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Page 1
Showing results for spiramycin
Search for spinamycin instead (3 results)
Spiramycin renaissance.
Rubinstein E, Keller N. Rubinstein E, et al. J Antimicrob Chemother. 1998 Nov;42(5):572-6. doi: 10.1093/jac/42.5.572. J Antimicrob Chemother. 1998. PMID: 9848439 Review. No abstract available.
[Spiramycin].
Vacek V. Vacek V. Cas Lek Cesk. 1994 Jan 17;133(2):56-60. Cas Lek Cesk. 1994. PMID: 8131182 Review. Czech.
Spiramycin is a 16-membered ring macrolide (antibiotic). It was discovered in 1952 as a product of Streptomyces ambofaciens. ...This difference between the effectiveness in vitro and in vivo is explained above all by the great affinity of spiramycin to tissues where
Spiramycin is a 16-membered ring macrolide (antibiotic). It was discovered in 1952 as a product of Streptomyces ambofaciens. ...This
SPIRAMYCIN.
[No authors listed] [No authors listed] Br Med J. 1956 Mar 17;1(4967):621. Br Med J. 1956. PMID: 13293407 Free article. No abstract available.
SPIRAMYCIN.
[No authors listed] [No authors listed] Can Med Assoc J. 1958 May 1;78(9):713-4. Can Med Assoc J. 1958. PMID: 13523517 Free PMC article. No abstract available.
Pharmacodynamics and pharmacokinetics of spiramycin and their clinical significance.
Brook I. Brook I. Clin Pharmacokinet. 1998 Apr;34(4):303-10. doi: 10.2165/00003088-199834040-00003. Clin Pharmacokinet. 1998. PMID: 9571302 Review.
Spiramycin is less metabolised than some of the other macrolides. The renal excretion of spiramycin is low, with 4 to 20% of the dose being excreted by this route. High concentrations of spiramycin are achieved in bile, which is an important route of eliminat
Spiramycin is less metabolised than some of the other macrolides. The renal excretion of spiramycin is low, with 4 to 20% of t
Evaluation of spiramycin for topical applications: a cell culture study.
Yagiz Aghayarov O, Bayar Muluk N, Vejselova Sezer C, Kutlu HM, Cingi C. Yagiz Aghayarov O, et al. Eur Rev Med Pharmacol Sci. 2023 Mar;27(2 Suppl):44-50. doi: 10.26355/eurrev_202303_31701. Eur Rev Med Pharmacol Sci. 2023. PMID: 36971220 Free article.
First, 105 NIH/3T3 cells were seeded onto coverslips in 6-well plates for morphological analysis of both untreated and spiramycin-treated cells. For 24 hours, NIH/3T3 cells were exposed to a 100 muM dosage of spiramycin. The cells in the control group were grown in …
First, 105 NIH/3T3 cells were seeded onto coverslips in 6-well plates for morphological analysis of both untreated and spiramycin-tre …
SPIRAMYCIN.
TURRISI E, SORGE F, POLOSA P. TURRISI E, et al. S Afr Med J. 1964 Feb 29;38:161-2. S Afr Med J. 1964. PMID: 14127210 No abstract available.
Spiramycin-induced cholestatic hepatitis.
Denie C, Henrion J, Schapira M, Schmitz A, Heller FR. Denie C, et al. J Hepatol. 1992 Nov;16(3):386. doi: 10.1016/s0168-8278(05)80677-4. J Hepatol. 1992. PMID: 1487619 No abstract available.
[SPIRAMYCIN].
[No authors listed] [No authors listed] Ann Pharm Fr. 1960 Mar;18:162-6. Ann Pharm Fr. 1960. PMID: 13856626 French. No abstract available.
Anti-Inflammatory Effects of Spiramycin in LPS-Activated RAW 264.7 Macrophages.
Kang JK, Kang HK, Hyun CG. Kang JK, et al. Molecules. 2022 May 17;27(10):3202. doi: 10.3390/molecules27103202. Molecules. 2022. PMID: 35630676 Free PMC article.
Spiramycin also inhibited the expression of NO synthase (iNOS), potentially explaining the spiramycin-induced decrease in NO production. ...In these assays, spiramycin did not induce any adverse reactions. In conclusion, our results demonstrate that spiram
Spiramycin also inhibited the expression of NO synthase (iNOS), potentially explaining the spiramycin-induced decrease in NO p
1,736 results