cyclo(leu leu)

Cyclo(Leu-Leu) is an efficient supramolecular catalyst.

Cyclo(L-Leu-L-Pro) 是一种来自芝麻假单胞菌BC42的化合物，具有抗真菌活性，抑制真菌病原体，抑制黄曲霉增殖。Cyclo(L-Leu-L-Pro) 抑制分生孢子的萌发和分生孢子的形成，可用于农业生物防治。

Cyclo(Leu-Ala) is the Diketopiperazine.

Cyclo(D-Leu-L-Pro) shows antitumour and antifungal activities.

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

Cyclo(Tyr-Leu) 是一种来自马齿苋 Portulaca oleracea Linn 的环状二肽，具有细胞毒性、抗真菌和抗凝血活性。

Cyclo(Leu-Val) is a cyclic dipeptide from the fermentation broth of F8712 strain.

Cyclo(L-Leu-trans-4-hydroxy-L-Pro) is a natural product from Phellinus igniarius.

Cyclo(Ile-Leu) shows cytotoxic activity in vitro.

Cyclo(Hpro-Leu) 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN6680，CAS号为 1016899-93-6。

Cyclo(Leu-Ala) (Cyclo(alanine-leucine)) 是一种从微生物中分离出的具有抗菌特性的化合物，能够与其他化合物协同，对一些植物病原体展示出抗菌活性。

Cyclo(L-Leu-L-Trp) is a diketopiperazine metabolite initially derived from Penicillium, exhibiting antibacterial (MICs = 125-1000 µg/ml) and antifungal activities (MICs = 8-64 µg/ml). It also demonstrates antioxidant properties by reducing the production of hydroxy radicals, as evidenced in an electron spin resonance (ESR) spectroscopy assay (IC50 = 1.8 µM). Additionally, Cyclo(L-Leu-L-Trp) has been identified as a bitter compound capable of quickly crossing rat taste cell membranes ex vivo at a 1 mM concentration. Furthermore, it acts as a melatonin receptor agonist in X. laevis melanophores, suppressing cAMP accumulation at a 20 µM concentration, with this effect being negated by the melatonin receptor antagonist luzindole.

Bisnafide is a Naphthalimide Analogue that acts as DNA intercalator and topo II inhibitor. It is also an antiangiogenic agent. Antiangiogenic agents can normalize tumor vessels and promote the delivery of cytotoxic agents to tumor sites.

Cyclo(Pro-Leu) (Cyclo-L-prolyl-L-leucine) 是一种源自海洋的天然产物，具有盐水虾的杀伤力。