leucyl leucyl leucine

L-Leucyl-L-Leucine methyl ester hydrochloride (Leu-Leu-ome hydrochloride) is a lysosomal condensation product that cytotoxic towards natural killer cells and CD4+ and CD8+ T lymphocytes.

N-[(1,1-Dimethylethoxy)carbonyl]-L-leucyl-L-leucine is a useful organic compound for research related to life sciences. The catalog number is T65042 and the CAS number is 73401-65-7.

The lysosomotropic dipeptide LLME has selective toxicity for NK cells, CTL, and M phi without adverse effects on a variety of other lymphoid or nonlymphoid cell types. See also E-2080.

Leucyl-leucyl-leucine is may be used for pH-dependent endosomal membrane disruption to release agents. Trileucine is used to evaluate the absorption characteristics of reversed phase liquid chromatography (HPLC) media.

[Leu5]-Enkephalin acetate(58822-25-6 free base) is an endogenous neuropeptide involved in nociception and an agonist of δ-opioid and μ-opioid receptors (Kis = 4.0 and 3.4 nM, respectively)

Diallyl G is a delta-opioid receptor antagonist agent.

L-Leucyl-L-alanine is a simple dipeptide composed of L-leucine and L-alanine>[1].

[Leu5]-Enkephalin (Leu-enkephalin) is an endogenous neuropeptide involved in nociception and an agonist of δ-opioid and μ-opioid receptors (Kis = 4.0 and 3.4 nM, respectively)

[Leu5]-Enkephalin TFA(58822-25-6(free bas)) (Leucyl-enkephalin) is the most potent δ-receptor ago

Leucyl-phenylalanine belongs to the class of organic compounds known as dipeptides.

Leucyl-leucyl-tyrosine is a bioactive chemical.

Leucyl-phenylalanine amide is an intermediate in the synthesis of γ-Secretase Inhibitor, the enzyme complex that catalyzes the cleavage of the amyloid precursor protein (APP) to produce amyloid β-peptide (Aβ) which is the major causative agent in Alzheime

L-Leucyl-L-prolyl-L-prolyl-L-seryl-L-arginine is a peptide.

Leucyl-valyl-isoleucinamide is a oligopeptide.

Tryptophyl-leucyl-glutamic acid is a tryptophan used for fluorescence spectroscopy.

DL-Leucyl-DL-phenylalanine, a dipeptide, serves as a substrate for detecting two distinct regions of dipeptidase staining on gels in both Drosophila simulans and Drosophila melanogaster.

Cyclo(L-leucyl-L-valyl) is a polymorphic compound isolated from the secondary metabolite of Streptomyces quinquefasciatus YIM, which has not yet shown antimicrobial activity.

Leu-AMS, a leucine analogue and potent inhibitor of leucyl-tRNA synthetase (LRS) with an IC50 of 22.34 nM, exhibits cytotoxic effects in both cancer and normal cells and hampers bacterial growth. It specifically inhibits LRS's catalytic activity without impacting the leucine-induced activation of mTORC1.