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Three undescribed dimeric ferulates from the culture broth of Phellinus linteus and their dengue virus type-2 inhibition activity Phytochem. Lett. (IF 1.7) Pub Date : 2024-03-09 Young-Hee Kim, Dae-Cheol Choi, Dae-Won Ki, Won-Gi Seo, Jae-Hyoung Song, Hyun-Jeong Ko, In-Kyoung Lee, Bong-Sik Yun
Several members of the genus have been used as traditional medicine for treating various diseases. They produce unique yellow pigments composed of a styrylpyrone class of compounds. Styrylpyrones exhibit various biological activities. The styryl group is derived from phenylalanine via cinnamic acid, -coumaric acid, and caffeoyl-CoA pathways, whereas the pyrone ring is derived from acetate. In a feeding
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Two undescribed compounds from Silybum marianum and their cytotoxicity activities Phytochem. Lett. (IF 1.7) Pub Date : 2024-03-08 Jing Wang, Juan Pan, Xin Meng, Zhi-Chao Hao, Jia-Tong Wu, Wei Guan, Hai-Xue Kuang, Qing-Shan Chen, Li-Li Zhang, Yan Liu, Bing-You Yang
A new amide dimer (), a new labdane-type diterpene (), and 18 known compounds were isolated from the seeds of (L.) Gaertn. The structures of the new compounds were elucidated by extensive spectroscopic data analyses and comparison with previously reported spectral date. The absolute configurations of compound was established by analysis of the electronic circular dichroism (ECD) data. In vitro bioassays
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A spectrofluorimetric approach for the quantification of naringin in biological fluids: Method development, validation and pharmacokinetic applications Phytochem. Lett. (IF 1.7) Pub Date : 2024-03-07 Sonal Pande, Chirag Patel, Jayesh Beladiya, Mukesh Kher, Sandip Dholakia
Naringin (NAR), a 4′,5,7-trihydroxyflavanone-7-rhamnoglucoside, is a prominent flavanone glycoside that has demonstrated promising therapeutic potential in both preclinical studies and clinical trials. However, its limited bioavailability has hindered its clinical translation as a medicine. To advance its therapeutic application and gain insights into its pharmacokinetic behavior in the body, it is
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Two new sesquiterpene lactones from the branches and leaves of Cinnamomum camphora chvar. Borneol Phytochem. Lett. (IF 1.7) Pub Date : 2024-03-07 Zhiyong Xu, Tao Jiang, Wei Xiong, Chuanqi Xie, Yunfei Liu, Xiaodan Han, Xuefang Wen, Jianping Fu, Junwei Xu, Yongsheng Guo, Lei Wu
In this study, two new sesquiterpene lactones, including one eudesmane-type borneolactone B (1), and one germacrane-type borneolactone C (2), and one known analog (3), were isolated from the ethyl acetate extract of the branches and leaves of chvar. Borneol. The planar structures and absolute configurations of compounds 1 and 2 were elucidated through comprehensive spectroscopic analysis, including
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Chemical constituents of Rubia yunnanensis and their cytotoxicity and anti-inflammatory activities Phytochem. Lett. (IF 1.7) Pub Date : 2024-03-05 Yi-Xue Zhang, Qiong Jin, Qi-Xiu Zhou, Ye Jin, Zhu-Ya Yang, Wen-Hong Tan, Yi-Fen Wang, Lu Liu
Two undescribed compounds, rubianthraquinone-3---glucopyranoside () and 28-hydroxyrubiyunnanol A (), along with thirteen known analogues (–), were isolated from the roots of . Structural carried out was elucidated on the basis of extensive 1D and 2D NMR spectroscopic data analyses and by comparison with the data described in the literature. The biological potential of all isolates was carried out through
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Two unprecedented neuroprotective 2-(2-phenylethyl)chromone derivatives from cultivated “Qi-Nan” agarwood of Aquilaria sinensis Phytochem. Lett. (IF 1.7) Pub Date : 2024-03-05 Lin Zhang, Hao Wang, Wen-Hua Dong, Jun Zeng, Li Yang, Wei Li, Hui-Qin Chen, Jing-Zhe Yuan, Cai-Hong Cai, Zhen-Yu Li, Wen-Li Mei, Hao-Fu Dai
