Dennis C. Liotta
American chemist
Dennis C. Liotta's AcademicInfluence.com Rankings
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Chemistry
Dennis C. Liotta's Degrees
- PhD Chemistry University of Maryland, College Park
- Bachelors Chemistry University of Notre Dame
Why Is Dennis C. Liotta Influential?
(Suggest an Edit or Addition)According to Wikipedia, Dennis Liotta is a chemistry professor at Emory University in Atlanta, Georgia, United States. He is noted for his work on the development of antiviral drugs. Career Liotta's fields of research are organic synthesis and medicinal chemistry. Along with Dr. Raymond F. Schinazi and Dr. Woo-Baeg Choi of Emory, he invented Emtricitabine, which is a breakthrough HIV drug. Emory University sold its royalties on the drug to Royalty Pharma and Gilead Sciences in July 2005 for $525 million. It is currently marketed under the name Emtriva. Emtriva is a component of a number of combination therapies used to treat HIV, including Truvada, Atripla, Complera, Stribild, Genvoya, Odefesey, Biktarvy, Descovy, and Symtuza. Truvada is the only combination therapy approved for Pre-Exposure Prophylaxis . Liotta, Choi and Schinazi also co-invented Epivir , which is a component of multiple combination therapies such as Combivir, Trizivir, Epzicom, Triumeq, Dutrebis and Delstrigo. It is estimated that >90% of HIV infected patients in the US take or have taken drug combinations that include either Emtriva or Epivir. In addition, he was one of the inventors of Epivir-HBV, the first drug approved to treat hepatitis B infections.
Dennis C. Liotta's Published Works
Published Works
- Inhibition of the replication of hepatitis B virus in vitro by 2',3'-dideoxy-3'-thiacytidine and related analogues. (1991) (496)
- Characterization of human immunodeficiency viruses resistant to oxathiolane-cytosine nucleosides (1993) (379)
- Thematic Review Series: Sphingolipids. Biodiversity of sphingoid bases (“sphingosines”) and related amino alcohols* (2008) (350)
- Synthesis and biological evaluation of novel curcumin analogs as anti-cancer and anti-angiogenesis agents. (2004) (345)
- Polyoxometalate HIV-1 protease inhibitors. A new mode of protease inhibition. (2001) (316)
- Quantitation of free sphingosine in liver by high-performance liquid chromatography. (1988) (296)
- Selectivity of ceramide-mediated biology. Lack of activity of erythro-dihydroceramide. (1993) (289)
- Deoxycytidine deaminase-resistant stereoisomer is the active form of (+/-)-2',3'-dideoxy-3'-thiacytidine in the inhibition of hepatitis B virus replication. (1992) (220)
- The anti-hepatitis B virus activities, cytotoxicities, and anabolic profiles of the (-) and (+) enantiomers of cis-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]cytosine (1992) (213)
- EF24, a novel synthetic curcumin analog, induces apoptosis in cancer cells via a redox-dependent mechanism (2005) (203)
- Fumonisins and fumonisin analogs as inhibitors of ceramide synthase and inducers of apoptosis. (2002) (176)
- Acylation of Naturally Occurring and Synthetic 1-Deoxysphinganines by Ceramide Synthase (1998) (152)
- Inhibition of the NF-κB signaling pathway by the curcumin analog, 3,5-Bis(2-pyridinylmethylidene)-4-piperidone (EF31): anti-inflammatory and anti-cancer properties. (2012) (151)
- Bimodal Regulation of Ceramidase by Interleukin-1β (1997) (151)
- Chemical synthesis and biological evaluation of cis- and trans-12,13-cyclopropyl and 12,13-cyclobutyl epothilones and related pyridine side chain analogues. (2001) (149)
- A subunit-selective potentiator of NR2C- and NR2D-containing NMDA receptors. (2010) (149)
- Inhibition of IκB Kinase-Nuclear Factor-κB Signaling Pathway by 3,5-Bis(2-flurobenzylidene)piperidin-4-one (EF24), a Novel Monoketone Analog of Curcumin (2008) (145)
- Disruption of sphingolipid metabolism and stimulation of DNA synthesis by fumonisin B1. A molecular mechanism for carcinogenesis associated with Fusarium moniliforme. (1994) (143)
- Highly active anticancer curcumin analogues. (2007) (141)
- Fumonisins: fungal toxins that shed light on sphingolipid function. (1996) (138)
