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Journal articles on the topic 'Grandiflorenic acid'

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Published: 4 June 2021
Last updated: 13 February 2022

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1

Zhang, Hongbin, Graham Wynne та Lewis N. Mander. "Synthesis of ent-9σ,15σ-cyclokaurene from grandiflorenic acid". Arkivoc 2001, № 8 (2001): 40–58. http://dx.doi.org/10.3998/ark.5550190.0002.806.

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2

Vieira, Henriete S., Jacqueline A. Takahashi, Lúcia P. S. Pimenta, and Maria Amélia D. Boaventura. "Effects of Kaurane Diterpene Derivatives on Germination and Growth of Lactuca sativa Seedlings." Zeitschrift für Naturforschung C 60, no. 1-2 (2005): 72–78. http://dx.doi.org/10.1515/znc-2005-1-214.

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Kaurenoic and grandiflorenic acid, isolated from Wedelia paludosa (Asteraceae), some derivatives from these acids (alcohols, esters, amides, lactones, oximes) and other naturally occurring kaurane diterpenes were tested for their action on the growth of radical and shoot of Lactuca sativa. Gibberellic acid, GA3, a commercially available phytohormone, belonging to the same class of diterpenes, was also tested. Some of the tested substances showed a remarkable activity either in the inhibition or in stimulation of L. sativa growth. The activity, in some cases, was even higher than that of GA3.
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3

Ruan, Y., B. J. Ma, L. Z. Li та X. L. Wang. "Specific 12α-hydroxylation of grandiflorenic acid by permeabilised fungus Fusarium graminearum". Natural Product Research 28, № 9 (2014): 677–79. http://dx.doi.org/10.1080/14786419.2014.891113.

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4

Truong, Nguyet Thi Hong, Thu Thi Hoai Nguyen, Quang That Ton, and Phung Kim Phi Nguyen. "SOME COMPOUNDS FROM FLOWER OF WEDELIA TRILOBATA (L.) HITCH. (ASTERACEAE)." Science and Technology Development Journal 14, no. 2 (2011): 20–27. http://dx.doi.org/10.32508/stdj.v14i2.1939.

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Wedelia trilobata Hitch. has not much been chemically and biologically studied. From the flower of Wedelia trilobata, ten compounds were isolated: friedelan-3β-ol (or epifriedelanol) (1), erythrodiol (2), 28-hydroxy-3β -tetradecanoyloxyolean-12-ene (or 3β -tetradecanoyloxyerythrodiol) (3), 3β-henicosanoyloxyolean-12-en-28-oic acid (4), 3β-pentadecanoyloxyolean-28(13)-lactone (5), kaura-9(11),16-dien-18-oic acid (or grandiflorenic acid) (6), 2-(3-hydroxy-3,7,11,15- tetramethylhexadecyl)-3,5,6-trimethyl-1,4-dihydroxybenzene (or tocopherolhydroquinone) (7), gramisterol (8), stigmasterol (9) and b
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5

Bejar, Ezra. "Preliminary investigation of the estrogenic potential of grandiflorenic acid from Montanoa tomentosa." Journal of Ethnopharmacology 23, no. 2-3 (1988): 329–31. http://dx.doi.org/10.1016/0378-8741(88)90013-x.

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6

Nakano, T., M. A. Maillo, A. C. Spinelli, Alfonso Martin, and A. Usubillaga. "Molecular rearrangements in derivatives of grandiflorenic acid [(-)-kaur-9(11),16-dien-19-oic acid]." Pure and Applied Chemistry 66, no. 10-11 (1994): 2357–60. http://dx.doi.org/10.1351/pac199466102357.

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7

Enriquez, Raul G., Julie Barajas, Benjamin Ortiz, et al. "Comparison of crystal and solution structures and 1H and 13C chemical shifts for grandiflorenic acid, kaurenoic acid, and monoginoic acid." Canadian Journal of Chemistry 75, no. 3 (1997): 342–47. http://dx.doi.org/10.1139/v97-039.

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The crystal structure of monoginoic acid, 3, is determined and compared with previously reported structures of kauradienoic acid, 1, and kaurenoic acid, 2. 1H and 13C chemical shifts are assigned for all three diterpenes and solution and crystal structure conformations are confirmed with the aid of solution NOE measurements. The overall shapes of 2 and 3 are very similar while 1 is significantly dissimilar. These differences may be partially responsible for the reported greater in vitro uterotropic activity of 1, relative to 2 and 3. Keywords: monoginoic acid, kaurodienoic acid, kaurenoic acid
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8

ENRIQUEZ, R. G., J. BARAJAS, B. ORTIZ, et al. "ChemInform Abstract: Comparison of Crystal and Solution Structures and 1H and 13C Chemical Shifts for Grandiflorenic Acid, Kaurenoic Acid, and Monoginoic Acid." ChemInform 28, no. 41 (2010): no. http://dx.doi.org/10.1002/chin.199741229.

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9

NAKANO, T. "ChemInform Abstract: Molecular Rearrangements in the Derivatives of Grandiflorenic Acid [(-)-Kaura-9(11),16-diene-19-oic Acid] and Some Related Diterpenes." ChemInform 29, no. 43 (2010): no. http://dx.doi.org/10.1002/chin.199843310.