Two unprecedented 2-(2-phenylethyl)chromone derivatives, ()-2-[2-hydroxy-2-(3-hydroxy-4-methoxyphenyl)ethyl]chromone () and ()-1-hydroxy-5-(4-hydroxyphenyl)-1-phenylpentane-3-one (), with one known compound were isolated from cultivated “Qi-Nan” agarwood of . Their structures were elucidated by analysis of 1D and 2D NMR as well as HRESIMS. TDDFT-ECD calculation was used to determine the absolute configuration
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Diverse sesquiterpenoid monomers from the leaves of Sarcandra glabra Phytochem. Lett. (IF 1.7) Pub Date : 2024-03-02 Zhenyu Zan, An Huang, Siyuan Wang, Xiaoli Wang, Mengmeng Yu, Danyang Zhang, Houli Jiang, Nan Wang, Jun Luo, Yi Li
The sarglalactones P and Q ( and ), two new lindenane sesquiterpenoid monomers, along with ten known sesquiterpenoid monomers and their derivatives (), were isolated from leaves. The structures, including the absolute configurations of and , were elucidated using comprehensive spectroscopic analyses, HRMS, ECD, and single-crystal X-ray diffraction. Compared with the reported lindenane sesquiterpenoid
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Cytotoxicities of cucurbitacins from the stem bark of Aquilaria sinensis Phytochem. Lett. (IF 1.7) Pub Date : 2024-03-02 Xiao-Yu Chen, Jun Yang, Xing-Zhi Yang, Ji-Feng Luo, Xiao-Yan Duan, Dong-Bao Hu, Yue-Hu Wang
One previously undescribed cucurbitacin, 11-hydrocucurbitacin B (), and five known analogs, 3-epicucurbitacin Q1 (), cucurbitacin Q1 (), cucurbitacin D (), isocucurbitacin D (), and hemslecin A (), were isolated from the stem bark of (Thymelaeaceae). The chemical structure of 11-hydrocucurbitacin B was elucidated by MS and NMR analysis and ECD calculations. All the isolates were evaluated for their
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Synthesis, antifungal activity, 3D-QSAR, and molecular docking study of novel anethole-derived hydroxamate compounds Phytochem. Lett. (IF 1.7) Pub Date : 2024-03-01 Yucheng Cui, Rong Li, Wengui Duan, Bo Cen, Guishan Lin, Kaiyue Wu
In an attempt to search for natural product-derived antifungal agents, a series of novel anethole-derived hydroxamate compounds were designed and synthesized. Their chemical structures were characterized by H NMR, C NMR, FT-IR, ESI-MS, and element analysis. It was found from the antifungal activity bioassay that some of the target compounds showed better antifungal activity than that of the commercial
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A pair of new enantiomeric alkaloids from Tinospora sinensis Phytochem. Lett. (IF 1.7) Pub Date : 2024-03-01 Yan Liang, Shaobo Guo, Yonghua Guo, Chang Xu, Guiyang Wang, Wei Zhang, Bin Liu
A pair of new enantiomeric alkaloids (+)- and (–)-, along with eight known compounds () were isolated from the stem of (Lour.) Merr. Their structures were elucidated on the basis of comprehensive analysis of HRESIMS and NMR spectroscopic data as well as CD spectroscopy methods. In addition, the isolated compounds were evaluated for their anti-inflammatory activity. Compounds (+)- and (–)- inhibited
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PRD: An integrated database solution for medicinal and aromatic plant research in pharmaceuticals and toxicology Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-28 Onur Kenan ULUTAŞ, Tuğba GÜNBATAN
Research in medicinal and aromatic science laboratories often involves isolation, identification, and characterization of bioactive compounds from natural sources, particularly those with potential applications in medicine and healthcare. A wide range of analytical techniques, including chromatography, spectroscopy, – bioassays, and also toxicity tests to investigate the chemical and biological properties
