Lista de obras - Nor Hadiani Ismail - Dominio Público Uruguay

(E)-2,4-Dimethyl-N'-(2-methyl-benzyl-idene)benzohydrazide.

artículo científico publicado en 2013

(E)-2-Meth-oxy-N'-(2,4,6-trihy-droxy-benzyl-idene)benzohydrazide.

artículo científico publicado en 2013

(E)-4-Meth-oxy-N'-(3,4,5-trihy-droxy-benzyl-idene)benzohydrazide methanol monosolvate.

artículo científico publicado en 2012

(E)-N'-(3,4-Dihy-droxy-benzyl-idene)-2,4-dimethyl-benzohydrazide monohydrate.

artículo científico publicado en 2013

(E)-N'-(3,4-Dimeth-oxy-benzyl-idene)-4-meth-oxy-benzohydrazide.

artículo científico publicado en 2012

(E)-N'-(4-Chloro-benzyl-idene)-2-meth-oxy-benzohydrazide.

artículo científico publicado en 2013

1,3-Dihydr-oxy-2-methoxy-methyl-9,10-anthraquinone from Rennellia elliptica Korth

artículo científico publicado en 2009

1,3-Dihydr-oxy-9,10-dioxo-9,10-di-hydro-anthracene-2-carbaldehyde.

artículo científico publicado en 2008

1-Hydr-oxy-2-meth-oxy-6-methyl-9,10-anthraquinone from Rennellia elliptica Korth

artículo científico publicado en 2009

1-Meth-oxy-4-methyl-9,10-anthraquinone

artículo científico publicado en 2011

2-Formyl-3-hydr-oxy-9,10-anthroquinone.

artículo científico publicado en 2008

2-{[2-(2-Hy-droxy-5-meth-oxy-benzyl-idene)hydrazin-1-yl-idene]meth-yl}-4-meth-oxy-phenol.

artículo científico publicado en 2014

3,4-Dimethoxybenzohydrazide derivatives as antiulcer: Molecular modeling and density functional studies.

artículo científico publicado en 2017

3-Acetyl-5-hydroxy-2-methylanthra[1,2-b]furan-6,11-dione ⬇️

artículo científico publicado el 16 de abril de 2011

3-[2-(Triphenyl-phosphanyl-idene)acet-yl]-2H-chromen-2-one.

artículo científico publicado en 2013

4-Phenylcoumarins from Mesua elegans with acetylcholinesterase inhibitory activity.

artículo científico publicado en 2010

5-Bromo-2-aryl benzimidazole derivatives as non-cytotoxic potential dual inhibitors of α-glucosidase and urease enzymes.

artículo científico publicado en 2017

6-[(2E)-3,7-Dimethyl-octa-2,6-dien-1-yl]-5,7-dihy-droxy-8-(2-methyl-butano-yl)-4-phenyl-2H-chromen-2-one-6-[(2E)-3,7-dimethyl-octa-2,6-dien-1-yl]-5,7-dihy-droxy-8-(3-methyl-butano-yl)-4-phenyl-2H-chromen-2-one (1/1) from Mesua elegans

artículo científico publicado en 2012

A Review of Bisindolylmethane as an Important Scaffold for Drug Discovery

artículo científico

A new xanthone from Garcinia nitida

artículo científico publicado en 2011

Acclimatisation-induced stress influenced host metabolic and gut microbial composition change.

artículo científico publicado en 2014

Alkaloids from Fissistigma latifolium (Dunal) Merr. ⬇️

artículo científico publicado en 2010

Anthraquinones with antiplasmodial activity from the roots of Rennellia elliptica Korth. (Rubiaceae). ⬇️

artículo científico publicado en 2010

Antioxidant properties of phenolic Schiff bases: structure-activity relationship and mechanism of action.

artículo científico publicado en 2013

Antiviral, cyototoxic and antimicrobial activities of anthraquinones isolated from the roots of morinda elliptica. ⬇️

artículo científico publicado en 2000

Benzimidazole derivatives as new α-glucosidase inhibitors and in silico studies.

artículo científico publicado en 2015

Benzimidazole derivatives protect against cytokine-induced apoptosis in pancreatic β-Cells

artículo científico publicado en 2015

Biology-oriented drug synthesis (BIODS) of 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl ether derivatives, in vitro α-amylase inhibitory activity and in silico studies.

artículo científico publicado en 2017

Biology-oriented drug synthesis (BIODS): In vitro β-glucuronidase inhibitory and in silico studies on 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl carboxylate derivatives.

