The activation effect of boric acid as an activator is good,and we investigate the best activation conditions for the boric acid impregnation method.To represent the structural characteristics and adsorption performan...The activation effect of boric acid as an activator is good,and we investigate the best activation conditions for the boric acid impregnation method.To represent the structural characteristics and adsorption performance of the Stellera Chamaejasme based carbon molecular sieves,we use Brunner-Emmet-Teller(BET)measurements,scan-ning electron microscope(SEM),Raman spectra(Raman),X-ray diffraction(XRD),and adsorption property measurement.When the loading ratio was 0.68:1,the specific surface area was 532.21 m^(2)/g,the total pore volume was 0.24 cm 3/g,the average pore size was 1.81 nm,the adsorption value of methylene blue was 145.28 mg/g,and the adsorption value of iodine was 713.33 mg/g,the results showed that boric acid had better activation effect.The carbon molecular sieves made from Stellera Chamaejasme and activated with boric acid produce two peaks on the aperture distribution graph that are densely distributed in the micropore range.This indicates that boric acid’s pore-forming tendency is primarily micropore.展开更多
Methanol extract of Stellera chamaejasme L wasassessed for antitumor activity by an antitumor activebioassay against murine leukemia P388 in vivo. Thebioassay-directed separation of the extract furnishedseven diterpen...Methanol extract of Stellera chamaejasme L wasassessed for antitumor activity by an antitumor activebioassay against murine leukemia P388 in vivo. Thebioassay-directed separation of the extract furnishedseven diterpene compounds (stellerarin, stelleramacrin,gnidimacrin, pimelea factor P2, subtoxin, huratoxin,simplexin ) and two biflavanone compounds (neochemae-jasmin A and B). Among them, gnidimacrin, stellerarinand stelleramacrin (a novel compound) were found tohave high antitumor and cytotoxic activities against P388,L1210 and K562 in vivo and in vitro. The results suggestedthat the diterpene compounds were the potent anti-tumor principles of Stellera chamaejame L展开更多
A new biflavonoid, stelleranol, was isolated from the roots of Stellera chamaejasme L.. Its structure was determined by the analysis of MS and NMR data, especially 2D NMR spectra.
A new chromone derivative, 3-[1- (2, 4, 6-trihydroxyphenyl) 3-di-(4-hydroxyphenyl) 1-propanone-2-yl] 5,7-dihydroxy-8-di(4-hydroxyphenyl)methyl-4H-1-benzopyran-4-one, named as isomohsenone was isolated from the roots o...A new chromone derivative, 3-[1- (2, 4, 6-trihydroxyphenyl) 3-di-(4-hydroxyphenyl) 1-propanone-2-yl] 5,7-dihydroxy-8-di(4-hydroxyphenyl)methyl-4H-1-benzopyran-4-one, named as isomohsenone was isolated from the roots of Stellera chamaejasme L. together with known chamaechromone. Its structure was determined by the analysis of MS and NMR data, especially 2D NMR spectra.展开更多
Gnidimacrin, a diterpene compound, isolated from the methanol extract of Stellera, chamaejasme L., showed significant antitumor activities against mouse leukemia P-388 and L-1210 in vivo, such as Lewis lung carcinoma,...Gnidimacrin, a diterpene compound, isolated from the methanol extract of Stellera, chamaejasme L., showed significant antitumor activities against mouse leukemia P-388 and L-1210 in vivo, such as Lewis lung carcinoma, B-16 melanoma and Colon cancer 26. It showed ILSs of 40%.49% and 41% at the dosages of 0.01-0.02 mg/kg ip,respectively. Gnidimacrin strongly inhibited cell Proliferation of human cancer cell lines such as leukemia K562, stomach cancers Kato-III, MKN-28, MKN-45, and mouse leukemia L-1210 by the MTT assay and colony forming assay in vitro. The IC50 of gnidimacrin was 0.007-0.00012 μg/ml. It is concluded that gnidimacrin is the principal antitumor element in Stellera chemaejasme L. with strong antitumor activities.展开更多
Stellera chamaejasme,widely distributed on the Qinghai-Tibet Plateau,is a poisonous plant causing serious harm to grassland.Activated carbons have been prepared from the roots of Stellera chamaejasme via phosphoric ac...Stellera chamaejasme,widely distributed on the Qinghai-Tibet Plateau,is a poisonous plant causing serious harm to grassland.Activated carbons have been prepared from the roots of Stellera chamaejasme via phosphoric acid and zinc chloride activation at500°C for 60 min with an impregnation ratio of 3:1.Yield(25.1%-27.6%),ash(4.5%-4.9%),methylene blue(195.0 mg/g-254.5 mg/g),iodine value(720.4 mg/g-810.5 mg/g),specific surface area(1023.3 m2/g-1216.7 m2/g),specific pore volume(2.13 cm3/g-2.26 cm3/g),mesopore volume(1.30 cm3/g-1.59 cm3/g)and average pore size(5.88nm-7.45 nm)of the products were determined.The results from both the zinc chloride and phosphoric acid activation processes showed that the activated carbons of S.chamaejasme roots exhibit a characterization of natural developed mesopores.展开更多
