نتائج البحث - "Maria S. Brown"

1

Academic Journal

Production of 6-Deoxy-13-cyclopropyl-Erythromycin B by Saccharopolyspora erythraea NRRL 18643

المؤلفون: BROOK K. MORSE, DIANNE M. RESCEK, ELLEN L. MCCORMICK, HAMISH A. I. MCARTHUR, JOHN P. DIRLAM, JOHN RUDDOCK, MARIA S. BROWN, MIKE PACEY, PAUL A. MURPHY, RICHARD G. WAX, THOMAS N. O'CONNELL

المصدر: The Journal of Antibiotics. 1999, 52(8):742

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2

Academic Journal

Biosynthesis of the Shikimate-derived Starter Unit of the Immunosuppressant Ascomycin: Stereochemistry of the 1, 4-Conjugate Elimination

المؤلفون: HAMISH A. I. MCARTHUR, HEINZ G. FLOSS, KEVIN A. REYNOLDS, KIMBERLEE K. WALLACE, MARIA S. BROWN, SANDEEP HANDA

المصدر: The Journal of Antibiotics. 1997, 50(8):701

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3

Academic Journal

Selective Production of Capreomycins through Mutation and Medium Development

المؤلفون: ALBERT E. DORO, BROOK K. MORSE, HAMISH A. I. MCARTHUR, MARIA S. BROWN, RICHARD G. WAX, T. KEVIN MURPHY

المصدر: The Journal of Antibiotics. 1997, 50(8):696

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4

Academic Journal

Production of Tuberactinamine A by Streptomyces griseovertidllatus var. tuberacticus NRRL 3482 Fed with (S)2-Aminoethyl-L-cysteine

المؤلفون: ADAM A. SMOGOWICZ, BROOK K. MORSE, DAVID A. PERRY, ELLEN L. MCCORMICK, HAMISH A. I. MCARTHUR, JOHN W. GAGNE, JOHN W. WONG, MARIA S. BROWN, MATT H. NARROL, RICHARD G. WAX, T. KEVIN MURPHY

المصدر: The Journal of Antibiotics. 1997, 50(8):698

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5

Optimization of Metal Affinity Ketoreductase Immobilization for Application in Batch and Flow Processes

المؤلفون: Alessandra Basso, Maria S. Brown, Alvaro Cruz-Izquierdo, Carlos A. Martinez, Simona Serban

المصدر: Organic Process Research & Development. 26:2075-2084

مصطلحات موضوعية: Organic Chemistry, Physical and Theoretical Chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::af3dd0ea67cc8b696312cdc78b7546e8
https://doi.org/10.1021/acs.oprd.1c00483

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6

Streamlined Synthesis of a Bicyclic Amine Moiety Using an Enzymatic Amidation and Identification of a Novel Solid Form

المؤلفون: Taegyo Lee, Richard A. Wisdom, Amber M. Johnson, Kevin M. Knopf, Giselle P. Reyes, Bryan Li, Ruggeri Sally G, Maria S. Brown, Gerald A. Weisenburger, Lulin Wei, Adam E. Goetz, Cuong V. Lu, Kris N. Jones, Angela L. A. Puchlopek-Dermenci, Michaella A. Caporello, Samir A. Kulkarni, Mengtan Zhang, Javier Magano

المصدر: Organic Process Research & Development. 25:1419-1430

مصطلحات موضوعية: chemistry.chemical_classification, Enzyme, Bicyclic molecule, Chemistry, Organic Chemistry, Moiety, Identification (biology), Amine gas treating, Physical and Theoretical Chemistry, Combinatorial chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::c07b7b0b7a0caed0edf5cb6b7b291c73
https://doi.org/10.1021/acs.oprd.1c00120

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7

Late-Stage Lead Diversification Coupled with Quantitative Nuclear Magnetic Resonance Spectroscopy to Identify New Structure–Activity Relationship Vectors at Nanomole-Scale Synthesis: Application to Loratadine, a Human Histamine H1 Receptor Inverse Agonist

المصدر: Journal of Medicinal Chemistry. 63:7268-7292

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::4a4f2cd830cd5ca3994e400969ad8fd2
https://doi.org/10.1021/acs.jmedchem.0c00483

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8

Late-Stage Microsomal Oxidation Reduces Drug-Drug Interaction and Identifies Phosphodiesterase 2A Inhibitor PF-06815189

المصدر: ACS Medicinal Chemistry Letters

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ebf76f135a3421c85311e525117027f
https://pubmed.ncbi.nlm.nih.gov/29456790

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9

Industrial Carbonyl Reduction

المؤلفون: John W. Wong, Thomas S. Moody, Jeremy Steflik, Maria S. Brown, Owen W. Gooding, Gjalt W. Huisman, David Mangan, Carlos A. Martinez, Jack Liang, Michael Paul Burns, Adam A. Smogowicz, Katarina S. Midelfort

