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Page 1
A novel brominated cuparene-derived sesquiterpene ether from the red alga Laurencia sp.
Su S, Sun WS, Wang B, Cheng W, Liang H, Zhao YY, Zhang QY, Wu J. Su S, et al. J Asian Nat Prod Res. 2010 Oct;12(10):916-20. doi: 10.1080/10286020.2010.506190. J Asian Nat Prod Res. 2010. PMID: 20924905
A novel brominated cuparene-derived sesquiterpene ether, 8,10-dibromo-3,7-epoxy-laur-13-ol (1), was isolated from Laurencia sp. collected in South China Sea. ...
A novel brominated cuparene-derived sesquiterpene ether, 8,10-dibromo-3,7-epoxy-laur-13-ol (1), was isolated from Laurencia sp. colle …
Antimicrobial cuparene-type sesquiterpenes, enokipodins C and D, from a mycelial culture of Flammulina velutipes.
Ishikawa NK, Fukushi Y, Yamaji K, Tahara S, Takahashi K. Ishikawa NK, et al. J Nat Prod. 2001 Jul;64(7):932-4. doi: 10.1021/np000593r. J Nat Prod. 2001. PMID: 11473426
Two new cuparene-type sesquiterpenes, enokipodins C (1) and D (2), were isolated from culture medium of an edible mushroom, Flammulina velutipes, along with enokipodins A (3) and B (4). ...
Two new cuparene-type sesquiterpenes, enokipodins C (1) and D (2), were isolated from culture medium of an edible mushroom, Flammulin …
Highly oxidized cuparene-type sesquiterpenes from a mycelial culture of Flammulina velutipes.
Ishikawa NK, Yamaji K, Tahara S, Fukushi Y, Takahashi K. Ishikawa NK, et al. Phytochemistry. 2000 Aug;54(8):777-82. doi: 10.1016/s0031-9422(00)00189-8. Phytochemistry. 2000. PMID: 11014265
Cuparene-type sesquiterpenes were isolated from a culture broth of Flammulina velutipes (Curt....
Cuparene-type sesquiterpenes were isolated from a culture broth of Flammulina velutipes (Curt....
Asymmetric intramolecular carbolithiation of achiral substrates: synthesis of enantioenriched (R)-(+)-cuparene and (R)-(+)-herbertene.
Luderer MR, Mealy MJ, Bailey WF. Luderer MR, et al. J Org Chem. 2014 Nov 7;79(21):10722-6. doi: 10.1021/jo502139m. Epub 2014 Oct 23. J Org Chem. 2014. PMID: 25303318
Concise syntheses of the sesquiterpenes (R)-(+)-cuparene and (R)-(+)-herbertene by asymmetric cyclization of achiral olefinic alkyllithium precursors in the presence of (-)-sparteine are reported. ...
Concise syntheses of the sesquiterpenes (R)-(+)-cuparene and (R)-(+)-herbertene by asymmetric cyclization of achiral olefinic alkylli …
Photomediated asymmetric synthesis of (-)-cuparene.
Grainger RS, Patel A. Grainger RS, et al. Chem Commun (Camb). 2003 May 7;(9):1072-3. Chem Commun (Camb). 2003. PMID: 12772908
Generation of a benzylic quaternary stereocentre via the photomediated cyclisation of a chiral alpha-(aminobutyl)styrene followed by a microwave-assisted Cope elimination has led to a total synthesis of the sesquiterpene (-)-cuparene....
Generation of a benzylic quaternary stereocentre via the photomediated cyclisation of a chiral alpha-(aminobutyl)styrene followed by a micro …
Use of aromatic radical-anions in the absence of THF. Tandem formation and cyclization of benzyllithiums derived from the attack of homo- and bishomoallyllithiums on alpha-methylstyrenes: two-pot synthesis of cuparene.
Cohen T, Kreethadumrongdat T, Liu X, Kulkarni V. Cohen T, et al. J Am Chem Soc. 2001 Apr 18;123(15):3478-83. doi: 10.1021/ja004353+. J Am Chem Soc. 2001. PMID: 11472119
A two-pot synthesis, the most efficient reported, of the sesquiterpene (+/-)-cuparene in 46% yield, using this technology is reported....
A two-pot synthesis, the most efficient reported, of the sesquiterpene (+/-)-cuparene in 46% yield, using this technology is reported …
Antifungal and Antimicroalgal Trichothecene Sesquiterpenes from the Marine Algicolous Fungus Trichoderma brevicompactum A-DL-9-2.
Shi ZZ, Liu XH, Li XN, Ji NY. Shi ZZ, et al. J Agric Food Chem. 2020 Dec 30;68(52):15440-15448. doi: 10.1021/acs.jafc.0c05586. Epub 2020 Dec 17. J Agric Food Chem. 2020. PMID: 33332117
Eight new trichothecene derivatives, trichodermarins G-N (1-8), and two new cuparene derivatives, trichocuparins A (9) and B (10), as well as six known trichothecenes (11-16) were isolated from the fungal strain Trichoderma brevicompactum A-DL-9-2 obtained from the inner t …
Eight new trichothecene derivatives, trichodermarins G-N (1-8), and two new cuparene derivatives, trichocuparins A (9) and B (10), as …
Predicting functions of putative fungal sesquiterpene synthase genes based on multiomics data analysis.
Nosenko T, Zimmer I, Ghirardo A, Köllner TG, Weber B, Polle A, Rosenkranz M, Schnitzler JP. Nosenko T, et al. Fungal Genet Biol. 2023 Mar;165:103779. doi: 10.1016/j.fgb.2023.103779. Epub 2023 Jan 24. Fungal Genet Biol. 2023. PMID: 36706978
We show that the STSs encoded by the L.bicolor mycorrhiza-induced genes emit either nerolidol or alpha-cuprenene and alpha-cuparene, and discuss the possible roles of these STs in the mycorrhiza formation....
We show that the STSs encoded by the L.bicolor mycorrhiza-induced genes emit either nerolidol or alpha-cuprenene and alpha-cuparene, …
Hitoyol A and B, Two Norsesquiterpenoids from the Basidiomycete Coprinopsis cinerea.
Otaka J, Hashizume D, Masumoto Y, Muranaka A, Uchiyama M, Koshino H, Futamura Y, Osada H. Otaka J, et al. Org Lett. 2017 Aug 4;19(15):4030-4033. doi: 10.1021/acs.orglett.7b01784. Epub 2017 Jul 20. Org Lett. 2017. PMID: 28726419
Compound 1 is possibly biosynthesized through decarboxylation-induced cyclization of lagopodin B, a known cuparene-type sesquiterpenoid. Compound 2 showed weak antimalarial activity with an IC(50) of 59 muM....
Compound 1 is possibly biosynthesized through decarboxylation-induced cyclization of lagopodin B, a known cuparene-type sesquiterpeno …
35 results