R. Vince

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Synthesis and biological evaluation of purine derivatives incorporating metal chelating ligands as HIV integrase inhibitors.

Xingnan Li, R. Vince, 2006, Bioorganic & medicinal chemistry.

Synthesis and activity of γ-(L-γ-azaglutamyl)-S-(p-bromobenzyl)-L-cysteinylglycine: A metabolically stable inhibitor of glyoxalase I

L. B. Akella, R. Vince, J. Brownell, 1999 .

NAD-based inhibitors with anticancer potential.

K. Pankiewicz, K. Felczak, R. Vince, 2014, Bioorganic & medicinal chemistry letters.

Guanabenz Attenuates Acetaminophen-Induced Liver Toxicity and Synergizes Analgesia in Mice.

Swati S. More, Jiashu Xie, R. Vince, 2020, Chemical research in toxicology.

Induction ofErythromycin Resistance inStaphylococcus aureus byErythromycin Derivatives

S. Pestka, R. LeMahieu, J. Unowsky, 1976 .

Inhibition of protein biosynthesis: the first active sparsomycin analog.

C. K. Lee, R. Vince, J. Brownell, 1977, Biochemical and biophysical research communications.

Vinyl and aryl metals

R. Vince, R. Muthyala, 2004 .

Studies on the inhibition of glyoxalase I by S-substituted glutathiones.

R. Vince, W. Wadd, S. Daluge, 1971, Journal of medicinal chemistry.

Dipeptide of ψ-GSH Inhibits Oxidative Stress and Neuroinflammation in an Alzheimer’s Disease Mouse Model

Swati S. More, R. Vince, Kwan-Hyun Kim, 2022, Antioxidants.

Development of sulfanegen for mass cyanide casualties

S. Patterson, H. Nagasawa, B. Logue, 2016, Annals of the New York Academy of Sciences.

Comparison of the efficacy of vidarabine, its carbocyclic analog (cyclaradine), and cyclaradine-5'-methoxyacetate in the treatment of herpes simplex virus type 1 encephalitis in mice

H. Lee, G. Arnett, R. Vince, 1983, Antimicrobial Agents and Chemotherapy.

The Amyloid Aggregation Accelerator Diacetyl Prevents Cognitive Decline in Alzheimer's Mouse Models.

Swati S. More, R. Vince, Wei Xie, 2021, Chemical research in toxicology.

Novel, orally effective cyanide antidotes.

S. Patterson, H. Nagasawa, R. Vince, 2007, Journal of medicinal chemistry.

Metabolism of the carbocyclic nucleoside analogue carbovir, an inhibitor of human immunodeficiency virus, in human lymphoid cells.

A. Fridland, J. Secrist, R. Vince, 1990, Biochemistry.

γ-Glutamyl-Transpeptidase-Resistant Glutathione Analog Attenuates Progression of Alzheimer’s Disease-like Pathology and Neurodegeneration in a Mouse Model

Swati S. More, Haizhou Zhu, Jiashu Xie, 2021, Antioxidants.

Binding of N-Substituted Erythromycylamines to Ribosomes

S. Pestka, R. Vince, D. Weiss, 1976, Antimicrobial Agents and Chemotherapy.

R. Vince, P. Pham, 2007 .

Sulfanegen stimulates 3-mercaptopyruvate sulfurtransferase activity and ameliorates Alzheimer's disease pathology and oxidative stress in vivo

Swati S. More, Jiashu Xie, Michael K. Lee, 2022, Redox biology.

Metabolism of carbovir, a potent inhibitor of human immunodeficiency virus type 1, and its effects on cellular metabolism

W. Parker, L. Bennett, S. Shaddix, 1993, Antimicrobial Agents and Chemotherapy.

Mechanism of inhibition of human immunodeficiency virus type 1 reverse transcriptase and human DNA polymerases alpha, beta, and gamma by the 5'-triphosphates of carbovir, 3'-azido-3'-deoxythymidine, 2',3'-dideoxyguanosine and 3'-deoxythymidine. A novel RNA template for the evaluation of antiretrovir

E. White, W. Parker, R. Buckheit, 1991, The Journal of biological chemistry.

Metabolism of O6-Propyl and N6-Propyl-carbovir in CEM Cells

W. Parker, S. Shaddix, L. Rose, 2000, Nucleosides, nucleotides & nucleic acids.

Lack of mitochondrial toxicity in CEM cells treated with carbovir.

