Setamycin, a 16-membered macrolide antibiotic. Identification and nematocidal activity.

نویسندگان

  • K Otoguro
  • A Nakagawa
  • S Omura
چکیده

Setamycin which has been isolated by Omura et al.,1*^ is a macrolide antibiotic possessing activities against trichomonads, some fungi and Gram-positive bacteria. The morphological and physiological properties of its producing organism led to a new genus designated as Kitasatosporia setae of the order ActinomycetalesP Recently, many unusual 16-memBered macrolides4) such as hygrolidins,5»6) L681,110 antibiotics,7) bafilomycins,8>9) leucanicidin10) and L-l55,175 antibiotic,n) have been reported. Setamycin also has been estimated as a macrolide belonging to this family from its spectral data and biological properties. In this paper we wish to describe the identification and biological properties of setamycin. The molecular formula, C42H61NO12for setamycin was tentatively proposed by the elementary analysis and 13C NMRspectral data, in our previous paper.13 However, the molecular formula was revised to be C44H65NO13 from the sub-

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Swalpamycin, a new macrolide antibiotic. II. Structure elucidation.

A new antibiotic swalpamycin (1) has been isolated from the culture broth of Streptomyces sp. Y-84,30967. The antibiotic has the molecular formula of C37H56O14 and belongs to the class of 16-membered neutral macrolide antibiotics. Its structure has been elucidated by an analysis of its spectral properties. It contains a novel aglycone herein called swalpanolide.

متن کامل

Structure activity relationship in sixteen membered macrolide antibiotics.

Leucomycin (Kitasamycin) is a macrolide antibiotic having activity against gram-positive bacteria and certain Mycoplasma strains. Comparison of antimicrobial activities of the variuos leucomycin congeners (I-X) indicates a clear structure-activity relationship among them. The acylation of the 3-hydroxy group somewhat reduces the in vitro activity while the acylation of the 4"-hydroxy group of m...

متن کامل

Absolute configurations of macrolide antibiotics of the bafilomycin and leucanicidin groups.

groups2) isolated from various microorganisms of the order Actinomycetales have been knownfor some years to possess a broad spectrum of biological activity against bacteria, fungi, yeasts, insects, protozoa, cestodes, and free-living nematodes. More recently they have been shown to have potent nematocidal activity against the free-living stages of intestinal parasitic nematodes of major importa...

متن کامل

TAN-1323 C and D, new concanamycin-group antibiotics; detection of the angiostatic activity with a wide range of macrolide antibiotics.

We detected potent angiostatic activity in a MeOH extract from the mycelia of microbial strain S-45628 in the chick chorioallantoic membrane (CAM) assay. The producer was taxonomically characterized as Streptomyces purpurascens. Active principles designated TAN-1323 A-D were isolated and determined to be 18-membered macrolide antibiotics; components C and D are new members of this group, while ...

متن کامل

PC-766B, a new macrolide antibiotic produced by Nocardia brasiliensis. II. Isolation, physico-chemical properties and structure elucidation.

A new macrolide antibiotic, PC-766B, was isolated from the cells of Nocardia brasiliensis SC-4710 by acetone extraction, and purified by gel filtration, silica gel chromatography, HPLC and TLC. The structure of PC-766B was determined by NMR spectral analysis to be a new class of the hygrolidin family antibiotics. PC-766B had a 16-membered macrocyclic lactone ring, a 6-membered hemiketal ring an...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • The Journal of antibiotics

دوره 41 2  شماره 

صفحات  -

تاریخ انتشار 1988