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R9002

Sigma-Aldrich

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:
29451-71-6
Molecular Weight:
1281.48
MDL number:
MFCD00167518
UNSPSC Code:
12352200
PubChem Substance ID:
24899412

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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.
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
S Itoh et al.
The Japanese journal of physiology, 45(1), 37-45 (1995-01-01)
Neuromedin B (NMB) and neuromedin C (NMC) are peptides found in the mammalian central nervous system, and their concentrations are particularly high in the hypothalamus. The amino acid sequences of these peptides are similar to that of bombesin, which is
J H Walsh et al.
Regulatory peptides, 3(1), 1-13 (1982-01-01)
Antibodies specific for the carboxyl-terminal regions of bombesin and of ranatensin were used to study the tissue distribution of substances immunochemically similar to these two peptides in three amphibian species. Brain extracts of Rana catesbeiana, Rana pipiens, and Xenopus laevis
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