E L Moss Jr
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Explore the profile of E L Moss Jr including associated specialties, affiliations and a list of published articles.
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21
Citations
167
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Recent Articles
1.
Cacciapuoti A, Loebenberg D, Corcoran E, Menzel Jr F, Moss Jr E, Norris C, et al.
Antimicrob Agents Chemother
. 2000 Jul;
44(8):2017-22.
PMID: 10898669
SCH 56592 (posaconazole), a new triazole antifungal agent, was tested in vitro, and its activity was compared to that of itraconazole against 39 Aspergillus strains and to that of fluconazole...
2.
Loebenberg D, Cacciapuoti A, PARMEGIANI R, Moss Jr E, Menzel Jr F, Antonacci B, et al.
Antimicrob Agents Chemother
. 1992 Feb;
36(2):498-501.
PMID: 1605621
SCH 39304, a new triazole antifungal agent, is a 50:50 racemic mixture of two enantiomers, SCH 42427 and SCH 42426. The activities of these three compounds were compared in a...
3.
Cacciapuoti A, Loebenberg D, PARMEGIANI R, Antonacci B, Norris C, Moss Jr E, et al.
Antimicrob Agents Chemother
. 1992 Jan;
36(1):64-7.
PMID: 1590702
SCH 39304 was compared with fluconazole and ketoconazole in a systemic Candida albicans infection in mice (10(6) CFU per mouse). Results were based on survival rates and CFU in kidneys...
4.
Cacciapuoti A, Loebenberg D, Moss Jr E, Menzel F, Rudeen J, Naples L, et al.
J Antibiot (Tokyo)
. 1990 Sep;
43(9):1131-6.
PMID: 2145254
A series of tylosins and acyl derivatives of 23-O-demycinosyltylosin (DMT) were initially tested for in vitro antibacterial activity and serum levels in squirrel monkeys (po) and mice (iv). Overall, the...
5.
Cacciapuoti A, Moss Jr E, Menzel Jr F, Cramer C, Weiss W, Loebenberg D, et al.
J Antibiot (Tokyo)
. 1987 Oct;
40(10):1426-30.
PMID: 3680008
The in vitro activities of three new 8-methoxychlortetracyclines, Sch 36969, 33256 and 34164 were compared to tetracycline, minocycline and doxycycline. Against aerobic Gram-negative rods Sch 36969 had a geometric mean...
6.
Loebenberg D, Moss Jr E, Rudeen J, Menzel Jr F, Hare R, Oden E, et al.
J Antimicrob Chemother
. 1985 Jun;
15 Suppl C:207-18.
PMID: 3897173
Sch 34343 showed a linear dose response (with respect to AUCs) in mice following both intravenous and subcutaneous administration. It was 100% bioavailable following subcutaneous administration. Peak serum levels, AUCs,...
7.
Loebenberg D, Miller G, Moss Jr E, Oden E, Hare R, Chung M, et al.
J Antimicrob Chemother
. 1982 Feb;
9 Suppl C:221-31.
PMID: 7061372
No abstract available.
8.
Hare R, Moss Jr E, Sabatelli F, Schaffer T, Waitz J
Scand J Infect Dis Suppl
. 1980 Jan;
Suppl 23:62-72.
PMID: 6937970
Data obtained with 30 micrograms netilmicin discs on Mueller-Hinton agar have been compared to MIC values obtained in Mueller-Hinton broth. Regression analysis was used to determine susceptibility cutoff points for...
9.
Davies D, Mallams A, COUNELIS M, Loebenberg D, Moss Jr E, Waitz J
J Med Chem
. 1978 Feb;
21(2):189-93.
PMID: 413921
The discovery of aminoglycoside 66-40C, a novel dimeric, unsaturated imine produced by Micromonospora inyoensis, afforded a versatile intermediate for the synthesis of a variety of sisomicin analogues modified at the...
10.
Waitz J, Sabatelli F, Menzel F, Moss Jr E
Antimicrob Agents Chemother
. 1974 Nov;
6(5):579-81.
PMID: 15825308
On the basis of parallel in vitro studies with antibiotic G-418, gentamicin, neomycin, and kanamycin, antibiotic G-418 was found to be less potent than gentamicin but more active than either...