CAS 13734-28-6

α-tert-butiloxicarbonil-L-lisina

Descripción:

α-tert-butiloxicarbonil-L-lisina, comúnmente conocido como Boc-L-lisina, es un derivado del aminoácido lisina, caracterizado por la presencia de un grupo protector de tert-butiloxicarbonilo (Boc). Este compuesto se utiliza típicamente en la síntesis de péptidos y en química orgánica como un grupo protector para el grupo amino de la lisina, lo que permite reacciones selectivas sin interferencia de la funcionalidad amino. Boc-L-lisina es un sólido cristalino blanco a blanco sucio que es soluble en disolventes orgánicos como el diclorometano y el dimetilsulfóxido, pero menos soluble en agua. Su estructura molecular incluye un esqueleto de lisina, que contribuye a sus propiedades básicas, y el grupo Boc, que mejora la estabilidad y reactividad bajo condiciones específicas. El compuesto es sensible a la humedad y debe almacenarse en un lugar fresco y seco para mantener su integridad. Además de su papel en la química sintética, Boc-L-lisina también se puede utilizar en el estudio de la estructura y función de proteínas debido a su incorporación en péptidos.

Fórmula: C₁₁H₂₂N₂O₄

InChI: InChI=1S/C11H22N2O4/c1-11(2,3)17-10(16)13-8(9(14)15)6-4-5-7-12/h8H,4-7,12H2,1-3H3,(H,13,16)(H,14,15)/t8-/m0/s1

Clave InChI: InChIKey=DQUHYEDEGRNAFO-QMMMGPOBSA-N

SMILES: [C@H](NC(OC(C)(C)C)=O)(CCCCN)C(O)=O

Sinónimos:

• (2S)-6-Amino-2-[[(tert-butoxy)carbonyl]amino]hexanoic acid
• (2S)-6-Azaniumyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoate
• (S)-6-Amino-2-(tert-butoxycarbonylamino)hexanoic acid
• <span class="text-smallcaps">L</span>-Lysine, N²-[(1,1-dimethylethoxy)carbonyl]-
• BOC-<span class="text-smallcaps">L</span>-Lys-OH
• Boc-L-lysine
• Boc-Lys-OH
• Lysine, N²-carboxy-, N²-tert-butyl ester, <span class="text-smallcaps">L</span>-
• N-Boc-L-Lysine
• N-tert-Butoxycarbonyllysine
• N-α-(tert-Butoxycarbonyl)-<span class="text-smallcaps">L</span>-lysine
• N_α-Boc-<span class="text-smallcaps">L</span>-lysine
• N²-[(1,1-Dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-lysine
• N²-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-lysine
• N^α-BOC-<span class="text-smallcaps">L</span>-lysine
• NSC 343721
• N~2~-(tert-butoxycarbonyl)lysine
• N~6~-(tert-butoxycarbonyl)-L-lysine
• α-N-Boc-lysine
• α-N-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-lysine
• α-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-lysine
• N2-tert-Butoxycarbonyl-L-lysine
• Lysine, N2-carboxy-, N2-tert-butyl ester, L-
• N2-[(1,1-Dimethylethoxy)carbonyl]-L-lysine

Nα-(tert-Butoxycarbonyl)-L-lysine

CAS: 13734-28-6

Fórmula: C₁₁H₂₂N₂O₄

Pureza: >98.0%(T)

Forma y color: White to Light yellow powder to lump

Peso molecular: 246.31

Ref: 3B-B1669

Nα-Boc-L-lysine, 97%

CAS: 13734-28-6

N-Boc-L-lysine is a protected analogue of a major amino acid participating in the binding of AcH to proteins. N-Boc-L-lysine as well as other t-butoxycarbonyl (Boc) amino acids can be converted to their respective amino acids via cleavage of the urethane bond. This Thermo Scientific Chemicals brand

Fórmula: C₁₁H₂₂N₂O₄

Pureza: 97%

Peso molecular: 246.31

Ref: 02-H63859

Boc-Lys-OH

CAS: 13734-28-6

Educt for the synthesis of Boc- and Fmoc-ε-azido-norleucine.

Fórmula: C₁₁H₂₂N₂O₄

Forma y color: White

Peso molecular: 246.31

Ref: 01-4000547

Boc-L-Lys-OH

CAS: 13734-28-6

Fórmula: C₁₁H₂₂N₂O₄

Pureza: 97%

Forma y color: Solid

Peso molecular: 246.3034

Ref: IN-DA0038XW

Boc-Lys-OH

CAS: 13734-28-6

Fórmula: C₁₁H₂₂N₂O₄

Pureza: ≥ 98.0%

Forma y color: White powder

Peso molecular: 246.30

Ref: 7W-GM9999

Boc-Lys-OH

CAS: 13734-28-6

Boc-Lys-OH

Fórmula: C₁₁H₂₂N₂O₄

Pureza: 98%

Forma y color: white solid

Peso molecular: 246.30g/mol

Ref: 54-OR36351

Boc-Lysine-OH

CAS: 13734-28-6

Fórmula: C₁₁H₂₂N₂O₄

Peso molecular: 246.31

Ref: 4Z-L-138033

N-Boc-L-lysine

Producto controlado

CAS: 13734-28-6

Fórmula: C₁₁H₂₂N₂O₄

Forma y color: White To Light Yellow

Peso molecular: 246.3

Ref: TR-B656900

N-Boc-L-Lysine

CAS: 13734-28-6

N-Boc-L-Lysine is a model of the amino acid lysine. This compound has been shown to inhibit the growth of cancer cells in vitro and in vivo. N-Boc-L-Lysine inhibits protein synthesis by blocking the formation of peptide bonds between amino acids, thus stopping the production of proteins vital for cell division. The inhibition of fatty acid synthesis by this compound may be due to its ability to inhibit the activity of fatty acid synthase, which catalyzes the conversion of acetyl coenzyme A into fatty acids. This product can also be synthesized from caproic acid and an ester hydrochloride or from a fatty acid and an ester hydrochloride.

Fórmula: C₁₁H₂₂N₂O₄

Pureza: Min. 95%

Forma y color: White Off-White Powder

Peso molecular: 246.3 g/mol

Ref: 3D-FB16295

Boc-Lys-OH

CAS: 13734-28-6

M03297 - Boc-Lys-OH

Fórmula: C₁₁H₂₂N₂O₄

Pureza: 95%

Forma y color: Solid

Peso molecular: 246.307

Ref: 10-M03297

N-Boc-L-lysine-d4

Producto controlado

CAS: 13734-28-6

Fórmula: C₁₁D₄H₁₈N₂O₄

Forma y color: Neat

Peso molecular: 250.328

Ref: TR-B656902