- The development of a selective cyclin-dependent kinase inhibitor that shows antitumor activity. (2009) (121)
- Development of a Unique Small Molecule Modulator of CXCR4 (2012) (118)
- In situ complexation directs the stereochemistry of N-glycosylation in the synthesis of oxathiolanyl and dioxolanyl nucleoside analogues (1991) (114)
- Total synthesis of SR 121463 A, a highly potent and selective vasopressin v(2) receptor antagonist. (2001) (106)
- New organoselenium methodology (1984) (106)
- EF24, a novel curcumin analog, disrupts the microtubule cytoskeleton and inhibits HIF-1 (2008) (106)
- Ceramide stimulates epidermal growth factor receptor phosphorylation in A431 human epidermoid carcinoma cells. Evidence that ceramide may mediate sphingosine action. (1991) (104)
- Discovery of small molecule CXCR4 antagonists. (2007) (102)
- A stereoselective synthesis of sphingosine, a protein kinase c inhibitor (1988) (96)
- Mechanism for Noncompetitive Inhibition by Novel GluN2C/D N-Methyl-d-aspartate Receptor Subunit-Selective Modulators (2011) (92)
- Affinity of the antiviral enantiomers of oxathiolane cytosine nucleosides for human 2'-deoxycytidine kinase. (1993) (92)
- Sphingoid bases and de novo ceramide synthesis: enzymes involved, pharmacology and mechanisms of action. (2003) (92)
- Fumonisin toxicity and sphingolipid biosynthesis. (1996) (90)
- Quinazolin-4-one derivatives: A novel class of noncompetitive NR2C/D subunit-selective N-methyl-D-aspartate receptor antagonists. (2010) (90)
- Suppression of aberrant colonic crypt foci by synthetic sphingomyelins with saturated or unsaturated sphingoid base backbones. (1997) (89)
- Pure nucleoside enantiomers of beta-2',3'-dideoxycytidine analogs are selective inhibitors of hepatitis B virus in vitro (1994) (88)
- Free sphingosine formation from endogenous substrates by a liver plasma membrane system with a divalent cation dependence and a neutral pH optimum. (1989) (87)
- Characteristics of the growth inhibition and cytotoxicity of long-chain (sphingoid) bases for Chinese hamster ovary cells: evidence for an involvement of protein kinase C. (1990) (85)
- The Ecstasy and Agony of Assay Interference Compounds. (2017) (83)
- Modulation of the free sphingosine levels in human neutrophils by phorbol esters and other factors. (1988) (82)
- A unified and quantitative receptor model for the microtubule binding of paclitaxel and epothilone. (1999) (80)
- Synthesis of EF24-tripeptide chloromethyl ketone: a novel curcumin-related anticancer drug delivery system. (2006) (79)
- A target site for template-based design of measles virus entry inhibitors. (2004) (76)
- Phenyl selenide anion, a superior reagent for the SN2 cleavage of esters and lactones (1981) (73)
- Stereoselectivity of electrophile-promoted cyclizations of .gamma.-hydroxyalkenes. An investigation of carbohydrate-derived and model substrates (1987) (72)
- GluN2D-Containing N-methyl-d-Aspartate Receptors Mediate Synaptic Transmission in Hippocampal Interneurons and Regulate Interneuron Activity (2016) (72)
- Origins of the enantioselectivity observed in oxazaborolidine-catalyzed reductions of ketones (1993) (71)
- Enzyme-mediated enantioselective preparation of pure enantiomers of the antiviral agent 2',3'-dideoxy-5-fluoro-3'-thiacytidine (FTC) and related compounds (1992) (69)
- The oxetane ring in taxol. (2000) (67)
- Novel NMDA receptor modulators: an update (2012) (66)
- Structural Determinants and Mechanism of Action of a GluN2C-selective NMDA Receptor Positive Allosteric Modulator (2014) (66)
- Monocarbonyl analogs of curcumin inhibit growth of antibiotic sensitive and resistant strains of Mycobacterium tuberculosis. (2015) (65)
- A novel pyrazolo[1,5-a]pyrimidine is a potent inhibitor of cyclin-dependent protein kinases 1, 2, and 9, which demonstrates antitumor effects in human tumor xenografts following oral administration. (2010) (64)
- A simple method for the efficient synthesis of unsaturated .beta.-dicarbonyl compounds (1981) (62)
- A COMPLETELY DIASTEREOSELECTIVE ELECTROPHILIC FLUORINATION OF A CHIRAL, NONCARBOHYDRATE SUGAR RING PRECURSOR : APPLICATION TO THE SYNTHESIS OF SEVERAL NOVEL 2'-FLUORONUCLEOSIDES (1998) (59)
