Xiaojie Jin

ORCID: 0000-0002-1467-6269
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About
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Research Areas
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Natural product bioactivities and synthesis
  • Cancer-related molecular mechanisms research
  • Phytochemistry and Biological Activities
  • MicroRNA in disease regulation
  • Molecular Sensors and Ion Detection
  • Sesquiterpenes and Asteraceae Studies
  • Crystallography and molecular interactions
  • Circular RNAs in diseases
  • Microbial Natural Products and Biosynthesis
  • Computational Drug Discovery Methods
  • RNA modifications and cancer
  • Redox biology and oxidative stress
  • Pharmacological Effects of Natural Compounds
  • Synthesis of Organic Compounds
  • Luminescence and Fluorescent Materials
  • Traditional Chinese Medicine Analysis
  • Catalytic C–H Functionalization Methods
  • Synthesis of Indole Derivatives
  • Biological Activity of Diterpenoids and Biflavonoids
  • Genomics, phytochemicals, and oxidative stress
  • Thyroid Cancer Diagnosis and Treatment
  • Oxidative Organic Chemistry Reactions
  • Plant Toxicity and Pharmacological Properties

Gansu University of Traditional Chinese Medicine
2019-2025

Ministry of Education of the People's Republic of China
2024

Nanchang University
2024

Renji Hospital
2000-2020

Lanzhou City University
2016-2020

Shanghai Jiao Tong University
2017

Lanzhou University
2011-2016

State Council of the People's Republic of China
2016

State Key Laboratory of Applied Organic Chemistry
2012-2014

Beijing Forestry University
2011

Trichalcogenasumanenes were synthesized on a multigram scale through two-step approach that takes advantage of non-pyrolytic cyclization and solventless ring contraction. Solid-state structure photophysical investigations demonstrate these compounds are promising candidates for electronic materials.

10.1002/anie.201308781 article EN Angewandte Chemie International Edition 2013-11-25

The well-known 8-aminoquinoline framework offers an ideal model for the development of fluorescence-enhanced chemosensors through simple and convenient syntheses. Herein, a novel molecule chemosensor, 5-diethylamino-2-(quinolin-8-yliminomethyl)-phenol (HL), has been designed by combining moiety 4-(diethylamino)salicylaldehyde in single to prove selectivity sensitivity Mg2+, Zn2+, Co2+ dual-channel mode (fluorescence emission UV/Vis). When binding HL not only showed obvious fluorescence...

10.1039/c3dt52618f article EN Dalton Transactions 2013-11-05

Traditional Chinese medicine (TCM) has been extensively employed for the treatment of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome 2 (SARS-CoV-2). However, there is demand discovering more SARS-CoV-2 Mpro inhibitors with diverse scaffolds to optimize anti-SARS-CoV-2 lead compounds. In this study, comprehensive in silico and vitro assays were utilized determine potential from TCM compounds against Mpro, which an important therapeutic target SARS-CoV-2. The...

10.1021/acs.jcim.3c01327 article EN Journal of Chemical Information and Modeling 2024-02-12

The rapid emergence of cross-resistance to the integrase strand transfer inhibitors (INSTIs) has become a serious problem in therapy human immunodeficiency virus type 1 (HIV-1) infection. Understanding detailed molecular mechanism INSTIs is therefore critical for development new effective against cross-resistance. On basis homology modeling constructed structure tetrameric HIV-1 intasome, mutation E138K/Q148K three important (Raltegravir (RAL, FDA approved 2007), Elvitegravir (EVG, 2012),...

10.1021/ci300541c article EN Journal of Chemical Information and Modeling 2012-12-11

Recent advances in nanotechnologies have led to wide use of nanomaterials biomedical field. However, nanoparticles are found interfere with protein misfolding and aggregation associated many human diseases. It is still a controversial issue whether inhibit or promote aggregation. In this study, we used molecular dynamics simulations explore the effects three kinds carbon including graphene, nanotube C₆₀ on behavior islet amyloid polypeptide fragment 22-28 (IAPP₂₂₋₂₈). The diverse behaviors...