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Tyrosinase inhibitors isolated from Iris bungei collected in Mongolia Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-26 Gyeong Han Jeong, Tae Hoon Kim
(Iridaceae) collected in Mongolia was subjected to bioassay-directed isolation using a tyrosinase inhibition assay. A dimeric stilbene (), two phenylpropanoid glycosides (, ), and a flavone glycoside (), along with fifteen known secondary metabolites (, ) were isolated from the methanolic extract of the whole plant. The structures of the new metabolites were elucidated by 1D and 2D NMR spectroscopic
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Isolation and identification of an undescribed isocoumarin derivative from endophytic fungus Thermothielavioides terrestris YB4 Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-16 Xinyuan Pan, Jinrui Ma, Zhuoyi Wang, Xiachang Wang, Zheng Ma, Junwei Sun, Yongyong Zhang
An undescribed isocoumarin derivative, named (±)-isothielavic acid (), was isolated from the metabolites of endophytic fungus YB4 together with two known compounds 4()-thielavic acid () and thymine (). The structure of (±)-isothielavic acid () was elucidated by comprehensive analysis of NMR spectroscopy and HRESIMS data as well as single-crystal X-ray diffraction experiment. Bioassay results indicated
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Isolation and biological activities of chemical constituents from Aspergillus niger Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-14 Jing Yi, Yu Zhang, Xuan Wang, Chao Wang, Chengpeng Sun, Jun Wu, Yuhzuo Wu
Fungi, a renewable natural product resource trove, have garnered increasing attention recently. ( niger) Ma001, a subspecies isolated from the human gut, exhibited moderate inhibition of carbapenem-resistant (CRAB). However, research on its active ingredients remains insufficient. Therefore, chemical investigations of Ma001 resulted in the isolation and identification of 19 natural products. Among
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Sesquiterpenes from Inula macrophylla and their anti-neuroinflammatory activity Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-09 Rui Ma, Bakhrom Komilov, Cheng-Bo Wang, Komila Alibekovna Eshbakova, Jun-Li Yang, Wei Ha, Yan-Ping Shi
A new sesquiterpene lactone dimer () and a new eremophilane sesquiterpene () together with nine known sesquiterpenes have been characterized from . The structure of macrophyllidimer D () and macrophallic acid F () were established by comprehensive analysis of spectroscopic data. The absolute configurations were determined by single-crystal X-ray diffraction analysis and calculated electronic circular
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Syntheses of (S)- and (R)-dihydromethysticin from two yeast-reduction products, which can be prepared from one racemic compound Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-09 Kento Tamada, Hisashi Nishiwaki, Satoshi Yamauchi
Biologically active ()-Dihydromethysticin (()-) with high enantiomeric purity (>99%ee) was synthesized from the optically active yeast-reduction product, (1 ,2 )-methyl 2-hydroxycyclohexyl acetate (), through the introduction of the 3,4-methylenedioxybenzyl group, Beayer-Villiger oxidation, and conversion to its enolate. Moreover, ()-Dihydromethysticin (()-) with high enantiomeric purity (>99%ee) was
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Novel quantitative method for sapogenins in yucca extracts by gas chromatography tandem mass spectrometry Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-09 Andreas Lehner, Zimu Wei, Adam Bush, Mike Rincker, John Buchweitz
