Literature DB >> 4597715

A quinoline methanol (WR 30090) for treatment of acute malaria.

D C Martin, J D Arnold, D F Clyde, M al-Ibrahim, P E Carson, K H Rieckmann, D Willerson.   

Abstract

WR 30090 at a dose of 230 mg every 8 hr for 6 days has proven to be a safe, well-tolerated compound with photosensitivity proving to be a minor consideration. WR 30090 was found to be an effective medication for the treatment of acute malaria caused by several strains of Plasmodium falciparum. At the dose of 230 mg every 8 hr for 6 days, all of six men infected with a chloroquine-susceptible strain (Uganda I) were cured, all of 13 subjects infected with moderately chloroquine-resistant strains (Malayan Camp, Malayan Taylor, and Philippine Per) were cured, and 19 of 23 subjects infected with strains highly resistant to chloroquine (Vietnam Smith and Vietnam Crocker) were cured. All of five subjects infected with the chloroquine-resistant Vietnam Marks strain were cured with only 3 days of therapy. Blood-induced P. vivax (Chesson strain) infection showed a mixed response. Six out of seven volunteers were cured when treated for 3 days with WR 30090. The one recrudescence responded to a repeated course of therapy for 3 days. However, recrudescence occurred in one volunteer treated for 6 days. Treatment with WR 30090 failed to cure sporozoite-induced P. vivax (Chesson strain) infection in any of four subjects. In all subjects treated, there was good suppression of parasitemia and relief of symptoms. The susceptibility of the strains of malaria to WR 30090 to some degree parallels their susceptibility to chloroquine.

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Year:  1973        PMID: 4597715      PMCID: PMC444389          DOI: 10.1128/AAC.3.2.214

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  5 in total

1.  Laboratory evaluation of the phototoxic potency of quinolinemethanols.

Authors:  W E Rothe; D P Jacobus
Journal:  J Med Chem       Date:  1968-03       Impact factor: 7.446

2.  Potential anti-infective agents. I. Quinoline, phenolic, and beta-aminoketone derivatives.

Authors:  R A Magarian; W L Nobles
Journal:  J Pharm Sci       Date:  1967-08       Impact factor: 3.534

3.  Hypotensive activity of several quinoline derivatives.

Authors:  B S Jandhyala; G J Grega; J P Buckley
Journal:  Arch Int Pharmacodyn Ther       Date:  1967-05

4.  [Studies on antiserotonin compounds in the group of quinoline derivatives. II. N,N-dimethylaminoacetaminoquinolines and their quaternary salts].

Authors:  J Kotler-Brajtburg
Journal:  Acta Pol Pharm       Date:  1967       Impact factor: 0.330

5.  A phenanthrene methanol (WR 33063) for treatment of acute malaria.

Authors:  J D Arnold; D C Martin; P E Carson; K H Rieckmann; D Willerson; D F Clyde; R M Miller
Journal:  Antimicrob Agents Chemother       Date:  1973-02       Impact factor: 5.191

  5 in total
  13 in total

1.  Clinical testing of new antimalarial compounds.

Authors:  C J Canfield; R S Rozman
Journal:  Bull World Health Organ       Date:  1974       Impact factor: 9.408

2.  Antimalarial activities of various 4-quinolonemethanols with special attention to WR-142,490 (mefloquine).

Authors:  L H Schmidt; R Crosby; J Rasco; D Vaughan
Journal:  Antimicrob Agents Chemother       Date:  1978-06       Impact factor: 5.191

Review 3.  Controlled Human Malaria Infection: Applications, Advances, and Challenges.

Authors:  Danielle I Stanisic; James S McCarthy; Michael F Good
Journal:  Infect Immun       Date:  2017-12-19       Impact factor: 3.441

4.  Utility of alkylaminoquinolinyl methanols as new antimalarial drugs.

Authors:  G S Dow; T N Heady; A K Bhattacharjee; D Caridha; L Gerena; M Gettayacamin; C A Lanteri; N Obaldia; N Roncal; T Shearer; P L Smith; A Tungtaeng; L Wolf; M Cabezas; D Yourick; K S Smith
Journal:  Antimicrob Agents Chemother       Date:  2006-09-11       Impact factor: 5.191

5.  Antimalarial activities of the 4-quinolinemethanols WR-184,806 and WR-226,253.

Authors:  L H Schmidt; R Crosby; J Rasco; D Vaughan
Journal:  Antimicrob Agents Chemother       Date:  1978-11       Impact factor: 5.191

6.  Antimalarial activities of various 4-pyridinemethanols with special attention to WR-172,435 and WR-180,409.

Authors:  L H Schmidt; R Crosby; J Rasco; D Vaughan
Journal:  Antimicrob Agents Chemother       Date:  1978-09       Impact factor: 5.191

7.  Antimalarial activities of WR-194,965, an alpha-amino-o-cresol derivative.

Authors:  L H Schmidt; R Crosby
Journal:  Antimicrob Agents Chemother       Date:  1978-11       Impact factor: 5.191

8.  Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique.

Authors:  R E Desjardins; C J Canfield; J D Haynes; J D Chulay
Journal:  Antimicrob Agents Chemother       Date:  1979-12       Impact factor: 5.191

9.  Prophylactic activity of mefloquine hydrochloride (WR 142490) in drug-resistant malaria.

Authors:  K H Rieckmann; G M Trenholme; R L Williams; P E Carson; H Frischer; R E Desjardins
Journal:  Bull World Health Organ       Date:  1974       Impact factor: 9.408

10.  Treatment of falciparum malaria from Vietnam with a phenanthrene methanol (WR 33063) and a quinoline methanol (WR 30090).

Authors:  C J Canfield; A P Hall; B S MacDonald; D A Neuman; J A Shaw
Journal:  Antimicrob Agents Chemother       Date:  1973-02       Impact factor: 5.191

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