5255-76-5 ((Skimmianine)

快速询单

结构式：

SkimmianineMOL文件

CAS号：

5255-76-5

英文名称：

Skimmianine

分子式：

C₁₄H₁₃NO₄

分子量：

259.257323980331

植物源：

黄缎木栎南香毛南香退热类药芸香

Skimmianine(5255-76-5)名称与标识符

名称

英文别名：

Skimmianine;Skimmianin;Chloroxylonine;4,7,8-Trimethoxyfuro[2,3-b]quinoline;Skimmiamine;beta-Fagarine;.beta.-Fagarine;Furo[2,3-b]quinoline, 4,7,8-trimethoxy-;4E1KLC380B;4,7,8-trimethoxyfurano[2,3-b]quinoline;b-fagarine;FURO(2,3-b)QUINOLINE, 4,7,8-TRIMETHOXY-;Furo[2, 4,7,8-trimethoxy-;Prestwick_184;Prestwick3_000668;Prestwick1_000668;Prestwick0_000668;Prestwick2_000668;CBMicro_015540;Skimmianine (beta-Fagarine);Oprea1_598261;Opre;

标识符

InChIKey：

SLSIBLKBHNKZTB-UHFFFAOYSA-N

Inchi：

1S/C14H13NO4/c1-16-10-5-4-8-11(13(10)18-3)15-14-9(6-7-19-14)12(8)17-2/h4-7H,1-3H3

SMILES：

O1C=CC2C1=NC1C(=C(C=CC=1C=2OC)OC)OC

BRN：

0028904

Skimmianine(5255-76-5)物化性质

计算特性

氢键供体数量 : 0
氢键受体数量 : 5
可旋转化学键数量 : 3
重原子数量 : 19
复杂度 : 314
拓扑分子极性表面积 : 53.7

Skimmianine(5255-76-5)国际标准相关数据

EINECS：

1585

Skimmianine(5255-76-5)相关文献

1. Biosynthesis of aromatic isoprenoids. Part I. The role of 3-prenylquinolines and of platydesmine in the biosnthesis of the furuquinoline alkaloid, dictamnine
James F. Collins,William J. Donnelly,Michael F. Grundon,Kevin J. James J. Chem. Soc. Perkin Trans. 1 1974 2177
2. Biphenyl dioxygenase-catalysed cis-dihydroxylation of tricyclic azaarenes: chemoenzymatic synthesis of arene oxide metabolites and furoquinoline alkaloids
Derek R. Boyd,Narain D. Sharma,Jonathan G. Carroll,Pui L. Loke,Colin R. O'Dowd,Christopher C. R. Allen RSC Adv. 2013 3 10944
3. Biosynthesis of aromatic isoprenoids. Part II. Aromatic hydroxylation in the biosynthesis of the furoquinoline alkaloids, skimmianine, evoxine, and choisyine
Michael F. Grundson,David M. Harrison,Caroline G. Sypropoulos J. Chem. Soc. Perkin Trans. 1 1974 2181
4. A one-pot, three-component reaction for the synthesis of novel 7-arylbenzo[c]acridine-5,6-diones
Shivani Mahajan,Sadhika Khullar,Sanjay K. Mandal,Inder Pal Singh Chem. Commun. 2014 50 10078
5. Biosynthesis of the furoquinoline alkaloids, skimmianine, evoxine, and choisyine: mechanism of formation of the furan ring. The timing of aromatic hydroxylation and of methylation
Michael F. Grundon,David M. Harrison,Caroline G. Spyropoulos J. Chem. Soc. Chem. Commun. 1974 51
6. Biosynthesis of the alkaloid skimmianine in Fagara coco from [4-14C]mevalonic acid, [5-14C] mevalonic acid, and [1-14C]dimethylallyl alcohol
Agustín O. Colonna,Eduardo G. Gros J. Chem. Soc. D 1970 674a
7. Aromatic hydroxylation in quinoline alkaloids. The biosynthesis of skimmianine from dictamnine, and a convenient synthesis of furanoquinoline alkaloids
J. F. Collins,W. J. Donnelly,M. F. Grundon,D. M. Harrison,C. G. Spyropoulos J. Chem. Soc. Chem. Commun. 1972 1029
8. Bioactive constituents from toxic seed plants in China
Jing Qu,Shi-Shan Yu,Dan Du,Ya-Dan Wang RSC Adv. 2013 3 10078
9. Natural cholinesterase inhibitors from marine organisms
Lindon?W. K. Moodie,Kristina Sep?i?,Tom Turk,Robert Frange?,Johan Svenson Nat. Prod. Rep. 2019 36 1053
10. Biosynthesis of aromatic isoprenoids. Part III. Mechanism of formation of the furan ring and origin of the 4-methoxy-group in the biosynthesis of furoquinoline alkaloids
Michael F. Grundon,David M. Harrison,Caroline G. Spyropoulos J. Chem. Soc. Perkin Trans. 1 1975 302