CAS 13588-94-8

Valylserine

Description:

Valylserine, with the CAS number 13588-94-8, is a dipeptide composed of the amino acids valine and serine. It is characterized by its structure, which includes a valine residue linked to a serine residue through a peptide bond. This compound is typically found in various biological systems and can play a role in protein synthesis and metabolism. Valylserine is known for its potential biological activities, including its involvement in cellular processes and signaling pathways. The presence of both hydrophobic (valine) and polar (serine) side chains contributes to its unique properties, influencing its solubility and interaction with other biomolecules. As a dipeptide, it may exhibit specific conformational characteristics that are important for its function in biological contexts. Valylserine is of interest in research related to peptide synthesis, drug design, and understanding the roles of amino acids in health and disease. However, detailed studies on its specific applications and effects are still ongoing in the scientific community.

Formula: C₈H₁₆N₂O₄

InChI: InChI=1S/C8H16N2O4/c1-4(2)6(9)7(12)10-5(3-11)8(13)14/h4-6,11H,3,9H2,1-2H3,(H,10,12)(H,13,14)/t5-,6-/m0/s1

InChI key: InChIKey=STTYIMSDIYISRG-WDSKDSINSA-N

SMILES: [C@@H](NC([C@H](C(C)C)N)=O)(C(O)=O)CO

Synonyms:

• (2S)-2-{[(2S)-2-ammonio-3-methylbutanoyl]amino}-3-hydroxypropanoate
• 22: PN: WO2014102101 SEQID: 322 claimed protein
• 22: PN: WO2014102104 SEQID: 121 claimed protein
• 50: PN: EP2161028 PAGE: 10 claimed protein
• 563: PN: EP2071334 SEQID: 602 claimed protein
• 563: PN: WO2009077864 SEQID: 602 claimed protein
• 92: PN: US20070066537 PAGE: 17 claimed protein
• <span class="text-smallcaps">L</smallcap>-Serine, <smallcap>L</span>-valyl-
• <span class="text-smallcaps">L</smallcap>-Serine, N-<smallcap>L</span>-valyl-
• <span class="text-smallcaps">L</smallcap>-Valyl-<smallcap>L</span>-serine
• H-Val-Ser-OH
• N-<span class="text-smallcaps">L</smallcap>-Valyl-<smallcap>L</span>-serine
• Nsc 339921
• Serine, N-<span class="text-smallcaps">L</smallcap>-valyl-, <smallcap>L</span>-
• Valylserine
• Serine, N-L-valyl-, L-
• L-Serine, L-valyl-
• L-Valyl-L-serine

H-Val-Ser-OH

CAS: 13588-94-8

Valylserine inhibited melanin synthesis in Mel-Ab cells through down-regulation of tyrosinase. The dipeptide forms nanotubes in the presence of trifluoroethanol.

Formula: C₈H₁₆N₂O₄

Purity: > 99%

Color and Shape: White Powder

Molecular weight: 204.23

Ref: 01-4002210

(S)-2-((S)-2-Amino-3-methylbutanamido)-3-hydroxypropanoic acid

CAS: 13588-94-8

Formula: C₈H₁₆N₂O₄

Color and Shape: Solid

Molecular weight: 204.2236

Ref: IN-DA0072AC

H-Val-Ser-OH

Controlled Product

CAS: 13588-94-8

Stability Hygroscopic
Applications H-VAL-SER-OH (cas# 13588-94-8) is a useful research chemical.

Formula: C₈H₁₆N₂O₄

Color and Shape: Neat

Molecular weight: 204.22

Ref: TR-V991708

H-Val-Ser-OH

CAS: 13588-94-8

L-Threonine is an amino acid that belongs to the branched-chain family of amino acids. It is a nonessential amino acid, meaning that it can be synthesized by the human body. L-Threonine is one of the two amino acids (along with L-Serine) that has a hydroxyl group on the alpha carbon atom. It is also used in certain metabolic pathways such as sphingolipid metabolism and tryptophan metabolism. L-Threonine is used in experimental models for bowel disease and intestinal cancer, but its role in these conditions has not been determined. The molecule can be found in both animal and plant proteins, but most often it occurs in animal sources. The compound can also be found as a component of skin condition treatments or as an additive to shampoos, lotions, and cosmetics.

Formula: C₈H₁₆N₂O₄

Purity: Min. 95%

Molecular weight: 204.22 g/mol

Ref: 3D-FV108233