Three series of novel 1,5-diphenyl-l-pentanone derivatives were designed and synthesized. Their structures were characterized by IR, IH NMR techniques, and elemental analysis. The insecticidal activities of the new co...Three series of novel 1,5-diphenyl-l-pentanone derivatives were designed and synthesized. Their structures were characterized by IR, IH NMR techniques, and elemental analysis. The insecticidal activities of the new compounds were preliminarily evaluated. The bioassay results indicated that the compounds Xll--X30 displayed better aphicidal activity against Aphis gossypii than compounds X1--X10 and the lead compound （E）-l,5-diphenyl-1- penten-1-one （A）. The inhibitory rates of compounds X6 and X29 were 100% against Plutella xylostella （L.） at 600 mgoL 1. Compounds X12, X13, X19, X24, X25, X26 and X27 showed higher insecticidal activity against Tetranychus cinnabarinus （Boisduval） at 600 mgoL 1 than the lead compound （A）. Keywords Stellera chamaejasme L, （E）-l,5-diphenyl-l-penten-l-one, analogue, synthesis, design, insecticidal activity展开更多
A series of novel daphneolone analogs was designed and synthesized on the basis of natural product 1,5-diphenyl-2-penten-1-one（I） from Stellera chamaejasme L. as lead compound, whereby 2,6-dimethylmorpholine moiety ...A series of novel daphneolone analogs was designed and synthesized on the basis of natural product 1,5-diphenyl-2-penten-1-one（I） from Stellera chamaejasme L. as lead compound, whereby 2,6-dimethylmorpholine moiety was introduced to replace 1-phenyl group. Their structures were confirmed by IR,1H NMR, and HRMS（ESI） or elemental analysis,13 C NMR for some representative compounds. The two isomers of target compounds were separated and identified by NOESY technique and chemical method.All of the synthesized compounds have been evaluated for anti-plant pathogenic fungi activities. The results showed that some compounds exhibited moderate to good antifungal activities against tested fungi at the concentration of 50 mg/L. Among them, compound 7d, with a 4-bromine-substituted phenyl group and cis-2,6-dimethylmorpholine moiety, displayed best activity with an EC50 of 23.87 mmol/L against Valsa mali, superior to lead compound I. In addition, preliminary structure–activity relationship analysis indicated that, between two isomers of target compounds, the antifungal activities of the isomer with cis-2,6-dimethylmorpholine were better than the trans-isomer.展开更多
基金Graduate Innovation Project of Qinghai University for Nationalities(2021XJXS12)Graduate Innovation Project of Qinghai University for Nationalities(12M2021018).
文摘The activation effect of boric acid as an activator is good,and we investigate the best activation conditions for the boric acid impregnation method.To represent the structural characteristics and adsorption performance of the Stellera Chamaejasme based carbon molecular sieves,we use Brunner-Emmet-Teller(BET)measurements,scan-ning electron microscope(SEM),Raman spectra(Raman),X-ray diffraction(XRD),and adsorption property measurement.When the loading ratio was 0.68:1,the specific surface area was 532.21 m^(2)/g,the total pore volume was 0.24 cm 3/g,the average pore size was 1.81 nm,the adsorption value of methylene blue was 145.28 mg/g,and the adsorption value of iodine was 713.33 mg/g,the results showed that boric acid had better activation effect.The carbon molecular sieves made from Stellera Chamaejasme and activated with boric acid produce two peaks on the aperture distribution graph that are densely distributed in the micropore range.This indicates that boric acid’s pore-forming tendency is primarily micropore.
文摘Methanol extract of Stellera chamaejasme L wasassessed for antitumor activity by an antitumor activebioassay against murine leukemia P388 in vivo. Thebioassay-directed separation of the extract furnishedseven diterpene compounds (stellerarin, stelleramacrin,gnidimacrin, pimelea factor P2, subtoxin, huratoxin,simplexin ) and two biflavanone compounds (neochemae-jasmin A and B). Among them, gnidimacrin, stellerarinand stelleramacrin (a novel compound) were found tohave high antitumor and cytotoxic activities against P388,L1210 and K562 in vivo and in vitro. The results suggestedthat the diterpene compounds were the potent anti-tumor principles of Stellera chamaejame L
文摘A new biflavonoid, stelleranol, was isolated from the roots of Stellera chamaejasme L.. Its structure was determined by the analysis of MS and NMR data, especially 2D NMR spectra.
