d[leu4,lys8]-vp

Selective vasopressin V1B receptor agonist (Ki values are 0.16, 64, 100 and 3800 nM for V1B, oxytocin, V2 and V1A receptors respectively). Displays weak antidiuretic, vasopressor and in vitro oxytocic activities.

d[Leu4,Lys8]-VP acetate is a selective vasopressin V1b receptor agonist. The Kis for rat, human and mouse V1b receptors are 0.16 nM, 0.52 nM and 0.1.38 nM, respectively. d[Leu4,Lys8]-VP acetate exhibits weak antidiuretic, vasopressor and oxytocic activiti

D[LEU4,LYS8]-VP TFA is a selective agonist for the vasopressin V1b receptor, with Ki values of 0.16 nM for rat, 0.52 nM for human, and 1.38 nM for mouse V1b receptors. This compound exhibits limited antidiuretic, vasopressor, and oxytocic activities in vitro [1] [2].

Neurokinin A(4-10) TFA(97559-35-8 free base) is a tachykinin NK2 receptor agonist[1].

(D-Ser2)-Leu-Enkephalin-Thr is a delta selective agent of opioid receptor and shows analgesic effects.

N-Formyl-Nle-Leu-Phe-Nle-Tyr-Lys TFA (For-Nle-Leu-Phe-Nle-Tyr-Lys-OH (TFA)) (For-Nle-Leu-Phe-Nle-Tyr-Lys-OH TFA) is a formyl peptide receptor (FPR) agonist and a potent chemoattractant for human neutrophils, with its radioiodinated form retaining full biological activity.

Leu-Tyr-Asp-Lys is a tetrapeptide compound that can be used to study metabolism-related diseases.

d[Cha4]-AVP acetate is a potent and selective human vasopressin V1B receptor agonist (Ki values are 1.2, 151, 240 and 750 nM for V1B, V1A, Oxytocin and V2 receptors respectively). Stimulates ACTH and corticosterone secretion and exhibits negligible vasopr

[Lys8, Lys9]-Neurotensin (8-13) acetate, a Neurotensin analog, exerts its analgesic effects through activation of the G protein-coupled receptors NTS1 and NTS2, with Ki values of 0.33 nM and 0.95 nM for hNTS1 and hNTS2 receptors, respectively[1].

N-Formyl-Met-Leu-Phe-Lys (fMLFK) is a peptide that acts as a potent and selective agonist of FPR1, with EC50s of 3.5 nM for FPR1, 6.7 μM for FPR2, and 0.88 μM for FPR2-D2817.32G. This chemotactic peptide binds specifically to receptors on leukocyte membranes and its uptake can contribute to the quantitative assessment of neutrophils in localized inflammatory processes, independent of associated edema formation or microcirculatory compromise.

Z-D-Leu-OH is a useful organic compound for research related to life sciences. The catalog number is T65908 and the CAS number is 28862-79-5.

Boc-D-Leu-OMe is a useful organic compound for research related to life sciences. The catalog number is T67216 and the CAS number is 133467-01-3.

D-Lys(Z)-Pro-Arg-pNA (diacetate) diacetate is a chromogenic substrate.

H-D-Phg(4-Cl)-OH has diverse applications in life science-related research.

[Deamino-4-valine, 8-D-arginine]-Vasopressin (dVDAVP) is a highly potent and specific antidiuretic agent with prolonged effects [1] [2].

(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-6-(5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)hexanoic acid is a useful organic compound for research related to life sciences. The catalog number is T65199 and the CAS number is 146987-10-2.

Boc-D-Lys(Boc)-OH is a useful organic compound for research related to life sciences. The catalog number is T66186 and the CAS number is 65360-27-2.

N-Formyl-Nle-Leu-Phe-Nle-Tyr-Lys TFA is a formyl peptide receptor (FPR) agonist.

Z-D-Lys(Boc)-OH is a valuable organic compound for life sciences research [CAS number: 66845-42-9, catalog number: T67537].

Fmoc-D-Lys(Ivdde)-OH is a valuable organic compound for life sciences research, catalog number T64743 and CAS number 1272755-33-5.

H-D-Leu-NH2.HCl is an amino acid derivative and has a wide range of applications in life science related research.

Boc-D-Phe(4-Br)-OH is an amino acid derivative and has a wide range of applications in life science related research.

Ac-Leu-Val-Lys-Aldehyde is a potent inhibitor of cathepsin B, with an inhibitory concentration (IC50) of 4 nM. It significantly reduces quinolinic acid-induced cell death in the striatum and results in the accumulation of LC3-II [1].

Tyr-(D-Dab4,Arg5,D-Trp8)-cyclo-Somatostatin-14 (4-11) is a somatostatin agonist used in cancer research [1].

