Relevant bibliographies by topics / Nordammarane

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Nordammarane'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

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Journal articles on the topic "Nordammarane"

1

Hu, Jiang, Hui Li, Ben-Shou Yang, Xia Mao, and Xiao-Dong Shi. "Nordammarane Triterpenoids fromSanguisorba officinalis." Helvetica Chimica Acta 98, no. 2 (2015): 273–78. http://dx.doi.org/10.1002/hlca.201400245.

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Hu, Jiang, Hui Li, Ben-Shou Yang, Xia Mao, and Xiao-Dong Shi. "ChemInform Abstract: Nordammarane Triterpenoids from Sanguisorba officinalis." ChemInform 46, no. 26 (2015): no. http://dx.doi.org/10.1002/chin.201526257.

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3

Esquivel, Baldomero, Francisco Guerrero, and R. A. Toscano. "Tri-Nordammarane Triterpenoids and Neoclerodane Diterpenoids From Salvia Aspera (Labiatae)." Natural Product Letters 16, no. 2 (2002): 129–35. http://dx.doi.org/10.1080/10575630290020046.

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4

Afiyatullov, Shamil Sh, Olesya I. Zhuravleva, Alexandr S. Antonov, et al. "New Metabolites from the Marine-Derived Fungus Aspergillus Fumigatus." Natural Product Communications 7, no. 4 (2012): 1934578X1200700. http://dx.doi.org/10.1177/1934578x1200700421.

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A new alkaloid, fumiquinazoline K (1), and a new nordammarane triterpenoid (2), together with three known diketopiperazines (3-5) and tryptoquivaline F (6) have been isolated from a marine strain of Aspergillus fumigatus KMM 4631 associated with the soft coral Sinularia sp. Their structures were determined by HR-MS and 1D and 2D NMR. Compounds 3-5 exhibit weak cytotoxicity against cytoplasm non-specific esterase in Ehrlich carcinoma cells. Compound 3 also induces early apoptosis of the same cells in a non-toxic range of concentrations.
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Zhang, Min, Wen-Liang Wang, Yu-Chun Fang, Tian-Jiao Zhu, Qian-Qun Gu, and Wei-Ming Zhu. "Cytotoxic Alkaloids and Antibiotic Nordammarane Triterpenoids from the Marine-Derived FungusAspergillus sydowi." Journal of Natural Products 71, no. 6 (2008): 985–89. http://dx.doi.org/10.1021/np700737g.

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Yang, Fei, Haiming Shi, Xiaowei Zhang, and Liangli (Lucy) Yu. "Two Novel Anti-Inflammatory 21-Nordammarane Saponins from Tetraploid Jiaogulan (Gynostemma pentaphyllum)." Journal of Agricultural and Food Chemistry 61, no. 51 (2013): 12646–52. http://dx.doi.org/10.1021/jf404726z.

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7

Zhang, Zhi-Bin, Si-Yao Du, Bo Ji, et al. "New Helvolic Acid Derivatives with Antibacterial Activities from Sarocladium oryzae DX-THL3, an Endophytic Fungus from Dongxiang Wild Rice (Oryza rufipogon Griff.)." Molecules 26, no. 7 (2021): 1828. http://dx.doi.org/10.3390/molecules26071828.

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Three new helvolic acid derivatives (named sarocladilactone A (1), sarocladilactone B (2) and sarocladic acid A (3a)), together with five known compounds (6,16-diacetoxy-25-hy- droxy-3,7-dioxy-29-nordammara-1,17(20)-dien-21-oic acid (3b), helvolic acid (4), helvolinic acid (5), 6-desacetoxy-helvolic acid (6) and 1,2-dihydrohelvolic acid (7)), were isolated from the endophytic fungus DX-THL3, obtained from the leaf of Dongxiang wild rice (Oryza rufipogon Griff.). The structures of the new compounds were elucidated via HR-MS, extensive 1D and 2D NMR analysis and comparison with reported data. Co
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Dissertations / Theses on the topic "Nordammarane"

1

Satiraphan, Malaï. "Etude phytochimique de deux Dipterocarpaceae de la forêt thaïlandaise : Hopea odorata Roxb. et Dipterocarpus costatus Gaertn.f." Thesis, Paris 5, 2012. http://www.theses.fr/2012PA05P623/document.

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Les extraits n-hexaniques respectivement des feuilles d’Hopea odorata Roxb. et du bois de Dipterocarpus costatus Gaertn.f. ont été sélectionnés sur la base d’un criblage biologique préliminaire. Ces extraits présentent des activités cytotoxiques significatives sur les lignées MCF-7 (cancer du sein) et NCI-H187 (cancer du poumon non à petite cellule). De plus, l’extrait du bois de D. costatus inhibe la croissance de la souche K1 de Plasmodium falciparum. L’étude phytochimique de l’extrait n-hexanique des feuilles d’Hopea odorata a permis d’isoler 19 composés terpéniques dont 16 triterpènes des
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