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Merck
CN

E7880

Eledoisin

≥97% (HPLC)

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关于此项目

经验公式(希尔记法):
C54H85N13O15S
化学文摘社编号:
分子量:
1188.40
UNSPSC Code:
12352200
MDL number:
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SMILES string

CCC(C)C(NC(=O)C(Cc1ccccc1)NC(=O)C(C)NC(=O)C(CC(O)=O)NC(=O)C(CCCCN)NC(=O)C(CO)NC(=O)C2CCCN2C(=O)C3CCC(=O)N3)C(=O)NCC(=O)NC(CC(C)C)C(=O)NC(CCSC)C(N)=O

assay

≥97% (HPLC)

storage temp.

−20°C

Biochem/physiol Actions

Tachykinin originally isolated from the salivary gland of octopus with structural homology to substance P; potent vasodilator and hypotensive agent; induces salivation and increases capillary permeability. Agonist at tachykinin NK-2/NK-3 receptors.

存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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M Bergstrom et al.
Scandinavian journal of clinical and laboratory investigation, 55(8), 679-689 (1995-12-01)
Tachykinins are a family of peptides that may be present in and secreted from carcinoid tumours of mid-gut origin. They are likely to play a role in the pathogenesis of, e.g. the flush, dyspnoea and valvular heart disease seen in
C Lippe et al.
Peptides, 19(8), 1435-1438 (1998-11-11)
The tachykinin-dependent stimulation of ion transport across frog skin was studied. Tachykinin stimulation was due to interaction with an NK1-like receptor as [Sar9-Met(O2)11]-Substance P (a very selective NK1 agonist) strongly stimulated SCC, whereas [beta-Ala8]-Neurokinin A 4-10 (a very selective NK2
G Hölzemann et al.
International journal of peptide and protein research, 44(2), 105-111 (1994-08-01)
The synthesis of 11 cyclic hexapeptides, some of which contain a carbohydrate side chain moiety, is described in this paper. A glycosylamine was coupled without hydroxyl protecting groups either directly or via a butyric acid spacer to the side chain
U Gether et al.
The Journal of biological chemistry, 268(11), 7893-7898 (1993-04-15)
The NK1 (substance P) and NK3 (neurokinin B) receptors are G protein-coupled receptors sharing approximately 70% identity within the membrane-spanning domains. However, they each have a distinct pharmacological profile in respect of peptide binding. To identify epitopes that determine their
P Björup et al.
Bioorganic & medicinal chemistry, 6(7), 891-901 (1998-09-08)
The influence of different reaction systems on alpha-chymotrypsin-catalyzed synthesis of eledoisin and LH-RH peptides from (7 + 4) and (5 + 5) fragments was investigated. The peptide yield was determined in the following systems: buffered aqueous media, frozen solutions, organic

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