文摘A new chromone derivative, 3-[1- (2, 4, 6-trihydroxyphenyl) 3-di-(4-hydroxyphenyl) 1-propanone-2-yl] 5,7-dihydroxy-8-di(4-hydroxyphenyl)methyl-4H-1-benzopyran-4-one, named as isomohsenone was isolated from the roots of Stellera chamaejasme L. together with known chamaechromone. Its structure was determined by the analysis of MS and NMR data, especially 2D NMR spectra.
文摘Gnidimacrin, a diterpene compound, isolated from the methanol extract of Stellera, chamaejasme L., showed significant antitumor activities against mouse leukemia P-388 and L-1210 in vivo, such as Lewis lung carcinoma, B-16 melanoma and Colon cancer 26. It showed ILSs of 40%.49% and 41% at the dosages of 0.01-0.02 mg/kg ip,respectively. Gnidimacrin strongly inhibited cell Proliferation of human cancer cell lines such as leukemia K562, stomach cancers Kato-III, MKN-28, MKN-45, and mouse leukemia L-1210 by the MTT assay and colony forming assay in vitro. The IC50 of gnidimacrin was 0.007-0.00012 μg/ml. It is concluded that gnidimacrin is the principal antitumor element in Stellera chemaejasme L. with strong antitumor activities.
基金the National Natural Science Foundation of China,Grant No.30760195the Natural Science Foundation of Qinghai Province,China,Grant No.2015-ZJ-909the Natural Science Project of Qinghai Nationalities University,Grant No.2015XJZ01.
文摘Stellera chamaejasme,widely distributed on the Qinghai-Tibet Plateau,is a poisonous plant causing serious harm to grassland.Activated carbons have been prepared from the roots of Stellera chamaejasme via phosphoric acid and zinc chloride activation at500°C for 60 min with an impregnation ratio of 3:1.Yield(25.1%-27.6%),ash(4.5%-4.9%),methylene blue(195.0 mg/g-254.5 mg/g),iodine value(720.4 mg/g-810.5 mg/g),specific surface area(1023.3 m2/g-1216.7 m2/g),specific pore volume(2.13 cm3/g-2.26 cm3/g),mesopore volume(1.30 cm3/g-1.59 cm3/g)and average pore size(5.88nm-7.45 nm)of the products were determined.The results from both the zinc chloride and phosphoric acid activation processes showed that the activated carbons of S.chamaejasme roots exhibit a characterization of natural developed mesopores.
文摘Three series of novel 1,5-diphenyl-l-pentanone derivatives were designed and synthesized. Their structures were characterized by IR, IH NMR techniques, and elemental analysis. The insecticidal activities of the new compounds were preliminarily evaluated. The bioassay results indicated that the compounds Xll--X30 displayed better aphicidal activity against Aphis gossypii than compounds X1--X10 and the lead compound （E）-l,5-diphenyl-1- penten-1-one （A）. The inhibitory rates of compounds X6 and X29 were 100% against Plutella xylostella （L.） at 600 mgoL 1. Compounds X12, X13, X19, X24, X25, X26 and X27 showed higher insecticidal activity against Tetranychus cinnabarinus （Boisduval） at 600 mgoL 1 than the lead compound （A）. Keywords Stellera chamaejasme L, （E）-l,5-diphenyl-l-penten-l-one, analogue, synthesis, design, insecticidal activity
基金supported by the National Natural Science Foundation of China (No. 21272266)the National High Technology Research and Development Program of China (No. 2011AA10A202)
文摘A series of novel daphneolone analogs was designed and synthesized on the basis of natural product 1,5-diphenyl-2-penten-1-one（I） from Stellera chamaejasme L. as lead compound, whereby 2,6-dimethylmorpholine moiety was introduced to replace 1-phenyl group. Their structures were confirmed by IR,1H NMR, and HRMS（ESI） or elemental analysis,13 C NMR for some representative compounds. The two isomers of target compounds were separated and identified by NOESY technique and chemical method.All of the synthesized compounds have been evaluated for anti-plant pathogenic fungi activities. The results showed that some compounds exhibited moderate to good antifungal activities against tested fungi at the concentration of 50 mg/L. Among them, compound 7d, with a 4-bromine-substituted phenyl group and cis-2,6-dimethylmorpholine moiety, displayed best activity with an EC50 of 23.87 mmol/L against Valsa mali, superior to lead compound I. In addition, preliminary structure–activity relationship analysis indicated that, between two isomers of target compounds, the antifungal activities of the isomer with cis-2,6-dimethylmorpholine were better than the trans-isomer.
