Welcome to LookChem.com Sign In|Join Free
  • or
H-TYR-TYR-TYR-OH, also known as tripeptide tyrosine, is a chemical compound composed of three molecules of the amino acid tyrosine linked together. It plays a crucial role in the production of several key neurotransmitters and hormones in the body, such as dopamine, adrenaline, and thyroid hormones. As a tripeptide, H-TYR-TYR-TYR-OH may have potential applications in the field of pharmaceuticals and biotechnology due to its ability to modulate physiological processes and potentially influence the function of the central nervous system. Furthermore, research suggests that tyrosine derivatives may possess antioxidant and anti-inflammatory properties, making H-TYR-TYR-TYR-OH a promising candidate for further exploration in drug development and therapeutic interventions.

7390-78-5

Post Buying Request

7390-78-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

7390-78-5 Usage

Uses

Used in Pharmaceutical Industry:
H-TYR-TYR-TYR-OH is used as a pharmaceutical compound for its potential to modulate physiological processes and influence the function of the central nervous system. Its involvement in the production of neurotransmitters and hormones makes it a valuable candidate for the development of drugs targeting various neurological and endocrine disorders.
Used in Biotechnology Industry:
H-TYR-TYR-TYR-OH is used as a biotechnological tool for its potential applications in modulating physiological processes. Its ability to influence the function of the central nervous system and its antioxidant and anti-inflammatory properties make it a promising candidate for the development of therapeutic interventions in various medical conditions.
Used in Drug Development:
H-TYR-TYR-TYR-OH is used as a drug development candidate due to its potential to modulate physiological processes and influence the function of the central nervous system. Its involvement in the production of neurotransmitters and hormones, as well as its antioxidant and anti-inflammatory properties, make it a valuable asset in the development of novel therapeutic agents for a wide range of medical conditions.
Used in Therapeutic Interventions:
H-TYR-TYR-TYR-OH is used as a therapeutic intervention for its potential to modulate physiological processes and influence the function of the central nervous system. Its antioxidant and anti-inflammatory properties, along with its involvement in the production of neurotransmitters and hormones, make it a promising candidate for the treatment of various medical conditions, including neurological and endocrine disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 7390-78-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7390-78:
(6*7)+(5*3)+(4*9)+(3*0)+(2*7)+(1*8)=115
115 % 10 = 5
So 7390-78-5 is a valid CAS Registry Number.

7390-78-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[2-[[2-amino-3-(4-hydroxyphenyl)propanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-3-(4-hydroxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names N-(N-L-tyrosyl-L-tyrosyl)-L-tyrosine

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:7390-78-5 SDS

7390-78-5Downstream Products

7390-78-5Relevant academic research and scientific papers

Peptide bond formation by aminolysin-A catalysis: A simple approach to enzymatic synthesis of diverse short oligopeptides and biologically active puromycins

Usuki, Hirokazu,Yamamoto, Yukihiro,Arima, Jiro,Iwabuchi, Masaki,Miyoshi, Shozo,Nitoda, Teruhiko,Hatanaka, Tadashi

supporting information; experimental part, p. 2327 - 2335 (2011/05/02)

A new S9 family aminopeptidase derived from the actinobacterial thermophile Acidothermus cellulolyticus was cloned and engineered into a transaminopeptidase by site-directed mutagenesis of catalytic Ser491 into Cys. The engineered biocatalyst, designated aminolysin-A, can catalyze the formation of peptide bonds to give linear homo-oligopeptides, hetero-dipeptides, and cyclic dipeptides using cost-effective substrates in a one-pot reaction. Aminolysin-A can recognize several C-terminal-modified amino acids, including the l- and d-forms, as acyl donors as well as free amines, including amino acids and puromycin aminonucleoside, as acyl acceptors. The absence of amino acid esters prevents the formation of peptides; therefore, the reaction mechanism involves aminolysis and not a reverse reaction of hydrolysis. The aminolysin system will be a beneficial tool for the preparation of structurally diverse peptide mimetics by a simple approach.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 7390-78-5