Kai‐Long Ji

ORCID: 0000-0003-4186-4086
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About
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Research Areas
  • Natural product bioactivities and synthesis
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Phytochemical compounds biological activities
  • Traditional and Medicinal Uses of Annonaceae
  • Bioactive Natural Diterpenoids Research
  • Phytochemistry and Biological Activities
  • Alkaloids: synthesis and pharmacology
  • Essential Oils and Antimicrobial Activity
  • Phytochemistry and Bioactive Compounds
  • Plant chemical constituents analysis
  • Biological Activity of Diterpenoids and Biflavonoids
  • Cholesterol and Lipid Metabolism
  • Microbial Metabolites in Food Biotechnology
  • Plant biochemistry and biosynthesis
  • Kidney Stones and Urolithiasis Treatments
  • Drug Transport and Resistance Mechanisms
  • Therapeutic Uses of Natural Elements
  • Ginger and Zingiberaceae research
  • Adipokines, Inflammation, and Metabolic Diseases
  • Phytochemistry and Bioactivity Studies
  • Phytochemicals and Medicinal Plants
  • Marine Sponges and Natural Products
  • Diet and metabolism studies
  • Bamboo properties and applications

Xishuangbanna Tropical Botanical Garden
2015-2025

Chinese Academy of Sciences
2014-2024

Shanghai Institute of Materia Medica
2018-2023

University of Chinese Academy of Sciences
2014-2022

Yunnan University of Traditional Chinese Medicine
2013

Abstract Dietary fiber has been shown to prevent high-fat diet induced obesity through modulating the gut microbiota; however, quality difference in type is largely unknown. We performed a 6 week study on C57BL/6J mice fed macronutrient matched with different types including cellulose (HFC), bamboo shoot (HFBS) and several other commonly consumed fibers. Our results showed that HFBS group exhibited lowest weight gain among all groups had improved lipid profiles glycemic control compared HFC...

10.1038/srep32953 article EN cc-by Scientific Reports 2016-09-07

A 17-membered macrocyclolipopeptide, named dysoxylactam (1) comprising an unprecedented branched C19 fatty acid and l-valine, was isolated from the plants of Dysoxylum hongkongense. The challenging relative configuration 1 established by means residual dipolar coupling-based NMR analysis. absolute determined single-crystal X-ray diffraction on its p-bromobenzoate derivative (2). Compound dramatically reversed multidrug resistance in cancer cells with fold-reversals ranging 28.4 to 1039.7 at...

10.1021/jacs.9b02259 article EN Journal of the American Chemical Society 2019-04-17

Ten quinoline alkaloids from Zanthoxylum avicennae , of which 1 possesses an unusual structure and 6 exhibits anti-inflammatory effect in macrophages.

10.1039/d2ob00711h article EN Organic & Biomolecular Chemistry 2022-01-01

A new class of potent liver injury protective compounds, phychetins A−D (1−4) featuring an unique 6/6/5/6/5 pentacyclic framework, were isolated and structurally characterized from a Chinese medicinal plant Phyllanthus franchetianus. Compounds 2−4 are three pairs enantiomers that initially obtained in racemic manner, further separated by chiral HPLC preparation. 1−4 proposed to be originated biosynthetically coexisting lignan via intramolecular Friedel–Crafts reaction as the key step....

10.1016/j.apsb.2023.05.001 article EN cc-by-nc-nd Acta Pharmaceutica Sinica B 2023-05-05

Nine new cedrelone limonoids, namely, walsuranolide B (1), 11β-hydroxy-23-O-methylwalsuranolide (2), yunnanolide A (3), yunnanol (4), 11β-hydroxyisowalsuranolide (5), 11β-hydroxy-1,2-dihydroisowalsuranolide (6), 1α,11β-dihydroxy-1,2-dihydroisowalsuranolide (7), 11β-hydroxy-1α-methoxy-1,2-dihydroisowalsuranolide (8), and (9), together with a cycloartane triterpenoid, (24S*,25R*)-cycloartane-3β,24,25,26-tetrol (10), were isolated from the leaves twigs of Walsura yunnanensis. Their structures...

10.1021/np400976p article EN Journal of Natural Products 2014-07-30

Chemical investigation of an EtOH extract the twigs and leaves Croton damayeshu afforded 10 new tigliane diterpenoids, crodamoids A–J (1–10), along with five known compounds. Their structures were elucidated by physical data analysis. Compounds 8, 9, 15 displayed cytotoxic effects against two human tumor cell lines, A549 HL-60 (IC50: 0.9–2.4 μM).

