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

(D-Ala2)-Leu-Enkephalin(Cas 64963-01-5) Usage

General Description

(D-Ala²)-Leu-Enkephalin is a synthetic peptide analog of the naturally occurring enkephalin, a type of endogenous opioid peptide that binds to opioid receptors in the brain. Enkephalins play a role in modulating pain and stress responses in the body. In this analog, the second amino acid in the sequence is modified, replacing glycine with D-alanine, which increases its stability against enzymatic degradation, prolonging its biological activity. Like natural enkephalins, (D-Ala²)-Leu-Enkephalin has potent analgesic effects by mimicking the action of endorphins, and it interacts primarily with delta-opioid receptors. Its structure includes five amino acids: D-alanine, tyrosine, glycine, phenylalanine, and leucine.

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

Shanghai Wibson Biotechnology Co., Ltd. is a high-tech enterprise that mainly develops and sells pharmaceutical and chemical raw materials and other related products. The company has advanced and perfect supporting system and has formed advanced chemical synthesis technology, which can quickly meet the personalized needs and series development from suitable testing to industrial production. Products are exported to Russia, Southeast Asia and other countries, in the world has a very high reputation and visibility. The company has strong financial strength and a good operating environment, can provide customers with high-quality, efficient and fast services.

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