首页|灰褐栓齿菌Phellodon cinereofuscus子实体化学成分及其对α-葡萄糖苷酶的抑制活性

灰褐栓齿菌Phellodon cinereofuscus子实体化学成分及其对α-葡萄糖苷酶的抑制活性

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糖尿病是最常见的慢性疾病之一,能够产生多种并发症.α-葡萄糖苷酶是治疗糖尿病的关键靶点,发掘新型α-葡萄糖苷酶抑制剂对糖尿病的治疗具有重要意义.本研究首次对野生食用菌灰褐栓齿菌Phellodon cinereofuscus子实体的化学成分及其α-葡萄糖苷酶抑制活性进行了研究.灰褐栓齿菌子实体的70%乙醇提取物通过硅胶柱色谱、HP20柱色谱、ODS柱色谱和高效液相色谱等现代色谱分离技术进行分离纯化,从中分离得到16个化合物,利用核磁共振波谱学方法对它们的结构进行了鉴定,分别为(22E,24R)-3β-hydroxy-24-methylcholesta-5,22-dien-7-one(1)、(22E,24R)-ergosta-4,6,8(14),22-tetraen-3,15-dion(2)、5α,8α-epidioxyergosta-6,9,22-trien-3β-ol(3)、(22E,24S)-cerevisterol(4)、20R,24R,9α-hydroxy-Δ4,6,8(14),22-tetraene-3,15-dione-ergosterol(5)、glaucoposterol B(6)、(22E,24R)-5α,6α-epoxyergosta-8(14),22-diene-3β,7α,15α-triol(7)、3β-Hydroxyl-(22E,24R)-ergosta-5,8,22-trien-7,15-dione(8)、5α,6α-epoxy-(22E,24R)-ergosta-8(14),22-diene-3β,7α-diol(9)、(22E,24R)-5α,6α-epoxy-ergosta-8,22-dien-3β,7α-diol(10)、demethylincisterol A3(11)、betulinic acid(12)、lup-20(29)-en-3α,28-diol(13)、(Z)-6-nonadecenoic acid(14)、tetradecanoic acid(15)、hexacosane(16).16 个化合物均为属内首次分离获得,对化合物1-16进行α-葡萄糖苷酶抑制活性测定,化合物3、6、11、13和14具有较好的抑制活性,其 IC50值分别(19.51±5.68)、(6.29±1.16)、(12.15±2.21)、(6.81±0.26)、(10.26±1.84)μmol/L,该研究结果为灰褐栓齿菌的药用功能提供了理论支持.
Chemical constituents from fruiting body of Phellodon cinereofuscus and their inhibitory activities against α-glucosidase
Diabetes is one of the most common chronic diseases,capable of generating various complications.α-Glucosidase serves as a crucial therapeutic target for diabetes,and the exploration of novel α-glucosidase inhibitors holds significant importance for diabetes treatment.The chemical constituents from fruiting body of Phellodon cinereofuscus and their inhibitory activities against α-glucosidase were studied.Sixteen compounds from 70%ethanol extract of P.cinereofuscus were isolated and purified by silica gel column,HP20 column chromatography,ODS column chromatography and high performance liquid chromatography(HPLC).The structures of them were identified by nuclear magnetic resonance(NMR)as(22E,24R)-3β-hydroxy-24-methylcholesta-5,22-dien-7-one(1),(22E,24R)-ergosta-4,6,8(14),22-tetraen-3,15-dion(2),5α,8α-epidioxyergosta-6,9,22-trien-3β-ol(3),(22E,24S)-cerevisterol(4),20R,24R,9α-hydroxy-Δ4,6,8(14),22-tetraene-3,15-dione-ergosterol(5),glaucoposterol B(6),(22E,24R)-5α,6α-epoxyergosta-8(14),22-diene-3β,7α,15α-triol(7),3β-Hydroxyl-(22E,24R)-ergosta-5,8,22-trien-7,15-dione(8),5α,6α-epoxy-(22E,24R)-ergosta-8(14),22-diene-3β,7α-diol(9),(22E,24R)-5α,6α-epoxy-ergosta-8,22-dien-3β,7α-diol(10),demethylincisterol A3(11),betulinic acid(12),lup-20(29)-en-3α,28-diol(13),(Z)-6-nonadecenoic acid(14),tetradecanoic acid(15),hexacosane(16).All the compounds were obtained from the genus of Phellodon for the first time.The inhibitory activities of compounds 1-16 against α-glucosidase were evaluated.Compounds 3,6,11,13 and 14 showed significant inhibitory activity against α-glucosidase with IC50 values of(19.51±5.68),(6.29±1.16),(12.15±2.21),(6.81±0.26),(10.26±1.84)μmol/L respectively.The results provide theoretical support for further research of the medicinal function of P.cinereofuscus.

Phellodon cinereofuscuschemical constituentsstructure identificationinhibitory activity against α-glucosidase

钟方琴、王雨曦、王慧丽、魏玉莲、袁海生

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辽宁大学生命科学院,辽宁 沈阳 110036

中国科学院沈阳应用生态研究所中国科学院森林生态与管理重点实验室,辽宁沈阳 110164

灰褐栓齿菌 化学成分 结构鉴定 α-葡萄糖苷酶抑制活性

2024

菌物学报
中科院微生物研究所 中国菌物学会

菌物学报

CSTPCD北大核心
影响因子:1.187
ISSN:1672-6472
年,卷(期):2024.43(12)