artículo científico publicado en 2016

Chemical characterizations dataset of flavonoid glycoside isomers and other constituents from Ficus deltoidea Jack

artículo científico publicado en 2024

Combinatorial Cytotoxic Effects of Damnacanthal and Doxorubicin against Human Breast Cancer MCF-7 Cells in Vitro.

artículo científico publicado en 2016

Comparative Study of the Volatile Components of Fresh and Fermented Flowers of Alnus sieboldiana (Betulaceae).

artículo científico publicado en 2016

Damnacanthal is a potent inducer of apoptosis with anticancer activity by stimulating p53 and p21 genes in MCF-7 breast cancer cells.

artículo científico publicado en 2014

Dihydropyrimidones: As novel class of β-glucuronidase inhibitors.

artículo científico publicado en 2016

Effects of Damnacanthal and Nordamnacanthal on Proliferation, Apoptosis, and Migration of Oral Squamous Cell Carcinoma Cells

artículo científico publicado en 2017

Evaluation of 2-indolcarbohydrazones as potent α-glucosidase inhibitors, in silico studies and DFT based stereochemical predictions.

artículo científico publicado en 2015

Goniolanceolatins A-H, Cytotoxic Bis-styryllactones from Goniothalamus lanceolatus

scientific article published on 21 August 2019

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

scientific article published on 24 March 2016

Hydrazinyl arylthiazole based pyridine scaffolds: Synthesis, structural characterization, in vitro α-glucosidase inhibitory activity, and in silico studies.

artículo científico publicado en 2017

In silico binding analysis and SAR elucidations of newly designed benzopyrazine analogs as potent inhibitors of thymidine phosphorylase.

artículo científico publicado en 2016

Inhibition of prostaglandin E(2) production by synthetic minor prenylated chalcones and flavonoids: synthesis, biological activity, crystal structure, and in silico evaluation

artículo científico publicado en 2014

Malaysianol A, a new trimer resveratrol oligomer from the stem bark of Dryobalanops aromatica.

artículo científico publicado en 2011

Medicinal uses, phytochemistry and pharmacology of Pongamia pinnata (L.) Pierre: a review.

artículo científico publicado en 2013

Methyl (E)-3,5-dimeth-oxy-2-{[2-(4-meth-oxy-benzo-yl)hydrazin-1-yl-idene]meth-yl}benzoate.

artículo científico publicado en 2012

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

artículo científico publicado en 2017

N'-[(E)-2,3-Dihy-droxy-benzyl-idene]-2-meth-oxy-benzohydrazide.

artículo científico publicado en 2012

N'-[(E)-2-Hy-droxy-5-meth-oxy-benzyl-idene]-2-meth-oxy-benzohydrazide.

artículo científico publicado en 2012

Nordamnacanthal potentiates the cytotoxic effects of tamoxifen in human breast cancer cells.

artículo científico publicado en 2014

Novel 2,5-disubtituted-1,3,4-oxadiazoles with benzimidazole backbone: a new class of β-glucuronidase inhibitors and in silico studies.

artículo científico publicado en 2015

Phenoxyacetohydrazide Schiff bases: β-glucuronidase inhibitors

artículo científico publicado en 2014

Rauniticine-allo-oxindole B and rauniticinic-allo acid B, new heteroyohimbine-type oxindole alkaloids from the stems of Malaysian Uncaria longiflora var. pteropoda ⬇️

artículo científico publicado en 2011

Rauniticine-allo-oxindole B methanol monosolvate.

artículo científico publicado en 2011

Subchronic toxicity, immunoregulation and anti-breast tumor effect of Nordamnacantal, an anthraquinone extracted from the stems of Morinda citrifolia L.

artículo científico publicado en 2018

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

artículo científico publicado en 2016

Synthesis and biological evaluation of indole derivatives as α-amylase inhibitor

artículo científico publicado en 2017

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

artículo científico publicado en 2016

Synthesis and in silico studies of novel sulfonamides having oxadiazole ring: As β-glucuronidase inhibitors.

artículo científico publicado en 2017

Synthesis and molecular modelling studies of phenyl linked oxadiazole-phenylhydrazone hybrids as potent antileishmanial agents.

artículo científico publicado en 2016

Synthesis of 2-methoxybenzoylhydrazone and evaluation of their antileishmanial activity

artículo científico publicado en 2013

Synthesis of 3,4,5-trihydroxybenzohydrazone and evaluation of their urease inhibition potential

