CAS 87392-13-0

H-4,5-Dehydro-Leu-OH

Description:

H-4,5-Dehydro-Leu-OH, with the CAS number 87392-13-0, is a synthetic amino acid derivative that is primarily used in biochemical research and peptide synthesis. This compound is characterized by the presence of a dehydro group, which indicates that it has undergone a reduction reaction resulting in the loss of hydrogen atoms, specifically at the 4 and 5 positions of the leucine structure. This modification can influence the compound's properties, such as its stability, reactivity, and interaction with biological systems. H-4,5-Dehydro-Leu-OH is often utilized in the study of protein folding, structure-function relationships, and the design of peptide-based therapeutics. Its unique structural features may also affect its hydrophobicity and overall solubility in various solvents. As with many amino acid derivatives, it is important to handle this compound with care in laboratory settings, following appropriate safety protocols.

Formula: C₆H₁₁NO₂

Synonyms:

• 4,5-Dehydro-Leucine

H-4,5-Dehydro-Leu-OH

CAS: 87392-13-0

Precursor amino acid for tritium-labeled L-leucine. Specifically labeled bioactive peptides such as oxytocin can be conveniently synthesized by using this compound.

Formula: C₆H₁₁NO₂

Purity: > 98%

Color and Shape: White Powder

Molecular weight: 129.16

Ref: 01-4018955

4,5-Dehydro-leucine

CAS: 87392-13-0

Formula: C₆H₁₁NO₂

Purity: 95%

Molecular weight: 129.1570

Ref: IN-DA004GPS

(S)-2-Methallylglycine

CAS: 87392-13-0

(S)-2-Methallylglycine

Purity: 95%

Molecular weight: 129.16g/mol

Ref: 54-OR962307

H-4,5-DEHYDRO-LEU-OH

CAS: 87392-13-0

Formula: C₆H₁₁NO₂

Purity: ≥97%

Color and Shape: Solid

Molecular weight: 129.159

Ref: 10-F475448

4,5-Dehydro-L-leucine

CAS: 87392-13-0

4,5-Dehydro-L-leucine (DHL) is a chemical compound that can be found naturally in the body. It has been shown to have anticancer properties in vitro and can activate photorhabdus, which are bacteria that infect insects. DHL is also capable of inhibiting acetylation, the process by which proteins are modified with an acetyl group. The ability of DHL to inhibit acetylation may be due to its ability to bind with histone H3 and prevent the acetylation of lysine residues on this protein. DHL has also been shown to inhibit dna replication and induce apoptosis of cancer cells in vitro.

Formula: C₆H₁₁NO₂

Purity: Min. 95%

Molecular weight: 129.16 g/mol

Ref: 3D-FD48625