r-gt

γ-GT (H-GLA(PNA)-OH) 是一种 γ-谷氨酰转移酶(glutamyl transferase)的底物。

RGT-068A 是一种有效，选择性和具有良好口服生物利用度的 MALT1抑制剂。

RGT-018 为一口服活性的SOS1抑制剂，其展现出强效的抗肿瘤能力。该化合物通过阻断KRAS活化，有效抑制癌细胞的增殖。

8-Br-GTP, an analog of GTP, functions as both a competitive inhibitor of FtsZ polymerization and GTPase activity (with a K i value of 31.8 μM). Moreover, it is capable of facilitating nucleic acid modification.

FMoc-Arg(Tos)-OH 是一种用于肽合成、生物化学和分子生物学的合成氨基酸。它是一种Fmoc 保护的氨基酸，作为肽和蛋白质合成的中间体，用于固相肽合成。

Cho-Arg is a steroid-based cationic lipid that contains a cholesterol skeleton coupled to an L-arginine head group. It forms a complex with plasmid DNA and decreases plasmid DNA migration in an agarose-gel retardant assay at charge ratios greater than or equal to 4. Cho-Arg facilitates transfection of plasmid DNA into H1299 and HeLa cells in the presence or absence of fetal bovine serum, an effect that is reversed by the lipid raft-mediated endocytosis inhibitor methyl-β-cyclodextrin and the caveolae-mediated endocytosis inhibitor genistein . It is cytotoxic to H1299 cells (IC50 = 88.5 μg/ml).

Dios-Arg is a steroid-based cationic lipid that contains a diosgenin skeleton coupled to an L-arginine head group. It forms a complex with plasmid DNA and decreases plasmid DNA migration in an agarose-gel retardant assay at charge ratio greater than or equal to 4. Dios-Arg facilitates transfection of plasmid DNA into H1299 and HeLa cells in the presence and absence of fetal bovine serum, an effect that is reversed by the lipid raft-mediated endocytosis inhibitor methyl-β-cyclodextrin and the caveolae-mediated endocytosis inhibitor genistein . It has been used, coupled to 1,2-dioleoyl-sn-glycero-3-PE , to bind siRNA and plasmid DNA to form cationic lipid nanoparticles for intracellular transport. Dios-Arg is cytotoxic to H1299 and HeLa cells (IC50s = 83.5 and 74.1 μg/ml, respectively).

2H-Cho-Arg is a steroid-based cationic lipid that contains a 2H-cholesterol skeleton coupled to an L-arginine head group and can be used to facilitate gene transfection. It forms a complex with plasmid DNA (pDNA) and decreases pDNA migration in an electrophoretic mobility shift assay at +/- charge ratios of 4 or higher. 2H-Cho-Arg facilitates transfection of a luciferase gene into H1299 cells, an effect that is reversed by the lipid raft-mediated endocytosis inhibitor methyl-β-cyclodextrin and the caveolae-mediated endocytosis inhibitor genistein , but not by inhibitors of clathrin- or micropinocytosis-mediated endocytosis. It induces cytotoxicity in H1299 cells (IC50 = 92.7 μg/ml).

(H-Tyr-Ile-Asn-Leu-Cys-Thr-Arg-Nva-Arg-Tyr-NH2)2 trifluoroacetate 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 T64688。

Boc-β-HoArg(Tos)-OH 是一种氨基酸衍生物，在生命科学相关研究中具有广泛的应用。

H-Arg(Tos)-OH 是一种氨基酸衍生物，在生命科学相关研究中具有广泛的应用。

(-)-Donepezil is an isomer of Donepezil -- a nootropic acting as an inhibitor of acetylcholinesterase.

ArgTX-48 is a highly potent and subfamily selective antagonist of the NMDARs and AMPARs.

Argtide is an luteinizing hormone releasing hormone (LHRH) antagonist.

DMJ-I-228 is a specific inhibitor of HIV-1 entry through interaction with the Env spike by virtue of the incorporation of a guandinium group.

AZD-3783 is a selective 5-hydroxytryptamine 1B receptor antagonist with probable antidepressant and anxiolytic activity.

ArgTX-93 is a highly potent and subfamily selective antagonist of the NMDARs and AMPARs.

Lys-Arg-Thr-Leu-Arg-Arg (KRTLRR) 是一种六肽。Lys-Arg-Thr-Leu-Arg-Arg 是EGF 受体蛋白激酶 C 的底物。Lys-Arg-Thr-Leu-Arg-Arg 可以用来测定蛋白激酶 C 的活性。

N-Myristoyl-Lys-Arg-Thr-Leu-Arg 是一种蛋白激酶 C (PKC) 抑制剂，其 IC50值为 75 μM。N-Myristoyl-Lys-Arg-Thr-Leu-Arg 抑制人白血病细胞系 Jurkat 中 IL-2受体的诱导和 IL-2的产生。

WLSEAGPVVTVTVRALGTGSW TFA 为心肌细胞特异性肽。该化合物通过表达外泌体，提高心肌细胞的特定摄取能力，降低心肌细胞凋亡率，并在体内心肌内注射后提升心脏潴留能力。

Arg-Trp 是由精氨酸和色氨酸组成的二肽，Arg-Trp 辛酯的类似物显示出抗菌活性。

Arg-Tyr 是一种具有强羟自由基和过氧化氢清除活性的二肽。

Pyr-Arg-Thr-Lys-Arg-AMC TFA为AMC肽类化合物，其结构由十肽组成，可经由特异性水解反应由如胰蛋白酶及凝血酶等蛋白酶作用下分解。该肽用于评估蛋白酶活性及酶抑制剂功效的检测。

Ergtoxin-1为钾离子通道阻断剂，源于墨西哥毒蝎Centruroides noxius的毒液。该化合物具有阻断神经、心脏及内分泌细胞ERG-K+通道的功能。