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H-SER-LEU-ILE-GLY-LYS-VAL-NH2

CAS No.
190383-13-2
Chemical Name:
H-SER-LEU-ILE-GLY-LYS-VAL-NH2
Synonyms
SLIGKV-NH2;Par-2 Ago;SLIGKVAMIDE;PAR-2 amide (1-6);PAR-2 AGONIST AMIDE;PAR-2 Agonist, amid;SLIGKV-NH2 TFA salt;PAR2 activating peptide;PAR-2 (1-6) AMIDE (HUMAN);SER-LEU-ILE-GLY-LYS-VAL-NH2
CBNumber:
CB7715297
Molecular Formula:
C28H54N8O7
Molecular Weight:
614.78
MDL Number:
MFCD02259590
MOL File:
190383-13-2.mol
MSDS File:
SDS
Last updated:2024-03-27 11:49:37

H-SER-LEU-ILE-GLY-LYS-VAL-NH2 Properties

Boiling point 1030.3±65.0 °C(Predicted)
Density 1.161±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility ≥13.48 mg/mL in EtOH with gentle warming and ultrasonic; ≥62.9 mg/mL in DMSO; ≥66.2 mg/mL in H2O
form solid
pka 12.04±0.10(Predicted)
Water Solubility Soluble to 1 mg/ml in water
Sequence H-Ser-Leu-Ile-Gly-Lys-Val-NH2

SAFETY

Risk and Safety Statements

Safety Statements  22-24/25
WGK Germany  3

H-SER-LEU-ILE-GLY-LYS-VAL-NH2 price More Price(16)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich S9192 Ser-Leu-Ile-Gly-Lys-Val-amide ≥95% (HPLC), solid 190383-13-2 1mg $57 2024-03-01 Buy
Tocris 3010 SLIGKV-NH2 190383-13-2 5 $165 2021-12-16 Buy
Usbiological 256692 SLIGKV-NH2 190383-13-2 5mg $403 2021-12-16 Buy
TRC S560020 SLIGKV-NH2 190383-13-2 5mg $145 2021-12-16 Buy
Biorbyt Ltd orb372666 PAR-2 Agonist amide > 95% 190383-13-2 5mg $552.5 2021-12-16 Buy
Product number Packaging Price Buy
S9192 1mg $57 Buy
3010 5 $165 Buy
256692 5mg $403 Buy
S560020 5mg $145 Buy
orb372666 5mg $552.5 Buy

H-SER-LEU-ILE-GLY-LYS-VAL-NH2 Chemical Properties,Uses,Production

Uses

SLIGKV-NH2 is a PAR2 agonist.

Definition

ChEBI: Ser-Leu-Ile-Gly-Lys-Val-Amide is an oligopeptide.

Biological Activity

sligkv-nh2 serves as a protease-activated receptor 2 (par2) agonist. pars are a group of g-protein-coupled receptors existing in several cell types. up to date, four par members including par1 to 4 have been identified, cloned and designated. par2 is expressed in the respiratory and gastrointestinal tracts. it is suggested that the activation of par2 is closely correlated with inflammatory evens in various cells and tissues. par2 has also been identified to induce protease activation and therefore result in systemic hypotension. [1]

Biochem/physiol Actions

Proteinase-activated receptor (PAR-2) is a member of proteolytically cleaved receptors. It is activated by a synthetic peptide (SLIGKV), that is exposed after trypsin cleavage of the amino terminus. PAR-2 stimulates an increase in cytosolic Ca2+ ion concentration.

in vitro

it was reported that sligkv-nh2 (the par2 activating peptide), by inducing express of par2, could slightly enhanced mucin secretion by human bronchial epithelial cells in vitro. according to this study, compared to cells treated with a control peptide with reversed amino acid sequence, exposure of cells to sligkv-nh2 for 30 mins resulted in a weak but statistically significant increase in mucin secretion at concentrations of 100 and 1000m. in addition, sligkv-nh2 was demonstrated to accelerate cell cycle progression and stimulate the growth of hepg2 cells. [1, 2]

in vivo

the ability of par2 agonists to induce contractile responses was investigated in vivo. it was found that mouse par2 activating (sligrl-nh2) and human par2 activating (sligkv-nh2) peptides triggered a concentration-dependent contractile response in guinea-pig gallbladder. [3]

IC 50

a protease-activated receptor 2 (par2) agonist with an ic50 of 10.4 m.

storage

Store at -20°C

References

[1] lin kw, park j, crews al, li yh, adler kb. protease-activated receptor-2 (par-2) is a weak enhancer of mucin secretion by human bronchial epithelial cells in vitro. int j biochem cell b. 2008. 40: 137988.
[2]xie l, zheng y, li x, zhao jy, chen xy, chen l, zhou j, hai o and li f. enhanced proliferation of human hepatoma cells by par-2 agonists via the erk/ap-1 pathway. oncol rep. 2012.28: 1665-72.
[3] tognetto m, trevisani m, maggiore b, navarra g, turini a, guerrini r, bunnett nw, geppetti p and harrison s. evidence that par-1 and par-2 mediate prostanoid-dependent contraction in isolated guinea-pig gallbladder. br.j.pharmacol. 2000.131: 689-94.
[4] robin j, kharbanda r, mclean p, campbell r, vallance p. protease-activated receptor 2–mediated vasodilatation in humans in vivo, role of nitric oxide and prostanoids. circulation. 2003;107:954-959.

H-SER-LEU-ILE-GLY-LYS-VAL-NH2 Preparation Products And Raw materials

Raw materials

Preparation Products

H-SER-LEU-ILE-GLY-LYS-VAL-NH2 Suppliers

Global( 94)Suppliers
Supplier Tel Email Country ProdList Advantage
Shenzhen Nexconn Pharmatechs Ltd
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Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
BOC Sciences
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Shanghai Longyu Biotechnology Co., Ltd.
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career henan chemical co
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Dideu Industries Group Limited
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Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471 sales@sarms4muscle.com China 10523 58
Hangzhou Go Top Peptide Biotech
0571-88211921 sales1@gotopbio.com CHINA 2609 58
Alfa Chemistry
+1-5166625404 Info@alfa-chemistry.com United States 21317 58

View Lastest Price from H-SER-LEU-ILE-GLY-LYS-VAL-NH2 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
H-SER-LEU-ILE-GLY-LYS-VAL-NH2 pictures 2020-02-14 H-SER-LEU-ILE-GLY-LYS-VAL-NH2
190383-13-2
US $7.00 / KG 1KG 99% 100KG Career Henan Chemical Co

190383-13-2(H-SER-LEU-ILE-GLY-LYS-VAL-NH2)Related Search:

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