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T 19. Suzuki T., Timofei S., Iuoras B.E., Uray G., Verdino P., Fabian W.M.

Quantitative structure-enantioselective retention relationships for chromatographic

separation of arylalkylcarbinols on Pirkle type chiral stationary phases.

J. Chromatogr. A. 922(1-2):13-23, 2001

C 33. Sievers-Engler A., Lindner W., Lämmerhofer M.

Ligand–receptor binding increments in enantioselective liquid chromatography



J. Chromatogr. A. 1363: 79–88, 2014
T 20. Funar-Timofei, S., Fabian, W.M.F., Kurunczi, L., Goodarzi, M., Ali, S.T., Heyden,

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Modelling heterocyclic azo dye affinities for cellulose fibres by computational approaches

Dyes Pigments 94(2): 278 – 289, 2012

C 34. Alencar J.M., Oliveira F.J.V.E., Airoldi C., Silva Filho E.C.

Organophilic nickel phyllosilicate for reactive blue dye removal



Chem. Eng. J. 236: 332 - 340, 2014

C 35. Valizadeh H., Shomali A., Nourshargh S., Mohammad-Rezaei R.

Carboxyl and nitrite functionalized graphene quantum dots as a highly active

reagent and catalyst for rapid diazotization reaction and synthesis of azo-dyes under

solvent-free conditions



Dyes Pigments 113: 522–528, 2015

C 36. Patel H. M., Noolvi M. N., Sharma P., Jaiswal V., Bansal S., Lohan S., Kumar S. S.,

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Quantitative structure–activity relationship (QSAR) studies as strategic approach in drug discovery

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C 37. Durán-Jiménez G., Hernández-Montoya V. , Montes-Morán,M.A., Bonilla-

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Adsorption of dyes with different molecular properties on activated carbons prepared from lignocellulosic wastes by Taguchi method

Micropor. Mesopor. Mat. 199: 99-107, 2014

C 38. Wang X.J., Sun Y.Y., Wu L., Gu S.J., Liu R.N., Liu L., Liu X., Xu J.

Quantitative structure-affinity relationship study of azo dyes for cellulose fibers by multiple linear regression and artificial neural network



Chemometr. Intell. Lab. 134: 1-9, 2014

C 39. Singh H., Sindhu J., Khurana J.M. , Sharma,C., Aneja K.R.

Syntheses, biological evaluation and photophysical studies of novel 1,2,3-triazole linked azo dyes



RSC Adv. 4(12): 5915-5926, 2014

C 40. Aguayo-Villarreal I.A., Hernandez-Montoya V. Rangel-Vazquez N.A., Montes-

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Determination of QSAR properties of textile dyes and their adsorption on novel carbonaceous adsorbents

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C 41. Bak A., Wyszomirski M., Magdziarz T., Smolinski A., Polanski J.

Structure-Based Modeling of Dye-Fiber Affinity with SOM-4D-QSAR Paradigm: Application to Set of Anthraquinone Derivatives



Comb. Chem. High. T. Scr. 17(6): 485-502, 2014
T 21. S. Funar-Timoftei, L. Crisan, S. Iliescu, G. Bandur, and E. Seclaman

Conformational analysis of an arylazo phosphate dimer by molecular and quantum mechanics approaches



Chemical Bulletin of Politehnica Timisoara University, 55(69):2–10, 2010.

C 42. Reiss A., Chifiriuc M. C., Amzoiu E., Spînu C. I.

Transition Metal(II) Complexes with Cefotaxime-Derived Schiff Base: Synthesis, Characterization, and Antimicrobial Studies



Bioinorg. Chem. Appl. 2014;2014:926287. doi: 10.1155/2014/926287. Epub 2014 Feb 12.
T 22. Fabian W. M. F., Timofei S., Kurunczi, L.

Comparative molecular field analysis (CoMFA), semiempirical (AM1) molecular orbital and multiconformational minimal steric difference (MTD) calculations of anthraquinone dye-fibre affinities.



J. Mol. Struc.-Theochem 340 (1): 73-81, 1995

C 43. Bak A., Wyszomirski M., Magdziarz T., Smolinski A., Polanski J.

