INHIBITORY AGENT FOR HUMAN ACQUIRED IMMUNODEFICIENCY SYNDROME VIRUS INFECTION
PURPOSE:To provide the subject inhibitor containing a specific spergualin-related compound as an active ingredient, low in toxicity, and excellent in safety, antitumor activity and immune-enhancing activity. CONSTITUTION:The objective inhibitor contains a spergualin-related compound (salt) of formul...
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creator | TOMIYOSHI TSUGIO SHIOZAWA AKIRA HOSHINO KOUROU IKEDA RYUJI |
description | PURPOSE:To provide the subject inhibitor containing a specific spergualin-related compound as an active ingredient, low in toxicity, and excellent in safety, antitumor activity and immune-enhancing activity. CONSTITUTION:The objective inhibitor contains a spergualin-related compound (salt) of formula I [Gu is guanidino; X0 is (CH2)1-5, (substituted)phenylene; (a) is 3-5; X1 (CH2)0-2-CH(CH00)(CH2)0-2 (R00 is H, OH, OCH3, etc); X2 is NH(CH2)4 NH (CH2)3NH-R02 (R02 is H, the OH-removed residue of the carboxyl group of an amino acid or peptide)] or a spergualin-related compound (salt) of formula II [X is (CH2)1-5, C6H4; (r) is 3-5; R6 is the residue produced by removing one H atom from the alpha-amino group and a hydroxyl group from the alpha-carboxyl group of an amino acid, etc.]. The compound is orally administered at a dose of preferably 5-500mg/kg.day. |
format | Patent |
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CONSTITUTION:The objective inhibitor contains a spergualin-related compound (salt) of formula I [Gu is guanidino; X0 is (CH2)1-5, (substituted)phenylene; (a) is 3-5; X1 (CH2)0-2-CH(CH00)(CH2)0-2 (R00 is H, OH, OCH3, etc); X2 is NH(CH2)4 NH (CH2)3NH-R02 (R02 is H, the OH-removed residue of the carboxyl group of an amino acid or peptide)] or a spergualin-related compound (salt) of formula II [X is (CH2)1-5, C6H4; (r) is 3-5; R6 is the residue produced by removing one H atom from the alpha-amino group and a hydroxyl group from the alpha-carboxyl group of an amino acid, etc.]. The compound is orally administered at a dose of preferably 5-500mg/kg.day.</description><edition>5</edition><language>eng</language><subject>HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><creationdate>1994</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19940712&DB=EPODOC&CC=JP&NR=H06192075A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19940712&DB=EPODOC&CC=JP&NR=H06192075A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>TOMIYOSHI TSUGIO</creatorcontrib><creatorcontrib>SHIOZAWA AKIRA</creatorcontrib><creatorcontrib>HOSHINO KOUROU</creatorcontrib><creatorcontrib>IKEDA RYUJI</creatorcontrib><title>INHIBITORY AGENT FOR HUMAN ACQUIRED IMMUNODEFICIENCY SYNDROME VIRUS INFECTION</title><description>PURPOSE:To provide the subject inhibitor containing a specific spergualin-related compound as an active ingredient, low in toxicity, and excellent in safety, antitumor activity and immune-enhancing activity. CONSTITUTION:The objective inhibitor contains a spergualin-related compound (salt) of formula I [Gu is guanidino; X0 is (CH2)1-5, (substituted)phenylene; (a) is 3-5; X1 (CH2)0-2-CH(CH00)(CH2)0-2 (R00 is H, OH, OCH3, etc); X2 is NH(CH2)4 NH (CH2)3NH-R02 (R02 is H, the OH-removed residue of the carboxyl group of an amino acid or peptide)] or a spergualin-related compound (salt) of formula II [X is (CH2)1-5, C6H4; (r) is 3-5; R6 is the residue produced by removing one H atom from the alpha-amino group and a hydroxyl group from the alpha-carboxyl group of an amino acid, etc.]. The compound is orally administered at a dose of preferably 5-500mg/kg.day.</description><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><subject>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1994</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNyjEKwjAUANAsDqLe4XuAQlVUHNPkx3whPzZNhEylSJxEC_X-uHgAp7e8uXDElhqKPmSQZ-QIxgewyUkGqdpEATWQc4m9RkOKkFWGLrMO3iHcKKQOiA2qSJ6XYvYYnlNZ_VyItcGobFXGd1-mcbiXV_n0l6utD5vTtj7u5e6f8wUfhi7h</recordid><startdate>19940712</startdate><enddate>19940712</enddate><creator>TOMIYOSHI TSUGIO</creator><creator>SHIOZAWA AKIRA</creator><creator>HOSHINO KOUROU</creator><creator>IKEDA RYUJI</creator><scope>EVB</scope></search><sort><creationdate>19940712</creationdate><title>INHIBITORY AGENT FOR HUMAN ACQUIRED IMMUNODEFICIENCY SYNDROME VIRUS INFECTION</title><author>TOMIYOSHI TSUGIO ; SHIOZAWA AKIRA ; HOSHINO KOUROU ; IKEDA RYUJI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_JPH06192075A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1994</creationdate><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><topic>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</topic><toplevel>online_resources</toplevel><creatorcontrib>TOMIYOSHI TSUGIO</creatorcontrib><creatorcontrib>SHIOZAWA AKIRA</creatorcontrib><creatorcontrib>HOSHINO KOUROU</creatorcontrib><creatorcontrib>IKEDA RYUJI</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>TOMIYOSHI TSUGIO</au><au>SHIOZAWA AKIRA</au><au>HOSHINO KOUROU</au><au>IKEDA RYUJI</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>INHIBITORY AGENT FOR HUMAN ACQUIRED IMMUNODEFICIENCY SYNDROME VIRUS INFECTION</title><date>1994-07-12</date><risdate>1994</risdate><abstract>PURPOSE:To provide the subject inhibitor containing a specific spergualin-related compound as an active ingredient, low in toxicity, and excellent in safety, antitumor activity and immune-enhancing activity. CONSTITUTION:The objective inhibitor contains a spergualin-related compound (salt) of formula I [Gu is guanidino; X0 is (CH2)1-5, (substituted)phenylene; (a) is 3-5; X1 (CH2)0-2-CH(CH00)(CH2)0-2 (R00 is H, OH, OCH3, etc); X2 is NH(CH2)4 NH (CH2)3NH-R02 (R02 is H, the OH-removed residue of the carboxyl group of an amino acid or peptide)] or a spergualin-related compound (salt) of formula II [X is (CH2)1-5, C6H4; (r) is 3-5; R6 is the residue produced by removing one H atom from the alpha-amino group and a hydroxyl group from the alpha-carboxyl group of an amino acid, etc.]. The compound is orally administered at a dose of preferably 5-500mg/kg.day.</abstract><edition>5</edition><oa>free_for_read</oa></addata></record> |
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subjects | HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS |
title | INHIBITORY AGENT FOR HUMAN ACQUIRED IMMUNODEFICIENCY SYNDROME VIRUS INFECTION |
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