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Syntheses of 2-Alkylthiopyrimidine Derivatives with Nitrofuran Nucleus and their Structure-Activity Relationship
Isamu Saikawa
1964 Volume 84 Issue 3 Pages
207-212
Published: March 25, 1964
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2-Alkylthio-4-(5-nitro-2-furylalkenyl)pyrimidines (VI) shown in Table I were readily obtained by an acid-catalyzed condensation of 2-alkylthio-4-methylpyrimidines (IV) with 5-nitro-2-furyl-aldehydes (V) in a fairly good yield. VI was highly susceptible to photodecomposition and some of them failed to show normal ultraviolet absorption spectra. Antibacterial activity of VI against
Escherichia coli O-18 and
Staphylococcus aureus 209P was tested in three kinds of bouillon medium, and the result (Table III) showed that 2-methylthio-4-[3-methyl-4-(5-nitro-2-furyl)-1, 3-butadienyl]pyrimidine had the highest activity among them.
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Syntheses of 2-Amino-1, 3, 4-oxadiazole Derivatives with Nitrofuran Nucleus and their Structure-Activity Relationship
Isamu Saikawa
1964 Volume 84 Issue 3 Pages
212-219
Published: March 25, 1964
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2-Amino-5-(5-nitro-2-furylalkenyl)-1, 3, 4-oxadiazoles (IV) were prepared by the known methods and their antibacterial activity was tested.
IV was less effective than 3-amino-6-(5-nitro-2-furylalkenyl)-1, 2, 4-triazines (II), but their structure-activity relationship was quite similar to that of II. IV (R
1=H,
n=0) was reacted with excess formaldehyde and 2-[bis(hydroxymethyl)amino]-5-[2-(5-nitro-2-furyl)vinyl]-1, 3, 4-oxadiazole (XVI) was obtained.
The protective effect of XVI in mice was tested and it was found to have stronger
in vivo activity than 3-[bis(hydroxymethyl)amino]-6-[2-(5-nitro-2-furyl)vinyl]-1, 2, 4-triazine (I).
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Syntheses of 2-(Substituted amino)-1, 3, 4-oxadiazole Derivatives with Nitrofuran Nucleus and their Structure-Activity Relationship
Isamu Saikawa, Akira Takai, Yutaka Kodama
1964 Volume 84 Issue 3 Pages
219-224
Published: March 25, 1964
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2-(Monosubstituted amino)-5-(5-nitro-2-furylalkenyl)-1, 3, 4-oxadiazoles (V) were prepared and their antibacterial activity was tested. Among them, the protective effect of 2-methylamino-5-[2-(5-nitro-2-furyl)vinyl]-1, 3, 4-oxadiazole (V:R
1=H,
n=0, R
3=CH
3) was tested in mice and it was found to have the same
in vivo activity spectrum as 2-[bis(hydroxymethyl)amino]-5-[2-(5-nitro-2-furyl)vinyl]-1, 3, 4-oxadiazole.
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Syntheses of 1, 3, 4-Oxadiazole Derivatives with Nitrofuran Nucleus and their Structure-Activity Relationship
Isamu Saikawa, Akira Takai, Yutaka Kodama
1964 Volume 84 Issue 3 Pages
225-229
Published: March 25, 1964
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2-Substituted 5-[2-(5-nitro-2-furyl)vinyl]-1, 3, 4-oxadiazoles (I), in which H, OH, SH, SCH
3, alkyl, or phenyl radical was substituted at 2-position in the oxadiazole ring, were prepared by the known methods and their antibacterial activity was tested, but none was so effective as 2-(amino-substituted)-1, 3, 4-oxadiazole derivatives
in vivo test.
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Heizaburo Hayashi, Shuzo Minami
1964 Volume 84 Issue 3 Pages
229-236
Published: March 25, 1964
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Examinations were made on the quantitative relationship between the repose angle, a flow property of powders measured by the tilting-box method, and various primary factors connected with that repose angle such as the length of powder tilting surface, interparticle cohesion, coefficient of internal friction, and apparent density of the powder.
1) The repose angle
i increased with decreasing the length of tilted surface,
i.e., the length of the tilting box,
L.2) If the values of the coefficient of internal friction and apparent density γ are not exceedingly different between two kinds of powders, fluidity of the powder expressed by the repose angle is closely correlated to the interparticle cohesion (
c).
3) When the apparent density is small, that powder has a poor fluidity.
