المؤلفون: Huan Wang, Han-Fei Liu, Xiao-Qiao Yang, Yu-Qiong Liao, Fen-Cong Pan, Jin-Yu Li, Hua-Yong Lou, Wei-Dong Pan

المصدر: Natural Products and Bioprospecting, Vol 15, Iss 1, Pp 1-10 (2025)

مصطلحات موضوعية: Teucrium quadrifarium, Lamiaceae, Neo-clerodane, Ferroptosis inhibitory activity, ROS, Botany, QK1-989

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2192-2195; https://doaj.org/toc/2192-2209

URL الوصول: https://doaj.org/article/5aa359279b3c4c75ab1135fbc7b06dd2

المؤلفون: Nancy Ortiz-Mendoza, Rubén San Miguel-Chávez, Martha Juana Martínez-Gordillo, Francisco Alberto Basurto-Peña, Mariana Palma-Tenango, Eva Aguirre-Hernández

المصدر: Metabolites; Volume 13; Issue 7; Pages: 866

مصطلحات موضوعية: Lamiaceae, terpenoids, flavonoids, neo-clerodane, variation secondary metabolism, antinociceptive effect

وصف الملف: application/pdf

Relation: Plant Metabolism; https://dx.doi.org/10.3390/metabo13070866

الاتاحة: https://doi.org/10.3390/metabo13070866

المؤلفون: Rubria Marlen Martínez-Casares, Liliana Hernández-Vázquez, Angelica Mandujano, Leonor Sánchez-Pérez, Salud Pérez-Gutiérrez, Julia Pérez-Ramos

المصدر: Molecules; Volume 28; Issue 12; Pages: 4744

مصطلحات موضوعية: clerodane, neo-clerodane, anti-inflammatory, cytotoxic activities

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Natural Products Chemistry; https://dx.doi.org/10.3390/molecules28124744

الاتاحة: https://doi.org/10.3390/molecules28124744

المؤلفون: Benedetta Fois, Angela Corona, Enzo Tramontano, Simona Distinto, Elias Maccioni, Rita Meleddu, Pierluigi Caboni, Costantino Floris, Filippo Cottiglia

المصدر: Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 749-757 (2021)

مصطلحات موضوعية: hiv, rnase h, reverse transcriptase, teucrium flavum, neo-clerodane diterpenes, flavonoids, Therapeutics. Pharmacology, RM1-950

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1475-6366; https://doaj.org/toc/1475-6374

URL الوصول: https://doaj.org/article/d6c2cdb23685453bad1bac9f008c7cb8

المؤلفون: Zahra Sadeghi (9303943), Jun-Li Yang (1656022), Alessandro Venditti (536550), Mahdi Moridi Farimani (739494)

مصطلحات موضوعية: Pharmacology, Biotechnology, Ecology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Teucrium genus, germander, neo-clerodane diterpenoids, ethnopharmacology

Relation: https://figshare.com/articles/journal_contribution/A_review_of_the_phytochemistry_ethnopharmacology_and_biological_activities_of_i_Teucrium_i_genus_Germander_/17913852

الاتاحة: https://doi.org/10.6084/m9.figshare.17913852.v1

المؤلفون: Raúl Argüello-García, Fernando Calzada, Bibiana Chávez-Munguía, Audifás-Salvador Matus-Meza, Elihú Bautista, Elizabeth Barbosa, Claudia Velazquez, Marta Elena Hernández-Caballero, Rosa Maria Ordoñez-Razo, José Antonio Velázquez-Domínguez

المصدر: Pharmaceuticals; Volume 15; Issue 7; Pages: 809

مصطلحات موضوعية: neo -clerodane diterpenes, Giardia intestinalis, ROS production, ultrastructural alterations, docking analysis, aldose reductase

وصف الملف: application/pdf

Relation: Medicinal Chemistry; https://dx.doi.org/10.3390/ph15070809

الاتاحة: https://doi.org/10.3390/ph15070809

المؤلفون: Aydogan, Fadime, Boga, Mehmet, Khan, Shabana I., Zulfiqar, Fazila, Khan, Ikhlas A., Ali, Zulfiqar

مصطلحات موضوعية: Lamiaceae, Teucrium Pruinosum, Chemotaxonomy, Neo -Clerodane, Abietane

Relation: Biochemical Systematics and Ecology; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://doi.org/10.1016/j.bse.2022.104545; https://hdl.handle.net/11468/15205; 105; WOS:000890305700007; 2-s2.0-85143064810; N/A; Q3

الاتاحة: https://hdl.handle.net/11468/15205
https://doi.org/10.1016/j.bse.2022.104545

المؤلفون: Dewu Zhang, Xiaoyu Tao, Guowei Gu, Yujia Wang, Wenxia Zhao, Wuli Zhao, Yan Ren, Shengjun Dai, Liyan Yu

المصدر: Frontiers in Microbiology, Vol 12 (2021)

مصطلحات موضوعية: neo-clerodane diterpene, scutebarbatine F, biotransformation, cytotoxicity, antiviral activity, Streptomyces, Microbiology, QR1-502

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fmicb.2021.662321/full; https://doaj.org/toc/1664-302X

URL الوصول: https://doaj.org/article/aa7d9981e205495cb311678046740f0f

المؤلفون: Hussien, Taha A., Mahmoud, Ahmed A., Mohamed, Naglaa S., Shahat, Abdelaaty A., El-Seedi, Hesham R., Hegazy, Mohamed-Elamir F.

