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Manufacturer Sells Best Quality Pentapeptide-18 64963-01-5 with stock
- 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
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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
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H-L-Tyr(Mpt)-D-Ala-Gly-L-Phe-L-Leu-OH
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60284-47-1,63631-40-3,64963-01-5,64963-05-9,64963-08-2,64975-66-2
D-Ala2-Leu5-enkephalin
| Conditions | Yield |
|---|---|
|
With
sodium hydroxide;
In
methanol;
at 0 ℃;
|
94% |
-
-
73965-71-6
Nα-(tert-butoxycarbonyl)-
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-
60284-47-1,63631-40-3,64963-01-5,64963-05-9,64963-08-2,64975-66-2
D-Ala2-Leu5-enkephalin
| Conditions | Yield |
|---|---|
|
With
methoxybenzene; trifluoroacetic acid;
|
47% |
64963-01-5 Upstream products
-
131124-60-2
-
73965-71-6
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-
86827-18-1
N-benzyloxycarbonyl-O-benzyl-L-tyrosine
-
139143-40-1
{(R)-2-[(S)-2-Benzyloxycarbonylamino-3-(4-benzyloxy-phenyl)-propionylamino]-propionylamino}-acetic acid methyl ester
