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1.
Fitoterapia ; 169: 105606, 2023 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-37442484

RESUMO

Fraxinifolines A-F (1-6), six new B-seco limonoids, together with four known A,D-di-seco ones, were isolated from the twigs with leaves of Tetradium fraxinifolium. Their structures with absolute configurations were elucidated on the basis of analysis of MS, NMR, single-crystal X-ray diffraction and biogenetic pathway. An anti-inflammatory bioassay in vitro showed limonoids 1-3 had significant immunosuppressive effect against the production of pro-inflammatory cytokines (IL-1ß and/or TNF-α) in lipopolysaccharide (LPS)-stimulated RAW264.7 cells.


Assuntos
Limoninas , Estrutura Molecular , Limoninas/farmacologia , Limoninas/química , Anti-Inflamatórios/farmacologia , Citocinas , Fator de Necrose Tumoral alfa/metabolismo
2.
Fitoterapia ; 157: 105118, 2022 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-34974140

RESUMO

Melodicochinines A - D (1-4), four new monoterpene indole alkaloids (MIAs), along with 21 known ones, were isolated from the stems and twigs of Melodinus cochinchinensis. Their structures were elucidated on the basis of extensive spectroscopic analysis. A ubiquitin-rhodamine 110 assay showed that 11-methyloxytabersonine had potential inhibitory effect against ubiquitin-specific protease 7 (USP7).


Assuntos
Apocynaceae/química , Extratos Vegetais/química , Alcaloides de Triptamina e Secologanina/isolamento & purificação , China , Cromatografia Líquida de Alta Pressão , Espectroscopia de Ressonância Magnética , Rotação Ocular , Extratos Vegetais/isolamento & purificação , Caules de Planta/química , Alcaloides de Triptamina e Secologanina/química , Espectrofotometria Infravermelho
3.
Nat Prod Res ; 35(2): 195-202, 2021 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-31148477

RESUMO

Twenty-one polycyclic polyprenylated acylphloroglucinols, including three new compounds named as hyperichoisins A (3), B (14) and C (21), were isolated from the aerial parts of Hypericum choisianum. The structures of those new compounds were elucidated by analysis of mass, NMR data, and chiroptical properties. A bioassay showed that otogirinin B had significant inhibitory effect on cell proliferation of A549.


Assuntos
Antineoplásicos Fitogênicos/química , Antineoplásicos Fitogênicos/farmacologia , Hypericum/química , Células A549 , Proliferação de Células/efeitos dos fármacos , Ensaios de Seleção de Medicamentos Antitumorais , Humanos , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Floroglucinol/química
4.
Fitoterapia ; 146: 104678, 2020 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-32593692

RESUMO

Hookerianones A - E (1-5), five new polyprenylated acylphloroglucinols (PPAPs), along with six known ones, were isolated from the aerial parts of Hypericum hookerianum. Their structures were elucidated by analyses of MS, NMR, chiroptical properties, biogenetic pathway, and/or single crystal X-ray diffraction. A ubiquitin-rhodamine 110 assay showed that furohyperforin and hypercalin C, two representative PPAPs in this plant, inhibited more than 90% USP7 at the concentration of 10 µM.


Assuntos
Hypericum/química , Floroglucinol/farmacologia , Inibidores de Proteases/farmacologia , Peptidase 7 Específica de Ubiquitina/antagonistas & inibidores , China , Estrutura Molecular , Floroglucinol/isolamento & purificação , Compostos Fitoquímicos/isolamento & purificação , Compostos Fitoquímicos/farmacologia , Componentes Aéreos da Planta/química , Inibidores de Proteases/isolamento & purificação
5.
Bioorg Chem ; 99: 103812, 2020 06.
Artigo em Inglês | MEDLINE | ID: mdl-32302796

RESUMO

Alopecines A-E (1-5), five unusual matrine-type alkaloids featuring with an additional dichlorocyclopropane (1-3) or a di/tri-chloromethyl (4/5) attached on the D ring, were isolated from the seeds of Sophora alopecuroides. Their structures and absolute configurations were elucidated by extensive spectroscopic techniques, and X-ray diffraction analyses or time-dependent density functional theory-based electronic circular dichroism (TDDFT-ECD) calculations. Alkaloid 4 exhibited potent inhibitory effects on the proliferation of ConA-induced T lymphocytes or LPS-induced B cells with IC50 value of 3.98 or 3.74 µM, respectively.


