Jinwen Huang

ORCID: 0000-0002-8473-2879
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About
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Research Areas
  • Cyclopropane Reaction Mechanisms
  • Catalytic Alkyne Reactions
  • Asymmetric Synthesis and Catalysis
  • Fluorine in Organic Chemistry
  • Chemical Synthesis and Reactions
  • Synthetic Organic Chemistry Methods
  • Proteoglycans and glycosaminoglycans research
  • Nitric Oxide and Endothelin Effects
  • Natural product bioactivities and synthesis
  • Carbon dioxide utilization in catalysis
  • Sulfur-Based Synthesis Techniques
  • Oxidative Organic Chemistry Reactions
  • Genomics, phytochemicals, and oxidative stress
  • Synthesis and biological activity
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Synthesis and Reactions of Organic Compounds
  • Synthesis and Catalytic Reactions
  • Skin Protection and Aging
  • Neurological Disease Mechanisms and Treatments
  • Chemical Synthesis and Analysis
  • Caveolin-1 and cellular processes
  • Crystallization and Solubility Studies
  • Liver Disease Diagnosis and Treatment
  • Peroxisome Proliferator-Activated Receptors
  • Organometallic Complex Synthesis and Catalysis

Shanghai Institute of Technology
2016-2025

Guangxi University of Chinese Medicine
2024

Wuyi University
2024

Kuaishou (China)
2023

Chang'an University
2023

Baoshan College
2023

Fujian Agriculture and Forestry University
2022

Green Technology
2022

Fluor (United States)
2022

Longhua Hospital Shanghai University of Traditional Chinese Medicine
2022

In the presence of catalytic amounts sodium iodide, triphenylphosphine, and phenol, carbon dioxide can efficiently react with epoxides to give corresponding five-membered cyclic carbonates in high yields. The mechanism this reaction was disclosed by (31)P NMR spectroscopic data deuterium labeling experiments.

10.1021/jo0348221 article EN The Journal of Organic Chemistry 2003-07-24

[reaction: see text] The attempted aza-Baylis-Hillman reaction of N-tosylated imines with ethyl 2,3-butadienoate or penta-3,4-dien-2-one gave azetidine derivatives in the presence DABCO. In case 2,3-butandieonate catalyzed by DMAP, novel dihydropyridine were formed.

10.1021/ol0359416 article EN Organic Letters 2003-11-01

Background and purpose: Silymarin, a standardized extract of the milk thistle seeds, has been widely used to treat chronic hepatitis, cirrhosis, other types toxic liver damage. Despite increasing studies on action silymarin its major active constituent, silybin in their therapeutic properties against insulin resistance, diabetes hyperlipidaemia vitro vivo, mechanism underlying remains unclear. Experimental approach: C57BL/6 mice were fed high-fat diet (HFD) for 3 months induce obesity,...

10.3389/fphar.2016.00345 article EN cc-by Frontiers in Pharmacology 2016-09-28

Background: The incidence of cerebral ischemia disease leading cause death in human population worldwide. Treatment remains a clinical challenge for researchers and mechanisms remain unknown. During the ischemia, inflammatory reaction oxidative stress plays an important role. current investigation scrutinized neuroprotective anti-inflammatory role pterostilbene against middle artery occlusion (MCAO) rodent model explore underlying mechanism. Methods: rats were divided into following groups...

10.3389/fphar.2021.770329 article EN cc-by Frontiers in Pharmacology 2021-11-02

Methylenecyclopropanes (MCPs) 1 can react with aldehydes and aldimines to give the corresponding indene, THF, pyrrolidine cycloaddition products in presence of BF3·OEt2 under mild reaction conditions.

10.1021/ol0498242 article EN Organic Letters 2004-03-04

[reactions: see text] Manganese(III)-mediated oxidative annulation of methylenecyclopropanes with 1,3-dicarbonyl compounds in acetic acid produces 4,5-dihydrofuran derivatives as [3+2] products moderate to good yields under mild conditions. The possible reaction mechanism is discussed on the basis previous mechanistic investigation.

10.1021/jo050181t article EN The Journal of Organic Chemistry 2005-04-02

New six C6-celastrol derivatives were designed, synthesized, and evaluated for their in vitro cytotoxic activities against nine human cancer cell lines (BGC-823, H4, Bel7402, H522, Colo 205, HepG2 MDA-MB-468). The results showed that most of the compounds displayed potent inhibition BGC823, with IC50s 1.84–0.39 μM. best compound NST001A was tested an vivo antitumor assay on nude mice bearing 205 xenografts, significant tumor growth at low concentrations. Therefore, celastrol C-6 are...

10.3390/molecules190710177 article EN cc-by Molecules 2014-07-14

Abstract The use of polymer‐supported Lewis bases such as PEG 4600 ‐(PPh 2 ) and poly(DMAP) in the Baylis–Hillman reactions N ‐tosylimines (ArCHNTs) 1 or corresponding arenecarbaldehydes with α,β‐unsaturated ketones has been investigated. adducts are obtained good yields. can be easily recovered by filtration base reproduced reduction LiAlH 4 CeCl 3 .

