“Scopolin”的意思、由来-开放百科全书

词条

Scopolin

释义

References
Bibliography

{{Chembox
| ImageFile = Scopolin.png
| ImageSize = 180px
| IUPACName =
| OtherNames =
|Section1={{Chembox Identifiers
| CASNo = 531-44-2
| PubChem = 439514
| SMILES = COC1=C(C=C2C(=C1)C=CC(=O)O2)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O
| ChemSpiderID = 388609
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 16065
| InChI = 1/C16H18O9/c1-22-9-4-7-2-3-12(18)23-8(7)5-10(9)24-16-15(21)14(20)13(19)11(6-17)25-16/h2-5,11,13-17,19-21H,6H2,1H3/t11-,13-,14+,15-,16-/m1/s1
| InChIKey = SGTCGCCQZOUMJJ-YMILTQATBT
| StdInChI = 1S/C16H18O9/c1-22-9-4-7-2-3-12(18)23-8(7)5-10(9)24-16-15(21)14(20)13(19)11(6-17)25-16/h2-5,11,13-17,19-21H,6H2,1H3/t11-,13-,14+,15-,16-/m1/s1
| StdInChIKey = SGTCGCCQZOUMJJ-YMILTQATSA-N
|Section2={{Chembox Properties
| C=16 | H=18 | O=9
| Appearance =
| Density =
| MeltingPtC =
| MeltingPt_notes =
| BoilingPt =
| Solubility =
|Section3={{Chembox Hazards
| MainHazards =
| FlashPt =
| AutoignitionPt =
}}Scopolin is a glucoside of scopoletin formed by the action of the enzyme scopoletin glucosyltransferase.^[1]

References

1. ^{{cite journal | author = Hino F, Okazaki M and Miura Y | year = 1982 | title = Effect of 2,4-dichlorophenoxyacetic acid on glucosylation of scopoletin to scopolin in tobacco tissue-culture | journal = Plant Physiol. | volume = 69 | pages = 810–813 | doi = 10.1104/pp.69.4.810 | pmid=16662301 | issue = 4 | pmc = 426310}}

Bibliography

{{cite journal|last1=Steck|first1=Warren|title=Biosynthesis of Scopolin in Tobacco|journal=Canadian Journal of Biochemistry|volume=45|issue=6|year=1967|pages=889–896|issn=1208-6002|doi=10.1139/o67-099}}
{{cite journal|last1=Steck|first1=Warren|title=The Biosynthetic Pathway from Caffeic Acid to Scopolin in Tobacco Leaves|journal=Canadian Journal of Biochemistry|volume=45|issue=12|year=1967|pages=1995–2003|issn=1208-6002|doi=10.1139/o67-233}}

2 : O-Methylated coumarins|Phenol glucosides

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