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Merck

R9002

Ranatensin

≥95% (HPLC)

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C61H84N16O13S
CAS Number:
Molecular Weight:
1281.48
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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assay

≥95% (HPLC)

storage temp.

−20°C

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

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

InChI key

AUOCWSNQHWTPIJ-JMYPGRSYSA-N



Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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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
Nakajama, T., et al.
Federation Proceedings, 29, 282-282 (1970)
B M Chronwall et al.
Neuroscience letters, 53(1), 109-114 (1985-01-07)
Previous studies have demonstrated a neuronal system containing an immunoreactive ranatensin-like peptide (irRT) in rat brain. The results of the present study describe the ascending projections of a prominent irRT cell group in the pons. A major pontine irRT fiber