The p-anisaldehyde reaction with yucca extract saponins has long been utilized for semi-quantitating saponins or sapogenins by reaction product UV–visible spectroscopy, likely by reaction with compound ketal functions. The methodology was easily implemented and enabled direct comparison with a new detection method generated from gas chromatography-tandem mass spectrometric (GC/MS/MS) analysis of yucca
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Styryllactones in the leaves of Goniothalamus lanceolatus Miq., molecular networking and their anti-dengue activity In vitro and In silico Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-09 Nor Nadirah Abdullah, Adlin Afzan, Nur Hana Jelas, Mohd Ridzuan Mohd Abd Razak, Nurulfazlina Edayah Rasol, Syahrul Imran Abu Bakar, Nur Vicky Bihud, Lam Kok Wai, Murizal Zainol, Fasihuddin Badruddin Ahmad, Geoffrey A. Cordell, Nor Hadiani Ismail
Due to dengue fever's swift global expansion and the lack of effective antiviral remedies, it is crucial to discover and develop new antiviral drugs. The study aimed to assess the antiviral potential of the extract and fractions from the leaves of Miq. (Annonaceae). New Guinea C strain DENV-2, at a multiplicity of infection of 0.4, was used to infect Vero cells. The assessment of antiviral effectiveness
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Coumarin hybrids for targeted therapies: A promising approach for potential drug candidates Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-08 Nameer Mazin Zeki, Yasser Fakri Mustafa
Phyto-coumarins demonstrate diverse biological actions, encompassing antiradical, anti-inflammatory, oncolytic, monoamine oxidase B (MAOB) suppression, and antibacterial properties. Researchers commonly employ these molecules to evolve innovative, fully or partially laboratory-made, medicinal products stemming from coumarin. Many of these medicines are crossbreed chemical compounds that have been strategically
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Anti-hyperlipidemia and anti-diabetic diarylheptanoids from the leaves of Aquilaria sinensis Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-07 Hong-Fang Cai, Kai-Wen Kang, Xu Gong, Xin-Yi Wu, Dong-Li Li, Jing-Wei Jin, Ri-Hui Wu, Li-She Gan
Nineteen compounds, including one new diarylheptanoid, (3 )− 1-(4-hydroxyphenyl)− 7-(4-methoxy-3-hydroxyphenyl)− 3-methoxyheptane () and one diarylheptanoid firstly found from nature, ()− 4-(3-hydroxy-7-(4-methoxyphenyl)heptyl)phenol (), together with four nor-sesquiterpenoids (-), five triterpenoids (-), five flavonoids (-), one benzophenone glycoside (), and two lignans (-), were isolated from 95%
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Two new phenolic glucosides from Curculigo orchioides and their cytotoxic effects Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-07 Nguyen Quoc Vuong, Nguyen Hoang Nam, Nguyen Thi Hue, Le Nguyen Thanh, Pham Van Cuong, Vu Mai Thao, Nguyen Thi Minh Hang, Vu Kim Thu, Nguyen Xuan Nhiem
Two new phenolic glucosides, curculigoside J () and K (), and seven known compounds, curculigoside B (), curculigoside (), curculigoside C (), orchioside B (), 3''-dehydroxynyasicoside (), curculigine J (), and curculigine B () were isolated from a methanolic extract of the roots of . The structures of these compounds were elucidated using spectroscopic methods and comparison of their NMR data with
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Synthesis and antifungal activity of 2,4-diacetylphloroglucinol analogues Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-06 Xi-Long Guo, Chun-Yan Zhao, Cui-Ping Zhang, Yi Zhu, Qing-Rong Wu, Yuan-Qing Zhou, Ya-Hong Fei, Fang Ge, Wei Shi
In this letter, we reported synthesis of 2,4-Diacetylphloroglucinol (DAPG) derivatives as a new class of anti fungal agents. A series of DAPG ester analogues with diverse length of acyl substitution on aromatic hydroxyls were synthesized and characterized by H, C NMR and ESI-MS. Their antifungal activities were evaluated against six important plant fungal pathogens using mycelial growth inhibitory