Structure-Based Modeling of Dye-Fiber Affinity with SOM-4D-QSAR Paradigm: Application to Set of Anthraquinone Derivatives



Comb. Chem. High. T. Scr. 17(6): 485-502, 2014
T 23. Goodarzi M. , Bora,A., Borota A., Funar-Timofei S., Avram S., Heyden,Y.V.

Modeling of 2-pyridin-3-yl-benzo[d][1,3]oxazin-4-one derivatives by several conformational searching tools and molecular docking



Curr. Pharm. Design 19(12): 2194-2203, 2013

C 44. Montesano C., Sergi M., Perez G.

Bio-inspired solid phase extraction sorbent material for cocaine: A cross reactivity study


Talanta 130: 382-387, 2014
T 24. Obiorah I., Sengupta S., Curpan R., Jordan V.C.

Defining the Conformation of the Estrogen Receptor Complex That Controls Estrogen-Induced Apoptosis in Breast Cancer



Mol. Pharmacol. 85(5): 789-799, 2014.

C 45. Obiorah I.E., Jordan V.C.

Differences in the Rate of Oestrogen-Induced Apoptosis in Breast Cancer by Oestradiol and the Triphenylethylene Bisphenol

Brit. J Pharmacol. 171(17,S1):4062-4072, 2014.
T 25. Lewis-Wambi J.S., Kim H., Curpan R., Grigg R., Sarker M.A., Jordan V.C.

The Selective Estrogen Receptor Modulator Bazedoxifene Inhibits Hormone-Independent Breast Cancer Cell Growth and Down-Regulates Estrogen Receptor alpha and Cyclin D1



Mol. Pharmacol. 80(4):610-620, 2011.

C 46. Fan P., Agboke F.A., Cunliffe H.E., Ramos P., Jordan V.C.

A Molecular Model for the Mechanism of Acquired Tamoxifen Resistance in Breast Cancer



Eur. J. Cancer, 50(16):2866-2876, 2014.

C 47. Komm B.S., Mirkin S.

An Overview of Current and Emerging Serms



J. Steroid Biochem. Mol. Biol. 143:207-222, 2014.

C 48. Pinkerton J.V., Komm B.S., Mirkin S.

Tissue Selective Estrogen Complex Combinations with Bazedoxifene/Conjugated Estrogens as a Model



Climacteric 16(6):618-628, 2013.

C 49. Santen R.J., Kagan R., Altomare C.J., Komm B., Mirkin S., Taylor H.S.

Current and Evolving Approaches to Individualizing Estrogen Receptor-Based Therapy for Menopausal Women



J. Clin. Endocrinol. Metab. 99(3):733-747, 2014.

C 50. Shoda T., Okuhira K., Kato M., et al.

Design and Synthesis of Tamoxifen Derivatives as a Selective Estrogen Receptor Down-Regulator



Bioorg. Med. Chem. Lett. 24(1):87-89, 2014.
T 26. Maximov P.Y., Myers C.B., Curpan R.F., Lewis-Wambi J.S., Jordan V.C.

Structure-Function Relationships of Estrogenic Triphenylethylenes Related to Endoxifen and 4-Hydroxytamoxifen



J. Med. Chem. 53(8):3273-3283, 2010.

C 51. Celeste Nicolao M., Celina Elissondo M., Denegri G.M., Goya A. B., Cumino A.C.

In Vitro and In Vivo Effects of Tamoxifen against Larval Stage Echinococcus granulosus



Antimicrob. Agents Chemother. 58(9):5146–5154, 2014.

C 52. Obiorah I.E., Jordan V.C.

Differences in the Rate of Oestrogen-Induced Apoptosis in Breast Cancer by Oestradiol and the Triphenylethylene Bisphenol



Br. J. Pharmacol. 171(17,S1):4062–4072, 2014.

C53. Stokes G.Y., Conboy J.C.

Measuring Selective Estrogen Receptor Modulator (SERM)-Membrane Interactions with Second Harmonic Generation



J. Am. Chem. Soc. 136(4):1409–1417, 2014.
T 27. Burai R., Ramesh C., Shorty M., Curpan R., Bologa C., Sklar L.A., Oprea T.,

Prossnitz E.R., Arterburn J.B.

