氯喹那多
氯喹那多结构式
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常用名 | 氯喹那多 | 英文名 | chlorquinaldol |
|---|---|---|---|---|
| CAS号 | 72-80-0 | 分子量 | 228.075 | |
| 密度 | 1.5±0.1 g/cm3 | 沸点 | 350.7±37.0 °C at 760 mmHg | |
| 分子式 | C10H7Cl2NO | 熔点 | 108-112 °C (dec.)(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 165.9±26.5 °C | |
| 符号 |
GHS07 |
信号词 | Warning |
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Purity determination of gynalgin bactericidal tablets with HPLC method.
Acta Pol. Pharm. 70(1) , 51-8, (2013) The study was aimed at developing a simple HPLC method for the determination of the content of impurities in Gynalgin, a two-component preparation. A satisfactory separation was performed on 250 x 4.6 mm Symmetry C8 column in a gradient elution system: mobile... |
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[Allergies to 8-hydroxyquinoline derivatives].
Derm. Beruf Umwelt. 36(3) , 86-90, (1988) Evaluation of our standardized test results from 1972 to 1983 indicated Vioform allergies in 1.2% of all cases and Sterosan allergies in 1.1%. Our results are within the spectrum found in the literature for Vioform between 0.3 and 5.1% and for Sterosan betwee... |
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In vitro activities of cloxyquin (5-chloroquinolin-8-ol) against Mycobacterium tuberculosis.
Antimicrob. Agents Chemother. 51 , 1105-6, (2007) The in vitro activities of cloxyquin (5-chloroquinolin-8-ol) against 9 standard strains and 150 clinical isolates of Mycobacterium tuberculosis were studied. The MICs ranged from 0.062 to 0.25 microg/ml. The MIC(50) and MIC(90) were 0.125 and 0.25 microg/ml, ... |
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Fluorimetric determination of chloroxine using manual and flow-injection methods.
J. Pharm. Biomed. Anal. 14(11) , 1505-11, (1996) A reliable and highly sensitive method is described for the determination of chloroxine in pharmaceutical preparations. It involves the formation of a complex between chloroxine and aluminum(III) in a micellar medium. The complex is a very fluorescent species... |
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Sensitivity to clioquinol and chlorquinaldol in the quinoline mix.
Contact Dermatitis 29(3) , 163, (1993)
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Experimental sensitization of guinea pigs by drugs. Comparison of the maximization test with the wholly intradermal test.
Contact Dermatitis 9(6) , 479-83, (1983) The capacity of tegobetain, pyrrolnitrin, tolcyclate and chlorquinaldol to induce delayed-type contact sensitization was studied in guinea pigs in 2 series of tests using the method of Magnusson & Kligman and the authors' modification of the wholly intraderma... |
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Therapeutic use of topical corticosteroids in the vesiculobullous lesions of incontinentia pigmenti.
Clin. Exp. Dermatol. 34(8) , e611-3, (2009) Incontinentia pigmenti (IP) is a rare genodermatosis caused by a mutation of nuclear factor kappa B essential modulator gene. There is no specific treatment for IP, therefore it has been claimed that there is no effective treatment to hasten resolution of any... |
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Prevention and treatment of atrophic rhinitis in pigs with Getroxel, chlorquinaldol and oxytetracycline.
Acta Vet. Hung. 39(3-4) , 127-35, (1991) The sensitivity of ten Bordetella bronchiseptica and ten Pasteurella multocida strains, each isolated from cases of atrophic rhinitis (AR), was examined in tube dilution test. Getroxel, chlorquinaldol and oxytetracycline and the former two ones combined with ... |
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Polymorphism and color dimorphism of chlorquinaldol (5,7-dichloro-8-hydroxy-2-methylquinoline).
Pharmazie 40(10) , 730, (1985)
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[In vitro activity of an antiseptic, chlorquinaldol, against Neisseria gonorrhoeae and Chlamydia trachomatis].
Pathol. Biol. 39(2) , 136-9, (1991) The activity of chlorquinaldol, a derivative of hydroxy-8-quinolein used for local antisepsy, was studied against Neisseria gonorrhoeae and Chlamydia trachomatis. The weak solubility of the product and the special growth conditions of the organisms made an ad... |