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2022-11
Selective and antagonist-dependent µ-opioid receptor activation by the combination of 2-{[2-(6-chloro-3,4-dihydro-1(2H)-quinolinyl)-2-oxoethyl]sulfanyl}-5-phenyl-4,6-(1H,5H)-pyrimidinedione and naloxone/naltrexone
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BPRDP056, a novel small molecule drug conjugate specifically targeting phosphatidylserine for cancer therapy
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2019-07
BPRDP056, a novel small molecule drug conjugate specifically targeting phosphatidylserine for cancer therapy
Cancer Research. 2019 Jul;79(13, Suppl.):Abstract number 227.
2019-04-01
A novel, potent, and orally bioavailable thiazole HCV NS5A inhibitor for the treatment of hepatitis C virus
European Journal of Medicinal Chemistry. 2019 Apr 1;167:245-268.
2019-04-01
The in vivo antinociceptive and mu-opioid receptor activating effects of the combination of N-phenyl-2′,4′-dimethyl-4,5′-bi-1,3-thiazol-2-amines and naloxone
European Journal of Medicinal Chemistry. 2019 Apr 1;167:312-323.
2019-03
Synthesis and biological evaluation of N-glucosyl indole derivatives as sodium-dependent glucose co-transporter 2 inhibitors
Bioorganic Chemistry. 2019 Mar;83:520-525.
2018-04
4-Bromophenylhydrazinyl benzenesulfonylphenylureas as indoleamine 2,3-dioxygenase inhibitors with in vivo target inhibition and anti-tumor efficacy
Bioorganic Chemistry. 2018 Apr;77:600-607.
2018-01-01
Identification of an oxime-containing C-glucosylarene as a potential inhibitor of sodium-dependent glucose co-transporter 2
European Journal of Medicinal Chemistry. 2018 Jan 1;143:611-620.
2017-06-22
Targeting coronaviral replication and cellular JAK2 mediated dominant NF-kappaB activation for comprehensive and ultimate inhibition of coronaviral activity
Scientific Reports. 2017 Jun 22;7:Article number 4105.
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