J. Sridhar

发表

Insights on Cytochrome P450 Enzymes and Inhibitors Obtained Through QSAR Studies

J. Sridhar, Jiawang Liu, M. Foroozesh, 2012, Molecules.

Selectivity and potency of cyclin-dependent kinase inhibitors

N. Pattabiraman, J. Sridhar, Nagaraju Akula, 2006, The AAPS Journal.

7-Ethynylcoumarins: selective inhibitors of human cytochrome P450s 1A1 and 1A2.

J. Sridhar, Jiawang Liu, M. Foroozesh, 2012, Chemical research in toxicology.

Identification of CYP 2A6 inhibitors in an effort to mitigate the harmful effects of the phytochemical nicotine

J. Sridhar, M. Foroozesh, M. Bratton, 2021, Journal of cancer metastasis and treatment.

Review of Ligand Specificity Factors for CYP1A Subfamily Enzymes from Molecular Modeling Studies Reported to-Date

J. Sridhar, Jiawang Liu, M. Foroozesh, 2017, Molecules.

Identification of quinones as HER2 inhibitors for the treatment of trastuzumab resistant breast cancer.

J. Sridhar, Cheryl L. Klein Stevens, M. Bratton, 2014, Bioorganic & medicinal chemistry letters.

New bivalent PKC ligands linked by a carbon spacer: enhancement in binding affinity.

J. Sridhar, P. Blumberg, A. Kozikowski, 2003, Journal of medicinal chemistry.

Cytochrome P450 Family 1 Inhibitors and Structure-Activity Relationships

J. Sridhar, Jiawang Liu, M. Foroozesh, 2013, Molecules.

DESIGN AND SYNTHESIS OF DIBENZYLFURAN BASED ETHER AND ESTER DERIVATIVES AS POTENTIAL P450 INHIBITORS.

J. Sridhar, M. Foroozesh, Navneet Goyal, 2018, Journal of undergraduate chemistry research.

Novel functionalized 5-(phenoxymethyl)-1,3-dioxane analogs exhibiting cytochrome P450 inhibition: a patent evaluation WO2015048311 (A1)

J. Sridhar, Jiawang Liu, M. Foroozesh, 2016, Expert opinion on therapeutic patents.

Ortho-Methylarylamines as Time-Dependent Inhibitors of Cytochrome P450 1A1 Enzyme.

Kevin E. Riley, J. Sridhar, Jiawang Liu, 2017, Drug metabolism letters.

In silico studies of polyaromatic hydrocarbon inhibitors of cytochrome P450 enzymes 1A1, 1A2, 2A6, and 2B1.

J. Sridhar, Jiawang Liu, M. Foroozesh, 2010, Chemical research in toxicology.

Osteoinductive effects of glyceollins on adult mesenchymal stromal/stem cells from adipose tissue and bone marrow.

Kevin E. Riley, Ryan S. Hunter, J. Sridhar, 2017, Phytomedicine : international journal of phytotherapy and phytopharmacology.

Coumarins and P450s, Studies Reported to-Date

J. Sridhar, Jiawang Liu, M. Foroozesh, 2019, Molecules.

Highly Potent and Specific GSK‐3β Inhibitors That Block Tau Phosphorylation and Decrease α‐Synuclein Protein Expression in a Cellular Model of Parkinson's Disease

T. Duka, J. Sridhar, A. Sidhu, 2006, ChemMedChem.

Synthetic Method to Form 2,2'-Bis(naphthoquinone) Compounds.

J. Sridhar, E. Stevens, V. Jha, 2017, The Journal of organic chemistry.

Modification and Biological Evaluation of Thiazole Derivatives as Novel Inhibitors of Metastatic Cancer Cell Migration and Invasion

J. Sridhar, Madhusoodanan Mottamal, Shilong Zheng, 2014, Journal of medicinal chemistry.

Pyranoflavones: a group of small-molecule probes for exploring the active site cavities of cytochrome P450 enzymes 1A1, 1A2, and 1B1.

Ming Zhao, J. Sridhar, Jiawang Liu, 2013, Journal of medicinal chemistry.

CDK Inhibitors as Anticancer Agents: Perspectives for the Future

N. Pattabiraman, J. Sridhar, E. Rosen, 2006 .

Binding modes of 6,7 di-substituted 4-anilinoquinoline-3-carbonitriles to EGFR.

N. Pattabiraman, J. Sridhar, Nagaraju Akula, 2004, Bioorganic & medicinal chemistry letters.

Identification of novel angiogenesis inhibitors.

Nagarajan Pattabiraman, N. Pattabiraman, J. Sridhar, 2005, Bioorganic & medicinal chemistry letters.

Cytochrome P450 Family 1 Inhibitors and Structure-Activity Relationships

J. Sridhar, Jiawang Liu, M. Foroozesh, 2013, Molecules.

Development of flavone propargyl ethers as potent and selective inhibitors of cytochrome P450 enzymes 1A1 and 1A2.

J. Sridhar, Jiawang Liu, M. Foroozesh, 2013, Drug metabolism letters.

Inhibition of cytochrome p450 enzymes by quinones and anthraquinones.

J. Sridhar, Jiawang Liu, M. Foroozesh, 2012, Chemical research in toxicology.

Identification of New Mono/Dihydroxynaphthoquinone as Lead Agents That Inhibit the Growth of Refractive and Triple-Negative Breast Cancer Cell Lines

J. Sridhar, R. Schroeder, F. Jones, 2019, ACS omega.

Ligands of Therapeutic Utility for the Liver X Receptors

Kevin E. Riley, J. Sridhar, Shilong Zheng, 2017, Molecules.

Synthesis and isozyme selectivity of small molecule protein kinase C inhibitors: a review of patents

N. Pattabiraman, J. Sridhar, 2005 .

Small Molecule Tyrosine Kinase Inhibitors of ErbB2/HER2/Neu in the Treatment of Aggressive Breast Cancer

J. Sridhar, R. Schroeder, C. Stevens, 2014, Molecules.

Identification of quinones as novel PIM1 kinase inhibitors.

J. Sridhar, M. Bratton, Ian K. Townley, 2016, Bioorganic & medicinal chemistry letters.

Effects of 7-O substitutions on estrogenic and anti-estrogenic activities of daidzein analogues in MCF-7 breast cancer cells.

J. Sridhar, D. Bhatnagar, J. McLachlan, 2010, Journal of medicinal chemistry.

QSAR models of cytochrome P450 enzyme 1A2 inhibitors using CoMFA, CoMSIA and HQSAR

J. Sridhar, M. Foroozesh, J Sridhar, 2011, SAR and QSAR in environmental research.

Ethynylflavones, Highly Potent, and Selective Inhibitors of Cytochrome P450 1A1

Ming Zhao, J. Sridhar, Jiawang Liu, 2014, Chemical research in toxicology.