These relationships found by experiments were found to agree well with the general formula for the repose angle, 2
c⋅cosφ/γ
L=sin
2{(
i-φ)/2}, (where φ is the angle of internal friction) derived kinetically from the equilibrium conditions of the force acting on tilted powder surface. Using this formula, the value of
c was calculated and the value was compared with that measured by the shear test.
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Synthesis of Methanesulfonates of Various Carbinols and Phenolic Compounds and their Pharmacological Activity
Tetsuji Kametani, Osamu Umezawa, Kiyoko Sekine, Takeshi Oda, Masako Is ...
1964 Volume 84 Issue 3 Pages
237-246
Published: March 25, 1964
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There have been numerous reports on Myleran among various alkyl methanesulfonates and 39 kinds of various derivatives of carbinols were synthesized to examine their antibacterial, antifungal, and antitumor actions. A large number of methanesulfonates of various phenolic compounds were synthesized and their antitumor action was examined. Among these compounds, 2-chloro-3′, 4′-dimethoxyacetophene was found to have considerable effect against Ehrlich ascites tumor.
Reaction of pyrocatechol with chloroacetyl chloride and chloropropionyl chloride was also examined.
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The Electrical Conductivity of Some Electrolytes and Anionic Surfactant
Masayuki Nakagaki, Skigeo Kawamura
1964 Volume 84 Issue 3 Pages
246-251
Published: March 25, 1964
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Electrical conductivity of sodium chloride, potassium chloride, and sodium lauryl sulfate in 0, 3, 10, 20, and 30% aqueous sucrose solutions was measured in concentration between 0.0002 and 0.04
M. The apparent radius of Na
+, K
+, and Cl
- was calculated from the limiting equivalent conductivity
Λ∞ of sodium and potassium chloride in aqueous sucrose solutions on the basis of Stokes' law. The apparent radius of these ions decreased linearly with increasing sucrose concentration. This is considered to be due to the partial dehydration of ions by the addition of sucrose.
The equivalent conductivity
Λ of sodium chloride, potassium chloride, and sodium lauryl sulfate decreased by the increase of sucrose concentration. The decrease of mobility of ions is considered to be due mainly to the increase of viscosity of the medium by the addition of sucrose.
Λη
0-√c curves, however, showed that
Λη
0 increased with sucrose concentration. This phenomenon seems to be due to the decrease of the radius of ions through dehydration by sucrose.
The critical micelle concentration of sodium lauryl sulfate decreased by the increase of sucrose concentration. This phenomenon is also considered to be due to dehydration by sucrose.
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Misao Kojima, Nobuo Nakamichi, Keiko Shiotani
1964 Volume 84 Issue 3 Pages
251-255
Published: March 25, 1964
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Reaction of allyl isothiocyanate with sugar reagents was examined and the compound was found to react with all reagents based on reducibility. Sugar reagents using copper sulfate produced a black precipitate which is probably due to the formation of copper (II) sulfide besides copper (I) oxide.
Allyl isothiocyanate can be quantitatively determined by the Bertrand method and is also possible by the 3, 5-dinitrosalicylic acid method if care is taken with reaction conditions (90±2°, heated for 30 min.).
Reduction of sugar reagents by allyl isothiocyanate is due to the reducibility of sodium sulfide which is formed on being heated with sodium hydroxide.
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Pharmacological Actions of Several Normorphines and 14-Hydroxynormorphinones
Isao Seki, Hiromu Takagi, Shinsaku Kobayashi
1964 Volume 84 Issue 3 Pages
255-267
Published: March 25, 1964
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The compounds having morphine rings on both ends of 2-butyne, 1, 4-bis(normorphino)-2-butyne dimethiodide (I), 1, 4-bis(norcodeino)-2-butyne dimethiodide (II), and 1, 4-bis(14-hydroxydihydronorcodeinono)-2-butyne dihydrochloride (III), did not show strong analgesic action or antagonism against morphine. Of these three compounds, III showed anti-barium action close to that of papaverine. Both N-allyl and N-propargyl compounds showed antagonism against morphine and this action was stronger in the former. Antagonism against morphine was seen in any of the actions such as analgesism, suppression of avoidance reactions, hypotension, respiration inhibition, and slowing of brain wave. Toxicity was the weakest in N-propargyl compound. The antagonistic action of N-propargyl-14-dihydroxydihydronormorphinone (RAM-302) against morphine was comparable to that of nalorphine and its toxicity was lower. This antagonistic action against morphine was the same as in the case of analgesic action and the 3-hydroxy compound had stronger action than the 3-methoxy compound.