10.1021/acs.jnatprod.9b00042 article EN Journal of Natural Products 2019-05-22

Eleven densely functionalized new dihydro-β-agarofuran sesquiterpenoid derivatives, named maytenoids A-K (1-11), as well one known analog, were isolated and characterized from Maytenus austroyunnanensis. Their structures assigned based on analysis of spectroscopic data X-ray crystallography. Compounds 1-9 are macrocyclic sesquiterpene pyridine alkaloids generated by the respective acylation hydroxy groups at C-3 C-13 sesquiterpenoids via diverse dicarboxylic acids. 1, 2, 5-10, 12 exhibited...

10.1021/acs.jnatprod.3c00504 article EN Journal of Natural Products 2023-09-20

Open AccessCCS ChemistryRESEARCH ARTICLE1 Feb 2021Macrocyclic Nonapeptides Incorporating Uncharacterized Amino Acids with Inhibitory Effects on Th17 Differentiation Kai-Long Ji, Yao-Yue Fan, Hio-Ha Kuok, Qun-Fang Liu, Ting Li and Jian-Min Yue Ji State Key Laboratory of Drug Research, Shanghai Institute Materia Medica, Chinese Academy Sciences, 201203 , Fan Kuok Quality Research in Medicines, Macau for Applied Medicine Health, University Science Technology, 999078 Liu *Corresponding author:...

10.31635/ccschem.020.202000265 article EN cc-by-nc CCS Chemistry 2020-06-17

Comprehensive Summary Five unreported and oxygenated ent ‐rosane diterpenoids ( ‐RDs), Euphomillanols A—E 1 — 5 ), were isolated from Euphorbia milii . Among them, compounds 2 are unprecedented 7/7/6‐fused tricyclic 5,10‐seco‐ ‐RDs possess a unique 11‐oxabicyclo[4.4.1]undeca‐1(10),5‐diene moiety, while 3 is characterized by 1‐methyl‐6‐oxabicyclo[3.2.1]oct‐2‐ene motif of ring A. Their structures with absolute configurations unambiguously determined the extensive spectroscopic methods, X‐ray...

10.1002/cjoc.202400749 article EN Chinese Journal of Chemistry 2024-09-10

Four highly rearranged labdane-type diterpenoids, maximumins A–D (1–4) possessing different new carbon skeletons, together with a biosynthetically related known analog 5 were isolated from Amomum maximum. The structures of compounds absolute configurations characterized by spectroscopic and computational approaches. plausible biogenetic pathways for 1–4 proposed. These showed moderate to weak activities against nuclear factor kappa B (NF-κB).

10.1021/acs.joc.8b02665 article EN The Journal of Organic Chemistry 2018-12-09

Two new limonoids, namely 14,15-didehydroruageanin A (1) and 3-O-methyl- butyrylseneganolide (2), were isolated from the fruits of Khaya ivorensis along with six known limonoids: seneganolide (3), 1,3-dideacetylkhivorin (4), 7-deacetylkhivorin (5), 3-deacetylkhivorin (6), 1-deacetylkhivorin (7), 3-deacetyl-7-oxokhivorin (8). All compounds evaluated for their cytotoxicity against five tumor cell lines.

10.3390/molecules19033004 article EN cc-by Molecules 2014-03-07

The 6-methoxy-cannabisin I (1), a new alkaloid, together with five known compounds oleraisoindole A (2), cannabisin F (3), apigenin (4), syringin (5) and ethyl-syringin (6) were isolated from Tinospora crispa stems. Their structures identified by the analysis of spectroscopic data. Compound 2 was T. for first time. Anti-inflammatory activity compound 1 detected against NO production in LPS-activated RAW 264.7 macrophages. However, no observed.

10.1080/14786419.2023.2272023 article EN Natural Product Research 2023-10-22

Alpinia hainanensis is an important food spice and ethnic medicine in Southwest China. In this study, we found that the EtOAc-soluble fraction (AHE) of A. rhizome ethanol extract could ameliorate dextran sulfate sodium-induced ulcerative colitis (UC). To explore active constituents, five pairs previously unreported enantiomers (1-5), together with nine known ones (6-14), were obtained. Structural characterization was achieved by comprehensive spectroscopic methods. Compounds 1 2 new...

10.1021/acs.jafc.1c08038 article EN Journal of Agricultural and Food Chemistry 2022-03-24

One novel pentacyclic triterpene, 24-dimethoxymethyl-3β,6β,19α- trihydroxy -12-en-28-oic acid (1), along with six known compounds 2-7, were isolated from the canes of Uncaria sessilifructus Roxb. Their structures determined according to spectroscopic and spectrometric analysis. The anti-inflammatory activities (1-7) scanned against NO production in LPS-activated RAW 264.7 macrophages by MTS assay, however no observed.

10.1080/14786419.2020.1795856 article EN Natural Product Research 2020-07-21
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