W. Parker, L. Bennett, S. Shaddix, 1997, Antiviral research.

6-Deoxycarbovir: A Xanthine Oxidase Activated Prodrug of Carbovir

R. Vince, J. Brownell, S. Beers, 1995 .

Synthesis and anti-HIV activity of carbocyclic 2',3'-didehydro-2',3'-dideoxy 2,6-disubstituted purine nucleosides.

R. Vince, M. Hua, 1990, Journal of medicinal chemistry.

2-Azabicyclo[2.2.1]hept-5-en-3-one: chemical profile of a versatile synthetic building block and its impact on the development of therapeutics.

Rohit Singh, R. Vince, 2012, Chemical reviews.

Resolution of racemic carbovir and selective inhibition of human immunodeficiency virus by the (-) enantiomer.

R. Vince, J. Brownell, 1990, Biochemical and biophysical research communications.

Glyoxalase inhibitors. A possible approach to anticancer agents.

R. Vince, S. Daluge, 1971, Journal of Medicinal Chemistry.

Potent and selective activity of a new carbocyclic nucleoside analog (carbovir: NSC 614846) against human immunodeficiency virus in vitro.

M. Boyd, R. Shoemaker, O. Weislow, 1988, Biochemical and biophysical research communications.

The design, synthesis and biological evaluations of C-6 or C-7 substituted 2-hydroxyisoquinoline-1,3-diones as inhibitors of hepatitis C virus.

Y. Sham, R. Geraghty, Jing Tang, 2012, Bioorganic & medicinal chemistry.

Design, asymmetric synthesis, and evaluation of pseudosymmetric sulfoximine inhibitors against HIV-1 protease.

Y. Sham, R. Vince, D. Lu, 2010, Bioorganic & medicinal chemistry.

Palladium-catalyzed synthesis of cis-2-[4-(9H-Purin-9-yl)-2-cyclopenten-1-yl]ethanol analogues

L. B. Akella, R. Vince, 1996 .

Conformationally restrained carbazolone-containing α,γ-diketo acids as inhibitors of HIV integrase

Xingnan Li, R. Vince, 2006 .

Palladium-Catalyzed Allylic Coupling of 1,2,3-Triazolo[4,5-d]pyrimidines (8-Azapurines).

R. Vince, M. Konkel, 1996, The Journal of organic chemistry.

Rationally designed dual inhibitors of HIV reverse transcriptase and integrase.

C. Salomon, Daniel J. Wilson, Zhengqiang Wang, 2007, Journal of medicinal chemistry.

Thiostrepton-resistant mutants of Bacillus subtilis: Localization of resistance to the 50S subunit

S. Pestka, I. Smith, G. Stöffler, 1976, Molecular and General Genetics MGG.

Binding of Thiostrepton to Ribosomes from Thiostrepton-Sensitive and -Resistant Bacillus subtilis Strains

S. Pestka, I. Smith, J. Gordon, 1976, Antimicrobial Agents and Chemotherapy.

Effect of sparsomycin analogues on the puromycin-peptidyl transferase reaction on ribosomes.

C. K. Lee, R. Vince, 1978, Journal of medicinal chemistry.

Synthesis of pyrimidine and quinolone conjugates as a scaffold for dual inhibitors of HIV reverse transcriptase and integrase.

Zhengqiang Wang, R. Vince, 2008, Bioorganic & medicinal chemistry letters.

Synthesis and biological evaluation of acyclic neplanocin analogues.