المصدر: Molecules. 25(9)

مصطلحات موضوعية: Stachys aegyptiaca, lamiaceae, herbal tea, nutrients, neo-clerodane diterpene peroxides

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-183132
https://doi.org/10.3390/molecules25092172

المؤلفون: Benedetta Fois (4517815), Angela Corona (847390), Enzo Tramontano (847397), Simona Distinto (847393), Elias Maccioni (847395), Rita Meleddu (847391), Pierluigi Caboni (631877), Costantino Floris (1684231), Filippo Cottiglia (37116)

مصطلحات موضوعية: Biochemistry, Medicine, Neuroscience, Pharmacology, Developmental Biology, Cancer, Virology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, HIV, RNase H, reverse transcriptase, Teucrium flavum, neo-clerodane diterpenes, flavonoids

Relation: https://figshare.com/articles/journal_contribution/Flavonoids_and_Acid-Hydrolysis_derivatives_of_i_Neo_i_-Clerodane_diterpenes_from_i_Teucrium_flavum_i_subsp_i_glaucum_i_as_inhibitors_of_the_HIV-1_reverse_transcriptase_associated_RNase_H_function/14191281

الاتاحة: https://doi.org/10.6084/m9.figshare.14191281.v1

المؤلفون: Chen, Xiaoyue, Berim, Anna, Dayan, Franck E., Gang, David R.

المصدر: Journal of Experimental Botany, 2017 Jan 01. 68(5), 1109-1122.

URL الوصول: https://www.jstor.org/stable/26391546

المؤلفون: Ali, Zülfiqar, Aydoğan, Fadime, Zülfiqar, Fazila, Karaalp, Canan, Khan, Ikhlas A., Bedir, Erdal

مصطلحات موضوعية: divaricatum, Teucrium divaricatum subsp, Lamiaceae, neo-clerodane, Antimicrobial, iNOS, Neoclerodane Diterpenoids, Furanoid Diterpenes, Chamaedrys, Phytochemistry, Glucoside, C-12

Relation: Phytochemistry Letters; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11454/89616; https://doi.org/10.1016/j.phytol.2023.01.010; 54; 45; 49

الاتاحة: https://hdl.handle.net/11454/89616
https://doi.org/10.1016/j.phytol.2023.01.010

المؤلفون: Costantino Floris, Angela Corona, Elias Maccioni, Filippo Cottiglia, Simona Distinto, Enzo Tramontano, Pierluigi Caboni, Rita Meleddu, Benedetta Fois

المصدر: Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 749-757 (2021)

مصطلحات موضوعية: Stereochemistry, Human immunodeficiency virus (HIV), Ethyl acetate, hiv, Fractionation, RM1-950, medicine.disease_cause, rnase h, 01 natural sciences, chemistry.chemical_compound, Drug Discovery, reverse transcriptase, medicine, RNase H, neo-clerodane diterpenes, Pharmacology, biology, 010405 organic chemistry, General Medicine, Teucrium flavum, Reverse transcriptase, 0104 chemical sciences, 010404 medicinal & biomolecular chemistry, chemistry, flavonoids, biology.protein, Acid hydrolysis, teucrium flavum, Therapeutics. Pharmacology, Function (biology)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::606adb076bfc0dfd8ba48187d2e90cd3
https://doaj.org/article/d6c2cdb23685453bad1bac9f008c7cb8

المؤلفون: Jorge Cárdenas, José Antonio Morales-Serna, Bernardo Antonio Frontana-Uribe, Manuel Salmón, Miguel Ángel Jaime-Vasconcelos

المصدر: Molecules, Vol 16, Iss 11, Pp 9109-9115 (2011)

مصطلحات موضوعية: Salvia occidentalis, Labiatae, diterpene, neo-clerodane, NMR, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: http://www.mdpi.com/1420-3049/16/11/9109/; https://doaj.org/toc/1420-3049

URL الوصول: https://doaj.org/article/25ba1d86d0a84a46b21e4e6e4e24e9b6

المؤلفون: Castro, Amaya, Coll, Josep, Pant, Anil K, Pakrash, Om

مصطلحات موضوعية: neo-clerodane diterpenoids

Relation: Sí; Natural product communications 10 (6):857-860 (2015); http://hdl.handle.net/10261/219404

الاتاحة: http://hdl.handle.net/10261/219404

المؤلفون: Simona Piccolella, Antonio Fiorentino, Brigida D'Abrosca, Assunta Esposito, Monica Scognamiglio, Severina Pacifico

المساهمون: Piccolella, S., Scognamiglio, M., D'Abrosca, B., Esposito, A., Fiorentino, A., Pacifico, S.