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New diketopiperazine alkaloids from the Haima cold seep-derived fungus Toxicocladosporium sp. CYH-18 Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-06 Yi-Hao Che, Jun-Feng Wang, Wen-Ping Ding, Zhi-Hui Xiao, Xue-Feng Shi, Jia-Min Wu, Fa-Zuo Wang, Si Zhang
The novel diketopiperazine alkaloid toxicocladine A (), two new natural products cyclo(L-Phe-ΔAla) () and cyclo(L-Tyr-ΔAla) (), and three known compounds protocatechuic acid (), protocatechuic acid methyl ester () and ergosterol peroxide (), were isolated from the fungus sp. CYH-18 collected from the Haima cold seep. The structures and absolute configurations of the compounds were determined via NMR
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Ergostane triterpenoids from cultures of basidiomycete Favolaschia minutissima Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-06 Somporn Palasarn, Patchanee Auncharoen, Natthawut Wiriyathanawudhiwong, Thitiya Boonpratuang, Chawanee Thongpanchang, Masahiko Isaka
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Announcements of the Phytochemical Society of Europe Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-05
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Comprehensive review on megastigmane glycosides: Sources, bioactivities, and 13C NMR spectroscopic data Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-02 Reham M. Samra, Ahmed Othman, Marwa Elsbaey, Yhiya Amen, Kuniyoshi Shimizu
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Prionitosides A and B – two iridoid glycosides with anti-inflammatory and cytotoxic activities from Barleria prionitis Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-02 Onesy Keomanykham, Le Thi Phuong Hoa, Tran Thi Bich Lien, Hoang Tuan Anh, Tran My Duyen, Nguyen Thi Hong Lien, Le Duc Long, Nguyen Xuan Nhiem, Tran Dinh Thang, Le Dang Quang, Vu Dinh Hoang, Dang Ngoc Quang
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Oleanolic acid glycosides from two species of Olax: Olax wildemanii and Olax subscorpioidea Phytochem. Lett. (IF 1.7) Pub Date : 2024-02-02 David Pertuit, Marc Sautour, Tomofumi Miyamoto, Clément Delaude, Mpuza Kapundu, Marie-Aleth Lacaille-Dubois, Anne-Claire Mitaine-Offer
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Carbazomycins I and J, two novel carbazole alkaloids isolated from Saccharopolyspora phattalungensis Phytochem. Lett. (IF 1.7) Pub Date : 2024-01-31 Wen Wang, Er Juan Zhao, Ting Peng, Zhang Yuan Yan, Zhi Kai Guo, Rui Hua Jiao
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Two new compounds from Rhodiola rosea and their anti-hypoxic activities Phytochem. Lett. (IF 1.7) Pub Date : 2024-01-31 Yan Liu, Shi-Qi Xu, Yu Mei, Juan Pan, Wei Guan, Meng-Meng Li, Hai-Xue Kuang, Bing-You Yang
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Exploring the potential of marine natural products in drug development: A comprehensive review Phytochem. Lett. (IF 1.7) Pub Date : 2024-01-19 Abid H. Banday, Noor ul Azha, Rehana Farooq, Sourab A. Sheikh, Muzafar A. Ganie, Mohammad N. Parray, Hina Mushtaq, Iqra Hameed, Muzaffar A. Lone
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Substituted pyrazole derivatives as potential fungicidal agents Phytochem. Lett. (IF 1.7) Pub Date : 2024-01-19 Daye Huang, Fang Liu, Shaohua Wen, Yueying Wang, Wei Fang, Zhigang Zhang, Shaoyong Ke
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Assessing the safety and efficacy of DIY-homemade sunscreens with natural, aromatic and herbal ingredients Phytochem. Lett. (IF 1.7) Pub Date : 2024-01-19 Onur Kenan ULUTAŞ, Figen KARADOGAN, Senem AKGÜL, Zeynep Gizem YILDIZ
