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Murugesan Natesan
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http://hub.abes.fr/acs/periodical/jacsat/1982/volume_104/issue_19/101021ja00383a045/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_1/101021jm049548x/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_1/101021jm020289q/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_18/101021jm020138n/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_16/101021jm000105c/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1985/volume_107/issue_13/101021ja00299a072/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1985/volume_107/issue_2/101021ja00288a037/authorship/1
http://hub.abes.fr/acs/periodical/inocaj/1984/volume_23/issue_11/101021ic00179a002/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1982/volume_104/issue_7/101021ja00371a049/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1989/volume_111/issue_1/101021ja00183a059/authorship/3
http://hub.abes.fr/acs/periodical/bichaw/1985/volume_24/issue_21/101021bi00342a008/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1994/volume_37/issue_3/101021jm00029a001/authorship/9
http://hub.abes.fr/acs/periodical/jacsat/1985/volume_107/issue_1/101021ja00287a052/authorship/4
http://hub.abes.fr/acs/periodical/bichaw/1988/volume_27/issue_1/101021bi00401a011/authorship/3
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Chemistry of the alkali-labile lesion formed from iron(II) bleomycin and d(CGCTTTAAAGCG)
Activation of oxygen and mediation of DNA degradation by manganese-bleomycin
Analysis of products formed during bleomycin-mediated DNA degradation
Deglycobleomycin: total synthesis and oxygen transfer properties of an active bleomycin analog
The chemistry of vicinal tricarbonyls. A stable vinyl tricarbonyl hydrate as a di- and trielectrophile
Oxygen transfer by bleomycin analogs dysfunctional in DNA cleavage
Dual Angiotensin II and Endothelin A Receptor Antagonists: Synthesis of2‘-Substituted N-3-Isoxazolyl Biphenylsulfonamides with Improved Potency andPharmacokinetics
Biphenylsulfonamide Endothelin Receptor Antagonists. 2. Discovery of4‘-Oxazolyl Biphenylsulfonamides as a New Class of Potent, Highly SelectiveETA Antagonists
Discovery of N-Isoxazolyl Biphenylsulfonamides as Potent Dual Angiotensin IIand Endothelin A Receptor Antagonists
Biphenylsulfonamide Endothelin Receptor Antagonists. 4. Discovery ofN-[[2‘-[[(4,5-Dimethyl-3-isoxazolyl)amino]sulfonyl]-4-(2-oxazolyl)[1,1‘-biphenyl]-2-yl]methyl]-N,3,3-trimethylbutanamide (BMS-207940), A Highly Potent andOrally Active ETA Selective Antagonist
Bleomycin as an oxene transferase. Catalytic oxygen transfer to olefins
Structure of the alkali-labile product formed during iron(II)-bleomycin-mediated DNA strand scission
Karachine: an unusual protoberberine alkaloid
The Discovery of Sulfonamide Endothelin Antagonists and the Development of the Orally Active ETA Antagonist 5-(Dimethylamino)-N-(3,4-dimethyl-5- isoxazolyl)-1-naphthalenesulfonamide
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