GLPBio

Bombesin

Catalog No.: GC14014Purity:>99.50%
Bombesin is a 14-amino acid peptide that belongs to the Bombesin-related peptide family and plays an important role in gastrin release and G protein receptor activation.

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Bombesin
Cas No.: 31362-50-2
1mgIn Stock
$63.00
1
5mgIn Stock
$126.00
1
10mgIn Stock
$176.00
1
25mgIn Stock
$280.00
1

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Description

Bombesin is a 14-amino acid peptide that belongs to the Bombesin-related peptide family and plays an important role in gastrin release and G protein receptor activation[1, 2]. Bombesin, with a carboxyl terminus ending in Gly-His-Leu-Met-NH2, was originally isolated from the skin of the European bell toad (Bombina bombina). Its homologous peptides (such as gastrin-releasing peptide (GRP) and neuromedin B (NMB)) were later found in mammals[3]. Bombesin is a multifunctional neuropeptide that can stimulate gastric and pancreatic secretion, gastrointestinal hormone release, gallbladder contraction, and bronchial contraction[4]. Bombesin is present in amphibian gastric endocrine cells, avian glandular stomach endocrine cells, and avian brain. In mammals, Bombesin is mainly present in nerve cells and fibers[5]. Bombesin can stimulate nuclear factor κB activation and the expression of proangiogenic factors in prostate cancer cells[6].

References:
[1] Vigna S R, Thorndyke M C. Bombesin[M]//The comparative physiology of regulatory peptides. Dordrecht: Springer Netherlands, 1989: 34-60.
[2] LaPelusa A, Jan A. Biochemistry, bombesin[J]. 2019.
[3] Tian Z. QUB-1073: A Bioactice Peptide from the Skin Secretion of Phyllomedusa Rohdei[D]. Queen's University Belfast. Faculty of Medicine, Health and Life Sciences, December, 2018.
[4] Cho W K. Role of the neuropeptide, bombesin, in bile secretion[J]. The Yale Journal of Biology and Medicine, 1997, 70(4): 409.
[5] Chejfec G, Lee I, Warren W H, et al. Bombesin in human neuroendocrine (NE) neoplasms[J]. Peptides, 1985, 6: 107-112.
[6] Levine L, Lucci III J A, Pazdrak B, et al. Bombesin stimulates nuclear factor κB activation and expression of proangiogenic factors in prostate cancer cells[J]. Cancer research, 2003, 63(13): 3495-3502.

Product Documents

Purity:>99.50%Appearance:A solid

Chemical Properties

CAS No.
31362-50-2
Chemical Name
(S,Z)-N'1-((5S,6Z,8S,9Z,11S,12Z,15Z,17S,18Z,20S,21Z,23S,24Z,26S,27Z,29S,30Z,33Z,35S,36Z,38S)-11-((1H-imidazol-5-yl)methyl)-23-((1H-indol-3-yl)methyl)-43-amino-7,10,13,16,19,22,25,28,31,34,37-undecahydroxy-5-(hydroxy(imino)methyl)-29-(2-hydroxy-2-iminoethy
SMILES
CC(C[C@@](/N=C(O)/[C@](/N=C(O)/[C@](/N=C(O)/[C@]1([H])CCC(O)=N1)([H])CCC(O)=N)([H])CCCNC(N)=N)([H])/C(O)=N/C/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/C/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](C(O)=N)([H])CCSC)([H])CC(C
Molecular Formula
C71H110N24O18S
Molecular Weight
1619.85
Solubility
Soluble to 1 mg/ml in sterile water
Storage
Desiccate at -20°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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