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ECKHARD THINES, HEIDRUN ANKE, OLOV STERNER
1998 Volume 51 Issue 4 Pages
387-393
Published: April 25, 1998
Released on J-STAGE: January 27, 2009
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From submerged cultures of
Scytalidium sp. 36-93, ten metabolites were isolated due to their effects on dihydroxynaphthalene (DHN) or DOPA melanin biosynthesis. Four of the compounds, scytalols A (
1a), B (
1b), C (
2), and D (
3), are new secondary metabolites, the structures of which were determined by spectroscopy, while the other compounds are known. Scytalols A (
1a) and D (
3) are selective inhibitors of DHN melanin biosynthesis and exhibit no antifungal or cytotoxic activities. Nectriapyrone, 6-methoxymellein and 4-chloro-6-methoxymellein stimulated the formation of DOPA melanin in B16-F1 melanoma cells in the absence of melanin-stimulating hormone.
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I. Taxonomy, Fermentation, Isolation and Physico-chemical and Biological Properties
TAKAYUKI KAJIURA, TAMOTSU FURUMAI, YASUHIRO IGARASHI, HIROSHI HORI, KA ...
1998 Volume 51 Issue 4 Pages
394-401
Published: April 25, 1998
Released on J-STAGE: January 27, 2009
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Strain TP-A0121 which produces a complex of novel tyrosine kinase inhibitors designated hibarimicins A, B, C, D and G was considered to be a new subspecies of
Microbispora rosea, and the name,
Microbispora rosea subsp.
hibaria, was proposed. Hibarimicins A, B, C and D specifically inhibited the
src tyrosine kinase activity without affecting protein kinase A or protein kinase C. They also showed
in vitro anti-Gram-positive bacterial and antitumor activities. The molecular formulae of hibarimicins A, B, C, D and G were assigned to be C
85H
112O
37, C
85H
112O
37, C
83H
110O
36, C
85H
112O
38, and C
85H
112O
39 respectively.
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II. Structural Studies
HIROSHI HORI, YASUHIRO IGARASHI, TAKAYUKI KAJIURA, TAMOTSU FURUMAI, KA ...
1998 Volume 51 Issue 4 Pages
402-417
Published: April 25, 1998
Released on J-STAGE: January 27, 2009
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The structure of hibarimicins A, B, C, D and G which are inhibitors for tyrosine specific protein kinase are determined using spectroscopic techniques. Hibarimicins described in this report consist of a common aglycon and six deoxyhexoses. The aglycon contains a highly oxidized naphtylnaphthoquinone as a chromophore. Among them, hibarimicin B was identical with angelmicin B
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Chemical Interrelation with a Homologous Peptide, Ustiloxin B
YUKIKO KOISO, NAOKO MORISAKI, YUKIKO YAMASHITA, YUKIKO MITSUI, RYUICHI ...
1998 Volume 51 Issue 4 Pages
418-422
Published: April 25, 1998
Released on J-STAGE: January 27, 2009
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Ustiloxin F, a microtubule inhibitor, was isolated as a minor metabolite of
Ustilaginoidea virens. The structure was determined from the spectral data and by chemical interrelation to ustiloxin B through reductive removal of the sulfoxide-containing side chain of ustiloxin B to give ustiloxin F. Ustiloxin F inhibited microtubule assembly with an IC
50 value of 10.3 μM.
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NAOKO MORISAKI, YUKIKO MITSUI, YUKIKO YAMASHITA, YUKIKO KOISO, RYUICHI ...
1998 Volume 51 Issue 4 Pages
423-427
Published: April 25, 1998
Released on J-STAGE: January 27, 2009
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Ustiloxin D, produced by the rice plant pathogen
Ustilaginoidea virens, exhibits potent anti-tubulin activity. In order to elucidate the effects of functional groups in ustiloxin D on its activity, several derivatives were synthesized and their anti-tubulin activities were estimated. The
N,
N-dimethylamino derivative and the 14-
O-methyl derivative were inactive (IC
50>50 μM). 20-Hydroxymethylated ustiloxin D showed decreased inhibitory activity compared with ustiloxin D.
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TATSUO TANIMOTO, SATOSHI OHYA, YOSHIO TSUJITA
1998 Volume 51 Issue 4 Pages
428-431
Published: April 25, 1998
Released on J-STAGE: January 27, 2009
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Recently we found novel zaragozic acids (ZAs), F-10863A (zaragozic acid D3, ZAD3), B, C and D in the culture broth of the fungus
Mollisia sp. SANK 10294 as potent inhibitors of squalene synthase. There are several other enzymes that use farnesylpyrophosphate as their substrate. Among them we chose farnesyl-protein transferase and examined whether ZAD3 and F-10863B inhibit this enzyme's activity. ZAD3 and F-10863B inhibited farnesyl-protein transferase with IC
50 values of 0.60 and 3.7 μM, respectively. They also inhibited geranylgeranyl-protein transferase at similar concentrations. In addition, they exhibited potent antifungal activity.
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TARO AMAGATA, KATSUHIKO MINOURA, ATSUSHI NUMATA
1998 Volume 51 Issue 4 Pages
432-434
Published: April 25, 1998
Released on J-STAGE: January 27, 2009
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TAKEO SUGAWARA, AKIHIRO TANAKA, KOICHI TANAKA, KOJI NAGAI, KENICHI SUZ ...
1998 Volume 51 Issue 4 Pages
435-438
Published: April 25, 1998
Released on J-STAGE: January 27, 2009
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Production, Isolation, Structure Elucidation and Biological Properties
TRIPTIKUMAR MUKHOPADHYAY, R. G. BHAT, KIRITY ROY, E. K. S. VIJAYAKUMAR ...
1998 Volume 51 Issue 4 Pages
439-441
Published: April 25, 1998
Released on J-STAGE: January 27, 2009
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HIROYUKI ONUKI, HARUMI MIYASHIGE, HIROSHI HASEGAWA, SHINYA YAMASHITA
1998 Volume 51 Issue 4 Pages
442-444
Published: April 25, 1998
Released on J-STAGE: January 27, 2009
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TOSHIYUKI KAMIGAUCHI, RYUJI SAKAZAKI, KAZUO NAGASHIMA, YOSHIMI KAWAMUR ...
1998 Volume 51 Issue 4 Pages
445-450
Published: April 25, 1998
Released on J-STAGE: January 27, 2009
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YOSHITAKE TANAKA, FANG FANG, CHENG GANG ZHANG, XIAN WU ZHANG, SATOSHI ...
1998 Volume 51 Issue 4 Pages
451-453
Published: April 25, 1998
Released on J-STAGE: January 27, 2009
JOURNAL
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