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1.
Fitoterapia ; 165: 105418, 2023 Mar.
Article in English | MEDLINE | ID: mdl-36587747

ABSTRACT

Fourteen new sulphur-containing amides, glycocramides A-N (1-14), as well as nine known analogues (15-23) were isolated and characterized from Glycosmis craibii Tanaka. The chemical structures of new sulphur-containing amides 1-14 were ambiguously elucidated by extensive spectroscopic methods, while the known compounds 15-23 were identified by the comparison of their experimental spectral data with those described data in the literatures. The antiproliferative effects of all isolated sulphur-containing amides were evaluated in vitro. As a result, part of sulphur-containing amides showed remarkable inhibitory effects against MGC-803 cell line with IC50 values ranging from 13.12 ± 0.10 to 20.03 ± 0.13 µM. These research results suggest that the sulphur-containing amides are potentially to be developed as a new natural anti-tumor drugs.


Subject(s)
Amides , Rutaceae , Amides/pharmacology , Amides/chemistry , Molecular Structure , Sulfur , Plant Extracts/chemistry , Rutaceae/chemistry , Cell Line, Tumor
2.
Nat Prod Res ; 36(1): 379-384, 2022 Jan.
Article in English | MEDLINE | ID: mdl-32619098

ABSTRACT

A phytochemical investigation on the stems of Glycosmis puberula var. craibii led to the isolation of a new indole alkaloid (named glycosmiscrol A, 1), together with four known compounds (2-5). The new structure was elucidated by detailed analysis of comprehensive spectroscopic methods. All isolated compounds were evaluated for their antiproliferative activities against five human cancer cell lines: HL-60, SMMC-7721, A-549, MCF-7 and SW480 in vitro. Compounds 1-5 showed significant antiproliferative effects with IC50 values ranging from 0.16 to 8.58 µM.


Subject(s)
Antineoplastic Agents, Phytogenic , Rutaceae , Antineoplastic Agents, Phytogenic/pharmacology , Cell Line, Tumor , Humans , Indole Alkaloids/pharmacology , Molecular Structure , Plant Stems
3.
Pharmacol Res ; 174: 105955, 2021 12.
Article in English | MEDLINE | ID: mdl-34715330

ABSTRACT

Severe Coronavirus Disease 2019 (COVID-19) is characterized by numerous complications, complex disease, and high mortality, making its treatment a top priority in the treatment of COVID-19. Integrated traditional Chinese medicine (TCM) and western medicine played an important role in the prevention, treatment, and rehabilitation of COVID-19 during the epidemic. However, currently there are no evidence-based guidelines for the integrated treatment of severe COVID-19 with TCM and western medicine. Therefore, it is important to develop an evidence-based guideline on the treatment of severe COVID-19 with integrated TCM and western medicine, in order to provide clinical guidance and decision basis for healthcare professionals, public health personnel, and scientific researchers involved in the diagnosis, treatment, and care of COVID-19 patients. We developed and completed the guideline by referring to the standardization process of the "WHO handbook for guideline development", the Grading of Recommendations Assessment, Development and Evaluation (GRADE) system, and the Reporting Items for Practice Guidelines in Healthcare (RIGHT).


Subject(s)
Antiviral Agents/therapeutic use , COVID-19 Drug Treatment , Drugs, Chinese Herbal/therapeutic use , Infectious Disease Medicine/trends , Medicine, Chinese Traditional/trends , SARS-CoV-2/drug effects , Antiviral Agents/adverse effects , COVID-19/diagnosis , COVID-19/virology , Consensus , Delphi Technique , Drugs, Chinese Herbal/adverse effects , Evidence-Based Medicine/trends , Host-Pathogen Interactions , Humans , Patient Acuity , SARS-CoV-2/pathogenicity , Treatment Outcome
4.
Chin J Nat Med ; 19(3): 225-230, 2021 Mar.
Article in English | MEDLINE | ID: mdl-33781456

ABSTRACT

The phytochemical investigation of the stems of Homalium stenophyllum afforded seven new phenolic glycosides (1-5 and 8-9) and two known compounds (6 and 7). Their structures were elucidated by comprehensive analyses of NMR spectroscopic, mass spectrometric data and chemical hydrolysis. Additionally, their anti-inflammatory activities against the NO production in LPS-induced macrophages were evaluated.


