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Identifying Predictive Risk Factors for Future Cognitive Impairment Among Chinese Older Adults: Longitudinal Prediction Study

JMIR aging, 2024-03, Vol.7, p.e53240-e53240

2024

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Association Between Sleep Efficiency Variability and Cognition Among Older Adults: Cross-Sectional Accelerometer Study

JMIR aging, 2024-04, Vol.7, p.e54353-e54353

2024

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Organic certification and the market: organic exports from and imports to China

British food journal (1966), 2011-09, Vol.113 (10), p.1200-1216

2011

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Nonlinear relationship of vegetation greening with nature and human factors and its forecast – A case study of Southwest China

Ecological indicators, 2020-04, Vol.111, p.106009, Article 106009

2020

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Bifunctional [2‘,6‘-Dimethyl-l-tyrosine]endomorphin-2 Analogues Substituted at Position 3 with Alkylated Phenylalanine Derivatives Yield Potent Mixed μ-Agonist/δ-Antagonist and Dual μ-Agonist/δ-Agonist Opioid Ligands

Journal of medicinal chemistry, 2007-06, Vol.50 (12), p.2753-2766

2007

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Nitric oxide-donating and reactive oxygen species-responsive prochelators based on 8-hydroxyquinoline as anticancer agents

European journal of medicinal chemistry, 2021-02, Vol.212, p.113153, Article 113153

2021

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Suitability of three seaweeds as feed in culturing strawberry conch Strombus luhuanus

Aquaculture, 2020-03, Vol.519, p.734761, Article 734761

2020

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Intracerebroventricular administration of CYX-6, a potent μ-opioid receptor agonist, a δ- and κ-opioid receptor antagonist and a biased ligand at μ, δ & κ-opioid receptors, evokes antinociception with minimal constipation and respiratory depression in rats in contrast to morphine

European journal of pharmacology, 2020-03, Vol.871, p.172918, Article 172918

2020

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Differentiation of opioid receptor preference by [Dmt 1]endomorphin-2-mediated antinociception in the mouse

European journal of pharmacology, 2005-02, Vol.509 (1), p.37-42

2005

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Enantioselective Synthesis of a Phenylalanine Library Containing Alkyl Groups on the Aromatic Moiety: Confirmation of Stereostructure by X-Ray Analysis

Chemical and Pharmaceutical Bulletin, 2006, Vol.54(6), pp.873-877

2006

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Oral Bioavailability of a New Class of μ-Opioid Receptor Agonists Containing 3,6-Bis[Dmt-NH(CH2) n ]-2(1H)-pyrazinone with Central-Mediated Analgesia

Journal of medicinal chemistry, 2004-05, Vol.47 (10), p.2599-2610

2004

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CYX-5, a G-protein biassed MOP receptor agonist, DOP receptor antagonist and KOP receptor agonist, evokes constipation but not respiratory depression relative to morphine in rats

Pharmacological reports, 2023-06, Vol.75 (3), p.634-646

2023

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Transformation of μ-opioid receptor agonists into biologically potent μ-opioid receptor antagonists

Bioorganic & medicinal chemistry, 2007-02, Vol.15 (3), p.1237-1251

2007

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Potent in vivo antinociception and opioid receptor preference of the novel analogue [Dmt 1]endomorphin-1

Pharmacology, biochemistry and behavior, 2006-06, Vol.84 (2), p.252-258

2006

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Neuroprotective Effect of N -Cyclohexylethyl-[A/G]-[D/E]-X-V Peptides on Ischemic Stroke by Blocking nNOS-CAPON Interaction

ACS chemical neuroscience, 2021-01, Vol.12 (1), p.244-255

2021

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Coordinate-Based Neural Network for Fourier Phase Retrieval

ICASSP 2024 - 2024 IEEE International Conference on Acoustics, Speech and Signal Processing (ICASSP), 2024, p.2585-2589

2024

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In Vitro Assessment of the Metabolic Stability of Two Novel Endomorphin-2 Analogs, CYX-5 and CYX-6, in Rat Liver Microsomes

European journal of drug metabolism and pharmacokinetics, 2023-07, Vol.48 (4), p.463-466

2023

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Design and synthesis of opioidmimetics containing 2′,6′-dimethyl- l-tyrosine and a pyrazinone-ring platform

Bioorganic & medicinal chemistry letters, 2007-11, Vol.17 (21), p.5768-5771

2007

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A highly dl-stereoselective pinacolization of aromatic aldehydes mediated by TiCl4–Zn

Chemical communications (Cambridge, England), 2000-01 (2), p.139-140

2000

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Synthesis of 3,6-bis[H-Tyr/H-Dmt-NH(CH 2) m, n ]-2(1 H)pyrazinone derivatives: Function of alkyl chain length on opioid activity