R. Vince, M. Hua, P. M. Korkowski, 1987, Journal of medicinal chemistry.

Cyclohexenyl nucleosides: Synthesis and biological activity of trans-3-(purin-9-yl)-4-cyclohexenylcarbinols

R. Vince, M. Konkel, 1996 .

Cyclohexenyl nucleosides: Synthesis of cis-4-(9H-purin-9-yl)-2-cyclohexenylcarbinols

R. Vince, M. Konkel, 1996 .

SYNTHESIS AND BIOLOGICAL ACTIVITY OF CYCLOHEXENYL NUCLEOSIDES. CIS-5-(9H-PURIN-9-YL)-3-CYCLOHEXENYL CARBINOLS AND THEIR 8-AZAPURINYL ANALOGS

R. Vince, M. Konkel, 1995 .

Design and synthesis of sulfoximine based inhibitors for HIV-1 protease.

Y. Sham, R. Vince, Abbas Raza, 2008, Bioorganic & medicinal chemistry letters.

Discovery of potent HIV-1 protease inhibitors incorporating sulfoximine functionality.

R. Vince, D. Lu, 2007, Bioorganic & medicinal chemistry letters.

Tight‐binding inhibitors efficiently inactivate both reaction centers of monomeric Plasmodium falciparum glyoxalase 1

Swati S. More, Marcel Deponte, R. Vince, 2012, The FEBS journal.

Design, synthesis, and binding studies of bidentate Zn-chelating peptidic inhibitors of glyoxalase-I.

Swati S. More, R. Vince, 2007, Bioorganic & medicinal chemistry letters.

A metabolically stable tight-binding transition-state inhibitor of glyoxalase-I.

Swati S. More, R. Vince, 2006, Bioorganic & medicinal chemistry letters.

Synthesis and biological evaluation of 4-purinylpyrrolidine nucleosides.

M. L. Peterson, R. Vince, M. Peterson, 1991, Journal of medicinal chemistry.

Cyanide antidotes for mass casualties: water-soluble salts of the dithiane (sulfanegen) from 3-mercaptopyruvate for intramuscular administration.

S. Patterson, H. Nagasawa, R. Vince, 2013, Journal of medicinal chemistry.

Cyanide Toxicity in Juvenile Pigs and Its Reversal by a New Prodrug, Sulfanegen Sodium

S. Patterson, H. Nagasawa, K. Belani, 2012, Anesthesia and analgesia.

Synthesis and antiviral activity of carbocyclic analogues of xylofuranosides of 2-amino-6-substituted-purines and 2-amino-6-substituted-8-azapurines.

G. Arnett, R. Vince, R. Turakhia, 1984, Journal of medicinal chemistry.

Synthesis of Carbocyclic Aminonucleosides

R. Vince, S. Daluge, 1978 .

Results of Hemodynamic Changes Observed During SNP Infusion , Followed Either by Placebo or Sulfanegen Sodium Given 2 Hours After SNP Infusion

S. Patterson, H. Nagasawa, K. Belani, 2012 .

Carbocyclic analogues of xylofuranosylpurine nucleosides. Synthesis and antitumor activity.

R. Vince, J. Brownell, S. Daluge, 1984, Journal of medicinal chemistry.

The butter flavorant, diacetyl, exacerbates β-amyloid cytotoxicity.

Swati S. More, Ashish P. Vartak, Robert Vince, 2012, Chemical research in toxicology.

The butter flavorant, diacetyl, forms a covalent adduct with 2-deoxyguanosine, uncoils DNA, and leads to cell death.

Swati S. More, R. Vince, Abbas Raza, 2012, Journal of agricultural and food chemistry.

Dehydroascorbic Acid Adducts of Guanosine Residues: Possible Biological Implications

R. Vince, Abbas Raza, 2011, Chembiochem : a European journal of chemical biology.

Novel substrate of adenosine deaminase.

H. Schaeffer, R. Vince, S. Gurwara, 1971, Journal of medicinal chemistry.

6-Benzoyl-3-hydroxypyrimidine-2,4-diones as dual inhibitors of HIV reverse transcriptase and integrase.