Highly Efficient Synthesis and Characterization of the GPR30-Selective Agonist G-1 and Related Tetrahydroquinoline Analogs

Org. Biomol. Chem., 8(9):2252-2259, 2010

C 54. Calleja J., Gonzalez-Perez A.B., de Lera A.R., Alvarez R., Fananas F.J., Rodriguez

Enantioselective Synthesis of Hexahydrofuro[3,2-C] Quinolines Through a Multicatalytic and Multicomponent Process. A New “Aromatic Sandwich” Model for BINOL-Phosphoric Acid Catalyzed Reactions



Chem. Sci. 5(3):996-1007, 2014.

C 55. Feldman R.D, Gros R.

Vascular Effects of Aldosterone: Sorting Out the Receptors and the Ligands



Clin. Exp. Pharmacol. Physiol. 40(12):916-921, 2013.

C 56. Ghosh M., Dhara S., Nuree Y., Ray J.K.

Synthesis of Bis-Exocyclic Conjugated Diene Containing 1,2,3,4-Tetrahydroquinoline Derivatives via Palladium-Catalyzed Intramolecular Heck Cyclization



RSC Adv. 4(78):41561-41564, 2014.

C 57. Kulkarni A.R, Thakur G.A.

Microwave-Assisted Expeditious and Efficient Synthesis of Cyclopentene Ring-Fused Tetrahydroquinoline Derivatives Using Three-Component Povarov Reaction



Tetrahedron Lett. 54(48):6592-6595, 2013.

C 58. Rodriguez F., Fananas F.J.

Constructing Molecular Complexity from Alkynol Derivatives: A Journey from Fischer Carbene Complexes to Tandem Catalysis with Gold and other Carbophilic Lewis Acids



Synlett 24(14):1757-1771, 2013.

C 59. Sarmah M.M., Prajapati D.

Aza-Diels-Alder Reaction: An Efficient Approach for Construction of Heterocycles



Curr. Org. Chem. 18(12):1586-1620, 2014.

C 60. Sarmah M.M., Prajapati D.

Exploration of Uracils: Pot and Step Economic Production of Pyridine Core Containing Templates by Multicomponent Aza-Diels-Alder Reaction



RSC Adv. 4(44):22955-22958, 2014.
T 28. Sengupta S., Obiorah I., Maximov P.Y., Curpan R., Jordan V.C.

Molecular Mechanism Of Action Of Bisphenol And Bisphenol A Mediated By Oestrogen Receptor Alpha In Growth And Apoptosis Of Breast Cancer Cells



British Journal of Pharmacology 169(1):167–178, 2013.

C 61. Fraczek T, Siwek A, Paneth P.

Assessing Molecular Docking Tools for Relative Biological Activity Prediction: A Case Study of Triazole HIV-1 NNRTIs



J. Chem. Inf. Model. 53(12):3326-3342, 2013.

C 62. Obiorah I., Sengupta S., Fan P., Jordan V.C.

Delayed Triggering of Oestrogen Induced Apoptosis that Contrasts with Rapid Paclitaxel-Induced Breast Cancer Cell Death



Br. J. Cancer 110(6):1488-1496, 2014.

C 63. Ziv-Gal A., Craig Z.R., Wang W., Flaws J.A.

Bisphenol A Inhibits Cultured Mouse Ovarian Follicle Growth Partially Via The Aryl Hydrocarbon Receptor Signaling Pathway



Reprod. Toxicol. 42:58-67, 2013.

C 64. Fan P, Agboke F.A., Cunliffe H.E., Ramos P., Jordan V.C.

A Molecular Model for the Mechanism of Acquired Tamoxifen Resistance in Breast Cancer



Eur. J. Cancer 50(16):2866-2876, 2014.

C 65. Jordan V.C.

Avoiding the Bad and Enhancing the Good of Soy Supplements in Breast Cancer. JNCI-Journal Natl. Cancer Inst. 106(9), 2014. doi:10.1093/jnci/dju233.



C 66. Obiorah I.E., Jordan V.C.

Differences in the Rate of Oestrogen-Induced Apoptosis in Breast Cancer by Oestradiol and the Triphenylethylene Bisphenol



Br. J. Pharmacol. 171(17, SI):4062-4072, 2014.

