摘要:
Es wird vorgeschlagen, 5-Chlor-1H-tetrazol-carbonsäureester durch Umsetzung von Dichlorisonitrilessigsäureestern mit Metallaziden herzustellen. Die hierzu erforderlichen Dichlorisonitrilessigsäureesterwerden durch Umsetzung von N-Formyl-aminocarbonsäureestern mit Chlor oder chlorabspaltenden Verbindungen gebildet.
摘要:
The present invention provides new physiological active substance erbstatin analogue compounds of a general formula (I), which have excellent tyrosine-specific protein-kinase inhibitory activity, antitumor activity and antimicrobial activity. in which R 1 represents a hydrogen atom, a lower alkanoyl group or a lower alkyl group; n represents a positive integer of 1 to3; X represents a hydrogen atom or a halogen atom; Y represents a group of formula -CH=CH-NC, -CH=CH-NHR 2 or-CH 2 -CH 2 -NHR 2 (where R 2 represents a formyl group or a lower alkanoyl group; with the exception of the cases where X is hydrogen atom, (R 1 0) n group is 2,5-dihydroxy group and Y is -CH=CH-NHCHO or-CH 2 -CH 2 -NHCHO). The present invention further provides a tyrosine-specific protein-kinase inhibitor, tumoricide or bactericide containing at least one compound of the said formula (I).
摘要:
A coordination complex is disclosed comprising a radionuclide selected from radioactive isotopes of Tc, Ru, Co. Pt and Re and an isonitrile ligand of the formula: where X is a lower alkyl group having 1 to 4 carbon atoms, wherein R is selected from COOR' and CONR 2 R 3 where R 1 can be H, a pharmaceutically acceptable cation, or a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, R 2 , and R 3 can be H, or a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, and R 2 and R 3 can be the same or different. Kits that can be used to form these complexes are also disclosed.
摘要:
This invention relates to a novel composition which is useful as an antitumor, antiviral and antifungal composition, a process of producing the composition and a method for inhibiting tumors, viruses, and fungi utilizing the composition. More particularly, the novel composition is an organic sesquiterpenoid isocyanide composition which is derived from marine sponge Bubaris sp., and has the general formula:
摘要翻译:本发明涉及一种可用作抗肿瘤,抗病毒和抗真菌组合物的新型组合物,该组合物的制备方法以及利用该组合物抑制肿瘤,病毒和真菌的方法。 更具体地说,新型组合物是衍生自海洋海绵Bubaris sp。的有机倍半萜烯异氰酸酯组合物,具有以下通式: a
摘要:
The present invention provides new physiological active substance erbstatin analogue compounds of a general formula (I), which have excellent tyrosine-specific protein-kinase inhibitory activity, antitumor activity and antimicrobial activity. in which R 1 represents a hydrogen atom, a lower alkanoyl group or a lower alkyl group; n represents a positive integer of
1 to3; X represents a hydrogen atom or a halogen atom; Y represents a group of formula -CH=CH-NC, -CH=CH-NHR 2 or-CH 2 -CH 2 -NHR 2 (where R 2 represents a formyl group or a lower alkanoyl group; with the exception of the cases where X is hydrogen atom, (R 1 0) n group is 2,5-dihydroxy group and Y is -CH=CH-NHCHO or-CH 2 -CH 2 -NHCHO).
The present invention further provides a tyrosine-specific protein-kinase inhibitor, tumoricide or bactericide containing at least one compound of the said formula (I).