Metabolites Annotation of Dichloromethane Extract of Kibatalia maingayi Woods using Orbitrap High-Resolution Mass Spectrometry

由 Abd Karim H.A., Rasol N.E., Ismail N.H., Wiart C., Osman C.P.
发表在 Malaysian Journal of Chemistry (2022)

Evaluation of a series of 9,10-anthraquinones as antiplasmodial agents

由 Osman C.P.; Ismail N.H.; Widyawaruyanti A.; Imran S.; Tumewu L.; Choo C.Y.; Ideris S.
发表在 Letters in Drug Design and Discovery (2019)

Molecular hybridization conceded exceptionally potent quinolinyl-oxadiazole hybrids through phenyl linked thiosemicarbazide antileishmanial scaffolds: In silico validation and SAR...

由 Taha M.; Ismail N.H.; Ali M.; Rashid U.; Imran S.; Uddin N.; Khan K.M.
发表在 Bioorganic Chemistry (2017)

Syntheses of new 3-thiazolyl coumarin derivatives, in vitro α-glucosidase inhibitory activity, and molecular modeling studies

由 Salar U.; Taha M.; Khan K.M.; Ismail N.H.; Imran S.; Perveen S.; Gul S.; Wadood A.
发表在 European Journal of Medicinal Chemistry (2016)

Synthesis of 2-(2-methoxyphenyl)-5-phenyl-1,3,4-oxadiazole derivatives and evaluation of their antiglycation potential

由 Taha M.; Ismail N.H.; Jamil W.; Imran S.; Rahim F.; Kashif S.M.; Zulkefeli M.
发表在 Medicinal Chemistry Research (2016)

Hybrid benzothiazole analogs as antiurease agent: Synthesis and molecular docking studies

由 Taha M.; Ismail N.H.; Imran S.; Wadood A.; Rahim F.; Khan K.M.; Riaz M.
发表在 Bioorganic Chemistry (2016)

Novel quinoline derivatives as potent in vitro α-glucosidase inhibitors: In silico studies and SAR predictions

由 Taha M.; Ismail N.H.; Imran S.; Wadood A.; Rahim F.; Ali M.; Rehman A.U.
发表在 MedChemComm (2015)

Synthesis of new oxadiazole derivatives as α-glucosidase inhibitors

由 Taha M.; Ismail N.H.; Imran S.; Rokei M.Q.B.; Saad S.M.; Khan K.M.
发表在 Bioorganic and Medicinal Chemistry (2015)

Thiadiazole derivatives as New Class of β-glucuronidase inhibitors

由 Salar U.; Taha M.; Ismail N.H.; Khan K.M.; Imran S.; Perveen S.; Wadood A.; Riaz M.
发表在 Bioorganic and Medicinal Chemistry (2016)

Synthesis and biological evaluation of novel N-arylidenequinoline-3-carbohydrazides as potent β-glucuronidase inhibitors

由 Taha M.; Sultan S.; Nuzar H.A.; Rahim F.; Imran S.; Ismail N.H.; Naz H.; Ullah H.
发表在 Bioorganic and Medicinal Chemistry (2016)

The metabolites of Piper sarmentosum and their biological properties: a recent update

由 Adib A.M.; Salmin N.N.; Kasim N.; Ling S.K.; Cordell G.A.; Ismail N.H.
发表在 Phytochemistry Reviews (2024)

A Comprehensive Analysis of Human CYP3A4 Crystal Structures as a Potential Tool for Molecular Docking-Based Site of Metabolism and Enzyme Inhibition Studies

由 Ridhwan M.J.M.; Bakar S.I.A.; Latip N.A.; Ghani N.A.; Ismail N.H.
发表在 Journal of Computational Biophysics and Chemistry (2022)

Synthesis of indole analogs as potent β-glucuronidase inhibitors

由 Baharudin M.S.; Taha M.; Imran S.; Ismail N.H.; Rahim F.; Javid M.T.; Khan K.M.; Ali M.
发表在 Bioorganic Chemistry (2017)

Novel thiosemicarbazide-oxadiazole hybrids as unprecedented inhibitors of yeast α-glucosidase and in silico binding analysis

由 Taha M.; Ismail N.H.; Imran S.; Wadood A.; Ali M.; Rahim F.; Khan A.A.; Riaz M.
发表在 RSC Advances (2016)

Alkaloids and Flavonoids Compositions of Traditional Medicinal Value Plants from Imbak Canyon Conservation Area (ICCA)

由 Salim F., Ismail N.H., Ghani N.Ab., Sidik N.J., Tajuddin A.M., Khalil A.K.B.
发表在 Malaysian Journal of Chemistry (2022)

Comprehensive studies of the anti-inflammatory effect of tetraprenyltoluquinone, a quinone from Garcinia cowa Roxb

由 Dewi I.P.; Dachriyanus; Aldi Y.; Ismail N.H.; Hefni D.; Susanti M.; Putra P.P.; Wahyuni F.S.
发表在 Journal of Ethnopharmacology (2024)

Lepiginosides A-D: three new triterpenoid saponins and a new farnesyl glycoside from the stembarks of Lepisanthes rubiginosa (roxb.) leenh

由 Zulkifli S.Z.; Ab Ghani N.; Rasol N.E.; Salleh W.M.N.H.W.; Ismail N.H.
发表在 Natural Product Research (2024)

Synthesis, β-glucuronidase inhibition and molecular docking studies of cyano-substituted bisindole hydrazone hybrids

由 Abid O.; Imran S.; Taha M.; Ismail N.H.; Jamil W.; Kashif S.M.; Khan K.M.; Yusoff J.
发表在 Molecular Diversity (2021)

Synthesis of piperazine sulfonamide analogs as diabetic-II inhibitors and their molecular docking study

由 Taha M.; Irshad M.; Imran S.; Chigurupati S.; Selvaraj M.; Rahim F.; Ismail N.H.; Nawaz F.; Khan K.M.
发表在 European Journal of Medicinal Chemistry (2017)

Synthesis, in vitro and Docking Studies of New Flavone Ethers as α-Glucosidase Inhibitors

由 Imran S.; Taha M.; Ismail N.H.; Kashif S.M.; Rahim F.; Jamil W.; Wahab H.; Khan K.M.
发表在 Chemical Biology and Drug Design (2016)