المصدر: Biomolecules
Volume 11
Issue 5
Biomolecules, Vol 11, Iss 690, p 690 (2021)

مصطلحات موضوعية: Teucrium chamaedrys L. subsp. chamaedry, Magnetic Resonance Spectroscopy, Antioxidant, medicine.medical_treatment, antioxidant activity, Chemical Fractionation, HeLa Cell, 01 natural sciences, Biochemistry, Teucrium, chemistry.chemical_compound, Glycosides, Teucrium chamaedrys L. subsp. chamaedrys, chemistry.chemical_classification, neo-clerodanes, Traditional medicine, biology, NMR-based metabolomic, Hep G2 Cells, Phenylethanoid, QR1-502, Phytochemical, cytotoxicity, Chemical and Drug Induced Liver Injury, Plant Leave, Cosmeceutical, Human, Cell Survival, Hep G2 Cell, Metabolomic, Fractionation, Microbiology, Article, Diterpenes, Clerodane, Plant Extract, Nutraceutical, Phenols, medicine, Humans, Metabolomics, A549 Cell, Molecular Biology, Cell Proliferation, Phenol, Plant Extracts, 010405 organic chemistry, Glycoside, biology.organism_classification, phenylethanoid glycosides, 0104 chemical sciences, Plant Leaves, 010404 medicinal & biomolecular chemistry, chemistry, A549 Cells, NMR-based metabolomics, Neo-clerodane, HeLa Cells, Phenylethanoid glycoside

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c170263bbb5c85f175c7c62ed3a63aa2

المؤلفون: Miguel Ángel Jaime-vasconcelos, Bernardo Antonio Frontana-uribe, José Antonio Morales-serna, Manuel Salmón, Jorge Cárdenas

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://www.mdpi.com/1420-3049/16/11/9109/pdf/.

مصطلحات موضوعية: Salvia occidentalis, Labiatae, diterpene, neo-clerodane, NMR

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.395.6104; http://www.mdpi.com/1420-3049/16/11/9109/pdf/

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.395.6104
http://www.mdpi.com/1420-3049/16/11/9109/pdf/

المؤلفون: Dewu Zhang, Xiaoyu Tao, Guowei Gu, Yujia Wang, Wenxia Zhao, Wuli Zhao, Yan Ren, Shengjun Dai, Liyan Yu

مصطلحات موضوعية: Microbiology, Microbial Genetics, Microbial Ecology, Mycology, neo-clerodane diterpene, scutebarbatine F, biotransformation, cytotoxicity, antiviral activity, Streptomyces

Relation: https://figshare.com/articles/dataset/Data_Sheet_1_Microbial_Transformation_of_neo-Clerodane_Diterpenoid_Scutebarbatine_F_by_Streptomyces_sp_CPCC_205437_pdf/14412548

الاتاحة: https://doi.org/10.3389/fmicb.2021.662321.s001
https://figshare.com/articles/dataset/Data_Sheet_1_Microbial_Transformation_of_neo-Clerodane_Diterpenoid_Scutebarbatine_F_by_Streptomyces_sp_CPCC_205437_pdf/14412548

المؤلفون: Caballero, Cristina, López-Olguin, Jesús Francisco, Ruíz, Marisa A., Ortego, Félix, Castañera, Pedro

مصطلحات موضوعية: Esterases, Glutathione S-transferases, Limonoids, Neo-clerodane diterpenes, Nutritional indexes, Scutellaria, Trichilia

Relation: http://dx.doi.org/10.5424/sjar/200806S1-386; http://hdl.handle.net/10261/57631

الاتاحة: http://hdl.handle.net/10261/57631
https://doi.org/10.5424/sjar/200806S1-386

المؤلفون: Estefanía Butassi, Matías Funes, Susana Zacchino, María Victoria Rodriguez

المصدر: CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET

مصطلحات موضوعية: Stereochemistry, Dimer, Plant Science, Trichophyton rubrum, 01 natural sciences, Ciencias Biológicas, purl.org/becyt/ford/1 [https], chemistry.chemical_compound, Drug Discovery, medicine, purl.org/becyt/ford/1.6 [https], SYNERGISM, Pharmacology, biology, 010405 organic chemistry, Baccharis, NEO-CLERODANE DIMER, General Medicine, biology.organism_classification, 0104 chemical sciences, 010404 medicinal & biomolecular chemistry, Monomer, Complementary and alternative medicine, chemistry, NEO-CLERODANE MONOMER, TERBINAFINE, TRICHOPHYTON RUBRUM, Terbinafine, Micología, CIENCIAS NATURALES Y EXACTAS, medicine.drug

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5428ba1f2b6776fbd508ce021a7e2f6
https://journals.sagepub.com/doi/abs/10.1177/1934578X1901400101