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Tephrosin: Difference between revisions

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Revision as of 18:53, 10 February 2011 editEdgar181 (talk | contribs)Extended confirmed users196,325 edits removed Category:Pyranodichromens using HotCat← Previous edit Latest revision as of 17:05, 16 July 2021 edit undoJJMC89 bot III (talk | contribs)Bots, Administrators3,706,494 editsm Moving Category:Heterocyclic compounds (5 rings) to Category:Heterocyclic compounds with 5 rings per Misplaced Pages:Categories for discussion/Log/2021 June 24#Category:Heterocyclic compounds (1 ring) 
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{{chembox {{chembox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 413150531
| ImageFile = Tephrosin.png | ImageFile = Tephrosin.png
| ImageSize = 200px | ImageSize = 200px
| IUPACName = 7a-Hydroxy-9,10-dimethoxy-3,3-dimethyl-13,13a-dihydro-3''H'',7a''H''-pyranodichromen-7-one | IUPACName = 7a-Hydroxy-9,10-dimethoxy-3,3-dimethyl-13,13a-dihydro-3''H'',7a''H''-pyranodichromen-7-one
| OtherNames = 12aβ-hydroxydeguelin<ref>{{cite journal| last=Cabizza | first=Maddalena | coauthors=Alberto Angioni, Marinella Melis, Marco Cabras, Carlo V. Tuberoso, and Paolo Cabras | year=2004 | title=Rotenone and rotenoids in cubè resins, formulations, and residues on olives | journal=Journal of Agriculture and Food Chemistry | volume=52 | issue=2 | pages=288–293 | doi=10.1021/jf034987a| pmid=14733510}}</ref> | OtherNames = 12aβ-hydroxydeguelin<ref>{{cite journal| last=Cabizza | first=Maddalena |author2=Alberto Angioni |author3=Marinella Melis |author4=Marco Cabras |author5=Carlo V. Tuberoso |author6=Paolo Cabras | year=2004 | title=Rotenone and rotenoids in cubè resins, formulations, and residues on olives | journal=Journal of Agricultural and Food Chemistry | volume=52 | issue=2 | pages=288–293 | doi=10.1021/jf034987a| pmid=14733510}}</ref>
| Section1 = {{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 76-80-2 | CASNo = 76-80-2
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 9C081V83CC
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 9442
| PubChem = 114909 | PubChem = 114909
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 241806
| SMILES = CC1(C=CC2=C(O1)C=CC3=C2O4COC5=CC(=C(C=C54(C3=O)O)OC)OC)C | SMILES = CC1(C=CC2=C(O1)C=CC3=C2O4COC5=CC(=C(C=C54(C3=O)O)OC)OC)C
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 102858
| InChI = 1/C23H22O7/c1-22(2)8-7-12-15(30-22)6-5-13-20(12)29-19-11-28-16-10-18(27-4)17(26-3)9-14(16)23(19,25)21(13)24/h5-10,19,25H,11H2,1-4H3/t19-,23-/m1/s1
| InChIKey = AQBZCCQCDWNNJQ-AUSIDOKSBD
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C23H22O7/c1-22(2)8-7-12-15(30-22)6-5-13-20(12)29-19-11-28-16-10-18(27-4)17(26-3)9-14(16)23(19,25)21(13)24/h5-10,19,25H,11H2,1-4H3/t19-,23-/m1/s1
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = AQBZCCQCDWNNJQ-AUSIDOKSSA-N
| RTECS =
| MeSHName =
| KEGG_Ref = {{keggcite|changed|kegg}}
| KEGG = C10535
}} }}
| Section2 = {{Chembox Properties |Section2={{Chembox Properties
| Formula = C<sub>23</sub>H<sub>22</sub>O<sub>7</sub> | Formula = C<sub>23</sub>H<sub>22</sub>O<sub>7</sub>
| MolarMass = 410.41658 g/mol | MolarMass = 410.41658 g/mol
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| BoilingPt = | BoilingPt =
| Solubility = }} | Solubility = }}
| Section3 = {{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards = | MainHazards =
| FlashPt = | FlashPt =
| Autoignition = }} | AutoignitionPt = }}
| Section8 = {{Chembox Related |Section8={{Chembox Related
| OtherAnions = | OtherAnions =
| OtherCations = | OtherCations =
| OtherFunctn = | OtherFunction =
| Function = | OtherFunction_label =
| OtherCpds = ], ]}} | OtherCompounds = ], ]}}
}} }}


'''Tephrosin''' is ]. It is a natural fish poison found in the leaves and seeds of '']''<ref>{{cite journal| last=Ahmad | first=V. U. | coauthors=Z. Ali, S. R. Hussaini, F. Iqbal, M. Zahid, M. Abbas, and N. Saba | date=1999-08-01 | title=Flavonoids of ''Tephrosia purpurea'' | journal=Fitoterapia | volume=70 | issue=4 | pages=443–445 | doi=10.1016/S0367-326X(99)00046-5}}</ref> and '']''<ref>Production of rotenoids by heterotrophic and photomixotrophic cell cultures of tephrosia vogelii. Nadine Lambert, Marie-France Trouslot, Claudine Nef-Campa and Hervé Chrestin, Phytochemistry, Volume 34, Issue 6, December 1993, Pages 1515-1520, {{doi|10.1016/S0031-9422(00)90838-0}}</ref>. '''Tephrosin''' is ]. It is a natural fish poison found in the leaves and seeds of '']''<ref>{{cite journal| last=Ahmad | first=V. U. |author2=Z. Ali |author3=S. R. Hussaini |author4=F. Iqbal |author5=M. Zahid |author6=M. Abbas |author7=N. Saba | date=1999-08-01 | title=Flavonoids of ''Tephrosia purpurea'' | journal=Fitoterapia | volume=70 | issue=4 | pages=443–445 | doi=10.1016/S0367-326X(99)00046-5}}</ref> and '']''.<ref>Production of rotenoids by heterotrophic and photomixotrophic cell cultures of tephrosia vogelii. Nadine Lambert, Marie-France Trouslot, Claudine Nef-Campa and Hervé Chrestin, Phytochemistry, Volume 34, Issue 6, December 1993, Pages 1515-1520, {{doi|10.1016/S0031-9422(00)90838-0}}</ref>




==See also== ==See also==
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