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Key Documents

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
Pricing and availability is not currently available.

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
102K09882
102K09881
102K0988
090H06132
016H1061

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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
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
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.
J Y Lin et al.
Brain research bulletin, 35(3), 241-246 (1994-01-01)
The effects of bombesin, gastrin-releasing peptide, neuromedin C, ranatensin, and neuromedin B on hypothalamic arcuate neurons were tested in this study using extracellular single-unit recording in fresh brain tissue slices. Adult ovariectomized Sprague-Dawley rats were used for preparation of brain
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
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