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10

Reynolds, W. F., A. J. Lough, J. F. Sawyer, R. G. Enriquez, B. Ortiz та F. Walls. "Structure of (4α)-kaura-9(11),16-dien-18-oic acid (grandiflorenic acid), an active ingredient of the Mexican medicinal plant zoapatle". Acta Crystallographica Section C Crystal Structure Communications 47, № 5 (1991): 973–77. http://dx.doi.org/10.1107/s0108270190008186.

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11

Bortoleti, Bruna Taciane da Silva, Manoela Daiele Gonçalves, Fernanda Tomiotto-Pellissier, et al. "Grandiflorenic acid promotes death of promastigotes via apoptosis-like mechanism and affects amastigotes by increasing total iron bound capacity." Phytomedicine 46 (July 2018): 11–20. http://dx.doi.org/10.1016/j.phymed.2018.06.010.

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12

REYNOLDS, W. F., A. J. LOUGH, J. F. SAWYER, R. G. ENRIQUEZ, B. ORTIZ та F. WALLS. "ChemInform Abstract: Structure of (4α)-Kaura-9(11),16-dien-18-oic Acid ( Grandiflorenic Acid) (I), an Active Ingredient of the Mexican Medicinal Plant Zoapatle." ChemInform 22, № 33 (2010): no. http://dx.doi.org/10.1002/chin.199133248.

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13

Cruz-Mondragón, Perla, M. Concepción Lozada, Benjamín Ortiz, Raúl G. Enríquez, and Manuel Soriano-García. "X-ray Crystal Structure of Grandiflorenic Acid [(−)-kaura-9(11)-16-dien-19-oic Acid] Methyl Ester, a Compound Formerly Considered as an Oily Derivative." Journal of Chemical Crystallography 39, no. 7 (2008): 474–77. http://dx.doi.org/10.1007/s10870-008-9507-7.

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14

Nakano, Tatsuhiko, Alfonso Martín та Alfredo Usubillaga. "Studies on Rearrangements in Derivatives of Grandiflorenic Acid, Part 2. Synthesis of Methyl (-)-20-Norkaur-9α-Methyl-5(10), 16-Dien-19-Oate, A New Tetracyclic Rosane-Type Diterpene". Journal of Natural Products 49, № 1 (1986): 62–66. http://dx.doi.org/10.1021/np50043a006.

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15

Batista, R., F. C. Braga, and A. B. Oliveira. "Quantitative determination by HPLC of ent-kaurenoic and grandiflorenic acids in aerial parts of Wedelia paludosa D.C." Revista Brasileira de Farmacognosia 15, no. 2 (2005): 119–25. http://dx.doi.org/10.1590/s0102-695x2005000200009.

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16

NAKANO, T., A. MARTIN, and A. USUBILLAGA. "ChemInform Abstract: Studies on Rearrangements in Derivatives of Grandiflorenic Acid." Chemischer Informationsdienst 17, no. 37 (1986). http://dx.doi.org/10.1002/chin.198637298.

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17

NAKANO, T., A. CASTALDI SPINELLI, A. MARTIN, A. USUBILLAGA, A. T. MCPHAIL, and K. D. ONAN. "ChemInform Abstract: Studies on Rearrangements in Derivatives of Grandiflorenic Acid. Part 1. Reaction of the Epoxides of Methyl (-)-Kaur-9(11)-en-19-oate and (-)-Kaur-9(11)-en-19-oic Acid with Boron Trifluoride-Diethyl Ether Either in the Absence or in t." Chemischer Informationsdienst 16, no. 48 (1985). http://dx.doi.org/10.1002/chin.198548311.

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18

Nakano, Tatsuhiko, Antonieta Castaldi Spinelli, Alfonso Martín, Alfredo Usubillaga, Andrew T. McPhail, and Kay D. Onan. "Studies on rearrangements in derivatives of grandiflorenic acid. Part 1. Reaction of the epoxides of methyl (–)-kaur-9(11)-en-19-oate and (–)-kaur-9(11)-en-19-oic acid with boron trifluoride-diethyl ether either in the absence or in the presence of N-nitrosomethylurea. Formation of two diterpenes of a new skeletal type." J. Chem. Soc., Perkin Trans. 1, 1985, 1693–97. http://dx.doi.org/10.1039/p19850001693.

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19

Duque Bautista, Horacio, Guilibaldo Gabriel Zurita Vásquez, Yesenia Pacheco Hernández, and Nemesio Villa Ruano. "Etiología de la mancha necrótica del Agave angustifolia: Una aproximación in vitro hacía su control biológico." Revista Mexicana de Fitopatología, Mexican Journal of Phytopathology 35, no. 2 (2017). http://dx.doi.org/10.18781/r.mex.fit.1701-2.

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<p>Presentamos la identificación molecular de una especie de Cladosporium aislada de las manchas necróticas de los tallos enfermos de Agave angustifolia, los cuales se colectaron en San Luis Amatlán Oaxaca, México. Los análisis de los espaciadores transcritos internos (ITS) del gen de RNA ribosomal 18S y de la secuencia parcial codificante (cDNA) de una proteína alergénica conservada de choque térmico 70 (HSP70), revelaron su similitud con Cladosporium herbarum (Pers.: Fr.) Link. La evaluación in vitro de los extractos etanólicos de las raíces Zaluzania montagnifolia y de sus principales
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