The Chemistry of Synthetic DrugsLongmans, Green and Company, 1911 - 229 páginas |
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Página 35
... position- isomerides , often show remarkable differences in their physio- logical action . Cocaine differs from its isomeride a - cocaine only in having a ( .CO.OCH2 ) group and a ( .O.CO.С¿Н5 ) group on adjacent carbon atoms , while in ...
... position- isomerides , often show remarkable differences in their physio- logical action . Cocaine differs from its isomeride a - cocaine only in having a ( .CO.OCH2 ) group and a ( .O.CO.С¿Н5 ) group on adjacent carbon atoms , while in ...
Página 38
... position to a previously present substituent group , but if the para position is already occupied , no hydroxylation takes place in the animal body . For example , aniline is oxidized to para - aminophenol , * HONH , Ortho compounds are ...
... position to a previously present substituent group , but if the para position is already occupied , no hydroxylation takes place in the animal body . For example , aniline is oxidized to para - aminophenol , * HONH , Ortho compounds are ...
Página 56
... position . For instance , substances containing CH3 tertiary amyl , -C - CH3 , or tertiary heptyl , —С ( C2H5 ) ̧ , are C2H5 more active than those containing tertiary butyl , -C ( CH3 ) 3 . NH – C ( CH3 ) 3 Tertiary - butyl - urea , CO ...
... position . For instance , substances containing CH3 tertiary amyl , -C - CH3 , or tertiary heptyl , —С ( C2H5 ) ̧ , are C2H5 more active than those containing tertiary butyl , -C ( CH3 ) 3 . NH – C ( CH3 ) 3 Tertiary - butyl - urea , CO ...
Página 63
... position to the quinoline nitrogen , CH2O Quinoline itself has an antipyretic action , but cannot be used as a drug , owing to its unpleasant by - effects . Para- methoxyquinoline has a weaker antipyretic action than quinó- line , but ...
... position to the quinoline nitrogen , CH2O Quinoline itself has an antipyretic action , but cannot be used as a drug , owing to its unpleasant by - effects . Para- methoxyquinoline has a weaker antipyretic action than quinó- line , but ...
Página 68
... An example of this class is Cosaprin , 2 NH.CO.CHg SO , H 1 Schmiedeberg , A. e . P. P. , 8 ( 1878 ) , 1 . 2 D. R. P. , 92,796 . > 1 Substances containing a sulphonic acid group in the w position 68 889 SYNTHETIC DRUGS.
... An example of this class is Cosaprin , 2 NH.CO.CHg SO , H 1 Schmiedeberg , A. e . P. P. , 8 ( 1878 ) , 1 . 2 D. R. P. , 92,796 . > 1 Substances containing a sulphonic acid group in the w position 68 889 SYNTHETIC DRUGS.
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Términos y frases comunes
acetyl acid group active adrenaline alcohol aldehyde aliphatic alkaline alkaloids alkyl groups amines amino group ANATOMY anesthetic aniline Annalen antimony antipyretic antiseptic aromatic arsenic atoms atoxyl atropine benzene by-effects carbon carboxyl CH.OH CH₂ CH2 CH2 CH₂O Chem chemical chloral chloride chloroform cocaine codeine compounds containing COOH Crown 8vo D.Sc derivatives drugs ecgonine entrance ester ether example formula guaiacol H₂C hydrogen hydrolyzed hydroxyl group hypnotic action Ibid Illustrations inert insoluble iodide iodine iodoform ketones large number less toxic medicine methyl groups methylamine MICHI molecule morphine mydriatic narcotic action narcotine NH.CO.CH NH₂ obtained OCH3 organism oxidized papaverine phenacetin phenetidine phenol physiol physiological action physiological effect piperidine poisonous potassium prepared Proc produced properties pyridine quinine radicles reduction resembles RSITY UNIV salicylic acid salol similar SITY sodium salt soluble in water solution substance sulphonic sulphuric acid synthesis synthetic therapeutic tissues tropine UNIV RSITY UNIV UNIVE yields он
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