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Results: 1-10 |
Results: 10
STRUCTURE OF SPOROSTATIN (M5032), AN INHIBITOR OF CYCLIC ADENOSINE-3',5'-MONOPHOSPHATE PHOSPHODIESTERASE
Authors: KINOSHITA K SASAKI T AWATA M TAKADA M YAGINUMA S
Citation: K. Kinoshita et al., STRUCTURE OF SPOROSTATIN (M5032), AN INHIBITOR OF CYCLIC ADENOSINE-3',5'-MONOPHOSPHATE PHOSPHODIESTERASE, Journal of antibiotics, 50(11), 1997, pp. 961-964
NEW NEPLANOCIN ANALOGS .9. A PRACTICAL PREPARATION OF (6'R)-6'-C-METHYLNEPLANOCIN-A (RMNPA), A POTENT ANTIVIRAL AGENT, AND THE DETERMINATION OF ITS 6'-CONFIGURATION - DIASTEREOSELECTIVE DEAMINATION BY ADENOSINE-DEAMINASE
Authors: SHUTO S OBARA T YAGINUMA S MATSUDA A
Citation: S. Shuto et al., NEW NEPLANOCIN ANALOGS .9. A PRACTICAL PREPARATION OF (6'R)-6'-C-METHYLNEPLANOCIN-A (RMNPA), A POTENT ANTIVIRAL AGENT, AND THE DETERMINATION OF ITS 6'-CONFIGURATION - DIASTEREOSELECTIVE DEAMINATION BY ADENOSINE-DEAMINASE, Chemical and Pharmaceutical Bulletin, 45(1), 1997, pp. 138-142
NEW NEPLANOCIN ANALOGS .5. A POTENT ADENOSYLHOMOCYSTEINE HYDROLASE INHIBITOR LACKING ANTIVIRAL ACTIVITY - SYNTHESIS AND ANTIVIRAL ACTIVITY OF 6'-CARBOXYLIC ACID-DERIVATIVES OF NEPLANOCIN-A
Authors: OBARA T SHUTO S SAITO Y TORIYA M OGAWA K YAGINUMA S SHIGETA S MATSUDA A
Citation: T. Obara et al., NEW NEPLANOCIN ANALOGS .5. A POTENT ADENOSYLHOMOCYSTEINE HYDROLASE INHIBITOR LACKING ANTIVIRAL ACTIVITY - SYNTHESIS AND ANTIVIRAL ACTIVITY OF 6'-CARBOXYLIC ACID-DERIVATIVES OF NEPLANOCIN-A, Nucleosides & nucleotides, 15(6), 1996, pp. 1157-1167
STACHYBOCINS, NOVEL ENDOTHELIN RECEPTOR ANTAGONISTS, PRODUCED BY STACHYBOTRYS SP M6222 .1. TAXONOMY, FERMENTATION, ISOLATION AND CHARACTERIZATION
Authors: NAKAMURA M ITO Y OGAWA K MICHISUJI Y SATO S TAKADA M HAYASHI M YAGINUMA S YAMAMOTO S
Citation: M. Nakamura et al., STACHYBOCINS, NOVEL ENDOTHELIN RECEPTOR ANTAGONISTS, PRODUCED BY STACHYBOTRYS SP M6222 .1. TAXONOMY, FERMENTATION, ISOLATION AND CHARACTERIZATION, Journal of antibiotics, 48(12), 1995, pp. 1389-1395
STACHYBOCINS, NOVEL ENDOTHELIN RECEPTOR ANTAGONISTS, PRODUCED BY STACHYBOTRYS SP M6222 .2. STRUCTURE DETERMINATION OF STACHYBOCIN-A, STACHYBOCIN-B AND STACHYBOCIN-C
Authors: OGAWA K NAKAMURA M HAYASHI M YAGINUMA S YAMAMOTO S FURIHATA K SHINYA K SETO H
