Stimulation of insulin secretion by 5-methylcoumarins and its sulfur analogues isolated from Clutia lanceolata Forssk

被引:10
作者
Ahmed, Sarfaraz [1 ]
Nur-e-Alam, Mohammad [1 ]
Parveen, Ifat [2 ]
Coles, Simon J. [3 ]
Hafizur, Rahman M. [4 ]
Hameed, Abdul [4 ,7 ]
Orton, James B. [3 ]
Threadgill, Michael D. [2 ,5 ]
Yousaf, Muhammad [1 ,6 ]
Alqahtani, Abdulaziz M. [1 ]
Al-Rehaily, Adnan J. [1 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmacognosy, POB 2457, Riyadh 11451, Saudi Arabia
[2] Aberystwyth Univ, IBERS, Aberystwyth SY23 3DA, Dyfed, Wales
[3] Univ Southampton, Sch Chem, UK Natl Crystallog Serv, Univ Rd, Southampton SO17 1BJ, Hants, England
[4] Univ Karachi, ICCBS, Dr Panjwani Ctr Mol Med & Drug Res, Karachi 75270, Pakistan
[5] Univ Bath, Dept Pharm & Pharmacol, Bath BA2 7AY, Avon, England
[6] Diteba Labs Inc, 1680 Tech Ave Unit 1, Mississauga, ON L4W 5S9, Canada
[7] COMSATS Univ Islamabad CUI, CADR, Abbottabad, Pakistan
基金
英国生物技术与生命科学研究理事会;
关键词
Clutia lanceolata Forssk; Peraceae; Coumarins; Methylthiocoumarins; Single X-ray crystallography; Murine islets; Insulin; MODIFIED LABDANE DITERPENOIDS; COUMARINS; DERIVATIVES; COMPONENTS; EXTRACTS; SKELETON; LEAVES; PLANTS;
D O I
10.1016/j.phytochem.2019.112213
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Clutia lanceolata Forssk. (C. lanceolata) is a medicinal plant native to sub-Saharan Africa and the Arabian Peninsula. Phytochemical investigation of the aerial parts of C. lanceolata yielded twenty-one coumarins including methylthio and methylsulfinyl-coumarins. Thirteen of these compounds are reported here for the first time, named as cluteolin A to M. The remaining eight compounds are known but have not been associated previously with C. lanceolata. The structures of the undescribed compounds were elucidated from their 2D NMR and MS spectra. Single crystal X-ray analyses confirmed the structures of eleven compounds. As, in Saudi Arabian tradition, C. lanceolata has been reported to have anti-diabetic and anti-fungal properties, the coumarins were examined for their biological activity. Seven compounds strongly enhanced the glucose-triggered release of insulin by murine pancreatic islets, with two compounds showing more than two-fold enhancement of insulin secretion, compared with the standard drug glimepiride.
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页数:9
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