- Dipyrimidine amines: a novel class of chemokine receptor type 4 antagonists with high specificity. (2010) (58)
- Nonpeptide inhibitors of measles virus entry. (2006) (58)
- Design of a Small-Molecule Entry Inhibitor with Activity against Primary Measles Virus Strains (2005) (56)
- DPC 817: a Cytidine Nucleoside Analog with Activity against Zidovudine- and Lamivudine-Resistant Viral Variants (2002) (54)
- Effects of substitution on intramolecular alkoxypalladation carbonylation reactions (1989) (54)
- Ceramide-beta-D-glucuronide: synthesis, digestion, and suppression of early markers of colon carcinogenesis. (1999) (54)
- The Ecstasy and Agony of Assay Interference Compounds (2017) (53)
- Activation of the p38 pathway by a novel monoketone curcumin analog, EF24, suggests a potential combination strategy. (2010) (53)
- An Orally Available, Small-Molecule Polymerase Inhibitor Shows Efficacy Against a Lethal Morbillivirus Infection in a Large Animal Model (2014) (52)
- Context-Dependent GluN2B-Selective Inhibitors of NMDA Receptor Function Are Neuroprotective with Minimal Side Effects (2015) (51)
- Curcumin analog cytotoxicity against breast cancer cells: exploitation of a redox-dependent mechanism. (2009) (51)
- A general method for controlling glycosylation stereochemistry in the synthesis of 2'-deoxyribose nucleosides (1990) (50)
- A simple, efficient synthesis of 3-substituted furans (1983) (50)
- The generation of uncomplexed phenyl selenide anion and its applicability to SN2 - type ester cleavages (1977) (50)
- Two Domains That Control Prefusion Stability and Transport Competence of the Measles Virus Fusion Protein (2006) (49)
- Stereoselectivity of induction of the retinoblastoma gene product (pRb) dephosphorylation by D-erythro-sphingosine supports a role for pRb in growth suppression by sphingosine. (1995) (49)
- Enigmol: A Novel Sphingolipid Analogue with Anticancer Activity against Cancer Cell Lines and In vivo Models for Intestinal and Prostate Cancer (2011) (48)
- Pharmacokinetics and metabolism of racemic 2',3'-dideoxy-5-fluoro-3'-thiacytidine in rhesus monkeys (1992) (47)
- Multiple Anticancer Activities of EF24, a Novel Curcumin Analog, on Human Ovarian Carcinoma Cells (2010) (47)
- Discovery of tetrahydroisoquinoline-based CXCR4 antagonists. (2013) (47)
- Synthesis and biological evaluation of 2',3'-didehydro-2',3'- dideoxy-5-fluorocytidine (D4FC) analogues: discovery of carbocyclic nucleoside triphosphates with potent inhibitory activity against HIV-1 reverse transcriptase. (1999) (46)
- Diastereoselective addition of chlorotitanium enolate of N-acyl thiazolidinethione to O-methyl oximes: A novel, stereoselective synthesis of α, β-disubstituted β-amino carbonyl compounds via chiral auxiliary mediated azetine formation (2003) (46)
- The Ecstasy and Agony of Assay Interference Compounds. (2017) (44)
- Mapping the Binding of GluN2B-Selective N-Methyl-d-aspartate Receptor Negative Allosteric Modulators (2012) (44)
- Cellular pharmacology and biological activity of 5-carboranyl-2'-deoxyuridine. (1994) (43)
- Autophagy and Apoptosis in Hepatocellular Carcinoma Induced by EF25-(GSH)2: A Novel Curcumin Analog (2014) (43)
- Infectious amplification of wild-type human immunodeficiency virus from patients' lymphocytes and modulation by reverse transcriptase inhibitors in vitro (1993) (42)
- Synthesis and structure activity relationship of tetrahydroisoquinoline-based potentiators of GluN2C and GluN2D containing N-methyl-D-aspartate receptors. (2013) (41)
- 3-Alkylfurans as useful synthetic equivalents for substituted δ2-butenolides (1983) (41)
- Design, Synthesis, and Structure–Activity Relationship of a Novel Series of GluN2C-Selective Potentiators (2014) (40)
- Biochemical and mechanistic basis for the activity of nucleoside analogue inhibitors of HIV reverse transcriptase. (2004) (39)
- Structure-activity relationships and pharmacophore model of a noncompetitive pyrazoline containing class of GluN2C/GluN2D selective antagonists. (2013) (37)
- Selenium in Organic Synthesis (1986) (37)
- Stereoselective hydrogen-transfer reactions involving acyclic radicals. A study of radical conformations using semiempirical calculations (1992) (37)
