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Maniyan P. Padmanilayam

Observed names: M.P. PADMANILAYAM, Maniyan P Padmanilayam, Maniyan Padmanilayam, Padmanilayam, M., Padmanilayam, M.P.
Observed institutions: AstraZeneca (United Kingdom), University of Alberta, Wayne State University, Rega Institute for Medical Research, University of Saskatchewan, AstraZeneca (United States), University of Nebraska Medical Center, KU Leuven
OpenAlex ID: A5048639235
Identification of an antimalarial synthetic trioxolane drug development candidate
2004 · Jonathan L. Vennerstrom, Sarah Arbe-Barnes, et al. · Nature · 632
A Conformational and Structure−Activity Relationship Study of Cytotoxic 3,5-Bis(arylidene)-4-piperidones and Related N-Acryloyl Analogues
2001 · Jonathan R. Dimmock, Maniyan P. Padmanilayam, et al. · Journal of Medicinal Chemistry · 218
The Structure−Activity Relationship of the Antimalarial Ozonide Arterolane (OZ277)
2009 · Yuxiang Dong, Sergio Wittlin, et al. · Journal of Medicinal Chemistry · 114
Cytotoxic analogues of 2,6-bis(arylidene)cyclohexanones
2003 · Jonathan R Dimmock, Maniyan P Padmanilayam, et al. · European Journal of Medicinal Chemistry · 95
Immunization to nicotine with a peptide-based vaccine composed of a conformationally biased agonist of C5a as a molecular adjuvant
2003 · Sam D Sanderson, Srinivasa R Cheruku, et al. · International Immunopharmacology · 68
Weak base dispiro-1,2,4-trioxolanes: Potent antimalarial ozonides
2006 · Yuanqing Tang, Yuxiang Dong, et al. · Bioorganic & Medicinal Chemistry Letters · 60
Antimalarial activity of N-alkyl amine, carboxamide, sulfonamide, and urea derivatives of a dispiro-1,2,4-trioxolane piperidine
2006 · Maniyan Padmanilayam, Bernard Scorneaux, et al. · Bioorganic & Medicinal Chemistry Letters · 59
Discovery of (+)-N-(3-Aminopropyl)-N-[1-(5-benzyl-3-methyl-4-oxo-[1,2]thiazolo[5,4-d]pyrimidin-6-yl)-2-methylpropyl]-4-methylbenzamide (AZD4877), a Kinesin Spindle Protein Inhibitor and Potential Anticancer Agent
2011 · Maria-Elena Theoclitou, Brian Aquila, et al. · Journal of Medicinal Chemistry · 48
Synthesis of 2H-pyrroles by treatment of pyrrolidines with DDQ
2003 · Srinivasa R. Cheruku, Maniyan P. Padmanilayam, et al. · Tetrahedron Letters · 33
Conversion of Substituted 1-Arylidene-2-tetralones to 2-Alkoxy-1-arylmethylnaphthalenes: An Example of Facile Aromatization
2002 · Amitabh Jha, Maniyan P. Padmanilayam, et al. · Synthesis · 14
Cytotoxic Mannich Bases of 1-Arylidene-2-tetralones
2003 · J.R. DIMMOCK, M.P. PADMANILAYAM, et al. · Journal of Enzyme Inhibition and Medicinal Chemistry · 10
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Cytotoxic Analogues of 2,6‐Bis(arylidene)cyclohexanones.
2003 · Jonathan R. Dimmock, Maniyan P. Padmanilayam, et al. · ChemInform · 3
1-(4-Carboethoxyphenylmethyl)-2-ethoxynaphthalene
2002 · Eliud O. Oloo, J. Wilson Quail, et al. · Acta Crystallographica Section E Structure Reports Online · 1
CCDC 298211: Experimental Crystal Structure Determination
2008 · Tang, Yuanqing, Dong, Yuxiang, et al. · The Cambridge Structural Database
cis-3-Phenyl-3,3a,4,5-tetrahydrobenzo[g]indazole-2-carboxamide
2004 · Eliud O. Oloo, Kurt Nienaber, et al. · Acta Crystallographica Section E Structure Reports Online
CCDC 238799: Experimental Crystal Structure Determination
2004 · Oloo, E.O., Nienaber, K., et al. · The Cambridge Structural Database
Synthesis of 2H‐Pyrroles by Treatment of Pyrrolidines with DDQ.
2003 · Srinivasa R. Cheruku, Maniyan P. Padmanilayam, et al. · ChemInform
ChemInform Abstract: Conversion of Substituted 1‐Arylidene‐2‐tetralones to 2‐Alkoxy‐1‐arylmethylnaphthalenes: An Example of Facile Aromatization.
2002 · Amitabh Jha, Maniyan P. Padmanilayam, et al. · ChemInform
(E)-1-(4-Carboxyphenylmethylene)-2-tetralone
2002 · Eliud O. Oloo, J. Wilson Quail, et al. · Acta Crystallographica Section E Structure Reports Online
CCDC 189410: Experimental Crystal Structure Determination
2002 · Oloo, E.O., Quail, J.W., et al. · The Cambridge Structural Database
CCDC 189409: Experimental Crystal Structure Determination
2002 · Oloo, E.O., Quail, J.W., et al. · The Cambridge Structural Database
Works count: 21
Citation count: 1,355
H-index: 10
I10-index: 11
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