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Results: 1-25 | 26-38
Results: 1-25/38
SYNTHETIC STUDY OF ALPHA-PYRONE MEROTERPE NOIDS, PYRIPYROPENES
Authors: SUNAZUKA T NAGAMITSU T
Citation: T. Sunazuka et T. Nagamitsu, SYNTHETIC STUDY OF ALPHA-PYRONE MEROTERPE NOIDS, PYRIPYROPENES, Yuki Gosei Kagaku Kyokaishi, 56(6), 1998, pp. 478-488
SOFTWARE PROCESS INNOVATION METHODOLOGY - MULTIPLE APPROACH INCLUDINGIS09001, MATURITY MODEL AND QC TECHNIQUE
Authors: HONDA K SUNAZUKA T MIYASHITA Y
Citation: K. Honda et al., SOFTWARE PROCESS INNOVATION METHODOLOGY - MULTIPLE APPROACH INCLUDINGIS09001, MATURITY MODEL AND QC TECHNIQUE, NEC research & development, 38(1), 1997, pp. 96-104
NEW ANALOGS OF THE PYRIPYROPENE FAMILY OF ACAT INHIBITORS VIA ALPHA-PYRONE FRAGMENTATION AND GAMMA-ACYLATION CYCLIZATION/
Authors: OBATA R SUNAZUKA T TIAN ZM TOMODA H HARIGAYA Y OMURA S SMITH AB
Citation: R. Obata et al., NEW ANALOGS OF THE PYRIPYROPENE FAMILY OF ACAT INHIBITORS VIA ALPHA-PYRONE FRAGMENTATION AND GAMMA-ACYLATION CYCLIZATION/, Chemistry Letters, (9), 1997, pp. 935-936
SYNTHESIS OF 4 CHIRAL ISOMERS OF BETA-LACTONE DU-6622 AND INHIBITION OF HMG-COA SYNTHASE BY THE SPECIFIC (2R,3R)-ISOMER
Authors: TOMODA H KUMAGAI H OGAWA Y SUNAZUKA T HASHIZUME H NAGASHIMA H OMURA S
Citation: H. Tomoda et al., SYNTHESIS OF 4 CHIRAL ISOMERS OF BETA-LACTONE DU-6622 AND INHIBITION OF HMG-COA SYNTHASE BY THE SPECIFIC (2R,3R)-ISOMER, Journal of organic chemistry, 62(7), 1997, pp. 2161-2165
SYNTHESES AND ABSOLUTE STRUCTURES OF NOVEL PROTEIN FARNESYLTRANSFERASE INHIBITORS, KURASOINS A AND B
Authors: SUNAZUKA T HIROSE T TIAN ZM UCHIDA R SHIOMI K HARIGAYA Y OMURA S
Citation: T. Sunazuka et al., SYNTHESES AND ABSOLUTE STRUCTURES OF NOVEL PROTEIN FARNESYLTRANSFERASE INHIBITORS, KURASOINS A AND B, Journal of antibiotics, 50(5), 1997, pp. 453-455
CHEMICAL MODIFICATION AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF PYRIPYROPENES .3. SYNTHETIC CONVERSION OF PYRIDINE-PYRONE MOIETY
Authors: OBATA R SUNAZUKA T TIAN ZM TOMODA H HARIGAYA Y OMURA S
Citation: R. Obata et al., CHEMICAL MODIFICATION AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF PYRIPYROPENES .3. SYNTHETIC CONVERSION OF PYRIDINE-PYRONE MOIETY, Journal of antibiotics, 50(3), 1997, pp. 229-236
EFFICIENT CHEMICAL CONVERSION OF LOUISIANIN-A TO LOUISIANIN-C AND LOUISIANIN-D, THE INHIBITOR OF ANGIOGENESIS