Y. Pommier, Y. Sham, Jing Tang, 2011, Bioorganic & medicinal chemistry letters.

3-Hydroxypyrimidine-2,4-diones as an inhibitor scaffold of HIV integrase.

Yves Pommier, Y. Pommier, Y. Sham, 2011, Journal of medicinal chemistry.

N-3 Hydroxylation of Pyrimidine-2,4-diones Yields Dual Inhibitors of HIV Reverse Transcriptase and Integrase.

Y. Pommier, Y. Sham, Jing Tang, 2011, ACS medicinal chemistry letters.

Pharmacophore and structure-activity relationships of integrase inhibition within a dual inhibitor scaffold of HIV reverse transcriptase and integrase.

C. Salomon, Jing Tang, Zhengqiang Wang, 2010, Bioorganic & medicinal chemistry.

Design and synthesis of dual inhibitors of HIV reverse transcriptase and integrase: introducing a diketoacid functionality into delavirdine.

Zhengqiang Wang, R. Vince, 2008, Bioorganic & medicinal chemistry.

Intramolecular Reactions of Some Cyclic β-Diketones1

H. Schaeffer, R. Vince, 1962 .

Synthesis of cyclohexyl carbocyclic puromycin and its inhibition of protein synthesis.

R. Vince, S. Daluge, 1977, Journal of Medicinal Chemistry.

Synthesis and antimicrobial activity of a carbocyclic puromycin analog. 6-Dimethylamino-9-(R(2R-hydroxy-3R-(p-methoxyphenyl-L alanylamino))-cyclopentyl)purine.

R. Vince, S. Daluge, 1972, Journal of Medicinal Chemistry.

Glyoxalase inhibitors as potential anticancer agents.

R. Vince, W. Wadd, Robert Vince, 1969, Biochemical and biophysical research communications.

Synthesis of conformationally restricted 2',3'-exo-methylene carbocyclic nucleosides built on a bicyclo[3.1.0]hexane template.

R. Vince, R. Bhushan, 2002, Bioorganic & medicinal chemistry.

Carbocyclic arabinosyladenine, an adenosine deaminase resistant antiviral agent.

R. Vince, S. Daluge, 1977, Journal of medicinal chemistry.

Puromycin based inhibitors of aminopeptidases for the potential treatment of hematologic malignancies.

Rohit Singh, R. Vince, Jessica M Williams, 2017, European journal of medicinal chemistry.

A synthetic route to carbocyclic aminonucleosides

R. Vince, S. Daluge, 1976 .

Puromycin analogs. Ribosomal binding and peptidyl transferase substrate activity of a carbocyclic analog of 8-azapuromycin.

R. Vince, C. L. Ritter, P. H. Duquette, 1974, Biochemistry.

The formation of arabino nucleosides from 3-acetamido-1,2-di-O-acetyl-3,5-dideoxy-d-ribofuranose during the fusion synthesis.

R. Vince, R. Almquist, 1974, Carbohydrate research.

Effect of Puromycin Analogues and Other Agents on Peptidyl-Puromycin Synthesis on Polyribosomes

S. Pestka, R. Vince, R. Harris, 1973, Antimicrobial Agents and Chemotherapy.

Inhibition of in vitro protein synthesis by a carbocyclic puromycin analog.

R. Vince, S. Daluge, M. Palm, 1972, Biochemical and biophysical research communications.

SYNTHESIS OF CYCLOHEXYL CARBOCYCLIC PUROMYCIN AND ITS INHIBITION OF PROTEIN SYNTHESIS

R. Vince, S. Daluge, 1977 .

Inhibition of glyoxalase I: the first low-nanomolar tight-binding inhibitors.

Swati S. More, R. Vince, 2009, Journal of medicinal chemistry.

Comparison of the effect of Carbovir, AZT, and dideoxynucleoside triphosphates on the activity of human immunodeficiency virus reverse transcriptase and selected human polymerases.

