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来自[来源]的异波蒙酮的凋亡诱导活性鉴定与评价:一种新型、罕见的含赤霉酸二萜的双环-[3.2.1]辛酮。

Identification and Evaluation of Apoptosis-Inducing Activity of Ipomone from : A Novel, Unusual Bicyclo-[3.2.1] Octanone Containing Gibberic Acid Diterpenoid.

作者信息

Goel Bharat, Chatterjee Essha, Dey Biswajit, Tripathi Nancy, Bhardwaj Nivedita, Khattri Arun, Guru Santosh Kumar, Jain Shreyans K

机构信息

Department of Pharmaceutical Engineering and Technology, Indian Institute of Technology (Banaras Hindu University), Varanasi 221005, Uttar Pradesh, India.

Department of Biological Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad 500037, Telangana, India.

出版信息

ACS Omega. 2021 Mar 15;6(12):8253-8260. doi: 10.1021/acsomega.0c06304. eCollection 2021 Mar 30.

Abstract

Ipomone (), a novel diterpenoid along with seven known compounds (-), was isolated for the first time from the acidified hydroalcoholic extract of seeds. The structures of the isolated compounds were elucidated via comprehensive NMR spectroscopic data. The absolute configuration of was ascertained through NOESY, NMR, and ECD analyses. Compound was found to contain an unusual bicyclo-[3.2.1] octanone, which appeared first time in any natural product that might be an artifact resulting from the acid-catalyzed 1,2 alkyl shift/rearrangement. The novel compound was screened for cytotoxic activity against a panel of 12 human cancer cell lines and exhibited weak cytotoxicity with IC values in the range of 34-86 μM (except for HEK-293 cells). Microscopic studies revealed that compound induced apoptosis and autophagy in A549 cells. To further explore the signaling pathway involved, immunoblot analysis was performed that confirmed inhibition of apoptotic proteins PARP-1 and caspase-3 expression and upregulation of LC3B expression by compound . The compound was further subjected to molecular docking studies to evaluate its binding affinity with p110α, PARP-1, and caspase-3 proteins.

摘要

首次从种子的酸化水醇提取物中分离出了异波莫酮(),它是一种新型二萜类化合物,还有七种已知化合物(-)。通过全面的核磁共振光谱数据阐明了分离出的化合物的结构。通过NOESY、核磁共振和ECD分析确定了的绝对构型。发现化合物含有一种不寻常的双环-[3.2.1]辛酮,这是在任何天然产物中首次出现,可能是酸催化的1,2烷基迁移/重排产生的假象。对该新型化合物针对一组12种人类癌细胞系进行了细胞毒性活性筛选,其表现出较弱的细胞毒性,IC值在34 - 86 μM范围内(HEK - 293细胞除外)。显微镜研究表明化合物在A549细胞中诱导了凋亡和自噬。为了进一步探索所涉及的信号通路,进行了免疫印迹分析,证实化合物抑制了凋亡蛋白PARP - 1和caspase - 3的表达,并上调了LC3B的表达。该化合物还进行了分子对接研究,以评估其与p110α、PARP - 1和caspase - 3蛋白的结合亲和力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea9/8015099/089b0dc2b092/ao0c06304_0002.jpg

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