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Merck
CN

R9002

Ranatensin

≥95% (HPLC)

别名:

pGlu-Val-Pro-Gln-Trp-Ala-Val-Gly-His-Phe-Met-NH2

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关于此项目

经验公式(希尔记法):
C61H84N16O13S
化学文摘社编号:
分子量:
1281.48
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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InChI

1S/C61H84N16O13S/c1-32(2)50(60(89)66-30-49(80)70-45(27-37-29-64-31-67-37)58(87)73-43(25-35-13-8-7-9-14-35)57(86)71-40(52(63)81)22-24-91-6)75-53(82)34(5)68-56(85)44(26-36-28-65-39-16-11-10-15-38(36)39)74-54(83)42(18-20-47(62)78)72-59(88)46-17-12-23-77(46)61(90)51(33(3)4)76-55(84)41-19-21-48(79)69-41/h7-11,13-16,28-29,31-34,40-46,50-51,65H,12,17-27,30H2,1-6H3,(H2,62,78)(H2,63,81)(H,64,67)(H,66,89)(H,68,85)(H,69,79)(H,70,80)(H,71,86)(H,72,88)(H,73,87)(H,74,83)(H,75,82)(H,76,84)/t34-,40-,41-,42-,43-,44-,45-,46-,50-,51-/m0/s1

SMILES string

CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc2c[nH]cn2)NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](Cc3c[nH]c4ccccc34)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]5CCCN5C(=O)[C@@H](NC(=O)[C@@H]6CCC(=O)N6)C(C)C)C(C)C)C(N)=O

InChI key

AUOCWSNQHWTPIJ-JMYPGRSYSA-N

assay

≥95% (HPLC)

storage temp.

−20°C

存储类别

11 - 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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Nakajama, T., et al.
Federation Proceedings, 29, 282-282 (1970)
P C Lee et al.
The American journal of physiology, 238(3), G213-G218 (1980-03-01)
Incubating dispersed acini from guinea pig pancreas with bombesin and then washing the cells to remove bombesin reduced the subsequent stimulation of amylase secretion caused by bombesin, litorin, or ranatensin by as much as 80%, but did not alter the
B M Chronwall et al.
Brain research, 338(1), 97-113 (1985-07-08)
An antibody to des-pyroglutamyl ranatensin (RT 2-11) has been prepared and has been used to histochemically and biochemically identify ranatensin-like immunoreactivity (irRT) in the rat brain. The most most prominent stained cell group was situated in the dorsal tegmental pons.
A Guglietta et al.
Peptides, 6 Suppl 3, 75-81 (1985-01-01)
The amphibian skin tetrapeptide bombesin shows potent action in reducing gastric acid secretion by intracerebral ventricular (ICV) administration in rats. In order to establish a relationship between this action and the amino acid composition of the bombesin-like peptides, most of
G de Caro et al.
Peptides, 5(3), 607-613 (1984-05-01)
The effects on ingestive behavior of the naturally occurring bombesin-like peptides ranatensin and litorin were studied in comparison to those of bombesin by intracerebroventricular pulse injection or by continuous infusion in the rat. Ranatensin and litorin, like bombesin, proved to

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