Isoquinoline alkaloid isolated from red clover, preparation method and use
A technology of isoquinoline alkaloids and red clover, applied in the field of medicine, can solve the problems of large side effects of aspirin, ineffective anti-platelet treatment effect, etc., and achieve the effects of less toxic and side effects, significant anti-platelet aggregation, and novel structure
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Embodiment 1
[0033] The present invention provides a kind of preparation method of the new isoquinoline alkaloid that is separated from red clover, comprises the steps:
[0034] S1. Grind the dried red clover, soak it in 95% ethanol for 20 hours, heat and reflux for extraction 3 times, 3 hours each time, dry the filtrate at low temperature until it has no alcohol smell, and obtain the thick paste of red clover ;
[0035] S2, uniformly disperse the thick red clover paste obtained in step S1 in a 1.0% HCl solution, sonicate for 50 minutes, let stand for 18 hours, and filter to obtain the supernatant;
[0036] S3. Adjust the supernatant liquid obtained in step S2 to pH=12 with aqueous ammonia, and extract with organic solvent in turn. The organic solvent is chloroform or acetone, and the extracts are concentrated and dried to obtain chloroform thick paste or acetone thick paste. Born turbidity is used. Determination of the platelet aggregation rate of chloroform thick paste and acetone thick...
Embodiment 2
[0050] The invention provides a preparation method of a novel isoquinoline alkaloid isolated from red clover, comprising the steps of:
[0051] S1. Grind the dried red clover, soak it in 95% ethanol for 20 hours, heat and reflux for extraction 3 times, 3 hours each time, dry the filtrate at low temperature until it has no alcohol smell, and obtain the thick paste of red clover ;
[0052] S2, uniformly disperse the thick red clover paste obtained in step S1 in a 1.0% HCl solution, sonicate for 50 minutes, let stand for 18 hours, and filter to obtain the supernatant;
[0053] S3. Adjust the supernatant obtained in step S2 to pH = 12 with aqueous ammonia, extract with an organic solvent in sequence, and concentrate and dry each extract to obtain a thick paste;
[0054] S4. Dissolve the active part, that is, the thick paste in step S3 with petroleum ether, put it on the silica gel column by wet method, and perform gradient elution with petroleum ether-ethyl acetate elution system...
Embodiment 3
[0067] This embodiment provides a method for preparing a new isoquinoline alkaloid isolated from red clover, comprising the following steps:
[0068] S1. Grind the dried red clover, soak it in 95% ethanol for 20 hours, heat and reflux for extraction 3 times, each time for 3 hours, and dry the filtrate in a low temperature environment until it has no alcohol smell, and the red clover thick paste is obtained ;
[0069] S2, uniformly disperse the thick red clover paste obtained in step S1 in a 1.0% HCl solution, sonicate for 50 minutes, let stand for 18 hours, and filter to obtain the supernatant;
[0070] S3. Adjust the supernatant obtained in step S2 to pH = 12 with aqueous ammonia, extract with an organic solvent in sequence, and concentrate and dry each extract to obtain a thick paste;
[0071] S4. Dissolving the active part, that is, the thick paste in step S3, with petroleum ether, put it on a silica gel column by a wet method, and use a petroleum ether-ethyl acetate eluti...
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