Bioorganic & medicinal chemistry letters, 2006-11, Vol.16 (22), p.5793-5796

2006

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Development of Potent μ-Opioid Receptor Ligands Using Unique Tyrosine Analogues of Endomorphin-2

Journal of medicinal chemistry, 2005-01, Vol.48 (2), p.586-592

2005

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[Dmt1]DALDA analogues modified with tyrosine analogues at position 1

Bioorganic & medicinal chemistry letters, 2016-08, Vol.26 (15), p.3629-3631

2016

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Development of Potent Bifunctional Endomorphin-2 Analogues with Mixed μ-/δ-Opioid Agonist and δ-Opioid Antagonist Properties

Journal of medicinal chemistry, 2004-07, Vol.47 (14), p.3591-3599

2004

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Application of liquid chromatography–tandem mass spectrometry for the determination of opioidmimetics in the brain dialysates from rats treated with opioidmimetics intraperitoneally

Journal of chromatography. B, 2004-06, Vol.806 (1), p.53-57

2004

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Novel µ opioid antagonists derived from the µ opioid agonists endomorphin and [Dmt1]DALDA (H‐Dmt‐D‐Arg‐Phe‐Lys‐NH2)

Chemical biology & drug design, 2020-11, Vol.96 (5), p.1305-1314

2020

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Identifying Predictive Risk Factors for Future Cognitive Impairment Among Chinese Older Adults: Longitudinal Prediction Study

Association Between Sleep Efficiency Variability and Cognition Among Older Adults: Cross-Sectional Accelerometer Study

Organic certification and the market: organic exports from and imports to China

Nonlinear relationship of vegetation greening with nature and human factors and its forecast – A case study of Southwest China

Bifunctional [2‘,6‘-Dimethyl-l-tyrosine]endomorphin-2 Analogues Substituted at Position 3 with Alkylated Phenylalanine Derivatives Yield Potent Mixed μ-Agonist/δ-Antagonist and Dual μ-Agonist/δ-Agonist Opioid Ligands

Nitric oxide-donating and reactive oxygen species-responsive prochelators based on 8-hydroxyquinoline as anticancer agents

Suitability of three seaweeds as feed in culturing strawberry conch Strombus luhuanus

Intracerebroventricular administration of CYX-6, a potent μ-opioid receptor agonist, a δ- and κ-opioid receptor antagonist and a biased ligand at μ, δ & κ-opioid receptors, evokes antinociception with minimal constipation and respiratory depression in rats in contrast to morphine

Differentiation of opioid receptor preference by [Dmt 1]endomorphin-2-mediated antinociception in the mouse

Enantioselective Synthesis of a Phenylalanine Library Containing Alkyl Groups on the Aromatic Moiety: Confirmation of Stereostructure by X-Ray Analysis

Oral Bioavailability of a New Class of μ-Opioid Receptor Agonists Containing 3,6-Bis[Dmt-NH(CH2) n ]-2(1H)-pyrazinone with Central-Mediated Analgesia

CYX-5, a G-protein biassed MOP receptor agonist, DOP receptor antagonist and KOP receptor agonist, evokes constipation but not respiratory depression relative to morphine in rats

Transformation of μ-opioid receptor agonists into biologically potent μ-opioid receptor antagonists

Potent in vivo antinociception and opioid receptor preference of the novel analogue [Dmt 1]endomorphin-1

Neuroprotective Effect of N -Cyclohexylethyl-[A/G]-[D/E]-X-V Peptides on Ischemic Stroke by Blocking nNOS-CAPON Interaction

Coordinate-Based Neural Network for Fourier Phase Retrieval

In Vitro Assessment of the Metabolic Stability of Two Novel Endomorphin-2 Analogs, CYX-5 and CYX-6, in Rat Liver Microsomes

Design and synthesis of opioidmimetics containing 2′,6′-dimethyl- l-tyrosine and a pyrazinone-ring platform

A highly dl-stereoselective pinacolization of aromatic aldehydes mediated by TiCl4–Zn

Synthesis of 3,6-bis[H-Tyr/H-Dmt-NH(CH 2) m, n ]-2(1 H)pyrazinone derivatives: Function of alkyl chain length on opioid activity

Development of Potent μ-Opioid Receptor Ligands Using Unique Tyrosine Analogues of Endomorphin-2

[Dmt1]DALDA analogues modified with tyrosine analogues at position 1

Development of Potent Bifunctional Endomorphin-2 Analogues with Mixed μ-/δ-Opioid Agonist and δ-Opioid Antagonist Properties

Application of liquid chromatography–tandem mass spectrometry for the determination of opioidmimetics in the brain dialysates from rats treated with opioidmimetics intraperitoneally

Novel µ opioid antagonists derived from the µ opioid agonists endomorphin and [Dmt1]DALDA (H‐Dmt‐D‐Arg‐Phe‐Lys‐NH2)

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