What is the TYR-D-ALA-GLY-PHE-LEU?

TYR-D-ALA-GLY-PHE-LEU is , while it's Molecular Formula is C 29 H 39 N 5 O 7 . Used in Pharmaceutical Research: TYR-D-ALA-GLY-PHE-LEU is used as a research compound for exploring its potential biological properties and functions. The unique sequence of amino acids in this peptide may contribute to its potential applications in various therapeutic areas. Used in Drug Development: TYR-D-ALA-GLY-PHE-LEU is used as a lead compound in the development of new drugs. Its specific amino acid sequence may provide insights into the design of novel therapeutic agents with targeted effects on specific biological pathways or diseases. Used in Diagnostic Applications: TYR-D-ALA-GLY-PHE-LEU may be used as a diagnostic marker or tool in the identification and monitoring of certain conditions or diseases. The peptide's unique properties could potentially be leveraged to develop assays or tests for medical diagnostics. Used in Cosmetics and Personal Care: TYR-D-ALA-GLY-PHE-LEU may also find applications in the cosmetics and personal care industry, where its potential biological activity could be harnessed for skin care, hair care, or other beauty products.

What is the CAS number for TYR-D-ALA-GLY-PHE-LEU?

The CAS number of TYR-D-ALA-GLY-PHE-LEU is 64963-01-5.

What is TYR-D-ALA-GLY-PHE-LEU (64963-01-5) used for?

TYR-D-ALA-GLY-PHE-LEU is a peptide consisting of the amino acids tyrosine (TYR), D-alanine (D-ALA), glycine (GLY), phenylalanine (PHE), and leucine (LEU) arranged in a specific sequence. This peptide possesses potential biological activity due to its unique arrangement of amino acids, making it a candidate for pharmaceutical research and development.InChI:InChI=1/C29H39N5O7/c1-17(2)13-24(29(40)41)34-28(39)23(15-19-7-5-4-6-8-19)33-25(36)16-31-26(37)18(3)32-27(38)22(30)14-20-9-11-21(35)12-10-20/h4-12,17-18,22-24,35H,13-16,30H2,1-3H3,(H,31,37)(H,32,38)(H,33,36)(H,34,39)(H,40,41)/t18-,22+,23+,24+/m1/s1

What is the TYR-D-ALA-GLY-PHE-LEU?

TYR-D-ALA-GLY-PHE-LEU is , while it's Molecular Formula is C 29 H 39 N 5 O 7 . Used in Pharmaceutical Research: TYR-D-ALA-GLY-PHE-LEU is used as a research compound for exploring its potential biological properties and functions. The unique sequence of amino acids in this peptide may contribute to its potential applications in various therapeutic areas. Used in Drug Development: TYR-D-ALA-GLY-PHE-LEU is used as a lead compound in the development of new drugs. Its specific amino acid sequence may provide insights into the design of novel therapeutic agents with targeted effects on specific biological pathways or diseases. Used in Diagnostic Applications: TYR-D-ALA-GLY-PHE-LEU may be used as a diagnostic marker or tool in the identification and monitoring of certain conditions or diseases. The peptide's unique properties could potentially be leveraged to develop assays or tests for medical diagnostics. Used in Cosmetics and Personal Care: TYR-D-ALA-GLY-PHE-LEU may also find applications in the cosmetics and personal care industry, where its potential biological activity could be harnessed for skin care, hair care, or other beauty products.

What is the CAS number for TYR-D-ALA-GLY-PHE-LEU?

The CAS number of TYR-D-ALA-GLY-PHE-LEU is 64963-01-5.

What is TYR-D-ALA-GLY-PHE-LEU (64963-01-5) used for?

