>>Signaling Pathways>> Ubiquitination/ Proteasome>> Proteasome>>(1S,2S)-Bortezomib

(1S,2S)-Bortezomib

Catalog No.GC62193

(1S,2S)-보르테조밉은 보르테조밉의 거울상 이성질체입니다. 보르테조밉은 세포 투과성, 가역성, 선택적 프로테아좀 억제제이며 트레오닌 잔기를 표적으로 하여 20S 프로테아좀(Ki 0.6nM)을 강력하게 억제합니다. Bortezomib은 세포주기를 방해하고 세포 사멸을 유도하며 NF-κB를 억제합니다. 보르테조밉은 항암제이자 인간에게 사용되는 최초의 치료적 프로테아좀 억제제이다.

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(1S,2S)-Bortezomib Chemical Structure

Cas No.: 1132709-14-8

Size 가격 재고 수량
1 mg
US$108.00
재고 있음
5 mg
US$315.00
재고 있음
10 mg
US$540.00
재고 있음

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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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