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(1S,2S)-Bortezomib

Catalog No.GC62193

Le (1S,2S)-bortézomib est un énantiomère du bortézomib. Le bortézomib est un inhibiteur du protéasome perméable aux cellules, réversible et sélectif, et inhibe puissamment le protéasome 20S (Ki de 0,6 nM) en ciblant un résidu thréonine. Le bortézomib perturbe le cycle cellulaire, induit l'apoptose et inhibe le NF-κB. Le bortézomib est un agent anticancéreux et le premier inhibiteur thérapeutique du protéasome À être utilisé chez l'homme.

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(1S,2S)-Bortezomib Chemical Structure

Cas No.: 1132709-14-8

Taille Prix Stock Qté
1 mg
108,00 $US
En stock
5 mg
315,00 $US
En stock
10 mg
540,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

(1S,2S)-Bortezomib is an enantiomer of Bortezomib. Bortezomib is a cell-permeable, reversible, and selective proteasome inhibitor, and potently inhibits 20S proteasome (Ki of 0.6 nM) by targeting a threonine residue. Bortezomib disrupts the cell cycle, induces apoptosis, and inhibits NF-κB. Bortezomib is an anti-cancer agent and the first therapeutic proteasome inhibitor to be used in humans[1][2][3].

[1]. Kamalzadeh Z, et al. Determination of Bortezomib in API Samples Using HPLC: Assessment of Enantiomeric and Diastereomeric Impurities. J Chromatogr Sci. 2017 Aug 1;55(7):697-705.
[2]. Adams J, et al. Proteasome inhibitors: a novel class of potent and effective antitumor agents. Cancer Res. 1999 Jun 1;59(11):2615-22.
[3]. Shahshahan MA, et al. Potential usage of proteasome inhibitor bortezomib (Velcade, PS-341) in the treatment of metastaticmelanoma: basic and clinical aspects. Am J Cancer Res. 2011;1(7):913-24.

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