Bonducellpin D

上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。

Bonducellpin D  纯度: ≥98.0%

Bonducellpin D 是一种从 Caesalpinia minax 中分离出来呋喃二萜类内酯。 Bonducellpin D 表现出对 SARS-CoV MproMERS-CoV Mpro 的广谱抑制能力,Ki 值分别为 467.11 和 284.86 nM。Bonducellpin D 在体外表现出中等的抗癌活性。

Bonducellpin D

Bonducellpin D Chemical Structure

CAS No. : 197781-85-4

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生物活性

Bonducellpin D is a furanoditerpenoid lactone isolated from Caesalpinia minax. Bonducellpin D exhibits broad-spectrum inhibition potential against SARS-CoV Mpro and MERS-CoV Mpro, with an Ki of 467.11 and 284.86 nM, respectively. Bonducellpin D also exhibits moderate anti-cancer activity in vitro[1][2][3].

IC50 & Target

Ki: 467.11 nM (SARS-CoV Mpro), 284.86 nM (MERS-CoV Mpro)[1]

分子量

404.45

Formula

C22H28O7

CAS 号

197781-85-4

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献
  • [1]. Gurung AB, et, al. Unravelling lead antiviral phytochemicals for the inhibition of SARS-CoV-2 M pro enzyme through in silico approach. Life Sci. 2020 Aug 15;255:117831.

    [2]. Zheng Y, et, al. Caesalminaxins A-L, cassane diterpenoids from the seeds of Caesalpinia minax. J Nat Prod. 2013 Dec 27; 76(12): 2210-8.

    [3]. Jiang RW, et, al. Molecular structures and antiviral activities of naturally occurring and modified cassane furanoditerpenoids and friedelane triterpenoids from Caesalpinia minax. Bioorg Med Chem. 2002 Jul;10(7):2161-70.

SARS-CoV MPro-IN-2

天然产物醌类Quinones

SARS-CoV MPro-IN-2 

SARS-CoV MPro-IN-2 (compound 15) 是一种有效的 SARS-CoV-2 Mpro 抑制剂,IC50 sub> 值为 72.07 nM。病毒的主要蛋白酶 Mpro 作为加工病毒多蛋白的主要酶,有助于 SARS-CoV-2 在宿主细胞中的复制和转录,并已被定性为药物发现的有吸引力的靶点。SARS-CoV MPro-IN-2 具有研究 COVID-19 的潜力。

SARS-CoV MPro-IN-2

SARS-CoV MPro-IN-2 Chemical Structure

CAS No. : 81418-42-0

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生物活性

SARS-CoV MPro-IN-2 (compound 15) is a potent inhibitor of SARS-CoV-2 Mpro with an IC50 value of 72.07 nM. The main protease (Mpro) of the virus as the major enzyme processing viral polyproteins contributes to the replication and transcription of SARS-CoV-2 in host cells, and has been characterized as an attractive target in drug discovery. SARS-CoV MPro-IN-2 has the potential for the research of COVID-19[1].

分子量

230.22

Formula

C13H10O4

CAS 号

81418-42-0

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Cui J, et al. Discovery of juglone and its derivatives as potent SARS-CoV-2 main proteinase inhibitors. Eur J Med Chem. 2021;225:113789.