Fmoc-D-Phe(4-I)-OH is an amino acid derivative with extensive applications in life science research.

[D-Pro4,D-Trp7,9] Substance P (4-11) acts as a potent Substance P antagonist, significantly reducing plasma aldosterone (ALDO) concentrations[1].

Boc-D-Leu-OH is a useful organic compound for research related to life sciences. The catalog number is T66581 and the CAS number is 16937-99-8.

[D-Leu-4]-OB3 suppresses the expression of genes associated with inflammation, proliferation, and metastasis, as well as the expression of PD-L1. Additionally, it promotes the expression of genes that induce apoptosis [1].

Ac-[Nle4,D-Phe7]-α-MSH (4-10)-NH2, a melanotropin derivative and melanocyte-stimulating hormone, activates tyrosinase and demonstrates a thermoregulatory effect in rat models [1][2].

N-Myristoyl-Lys-Arg-Thr-Leu-Arg is a protein kinase C (PKC) inhibitor (IC50 = 75 μM) that effectively inhibits IL-2 receptor induction and IL-2 production in the human leukemic cell line Jurkat [1].

E-2078, known chemically as (N-Me-Tyr1,N-Me-Arg7,D-Leu-NHEt8)-Dynorphin A (1-8), is a stable analog of Dynorphin A (1–8) and functions as a kappa opioid receptor (KOR) agonist [1].

Fmoc-D-4-Pal-OH (Catalog No: T65478, CAS No: 205528-30-9) is an essential organic compound for life sciences research.

Fmoc-D-Lys(Fmoc)-OH is a useful organic compound for research related to life sciences. The catalog number is T66832 and the CAS number is 75932-02-4.

Fmoc-D-Phe(4-F)-OH is an amino acid derivative with broad applications in life sciences research.

H-D-Phe(4-CN)-OH is an important organic compound utilized in life sciences research, catalog number T65897 and CAS number 263396-44-7.

D-Val-Leu-Lys-chloromethylketone, a tripeptide, functions as an anticoagulant [1].

Acetyl-(D-Phe2,Lys15,Arg16,Leu27)-VIP(1-7)-GRF(8-27) is a selective antagonist for the vasoactive intestinal peptide 1 (VIP 1) receptor.

[D-Ala2] Leu-Enkephalinamide, an enkephalin analog, exhibits significant corneal permeability and analgesic properties, making it suitable for ocular disease research [1] [2].

[D-Pro4,D-Trp7,9,10] Substance P (4-11) is a potent antagonist of the tachykinin family of neuropeptides [1].

D-Ala-Lys-AMCA hydrochloride, a known substrate of proton-coupled oligopeptide transporter 1 (PEPT1), emits blue fluorescence and may be transported into Caco-2 cells and liver cancer cells.

[Lys8, Lys9]-Neurotensin (8-13) (JMV438) is a Neurotensin analog that elicits analgesic effects by activating the G protein-coupled receptors NTS1 and NTS2, with K i values of 0.33 nM and 0.95 nM for hNTS1 and hNTS2 receptors, respectively.

H-Leu-Ser-Lys-Leu-OH (LSYL), a latency-associated peptide located at the amino terminus of LAP, inhibits TGF-β1 activation by binding with KRFK, thereby obstructing TGF-β1 signal transduction and inhibiting the progression of hepatic damage and fibrosis [1].

(D-Phe6,Leu-NHEt13,des-Met14)-Bombesin (6-14), a bombesin (BBN) antagonist, holds potential for cancer research applications [1].

Fmoc-D-Leu-OH, catalog number T67556 and CAS number 114360-54-2, is a valuable organic compound for life sciences research.

Z-D-Lys-OH is a valuable organic compound for life sciences research (catalog number T66827; CAS number 70671-54-4).

[D-Arg2]Dermorphin-(1-4) amide is an N-terminal truncated peptide of [D-Arg2]dermorphin known for its hypothermic and analgesic effects, and it demonstrates degradation when exposed to soluble mouse liver and brain extracts [1].

H-D-4-Pal-OH.2HCl, an amino acid derivative, has a wide range of applications in life science research.

H-D-Lys(Z)-OH is an essential organic compound for life sciences research, identified by catalog number T66768 and CAS number 34404-32-5.

Fmoc-D-Lys-OH is a useful organic compound for research related to life sciences. The catalog number is T65525 and the CAS number is 110990-08-4.

[D-Pro4,D-Trp7,9,Nle11] Substance P (4-11) is a potent neurokinin NK1 antagonist that effectively inhibits the actions of gold-protein-substance P (GPSP) and substance P (SP), demonstrating its efficacy in neutralizing their effects [1].