E. White, W. Parker, J. Secrist, 1989, Biochemical and biophysical research communications.

Substrate specificity of human glycinamide ribonucleotide transformylase.

R. Vince, V. Antle, M. Hua, 1999, Archives of biochemistry and biophysics.

Enzyme inhibitors. XIX. The synthesis of some 1-hydroxy-2-hydroxymethyl-4-(6-substituted-9-purinyl)cyclohexanes as nucleoside analogs.

H. Schaeffer, R. Vince, 1968, Journal of medicinal chemistry.

Synthesis of Carbocyclic Aminonucleosides

R. Vince, S. Daluge, 1978 .

Carbocyclic arabinofuranosyladenine (cyclaradine): efficacy against genital herpes in guinea pigs.

H. Lee, G. Arnett, P. Reichert, 1983, Science.

Puromycin analogs. Studies on ribosomal binding with diastereomeric carbocyclic puromycin analogs.

R. Vince, S. Daluge, 1974, Journal of Medicinal Chemistry.

Enantioselective synthesis of 2-[5-(9H-purin-9-yl)-2-cyclopenten-1-yl]-ethanol analogues as potential antiviral agents

R. Vince, L. Akella, 1996 .

SYNTHESIS AND BIOLOGICAL EVALUATION OF ENDOCYCLIC 2′,3′-DIDEHYDRO- 2′,3′-DIDEOXYMETHANOCARBA ADENOSINE

R. Vince, D. Q. Dorr, 2002, Nucleosides, nucleotides & nucleic acids.

Facile Synthesis of Carbocyclic Lyxo- and Ribonucleosides

R. Vince, S. Daluge, 1980 .

Carbocyclic analogs of arabinosylpurine nucleosides.

H. Lee, R. Vince, 1980, Journal of pharmaceutical sciences.

(±) 4β-amino-2α,3α-dihydroxy-1β-cyclopentanemethanol hydrochloride. Carbocyclic ribofuranosylamine for the synthesis of carbocyclic nucleosides.

R. Vince, R. Cermak, 1981 .

Synthesis and biological evaluation of 5'-sulfamoylated purinyl carbocyclic nucleosides.

R. Vince, J. Brownell, E. Peterson, 1992, Journal of medicinal chemistry.

ENZYME INHIBITORS. VI. STUDIES ON THE BULK TOLERANCE OF ADENOSINE DEAMINASE FOR 6-SUBSTITUTED AMINO-9-(3-HYDROXYPROPYL)PURINES.

H. Schaeffer, R. Vince, 1965, Journal of Medicinal Chemistry.

Pharmacokinetics and Bioavailability of Carbovir,

Yoon-hee, R. Remmel, R. Vince, 2003 .

Pharmacokinetics and bioavailability of carbovir, a carbocyclic nucleoside active against human immunodeficiency virus, in rats

Y. Yeom, R. Remmel, R. Vince, 1989, Antimicrobial Agents and Chemotherapy.

PUROMYCIN ANALOGS, STUDIES ON RIBOSOMAL BINDUNG WITH DIASTEREOMERIC CARBOCYCLIC PUROMYCIN ANALOGS

R. Vince, S. Daluge, 1974 .

Puromycin analogs. Synthesis and biological activity of 5'-deoxypuromycin and its aminonucleoside, 6-dimethylamino-9(3'-amin-3',5-dideoxy-beta-D-ribofuranosyl)purine.

R. Vince, R. Almquist, 1973, Journal of medicinal chemistry.

Deamination of cyclaradine by adenosine deaminase under high pressure.

R. Vince, N. Katagiri, C. Kaneko, 1998, Nucleosides & nucleotides.

Enzyme inhibitors. 18. Studies on the stereoselectivity of inhibition of adenosine deaminase by DL-, D-, and L-9-(2-hydroxypropyl)adenine.

H. Schaeffer, R. Vince, 1967, Journal of medicinal chemistry.

Enantioselective Synthesis of 2‐(5‐(9H‐Purin‐9‐yl)‐2‐cyclopenten‐1‐yl) ethanol Analogues as Potential Antiviral Agents.