Authors: SUNAZUKA T ZHIMING T HARIGAYA Y TAKAMATSU S HAYASHI M KOMIYAMA K OMURA S
Citation: T. Sunazuka et al., EFFICIENT CHEMICAL CONVERSION OF LOUISIANIN-A TO LOUISIANIN-C AND LOUISIANIN-D, THE INHIBITOR OF ANGIOGENESIS, Journal of antibiotics, 50(3), 1997, pp. 274-275
CHLOROPEPTINS, NEW ANTI-HIV ANTIBIOTICS INHIBITING GP120-CD4 BINDING FROM STREPTOMYCES SP .2. STRUCTURE ELUCIDATION OF CHLOROPEPTIN-I
Authors: MATSUZAKI K OGINO T SUNAZUKA T TANAKA H OMURA S
Citation: K. Matsuzaki et al., CHLOROPEPTINS, NEW ANTI-HIV ANTIBIOTICS INHIBITING GP120-CD4 BINDING FROM STREPTOMYCES SP .2. STRUCTURE ELUCIDATION OF CHLOROPEPTIN-I, Journal of antibiotics, 50(1), 1997, pp. 66-69
RELATIVE AND ABSOLUTE STEREOCHEMISTRIES AND TOTAL SYNTHESIS OF (-MACROSPHELIDE-A AND (+)-MACROSPHELIDE-B, POTENT, ORALLY BIOAVAILABLE INHIBITORS OF CELL-CELL ADHESION())
Authors: SUNAZUKA T HIROSE T HARIGAYA Y TAKAMATSU S HAYASHI M KOMIYAMA K OMURA S SPRENGELER PA SMITH AB
Citation: T. Sunazuka et al., RELATIVE AND ABSOLUTE STEREOCHEMISTRIES AND TOTAL SYNTHESIS OF (-MACROSPHELIDE-A AND (+)-MACROSPHELIDE-B, POTENT, ORALLY BIOAVAILABLE INHIBITORS OF CELL-CELL ADHESION()), Journal of the American Chemical Society, 119(42), 1997, pp. 10247-10248
SYNTHESIS AND ACTIVITY OF STAUROSPORINE ANALOGS WITH A LACTONE FUNCTIONALITY
Authors: YAMADA R FUKUDA K KAWANISHI M OHMORI Y NASU M SETO M SASAKI Y SUNAZUKA T ZHUORONG L FUNATO N IGUCHI M HARIGAYA Y IWAI Y OMURA S
Citation: R. Yamada et al., SYNTHESIS AND ACTIVITY OF STAUROSPORINE ANALOGS WITH A LACTONE FUNCTIONALITY, Bioorganic & medicinal chemistry letters, 6(16), 1996, pp. 1893-1896
CHEMISTRY AND SYNTHETIC STUDY OF LACTACYSTIN, THE FIRST NONPROTEIN NEUROTROPHIC FACTOR
Authors: SUNAZUKA T NAGAMITSU T OMURA S
Citation: T. Sunazuka et al., CHEMISTRY AND SYNTHETIC STUDY OF LACTACYSTIN, THE FIRST NONPROTEIN NEUROTROPHIC FACTOR, Yuki Gosei Kagaku Kyokaishi, 54(9), 1996, pp. 740-751
BIOSYNTHESIS OF PYRIPYROPENE-A
Authors: TOMODA H TABATA N NAKATA Y NISHIDA H KANEKO T OBATA R SUNAZUKA T OMURA S
Citation: H. Tomoda et al., BIOSYNTHESIS OF PYRIPYROPENE-A, Journal of organic chemistry, 61(3), 1996, pp. 882-886
KURASOIN-A AND KURASOIN-B, NEW-PROTEIN FARNESYLTRANSFERASE INHIBITORSPRODUCED BY PAECILOMYCES SP FO-3684 .2. STRUCTURE ELUCIDATION AND TOTAL SYNTHESIS
Authors: UCHIDA R SHIOMI K SUNAZUKA T INOKOSHI J NISHIZAWA A HIROSE T TANAKA H IWAI Y OMURA S