Assuntos
Alcaloides/farmacologia , Imunossupressores/farmacologia , Extratos Vegetais/farmacologia , Sophora/química , Alcaloides/química , Alcaloides/isolamento & purificação , Animais , Linfócitos B/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Sobrevivência Celular/efeitos dos fármacos , Células Cultivadas , Concanavalina A/antagonistas & inibidores , Concanavalina A/farmacologia , Relação Dose-Resposta a Droga , Feminino , Imunossupressores/química , Imunossupressores/isolamento & purificação , Lipopolissacarídeos/antagonistas & inibidores , Lipopolissacarídeos/farmacologia , Camundongos , Camundongos Endogâmicos BALB C , Conformação Molecular , Extratos Vegetais/química , Extratos Vegetais/isolamento & purificação , Sementes/química , Estereoisomerismo , Relação Estrutura-Atividade , Linfócitos T/efeitos dos fármacos
6.
Fitoterapia ; 134: 96-100, 2019 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-30794918

RESUMO

Seventeen structurally diverse lignans, comprising six new compounds, ecdysanols A (1), B (11), C - E (13-15), and F (17), were isolated from the caulis of Urceola rosea. The structures and absolute configurations of these new compounds were elucidated by means of extensive analysis of mass and NMR data, as well as chiroptical properties. A bioassay in vitro showed that all lignans possessed anti-inflammatory effects by inhibiting the production of TNF-α, NO and/or IL-6 in LPS-stimulated RAW264.7 cells. Ecdysanol F (17) showed the most strongly effect against NO and IL-6 levels.


Assuntos
Anti-Inflamatórios/farmacologia , Apocynaceae/química , Lignanas/farmacologia , Animais , Anti-Inflamatórios/isolamento & purificação , Sobrevivência Celular , China , Feminino , Interleucina-6/metabolismo , Lignanas/isolamento & purificação , Camundongos , Estrutura Molecular , Óxido Nítrico/metabolismo , Compostos Fitoquímicos/isolamento & purificação , Compostos Fitoquímicos/farmacologia , Células RAW 264.7 , Fator de Necrose Tumoral alfa/metabolismo
7.
Fitoterapia ; 133: 96-101, 2019 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-30605781

RESUMO

A phytochemical investigation on the twigs and leaves of Flueggea virosa (Euphorbiaceae) led to the isolation of flueggenoids A - E (1-5), five new 13-methyl-ent-podocarpanes, together with eleven known compounds (6-16). Their structures and absolute configurations were elucidated on the basis of extensive MS and NMR data analysis, and/or single-crystal X-ray diffraction, time-dependent density functional theory (TDDFT)-based electronic circular dichroism (ECD) calculations, and chemical transformation. All isolates were evaluated for anti-HCV activity, the results showed that terpenoids of F. virosa had nonnegligible contribution for the anti-HCV activity.


Assuntos
Malpighiales/química , Terpenos/química , Linhagem Celular Tumoral , China , Hepacivirus , Humanos , Estrutura Molecular , Compostos Fitoquímicos/química , Compostos Fitoquímicos/isolamento & purificação , Componentes Aéreos da Planta/química , Terpenos/isolamento & purificação
8.
Nat Prod Res ; 33(1): 41-46, 2019 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-29382221

RESUMO

Six triterpenoids (1-6), four megastigmanes (7-10) and five hydroxycinnamic acid derivatives (11-15) were isolated from the aerial part of Anisomeles indica (Lamiaceae). Of these components, compound 1 was identified to be a new triterpenoid with the structure of 2α,3α,19α-trihydroxyurs-12,20(30)-dien-28-oic acid based on extensive analysis of MS, 1D and 2D NMR spectroscopic data, while compounds 2-13 were obtained for the first time from Anisomeles species.