Synthesis of 4-methoxybenzoylhydrazones and evaluation of their antiglycation activity

artículo científico publicado en 2014

Synthesis of 6-chloro-2-Aryl-1H-imidazo[4,5-b]pyridine derivatives: Antidiabetic, antioxidant, β-glucuronidase inhibiton and their molecular docking studies

artículo científico publicado en 2016

Synthesis of alpha amylase inhibitors based on privileged indole scaffold

artículo científico publicado en 2017

Synthesis of benzimidazole derivatives as potent β-glucuronidase inhibitors

artículo científico publicado en 2015

Synthesis of indole analogs as potent β-glucuronidase inhibitors.

artículo científico publicado en 2017

Synthesis of new oxadiazole derivatives as α-glucosidase inhibitors

scientific article published on 02 July 2015

Synthesis of novel benzohydrazone-oxadiazole hybrids as β-glucuronidase inhibitors and molecular modeling studies

scientific article published on 26 October 2015

Synthesis of novel bisindolylmethane Schiff bases and their antibacterial activity.

artículo científico publicado en 2014

Synthesis of novel bisindolylmethanes: New carbonic anhydrase II inhibitors, docking, and 3D pharmacophore studies.

artículo científico publicado en 2016

Synthesis of novel derivatives of 4-methylbenzimidazole and evaluation of their biological activities.

artículo científico publicado en 2014

Synthesis of novel derivatives of oxindole, their urease inhibition and molecular docking studies

artículo científico publicado en 2015

Synthesis of novel disulfide and sulfone hybrid scaffolds as potent β-glucuronidase inhibitor.

artículo científico publicado en 2016

Synthesis of novel flavone hydrazones: in-vitro evaluation of α-glucosidase inhibition, QSAR analysis and docking studies.

artículo científico publicado en 2015

Synthesis of novel inhibitors of α-glucosidase based on the benzothiazole skeleton containing benzohydrazide moiety and their molecular docking studies

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Synthesis of potent urease inhibitors based on disulfide scaffold and their molecular docking studies.

artículo científico publicado en 2015

Synthesis of unsymmetrical monocarbonyl curcumin analogues with potent inhibition on prostaglandin E2 production in LPS-induced murine and human macrophages cell lines.

artículo científico publicado en 2016

Synthesis, biological evaluation, and docking studies of novel thiourea derivatives of bisindolylmethane as carbonic anhydrase II inhibitor

artículo científico publicado en 2015

Synthesis, crystal structure, DFT studies and evaluation of the antioxidant activity of 3,4-dimethoxybenzenamine schiff bases.

artículo científico publicado en 2014

Synthesis, evaluation of antioxidant activity and crystal structure of 2,4-dimethylbenzoylhydrazones.

artículo científico publicado en 2013

Synthesis, in vitro evaluation and molecular docking studies of biscoumarin thiourea as a new inhibitor of α-glucosidases

artículo científico publicado en 2015

Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking studies of new thiazole derivatives

artículo científico publicado en 2016

Synthesis, in vitro β-glucuronidase inhibitory activity and in silico studies of novel (E)-4-Aryl-2-(2-(pyren-1-ylmethylene)hydrazinyl)thiazoles.

artículo científico publicado en 2016

Synthesis, in vitro β-glucuronidase inhibitory potential and molecular docking studies of quinolines

artículo científico publicado en 2017

Synthesis, molecular docking and α-glucosidase inhibition of 5-aryl-2-(6'-nitrobenzofuran-2'-yl)-1,3,4-oxadiazoles

artículo científico publicado en 2016

Synthesis, molecular docking studies of hybrid benzimidazole as α-glucosidase inhibitor

artículo científico publicado en 2016

Synthesis, α-glucosidase inhibitory activity and in silico study of tris-indole hybrid scaffold with oxadiazole ring: As potential leads for the management of type-II diabetes mellitus.

artículo científico publicado en 2017

Synthesis, α-glucosidase inhibitory, cytotoxicity and docking studies of 2-aryl-7-methylbenzimidazoles

artículo científico publicado en 2016

Synthesis, β-glucuronidase inhibition and molecular docking studies of hybrid bisindole-thiosemicarbazides analogs

artículo científico publicado en 2016

Synthesis,In vitroand Docking Studies of New Flavone Ethers asα-Glucosidase Inhibitors

artículo científico publicado en 2015

Thiadiazole derivatives as New Class of β-glucuronidase inhibitors.

artículo científico publicado en 2016

UV/Visible spectra of a series of natural and synthesised anthraquinones: experimental and quantum chemical approaches

artículo científico publicado en 2014

Xanthones from Garcinia mangostana (Guttiferae).

artículo científico publicado en 2006

Lista de obras de Nor Hadiani Ismail

(E)-2,4-Dimethyl-N'-(2-methyl-benzyl-idene)benzohydrazide.