R. Vince, L. Akella, 1996 .

Synthesis and Biological Evaluation of Endocyclic 2′,3′‐Didehydro‐2′,3′‐dideoxymethanocarba Adenosine.

Robert Vince, R. Vince, Danae Quirk Dorr, 2003 .

A synthetic route to carbocyclic aminonucleosides

R. Vince, S. Daluge, 1976 .

Nucleoside analogs. Synthesis of 6-(6-amino-9-purinyl)-1,5-anhydro-6-deoxy-l-allitol.

R. Vince, J. Donovan, 1969, Journal of medicinal chemistry.

Substrate Specificity of Glycinamide Ribonucleotide Transformylase from Chicken Liver

R. Vince, V. Antle, C. Caperelli, 1996, The Journal of Biological Chemistry.

Synthesis and biological evaluation of carboacyclic nucleosides with (Z) and (E)-9-[4,4-bis(hydroxymethyl)]-2-butenyl side chain.

R. Vince, R. Muthyala, Ye Tang, 2006, Bioorganic & medicinal chemistry.

CARBOCYCLIC ANALOGS OF ARABINOSYLPURINE NUCLEOSIDES

Hee‐Yoon Lee, R. Vince, 1981 .

PHOSPHONATE ANALOGS OF CARBOCYCLIC PHOSPHORIBOSYLAMINE AND CARBOCYCLIC GLYCINAMIDE RIBONUCLEOTIDE

R. Vince, C. Caperelli, M. Hua, 1996 .

6-Substituted Derivatives of Carbovir: Anti-HIV Activity

W. Parker, R. Vince, B. Bowdon, 1995 .

Comparative Brain Exposure to (-)-Carbovir After (-)-Carbovir or (-)-6-Aminocarbovir Intravenous Infusion in Rats

R. Remmel, R. Vince, C. Zimmerman, 1995, Pharmaceutical Research.

1,2,4-Triazole amino nucleosides. 1-beta-D-3'-Amino-3'-deoxyribofuranosyl-1,2,4-triazole-3-carboxamide and related nucleosides.

R. Vince, A. Narang, 1977, Journal of medicinal chemistry.

Poly(2-fluoroadenylic acid). The role of basicity in the stabilization of complementary helices.

V. Amarnath, R. Vince, A. D. Broom, 1979, Biochimica et biophysica acta.

Glutaryl-S-(p-bromobenzyl)-L-cysteinylglycine. A metabolically stable inhibitor of glyoxalase I.

R. Vince, M. Wolf, C. Sanford, 1973, Journal of medicinal chemistry.

Synthesis and kinetic evaluation of S- and N-substituted cysteinylglycines as inhibitors of glyoxalase I.

R. Vince, P. A. Lyon, 1977, Journal of medicinal chemistry.

Ribosomal protein alterations in thiostrepton- and Micrococcin-resistant mutants of Bacillus subtilis.

S Pestka, S. Pestka, I. Smith, 1979, The Journal of biological chemistry.

Potential of a γ-glutamyl-transpeptidase-stable glutathione analogue against amyloid-β toxicity.

Swati S. More, R. Vince, 2012, ACS chemical neuroscience.

Pharmacokinetic evaluation of (-)-6-aminocarbovir as a prodrug for (-)-carbovir in rats.

R. Remmel, S. S. Ibrahim, R. Vince, 1992, Drug metabolism and disposition: the biological fate of chemicals.

Photoprotection of DNA (in vitro) by acyclothymidine dinucleosides.

R. Vince, Abbas Raza, Christine D. Dreis, 2013, Bioorganic & medicinal chemistry letters.

Partition of ribosomes in two-polymer aqueous phase systems.

S. Pestka, R. Vince, D. Weiss, 1976, Analytical biochemistry.

Topical Acyclothymidine Dinucleosides (aTds) Promote Non-UV-Mediated Endogenous Defense Mechanisms in Guinea Pig Skin.