Assuntos
Ácidos Cumáricos/isolamento & purificação , Lamiaceae/química , Norisoprenoides/isolamento & purificação , Triterpenos/isolamento & purificação , Ácidos Cumáricos/química , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Norisoprenoides/química , Componentes Aéreos da Planta/química , Extratos Vegetais/química , Triterpenos/química
9.
Fitoterapia ; 129: 179-184, 2018 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-29981396

RESUMO

The fruits of Swietenia macrophylla (skyfruits) are commercially used as healthcare products to improve blood circulation. An investigation of active ingredients of skyfruits led to the isolation of four new limonoids, swietemacrolides A-D (1-4), together with ten known limonoids (5-14) and one proto-limonoid (15). Their structures were elucidated on the basis of MS and NMR data analysis. Swietemacrolide C (3) at the concentration of 10 µM showed significant protective effect on H2O2-induced apoptosis in human umbilical vascular endothelial cells (HUVECs), while swieteliacate D (5) displayed moderate anti-apoptotic activity.


Assuntos
Apoptose/efeitos dos fármacos , Frutas/química , Células Endoteliais da Veia Umbilical Humana/efeitos dos fármacos , Limoninas/farmacologia , Meliaceae/química , Humanos , Peróxido de Hidrogênio , Limoninas/isolamento & purificação , Melanesia , Estrutura Molecular
10.
Ying Yong Sheng Tai Xue Bao ; 29(3): 976-986, 2018 Mar.
Artigo em Chinês | MEDLINE | ID: mdl-29722243

RESUMO

Using land use data in the year 1995, 2005 and 2014, this study estimated the ecosystem service value (ESV) in each county located in the middle reach of Yangtze River and analyzed its spatiotemporal variation features and terrain gradient effects based on "the equivalent value per unit area of ecosystem services in China". The results showed that ESV in the middle reach of Yangtze River was generally higher in mountainous area but lower in plain region, with an obvious terrain gradient effect. Specifically, the relationship of the relief degree of land surface (RDLS) and the ESV showed significant logarithm function at county scale with a high curve fitting degree of 0.53. The ESV increased from 400.35×104 yuan·km-2 to 554.57×104 yuan·km-2 with the increasing RDLS (grade 1-5) in 2014. During 1995-2004, the ecosystem service value variation changed from decreasing to stable with the increases of the RDLS. With a perspective of ecosystem service values, the value of food production and waste treatment service value decreased with the increase of the RDLS, while the others increased in general, such as the production of raw materials and gas regulation service value, because of the influences of dynamic land use structure in varied topography and distinct dominant ecosystem services from different land types.


Assuntos
Conservação dos Recursos Naturais , Ecossistema , China , Monitoramento Ambiental , Eliminação de Resíduos , Rios
11.
Phytochemistry ; 145: 93-102, 2018 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-29107811

RESUMO

A phytochemical investigation on the aerial part of Euphorbia helioscopia (Euphorbiaceae) led to the isolation of 22 highly oxygenated diterpenoids with structural types of ent-abietane, ent-kaurane, lathyrane, ent-atisane and ingenane. 17 of them, named euphelionolides A - N, 16-epi-18-hydroxy-abbeokutone, as well as eupheliotriols A and B, were identified to be previously undescribed compounds by extensive analysis of spectroscopic data. The stereostructures of euphelionolides A - K were determined by single crystal X-ray diffraction combined with analysis of substituent effects and comparison of optical characteristics. Eupheliotriol B is the first example of natural occurring lathyrol with 12Z-ene, while ent-atisanes are the first reported from the title plant. Furthermore, euphelionolides F and L exhibited significant cytotoxicity against MCF-7 and PANC-1 cell lines.