(E)-2-Meth-oxy-N'-(2,4,6-trihy-droxy-benzyl-idene)benzohydrazide.

(E)-4-Meth-oxy-N'-(3,4,5-trihy-droxy-benzyl-idene)benzohydrazide methanol monosolvate.

(E)-N'-(3,4-Dihy-droxy-benzyl-idene)-2,4-dimethyl-benzohydrazide monohydrate.

(E)-N'-(3,4-Dimeth-oxy-benzyl-idene)-4-meth-oxy-benzohydrazide.

(E)-N'-(4-Chloro-benzyl-idene)-2-meth-oxy-benzohydrazide.

1,3-Dihydr-oxy-2-methoxy-methyl-9,10-anthraquinone from Rennellia elliptica Korth

1,3-Dihydr-oxy-9,10-dioxo-9,10-di-hydro-anthracene-2-carbaldehyde.

1-Hydr-oxy-2-meth-oxy-6-methyl-9,10-anthraquinone from Rennellia elliptica Korth

1-Meth-oxy-4-methyl-9,10-anthraquinone

2-Formyl-3-hydr-oxy-9,10-anthroquinone.

2-{[2-(2-Hy-droxy-5-meth-oxy-benzyl-idene)hydrazin-1-yl-idene]meth-yl}-4-meth-oxy-phenol.

3,4-Dimethoxybenzohydrazide derivatives as antiulcer: Molecular modeling and density functional studies.

3-Acetyl-5-hydroxy-2-methylanthra[1,2-b]furan-6,11-dione ⬇️

3-[2-(Triphenyl-phosphanyl-idene)acet-yl]-2H-chromen-2-one.

4-Phenylcoumarins from Mesua elegans with acetylcholinesterase inhibitory activity.

5-Bromo-2-aryl benzimidazole derivatives as non-cytotoxic potential dual inhibitors of α-glucosidase and urease enzymes.

6-[(2E)-3,7-Dimethyl-octa-2,6-dien-1-yl]-5,7-dihy-droxy-8-(2-methyl-butano-yl)-4-phenyl-2H-chromen-2-one-6-[(2E)-3,7-dimethyl-octa-2,6-dien-1-yl]-5,7-dihy-droxy-8-(3-methyl-butano-yl)-4-phenyl-2H-chromen-2-one (1/1) from Mesua elegans

A Review of Bisindolylmethane as an Important Scaffold for Drug Discovery

A new xanthone from Garcinia nitida

Acclimatisation-induced stress influenced host metabolic and gut microbial composition change.

Alkaloids from Fissistigma latifolium (Dunal) Merr. ⬇️

Anthraquinones with antiplasmodial activity from the roots of Rennellia elliptica Korth. (Rubiaceae). ⬇️

Antioxidant properties of phenolic Schiff bases: structure-activity relationship and mechanism of action.

Antiviral, cyototoxic and antimicrobial activities of anthraquinones isolated from the roots of morinda elliptica. ⬇️

Benzimidazole derivatives as new α-glucosidase inhibitors and in silico studies.

Benzimidazole derivatives protect against cytokine-induced apoptosis in pancreatic β-Cells

Biology-oriented drug synthesis (BIODS) of 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl ether derivatives, in vitro α-amylase inhibitory activity and in silico studies.

Biology-oriented drug synthesis (BIODS): In vitro β-glucuronidase inhibitory and in silico studies on 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl carboxylate derivatives.

Chemical characterizations dataset of flavonoid glycoside isomers and other constituents from Ficus deltoidea Jack

Combinatorial Cytotoxic Effects of Damnacanthal and Doxorubicin against Human Breast Cancer MCF-7 Cells in Vitro.

Comparative Study of the Volatile Components of Fresh and Fermented Flowers of Alnus sieboldiana (Betulaceae).

Damnacanthal is a potent inducer of apoptosis with anticancer activity by stimulating p53 and p21 genes in MCF-7 breast cancer cells.

Dihydropyrimidones: As novel class of β-glucuronidase inhibitors.

Effects of Damnacanthal and Nordamnacanthal on Proliferation, Apoptosis, and Migration of Oral Squamous Cell Carcinoma Cells

Evaluation of 2-indolcarbohydrazones as potent α-glucosidase inhibitors, in silico studies and DFT based stereochemical predictions.

