Jun Chang

ORCID: 0000-0001-6481-7130
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About
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Research Areas
  • Natural product bioactivities and synthesis
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Phytochemistry and Biological Activities
  • Plant chemical constituents analysis
  • Pharmacological Effects of Natural Compounds
  • Traditional and Medicinal Uses of Annonaceae
  • Bioactive natural compounds
  • Cancer Treatment and Pharmacology
  • Antimicrobial Resistance in Staphylococcus
  • Synthesis and biological activity
  • Sirtuins and Resveratrol in Medicine
  • Ginger and Zingiberaceae research
  • Essential Oils and Antimicrobial Activity
  • Antimicrobial Peptides and Activities
  • Phytochemical compounds biological activities
  • Phytochemical Studies and Bioactivities
  • Alkaloids: synthesis and pharmacology
  • Sesquiterpenes and Asteraceae Studies
  • Synthesis and Characterization of Heterocyclic Compounds
  • Carbohydrate Chemistry and Synthesis
  • Food Safety and Hygiene
  • Synthesis and Biological Activity
  • Cancer, Hypoxia, and Metabolism
  • Berberine and alkaloids research

Fudan University
2015-2024

Tongren University
2024

Pudong Medical Center
2024

Nanjing Normal University
2024

First Affiliated Hospital of Anhui Medical University
2024

Anhui Medical University
2024

Tianjin University of Traditional Chinese Medicine
2021

Beijing Sport University
2018

Purdue University West Lafayette
2014-2017

Huashan Hospital
2016

A Mannich–Michael combo: An efficient and highly enantioselective cascade process by H-bonding catalysis for the synthesis of functionalized tetrahydroquinolines has been developed. indane amine-thiourea small molecule discovered to catalyze this in high yields with good diastereomeric ratios excellent enantioselectivities (see scheme). Detailed facts importance specialist readers are published as ”Supporting Information”. Such documents peer-reviewed, but not copy-edited or typeset. They...

10.1002/chem.201103136 article EN Chemistry - A European Journal 2012-02-29

Treating staphylococcal biofilm-associated infections is challenging. Based on the findings that compound 2 targeting HK domain of Staphylococcus epidermidis YycG has bactericidal and antibiofilm activities against staphylococci, six newly synthesized derivatives were evaluated for their antibacterial activities. The inhibited autophosphorylation recombinant YycG' IC50 values ranged from 24.2 to 71.2 μM. displayed activity planktonic S. or aureus strains in MIC range 1.5-3.1 All had 6- 24-h...

10.1007/s00253-014-5685-8 article EN cc-by Applied Microbiology and Biotechnology 2014-04-16

The accumulation and deposition of beta-amyloid (Aβ) are key neuropathological hallmarks Alzheimer's disease (AD). PARP16, a Poly(ADP-ribose) polymerase, is known tail-anchored endoplasmic reticulum (ER) transmembrane protein that transduces ER stress during pathological processes. Here, we found PARP16 was significantly increased in the hippocampi cortices APPswe/PS1dE9 (APP/PS1) mice hippocampal neuronal HT22 cells exposed to Aβ, suggesting positive correlation between progression AD...

10.14336/ad.2023.0119 article EN cc-by Aging and Disease 2023-01-01

Five new compounds, two degraded terpene glycosides, dasycarpusides A and B (1, 2), three phenolic 2-methoxy-4-hydroxymethylphenol 1-O-alpha-rhamnopyranosyl-(1"-->6')- beta-glucopyranoside ( 3), 2-methoxy-4-acetylphenol 1-O-alpha-rhamnopyranosyl-(1"-->6')-beta-glucopyranoside (4), 2-methoxy-4-(8-hydroxyethyl)-phenol (5), were isolated from the water-soluble constituents of root bark Dictamnus dasycarpus Turcz.(Rutaceae). Their structures elucidated by spectroscopic analysis chemical...

10.1055/s-2002-32077 article EN Planta Medica 2002-05-01

A new lignan glycoside, (7S,8R)-guaiacylglycerol-ferulic acid ether-7-O-β-D-glucopyranoside (1), along with five known phenylpropanoids (2-6) and seven phenylpropanoid glycosides (7-13), were isolated from the stems of Zanthoxylum armatum DC. Their structures elucidated by spectroscopic analysis. Compounds 2-8 11-13 first Rutaceae others for time Z. armatum.

10.1080/14786419.2016.1205064 article EN Natural Product Research 2016-07-20

Twelve phenolic compounds, including four novel skeleton planchols A-D (1-4), together with pairs of isomeric flavanoids (5-12) were isolated from the root Actinidia chinensis Planch (Actinidiaceae). Their structures elucidated by spectroscopic analysis and chemical evidence. The structure 1 was further confirmed a single-crystal X-ray diffraction determination. Moreover, it found that 2 showed remarkable cytotoxic activity against P-388 A-549 cell lines.

10.1055/s-2005-871225 article EN Planta Medica 2005-07-01

Two new flavonoids, 6,8,3′,4′-tetrahydroxy-2′-methoxy-7-methylisoflavanone (1) and 6,8,3′,4′-tetrahydroxy-2′-methoxy-6′-(1,1-dimethylallyl)-isoflavone (2), were isolated from the 95% ethanolic extract of dried roots Lespedeza cuneata together with betulinic acid (3), β-sitosterol (4), hexacosanoic 2,3-dihydroxy-propyl ester (5), which this plant for first time. Their structures elucidated by spectral analysis.

10.1080/10286020600979894 article EN Journal of Asian Natural Products Research 2007-10-01

Two new phenolic glycoside, 2-methoxy-4-hydroxylphenyl-1-O-α-L-rhamnopyranosyl- (1″ → 6')-β-D-glucopyranoside. (1) and threo-3-methoxy-5-hydroxy-phenylpropanetriol-8-O-β-D-glucopyranoside (2), were isolated from the stems of Zanthoxylum armatum. The compounds 1 2 showed weak scavenging activity in DPPH free radical assay with IC50 values 323 114 mM, respectively.

10.1080/14786419.2017.1303695 article EN Natural Product Research 2017-03-21

From the water-soluble constituents of root bark Dictamnus dasycarpus, six new eudesmane-type sesquiterpene glycosides, dictamnosides H-M (1-6), and a trinorguaiane-type glycoside, dictamnoside N (7), together with four known A (8), B (9), D (10), G (11), were isolated. Their structures elucidated by spectroscopic analyses chemical evidence. In vitro tests for immunological activity showed (8) to possess remarkable in stimulating proliferation T-cells.

10.1021/np000567t article EN Journal of Natural Products 2001-07-01

Six novel 4,5-seco-rearranged abietane diterpenoids, including one tetracyclic diterpenoid, prionoid A (1), two tricyclic prionoids B (2) and C (3), three dicyclic D (4), E (5), F (6), were isolated from the roots of Salvia prionitis Hance (Labiatae). Their structures elucidated using spectroscopic analysis. The structure 1 was further confirmed by a single-crystal X-ray diffraction determination. Moreover, it found that 4 (IC50 = 0.41 microM) 5 0.72 showed significant cytotoxic activity...

10.1055/s-2005-871279 article EN Planta Medica 2005-09-01
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