Glu-glu

Glutamyl-glutamic acid (Glu-glu) 是一些微球菌和节杆菌属菌的胞壁中的肽桥。

Ac-Tyr(PO3H2)-Glu-Glu-Ile-Glu-OH TFA（化合物1）是一种与srcSH2域具有高亲和性的五肽，IC50约为1 µM。它同样作为srcSH3-SH2：磷酸蛋白相互作用的抑制剂。

Phosphopeptide ligand for the src SH2 domain (IC50 = 1 μM). Blocks src interactions with EGFR and FAK.

[Leu15]-Gastrin I, human 是一种 Gastrin I 的变体，它的第15位氨基酸残基被亮氨酸（Leu）替代了。[Leu15]-Gastrin I (human) 可调节促胰液素与粘膜质膜的结合。

H-Glu(OEt)-OEt.HCl (Diethyl L-glutamate hydrochloride) 是一种谷氨酸衍生物。

Fmoc-L-glutamic acid 5-tert-butyl ester是一种谷氨酸衍生物。

Boc-Glu(OBzl)-OH (Boc-Glu(OBzl)-OH) 是一种谷氨酸衍生物。

H-Glu-OtBu 是一种不可裂解的抗体药物偶联物（ADC）链接子，用于 ADC 合成；同时也是一种基于烷基链的 PROTAC 链接子，可用于PROTAC制备。

H-Glu(OMe)-OH 是一种谷氨酸衍生物，可用于合成多种化合物且与机体免疫和代谢有关。

Oglufanide (H-Glu-Trp-OH) 是一种从小牛胸腺中分离出来的二肽免疫调节剂，可抑制血管内皮生长因子，可刺激细胞内细菌感染和对丙型肝炎病毒的免疫反应。

HAE (His-Ala-Glu) 由组氨酸、丙氨酸和谷氨酸组成。

Arg-Gly-Glu-Ser acetate(93674-97-6 free base) 是一种 RGD 相关肽，可控制纤维蛋白原与活化血小板结合的 RGDS 活性。

Troriluzole 是一种具有口服活性谷氨酸调节剂，具有抗癌活性。Troriluzole 可提高位于神经胶质细胞的兴奋性氨基酸转运体的表达，可用于研究脊髓小脑性共济失调、阿尔茨海默病和广泛性焦虑症 (GAD) 。

Alanine glutamate is an agent of the dipeptide.

Levitide is a neurohormone-like peptide which is from the skin of Xenopus laevis.

Splenopentin diacetate (Splenin pentapeptide (32-36)) 是一种合成的免疫调节肽，可以再现脾和胸腺激素胸腺生成素的生物活性。

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

Antho-rwamide I is an anthozoan neuropeptide.

Prolylglutamic acid（H-Pro-Glu-OH）是一种脯氨酸和谷氨组成的酸二肽和内源性代谢物，能够通过ESX-5通路将致病性分枝杆菌的LipY脂肪酶靶向到细胞表面。

Z-AEVD-FMK (Z-Ala-Glu-Val-Asp-Fluoromethyl Ketone) 是一种可降解的 ADC links，是一种 caspase-10 抑制剂，降低 TNF-α/丁酸盐诱导的细胞凋亡，抑制 Gal-9 诱导的细胞凋亡。

Pro-Adrenomedullin(153-185),human, (C143H224N42O43), a peptide with the sequence H2N-SLPEAGPGRTLVSSKPQAHGAPAPPSGSAPHFL-OH, MW= 3219.6. Adrenomedullin (AM) is a ubiquitously expressed peptide initially isolated from phaechromyctoma in 19931. AM was initially identified as a vasodilator, some have cited this as the most potent endogenous vasodilatory peptide found in the body2. Differences in opinion regarding the ability of AM to relax vascular tone arises from the differences in the model system used3. Other effects of AM include increasing the tolerance of cells to oxidative stress and hypoxic injury and angiogenesis. AM is seen as a positive influence in diseases such as hypertension, myocardial infarction, chronic obstructive pulmonary disease and other cardiovascular diseases, whereas it can be seen as a negative factor in potentiating the potential of cancerous cells to extend their blood supply and cause cell proliferation.

Boc-Glu-OBzl is an amino acid building block.1,2It has been used in the synthesis of peptide-based inhibitors of human caspases and human rhinovirus (HRV) 3C protease that have enzyme inhibitory activityin vitro. 1.Garcia-Calvo, M., Peterson, E.P., Leiting, B., et al.Inhibition of human caspases by peptide-based and macromolecular inhibitorsJ. Biol. Chem.273(49)32608-32613(1998) 2.Dragovich, P.S., Webber, S.E., Babine, R.E., et al.Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 2. peptide structure-activity studiesJ. Med. Chem.41(15)2819-2934(1998)

Fmoc-Ala-Glu-Asn-Lys-NH2 is a peptide inhibitor that selectively targets asparagine endopeptidase (AEP) and inhibits the cleavage of amyloid precursor protein (APP). AEP, a pH-controlled cysteine proteinase, plays a crucial role in the proteolytic processing of APP, and its activity is enhanced during the aging process [1].

Suc-Ile-Glu(γ-pip)-Gly-Arg-pNA hydrochloride is a factor Xa specific chromogenic substrate.