About: http://hub.abes.fr/acs/periodical/jmcmar/1975/volume_18/issue_9/w

Documentation

scienceplus.abes.fr version Bêta

scienceplus.abes.fr | explorer

À propos de : http://hub.abes.fr/acs/periodical/jmcmar/1975/volume_18/issue_9/w Goto Sponge NotDistinct Permalink

Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/1975/volume_18
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/1975/volume_18/issue_9/m/print http://hub.abes.fr/acs/periodical/jmcmar/1975/volume_18/issue_9/m/web
issue	9
is Is Part Of of	Preparation and biological activity of some aminoacyl and peptidyl derivatives of 2'-amino-2'-deoxyuridine 1-[[(5-Nitrofuranyl)methylene]amino]-4- and/or -5-substituted 2-imidazolidinones Synthesis and hypoglycemic activity of phenacyltriphenylphosphoranes and phosphonium salts Rm values of phenols. Their relation with log P values and activity 4-Trifluoromethylimidazoles and 5-(4-pyridyl)-1,2,4-triazoles, new classes of xanthine oxidase inhibitors Antifertility agents. 8. Seco steroids. 2. 5,6-Secoestradiol and some related compounds Inhibitors of polyamine biosynthesis. 3. (+-)-5-Amino-2-hydrazino-2-methylpentanoic acid, an inhibitor of ornithine decarboxylase Chemical differentiation of histamine H1- and H2-receptor agonists 3,5-Disubstituted 1,2,4-triazoles, a new class of xanthine oxidase inhibitor Structure-activity relation in synthetic fibrinolytics. 2-Phenethynylcyclopropanecarboxylates Masthead Methotrexate analogs. 6. Replacement of glutamic acid by various amino acid esters and amines Potential inhibitors of L-asparagine biosynthesis. 3. Aromatic sulfonyl fluoride analogs of L-asparagine and L-glutamine Book Reviews Potential filaricides. 6. Synthesis of 3,8-disubstituted 1,3,8-triazabicyclo[4.4.0]decan-2-ones and -thiones Oxanilic acids, a new series of orally active antiallergic agents Benzoxocin and benzoxonin derivatives. Novel groups of terpenophenols with central nervous system activity. Correction Rm values of steroids as an expression of their lipophilic character in structure-activity studies Calculation of hydrophobic constant (log P) from .pi. and f constants Ergot alkaloids. Synthesis of 6-methyl-8-ergolenes as inhibitors of prolactin release Potential bioreductive alkylating agents. 5. Antineoplastic activity of quinoline-5,8-diones, naphthazarins, and naphthoquinones Synthesis and biological properties of the 2-L-.beta.-(pyrazolyl-1)alanine analogs of luteinizing hormone-releasing hormone and thyrotropin-releasing hormone Regression analysis of the relation between physical properties and the in vitro inhibition of monoamine oxidase by propynylamines Synthesis of ethyl 6-substituted-chroman- and -chromone-2-carboxylates. Comparative structure-activity study employing the 6-phenyl and phenoxy analogs in the triton hyperlipidemic rat model

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata