synthesis of γ-Secretase Inhibitor, the enzyme complex that catalyzes the cleavage of the amyloid precursor protein (APP) to produce amyloid β-peptide (Aβ) which is the major causative agent in Alzheime