Goniolanceolatins A-H, Cytotoxic Bis-styryllactones from Goniothalamus lanceolatus

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

Hydrazinyl arylthiazole based pyridine scaffolds: Synthesis, structural characterization, in vitro α-glucosidase inhibitory activity, and in silico studies.

In silico binding analysis and SAR elucidations of newly designed benzopyrazine analogs as potent inhibitors of thymidine phosphorylase.

Inhibition of prostaglandin E(2) production by synthetic minor prenylated chalcones and flavonoids: synthesis, biological activity, crystal structure, and in silico evaluation

Malaysianol A, a new trimer resveratrol oligomer from the stem bark of Dryobalanops aromatica.

Medicinal uses, phytochemistry and pharmacology of Pongamia pinnata (L.) Pierre: a review.

Methyl (E)-3,5-dimeth-oxy-2-{[2-(4-meth-oxy-benzo-yl)hydrazin-1-yl-idene]meth-yl}benzoate.

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

N'-[(E)-2,3-Dihy-droxy-benzyl-idene]-2-meth-oxy-benzohydrazide.

N'-[(E)-2-Hy-droxy-5-meth-oxy-benzyl-idene]-2-meth-oxy-benzohydrazide.

Nordamnacanthal potentiates the cytotoxic effects of tamoxifen in human breast cancer cells.

Novel 2,5-disubtituted-1,3,4-oxadiazoles with benzimidazole backbone: a new class of β-glucuronidase inhibitors and in silico studies.

Phenoxyacetohydrazide Schiff bases: β-glucuronidase inhibitors

Rauniticine-allo-oxindole B and rauniticinic-allo acid B, new heteroyohimbine-type oxindole alkaloids from the stems of Malaysian Uncaria longiflora var. pteropoda ⬇️

Rauniticine-allo-oxindole B methanol monosolvate.

Subchronic toxicity, immunoregulation and anti-breast tumor effect of Nordamnacantal, an anthraquinone extracted from the stems of Morinda citrifolia L.

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

Synthesis and biological evaluation of indole derivatives as α-amylase inhibitor

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

Synthesis and in silico studies of novel sulfonamides having oxadiazole ring: As β-glucuronidase inhibitors.

Synthesis and molecular modelling studies of phenyl linked oxadiazole-phenylhydrazone hybrids as potent antileishmanial agents.

Synthesis of 2-methoxybenzoylhydrazone and evaluation of their antileishmanial activity

Synthesis of 3,4,5-trihydroxybenzohydrazone and evaluation of their urease inhibition potential

Synthesis of 4-methoxybenzoylhydrazones and evaluation of their antiglycation activity

Synthesis of 6-chloro-2-Aryl-1H-imidazo[4,5-b]pyridine derivatives: Antidiabetic, antioxidant, β-glucuronidase inhibiton and their molecular docking studies

Synthesis of alpha amylase inhibitors based on privileged indole scaffold

Synthesis of benzimidazole derivatives as potent β-glucuronidase inhibitors

Synthesis of indole analogs as potent β-glucuronidase inhibitors.

Synthesis of new oxadiazole derivatives as α-glucosidase inhibitors

Synthesis of novel benzohydrazone-oxadiazole hybrids as β-glucuronidase inhibitors and molecular modeling studies

Synthesis of novel bisindolylmethane Schiff bases and their antibacterial activity.

Synthesis of novel bisindolylmethanes: New carbonic anhydrase II inhibitors, docking, and 3D pharmacophore studies.

Synthesis of novel derivatives of 4-methylbenzimidazole and evaluation of their biological activities.

Synthesis of novel derivatives of oxindole, their urease inhibition and molecular docking studies

Synthesis of novel disulfide and sulfone hybrid scaffolds as potent β-glucuronidase inhibitor.

Synthesis of novel flavone hydrazones: in-vitro evaluation of α-glucosidase inhibition, QSAR analysis and docking studies.

Synthesis of novel inhibitors of α-glucosidase based on the benzothiazole skeleton containing benzohydrazide moiety and their molecular docking studies

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

Synthesis of potent urease inhibitors based on disulfide scaffold and their molecular docking studies.

Synthesis of unsymmetrical monocarbonyl curcumin analogues with potent inhibition on prostaglandin E2 production in LPS-induced murine and human macrophages cell lines.

Synthesis, biological evaluation, and docking studies of novel thiourea derivatives of bisindolylmethane as carbonic anhydrase II inhibitor

Synthesis, crystal structure, DFT studies and evaluation of the antioxidant activity of 3,4-dimethoxybenzenamine schiff bases.