Citation: K. Ogawa et al., STACHYBOCINS, NOVEL ENDOTHELIN RECEPTOR ANTAGONISTS, PRODUCED BY STACHYBOTRYS SP M6222 .2. STRUCTURE DETERMINATION OF STACHYBOCIN-A, STACHYBOCIN-B AND STACHYBOCIN-C, Journal of antibiotics, 48(12), 1995, pp. 1396-1400
NUCLEOSIDES AND NUCLEOTIDES .129. NEW NEPLANOCIN ANALOGS .3. 6'R-CONFIGURATION IS ESSENTIAL FOR THE ANTIVIRAL ACTIVITY OF 6'-C-METHYL-3-DEAZANEPLANOCIN AS
Authors: SHUTO S OBARA T KOSUGI Y SAITO Y TORIYA M YAGINUMA S SHIGETA S MATSUDA A
Citation: S. Shuto et al., NUCLEOSIDES AND NUCLEOTIDES .129. NEW NEPLANOCIN ANALOGS .3. 6'R-CONFIGURATION IS ESSENTIAL FOR THE ANTIVIRAL ACTIVITY OF 6'-C-METHYL-3-DEAZANEPLANOCIN AS, Bioorganic & medicinal chemistry letters, 4(4), 1994, pp. 605-608
USE OF TRANSCRIPTIONAL-ENHANCER ELEMENTS RESPONSIVE TO RAS, PROTEIN KINASE-A AND PROTEIN-KINASE-C TO EVALUATE INHIBITORS OF SPECIFIC SIGNAL-TRANSDUCTION PATHWAYS
Authors: KANBE T TSUCHIYA KS HORI M YAGINUMA S MURAKAMI Y MIZUNO S UEHARA Y
Citation: T. Kanbe et al., USE OF TRANSCRIPTIONAL-ENHANCER ELEMENTS RESPONSIVE TO RAS, PROTEIN KINASE-A AND PROTEIN-KINASE-C TO EVALUATE INHIBITORS OF SPECIFIC SIGNAL-TRANSDUCTION PATHWAYS, Biological & pharmaceutical bulletin, 17(6), 1994, pp. 779-783
AM4299-A AND AM4299-B, NOVEL THIOL PROTEASE INHIBITORS
Authors: MORISHITA A ISHIKAWA S ITO Y OGAWA K TAKADA M YAGINUMA S YAMAMOTO S
Citation: A. Morishita et al., AM4299-A AND AM4299-B, NOVEL THIOL PROTEASE INHIBITORS, Journal of antibiotics, 47(9), 1994, pp. 1065-1068
NEW NEPLANOCIN ANALOGS .4. 2-FLUORONEPLANOCIN-A - AN ADENOSINE DEAMINASE-RESISTANT EQUIVALENT OF NEPLANOCIN-A
Authors: SHUTO S OBARA T ITOH H KOSUGI Y SAITO Y TORIYA M YAGINUMA S SHIGETA S MATSUDA A
Citation: S. Shuto et al., NEW NEPLANOCIN ANALOGS .4. 2-FLUORONEPLANOCIN-A - AN ADENOSINE DEAMINASE-RESISTANT EQUIVALENT OF NEPLANOCIN-A, Chemical and Pharmaceutical Bulletin, 42(8), 1994, pp. 1688-1690
METHOD OF IDENTIFYING INHIBITORS OF ONCOGENIC TRANSFORMATION - SELECTIVE-INHIBITION OF CELL-GROWTH IN SERUM-FREE MEDIUM
Authors: LI PM FUKAZAWA H YAMAMOTO C MIZUNO S TANAKA K HORI M YAGINUMA S SAITO T UEHARA Y
Citation: Pm. Li et al., METHOD OF IDENTIFYING INHIBITORS OF ONCOGENIC TRANSFORMATION - SELECTIVE-INHIBITION OF CELL-GROWTH IN SERUM-FREE MEDIUM, Oncogene, 8(7), 1993, pp. 1731-1735
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