C 67. Craig Z.R., Singh J., Gupta R.K., Flaws J.A.

Co-Treatment of Mouse Antral Follicles with 17 Beta-Estradiol Interferes with Mono-2-Ethylhexyl Phthalate (MEHP)-Induced Atresia and Altered Apoptosis Gene Expression



Reprod. Toxicol. 45:45-51, 2014.

C 68. Heger Z., Rodrigo M.A.M., Krizkova S, et al.

Identification of Estrogen Receptor Proteins in Breast Cancer Cells Using Matrix-Assisted Laser Desorption/Ionization Time of Flight Mass Spectrometry



Oncol. Lett. 7(5):1341-1344, 2014.

C 69. Peyre L., Rouimi P., de Sousa G., et al.

Comparative Study of Bisphenol A and Its Analogue Bisphenol S on Human Hepatic Cells: A Focus on Their Potential Involvement in Nonalcoholic Fatty Liver Disease



FOOD Chem. Toxicol. 70:9-18, 2014.

C 70. Sengupta S., Biarnes M.C., Jordan V.C.

Cyclin Dependent Kinase-9 Mediated Transcriptional De-regulation of cMYC as a Critical Determinant of Endocrine-Therapy Resistance in Breast Cancers



Breast Cancer Res. Treat. 143(1):113-124, 2014.
T 29. Curpan R.F., Simons P.C., Zhai D., Young S.M., Carter M.B., Bologa C.G., Sklar

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High-Throughput Screen for the Chemical Inhibitors of Antiapoptotic Bcl-2 Family Proteins by Multiplex Flow Cytometry

Assay Drug Devel. Technol. 9(5), 465–474, 2011.

C 71. Mathieu A.-L., Sperandio O., Pottiez V., et al.

Identification of Small Inhibitory Molecules Targeting the Bfl-1 Anti-Apoptotic Protein That Alleviates Resistance to ABT-737



J. Biomol. Screen. 19(7):1035-1046, 2014.

C 72. Smurthwaite C.A., Hilton B.J., O’Hanlon R., et al.

Fluorescent Genetic Barcoding in Mammalian Cells for Enhanced Multiplexing Capabilities in Flow Cytometry



Cytom. PART A 85A(1):105-113, 2014.

C 73. Song S.-S., Lee W.-K., Aluvila S., Oh K.J., Yu Y.G.

Identification of Inhibitors Against BAK Pore Formation using an Improved in vitro Assay System



Bull. KOREAN Chem. Soc. 35(2):419-424, 2014.
T 30. Haynes M.K., Strouse J.J., Waller A., Leitao A., Curpan R.F., Bologa C., Thompson,

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Detection of Intracellular Granularity Induction in Prostate Cancer Cell Lines by Small Molecules Using the HyperCyt (R) High-Throughput Flow Cytometry System

J. Biomol. Screen. 14(6), 596–609, 2009.

C 74. Smurthwaite C.A., Hilton B.J., O’Hanlon R., et al.

Fluorescent Genetic Barcoding in Mammalian Cells for Enhanced Multiplexing Capabilities in Flow Cytometry



Cytom. PART A 85A(1):105-113, 2014.
T 31. Oprea T.I., Allu T.K., Fara D.C., Rad R.F., Ostopovici L., Bologa C.G.

Lead-like, drug-like or "pub-like": how different are they?



J. Comp.-Aid. Mol. Design 21(1-3):113-119, 2007.

C 75. Camp D., Newman S., Pham N.B., Quinn R.J.

Nature Bank and the Queensland Compound Library: Unique International Resources at the Eskitis Institute for Drug Discovery.



Comb. Chem. High Throughput Screen. 17(3):201-209, 2014.

C 76. Kell D.B.

Finding Novel Pharmaceuticals in the Systems Biology Era Using Multiple Effective Drug Targets, Phenotypic Screening and Knowledge of Transporters: Where Drug Discovery Went Wrong and How to Fix It



FEBS J. 280(23):5957-5980, 2013.

C 77. Pascolutti M., Quinn R.J.

Natural Products as Lead Structures: Chemical Transformations to Create Lead-Like Libraries



Drug Discov. Today 19(3):215-221, 2014.

C 78. Skariyachan S., Jayaprakash N., Bharadwaj N., Narayanappa R.

Exploring Insights for Virulent Gene Inhibition of Multidrug Resistant Salmonella Typhi, Vibrio Cholerae, and Staphylococcus Areus by Potential Phytoligands Via in Silico Screening



J. Biomol. Struct. Dyn. 32(9):1379-1395, 2014.
T 32. Ostopovici L., Mracec M., Mracec M., Borota A.

Exploring the binding site of the human muscarinic M3 receptor: homology

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C 79. Bhandare R.R., Canney D.J.

Bioisosteric Replacement and Related Analogs in the Design, Synthesis and Evaluation of Ligands for Muscarinic Acetylcholine Receptors



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T 33. Oprea T.I., Bologa C.G., Boyer S., Curpan R.F., Glen R.C., Hopkins A.L., Lipinski

C.A., Marshall G.R., Martin Y.C., Ostopovici-Halip L., Rishton G., Ursu O., Vaz

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A crowdsourcing evaluation of the NIH chemical probes.

Nat. Chem. Biol. 5(7):441-447, 2009

C 80. Eskiocak B., Ali A., White M.A.

The Estrogen-Related Receptor alpha Inverse Agonist XCT 790 Is a Nanomolar

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Biochemistry 53(29): 4839-4846, 2014

C 81. Dahlin J.L.,Walters M.A.

The essential roles of chemistry in high-throughput screening triage



Future Med. Chem. 6(11): 1265-1290, 2014

C 82. Curpăn R., Avram S., Vianello R., Bologa C.

Exploring the biological promiscuity of high-throughput screening hits through

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Bioorg. Med Chem. 22(8): 2461-2468, 2014

C 83. Franco P., Porta N., Holliday J.D., Willett P.

The use of 2D fingerprint methods to support the assessment of structural similarity

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J. Cheminformatics 6(1):5, 2014

C 84. Litterman N.K., Lipinski C.A., Bunin B.A., Ekins S.

Computational Prediction and Validation of an Expert's Evaluation of Chemical Probes



J. Chem. Inf. Model. 54(10):2996-3004., 2014
T 34. Slack J.P., Brockhoff A., Batram C., Menzel S., Sonnabend C., Born S., Galindo

M.M., Kohl S., Thalmann S., Ostopovici-Halip L., Simons C.T., Ungureanu I.,

Duineveld K., Bologa C.G., Behrens M., Furrer S., Oprea T.I., Meyerhof W.

Modulation of Bitter Taste Perception by a Small Molecule hTAS2R Antagonist



Curr. Biol. 20(12): 1104-1109, 2010

C 85. Pydi S.P., Sobotkiewicz T., Billakanti R., Bhullar R.P., Loewen M.C., Chelikani P.

Amino Acid Derivatives as Bitter Taste Receptor (T2R) Blockers



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C 86. Li J., Pan L., Fletcher J.N., Lv W., Deng Y., Vincent M.A., Slack J.P., McCluskey

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In Vitro Evaluation of Potential Bitterness-Masking Terpenoids from the Canada Goldenrod (Solidago canadensis)

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C 87. Bachmanov A.A., Bosak N.P., Lin C., Matsumoto I., Ohmoto M., Reed D.R.,

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Curr. Pharm. Design 20(16): 2669-2683, 2014

C 88. Roland W.S., Gouka R.J., Gruppen H., Driesse M., van Buren L., Smit G., Vincken

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6-Methoxyflavanones as Bitter Taste Receptor Blockers for hTAS2R39

Plos One 9(4): e94451,2014

C 89. Foster,S.R., Roura E., Thomas W.G.

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Pharmacol. Therapeut. 142(1): 41-61, 2014

C 90. Levit A., Nowak S., Peters M., Wiener A., Meyerhof W., Behrens M., Niv M.Y.

The bitter pill: clinical drugs that activate the human bitter taste receptor TAS2R14



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C 91. Pydi S.P., Bhullar R.P., Chelikani P.

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Adv Pharmacol. 70: 303-26, 2014.

C 92. Giorgetti A

Membrane Proteins: Insights from Computational Biology



Biol. Med. J. 6:1000e101, 2014

C 93 Sanematsu K., Yoshida R., Shigemura N., Ninomiya Y.

Structure, Function, and Signaling of Taste G-Protein-Coupled Receptors



Curr. Pharm. Biotechnol.15(10): 951-61, 2014

C 94. Foster S.R., Blank K., See Hoe L.E., Behrens M., Meyerhof W., Peart J.N., Thomas

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Bitter taste receptor agonists elicit G-protein-dependent negative inotropy in the murine heart

Faseb J. 28(10): 4497-4508, 2014
T 35. Chigaev A., Waller A., Amit O., Halip L., Bologa C., Sklar L

Real-time analysis of conformation-sensitive antibody binding provides newinsights into integrin conformational regulation



J. Biol. Chem. 284(21): 14337-143346, 2008

C 95. Chigaev A., Smagley Y., Sklar L.A.

Carbon monoxide down-regulates α4β1 integrin-specific ligand binding and cell adhesion: a possible mechanism for cell mobilization



BMC Immunol. 15(1): 52, 2014

C 96. Yoon S.O., Lee I.Y., Zhang X., Zapata M.C., Choi Y.S.

CD9 may contribute to the survival of human germinal center B cells by facilitating the interaction with follicular dendritic cells



FEBS Open Bio. 4: 370-6, 2014

C 97. Liu C.H., Hu R.H., Huang M.J., Lai I.R., Chen C.H., Lai H.S., Wu Y.M., Huang M.C..

C1GALT1 Promotes Invasive Phenotypes of Hepatocellular Carcinoma Cells by Modulating Integrin beta 1 Glycosylation and Activity



Plos One 9(8): e94995, 2014
T 36. Njus B., Chigaev A., Waller A., Wlodek D., Ostopovici-Halip L., Ursu U., Wang W.,

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Conformational mAb as a Tool for Integrin Ligand Discovery

Assay Drug Dev Technol. 7(5): 507-15, 2009

C 98. Chigaev A., Smagley Y., Sklar L.A.

Carbon monoxide down-regulates α4β1 integrin-specific ligand binding and cell adhesion: a possible mechanism for cell mobilization



BMC Immunol. 15(1): 52, 2014
T 37. Olah M., Mracec M., Ostopovici L., Rad R., Bora A., Hadaruga N., Olah I., Banda M.,

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Pharmacological Reviews, 66(1): 334-395, 2014

C 100. Cherkasov A., Muratov E.N., Fourches D., Varnek A., Baskin I.I., Cronin M., Dearden

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J. Med. Chem. 57(12): 4977-5010, 2014

C 101. Krishna S., Singh D.K., Meena S., Datta D., Siddiqi M.I., Banerjee D.

Pharmacophore-based screening and identification of novel human ligase I inhibitors with potential anticancer activity.



J. Chem. Inf. Model. 54(3): 781-92, 2014

C 102. Anger L.T., Wolf A., Schleifer K.J., Schrenk D., Rohrer S.G.

Generalized Workflow for Generating Highly Predictive in Silico Off-Target Activity Models



J. Chem. Inf. Model. 54(9): 2411-22, 2014

C 103. Reddy A,S., Tan Z., Zhang S.

Curation and analysis of multitargeting agents for polypharmacological modeling.



J. Chem. Inf. Model. 54(9): 2536-43, 2014

C 104. Flachner B., Tömöri T., Hajdú I., Dobi K., Lőrincz Z., Cseh S., Dormán G.

Rapid in silico selection of an MCHR1 antagonists’ focused library from multi-million compounds’ repositories: biological evaluation



Med. Chem. Res. 23(3): 1234-1247, 2014

C 105. García-Jacas C.R., Marrero-Ponce Y., Acevedo-Martínez L., Barigye S.J., Valdés-

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QuBiLS-MIDAS: a parallel free-software for molecular descriptors computation based on multilinear algebraic maps.

J. Comput.Chem. 35(18): 1395-409, 2014
T 38. Taboureau O., Nielsen S.K., Audouze K., Weinhold N., Edsgard D., Roque F.S.,

Kouskoumvekaki I., Bora A., Curpan R., Jensen T.S., Brunak,S., Oprea T.I.

ChemProt: a disease chemical biology database

Nucleic Acids Res. 39 (1): D367–D372, 2011

C 106. Kell D.B, Goodacre R.

Metabolomics and systems pharmacology: why and how to model the human metabolic network for drug discovery

Drug Discov. Today 19(2): 171-182, 2014

C 107. Nicolaes G.A., Kulharia M., Voorberg J., Kaijen P.H., Wroblewska A., Wielders S.,

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Rational design of small molecules targeting the C2 domain of coagulation factor VIII

Blood. 123(1): 113-120, 2014



C 108. Audouze K., Tromelin A., Le Bon A.M., Belloir C., Petersen R.K., Kristiansen K.,

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Identification of odorant-receptor interactions by global mapping of the human odorome

PLoS One 9(4): e93037, 2014

C 109. Tang J., Aittokallio T.

Network pharmacology strategies toward multi-target anticancer therapies: from computational models to experimental design principles

Curr. Pharm. Des. 20(1): 23-36, 2014

C 110. Azmi A.S., Mohammad R.M.

Rectifying cancer drug discovery through network pharmacology

Future Med. Chem. 6(5): 529-539, 2014

C 111. Liu L.L., Lu J., Lu Y., Zheng M.Y., Luo X.M., Zhu W.L., Jiang H.L., Chen K.X.

Novel Bayesian classification models for predicting compounds blocking hERG potassium channels

Acta Pharmacol. Sin. 35(8): 1093-1102, 2014

C 112. Allarakhia M.

The successes and challenges of open-source biopharmaceutical innovation

Expert Opin. Drug Discov. 9(5): 459-465, 2014

C 113. Allarakhia M.

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Expert Opin. Drug Discov. 9(5): 459-465, 2014
T 39. Olah M., Rad R., Ostopovici L., Bora A., Hadaruga N., Hadaruga D., Moldovan R.,

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WOMBAT and WOMBAT PK: Bioactivity Databases for Lead and Drug Discovery

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C 114. Luo M., Wang X.S., Roth B.L., Golbraikh A., Tropsha A.

Application of quantitative structure-activity relationship models of 5-HT1A receptor binding to virtual screening identifies novel and potent 5-HT1A ligands

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Polyhedron 76: 94-101, 2014
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C181. Kumar R., Obrai S., Jassal A. K., Hundal M. S.

Supramolecular architectures of N,N,N′,N′-tetrakis-(2-hydroxyethyl)ethylenediamine and tris(2-hydroxyethyl)amine with La(III) picrate



RSC Adv. 4: 59248-59264, 2014
T76. Crisan M., Grozav M., Bertea C.

Arabidopsis thaliana seed germination and early seedling growth are inhibited by monoethanolamine salts of para-halogenated benzoic acids

J. Plant Interact. 4(4): 271-277, 2009

C182. Waqas M., Khan A. L., Ali L., Kang S. M., Kim Y. H., Lee I. J.

Seed Germination-Influencing Bioactive Secondary Metabolites Secreted by the Endophyte Cladosporium cladosporioides LWL5



Molecules 18(12): 15519-15530, 2013
T77. Muntean S.G., Simu G.M., Kurunczi L., Szabadai Z.

Investigation of the aggregation of three disazo direct dyes by UV-vis spectroscopy and mathematical analysis



Rev. Chim.-Bucharest 60(2): 152-155, 2009

C183 . Ingale G., Seo Y.J.

Azo compounds with different sized fluorophores and characterization of their photophysical properties based on trans to cis conformational change



Tetrahedron Lett. 55(38): 5247-5250, 2014
T78. Muntean S.G., Simu G., Sfarloaga P., Bologa C.

Study of a trisazo direct dye adsorption on wood fibre using a comparison of different adsorption isotherms



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C184. Mohan D., Kumar H., Sarswat A., Alexandre-Franco M., Pittman Jr C.U.

Cadmium and lead remediation using magnetic oak wood and oak bark fast pyrolysis bio-chars



Chem. Eng. J. 236: 513-528, 2014
T79. Muntean S.G., Paska O., Coseri S., Simu G.M., Grad M.E., Ilia, G

Evaluation of a functionalized copolymer as adsorbent on direct dyes removal process: Kinetics and equilibrium studies



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