- Dynamics and fluidity of amyloid fibrils: a model of fibrous protein aggregates. (2002) (37)
- Directed evolution of an orthogonal nucleoside analog kinase via fluorescence-activated cell sorting (2009) (36)
- The 5'-triphosphates of the (-) and (+) enantiomers of cis-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxathiolane-5-yl]cytosine equally inhibit human immunodeficiency virus type 1 reverse transcriptase (1993) (36)
- Non-nucleoside inhibitors of the measles virus RNA-dependent RNA polymerase: synthesis, structure-activity relationships, and pharmacokinetics. (2012) (36)
- Pharmacokinetics, oral bioavailability, and metabolic disposition in rats of (-)-cis-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl] cytosine, a nucleoside analog active against human immunodeficiency virus and hepatitis B virus (1993) (36)
- Pyrazolo-Piperidines Exhibit Dual Inhibition of CCR5/CXCR4 HIV Entry and Reverse Transcriptase. (2015) (35)
- 1-Deoxy-5-hydroxysphingolipids as new anticancer principles: an efficient procedure for stereoselective syntheses of 2-amino-3,5-diols. (2005) (35)
- NMDA receptor modulators: an updated patent review (2013 – 2014) (2014) (34)
- Recent advances in the development of HBV capsid assembly modulators. (2019) (33)
- Development and screening of water-soluble analogues of progesterone and allopregnanolone in models of brain injury. (2009) (32)
- Nitrogen Glycosylation Reactions Involving Pyrimidine and Purine Nucleoside Bases with Furanoside Sugars (1995) (32)
- Simple, inexpensive procedure for the large-scale production of alkyl quinones (1983) (32)
- A Novel Negative Allosteric Modulator Selective for GluN2C/2D-Containing NMDA Receptors Inhibits Synaptic Transmission in Hippocampal Interneurons. (2017) (32)
- The Ecstasy and Agony of Assay Interference Compounds. (2017) (32)
- Use of magnesium cation in aldol additions - a convenient method for achieving anti-aldol selectivity (1991) (31)
- Novel Cyclopropyl-Indole Derivatives as HIV Non-Nucleoside Reverse Transcriptase Inhibitors. (2012) (31)
- Synthesis, structural activity-relationships, and biological evaluation of novel amide-based allosteric binding site antagonists in NR1A/NR2B N-methyl-D-aspartate receptors. (2009) (31)
- Monocarbonyl curcumin analogues: heterocyclic pleiotropic kinase inhibitors that mediate anticancer properties. (2013) (31)
- CCR5 receptor antagonists in preclinical to phase II clinical development for treatment of HIV (2016) (30)
- Ligand-assisted nucleophilic additions. Control of site and face attack of nucleophiles on 4-oxido enones (1988) (30)
- Targeting tissue factor-expressing tumor angiogenesis and tumors with EF24 conjugated to factor VIIa. (2008) (30)
- Recent patents regarding the discovery of small molecule CXCR4 antagonists (2009) (30)
- Structural elements of a pH-sensitive inhibitor binding site in NMDA receptors (2019) (30)
- A structurally derived model of subunit‐dependent NMDA receptor function (2018) (30)
- Nucleophilic ring opening of lactones via SN2-type reaction with uncomplexed phenyl selenide anion (1978) (29)
- A Real-Time Method for Measuring cAMP Production Modulated by Gαi/o-Coupled Metabotropic Glutamate Receptors (2014) (29)
- Origins of regio- and stereoselectivity in additions of phenylselenenyl chloride to allylic alcohols and the applicability of these additions to a simple 1,3-enone transposition sequence (1982) (28)
- Stereoselective synthesis of quaternary center bearing azetines and their beta-amino acid derivatives. (2008) (27)
- MECHANISTIC ASPECTS OF THE LIGAND-ASSISTED NUCLEOPHILIC ADDITION REACTION (1990) (27)
- Enantiomeric propanolamines as selective N-methyl-D-aspartate 2B receptor antagonists. (2008) (27)
- Transition-state pliability in nitrogen-to-nitrogen proton transfer (1983) (27)
- Synthesis of sphingosine and sphingoid bases. (2000) (26)
- Novel synthesis and biological evaluation of enigmols as therapeutic agents for treating prostate cancer. (2011) (26)
- An NMDAR positive and negative allosteric modulator series share a binding site and are interconverted by methyl groups (2018) (26)
