• Product NamePro-Leu-Gly-NH2
  • CasNo. 2002-44-0
  • MFC13H24N4O3
  • MW284.359
  • Purity
  • Appearance
  • Packing
  • Contact usInquiry

Product Details

CasNo: 2002-44-0

MF: C13H24N4O3

Offer Chemical Raw Material Pro-Leu-Gly-NH2 2002-44-0 In Stock

  • Molecular Formula:C13H24N4O3
  • Molecular Weight:284.359
  • Vapor Pressure:1.34E-15mmHg at 25°C 
  • Melting Point:122-123 °C(Solv: water (7732-18-5)) 
  • Refractive Index:1.51 
  • Boiling Point:626.2 °C at 760 mmHg 
  • PKA:14.10±0.20(Predicted) 
  • Flash Point:332.5 °C 
  • PSA:113.32000 
  • Density:1.147 g/cm3 
  • LogP:0.68170 

H-PRO-LEU-GLY-NH2(Cas 2002-44-0) Usage

Biological Activity

melanocyte stimulating hormone release inhibiting factor,(c13h24n4o3), a tri-peptide with the sequence h2n-pro-leu-gly-amide, mw= 284.35. melanocyte-inhibiting factor (also known as pro-leu-gly-nh2, melanostatin, msh release-inhibiting hormone or mif-1) is an endogenous peptide fragment derived from cleavage of the hormone oxytocin, but having generally different actions in the body(1). mif-1 produces multiple effects, both blocking the effects of opioid receptor activation(2), while at the same time acting as a positive allosteric modulator of the d2 and d4 dopamine receptor subtypes, as well as inhibiting release of other neuropeptides such as alpha-msh, and potentiating melatonin activity(3). mif-1 is unusually resistant to metabolism in the bloodstream, and crosses the blood–brain barrier easily, though it is poorly active orally and is usually injected.figure1 formula of melanocyte stimulating hormone release inhibiting factor

references

1. Celis ME, Taleisnik S, Walter R (July 1971). "Regulation of formation and proposed structure of the factor inhibiting the release of melanocyte-stimulating hormone". Proceedings of the National Academy of Sciences of the United States of America 68 (7): 1428–33.2. Contreras PC, Takemori AE (June 1984). "Effect of prolyl-leucyl-glycinamide and alpha-melanocyte-stimulating hormone on levorphanol-induced analgesia, tolerance and dependence". Life Sciences 34 (26): 2559–66.3. Sandyk R (May 1990). "MIF-induced augmentation of melatonin functions: possible relevance to mechanisms of action of MIF-1 inmovement disorders". The International Journal of Neuroscience 52 (1-2): 59–65.

InChI:InChI=1/C13H24N4O3/c1-8(2)6-10(12(19)16-7-11(14)18)17-13(20)9-4-3-5-15-9/h8-10,15H,3-7H2,1-2H3,(H2,14,18)(H,16,19)(H,17,20)/t9-,10-/m0/s1

2002-44-0 Relevant articles

PROCESS FOR LARGE SCALE LIQUID PHASE SYNTHESIS OF CARBETOCIN AND ITS NOVEL INTERMEDIATES

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Page/Page column 16; 23, (2017/11/06)

A process for large scale liquid phase s...

SYNTHESIS OF THE AMIDE OF THE C-TERMINAL TETRAPEPTIDE OF THE SEQUENCE OF OXYTOCIN

Ivanov, A. K.,Antonov, A. A.,Donetskii, I. A.

, p. 344 - 349 (2007/10/02)

The synthesis has been effected of the a...

BEHAVIORAL EFFECTS OF THYROLIBERIN, MELANOSTATIN, AND ITS ANALOGS

Mazurov, A. A.,Andronati, S. A.,Lobasyuk, B. A.,Kabanov, V. M.,Korotenko, T. I.

, p. 106 - 110 (2007/10/02)

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Peptide syntheses with the N-PChd protective group. Synthesis of the hydrophobic segment 14-20 L-Ala-Leu-Ile-Leu-Leu-Ala-Gln of human lymphoblastoid interferon

Khalifa,Jung,Rieker

, p. 1068 - 1090 (2007/10/02)

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2002-44-0 Process route

PChd-L-Pro-L-Leu-Gly-NH<sub>2</sub>
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PChd-L-Pro-L-Leu-Gly-NH2

2,6-di(t-butyl)-4-phenylphenol
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2,6-di(t-butyl)-4-phenylphenol

melanostatin
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melanostatin

Conditions
Conditions Yield
With hydrogen; palladium on activated charcoal; In methanol; for 3h;
90%
85%
benzoyloxycarbonylprolyl-leucyl-glycine amide
14485-80-4

benzoyloxycarbonylprolyl-leucyl-glycine amide

melanostatin
2002-44-0

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Conditions
Conditions Yield
With 5%-palladium/activated carbon; hydrogen; In methanol;
99.7%
With hydrogen; palladium; In ethanol;
80%

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