NEW SESQUITERPENE DERIVATIVE

PURPOSE:To obtain a new compound having excellent retrovirus protease inhibiting action and useful as an anti-human immunodeficiency virus agent, etc. CONSTITUTION:A compound of formula I (R is hydroxymethyl and R is OH, or R is hydroxymethyl or formyl and R is H), e.g. the compound of formula II ha...

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Hauptverfasser: MIZUNO SUKETOSHI, OKAMOTO ROKURO, SHIBAMOTO NORIO, WATANABE YOSHIO, KUMAMOTO TOSHIHIKO, KOJIMA IKUO, AKAGAWA HISAYOSHI, DOBASHI KAZUYUKI, KOMINATO KAICHIRO, NISHIDA HIROSHI
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creator MIZUNO SUKETOSHI
OKAMOTO ROKURO
SHIBAMOTO NORIO
WATANABE YOSHIO
KUMAMOTO TOSHIHIKO
KOJIMA IKUO
AKAGAWA HISAYOSHI
DOBASHI KAZUYUKI
KOMINATO KAICHIRO
NISHIDA HIROSHI
description PURPOSE:To obtain a new compound having excellent retrovirus protease inhibiting action and useful as an anti-human immunodeficiency virus agent, etc. CONSTITUTION:A compound of formula I (R is hydroxymethyl and R is OH, or R is hydroxymethyl or formyl and R is H), e.g. the compound of formula II having the following properties. Color and form, light yellow powder; melting point, slowly decomposing at 180 deg.C without exhibiting a definite melting point; molecular formula, C23H30O5; color reactions, positive to Gibbs reaction and 2,4-dinitrophenylhydrazine reagent; solubility, soluble in methanol, acetone, etc., and insoluble in water and n-hexane; classification by basic, neutral and acidic, acidic. This compound can be prepared by culturing a microorganism belonging to the genus Stachybotrys and capable of producing the compound of formula I [e.g. Stachybotrys sp. Mer-NF5O03 (FERM P-12344)] preferably under aerobic condition at 28 deg.C for usually 2-10 days and separating and purifying the compound from the cultured product.
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Color and form, light yellow powder; melting point, slowly decomposing at 180 deg.C without exhibiting a definite melting point; molecular formula, C23H30O5; color reactions, positive to Gibbs reaction and 2,4-dinitrophenylhydrazine reagent; solubility, soluble in methanol, acetone, etc., and insoluble in water and n-hexane; classification by basic, neutral and acidic, acidic. This compound can be prepared by culturing a microorganism belonging to the genus Stachybotrys and capable of producing the compound of formula I [e.g. Stachybotrys sp. 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Color and form, light yellow powder; melting point, slowly decomposing at 180 deg.C without exhibiting a definite melting point; molecular formula, C23H30O5; color reactions, positive to Gibbs reaction and 2,4-dinitrophenylhydrazine reagent; solubility, soluble in methanol, acetone, etc., and insoluble in water and n-hexane; classification by basic, neutral and acidic, acidic. This compound can be prepared by culturing a microorganism belonging to the genus Stachybotrys and capable of producing the compound of formula I [e.g. Stachybotrys sp. Mer-NF5O03 (FERM P-12344)] preferably under aerobic condition at 28 deg.C for usually 2-10 days and separating and purifying the compound from the cultured product.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record>
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subjects BEER
BIOCHEMISTRY
CHEMISTRY
ENZYMOLOGY
FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
MICROBIOLOGY
MUTATION OR GENETIC ENGINEERING
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
PROCESSES USING MICROORGANISMS
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
SPIRITS
VINEGAR
WINE
title NEW SESQUITERPENE DERIVATIVE
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