Citation: R. Uchida et al., KURASOIN-A AND KURASOIN-B, NEW-PROTEIN FARNESYLTRANSFERASE INHIBITORSPRODUCED BY PAECILOMYCES SP FO-3684 .2. STRUCTURE ELUCIDATION AND TOTAL SYNTHESIS, Journal of antibiotics, 49(9), 1996, pp. 886-889
ARISUGACIN-A AND ARISUGACIN-B, NOVEL AND SELECTIVE ACETYLCHOLINESTERASE INHIBITORS FROM PENICILLIUM SP FO-4259 .2. STRUCTURE ELUCIDATION
Authors: KUNO F SHIOMI K OTOGURO K SUNAZUKA T OMURA S
Citation: F. Kuno et al., ARISUGACIN-A AND ARISUGACIN-B, NOVEL AND SELECTIVE ACETYLCHOLINESTERASE INHIBITORS FROM PENICILLIUM SP FO-4259 .2. STRUCTURE ELUCIDATION, Journal of antibiotics, 49(8), 1996, pp. 748-751
CHLOVALICIN, A NEW CYTOCIDAL ANTIBIOTIC PRODUCED BY SPOROTHRIX SP FO-4649 .2. PHYSICOCHEMICAL PROPERTIES AND STRUCTURAL ELUCIDATION
Authors: TAKAMATSU S KIM YP KOMIYA T SUNAZUKA T HAYASHI M TANAKA H KOMIYAMA K OMURA S
Citation: S. Takamatsu et al., CHLOVALICIN, A NEW CYTOCIDAL ANTIBIOTIC PRODUCED BY SPOROTHRIX SP FO-4649 .2. PHYSICOCHEMICAL PROPERTIES AND STRUCTURAL ELUCIDATION, Journal of antibiotics, 49(7), 1996, pp. 635-638
ANDRASTINS A-SIMILAR-TO-C, NEW-PROTEIN FARNESYLTRANSFERASE INHIBITORSPRODUCED BY PENICILLIUM SP FO-3929 .2. STRUCTURE ELUCIDATION AND BIOSYNTHESIS
Authors: UCHIDA R SHIOMI K INOKOSHI J SUNAZUKA T TANAKA H IWAI Y TAKAYANAGI H OMURA S
Citation: R. Uchida et al., ANDRASTINS A-SIMILAR-TO-C, NEW-PROTEIN FARNESYLTRANSFERASE INHIBITORSPRODUCED BY PENICILLIUM SP FO-3929 .2. STRUCTURE ELUCIDATION AND BIOSYNTHESIS, Journal of antibiotics, 49(5), 1996, pp. 418-424
CHEMICAL MODIFICATION AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF PYRIPYROPENES .1. MODIFICATION AT THE 4 HYDROXYL-GROUPS
Authors: OBATA R SUNAZUKA T LI ZR TIAN ZM HARIGAYA Y TABATA N TOMODA H OMURA S
Citation: R. Obata et al., CHEMICAL MODIFICATION AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF PYRIPYROPENES .1. MODIFICATION AT THE 4 HYDROXYL-GROUPS, Journal of antibiotics, 49(11), 1996, pp. 1133-1148
CHEMICAL MODIFICATION AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF PYRIPYROPENES .2. 1,11-CYCLIC ANALOGS
Authors: OBATA R SUNAZUKA T KATO Y TOMODA H HARIGAYA Y OMURA S
Citation: R. Obata et al., CHEMICAL MODIFICATION AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF PYRIPYROPENES .2. 1,11-CYCLIC ANALOGS, Journal of antibiotics, 49(11), 1996, pp. 1149-1156
SYNTHESIS AND ANTIPLATETLET AGGREGATION ACTIVITY OF WATER-SOLUBLE STAUROSPORINE DERIVATIVES
Authors: YAMADA R SETO M SASAKI Y SUNAZUKA T HARIGAYA Y IWAI Y OMURA S