- Human acid beta-glucosidase: use of sphingosyl and N-alkyl-glucosylamine inhibitors to investigate the properties of the active site. (1990) (25)
- Diels-Alder reactions involving cross-conjugated dienones. Effects of substitution on reactivity (1981) (25)
- Inhibition of skin carcinomas but not papillomas by sphingosine, N-methylsphingosine, and N-acetylsphingosine. (1998) (25)
- Discovery of aminoquinolines as a new class of potent inhibitors of heat shock protein 90 (Hsp90): Synthesis, biology, and molecular modeling. (2008) (24)
- Synthesis of C-arabinofuranosyl compounds. Phosphonate and carboxylate isosteres of d-arabinose 1,5-bisphosphate (1987) (24)
- Highly diastereoselective aldol reactions of chiral methyl ketones (1993) (24)
- Pyridinium dichromate-induced 1,3-oxidative rearrangements of enynols (1987) (23)
- Phosphatidyl-2',3'-dideoxy-3'-thiacytidine: synthesis and antiviral activity in hepatitis B-and HIV-1-infected cells. (1995) (23)
- Discovery and Development of the Anti-Human Immunodeficiency Virus Drug, Emtricitabine (Emtriva, FTC). (2016) (23)
- Cyclization protocols for controlling the glycosidic stereochemistry of nucleosides. Application to the synthesis of the antiviral agent 3'-azido-3'-deoxythymidine (AZT) (1991) (23)
- Complementary Facial Selectivity in Conjugate Additions to γ-Hydroxyenones (1992) (23)
- Episulfonium ions may not be the stereodeterminants in glycosylations of 2-thioalkyl pyranosides (1993) (23)
- The synthesis and anti-hiv activity of pyrimidine dioxolanyl nucleosides (1993) (22)
- Photoelectron spectra of alkyl aryl selenides. Electronic and steric factors in the observation of rotamers (1981) (22)
- Discovery of Tetrahydroisoquinoline-Containing CXCR4 Antagonists with Improved in Vitro ADMET Properties. (2018) (22)
- Synthesis and Metabolic Studies of Host Directed Inhibitors for Anti Viral Therapy. (2013) (22)
- An efficient synthesis of 3′-fluoro-3′-deoxythymidene (FLT) (1992) (22)
- NMDA receptor channel gating control by the pre-M1 helix (2020) (21)
- A two-step chemical and circular dichroic method for assigning the absolute configurations of sphingosines (1995) (21)
- Targeting tissue factor-expressing tumor angiogenesis and tumors with EF24 conjugated to factor VIIa (2008) (21)
- Synthetic applications of 2-phenylselenenylenones—III (1985) (21)
- Anti‐HIV Small‐Molecule Binding in the Peptide Subpocket of the CXCR4:CVX15 Crystal Structure (2014) (21)
- A synthesis of the abietane diterpenoid quinone (±)-royleanone via maleoylcobalt technology. (1990) (21)
- Design, Synthesis, and Pharmacological Evaluation of Second-Generation Tetrahydroisoquinoline-Based CXCR4 Antagonists with Favorable ADME Properties. (2018) (21)
- Synthetic applications of phenyltrimethylsilylselenide (1978) (20)
- Regulation of sphingosine-activated protein kinases: selectivity of activation by sphingoid bases and inhibition by non-esterified fatty acids. (1993) (20)
- Molecular aggregation and its applicability to synthesis. The Diels-Alder reaction (1988) (20)
- Diastereoselective sulfenylation reactions employing N-phenylthio lactams under nonbasic conditions (1992) (20)
- A General Synthesis of 2-Phenylselenenylenones. The Reaction of Unsaturated Ketones with a Phenylselenenyl Chloride/Pyridine Complex (1980) (19)
- Stereocontrolled glycosylations via additions of sulfur electrophiles to glycals (1993) (19)
- Calculated conformer energies for organic molecules with multiple polar functionalities are method dependent: Taxol (case study) (2001) (19)
- Pharmacokinetics of the Antiviral Agent β-d-2′,3′-Didehydro-2′,3′-Dideoxy-5-Fluorocytidine in Rhesus Monkeys (1999) (19)
- Small molecule and peptide-based CXCR4 modulators as therapeutic agents. A patent review for the period from 2010 to 2018 (2019) (19)
- Design and synthesis of C6-C8 bridged epothilone A. (2008) (18)
- Biased modulators of NMDA receptors control channel opening and ion selectivity (2019) (18)
- In situ Complexation Directs the Stereochemistry of N‐Glycosylation in the Synthesis of Oxathiolanyl and Dioxolanyl Nucleoside Analogues. (1992) (18)
