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Items: 1 to 20 of 87

1.

Ramoplanin: a lipoglycodepsipeptide antibiotic.

Farver DK, Hedge DD, Lee SC.

Ann Pharmacother. 2005 May;39(5):863-8. Epub 2005 Mar 22. Review.

PMID:
15784805
2.

Ramoplanin: a topical lipoglycodepsipeptide antibacterial agent.

Fulco P, Wenzel RP.

Expert Rev Anti Infect Ther. 2006 Dec;4(6):939-45. Review.

PMID:
17181409
3.

In-vitro activity of vancomycin, teicoplanin, daptomycin, ramoplanin, MDL 62873 and other agents against staphylococci, enterococci and Clostridium difficile.

Bartoloni A, Colao MG, Orsi A, Dei R, Giganti E, Parenti F.

J Antimicrob Chemother. 1990 Nov;26(5):627-33.

PMID:
1688341
4.

In vitro activity of ramoplanin against Clostridium difficile, including strains with reduced susceptibility to vancomycin or with resistance to metronidazole.

Peláez T, Alcalá L, Alonso R, Martín-López A, García-Arias V, Marín M, Bouza E.

Antimicrob Agents Chemother. 2005 Mar;49(3):1157-9.

5.

Efficacy of oral ramoplanin for inhibition of intestinal colonization by vancomycin-resistant enterococci in mice.

Stiefel U, Pultz NJ, Helfand MS, Donskey CJ.

Antimicrob Agents Chemother. 2004 Jun;48(6):2144-8.

6.
7.

In vitro activities of ramoplanin, teicoplanin, vancomycin, linezolid, bacitracin, and four other antimicrobials against intestinal anaerobic bacteria.

Citron DM, Merriam CV, Tyrrell KL, Warren YA, Fernandez H, Goldstein EJ.

Antimicrob Agents Chemother. 2003 Jul;47(7):2334-8.

8.

Ambush of Clostridium difficile spores by ramoplanin: activity in an in vitro model.

Kraus CN, Lyerly MW, Carman RJ.

Antimicrob Agents Chemother. 2015 May;59(5):2525-30. doi: 10.1128/AAC.04853-14. Epub 2015 Feb 17.

9.

The mechanism of action of ramoplanin and enduracidin.

Fang X, Tiyanont K, Zhang Y, Wanner J, Boger D, Walker S.

Mol Biosyst. 2006 Jan;2(1):69-76. Epub 2005 Nov 29.

PMID:
16880924
10.

Functional analysis of the lipoglycodepsipeptide antibiotic ramoplanin.

Cudic P, Behenna DC, Kranz JK, Kruger RG, Wand AJ, Veklich YI, Weisel JW, McCafferty DG.

Chem Biol. 2002 Aug;9(8):897-906.

11.

Ramoplanin. A 16686, a 16686a, MDL 62198.

[No authors listed]

Drugs R D. 2002;3(1):61-4. Review. No abstract available.

PMID:
11881535
12.

Fidaxomicin: a macrocyclic antibiotic for the management of Clostridium difficile infection.

Sullivan KM, Spooner LM.

Ann Pharmacother. 2010 Feb;44(2):352-9. doi: 10.1345/aph.1M351. Epub 2010 Jan 13. Review.

PMID:
20071495
13.

Bactericidal activity of ramoplanin against antibiotic-resistant enterococci.

Johnson CC, Taylor S, Pitsakis P, May P, Levison ME.

Antimicrob Agents Chemother. 1992 Oct;36(10):2342-5.

14.

Comparison of the efficacy of ramoplanin and vancomycin in both in vitro and in vivo models of clindamycin-induced Clostridium difficile infection.

Freeman J, Baines SD, Jabes D, Wilcox MH.

J Antimicrob Chemother. 2005 Oct;56(4):717-25. Epub 2005 Sep 5.

PMID:
16143709
15.

Dalbavancin: a new option for the treatment of gram-positive infections.

Lin SW, Carver PL, DePestel DD.

Ann Pharmacother. 2006 Mar;40(3):449-60. Epub 2006 Feb 28. Review.

PMID:
16507624
16.

In-vitro studies with ramoplanin (MDL 62,198): a novel lipoglycopeptide antimicrobial.

O'Hare MD, Ghosh G, Felmingham D, Grüneberg RN.

J Antimicrob Chemother. 1990 Feb;25(2):217-20.

PMID:
2139436
17.

Ramoplanin at bactericidal concentrations induces bacterial membrane depolarization in Staphylococcus aureus.

Cheng M, Huang JX, Ramu S, Butler MS, Cooper MA.

Antimicrob Agents Chemother. 2014 Nov;58(11):6819-27. doi: 10.1128/AAC.00061-14. Epub 2014 Sep 2.

18.

Production of the Ramoplanin Activity Analogue by Double Gene Inactivation.

Han J, Chen J, Shao L, Zhang J, Dong X, Liu P, Chen D.

PLoS One. 2016 May 5;11(5):e0154121. doi: 10.1371/journal.pone.0154121. eCollection 2016.

19.

Functional and biochemical analysis of a key series of ramoplanin analogues.

Fang X, Nam J, Shin D, Rew Y, Boger DL, Walker S.

Bioorg Med Chem Lett. 2009 Nov 1;19(21):6189-91. doi: 10.1016/j.bmcl.2009.09.001. Epub 2009 Sep 6.

20.

Dissecting ramoplanin: mechanistic analysis of synthetic ramoplanin analogues as a guide to the design of improved antibiotics.

Chen L, Yuan Y, Helm JS, Hu Y, Rew Y, Shin D, Boger DL, Walker S.

J Am Chem Soc. 2004 Jun 23;126(24):7462-3.

PMID:
15198592

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