glu

Jujuboside A 是从中药酸枣仁中提取的一种糖苷，可用于失眠和焦虑的相关研究。

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) 。

H-GLU(OTBU)-NH2 HCL 是一种氨基酸衍生物。

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。

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。

Tectorigenin, 7-O-[?-D-Apiofuranosyl-(1-6)-?-D-glu 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 T124939，CAS号为 365544-05-4。

Formononetin, 7-O-[?-D-Apiofuranosyl-(1?6)-?-D-glu 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 T129516。

Mal-PEG4-Glu(OH)-NH-m-PEG24 is a polyethylene glycol-based (PEG-based) linker, specifically designed for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

Mal-PEG4-Glu(TFP ester)-NH-m-PEG24 is a polyethylene glycol (PEG)-based linker essential for the synthesis of proteolysis targeting chimeras (PROTACs)[1].

G-Glu-Glu is an endogenous constituent of the brain. G-Glu-Glu activates N-methyl-D-aspartate receptors in rats.

Glu-AMS TEA，一种Ki为2.8 nM的大肠杆菌谷氨酰-tRNA合成酶（GluRS）竞争性抑制剂。

Gamma-Glu-AbuTFA为Gamma-Glu-Abu的TFA盐状化合物，充当钙敏感受体（calcium sensing receptor，CaSR）的激动剂。该化合物在HEK-293细胞中能有效激活CaSR，其EC50值为0.21 μM。

H-Glu-Thr-OH (L-α-Glutamyl-L-threonine) 是由两种氨基酸组成的二肽，这两个氨基酸分别为谷氨酸 (Glu) 和苏氨酸 (Thr)，它们通过肽键形成。此化合物是细胞外钙敏感受体 (CaSR) 的激动剂。

Alanine glutamate is an agent of the dipeptide.

OSu-Glu-VC-PAB-MMAE 是一种氨基反应型 Drug-linker,可降解连接子，MMAE 是一种 tubulin 抑制剂，抑制有丝分裂，常用于抗体-药物偶联物（ADC）的合成。

Mal((3S,3aR,6S,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diamine-PEG12)-β-Glu-PAB-Exatecan (LP1) 是一种用于ADC（抗体偶联药物）的药物-连接体偶联物。它由DNA拓扑异构酶 I 的强效抑制剂Exatecan和连接子Mal((3S,3aR,6S,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diamine-PEG12)-β-Glu-PAB构成，用于制备抗体偶联物AZD0516。

β-Glu-PAB(CH2NH2)-Exatecan (Compound 9a) 是一种拓扑异构酶 I (topoisomerase I) 抑制剂。它通过与拓扑异构酶 I-DNA 复合物结合来阻止 DNA 链的重新连接，从而导致 DNA 断裂和细胞凋亡。该化合物可在肿瘤微环境中通过高表达的 β-葡萄糖醛酸酶特异性切割，释放出具有细胞毒性的 Exatecan。β-Glu-PAB(CH2NH2)-Exatecan 还是 Mal((3S,3aR,6S,6aR)-Hexahydrofuro[3,2-b]furan-3,6-diamine-PEG12)-β-Glu-PAB-Exatecan 的中间体，具有研究癌症的潜力。

DDCPPB-Glu is a 6-5 fused ring heterocycle antifolate that shows antitumor activity.

G-Glu-Val (γ-glutamyl-L-valine, H-Glu-Val -OH), a flavour-regulating dipeptide, is a major contributor to mellow .

γ-Glu-Gly TFA, a γ-glutamyl dipeptide, is a human lipid metabolite with a structure resembling GABA (γ-aminobutyric acid). It serves as an excitatory amino acid antagonist [1][2][3].

γ-Glu-Cys is an intermediate in glutathione (GSH) synthesis.1It is formed by ATP-dependent condensation of cysteine and glutamate by γ-glutamylcysteine synthetase. γ-Glu-Cys is also an essential component of phytochelatins, the heavy metal detoxifying enzymes in plants.2

Abz-Ala-Pro-Glu-Glu-Ile-Met-Arg-Arg-Gln-EDDnp is a fluorescence-quenched peptide substrate for human neutrophil elastase (kcat/Km = 531 mM-1s-1). Enzymatic peptide hydrolysis disrupts the Abz:EDDnp donor-acceptor pair allowing fluorescence measurement of Abz (ex = 320 nm; em = 420 nm).

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)