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Title:
AUREOBASIDINS
Document Type and Number:
WIPO Patent Application WO/1995/018147
Kind Code:
A1
Abstract:
Aureobasidins useful as a wide-spectrum antimycotic. They are cyclodepsipeptides composed of one hydroxy acid residue having group A1, three amino acid residues having groups C1, F1 and H1, four N-methylamino acid residues having groups B1, D1, G1 and I1, and one cyclic amino acid residue having E1. A representative example thereof is one wherein A1 is CH3CH2CH(CH3)-, B1 is (CH3)2CH-, C1 is benzyl, cyclohexylmethyl, p-fluorobenzyl, benzyloxymethyl, benzyloxybenzyl, methoxybenzyl, cyclohexylmethyloxybenzyl, etc., D1 is methyl, benzyl, hydroxymethyl, etc., E1 is propylene, F1 is CH3CH2CH(CH3)-, G1 is (CH3)2CH-, H1 is (CH3)2CHCH2-, and I1 is (CH3)2C(OH)-. They have excellent activities against not only candida but also cryptococcus and aspergillus.

Inventors:
KUROME TORU (JP)
INOUE TETSUYA (JP)
TAKESAKO KAZUTOH (JP)
INAMI KAORU (JP)
KATO IKUNOSHIN (JP)
Application Number:
PCT/JP1994/002201
Publication Date:
July 06, 1995
Filing Date:
December 26, 1994
Export Citation:
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Assignee:
TAKARA SHUZO CO (JP)
KUROME TORU (JP)
INOUE TETSUYA (JP)
TAKESAKO KAZUTOH (JP)
INAMI KAORU (JP)
KATO IKUNOSHIN (JP)
International Classes:
C07K11/02; A61K38/00; (IPC1-7): C07K11/02; A61K38/15
Foreign References:
JPH0665291A1994-03-08
JPH0539204A1993-02-19
JPH03220199A1991-09-27
Other References:
J. Antibiot., Vol. 46, No. 9 (1993), "Isolation, Structures, and Antifungal Activities of New Aureobasidins", pp. 1347-1354.
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