المصدر: Practical Methods for Biocatalysis and Biotransformations 2

مصطلحات موضوعية: Chemistry, Carbonyl reduction, Organic chemistry, Photochemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::7e5c3172496feec5a814a3e282c19870
https://doi.org/10.1002/9781119943426.ch4

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10

ChemInform Abstract: Biosynthesis of the Shikimate-Derived Starter Unit of the Immunosuppressant Ascomycin: Stereochemistry of the 1,4-Conjugate Elimination

المؤلفون: Kimberlee K. Wallace, Heinz G. Floss, Kevin A. Reynolds, Hamish A. I. McArthur, Maria S. Brown, Sandeep Handa

المصدر: ChemInform. 29

مصطلحات موضوعية: chemistry.chemical_compound, Starter, Biosynthesis, Chemistry, Stereochemistry, medicine, General Medicine, Ascomycin, medicine.drug, Conjugate

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d5d879df1cd49e9c974cfe81af586caa
https://doi.org/10.1002/chin.199803241

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11

ChemInform Abstract: Production of 6-Deoxy-13-cyclopropyl-erythromycin B by Saccharopolyspora erythraea NRRL 18643

المؤلفون: Maria S. Brown, et al. et al.

المصدر: ChemInform. 31

مصطلحات موضوعية: 6-deoxy-13-cyclopropyl-erythromycin B, biology, Chemistry, Stereochemistry, medicine.drug_class, Antibiotics, medicine, Saccharopolyspora erythraea, General Medicine, biology.organism_classification

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::07a8277853a0c78c2d470474de624979
https://doi.org/10.1002/chin.200003243

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12

Production of 6-deoxy-13-cyclopropyl-erythromycin B by Saccharopolyspora erythraea NRRL 18643

المؤلفون: Hamish A. I. McArthur, Ellen L. McCormick, Mike Pacey, Thomas N. O'Connell, John C. Ruddock, John P. Dirlam, Paul A. Murphy, Maria S. Brown, Brook Knight Morse, Richard Gerald Wax, Dianne M. Rescek

المصدر: The Journal of antibiotics. 52(8)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8db122089fa02833059677309da2751d
https://pubmed.ncbi.nlm.nih.gov/10580387

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13

Academic Journal

Streamlined Synthesis of a Bicyclic Amine Moiety Using an Enzymatic Amidation and Identification of a Novel Solid Form

المؤلفون: Maria S. Brown (10880964), Michaella A. Caporello (10531618), Adam E. Goetz (1309353), Amber M. Johnson (2164633), Kris N. Jones (1857169), Kevin M. Knopf (6620207), Samir A. Kulkarni (1516072), Taegyo Lee (1591999), Bryan Li (1997587), Cuong V. Lu (2999454), Javier Magano (1608052), Angela L. A. Puchlopek-Dermenci (3865009), Giselle P. Reyes (10880967), Sally Gut Ruggeri (10048410), Lulin Wei (2320732), Gerald A. Weisenburger (2407798), Richard A. Wisdom (10880970), Mengtan Zhang (10880973)

Relation: https://figshare.com/articles/journal_contribution/Streamlined_Synthesis_of_a_Bicyclic_Amine_Moiety_Using_an_Enzymatic_Amidation_and_Identification_of_a_Novel_Solid_Form/14684358

الاتاحة: https://doi.org/10.1021/acs.oprd.1c00120.s001

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14

Stereochemical Analyses of the Streptomyces hygroscopicus var. ascomyceticus Type-II Dehydroquinate Dehydratase and Evidence for a Role of the Enzyme in the Biosynthesis of the Shikimate-Derived Moiety of Ascomycin

المؤلفون: Claudio D. Denoya, Maria S. Brown, Hamish A. I. McArthur, Kevin A. Reynolds, Yuko M. Lindsay, Galina Florova

المصدر: The Journal of Organic Chemistry. 63:8098-8099

مصطلحات موضوعية: chemistry.chemical_classification, biology, Stereochemistry, Chemistry, Organic Chemistry, biology.organism_classification, chemistry.chemical_compound, Enzyme, Biochemistry, Biosynthesis, Dehydratase, medicine, Moiety, Ascomycin, Streptomyces hygroscopicus, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::10251d3241c10bbe062844f196b4da33
https://doi.org/10.1021/jo981712z

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15

Biosynthetic studies of ascomycin (FK520): formation of the (1R,3R,4R)-3,4-dihydroxycyclohexanecarboxylic acid-derived moiety

المؤلفون: Richard Gerald Wax, Hamish A. I. McArthur, Kevin A. Reynolds, Maria S. Brown, Bradley S. Moore, Kevin Koch, Kimberlee K. Wallace

المصدر: Journal of the American Chemical Society. 116:11600-11601

مصطلحات موضوعية: Colloid and Surface Chemistry, Chemistry, Stereochemistry, medicine, Moiety, General Chemistry, Ascomycin, Biochemistry, Catalysis, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::5dd56aca6be43437e0e5ca9bd272eaa7
https://doi.org/10.1021/ja00104a063

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