- Discovery of novel N-aryl piperazine CXCR4 antagonists. (2015) (18)
- Synthesis and evaluation of 2'-substituted cyclobutyl nucleosides and nucleotides as potential anti-HIV agents. (2007) (18)
- Bioactive Properties of Sphingosine and Structurally Related Compounds (1996) (18)
- Fluorimetric studies of protein kinase C interactions with phospholipids. (1989) (17)
- A diastereoselective synthesis of (2S, 3R, 4S)-2-amino-1-cyclohexyl-6-methylheptane-3,4-diol, the Abbott aminodiol☆ (1996) (17)
- Synthetic applications of 2-phenylselenenyl enones. Selective formation of exocyclic or endocyclic enones from a common intermediate (1980) (17)
- Reactions involving selenium metal as an electrophile. The enolate - selenolate transformation (1980) (17)
- New probes for electron-transfer processes. Evidence supporting the single-electron-transfer mechanism in additions of carbanions to dienones (1983) (17)
- Based-induced rearrangements of .alpha.-phenylselenenyl ketones (1982) (17)
- Phosphonosilylations of cyclic enones (1982) (17)
- Enantioselective synthesis of the carbocyclic nucleoside (-)-abacavir. (2012) (16)
- Triene Cyclizations. The Total Synthesis of Pallescensin A (1987) (16)
- Bimodal Regulation of Ceramidase by Interleukin-1 b IMPLICATIONS FOR THE REGULATION OF CYTOCHROME P 450 2 C 11 ( CYP 2 C 11 ) * (1997) (16)
- Acetylide Additions to Enediones. Regioselectivity Based on Stereoelectronic Control. (1985) (16)
- SYNTHETIC APPLICATIONS OF 2-PHENYLSELENENYLENONES. 2. SYNTHESIS OF DIHYDROJASMONE AND CIS-JASMONE (1981) (16)
- Reactions involving selenium metal as an electrophile. 2. A general procedure for the preparation of unsaturated β-dicarbonyl compounds (1981) (16)
- Discovery of a Fluorinated Enigmol Analog with Enhanced in Vivo Pharmacokinetic and Anti-Tumor Properties. (2016) (16)
- Absolute Configuration of the Antiviral Agent (−)-cis-5-Fluoro-1-[2-Hydroxymethyl)-1,3-Oxathiolan-5-yl]Cytosine (1993) (16)
- Synthetic applications of phenylselenenyl chloride additions. A simple 1,3-enone transposition sequence (1980) (15)
- Aldol reactions of α-(N,N-dibenzylamino) ethyl ketones (1994) (15)
- Solvation-controlled diastereofacial selectivity in alkylations of bicyclic lactam enolates (1990) (15)
- Pharmacokinetics of 5-carboranyl-2'-deoxyuridine in rats. (1994) (15)
- Synthesis of 1-deoxysphingosine derivatives with conformationally restricted pyrrolidinediol head groups. (2006) (15)
- The GluN2B‐Glu413Gly NMDA receptor variant arising from a de novo GRIN2B mutation promotes ligand‐unbinding and domain opening (2018) (15)
- Computational studies of transition metal selectivity of octapeptide repeat region of prion protein (PrP). (2010) (14)
- SELECTIVE REACTIONS OF CARBANIONS WITH P-QUINONES. THE AGGREGATE MODEL (1981) (14)
- Potent SARS-CoV-2 Direct-Acting Antivirals Provide an Important Complement to COVID-19 Vaccines (2021) (14)
- Influences of sphingosine on two-stage skin tumorigenesis in Sencar mice. (1992) (14)
- An efficient asymmetric synthesis of Enigmols (1-deoxy-5- hydroxysphingoid bases), an important class of bioactive lipid modulators (2010) (13)
- Chloride is an Agonist of Group II and III Metabotropic Glutamate Receptors (2015) (13)
- Diastereoselective synthesis of the key lactone intermediate for the preparation of hydroxyethylene dipeptide isosteres (1994) (13)
- The reaction of β,γ-unsaturated acids with phenylselenenyl chloride.: Decarboxylative elimination vs phenylselenolactonization. (1979) (13)
- An examination of the synthetic utility of phenylselenenyl chloride additions to olefins (1979) (13)
- Asymmetric synthesis of host-directed inhibitors of myxoviruses (2013) (13)
- Remote asymmetric induction in organocopper conjugate additions to 3-ketoacrylates (1996) (12)
- Evaluating the neurotherapeutic potential of a water-soluble progesterone analog after traumatic brain injury in rats (2016) (12)
- Negative allosteric modulation of GluN1/GluN3 NMDA receptors (2020) (12)
- Tumor Angiogenesis Therapy Using Targeted Delivery of Paclitaxel to the Vasculature of Breast Cancer Metastases (2014) (12)
- Aryl Substituted Benzimidazolones as Potent HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors. (2019) (12)
