Enade Perdana Istyastono

Author

Also Known As

E. Istyastono, E. P. Istyastono, ENADE PERDANA ISTYASTONO, Enade Istyastono, Enade P Istyastono, Enade P. Istyastono, Enade Perdana ISTYASTONO, Enade Perdana Istyastono, Enade Perdana PerdanIstyastono, Istyastono, Enade Perdana

112

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Sanata Dharma University Universitas Gadjah Mada Vrije Universiteit Amsterdam Atma Jaya Catholic University of Indonesia Institute of Medicinal Plant Development

About

Enade Perdana Istyastono is an author at Sanata Dharma University specializing in medicine, drug discovery, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	17	500
2	Natural Sciences	11	11	342
3	Engineering	5	5	66
4	Health Sciences	1	1	13
5	Language Studies	1	1	17

Enade Perdana Istyastono

Publications

891

Citations

H-Index

Page 1

	Year	Citations
Synthesis and QSAR of Quinazoline Sulfonamides As Highly Potent Human Histamine H<sub>4</sub> Receptor Inverse Agonists Rogier A. Smits, Maristella Adami, Enade Perdana Istyastono, Journal of Medicinal Chemistry Drug TargetPharmacotherapyChemical BiologyPharmaceutical ChemistryMolecular Pharmacology	2010	123
PyPLIF: Python-based Protein-Ligand Interaction Fingerprinting Muhammad Radifar, Nunung Yuniarti, Enade Perdana Istyastono Bioinformation	2013	68
Matrix metalloproteinase 9 (MMP9) in wound healing of diabetic foot ulcer: Molecular target and structure-based drug design Maywan Hariono, Sri Hartati Yuliani, Enade Perdana Istyastono, Wound Medicine Matrix Metalloproteinase 9MetalloproteinDiabetesLower Extremity WoundDiabetic Foot Ulcer	2018	67
Virtual Fragment Screening: Discovery of Histamine H<sub>3</sub> Receptor Ligands Using Ligand-Based and Protein-Based Molecular Fingerprints Francesco Sirci, Enade Perdana Istyastono, Henry F. Vischer, Journal of Chemical Information and Modeling Molecular PharmacologyVirtual ScreeningHit IdentificationDrug TargetBiochemistry	2012	64
Molecular Determinants of Ligand Binding to H4R Species Variants Herman D. Lim, Chris de Graaf, Wen Jiang, Molecular Pharmacology	2010	55
Molecular Determinants of Ligand Binding Modes in the Histamine H<sub>4</sub>Receptor: Linking Ligand-Based Three-Dimensional Quantitative Structure–Activity Relationship (3D-QSAR) Models to in Silico Guided Receptor Mutagenesis Studies Enade Perdana Istyastono, Saskia Nijmeijer, Herman D. Lim, Journal of Medicinal Chemistry	2011	52
Triazole Ligands Reveal Distinct Molecular Features That Induce Histamine H<sub>4</sub> Receptor Affinity and Subtly Govern H<sub>4</sub>/H<sub>3</sub> Subtype Selectivity Maikel Wijtmans, Chris de Graaf, Gerdien de Kloe, Journal of Medicinal Chemistry	2011	44
Inhibition of human glutathione<i>S</i>-transferases by curcumin and analogues Regina Appiah‐Opong, Jan N. M. Commandeur, Enade Perdana Istyastono, Xenobiotica	2009	41
Clobenpropit analogs as dual activity ligands for the histamine H3 and H4 receptors: Synthesis, pharmacological evaluation, and cross-target QSAR studies Herman D. Lim, Enade Perdana Istyastono, Andrea van de Stolpe, Bioorganic & Medicinal Chemistry Medicinal ChemistryDrug TargetAllergyMedicineMechanism Of Action	2009	34
Structure-based virtual screening for fragment-like ligands of the G protein-coupled histamine H<sub>4</sub>receptor Enade Perdana Istyastono, Albert J. Kooistra, Henry F. Vischer, MedChemComm BiochemistryBiomolecular Structure PredictionNatural SciencesMedicineStructural Bioinformatics	2015	34

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