Assuntos
Antineoplásicos Fitogênicos/farmacologia , Diterpenos/farmacologia , Euphorbia/química , Oxigênio/química , Antineoplásicos Fitogênicos/química , Antineoplásicos Fitogênicos/isolamento & purificação , Linhagem Celular Tumoral , Proliferação de Células/efeitos dos fármacos , Sobrevivência Celular/efeitos dos fármacos , Diterpenos/química , Diterpenos/isolamento & purificação , Relação Dose-Resposta a Droga , Ensaios de Seleção de Medicamentos Antitumorais , Humanos , Estrutura Molecular , Relação Estrutura-Atividade
12.
J Asian Nat Prod Res ; 19(6): 602-609, 2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-28485622

RESUMO

The first synthesis of dendroflorin has been achieved in 10 steps with an overall yield of 5.5%. The key step in the synthesis features the biphenyl structure is built through Suzuki-Miyaura reaction. In addition, the ortho-localization effect induced by aromatic substituent during the bromination of intermediate 8 is also observed and discussed.


Assuntos
Benzoatos/síntese química , Dendrobium/química , Fluorenos/isolamento & purificação , Benzoatos/química , Compostos de Bifenilo/química , Catálise , Fluorenos/química , Hidroquinonas/química , Estrutura Molecular
13.
J Asian Nat Prod Res ; 17(10): 996-1001, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26120736

RESUMO

Two new triterpenoids, termichebuloside A (1), an unusual dimeric triterpenoid saponin, and termichebulolide (2), an oleanolic acid-type lactone, along with 11 known triterpenoids, were isolated from MeOH extract of the barks of Terminalia chebula. The structures of 1 and 2 were elucidated to be arjunglucoside I-(3-O-19',23-O-19')-18,19-seco-19-hydroxyarjunglucoside I (1) and 2α,3ß,23-trihydroxyolean-11,13(18)-dien-28,19ß-olide (2), respectively, on the basis of spectroscopic evidences and biogenetic consideration.


Assuntos
Saponinas/isolamento & purificação , Terminalia/química , Triterpenos/isolamento & purificação , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular , Casca de Planta/química , Saponinas/química , Estereoisomerismo , Triterpenos/química
14.
J Asian Nat Prod Res ; 15(1): 89-93, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23324033

RESUMO

Aglinin A (1) is a mixture of C(24)-epimeric 20S,24-epoxy-24,25-dihydroxy-3,4-secodammar-4(28)-en-3-oic acid and present in plants of the family Meliaceae. The two epimers of 1 were resolved through an acetonide reaction, and the absolute configurations of two derivatives were deduced by the analysis of their (13)C NMR differences induced by γ-gauche or steric effect. Based on it, the (13)C NMR assignment of 24R-1 and 24S-1 was also established.


Assuntos
Medicamentos de Ervas Chinesas/química , Medicamentos de Ervas Chinesas/isolamento & purificação , Meliaceae/química , Triterpenos/química , Triterpenos/isolamento & purificação , Medicamentos de Ervas Chinesas/farmacologia , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular , Estereoisomerismo , Triterpenos/farmacologia
15.
J Asian Nat Prod Res ; 14(11): 1073-7, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22924384

RESUMO

Two new arylnaphthalene lignan glycosides, named reticulatusides A (1) and B (2), together with eight known compounds were isolated from the 95% EtOH extract of the whole plant of Phyllanthus reticulatus. The structures of the new compounds were elucidated by spectroscopic methods.


Assuntos
Medicamentos de Ervas Chinesas/isolamento & purificação , Glicosídeos/isolamento & purificação , Lignanas/isolamento & purificação , Naftalenos/isolamento & purificação , Phyllanthus/química , Medicamentos de Ervas Chinesas/química , Glicosídeos/química , Lignanas/química , Estrutura Molecular , Naftalenos/química , Ressonância Magnética Nuclear Biomolecular
16.
Nat Prod Res ; 26(13): 1213-7, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-21895463

RESUMO

Lamiolactone (1), a new iridoid lactone, together with five known iridoids, were isolated from the 95% EtOH extract of the roots of Lamiophlomis rotata. The structure of 1 was elucidated to be methyl antirrhinolide-4-carboxylate on the basis of spectroscopic analysis.