- Opening of tartrate acetals using dialkylboron bromide: evidence for stereoselectivity downstream from ring fission. (2003) (12)
- Stereocontrolled synthesis of β-2′-deoxypyrimidine nucleosides via intramolecular glycosylations (1997) (12)
- The Ecstasy and Agony of Assay Interference Compounds. (2017) (12)
- The case favoring direct C-alkylation of heteroatom-substituted enolates (1988) (12)
- Surprisingly high diastereoselection in the aldol reactions of sodium enolates of α-amino methyl ketones (1994) (12)
- Water-soluble progesterone analogues are effective, injectable treatments in animal models of traumatic brain injury. (2012) (12)
- Synthesis of Novel Tetrahydroisoquinoline CXCR4 Antagonists with Rigidified Side-Chains. (2018) (11)
- The Structure-Activity Relationship of a Tetrahydroisoquinoline Class of N-Methyl-d-Aspartate Receptor Modulators that Potentiates GluN2B-Containing N-Methyl-d-Aspartate Receptors. (2017) (11)
- Pharmacokinetics of 2',3'-dideoxy-5-fluoro-3'-thiacytidine in rats. (1994) (11)
- REVERSAL OF STEREOSPECIFICITY DURING ALLYLIC HYDROPEROXIDATION OF 3-NORCARENE AND BICYCLO(4.2.0)OCT-3-ENE DERIVATIVES ARISING FROM STRUCTURALLY ENFORCED QUENCHING OF SINGLET OXYGEN BY THE HYDRAZIDE FUNCTIONALITY (1976) (11)
- Synthesis and SAR of 1,2,3,4-Tetrahydroisoquinoline-Based CXCR4 Antagonists. (2018) (11)
- Structural analysis of CXCR4 - Antagonist interactions using saturation-transfer double-difference NMR. (2015) (11)
- Inhibition of breast cancer metastasis to the lungs with UBS109 (2018) (10)
- A novel class of negative allosteric modulators of NMDA receptor function. (2015) (10)
- Comparison of collisional activation spectra of some positive ions produced both by charge reversal of negative ions and by decomposition of positive ions (1982) (10)
- In Vitro Metabolic Stability and in Vivo Biodistribution of 3-Methyl-4-furoxancarbaldehyde Using PET Imaging in Rats. (2016) (10)
- Trajectories of proton transfer reactions. Experimental determination of the magnitude of primary deuterium isotope effects for proton-transfers occuring at acute angles (1988) (10)
- A General Synthetic Method of 5-Carboranyluracil Nucleosides with Potential Antiviral Activity and use in Neutron Capture Therapy (1997) (9)
- Synthesis of fluorescent nucleoside analogs as probes for 2'-deoxyribonucleoside kinases. (2010) (9)
- Frontier molecular orbital basis for the structurally dependent regiospecific reactions of singlet (1Δg) oxygen with polyolefins (1976) (9)
- Adamantane and nipecotic acid derivatives as novel β-Turn mimics (1994) (9)
- C6-C8 bridged epothilones: consequences of installing a conformational lock at the edge of the macrocycle. (2011) (9)
- Synthesis, anti-human immunodeficiency virus, and anti-hepatitis B virus activity of pyrimidine oxathiolane nucleosides (1993) (9)
- Reduction Sensitive Lipid Conjugates of Tenofovir: Synthesis, Stability, and Antiviral Activity. (2016) (8)
- The Discovery of Dihydropyrrolo[1,2-a]pyrazin-3(4H)-one-Based Second-Generation GluN2C- and GluN2D-Selective Positive Allosteric Modulators (PAMs) of the N-Methyl-D-Aspartate (NMDA) Receptor. (2020) (8)
- A Machine Learning Approach for Predicting HIV Reverse Transcriptase Mutation Susceptibility of Biologically Active Compounds (2018) (8)
- Small molecule CXCR4 antagonists block the HIV-1 Nef/CXCR4 axis and selectively initiate the apoptotic program in breast cancer cells (2018) (8)
- Distinct GluN1 and GluN2 Structural Determinants for Subunit-Selective Positive Allosteric Modulation of N-Methyl-d-aspartate Receptors. (2020) (8)
- A Facially-Selective Protonation Controls the Stereochemistry of a Key Intermediate in the Synthesis of 1.beta.-Methylcarbapenems (1994) (8)
- Synthesis of enantiomerically pure D-FDOC, an anti-HIV agent. (2004) (8)
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- Editorial Confronting Racism in Chemistry Journals (2020) (0)
- Update to Our Reader, Reviewer, and Author Communities-April 2020. (2020) (0)
- Confronting Racism in Chemistry Journals. (2020) (0)
- Stereocontrolled Glycosylations via Addition of Sulfur Electrophiles to Glycals. (1993) (0)