TYR-D-ALA-GLY-PHE-LEU is a peptide consisting of the amino acids tyrosine (TYR), D-alanine (D-ALA), glycine (GLY), phenylalanine (PHE), and leucine (LEU) arranged in a specific sequence. This peptide possesses potential biological activity due to its unique arrangement of amino acids, making it a candidate for pharmaceutical research and development.InChI:InChI=1/C29H39N5O7/c1-17(2)13-24(29(40)41)34-28(39)23(15-19-7-5-4-6-8-19)33-25(36)16-31-26(37)18(3)32-27(38)22(30)14-20-9-11-21(35)12-10-20/h4-12,17-18,22-24,35H,13-16,30H2,1-3H3,(H,31,37)(H,32,38)(H,33,36)(H,34,39)(H,40,41)/t18-,22+,23+,24+/m1/s1

Product classification

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(D-Ala2)-Leu-Enkephalin

Product Name: (D-Ala2)-Leu-Enkephalin
CasNo: 64963-01-5
Purity:
Appearance:

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CasNo： 64963-01-5

Molecular Formula： C₂₉H₃₉N₅O₇

Buy Quality (D-Ala2)-Leu-Enkephalin 64963-01-5 In Stock with Immediately Delivery

Molecular Formula:C₂₉H₃₉N₅O₇
Molecular Weight:569.658
Vapor Pressure:0mmHg at 25°C
Melting Point:160-163.5 °C
Refractive Index:1.582
Boiling Point:991.9 °C at 760 mmHg
PKA:3.40±0.10(Predicted)
Flash Point:553.7 °C
PSA：199.95000
Density:1.257 g/cm³
LogP:2.48980

TYR-D-ALA-GLY-PHE-LEU(Cas 64963-01-5) Usage

General Description

TYR-D-ALA-GLY-PHE-LEU is a peptide composed of the amino acids tyrosine (TYR), D-alanine (D-ALA), glycine (GLY), phenylalanine (PHE), and leucine (LEU). These amino acids are arranged in a specific sequence to form a peptide with potential biological activity. TYR-D-ALA-GLY-PHE-LEU may have applications in pharmaceutical research, as it could potentially exhibit certain properties or functions due to its unique sequence of amino acids. Further research and testing would be necessary to fully understand the potential uses and effects of this peptide.

InChI:InChI=1/C29H39N5O7/c1-17(2)13-24(29(40)41)34-28(39)23(15-19-7-5-4-6-8-19)33-25(36)16-31-26(37)18(3)32-27(38)22(30)14-20-9-11-21(35)12-10-20/h4-12,17-18,22-24,35H,13-16,30H2,1-3H3,(H,31,37)(H,32,38)(H,33,36)(H,34,39)(H,40,41)/t18-,22+,23+,24+/m1/s1

64963-01-5 Relevant articles

Synthesis and antinociceptive activity of [D-Ala2]Leu-enkephalin derivatives conjugated with the adamantane moiety

Kitagawa, Kouki,Mizobuchi, Noriko,Hama, Teruo,Hibi, Tohru,Konishi, Ryoji,Futaki, Shiroh

, p. 1782 - 1787 (2007/10/03)

Based on the physicochemical and pharmac...

Synthesis of 2>Leu-enkephalin and 2,D-Leu5>Leu-enkephalin with High Specific Tritiated Activity in the Leucine Residue

Hasegawa, Hiroshi,Shinohara, Yoshihiko,Baba, Shigeo

, p. 2641 - 2644 (2007/10/02)

2>Leu-enkephalin and 2,D-Leu5>Leu-enkep...

A photoaffinity reagent to label the opiate receptors of guinea pig ileum and mouse vas deferens

Fujioka,Matsunaga,Nakayama,Kanaoka,Hayashi,Kangawa,Matsuo

, p. 836 - 840 (2007/10/02)

An enkephalin derivative, [D-Ala2,Leu5]e...

Phosphinyl- and Phosphinothioylamino Acids and Peptides. VI. The Protection of the Hydroxyl Function in the Tyrosine Side-chain by the Dimethylphosphinothioyl Group

Ueki, Masaaki,Inazu, Toshiyuki

, p. 204 - 207 (2007/10/02)

The use of the dimethylphosphinothioyl (...

64963-01-5 Process route

: H-L-Tyr(Mpt)-D-Ala-Gly-L-Phe-L-Leu-OH

: 60284-47-1,63631-40-3,64963-01-5,64963-05-9,64963-08-2,64975-66-2
D-Ala₂-Leu₅-enkephalin

Conditions

Conditions	Yield
With sodium hydroxide; In methanol; at 0 ℃;	94%

: 73965-71-6
N^α-(tert-butoxycarbonyl)-2,Leu⁵>enkephalin

: 60284-47-1,63631-40-3,64963-01-5,64963-05-9,64963-08-2,64975-66-2
D-Ala₂-Leu₅-enkephalin