R. Vince, Abbas Raza, J. Nugent, 2015, The Journal of investigative dermatology.

In Vivo Assessment of Retinal Biomarkers by Hyperspectral Imaging: Early Detection of Alzheimer's Disease.

Swati S. More, J. Beach, Collin M. McClelland, 2019, ACS chemical neuroscience.

Early Detection of Amyloidopathy in Alzheimer's Mice by Hyperspectral Endoscopy.

Swati S. More, J. Beach, R. Vince, 2016, Investigative ophthalmology & visual science.

Cofactor-type inhibitors of inosine monophosphate dehydrogenase via modular approach: targeting the pyrophosphate binding sub-domain.

R. Petrelli, P. Kusumanchi, Daniel J. Wilson, 2011, Bioorganic & medicinal chemistry.

The distance between two functionally significant regions of the 50 S Escherichia coli ribosome: the erythromycin binding site and proteins L7/L12.

S. Pestka, C. Cantor, R. Langlois, 1976, Journal of molecular biology.

C-6 aryl substituted 4-quinolone-3-carboxylic acids as inhibitors of hepatitis C virus.

Jeana Zacharias, R. Geraghty, Zhengqiang Wang, 2012, Bioorganic & medicinal chemistry.

An Orally Bioavailable (Mice) Prodrug of Glutathione.

H. Nagasawa, R. Vince, D. Crankshaw, 2021, Antioxidants.

Photoaffinity labeling of the ribosomal peptidyl transferase site with synthetic puromycin analogues.

R. Vince, J. Brownell, K. Fong, 1978, Biochemistry.

Interaction between the erythromycin and chloramphenicol binding sites on the Escherichica coli ribosome.

S. Pestka, C. Cantor, R. Langlois, 1977, Biochemistry.

Peptidyl transferase substrate activity and inhibition of protein biosynthesis by a hydrophilic-aminoacyl analogue of puromycin.

R. Vince, K. Fong, 1978, Biochemical and biophysical research communications.

Restoration of glyoxalase enzyme activity precludes cognitive dysfunction in a mouse model of Alzheimer's disease.

Swati S. More, Ashish P. Vartak, R. Vince, 2013, ACS chemical neuroscience.

Design, synthesis and biological evaluation of glutathione peptidomimetics as components of anti-Parkinson prodrugs.

Swati S. More, R. Vince, 2008, Journal of medicinal chemistry.

Orally Bioavailable Prodrugs of ψ-GSH: A Potential Treatment for Alzheimer’s Disease

Swati S. More, Haizhou Zhu, Jiashu Xie, 2022, Journal of medicinal chemistry.

Hyperspectral imaging signatures detect amyloidopathy in Alzheimer's mouse retina well before onset of cognitive decline.

Swati S. More, Robert Vince, Swati S More, 2015, ACS chemical neuroscience.

Induction of Erythromycin Resistance in Staphylococcus aureus by Erythromycin Derivatives

S. Pestka, R. LeMahieu, J. Unowsky, 1976, Antimicrobial Agents and Chemotherapy.

Hepatoprotective Effect of ψ-Glutathione in a Murine Model of Acetaminophen-Induced Liver Toxicity.

Swati S. More, Ashish P. Vartak, R. Vince, 2017, Chemical research in toxicology.

Geometric Isomer of Guanabenz Confers Hepatoprotection to a Murine Model of Acetaminophen Toxicity.

Swati S. More, Jiashu Xie, Rongrong Jiang, 2023, Chemical research in toxicology.

Hemolytic and antimalarial effects of tight-binding glyoxalase 1 inhibitors on the host-parasite unit of erythrocytes infected with Plasmodium falciparum

Swati S. More, Marcel Deponte, R. Vince, 2016, Redox biology.

Could the artificial butter flavoring, diacetyl, cause Alzheimer's disease?

Swati S. More, Ashish P. Vartak, R. Vince, 2012 .