- Organoselenium Chemistry I. Functional Group Transformations (1989) (0)
- Update to Our Reader, Reviewer, and Author Communities-April 2020. (2020) (0)
- Confronting Racism in Chemistry Journals. (2020) (0)
- Pharmacokinetics of the Antiviral Agent bD-2 9 , 3 9-Didehydro-2 9 , 3 9-Dideoxy-5-Fluorocytidine in Rhesus Monkeys (1999) (0)
- Confronting Racism in Chemistry Journals. (2020) (0)
- Confronting Racism in Chemistry Journals. (2020) (0)
- Confronting Racism in Chemistry Journals. (2020) (0)
- Molecular Aggregation and Its Applicability to Synthesis. The Diels-Alder Reaction. (1989) (0)
- Effects of Substitution on Intramolecular Alkoxypalladation Carbonylation Reactions. (1990) (0)
- Confronting Racism in Chemistry Journals. (2020) (0)
- Confronting Racism in Chemistry Journals. (2020) (0)
- Process for the preparation of therapeutically useful beta-2-hydroxymethyl-5- (5-fluorocytosin-1-yl) -1,3-oxathiolane enantiomers (1993) (0)
- Pyridinium Dichromate-Induced 1,3-Oxidative Rearrangements of Enynols. (1987) (0)
- Long-chain (sphingoid) bases cause growth changes and cytotoxicity in Chinese hamster ovary cells (1987) (0)
- Recent Reviews. 39 (1996) (0)
- The method of the nucleoside 2 ', 3'-dideoxy-3' -tiapyrimidiini beta-isomer valmistamiseski (1992) (0)
- Development of novel small molecule inhibitors targeting CXCR4 against cancer metastasis (2006) (0)
- Ligand Assisted Nucleophilic Additions. Control of Site and Face Attack of Nucleophiles on 4‐Oxidoenones. (1988) (0)
- Update to Our Reader, Reviewer, and Author Communities-April 2020. (2020) (0)
- Photoelectron Spectra of Alkyl Aryl Selenides. Electronic and Steric F actors in the Observation of Rotamers. (1982) (0)
- Synthesis of Enantiomerically Pure D‐FDOC, an anti‐HIV Agent. (2005) (0)
- Salts of amides of (-) cis 5-fluoro-2'-3'-thiacytidine dedoxi useful for the treatment of hepatitis b. (1992) (0)
- Selenium in Organic Syntheses (1986) (0)
- Confronting Racism in Chemistry Journals. (2020) (0)
- Update to Our Reader, Reviewer, and Author Communities-April 2020. (2020) (0)
- Coal liquefaction in a fluorocarbon medium. Final report, August 1982-November 1985. [1,2,3,4-tetrahydroquinoline] (1985) (0)
- Diastereoselective Addition of Chlorotitanium Enolates of N-Acyl Thiazolidinethione to Activated Imines — A Novel Synthesis of β-Lactams. (2007) (0)
- 236 GROWTH INHIBITORY EFFECTS OF ENIGMOL, (2-AMINO-3,5-DIHYDROXYOCTADECANE[2S,3S,5S]), ON ANDROGEN-DEPENDENT AND ANDROGEN-INDEPENDENT PROSTATE CANCER (2010) (0)
- Confronting Racism in Chemistry Journals. (2020) (0)
- Empirical Derivation of Molecular Mechanics Parameter Sets: Application to β-Lactams (2010) (0)
- Recent Reviews. 47. (1998) (0)
- Therapeutic Discovery Enigmol : A Novel Sphingolipid Analogue with Anticancer Activity against Cancer Cell Lines and In vivo Models for Intestinal and Prostate Cancer (2011) (0)
- Virtual Special Issue: Epigenetics 2022. (2022) (0)
- Using 5-fluoro-2'-deoxy-3'-thiacytidine for the treatment of hepatitis B (1992) (0)
- A Synthesis of the Abietane Diterpenoid Quinone (.+-.)-Royleanone via Maleoylcobalt Technology. (1991) (0)
- Confronting Racism in Chemistry Journals. (2020) (0)
- Design and Evaluation of Nonpeptide Fibrinogen y-Chain Based GPIIbDIIa Antagonists (2001) (0)
- Update to Our Reader, Reviewer, and Author Communities-April 2020. (2020) (0)
- Confronting Racism in Chemistry Journals. (2020) (0)
- Channel Open Probability Controls Allosteric Modulation of Potency and Efficacy (2017) (0)
- Update to Our Reader, Reviewer, and Author Communities—April 2020 (2020) (0)
- Salts and amides of the (-) cis-5-fluoro-2'-deoxy-thiacytidine which are suitable for the treatment of hepatitis B (1992) (0)
- Correction to Reduction Sensitive Lipid Conjugates of Tenofovir: Synthesis, Stability, and Antiviral Activity. (2017) (0)
- Update to Our Reader, Reviewer, and Author Communities-April 2020. (2020) (0)
- A Uniquely Accessible Route to the Diastereoselective Synthesis of Azetine Derivatives. (2004) (0)
- Virtual Special Issue: Epigenetics 2022. (2022) (0)
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