What is the H-TYR-GLY-GLY-PHE-MET-OH?

H-TYR-GLY-GLY-PHE-MET-OH is White lyophilised solid, while it's Molecular Formula is C27H35 N5 O7 S. White lyophilised solid Endogenous opioid peptide that also functions as a growth factor on many cell types at a receptor that is distinct from the neuronal opioid receptors

What is the CAS number for H-TYR-GLY-GLY-PHE-MET-OH?

The CAS number of H-TYR-GLY-GLY-PHE-MET-OH is 58569-55-4.

What is the H-TYR-GLY-GLY-PHE-MET-OH?

H-TYR-GLY-GLY-PHE-MET-OH is White lyophilised solid, while it's Molecular Formula is C27H35 N5 O7 S. White lyophilised solid Endogenous opioid peptide that also functions as a growth factor on many cell types at a receptor that is distinct from the neuronal opioid receptors

What is the CAS number for H-TYR-GLY-GLY-PHE-MET-OH?

The CAS number of H-TYR-GLY-GLY-PHE-MET-OH is 58569-55-4.

58569-55-4

Product NameMet-Enkephalin
Molecular FormulaC27H35 N5 O7 S
Molecular Weight573.67
Purity99%
AppearanceWhite lyophilised solid

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Product Details

Quick Details

CasNo： 58569-55-4
Molecular Formula： C27H35 N5 O7 S
Appearance： White lyophilised solid
Purity： 99%

Factory Supply High Purity Met-Enkephalin 58569-55-4 Efficient Shipping

Molecular Formula:C27H35 N5 O7 S
Molecular Weight:573.67
Appearance/Colour:White lyophilised solid
Vapor Pressure:0mmHg at 25°C
Melting Point:174-177 °C
Refractive Index:1.608
Boiling Point:1052.9 °C at 760 mmHg
PKA:3.23±0.10(Predicted)
Flash Point:590.6 °C
PSA：225.25000
Density:1.324 g/cm³
LogP:1.80830

H-TYR-GLY-GLY-PHE-MET-OH(Cas 58569-55-4) Usage

Uses	Endogenous opioid peptide that also functions as a growth factor on many cell types at a receptor that is distinct from the neuronal opioid receptors

InChI:InChI=1/C27H35N5O7S/c1-40-12-11-21(27(38)39)32-26(37)22(14-17-5-3-2-4-6-17)31-24(35)16-29-23(34)15-30-25(36)20(28)13-18-7-9-19(33)10-8-18/h2-10,20-22,33H,11-16,28H2,1H3,(H,29,34)(H,30,36)(H,31,35)(H,32,37)(H,38,39)/t20-,21-,22-/m0/s1

58569-55-4 Relevant articles

Neutrophil-mediated oxidation of enkephalins via myeloperoxidase-dependent addition of superoxide

Nagy, Péter,Kettle, Anthony J.,Winterbourn, Christine C.

, p. 792 - 799 (2010)

Neutrophils play a major role in acute i...

IMPROVED DEPROTECTION IN SOLID PHASE PEPTIDE SYNTHEIS: QUANTITATIVE REDUCTION OF METHIONINE SULFOXIDE TO METHIONINE DURING HF CLEAVAGE

Tam, James P.,Heath, William F.,Merrifield, R. B.

, p. 2939 - 2942 (1982)

The reduction of methionine sulfoxide re...

Sustainable Peptide Synthesis Enabled by a Transient Protecting Group

Avrutina, Olga,Knauer, Sascha,Koch, Niklas,Kolmar, Harald,Meusinger, Reinhard,Uth, Christina

supporting information, p. 12984 - 12990 (2020/06/01)

The growing interest in synthetic peptid...

Synthesis of Met-enkephalin by solution-phase peptide synthesis methodology utilizing para-toluene sulfonic acid as N-terminal masking of l-methionine amino acid

Khan, Riaz A.

, p. 884 - 888 (2016/11/11)

The Met-enkephalin, Tyr-Gly-Gly-Phe-Met,...

Nicotinoyl peptide derivatives and cosmetic composition comprising the same

-

, (2012/03/11)

The present invention relates to nicotin...

58569-55-4 Process route

: C₁₇H₁₃NO₁₀S₂^(2-)*2Na⁽¹⁺⁾

: C₂₀H₁₉NO₁₀S₃^(2-)*2Na⁽¹⁺⁾

: C₂₄H₁₉NO₁₀S₂^(2-)*2Na⁽¹⁺⁾

: C₂₄H₁₉NO₁₁S₂^(2-)*2Na⁽¹⁺⁾

: 58569-55-4
met-enkephalin

Conditions

Conditions	Yield
C₂₀H₁₉NO₁₀S₃^(2-)2Na⁽¹⁺⁾; With* sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; ethyl cyanoglyoxylate-2-oxime; In water; acetonitrile; at 20 ℃; for 0.75h; With ethanolamine; In water; for 0.166667h; C₁₇H₁₃NO₁₀S₂^(2-)2Na⁽¹⁺⁾; C₂₄H₁₉NO₁₀S₂^(2-)2Na⁽¹⁺⁾; C₂₄H₁₉NO₁₁S₂^(2-)*2Na⁽¹⁺⁾; Further stages;	63%

Yield

C₂₀H₁₉NO₁₀S₃^(2-)*2Na⁽¹⁺⁾; With sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; ethyl cyanoglyoxylate-2-oxime; In water; acetonitrile; at 20 ℃; for 0.75h;

With ethanolamine; In water; for 0.166667h;