Citation: R. Yamada et al., SYNTHESIS AND ANTIPLATETLET AGGREGATION ACTIVITY OF WATER-SOLUBLE STAUROSPORINE DERIVATIVES, Journal of antibiotics, 49(10), 1996, pp. 1070-1072
TOTAL SYNTHESIS OF (+)-LACTACYSTIN
Authors: NAGAMITSU T SUNAZUKA T TANAKA H OMURA S SPRENGELER PA SMITH AB
Citation: T. Nagamitsu et al., TOTAL SYNTHESIS OF (+)-LACTACYSTIN, Journal of the American Chemical Society, 118(15), 1996, pp. 3584-3590
CHEMICAL MODIFICATION AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF PYRIPYROPENES - POTENT, BIOAVAILABLE INHIBITOR OF ACYL-COA-CHOLESTEROL O-ACYLTRANSFERASE (ACAT)
Authors: OBATA R SUNAZUKA T TOMODA H HARIGAYA Y OMURA S
Citation: R. Obata et al., CHEMICAL MODIFICATION AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF PYRIPYROPENES - POTENT, BIOAVAILABLE INHIBITOR OF ACYL-COA-CHOLESTEROL O-ACYLTRANSFERASE (ACAT), Bioorganic & medicinal chemistry letters, 5(22), 1995, pp. 2683-2688
TOTAL SYNTHESIS OF (-PYRIPYROPENE-A - A POTENT, ORALLY BIOAVAILABLE INHIBITOR OF ACYL-COA-CHOLESTEROL ACYLTRANSFERASE())
Authors: NAGAMITSU T SUNAZUKA T OBATA R TOMODA H TANAKA H HARIGAYA Y OMURA S SMITH AB
Citation: T. Nagamitsu et al., TOTAL SYNTHESIS OF (-PYRIPYROPENE-A - A POTENT, ORALLY BIOAVAILABLE INHIBITOR OF ACYL-COA-CHOLESTEROL ACYLTRANSFERASE()), Journal of organic chemistry, 60(25), 1995, pp. 8126-8127
ARISUGACIN, A NOVEL AND SELECTIVE INHIBITOR OF ACETYLCHOLINESTERASE FROM PENICILLIUM SP FO-4259
Authors: OMURA S KUNO F OTOGURO K SUNAZUKA T SHIOMI K MASUMA R IWAI Y
Citation: S. Omura et al., ARISUGACIN, A NOVEL AND SELECTIVE INHIBITOR OF ACETYLCHOLINESTERASE FROM PENICILLIUM SP FO-4259, Journal of antibiotics, 48(7), 1995, pp. 745-746
STRUCTURE-ACTIVITY-RELATIONSHIPS OF LACTACYSTIN, THE FIRST NONPROTEINNEUROTROPHIC FACTOR
Authors: NAGAMITSU T SUNAZUKA T STUMP H OBATA R ARIMA S MATSUZAKI K TANAKA H OMURA S
Citation: T. Nagamitsu et al., STRUCTURE-ACTIVITY-RELATIONSHIPS OF LACTACYSTIN, THE FIRST NONPROTEINNEUROTROPHIC FACTOR, Journal of antibiotics, 48(7), 1995, pp. 747-748
STRUCTURE-ACTIVITY-RELATIONSHIPS OF PYRIPYROPENES FUNGAL ACYL-COA - CHOLESTEROL ACYLTRANSFERASE INHIBITORS
Authors: OBATA R SUNAZUKA T LI ZR TOMODA H OMURA S
Citation: R. Obata et al., STRUCTURE-ACTIVITY-RELATIONSHIPS OF PYRIPYROPENES FUNGAL ACYL-COA - CHOLESTEROL ACYLTRANSFERASE INHIBITORS, Journal of antibiotics, 48(7), 1995, pp. 749-750
Risultati: 1-25 | 26-38