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Structural diversity derivatization and studies on the nematicidal activity of tropane derivatives Phytochem. Lett. (IF 1.7) Pub Date : 2024-01-19 Aoyun Lu, Yiting Zheng, Tao Li, Jiayi Wang, Gonghua Song
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Bioguided antiplasmodial isolation of six new labdane-type diterpenoids from the stem bark of Croton sylvaticus Hochst. Ex. Krauss Phytochem. Lett. (IF 1.7) Pub Date : 2024-01-12 Clémence Donfack Gouni, Yannick Stéphane Fotsing Fongang, Darline Dize, Georges Bellier Tabekoueng, Donald Ulrich Kenou Kagho, Gabin Thierry Mbahbou Bitchagno, Jean Jules Kezetas Bankeu, Bruno Ndjakou Lenta, Fabrice Boyom Fekam, Norbert Sewald, Silvère Augustin Ngouela
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Homoerythrina-type alkaloids with neuroprotective activity from the branches of Cephalotaxus hainanensis Li Phytochem. Lett. (IF 1.7) Pub Date : 2023-12-29 Hao Yan, Hao Wang, Peng-Wei Chen, Li Yang, Hui-Qin Chen, Fei Wu, Pei Wang, Hao-Fu Dai, Xiao-Long Huang, Shuang-Qing Zhou, Wen-Li Mei
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A new phthalides derivative pestalotiophthalide a with α-glucosidase inhibitory activity from Pestalotiopsis palmarum Phytochem. Lett. (IF 1.7) Pub Date : 2023-12-29 Li-Bin Lin, Guang-Yu Bai, Xiang Zhao, Wei shi, Jia-Yao Hu, Jin-Ye Bai, Rui-Hua Wang, Xiao-Ling Wang, Jian Xiao
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Laxilignans A-C from the leaves of Terminalia laxiflora Engl. and their α-glucosidase inhibitory activity Phytochem. Lett. (IF 1.7) Pub Date : 2023-12-29 Ann G. Boulis, Soheir M. El Zalabani, Neveen S. Ghaly, Omar M. Sabry, May A. El-Manawaty, Ahmed H. Afifi, Farouk R. Melek
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Two unprecedented 2-(2-phenethyl)chromone dimers from red soil agarwood of Aquilaria crassna Phytochem. Lett. (IF 1.7) Pub Date : 2023-12-30 Hong-Xing Chai, Hao Wang, Jun Zeng, Wen-Hua Dong, Wen-Li Mei, Bei Jiang, Wei Li, Hao-Fu Dai
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Natural products from the culture broth of an actinobacteria Streptomyces sp. M5205 and evaluation of their antifungal activity Phytochem. Lett. (IF 1.7) Pub Date : 2023-12-22 Jih-Jung Chen, Ming-Jen Cheng, Min Tseng, Ming-Der Wu, Jing-Ru Weng
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UPLC–QTOF-MS/MS analysis of saponin-enriched fractions from Calliandra umbellifera Benth and evaluation of antibacterial activity against multidrug-resistant bacteria Phytochem. Lett. (IF 1.7) Pub Date : 2023-12-22 Maria do Socorro Costa, Ana Raquel Pereira da Silva, Nara Juliana Santos Araújo, Cícera Laura Roque Paulo, Paulo Roberto Vieira Ribeiro, Josean Fechine Tavares, Jacqueline Cosmo Andrade Pinheiro, Henrique Douglas Melo Coutinho
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Bioactive constituents of the stem bark of Bersama abyssinica Fresen subsp. abyssinica Verdc. (Melianthaceae) Phytochem. Lett. (IF 1.7) Pub Date : 2023-12-18 Vanessa Charnele Tsafack, Appolinaire Kene Dongmo, Raymond Ngansop Nono, Georges Bellier Tabekoueng, Beate Neumann, Hans-Georg Stammler, Jean Jules Kezetas Bankeu, Siméon Fogué Kouam, Pépin Nkeng-Efouet-Alango, Bruno Ndjakou Lenta, Norbert Sewald, Jean Rodolphe Chouna
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The antiproliferative activity of Varronia dardani (Taroda) J.S. Mill. roots against human melanoma cells and the isolation of a new hydroanthraquinone Phytochem. Lett. (IF 1.7) Pub Date : 2023-12-15 Carlos Arthur Gouveia Veloso, César Augusto Gonçalves Dantas, Raimundo Gonçalves de Oliveira Júnior, Vicente Carlos de Oliveira Costa, Luiz Antonio Miranda de Souza Duarte-Filho, José Iranildo Miranda de Melo, Pierre Edouard Bodet, Josean Fechine Tavares, Marcelo Sobral da Silva, Laurent Picot
