Literature DB >> 33850244

A neoclerodane orthoester and other new neoclerodane diterpenoids from Teucrium yemense chemistry and effect on secretion of insulin.

Mohammad Nur-E-Alam1, Ifat Parveen2, Barrie Wilkinson3, Sarfaraz Ahmed4, Rahman M Hafizur5, Ahmed Bari6, Timothy J Woodman7, Michael D Threadgill2,7, Adnan J Al-Rehaily4.   

Abstract

Teucrium yemense, a medicinal plant commonly grown in Saudi Arabia and Yemen, is traditionally used to treat infections, kidney diseases, rheumatism, and diabetes. Extraction of the dried aerial parts of the plant with methanol, followed by further extraction with butanol and chromatography, gave twenty novel neoclerodanes. Their structures, relative configurations and some conformations were determined by MS and 1-D and 2-D NMR techniques. Most were fairly conventional but one contained an unusual stable orthoester, one had its (C-16)-(C-13)-(C-14)-(C-15) (tetrahydro)furan unit present as a succinic anhydride and one had a rearranged carbon skeleton resulting from ring-contraction to give a central octahydroindene bicyclic core, rather than the usual decalin. Mechanisms are proposed for the biosynthetic formation of the orthoester and for the ring-contraction. Four novel neoclerodanes increased the glucose-triggered release of insulin from isolated murine pancreatic islets by more than the standard drug tolbutamide, showing that they are potential leads for the development of new anti-diabetic drugs.

Entities:  

Year:  2021        PMID: 33850244     DOI: 10.1038/s41598-021-87513-3

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


  16 in total

1.  Medicinal plant diversity in the flora of Saudi Arabia 1: a report on seven plant families.

Authors:  M Atiqur Rahman; Jaber S Mossa; Mansour S Al-Said; Mohammed A Al-Yahya
Journal:  Fitoterapia       Date:  2004-03       Impact factor: 2.882

Review 2.  Plant orthoesters.

Authors:  Shang-Gao Liao; Hua-Dong Chen; Jian-Min Yue
Journal:  Chem Rev       Date:  2009-03-11       Impact factor: 60.622

Review 3.  Chemical constituents and biological activities of the genus Linaria (Scrophulariaceae).

Authors:  Thamere Cheriet; Ines Mancini; Ramdane Seghiri; Fadila Benayache; Samir Benayache
Journal:  Nat Prod Res       Date:  2015-02-12       Impact factor: 2.861

4.  Neo-clerodane diterpenes from the hallucinogenic sage Salvia divinorum.

Authors:  Osamu Shirota; Kumi Nagamatsu; Setsuko Sekita
Journal:  J Nat Prod       Date:  2006-12       Impact factor: 4.050

Review 5.  A review of salvinorin analogs and their kappa-opioid receptor activity.

Authors:  Jeremy J Roach; Ryan A Shenvi
Journal:  Bioorg Med Chem Lett       Date:  2018-03-12       Impact factor: 2.823

6.  Acylated neo-clerodanes and 19-nor-neo-clerodanes from the aerial parts of Scutellaria coleifolia (Lamiaceae).

Authors:  Shin-Ichiro Kurimoto; Jian-Xin Pu; Han-Dong Sun; Yoshihisa Takaishi; Yoshiki Kashiwada
Journal:  Phytochemistry       Date:  2015-05-27       Impact factor: 4.072

7.  Neoclerodane Diterpenoids from Reehal Fatima, Teucrium yemense.

Authors:  Mohammad Nur-E-Alam; Muhammad Yousaf; Sarfaraz Ahmed; Ebtesam S Al-Sheddi; Ifat Parveen; David M Fazakerley; Ahmed Bari; Hazem A Ghabbour; Michael D Threadgill; Kezia C L Whatley; Karl F Hoffmann; Adnan J Al-Rehaily
Journal:  J Nat Prod       Date:  2017-06-05       Impact factor: 4.050

8.  Teucrium polium improves endothelial dysfunction by regulating eNOS and VCAM-1 genes expression and vasoreactivity in diabetic rat aorta.

Authors:  Sakineh Khodadadi; Narges Amel Zabihi; Saeed Niazmand; Abbasali Abbasnezhad; Maryam Mahmoudabady; Seyed Abdolrahim Rezaee
Journal:  Biomed Pharmacother       Date:  2018-05-07       Impact factor: 6.529

9.  Enantioselective Michael addition of water.

Authors:  Bi-Shuang Chen; Verena Resch; Linda G Otten; Ulf Hanefeld
Journal:  Chemistry       Date:  2014-12-21       Impact factor: 5.236

10.  Synthesis and κ-opioid receptor activity of furan-substituted salvinorin A analogues.

Authors:  Andrew P Riley; Chad E Groer; David Young; Amy W Ewald; Bronwyn M Kivell; Thomas E Prisinzano
Journal:  J Med Chem       Date:  2014-12-09       Impact factor: 7.446

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