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Pharmacological Actions of Several 14-Hydroxy-6-deoxymorphine Derivatives
Isao Seki, Hiromu Takagi, Shinsaku Kobayashi, Takehiko Deguchi, Seizi ...
1964 Volume 84 Issue 3 Pages
268-279
Published: March 25, 1964
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Physiological action of 14-hydroxy-6-deoxy morphine derivatives was examined; analgesic action, suppression of avoidance reactions, fortification of thiopental anesthesia, action on brain wave of rabbit cerebral cortex, actions on blood pressure and respiration, and action on excised intestine. N-Phenethyl-14-hydroxydeoxydihydronormorphine (RAM-315) has analgesic action 70 times that of morphine, as well as stronger actions in other points. The N-methyl compound (RAM-307) shows 10 times stronger action than morphine. In general, 6-deoxy compounds have stronger action and stronger toxicity. N-Allyl and N-propargyl compounds show antagonism against morphine, that of N-allyl-14-hydroxydeoxydihydronormorphine (RAM-313) being five times that of nalorphine.
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On the Chemical Structure-Activity Relationships of 14-Hydroxymorphine Derivatives
Isao Seki, Hiromu Takagi, Shinsaku Kobayashi
1964 Volume 84 Issue 3 Pages
280-286
Published: March 25, 1964
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About 80 kinds of new derivatives of morphine possessing a hydroxyl in 14-position were synthesized and the effect of this introduction of hydroxyl on acute toxicity, analgesic action, and antitussive action was examined. in general, the introduction of hydroxyl resulted in reduction of toxicity and increased analgesic and antitussive actions. In N-substituted compounds, N-phenethyl compound had stronger toxicity than the N-methyl compound, and analgesic action was also stronger. N-Pentyl, N-phenacyl, and non-substituted compounds had weak actions. Etherification of the hydroxyl in 3-position resulted in decreased analgesic and antitussive actions. Etherification of hydroxyl in 4-position of morphinan derivatives results in fortification of toxicity, analgesic and antitussive actions, the action being marked in methyl ethers. Both the analgesic and antitussive actions, and toxicity become stronger in 6-oxo and 6-deoxy compounds than in 6-hydroxy compounds. These tendencies are approximately the same as those of compounds not possessing a hydroxyl in 14-position.
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Reaction of α-Picoline N-Oxide with α-Halo Ketone
Tetsuzo Kato, Yoshinobu Goto, Yutaka Yamamoto
1964 Volume 84 Issue 3 Pages
287-289
Published: March 25, 1964
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When α-picoline 1-oxide and phenacyl bromide are mixed under cooling and the solidified crystals are washed with anhydrous ether and benzene, O-phenacyl compound (I), m.p. 70°, of α-picoline 1-oxide is obtained. Basification of this product (I) with sodium carbonate gives phenylglyoxal easily in ca. 50% yield. If a solvent is used and the mixture is heated, this yield becomes lower. The use of acetone produces α-picoline 1-oxide 1/2hydrobromide (II), m.p. 142°. Reaction of α-picoline 1-oxide and α-bromoacetone in benzene gave pyruvic aldehyde in 26% yield.
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Tetsuzo Kato, Yoshinobu Goto, Masatsugu Kondo
1964 Volume 84 Issue 3 Pages
290-292
Published: March 25, 1964
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Quinaldine 1-oxide reacts with amyl nitrite in liquid ammonia, in the presence of metal amide, and produces quinaldaldehyde 1-oxide oxime (II) in 27-51% yield, with by-product formation of quinaldonitrile 1-oxide (III), quinaldamide 1-oxide (IV), qninaldonitrile (V), and quinaldamide.
The same reaction of lepidine 1-oxide resulted in the difficulty of separating the product but formation of cinchoninaldehyde 1-oxide oxime was proved by its isolation.
Quinaldine and lepidine both easily afforded the corresponding quinolinecarboxaldehyde oxime in a good yield of 55-67%.
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[in Japanese]
1964 Volume 84 Issue 3 Pages
APreface1
Published: March 25, 1964
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1964 Volume 84 Issue 3 Pages
A1-A4
Published: March 25, 1964
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1964 Volume 84 Issue 3 Pages
A5-A18
Published: March 25, 1964
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1964 Volume 84 Issue 3 Pages
A19-A32
Published: March 25, 1964
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1964 Volume 84 Issue 3 Pages
A33-A44
Published: March 25, 1964
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1964 Volume 84 Issue 3 Pages
A45-A55
Published: March 25, 1964
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1964 Volume 84 Issue 3 Pages
A56-A58
Published: March 25, 1964
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