cyclo(his-pro)

Cyclo(his-pro) 是一种口服具有活力的，结构上与促甲状腺激素释放激素相关的环状二肽。它能够抑制NF-κB 核积累，也能够穿越脑血屏障并影响多种炎症和应激反应。

Cyclo(his-pro) TFA, an orally active cyclic dipeptide structurally related to tyreotropin-releasing hormone, has shown inhibitory effects on NF-κB nuclear accumulation. Additionally, it possesses the ability to cross the blood-brain barrier and impact various inflammatory and stress responses [1, 2].

Cyclo(L-Pro-L-Ile) 是一种来自苏云金芽孢杆菌双酮哌嗪，可诱发中度超敏反应，可用于研究松树枯萎病。

Cyclo(L-Phe-trans-4-hydroxy-L-Pro) (Cyclo(L-phenylalanyl-trans-4-hydroxy-L-proline))是一种存在于Phellinus igniarius 中的天然产物。

cyclo(L-Pro-L-Tyr) 是真菌和细菌的次生代谢产物。

Cyclo(Pro-Ala) 是一种天然产品。

Cyclo(Tyr-Pro) shows antibacterial activity towards several marine bacterial species, it also shows weak antagonistic activity against VEGFR2 -CD. Cyclo(Tyr-Pro) and cyclo(Pro-Val) are toxic to both suspension cells and seedlings of Pinus thunbergii, whic

Cyclo(D-Phe-L-Pro) is a natural product from Phellinus igniarius.

Cyclo(Pro-Trp) and cyclo(Phe-Pro) show broad spectrum antibacterial properties.

Cyclo(Phe-Pro) acetate(14705-60-3 free base) 是一些细菌和真菌的次级代谢产物，也是由创伤弧菌产生的。

Cyclo(D-Val-L-Pro) 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 TN6670，CAS号为 27483-18-7。

Cyclo(D-Ala-L-Pro) 在生命科学相关研究中具有广泛的应用。

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

Cyclo(Pro-Pro) tasted bitter.Verpacamides A-D, a sequence of C11N5 diketopiperazines relating cyclo(Pro-Pro) to cyclo(Pro-Arg), from the marine sponge Axinella vaceleti is possible biogenetic precursors of pyrrole-2-aminoimidazole alkaloids.

Cyclo(L-Ala-L-Pro) and cyclo(L-Val-L-Pro) inhibit aflatoxin production of Aspergillus parasiticus and Aspergillus flavus in liquid medium at concentrations of several hundred uM without affecting fungal growth.

Cyclo(Gly-(L)-Pro) shows immunostimulatory properties. Cyclo(Gly-l-Pro) exhibits potent inhibition of TNF-α release with the IC50 values of 4.5 ug/mL, respectively, it also exhibits significant diminution of IL-1β and IL-6 mRNA-expression levels and NO pr

Cyclo(Pro-Gly) is an active metabolite of piracetam-N-phenylacetyl-L-prolylglycine (GWS-111), it shows a greater resistance to an enzymatic effect than natural neuropeptides. Cyclo-(Gly-Pro) shows cytotoxicity at the concentration of 10 umol L, it inhibit

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

Cyclo(L-Pro-L-Val) 是从辣椒溶杆菌AZ2和白斑分枝杆菌果实中提取出的 2,5-二酮哌嗪，具有抗炎活性，对植物病原微生物 (如 R. fascians LMG 3605) 具有毒性活性，能抑制革兰氏阳性植物病原菌。Cyclo(L-Pro-L-Val) 以浓度依赖性方式显著抑制了IKKα、IKKβ、IκBα和NF-κB 的磷酸化以及iNOS 和COX-2的活化，是治疗炎症相关疾病的潜在治疗剂。