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2-Amino-D-Phenylalanine is a chemical compound that is part of the amino acid group. It is a derivative of the essential amino acid phenylalanine, characterized by a 2-amino substituent on the D-phenylalanine molecule. This unique structure endows it with potential applications in pharmaceuticals and biochemistry, where it may contribute to the synthesis of peptides, proteins, and other biologically active molecules. Its therapeutic and medicinal uses are currently under investigation, with the need for further research and clinical trials to elucidate its pharmacological properties and potential applications fully.

35987-77-0

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35987-77-0 Usage

Uses

Used in Pharmaceutical and Biochemical Applications:
2-Amino-D-Phenylalanine is used as a building block for the synthesis of peptides and proteins, playing a crucial role in the development of new drugs and therapeutic agents. Its unique structure allows for the creation of novel biologically active molecules with potential applications in various medical fields.
Used in Research and Development:
In the scientific community, 2-Amino-D-Phenylalanine serves as an important compound for research purposes. It is utilized in the study of amino acid derivatives, their interactions with biological systems, and their potential roles in disease mechanisms and treatment strategies.
Used in Therapeutic and Medicinal Applications:
Although still in the exploratory phase, 2-Amino-D-Phenylalanine may have therapeutic and medicinal uses. Its potential applications could include the treatment of various diseases and conditions, pending the results of ongoing research and clinical trials that will provide a deeper understanding of its pharmacological properties and efficacy.
Used in Drug Synthesis:
2-Amino-D-Phenylalanine is used as a key component in the synthesis of pharmaceutical drugs. Its unique properties may contribute to the development of innovative medications with improved efficacy and reduced side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 35987-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,8 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35987-77:
(7*3)+(6*5)+(5*9)+(4*8)+(3*7)+(2*7)+(1*7)=170
170 % 10 = 0
So 35987-77-0 is a valid CAS Registry Number.

35987-77-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-amino-3-(2-aminophenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names 2-AMINO-D-PHENYLALANINE

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:35987-77-0 SDS

35987-77-0Relevant academic research and scientific papers

Immunomodulatory peptides

-

, (2014/12/12)

The invention relates to peptides derivatized with a hydrophilic polymer which, in some embodiments, bind to human FcRn and inhibit binding of the Fc portion of an IgG to an FcRn, thereby modulating serum IgG levels. The disclosed compositions and methods may be used in some embodiments, for example, in treating autoimmune diseases and inflammatory disorders. The invention also relates, in further embodiments, to methods of using and methods of making the peptides of the invention.

An unnatural amino acid based fluorescent probe for phenylalanine ammonia lyase

Tian, Zhenlin,Zhu, Weiping,Xu, Yufang,Qian, Xuhong

supporting information, p. 5818 - 5821 (2014/08/05)

A fluorescent probe (2a-LP) based on an unnatural amino acid (UAA) is developed for the detection of phenylalanine ammonia lyase (PAL). In the presence of PAL, 2a-LP is catalytically deaminated to ortho-amino-transcinnamic acid (o-a-CA), which shows a rem

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