10.1002/adsc.200303072 article EN Advanced Synthesis & Catalysis 2003-08-01

Methylenecyclopropanes (MCPs 1) react with aldehydes, N-tosyl aldimines, and acetals to give the corresponding indene, THF, pyrrolidine cycloaddition products in presence of BF3 x OEt2 under mild reaction conditions. Some special transformations MCPs 1 aldehydes have been reported this paper. A plausible mechanism has discussed, which is based on a deuterium-labeling experiment Prins-type mechanism.

10.1002/chem.200500447 article EN Chemistry - A European Journal 2005-09-15

Ultra Violet (UV) radiation induces reactive oxygen species (ROS) production, DNA oxidation and single strand breaks (SSBs), which will eventually lead to skin cell damages or even cancer. Here, we tested the potential activity of gremlin, a novel vascular endothelial growth factor (VEGF) receptor 2 (VEGFR2) agonist, against UV-induced damages. We show that gremlin activated VEGFR2 significantly inhibited death apoptosis keratinocytes fibroblasts. Pharmacological inhibition shRNA-mediated...

10.18632/oncotarget.12454 article EN Oncotarget 2016-10-04

Postoperative cognitive dysfunction (POCD) is a common complication in elderly patients who undergo surgery involving anesthesia. Its underlying mechanisms remain unclear. Autophagy plays an important role the damage and repair of nervous system associated with development POCD. Using rat model, adenosine monophosphate-activated protein kinase α1 (AMPKα1), autophagy regulator, was found to be significantly downregulated rats POCD that induced by sevoflurane anesthesia or appendectomy....

10.1002/jcb.28443 article EN Journal of Cellular Biochemistry 2019-02-18

[reaction: see text] Pd(PPh3)4-catalyzed isomerization of MCPs 1 in acetic acid proceeds smoothly at 80 degrees C toluene to give the corresponding 1-substituted or 1,1-disubstituted dienes 2 good excellent yields under mild conditions. The plausible mechanism has been disclosed on basis a deuterium-labeling experiment.

10.1021/jo050560m article EN The Journal of Organic Chemistry 2005-06-01

Background: Although there have been many magnetic resonance spectroscopy (MRS) studies of migraine, few focused on migraines during an attack. Here, we aimed to assess metabolite changes in the brain patients with both attack and interictal phase. Methods: Six (one man five women, mean age: 39 ± 10 years) migraine without aura (MWoA-DA), 13 (three men 31 9 period (MWoA-DI), healthy controls (HC) (four nine were studied. All subjects underwent MRS examination focusing occipital lobe....

10.3389/fneur.2021.656349 article EN cc-by Frontiers in Neurology 2021-05-20

Two new steroid saponins, named terrestrinins A (1) and B (2), along with six known compounds were isolated from the Chinese medicine herb Tribulus terrestris, their chemical structures elucidated as 26-O-beta-D-glucopyranosyl-(25S)-furostan-4(5),20(22)-diene-3,12-dione 26-O-beta-D-glucopyranosyl-(25S)-5alpha-furostane-3beta,22alpha,26-triol-3-O-beta-D-xylopyranosyl(1 --> 3)-[(beta-D-xylopyranosyl(1 2)]-beta-D-glucopyranosyl(1 4)-[alpha-L-rhamnopyranosyl(1 2)]-beta-D-galactopyranoside (2) on...

10.1080/1028602031000111996 article EN Journal of Asian Natural Products Research 2003-10-02

A new class of C(6)-indole substituted celastrol derivatives were designed and synthesized. Among all these synthesized molecules, compound<bold>4f</bold>and<bold>4h</bold>displayed excellent<italic>in vitro</italic>antiproliferative activities against Bel7402 cancer cells.

10.1039/c4ra15414b article EN RSC Advances 2015-01-01

To investigate the effects of liraglutide combined with insulin on oxidative stress and expression levels serum monocyte chemoattractant protein-1 (MCP-1) nuclear factor-kB (NF-kB) in patients type 2 diabetes.An experimental study.Department Endocrinology, Second Hospital Affiliated to Lanzhou University, China, from September 2016 January 2018.Ninety-two diabetes were selected as objects study. They randomly divided into observation group control group, 46 cases each group. The was treated...

10.29271/jcpsp.2019.03.218 article EN Journal of College of Physicians And Surgeons Pakistan 2019-03-01

Melanoma is known as the most aggressive and lethal type of cutaneous cancer due to its rapid development drug resistance chemotherapy drugs.In our study, we conducted a variety studies, including quantitative PCR, Western blot, autophagy apoptosis assays investigate involvement miR-26a HMGB1 in modulation dabrafenib sensitivity human melanoma cell lines.Our studies revealed that expressions were altered two lines after treatment. Additionally, caused this autophagic process was regulated by...

10.2147/dddt.s225671 article EN cc-by-nc Drug Design Development and Therapy 2019-10-01
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