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A new oligostilbenoid isolated from the stems of Ochna integerrima Phytochem. Lett. (IF 1.7) Pub Date : 2023-12-14 Ratchanaporn Chokchaisiri, Waraluck Chaichompoo, Sareeya Bureekaew, Chutamas Thepmalee, Lucksagoon Ganranoo, Sarot Cheenpracha, Apichart Suksamrarn
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Vasorelaxant effect of a phenylethylamine analogue based on schwarzinicine A an alkaloid isolated from the leaves of Ficus schwarzii Phytochem. Lett. (IF 1.7) Pub Date : 2023-12-09 Kayatri Govindaraju, Yin Ying Mak, Fong Kai Lee, Claudia C. Bauer, Kuan Hon Lim, Robin S. Bon, Cin Kong, Sue Mian Then, Kang Nee Ting
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Two new monoterpenoids from the roots of Paeonia lactiflora and their neuroprotective activities Phytochem. Lett. (IF 1.7) Pub Date : 2023-12-12 Bo Fu, Jin-Ling Zhang, Xin Meng, Jia-Tong Wu, Yan Liu, Yu-Qing Wang, Yi-Qiang Zhang, Juan Pan, Wei Guan, Rui-Feng Fan, Anam Naseem, Hai-Xue Kuang, Bing-You Yang
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Synthesis and antifungal activity of 2,4-dihydroxy-5-methylphenyl ethanone derivatives against phytopathogenic fungi in vitro Phytochem. Lett. (IF 1.7) Pub Date : 2023-12-09 Lin Jia, Cui-Ping Zhang, Yi Zhu, Chun-Yan Zhao, Zeng-Hui Han, Dong-Bao Hu, Wei Shi
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Iridoid and lignan glycosides from Lancea tibetica Phytochem. Lett. (IF 1.7) Pub Date : 2023-11-25 Yi Zhu, Junlin Wang, Lu Tang, Yuxin Shang, Weiyi Zhao, Wei Zhang, Ping Hai, Yongbiao Zheng, Wenbo Li, Yanfang Su
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Two new steroids from the medicinal plant Physalis peruviana L. Phytochem. Lett. (IF 1.7) Pub Date : 2023-11-22 Léannick W. Demgne, Paul Eckhardt, Boris Y. Kianfé, Roland T. Tchuenguem, Jean P. Dzoyem, Beaudelaire K. Ponou, Rémy B. Teponno, Luciano Barboni, Till Opatz, Léon A. Tapondjou
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Design, synthesis, and anti–tobacco mosaic virus activity evaluation of quinazolinone derivatives containing purine moieties Phytochem. Lett. (IF 1.7) Pub Date : 2023-11-22 Yi Deng, Minghua Chen, Junming Yi, Yuguo Zheng
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Phenolic glycosides from Yua thomsonii Phytochem. Lett. (IF 1.7) Pub Date : 2023-11-18 Dang Viet Cuong, Tran Thi Hong Hanh, Pham Thi Mai Huong, Nguyen Thi Huong, Tran Hong Quang, Nguyen Xuan Cuong
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Announcements of the Phytochemical Society of Europe Phytochem. Lett. (IF 1.7) Pub Date : 2023-11-17
Abstract not available
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Two new ketene derivatives from the endophytic fungus Daldinia eschscholtzii J11 Phytochem. Lett. (IF 1.7) Pub Date : 2023-11-08 Song-Mei Lu, Cheng-Juan Liao, Yuan Xu, Teng-Yuan Gui, He-Lin Sui, Min Zhou
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Biotransformation of norethisterone by Rhizopus microsporus PT2906 Phytochem. Lett. (IF 1.7) Pub Date : 2023-11-02 Xiulan Xin, Jia Liu, Shengqiao Luan, Meirong Zhou, Wenxin Wang, Yuzhuo Wu, Xiaochi Ma, Chao Wang, Ping Guo, Dawei Li
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Lanostane triterpenoids from artificially cultivated fruiting bodies of Ganoderma wiiroense Phytochem. Lett. (IF 1.7) Pub Date : 2023-10-29 Arunrat Yangchum, Kitlada Srichomthong, Tuksaporn Thummarukcharoen, Sujinda Sommai, Masahiko Isaka
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Procaine treatment altered metabolite profiles of endophytic fungus Talaromyces wortmannii collected from Morus cathayana Hemsl Phytochem. Lett. (IF 1.7) Pub Date : 2023-10-20 Nizar Happyana, Elvira Hermawati, Suzany Dwi Ellita, Lia Dewi Juliawaty, Yana Maolana Syah, Euis Holisotan Hakim