Assuntos
Iridoides/química , Lactonas/química , Lamiaceae/química , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Raízes de Plantas/química
17.
Bioorg Med Chem ; 19(10): 3120-7, 2011 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-21524588

RESUMO

A series of tryptamine derivatives were synthesized and evaluated for their anti-hepatitis B virus (HBV) activity and cytotoxicity in the HepG2.2.15 cell line. The preliminary SAR was discussed. Compounds 2e and 4a showed potent antiviral activity (IC(50)=0.4 and <1 µM, respectively) and low cytotoxicity (CC(50)=40.6 and >25 µM, respectively).


Assuntos
Antivirais/química , Antivirais/farmacologia , Vírus da Hepatite B/efeitos dos fármacos , Hepatite B/tratamento farmacológico , Triptaminas/química , Triptaminas/farmacologia , Sobrevivência Celular/efeitos dos fármacos , DNA Viral/metabolismo , Células Hep G2 , Humanos , Relação Estrutura-Atividade
18.
J Asian Nat Prod Res ; 13(2): 178-81, 2011 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21279882

RESUMO

A new dammarane-type triterpenoid saponin, (20R)-ginsenoside ST(2) (1), along with five known saponins was isolated from the hongshen extract of Shenmai injection. The structure of 1 was elucidated to be (20R)-dammar-23(E)-ene-3ß,6α,12ß,20,25-pentol 6-O-ß-D-glucopyranoside by means of spectroscopic methods.


Assuntos
Medicamentos de Ervas Chinesas/isolamento & purificação , Ginsenosídeos/isolamento & purificação , Panax/química , Plantas Medicinais/química , Triterpenos/isolamento & purificação , Medicamentos de Ervas Chinesas/química , Medicamentos de Ervas Chinesas/farmacologia , Ginsenosídeos/química , Ginsenosídeos/farmacologia , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular , Estereoisomerismo , Triterpenos/química , Triterpenos/farmacologia , Damaranos
19.
J Asian Nat Prod Res ; 12(11): 1005-9, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-21061224

RESUMO

A new lycopodane-type Lycopodium alkaloid, 6α-hydroxy-5,15-oxide-lycopodane (1), and seven known alkaloids were isolated from the whole plants of Huperzia serrata. Their structures were elucidated by means of spectroscopic methods. 12-Deoxyhuperzine O (2) was reported as a naturally occurring alkaloid for the first time, and showed an antagonist effect on the N-methyl-d-aspartate receptor with an IC(50) value of 0.92 µM.


Assuntos
Alcaloides/isolamento & purificação , Medicamentos de Ervas Chinesas/isolamento & purificação , Huperzia/química , Alcaloides/química , Alcaloides/farmacologia , Animais , Córtex Cerebral/efeitos dos fármacos , Medicamentos de Ervas Chinesas/química , Medicamentos de Ervas Chinesas/farmacologia , Concentração Inibidora 50 , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular , Ratos , Ratos Sprague-Dawley , Receptores de N-Metil-D-Aspartato/antagonistas & inibidores , Membranas Sinápticas/efeitos dos fármacos
20.
Nat Prod Res ; 23(15): 1363-6, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19809906

RESUMO

Two new Lycopodium alkaloids, N-oxidehuperzine E (1) and N-oxidehuperzine F (2), along with two known alkaloids, huperzines E (3) and F (4), were isolated from Huperzia serrata (Thunb.) Trev. Their structures were elucidated by spectroscopic and chemical transformations.


Assuntos
Alcaloides/química , Huperzia/química , Extratos Vegetais/química , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular
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