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Attributs	Valeurs
type	work Journal
Title	Journal of Medicinal Chemistry
bibo:shortTitle	J. Me. Chem. J. Med. Chem.
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/m/print http://hub.abes.fr/acs/periodical/jmcmar/m/web
publisher identifier	jm
is Is Part Of of	http://hub.abes.fr/acs/periodical/jmcmar/1996/volume_39 http://hub.abes.fr/acs/periodical/jmcmar/1997/volume_40 http://hub.abes.fr/acs/periodical/jmcmar/1998/volume_41 http://hub.abes.fr/acs/periodical/jmcmar/1999/volume_42 http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43 http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44 http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45 http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46 http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47 http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48 http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49 http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50 http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51 http://hub.abes.fr/acs/periodical/jmcmar/1959/volume_1 http://hub.abes.fr/acs/periodical/jmcmar/1959/volume_2 http://hub.abes.fr/acs/periodical/jmcmar/1960/volume_2 http://hub.abes.fr/acs/periodical/jmcmar/1961/volume_3 http://hub.abes.fr/acs/periodical/jmcmar/1961/volume_4 http://hub.abes.fr/acs/periodical/jmcmar/1962/volume_5 http://hub.abes.fr/acs/periodical/jmcmar/1963/volume_6 http://hub.abes.fr/acs/periodical/jmcmar/1964/volume_7 http://hub.abes.fr/acs/periodical/jmcmar/1965/volume_8 http://hub.abes.fr/acs/periodical/jmcmar/1966/volume_9 http://hub.abes.fr/acs/periodical/jmcmar/1967/volume_10 http://hub.abes.fr/acs/periodical/jmcmar/1968/volume_11 http://hub.abes.fr/acs/periodical/jmcmar/1969/volume_12 http://hub.abes.fr/acs/periodical/jmcmar/1970/volume_13 http://hub.abes.fr/acs/periodical/jmcmar/1971/volume_14 http://hub.abes.fr/acs/periodical/jmcmar/1972/volume_15 http://hub.abes.fr/acs/periodical/jmcmar/1973/volume_16 http://hub.abes.fr/acs/periodical/jmcmar/1974/volume_17 http://hub.abes.fr/acs/periodical/jmcmar/1975/volume_18 http://hub.abes.fr/acs/periodical/jmcmar/1976/volume_19 http://hub.abes.fr/acs/periodical/jmcmar/1977/volume_20 http://hub.abes.fr/acs/periodical/jmcmar/1978/volume_21 http://hub.abes.fr/acs/periodical/jmcmar/1979/volume_22 http://hub.abes.fr/acs/periodical/jmcmar/1980/volume_23 http://hub.abes.fr/acs/periodical/jmcmar/1981/volume_24 http://hub.abes.fr/acs/periodical/jmcmar/1982/volume_25 http://hub.abes.fr/acs/periodical/jmcmar/1983/volume_26 http://hub.abes.fr/acs/periodical/jmcmar/1984/volume_27 http://hub.abes.fr/acs/periodical/jmcmar/1985/volume_28 http://hub.abes.fr/acs/periodical/jmcmar/1986/volume_29 http://hub.abes.fr/acs/periodical/jmcmar/1987/volume_30 http://hub.abes.fr/acs/periodical/jmcmar/1988/volume_31 http://hub.abes.fr/acs/periodical/jmcmar/1989/volume_32 http://hub.abes.fr/acs/periodical/jmcmar/1990/volume_33 http://hub.abes.fr/acs/periodical/jmcmar/1991/volume_34 http://hub.abes.fr/acs/periodical/jmcmar/1992/volume_35 http://hub.abes.fr/acs/periodical/jmcmar/1993/volume_36 http://hub.abes.fr/acs/periodical/jmcmar/1994/volume_37 http://hub.abes.fr/acs/periodical/jmcmar/1995/volume_38
is is part of this journal of	Hypotensive Hydrazinophthalazines and Related Compounds Alpha- and Beta-Prodine Type Compounds Synthsis and Radioprotective Properties of Chlorinated O-Dialkylaminopropionamido- and O-Dialkylaminopropylaminodiphenyl Sulphide Derivatives Book Reviews Synthesis of Diethylaminoethyl Esters of p-Carboxyphenylphenylcarbinols Heterocyclic Disulphonamides and Their Diuretic Properties Potential Anticancer Agents--XXXL. The Relationship of Analogues of 1-Methyl-3-nitro-1-nitrosoguanidine (NSC-9369) A Study of the Nicotinic Action of 3-Phenyltropane and Related Compounds Synthesis Experiments in the Group of Hypotensive Alkaloids--XXI. Chemistry of 1,2,3,4-Tetra-hydronorharmane-1-carboxylic Acid and Derivatives Local Anaesthetic Studies with Some Alkoxy-dialkylaminoalkoxyanilines Indanols. IV.1 Indanoxypropanolamines Potential Uricosuric Agents Derived from 1,3-Diphenylbarbituric Acid Synthesis of Sulfonylhydrazine Derivatives with Monoamine Oxidase Inhibitory Activity Synthetic Amebicides. VII. 6,6′-Diallyl-α,α′-bis(dialkylaminoalkylamino)-4,4′-bi-o -cresols Synthesis of Certain 16α-Substituted Derivatives of 9α-Fluoro-11-dehydrocorticosterone, Progesterone and Deoxycorticosterone Sulfanilamidopyrimidines. II.1 4-Sulfanilamidopyrimidines and Certain 4,6-Disubstituted Pyrimidines2 Methanesulfonates of Tertiary and Quaternary Amino Alcohols The Binding of Tetracycline Analogs to Conalbumin in the Absence and Presence of Cupric Ions Masthead Synthetic Analgesics. IV. Synthesis of Enantiomers of Basic Anilides Containing the Phenalkyl Moiety1,2 Anaphylactic Microshock in the Screening of Some Theophyllines and Benzylphenoxyaminoalkanes for Antiasthmatic Activity Steroids. CCXIII.1 Synthesis of Some 6-Chlorotestosterone Derivatives Compounds Related to Carnitine: Derivatives of 4-Dimethylamino-3-hydroxybutyric Acid Sympathetic Nervous System Blocking Agents. Derivatives of Guanidine and Related Compounds1 1,4-Di(D-glycosyl)piperazine Derivatives as Oxyuricidal Agents Spiranes. III.1a,b Azaspiranes and Intermediates1c Iodination of 2'-Deoxycytidine and Related Substances1 Subsidiary Constituents from Amanita Muscaria1a,b The Synthesis of Halogenated Tuberculostatic Thiocarbanilides Aldosterone Antagonists. 2'3'α-Tetrahydrofuran-2'-spiro-17-(4-androsten-3-one) and Related Compounds Synthesis and Pharmacological Activity of Fluorinated Tryptamine Derivatives Dibenzo[b,e][1,4]diazepines Antiviral Activity of Glyoxals and Derivatives Nitrogen Substituted Phenoxazines Derivatives of Purinethiols. Purine Thiolcarbonates and Related Compounds1 α-Alkyloximinocarboxamides for Biological Testing Hydrazino Acids. II. Alkyl-, Aralkyl-, and Hydroxyalkyl-α-hydrazino Acids Central Nervous System Depressants. VI. Polymethoxyphenyl Esters and Amides Monoamine Oxidase Inhibitors. Hydrazine Derivatives Synthesis and Biological Properties of Aminoalkylhydrazines. A Unique Nitrogen-Nitrogen Scission of 1-(2-Diethylaminoethyl)-2-(1-phenyl-2-propyl)hydrazine

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