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Age-related decline in melatonin contributes to enhanced osteoclastogenesis via disruption of redox homeostasis

Molecular medicine (Cambridge, Mass.), 2024-01, Vol.30 (1), p.10-10, Article 10

2024

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A bibliometric analysis of exertional heat stroke research in Web of Science

Military Medical Research, 2016-10, Vol.3 (1), p.31, Article 31

2016

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Tanshinone IIA attenuates osteoarthritis via inhibiting aberrant angiogenesis in subchondral bone

Archives of biochemistry and biophysics, 2024-03, Vol.753, p.109904, Article 109904

2024

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Finite element analysis of an intramedulary anatomical strut for proximal humeral fractures with disrupted medial column instability: A cohort study

International journal of surgery (London, England), 2020-01, Vol.73, p.50-56

2020

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Nonclinical pharmacokinetics and in vitro metabolism of H3B-6545, a novel selective ERα covalent antagonist (SERCA)

Cancer chemotherapy and pharmacology, 2019-01, Vol.83 (1), p.151-160

2019

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In Vitro Structure−Activity Relationship and In Vivo Characterization of 1-(Aryl)-3-(4-(amino)benzyl)urea Transient Receptor Potential Vanilloid 1 Antagonists

Journal of medicinal chemistry, 2007-07, Vol.50 (15), p.3651-3660

2007

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Tetrahydropyridine-4-carboxamides as novel, potent transient receptor potential vanilloid 1 (TRPV1) antagonists

Bioorganic & medicinal chemistry, 2008-09, Vol.16 (18), p.8516-8525

2008

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Toxic Response of Daphnia magna to Microcystis aeruginosa

Asian journal of chemistry, 2013, Vol.25 (6), p.2965-2969

2013

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Structure−Activity Relationship of Triazafluorenone Derivatives as Potent and Selective mGluR1 Antagonists

Journal of medicinal chemistry, 2005-11, Vol.48 (23), p.7374-7388

2005

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Catalytic reactions of samarium (II) iodide

Tetrahedron letters, 1997-03, Vol.38 (12), p.2045-2048

1997

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Correlation between brain/plasma ratios and efficacy in neuropathic pain models of selective metabotropic glutamate receptor 1 antagonists

Bioorganic & medicinal chemistry letters, 2006-09, Vol.16 (18), p.4936-4940

2006

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Structure–activity studies of a novel series of 5,6-fused heteroaromatic ureas as TRPV1 antagonists

Bioorganic & medicinal chemistry, 2006-07, Vol.14 (14), p.4740-4749

2006

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Dynamic response of shallow-buried circular composite lining tunnel with imperfect interface under SV waves

Waves in random and complex media, 2023-08, p.1-26

2023

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Accumulation of β-aminoisobutyric acid mediates hyperalgesia in ovariectomized mice through Mas-related G protein-coupled receptor D signaling

Biochimica et biophysica acta. Molecular basis of disease, 2024-08, Vol.1870 (6), p.167269, Article 167269

2024

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Studies on the ingestion characteristics of giant freshwater prawn, Chinese prawn and giant tiger prawn

Chinese journal of oceanology and limnology, 2000-12, Vol.18 (4), p.338-344

2000

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Covalent ERα Antagonist H3B-6545 Demonstrates Encouraging Preclinical Activity in Therapy-Resistant Breast Cancer

Molecular cancer therapeutics, 2022-06, Vol.21 (6), p.890-902

2022

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Pyridopyrimidine analogues as novel adenosine kinase inhibitors

Bioorganic & medicinal chemistry letters, 2001-08, Vol.11 (16), p.2071-2074

2001

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A Historic View of the US Business Ethical Laws and Implications for Developing Countries like China

Review of European studies, 2016-06, Vol.8 (3), p.49

2016

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Fatty acid amide hydrolase inhibitors display broad selectivity and inhibit multiple carboxylesterases as off-targets

Neuropharmacology, 2007-03, Vol.52 (4), p.1095-1105

2007

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Abstract DDT01-04: Discovery and development of H3B-6545: A novel, oral, selective estrogen receptor covalent antagonist (SERCA) for the treatment of breast cancer

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.DDT01-04-DDT01-04

2017

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Enantioselective Deprotonation of Tropinone and Reactions of Tropinone Lithium Enolate

Synlett, 1991-03, Vol.1991 (3), p.173-175

1991

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Discovery of Selective Estrogen Receptor Covalent Antagonists for the Treatment of ERα WT and ERα MUT Breast Cancer

Cancer discovery, 2018-09, Vol.8 (9), p.1176-1193

2018

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Age-related decline in melatonin contributes to enhanced osteoclastogenesis via disruption of redox homeostasis

A bibliometric analysis of exertional heat stroke research in Web of Science

Tanshinone IIA attenuates osteoarthritis via inhibiting aberrant angiogenesis in subchondral bone

Finite element analysis of an intramedulary anatomical strut for proximal humeral fractures with disrupted medial column instability: A cohort study

Nonclinical pharmacokinetics and in vitro metabolism of H3B-6545, a novel selective ERα covalent antagonist (SERCA)

In Vitro Structure−Activity Relationship and In Vivo Characterization of 1-(Aryl)-3-(4-(amino)benzyl)urea Transient Receptor Potential Vanilloid 1 Antagonists

5-(3-Bromophenyl)-7-(6-morpholin-4-ylpyridin-3-yl)pyrido[2,3-d]pyrimidin-4-ylamine: structure–activity relationships of 7-substituted heteroaryl analogs as non-nucleoside adenosine kinase inhibitors

Total Synthesis of 6‑Deoxypladienolide D and Assessment of Splicing Inhibitory Activity in a Mutant SF3B1 Cancer Cell Line

Tetrahydropyridine-4-carboxamides as novel, potent transient receptor potential vanilloid 1 (TRPV1) antagonists

Toxic Response of Daphnia magna to Microcystis aeruginosa

Structure−Activity Relationship of Triazafluorenone Derivatives as Potent and Selective mGluR1 Antagonists

Catalytic reactions of samarium (II) iodide

Correlation between brain/plasma ratios and efficacy in neuropathic pain models of selective metabotropic glutamate receptor 1 antagonists

Structure–activity studies of a novel series of 5,6-fused heteroaromatic ureas as TRPV1 antagonists

Dynamic response of shallow-buried circular composite lining tunnel with imperfect interface under SV waves

Accumulation of β-aminoisobutyric acid mediates hyperalgesia in ovariectomized mice through Mas-related G protein-coupled receptor D signaling

Studies on the ingestion characteristics of giant freshwater prawn, Chinese prawn and giant tiger prawn

Covalent ERα Antagonist H3B-6545 Demonstrates Encouraging Preclinical Activity in Therapy-Resistant Breast Cancer

Pyridopyrimidine analogues as novel adenosine kinase inhibitors

A Historic View of the US Business Ethical Laws and Implications for Developing Countries like China

Fatty acid amide hydrolase inhibitors display broad selectivity and inhibit multiple carboxylesterases as off-targets

Abstract DDT01-04: Discovery and development of H3B-6545: A novel, oral, selective estrogen receptor covalent antagonist (SERCA) for the treatment of breast cancer

Enantioselective Deprotonation of Tropinone and Reactions of Tropinone Lithium Enolate

Discovery of Selective Estrogen Receptor Covalent Antagonists for the Treatment of ERα WT and ERα MUT Breast Cancer

Novel Transient Receptor Potential Vanilloid 1 Receptor Antagonists for the Treatment of Pain: Structure−Activity Relationships for Ureas with Quinoline, Isoquinoline, Quinazoline, Phthalazine, Quinoxaline, and Cinnoline Moieties

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