Subject(s)
Glycosides , Phenols , Salicaceae/chemistry , Anti-Inflammatory Agents/pharmacology , Glycosides/isolation & purification , Glycosides/pharmacology , Macrophages/drug effects , Molecular Structure , Phenols/isolation & purification , Phenols/pharmacology , Phytochemicals/isolation & purification , Phytochemicals/pharmacology , Plant Stems/chemistry
5.
Nat Prod Res ; 35(21): 3562-3568, 2021 Nov.
Article in English | MEDLINE | ID: mdl-32037889

ABSTRACT

A preliminary phytochemical investigation of the stems of the endangered plant Ulmus elongata led to the isolation of a new coumarin derivative (named ulmuselactone A, 1) and eight known compounds (2-9). The new structure was elucidated by detailed analysis of comprehensive spectroscopic methods, and its absolute configuration was established by comparing experimental and calculated electronic circular dichroism (ECD) spectra. The isolated compounds were evaluated for their antibacterial activities.


Subject(s)
Ulmus , Anti-Bacterial Agents/pharmacology , Coumarins/pharmacology , Phytochemicals , Plant Extracts
6.
Nat Prod Res ; 33(16): 2300-2307, 2019 Aug.
Article in English | MEDLINE | ID: mdl-29468894

ABSTRACT

Phytochemical investigation of the stems of Vatica mangachapoi (Dipterocarpaceae) led to the isolation and structural elucidation of twenty-seven oligostilbenes (1-27), including a new natural compound 1. The structure of 1 was elucidated on the basis of spectroscopic analyses including NMR, MS and ECD data, and the known compounds were identified by comparisons with those reported in the literature. The absolute configuration of 1 was first time determined by a combination of NOESY spectrum and quantum chemical computation. Among of isolates were tested for their anti-osteoporosis and anti-HIV-1 activities in vitro by the MTT method. Moreover, the chemotaxonomic significance of these compounds was summarised.


Subject(s)
Dipterocarpaceae/chemistry , Stilbenes/isolation & purification , Anti-HIV Agents/pharmacology , Magnetic Resonance Spectroscopy , Osteoporosis/drug therapy , Plant Stems/chemistry , Stilbenes/chemistry , Stilbenes/classification , Stilbenes/pharmacology
7.
Nat Prod Res ; 33(3): 374-379, 2019 Feb.
Article in English | MEDLINE | ID: mdl-29630409

ABSTRACT

A new morphinandienone alkaloid, fissistigmine A (1), together with three known alkaloids (2-4), were isolated and identified from the stems of Fissistigma tungfangense. Among them, fissistigmine A (1) represents the first example of a novel naturally occurring morphinandienone alkaloid with a unique cleavage of the C-9-N-17 bond. All isolated compounds were evaluated for their anti-rheumatoid arthritis activities via examining their anti-proliferative effects on synoviocytes in vitro. Compound 1 exhibited inhibitory effect on the proliferation of synoviocytes with an IC50 value of 114.6 ± 2.2 µM.


Subject(s)
Alkaloids/isolation & purification , Annonaceae/chemistry , Morphinans/isolation & purification , Alkaloids/chemistry , Antirheumatic Agents/isolation & purification , Cell Proliferation/drug effects , Morphinans/chemistry , Plant Stems/chemistry , Synoviocytes/drug effects
8.
Nat Prod Res ; 33(9): 1292-1297, 2019 May.
Article in English | MEDLINE | ID: mdl-29737877

ABSTRACT

One new norisoprenoid 3,9-dihydroxy dihydro actinidiolide (1), together with eleven known compounds (2-12), were isolated from ethanol extract of the leaves of Ficus pumila collected in Hainan Province, China. Their structures were elucidated by the detailed analysis of comprehensive spectroscopic data. Compounds 1, 2, 4, 5, 8 and 10-12 were isolated from the F. pumila for the first time. All compounds were evaluated for their cytotoxic activity. Compounds 3 and 9 showed weak cytotoxic activity against Hela, MCF-7 and A549 cell lines.


Subject(s)
Ficus/chemistry , Norisoprenoids/isolation & purification , Cell Line, Tumor , Humans , Norisoprenoids/chemistry , Plant Extracts/analysis , Plant Leaves/chemistry
9.
Nat Prod Res ; 33(19): 2784-2788, 2019 Oct.
Article in English | MEDLINE | ID: mdl-30445847

ABSTRACT

One new lignan derivative 2,3-dimethyl-4-(4'-hydroxy-3',5'-dimethoxyphenyl)-6-hydroxy-7-methoxy-naphthalene (1), together with four known analogues (2-5), were isolated from acetone extract of the fruiting bodies of Ganoderma lipsiense collected in the Hainan Province, China. Their structures were elucidated by the detailed analysis of comprehensive spectroscopic data. Compound 1 showed insecticidal activity against newly hatched karvae of Helicoverpa armigera Hubner. Compounds 1-5 showed moderate antibacterial activity against Staphylococcus aureus with the same MIC value of 1.25 µg/mL.


