N-Boc-L-b-homoproline

CAS: 56502-01-3

Ref. 3D-FB11379

Información del producto

• Nombre: N-Boc-L-b-homoproline
• Sinónimos: (S)-2-(1-Boc-2-pyrrolidinyl)acetic acidBoc-b3-Homopro-OH, (2S)-1-[(1,1-Dimethylethoxy)carbonyl]-2-pyrrolidineacetic acid, (S)-1-(tert-Butoxycarbonyl)-2-pyrrolidineacetic acid, (S)-2-(Carboxymethyl)pyrrolidine-1-carboxylic acid tert-butyl ester, (S)-2-Carboxymethylpyrrolidine-1-carboxylic acid tert-butyl ester, (S)-2-[1-(tert-Butoxycarbonyl)pyrrolidin-2-yl]acetic acid, (S)-2-[1-(tert-Butoxycarbonyl)pyrrolidin-2-yl]ethanoic acid, (S)-[1-(tert-Butoxycarbonyl)pyrrolidin-2-yl]acetic acid, 2-Pyrrolidineacetic acid, 1-[(1,1-dimethylethoxy)carbonyl]-, (2S)-, 2-Pyrrolidineacetic acid, 1-[(1,1-dimethylethoxy)carbonyl]-, (S)-, 2-[(2S)-(1-tert-Butoxycarbonyl)pyrrolidin-2-yl]acetic acid, 2-[(2S)-1-[(2-Methylpropan-2-yl)oxycarbonyl]pyrrolidin-2-yl]acetic acid, 2-[(2S)-1-[(tert-Butoxy)carbonyl]pyrrolidin-2-yl]acetic acid, <span class="text-smallcaps">L</span>-Boc-β-homoproline, Boc-β-HoPro-OH, [(2S)-1-(tert-butoxycarbonyl)pyrrolidin-2-yl]acetic acid
• CAS: 56502-01-3

Descripción

N-Boc-L-b-homoproline is an analog of homoproline that has cytotoxic properties. It is a racemic mixture of two enantiomers, L-b-homoproline and D-b-homoproline. N-Boc-L-b-homoproline has been shown to inhibit the growth of colon cancer cells in vitro and has been used as a lead compound for the development of novel anticancer drugs. This chemical can be used in biological assays to study the effects of homoproline analogs on colon cancer cells. The cytotoxicity observed may be due to the inhibition of DNA synthesis or protein biosynthesis by N-Boc-L-b-homoproline, which prevents the production of new cells.

• Marca: Biosynth

Propiedades químicas

• Peso molecular: 229.27 g/mol
• Fórmula: C₁₁H₁₉NO₄
• Pureza: Min. 95%
• Color/Forma: White To Beige Solid
• InChI: InChI=1S/C11H19NO4/c1-11(2,3)16-10(15)12-6-4-5-8(12)7-9(13)14/h8H,4-7H2,1-3H3,(H,13,14)/t8-/m0/s1
• Clave InChI: InChIKey=GDWKIRLZWQQMIE-QMMMGPOBSA-N
• SMILES: CC(C)(C)OC(=O)N1CCC[C@H]1CC(=O)O