10.1371/journal.pone.0065579 article EN cc-by PLoS ONE 2013-06-05

Fusarium, a large genus of filamentous fungi, is widely distributed in soil and plants. Fusarium prolific source novel chemical constituents with various bioactivities. In search for antibiotics from endophytic the secondary metabolites avenaceum SF-1502 proliferatum AF-04 were investigated. An alkaloid (1), depsipeptide (6), five sesquiterpenoids (7–11) isolated extracts fungus F. SF-1502. Three alkaloids (2–4), (5), three (9, 11, 12), sesterterpene (13), four 1,4-naphthoquinones (14–17)...

10.1021/acs.jafc.8b05576 article EN Journal of Agricultural and Food Chemistry 2019-01-28

Background: PARP1 (poly ADP-ribose polymerase 1, also known as ADPRT1) plays a significant role in DNA repair and has become an attractive target for treating PARP1-related diseases, such cancer. Objective: This study aimed to discover inhibitors targeting from the phytochemicals of Huangbai (Phellodendron chinense Schneid.), Baixianpi (Dictamnus dasycarpus Turcz.), Shechuangzi (Cnidium monnieri (L.) Spreng.). Methods: The chemical compositions Huangbai, Baixianpi, were extracted HERB...

10.2174/0115734064350048241121110017 article EN Medicinal Chemistry 2025-02-07

Caffeic acid (CA) is a prevalent polyphenolic compound commonly found in various plant-derived foods. Due to its diverse pharmacological properties, including antioxidant activity, cardiovascular protection, and immune regulation, CA has garnered significant attention. Ionizing radiation (IR) extensively utilized across industrial sectors, agriculture, defense applications, scientific research, clinical medicine; however, the detrimental effects of on human health cannot be ignored. IR can...

10.1016/j.brainresbull.2025.111325 article EN cc-by Brain Research Bulletin 2025-03-01

Abstract Trichalcogenasumanenes were synthesized on a multigram scale through two‐step approach that takes advantage of non‐pyrolytic cyclization and solventless ring contraction. Solid‐state structure photophysical investigations demonstrate these compounds are promising candidates for electronic materials.

10.1002/ange.201308781 article EN Angewandte Chemie 2013-11-25

A tumor-related hypoxic microenvironment can promote the proliferation of gastric cancer cells, and hypoxic-induced autophagy is main mechanism protection against hypoxia in cells. Isorhamnetin (ISO) a chemical substance derived from plants, mainly sea buckthorn. Previous studies have shown that ISO has antitumor effects, but effects environment are still unknown. In this study, we investigated mechanisms underlying ISO-induced cell death. The results show targeted PI3K blocked PI3K–AKT–mTOR...

10.1021/acs.jafc.1c02620 article EN Journal of Agricultural and Food Chemistry 2021-07-16

Five new polyketides, plakortoxides A (1) and B (2), simplextones C (3) D (4), plakorsin (5), together with six known analogues (6–11) were isolated from the South China Sea sponge Plakortis simplex. Their structures identified by spectroscopic chemical methods, including NMR, MS, IR. Experimental calculated ECD spectra modified Mosher's method used to determine absolute configurations. Structurally, both feature a butenolide coupled an epoxide moiety, while consist of γ-butyrolactone...

10.1021/np300771p article EN Journal of Natural Products 2013-03-25

Cutaneous melanoma is a highly malignant skin tumor, and most patients have poor prognosis. In recent years, immunotherapy has assumed an important role in the treatment of advanced cutaneous melanoma, but only small percentage benefit from immunotherapy. A growing number studies demonstrated that prognosis with closely related to long non-coding RNA tumor immune microenvironment.We downloaded expression data immune-related gene lists separately The Cancer Genome Atlas database ImmPort...

10.2147/ijgm.s335266 article EN cc-by-nc International Journal of General Medicine 2021-10-01

The Huashi Baidu Formula (HSBDF), a key Chinese medical drug, has remarkable clinical efficacy in treating acute lung injury (ALI), and it been officially approved by the National Medical Products Administration of China for drug trials. Nevertheless, regulated mechanisms HSBDF its active compounds plasma against ALI were rarely studied. Based on these considerations, anti-inflammatory screened molecular docking binding free energy. further identified LC/MS. Network pharmacology was employed...

10.3389/fphar.2022.879268 article EN cc-by Frontiers in Pharmacology 2022-06-02
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