Subject(s)
Anti-Bacterial Agents/pharmacology , Ganoderma/chemistry , Insecticides/pharmacology , Lignans/pharmacology , Animals , Anti-Bacterial Agents/chemistry , China , Drug Evaluation, Preclinical , Fruiting Bodies, Fungal/chemistry , Insecticides/chemistry , Lignans/chemistry , Magnetic Resonance Spectroscopy , Microbial Sensitivity Tests , Molecular Structure , Moths/drug effects , Spectrometry, Mass, Electrospray Ionization , Staphylococcus aureus/drug effects
10.
Molecules ; 23(2)2018 Feb 22.
Article in English | MEDLINE | ID: mdl-29470386

ABSTRACT

Two new phenolic glycosides (1 and 2) and two new isocoumarin glycosides (3 and 4), along with 14 known compounds (5-18), were isolated from the stems of Homalium paniculiflorum. Their structures were established on the basis of extensive spectroscopic analyses and chemical methods. All new compounds were evaluated for their anti-inflammatory activities via examining the inhibitory activity on nitric oxide (NO) production induced by lipopolysaccharide (LPS) in mouse macrophage RAW 264.7 cells in vitro. Compounds 1 and 4 exhibited inhibitory activities with IC50 values of 30.23 ± 1.23 µM and 19.36 ± 0.19 µM, respectively.


Subject(s)
Glycosides/chemistry , Inflammation/drug therapy , Isocoumarins/chemistry , Salicaceae/chemistry , Animals , Humans , Inflammation/chemically induced , Lipopolysaccharides/toxicity , Mice , Nitric Oxide/antagonists & inhibitors , Nitric Oxide/biosynthesis , Phenol/chemistry , Plant Stems/chemistry , RAW 264.7 Cells/drug effects
11.
Nat Prod Res ; 32(8): 953-958, 2018 Apr.
Article in English | MEDLINE | ID: mdl-28906141

ABSTRACT

A new dihydrochalcone glycoside, phloretin-4-O-ß-D-glucopyranoside (1), together with seven known flavonoids (2-8), were isolated from the stems of Homalium stenophyllum. The structure of 1 was elucidated by extensive spectroscopic methods and the known compounds were identified by comparisons with data reported in the literature. The known compounds (2-8) were isolated from the genus Homalium for the first time. All compounds were evaluated for their antibacterial activities against six pathogenic bacteria in vitro.


Subject(s)
Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Chalcones/chemistry , Glycosides/chemistry , Salicaceae/chemistry , Anti-Bacterial Agents/isolation & purification , Flavonoids/chemistry , Magnetic Resonance Spectroscopy , Microbial Sensitivity Tests , Molecular Structure , Plant Stems/chemistry
12.
Nat Prod Res ; 31(9): 1022-1027, 2017 May.
Article in English | MEDLINE | ID: mdl-27966385

ABSTRACT

One new lignan derivative 2,3-dimethyl-4-(4-methoxyphenyl)-6,7-dihydroxynaphthalene (1), together with five known compounds (2-6), were isolated from ethanol extract of the branches and leaves of Combretum alfredii Hance collected in Hainan Province, China. Their structures were elucidated by the detailed analysis of comprehensive spectroscopic data. Compounds 1, 2, 5 and 6 were isolated from the genus of Combretum for the first time. All compounds were evaluated for their antibacterial activities. Compounds 1 and 2 showed significant antibacterial activities against six pathogenic bacteria.


Subject(s)
Anti-Bacterial Agents/isolation & purification , Combretum/chemistry , Lignans/isolation & purification , Lignans/chemistry , Lignans/pharmacology , Naphthols , Plant Extracts/analysis , Plant Leaves/chemistry
13.
Nat Prod Res ; 30(20): 2285-90, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27093519

ABSTRACT

One new alkaloid consanguine B (1), together with 10 known alkaloids (2-11), were isolated from ethanol extract of the branches and leaves of Polyalthia obliqua Hook.f. & Thomson collected in the Hainan Province, China. Their structures were elucidated by the detailed analysis of comprehensive spectroscopic data. All compounds were evaluated for their cytotoxic activities. Compound 1 showed weak cytotoxic activities against Hela and MCF-7 human cancer cell lines.


Subject(s)
Antineoplastic Agents, Phytogenic/pharmacology , Polyalthia/chemistry , Alkaloids/chemistry , Alkaloids/isolation & purification , Alkaloids/pharmacology , Antineoplastic Agents, Phytogenic/chemistry , Berberine/chemistry , Berberine Alkaloids/isolation & purification , Berberine Alkaloids/pharmacology , China , Drug Screening Assays, Antitumor , HeLa Cells/drug effects , Humans , MCF-7 Cells/drug effects , Molecular Structure , Plant Extracts/chemistry , Plant Leaves/chemistry
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