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L-Leucine,O-sulfo-L-tyrosylglycylglycyl-L-phenylalanylis a complex chemical compound consisting of amino acids L-Leucine and L-Phenylalanyl, with an O-sulfo group attached to a tyrosine amino acid. This sulfated form may be involved in various biochemical reactions and functions within the body, leveraging the properties of its constituent amino acids. L-Leucine is crucial for protein synthesis and metabolic regulation, while L-Phenylalanyl is essential for the production of other amino acids and biologically active compounds. The specific context and role of L-Leucine,O-sulfo-L-tyrosylglycylglycyl-L-phenylalanyl- would depend on further research or the context in which it is studied.

80632-52-6

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80632-52-6 Usage

Uses

Since the provided materials do not specify any particular applications for L-Leucine,O-sulfo-L-tyrosylglycylglycyl-L-phenylalanyl-, it is not possible to list its uses based on the given information. However, given the roles of its constituent amino acids, it can be hypothesized that L-Leucine,O-sulfo-L-tyrosylglycylglycyl-L-phenylalanyl- may have potential applications in various industries, such as pharmaceuticals, nutrition, or cosmetics, depending on its specific properties and functions once identified through further research.

Check Digit Verification of cas no

The CAS Registry Mumber 80632-52-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,3 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80632-52:
(7*8)+(6*0)+(5*6)+(4*3)+(3*2)+(2*5)+(1*2)=116
116 % 10 = 6
So 80632-52-6 is a valid CAS Registry Number.
InChI:InChI=1/C28H37N5O10S/c1-17(2)12-23(28(38)39)33-27(37)22(14-18-6-4-3-5-7-18)32-25(35)16-30-24(34)15-31-26(36)21(29)13-19-8-10-20(11-9-19)43-44(40,41)42/h3-11,17,21-23H,12-16,29H2,1-2H3,(H,30,34)(H,31,36)(H,32,35)(H,33,37)(H,38,39)(H,40,41,42)/t21-,22-,23-/m0/s1

80632-52-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[[(2S)-2-[[2-[[2-[[(2S)-2-amino-3-(4-sulfooxyphenyl)propanoyl]amino]acetyl]amino]acetyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoic acid

1.2 Other means of identification

Product number -
Other names Tyr-O-sulfated leucine enkephalin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:80632-52-6 SDS

80632-52-6Downstream Products

80632-52-6Relevant academic research and scientific papers

Sulfation of various alcoholic groups by an arylsulfate sulfotransferase from desulfitobacterium hafniense and synthesis of estradiol sulfate

Van Der Horst, Michael A.,Van Lieshout, Johan F. T.,Bury, Aleksandra,Hartog, Aloysius F.,Wever, Ron

supporting information, p. 3501 - 3508 (2013/02/22)

Bacterial arylsulfate sulfotransferases (AST) are enzymes that catalyse the transfer of a sulfate group from p-nitrophenyl sulfate (p-NPS) to a phenolic acceptor molecule. By screening of the NCBI protein database a gene coding for an AST was found in Desulfitobacterium hafniense. After expression the enzyme was purified and characterised. This AST efficiently sulfates various acceptor molecules (estrone, estradiol, enkephalin and non-phenolic alcohols) using p-NPS as sulfate donor. The purified AST has a pH optimum of 9.6, it is stable in the presence of 10% of DMSO, and depending on the conditions it has a melting temperature of up to 47°C. Surprisingly, and in great contrast to all other known bacterial ASTs, this enzyme was able to use a variety of non-phenolic alcohols as sulfate acceptor. Because of these properties, this unique enzyme is a promising tool for biotransformation processes, providing a green and simple method to specifically sulfate compounds without need for functional group protection.

Use of Dimethylformamide-Sulphur Trioxide Complex as a Sulphating Agent of Tyrosine

Futaki, Shiroh,Taike, Takashi,Yagami, Takeshi,Ogawa, Toyoko,Akita, Tadashi,Kitagawa, Kouki

, p. 1739 - 1744 (2007/10/02)

Dimethylformamide-sulphur trioxide (DMF-SO3) complex was found to be more suitable for tyrosine sulphation than pyridine-sulphur trioxide (Pyr-SO3) complex, the most commonly used sulphur trioxide complex for sulphation.The work-up after sulphation using

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