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Oligo-beta-(1,3)-glukano-(1,3)-mannoza, oligo-beta-(1.3)-glukano-(1,3)-manitol oraz ich pochodne do leczenia chorób układu immunologicznego, sposoby ich otrzymywania oraz zawierające je środki lecznicze
专利权人:
ASE & BIO
发明人:
YVIN, JEAN-CLAUDE,DESCROIX, KARINE,FERRIERES, VINCENT,JAMOIS, FRANK,LAURENT, ISABELLE,VETVICKA, VACLAV,YVIN JEAN-CLAUDE,DESCROIX KARINE,FERRIERES VINCENT,JAMOIS FRANK,LAURENT ISABELLE,VETVICKA VACLAV
申请号:
PL07872005
公开号:
PL2102222T3
申请日:
2007.12.20
申请国别(地区):
PL
年份:
2012
代理人:
摘要:
The use of oligosaccharides (I) and (II), i.e. oligo-beta -glucan-(1,3)-mannose, -mannitol, -glucose and -glucitol compounds and their 4-deoxy derivatives, as medicaments for treating tumor, cancer, viral, bacterial, fungal, immune system, autoimmune or immunostimulation deficiency-associated diseases is new. Some compounds (I) and (II) (i.e. the mannose and mannitol derivatives) are new, as are various intermediates. The use of oligosaccharides of formulae (I) and (II) is claimed in the preparation of a medicament for treating tumor, cancer, viral, bacterial, fungal, immune system, autoimmune or immunostimulation deficiency-associated diseases in humans and warm-blooded animals. R 1H or OH; n : 2-10 (preferably 2-7, especially 3-5). Independent claims are included for: (1) oligo-beta -glucan-(1,3)-mannose (I') and oligo-beta -glucan-(1,3)-mannitol compounds (II') (including 4-deoxy derivatives), of formulae (I; terminal 2-OH in beta -configuration) and (II; terminal 2-OH in beta -configuration) respectively, as new compounds; (2) the preparation of (I') and (II'); and (3) new intermediate saccharide and oligosaccharide compound intermediates of formulae (III) - (VI). p : 0-9 (preferably 0-6, especially 2-4); R 2H, allyl, methylnaphthyl, benzyl, p-methoxybenzyl, COCH 2Cl, COCH 2Br or COCH 2I; or R 3, R 4, R 3', R 4' : benzyl (Bn), chlorobenzyl, nitrobenzyl, allyl, triarylmethyl, trialkylsilyl (e.g. SiEt 3, Si(CHMe 2) 3or Si(Me) 2tBu) or ester group (e.g. COMe, COCH 2Cl, COPh or pivaloyl); or R 3+ R 4, R 3'+ R 4' : CHMe, CMe 2, C(CF 3) 2, 5-7C cycloalkylidene, butylidene, 1-tert. butylethylidene, benzylidene, methoxybenzylidene or 1-phenylbenzylidene; R 5H, levinoyl (preferred), COMe, COCH 2Cl, fluorenylmethoxycarbonyl or trialkylsilyl (e.g. SiEt 3, Si(CHMe 2) 3or Si(Me) 2tBu); provided that R 3, R 4, R 3', R 4'are all different from R 5; R 7ester group, specifically COMe, COPh (preferred) or pivaloyl; R 8group orthogonal to all the other protecting groups, selected
来源网站:
中国工程科技知识中心
来源网址:
http://www.ckcest.cn/home/

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