CAS 20859-02-3

L-tert-Leucina

Descrizione:

L-tert-Leucina, con il numero CAS 20859-02-3, è un derivato di aminoacido caratterizzato dalla sua struttura a catena ramificata, che è un marchio distintivo della leucina e dei suoi derivati. È un composto non polare e idrofobico, rendendolo meno solubile in acqua rispetto ad aminoacidi più polari. L-tert-Leucina presenta un gruppo tert-butilico attaccato al carbonio alfa, che contribuisce alle sue uniche proprietà steriche e influenza le sue interazioni nei sistemi biologici. Questo composto è spesso utilizzato nella sintesi di peptidi e come mattoncino nella sviluppo di farmaci e biochimici. La sua chiralità, essendo la forma L, è significativa in contesti biologici, poiché può influenzare l'attività e la funzione di peptidi e proteine. Inoltre, L-tert-Leucina può partecipare a varie reazioni chimiche, tra cui acilazione e amidazione, rendendolo un reagente versatile nella sintesi organica. Nel complesso, le sue caratteristiche strutturali e proprietà rendono L-tert-Leucina un composto importante sia nelle applicazioni di ricerca che industriali.

Formula: C₆H₁₃NO₂

InChI: InChI=1/C6H13NO2/c1-6(2,3)4(7)5(8)9/h4H,7H2,1-3H3,(H,8,9)

InChI key: InChIKey=NPDBDJFLKKQMCM-SCSAIBSYSA-N

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

Sinonimi:

• (2S)-2-Amino-3,3-dimethylbutanoic acid
• (S)-2-Amino-3,3-dimethylbutanoic acid
• (S)-2-Amino-3,3-dimethylbutyric acid
• (S)-tert-Butylglycine
• (S)-tert-Leucine
• 2-Amino-3,3-Dimethyl-Butanoic Acid
• 3-Methyl-<span class="text-smallcaps">L</span>-valine
• 3-Methyl-l-valine
• 3-Methylvaline
• <span class="text-smallcaps">L</span>-2-Amino-3,3-dimethylbutyric acid
• <span class="text-smallcaps">L</span>-Pseudoleucine
• <span class="text-smallcaps">L</span>-Valine, 3-methyl-
• <span class="text-smallcaps">L</span>-tert-Butylglycine
• <span class="text-smallcaps">L</span>-tert-Leucine
• Butyric acid, 2-amino-3,3-dimethyl-, <span class="text-smallcaps">L</span>-
• D-t-Butylglycine
• H-Tle-OH
• L-tert-Leucine
• L-valine,3-methyl
• NSC 203785
• Nsc203785
• tert-<span class="text-smallcaps">L</span>-Leucine
• tert-Butyl-<span class="text-smallcaps">L</span>-glycine
• β-Methyl-<span class="text-smallcaps">L</span>-valine
• Butyric acid, 2-amino-3,3-dimethyl-, L-
• β-Methyl-L-valine
• L-LEUCINE
• LEU
• L-α-tert-Butylglycine
• L-2-AMINO-4-METHYLVALERIC ACID
• L-2-(T-BUTYL)GLYCINE
• (2S)-2-Amino-3,3-dimethylbutanoicacid
• L-2-AMINO-4-METHYLPENTANOIC ACID
• L-TERT-LEUCINE, 99% (99% EE/GLC)
• FEMA 3297
• L-A-AMINO-G-METHYL VALERIC ACID
• LEUCINE
• H-LEU-OH
• (S)-(+)-LEUCINE
• L-LEU
• H-L-LEU-OH
• (S)-2-AMINO-4-METHYLPENTANOIC ACID
• LEUCINE, L-
• RARECHEM AB PP 3754
• L-A-AMINOISOCAPROIC ACID

L-tert-Leucine

CAS: 20859-02-3

Formula: C₆H₁₃NO₂

Purezza: >98.0%(T)

Colore e forma: White to Almost white powder to crystal

Peso molecolare: 131.18

Ref: 3B-L0147

L-tert-Leucine, 99%

CAS: 20859-02-3

L-tert-Leucine is an essential amino acid and makes up one third of our muscle protein. It can be used as a food additive. It is used in the formation of sterols. It is used in the production of cobalt oxazoline palladacycles complex, which acts as a catalyst in the rearrangement of prochiral N-aryl

Formula: C₆H₁₃NO₂

Purezza: 99%

Colore e forma: White, Crystals or powder or crystalline powder

Peso molecolare: 131.18

Ref: 02-L13707

L-Valine, 3-methyl-

CAS: 20859-02-3

Formula: C₆H₁₃NO₂

Purezza: 97%

Colore e forma: Solid

Peso molecolare: 131.1729

Ref: IN-DA002JSN

L-tert-Leucine

CAS: 20859-02-3

Formula: C₆H₁₃NO₂

Peso molecolare: 131.18

Ref: 4Z-L-117020

3-Methyl-L-valine

CAS: 20859-02-3

3-Methyl-L-valine

Formula: C₆H₁₃NO₂

Purezza: 97%

Colore e forma: light beige powder

Peso molecolare: 131.17g/mol

Ref: 54-OR0572

L-tert-Leucine

CAS: 20859-02-3

Formula: C₆H₁₃NO₂

Peso molecolare: 131.18

Ref: 7W-GM4241

L-tert-Leucine

CAS: 20859-02-3

Formula: C₆H₁₃NO₂

Purezza: 98%

Colore e forma: Solid

Peso molecolare: 131.175

Ref: 10-F044734

L-tert-Leucine

CAS: 20859-02-3

L-tert-Leucine is a chiral compound that inhibits the activity of metalloproteases, enzymes that catalyze the breakdown of proteins. L-tert-Leucine has been shown to inhibit proteolytic activity in recombinant cells and bacterial strain such as Escherichia coli, Pseudomonas aeruginosa, and Bacillus subtilis. L-tert-Leucine binds to the active site of metalloproteases by competitive inhibition, inhibiting the breakdown of proteins. This compound also prevents degradation of dinucleotide phosphate and chiral synthesis. The enantiopure form of this compound is used as a substrate for kinetic studies with type strains of various metalloprotease enzymes.

Formula: C₆H₁₃NO₂

Purezza: (%) Min. 95%

Colore e forma: White Powder

Peso molecolare: 131.17 g/mol

Ref: 3D-FL12004

L-tert-Leucine

Prodotto controllato

CAS: 20859-02-3

Applications L-tert-Leucine acts as a catalyst for the enantioselective oxidative coupling and cyclization of benzophenathrenols to oxa[9]helicenes.
References Sako, M., et al.: J. Amer. Chem. Society., 138, 11481-11484 (2016)

Formula: C₆H₁₃NO₂

Colore e forma: Neat

Peso molecolare: 131.17

Ref: TR-L330135

L-tert-Leucine

CAS: 20859-02-3

Formula: C₆H₁₃NO₂

Peso molecolare: 131.18

Ref: ST-EA-CP-L28006