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S-phosphocysteine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115562-30-6 Structure
  • Basic information

    1. Product Name: S-phosphocysteine
    2. Synonyms: S-phosphocysteine;S-phospho-L-cysteine
    3. CAS NO:115562-30-6
    4. Molecular Formula: C3H8NO5PS
    5. Molecular Weight: 201.14
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115562-30-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 503.5°Cat760mmHg
    3. Flash Point: 258.3°C
    4. Appearance: /
    5. Density: 1.83g/cm3
    6. Vapor Pressure: 1.66E-11mmHg at 25°C
    7. Refractive Index: 1.627
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: S-phosphocysteine(CAS DataBase Reference)
    11. NIST Chemistry Reference: S-phosphocysteine(115562-30-6)
    12. EPA Substance Registry System: S-phosphocysteine(115562-30-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 115562-30-6(Hazardous Substances Data)

115562-30-6 Usage

Definition

ChEBI: A phosphoamino acid consisting of L-cysteine carrying an S-phospho substituent.

Check Digit Verification of cas no

The CAS Registry Mumber 115562-30-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,5,6 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 115562-30:
(8*1)+(7*1)+(6*5)+(5*5)+(4*6)+(3*2)+(2*3)+(1*0)=106
106 % 10 = 6
So 115562-30-6 is a valid CAS Registry Number.
InChI:InChI=1/C3H8NO5PS/c4-2(3(5)6)1-11-10(7,8)9/h2H,1,4H2,(H,5,6)(H2,7,8,9)/t2-/m0/s1

115562-30-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name S-phospho-L-cysteine

1.2 Other means of identification

Product number -
Other names S3-phosphocysteine

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:115562-30-6 SDS

115562-30-6Upstream product

115562-30-6Downstream Products

115562-30-6Relevant articles and documents

Peptide Tyrosinase Activators

-

, (2015/06/10)

Peptides that increase melanin synthesis are provided. These peptides include pentapeptides YSSWY, YRSRK, and their variants. The peptides may activate the enzymatic activity of tyrosinase to increase melanin synthesis. The pharmaceutical, cosmetic, and other compositions including the peptides are also provided. The methods of increasing melanin production in epidermis of a subject are provided where the methods include administering compositions comprising an amount of one or more peptides effective to increase the melanin production. The methods also include treating vitiligo or other hypopigmentation disorders with compositions including one or more peptides.

Thiophosphorylation of free amino acids and enzyme protein by thiophosphoramidate ions

Ruman, Tomasz,Dlugopolska, Karolina,Jurkiewicz, Agata,Rut, Dagmara,Fraczyk, Tomasz,Ciesla, Joanna,Les, Andrzej,Szewczuk, Zbigniew,Rode, Wojciech

experimental part, p. 74 - 80 (2010/05/17)

In search of an activity-preserving protein thiophosphorylation method, with thymidylate synthase recombinant protein used as a substrate, potassium thiophosphoramidate and diammonium thiophosphoramidate salts in Tris- and ammonium carbonate based buffer solutions were employed, proving to serve as a non-destructive environment. Using potassium phosphoramidate or diammonium thiophosphoramidate, a series of phosphorylated and thiophosphorylated amino acid derivatives was prepared, helping, together with computational (using density functional theory, DFT) estimation of 31P NMR chemical shifts, to assign thiophosphorylated protein NMR resonances and prove the presence of thiophosphorylated lysine, serine and histidine moieties. Methods useful for prediction of 31P NMR chemical shifts of thiophosphorylated amino acid moieties, and thiophosphates in general, are also presented. The preliminary results obtained from trypsin digestion of enzyme shows peak at m/z 1825.805 which is in perfect agreement with the simulated isotopic pattern distributions for monothiophosphate of TVQQQVHLNQDEYK where thiophosphate moiety is attached to histidine (His26) or lysine (Lys33) side-chain.

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