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Flavogallonic acid dilactone: Difference between revisions

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Revision as of 15:41, 31 July 2011 editLilHelpa (talk | contribs)Extended confirmed users, Pending changes reviewers413,676 editsm Typo fixing, replaced: Refernce → Reference using AWB← Previous edit Latest revision as of 10:39, 23 December 2024 edit undoGraeme Bartlett (talk | contribs)Administrators250,106 edits chemspider 
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{{chembox {{chembox
| Watchedfields = changed
| verifiedrevid = 441178083 | verifiedrevid = 442366566
| Name = Flavogallonic acid dilactone | Name = Flavogallonic acid dilactone
| ImageFile = Flavogallonic acid dilactone.png | ImageFile = Flavogallonic acid dilactone.svg
| ImageSize = 200px | ImageSize = 200px
| ImageName = Chemical structure of flavogallonic acid dilactone | ImageName = Chemical structure of flavogallonic acid dilactone
| ImageAlt = Chemical structure of flavogallonic acid dilactone | ImageAlt = Chemical structure of flavogallonic acid dilactone
| PIN = 3,4,5-Trihydroxy-2-(1,6,7-trihydroxy-4,9-dioxo-4,9-dihydrobenzopyranobenzopyran-2-yl)benzoic acid
| IUPACName =
| OtherNames = <!-- <br> --> | OtherNames = <!-- <br> -->
|Section1= {{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 103744-88-3 | CASNo = 103744-88-3
| ChemSpiderID = 57539155
| CASNo_Ref =
| CASOther = | PubChem = 71308199
| StdInChI=1S/C21H10O12/c22-8-2-5(19(28)29)10(16(27)14(8)25)4-1-6-11-12-7(21(31)32-17(11)13(4)24)3-9(23)15(26)18(12)33-20(6)30/h1-3,22-27H,(H,28,29)
| PubChem =
| StdInChIKey = ICEBGCDIMFYRLU-UHFFFAOYSA-N
| SMILES = O=c4oc3c1c(c(c2O)oc(=O)c1cc(O)c3O)c4cc2-c(c(O)c5O)c(C(O)=O)cc5O | SMILES = O=c4oc3c1c(c(c2O)oc(=O)c1cc(O)c3O)c4cc2-c(c(O)c5O)c(C(O)=O)cc5O

| InChI =
| MeSHName =
}} }}
|Section2= {{Chembox Properties |Section2={{Chembox Properties
| Formula = C<sub>21</sub>H<sub>10</sub>O<sub>12</sub> | Formula = C<sub>21</sub>H<sub>10</sub>O<sub>12</sub>
| MolarMass = 454.29 g/mol | MolarMass = 454.29 g/mol
| ExactMass = 454.017225 u
| Appearance = | Appearance =
| Density = | Density =
| MeltingPt = <!-- °C --> | MeltingPt =
| BoilingPt = <!-- °C --> | BoilingPt =
| Solubility = | Solubility =
}} }}
| Section3 = {{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards = | MainHazards =
| FlashPt = | FlashPt =
| Autoignition = | AutoignitionPt =
| RPhrases = <!-- {{R10}}, {{R23}}, {{R34}}, {{R50}} etc. --> | GHS_ref=<!-- no GHS data in PubChem Dec2021 -->
| SPhrases = <!-- {{S1/2}}, {{S9}}, {{S16}}, {{S26}}, {{S36/37/39}}, {{S45}}, {{S61}} etc. -->
}} }}
}} }}
'''Flavogallonic acid dilactone''' is a ] that can be found in '']'' seeds,<ref>Antiproliferative constituents in the plant 8. Seeds of Rhynchosia volubilis. Kinjo Junei, Nagao Tsuneatsu, Tanaka Takashi, Nonaka Gen-Ichiro and Okabe Hikaru, Biological & pharmaceutical bulletin, 2001, vol. 24, no12, pp. 1443-1445, {{INIST|13400364}}, {{doi|10.1248/bpb.24.1443}}</ref> in '']'',<ref>5A-Reductase inhibitory tannin-related compounds isolated from Shorea laeviforia. Yoshio Hirano, Ryuichiro Kondo and Kokki Sakai, Journal of wood science, Volume 49, Number 4, pp. 339-343, {{doi|10.1007/s10086-002-0481-y}}</ref> in '']'' and '']''.<ref>The use of microfluorometric method for activity-guided isolation of antiplasmodial compound from plant extracts. M. N. Shuaibu, P. A. Wuyep, T. Yanagi, K. Hirayama, T. Tanaka and I. Kouno, Parasitol Res (2008) 102, pp. 1119–1127, {{doi|10.1007/s00436-008-0879-6}}</ref> '''Flavogallonic acid dilactone''' is a ] that can be found in '']'' seeds,<ref>Antiproliferative constituents in the plant 8. Seeds of Rhynchosia volubilis. Kinjo Junei, Nagao Tsuneatsu, Tanaka Takashi, Nonaka Gen-Ichiro and Okabe Hikaru, Biological & pharmaceutical bulletin, 2001, vol. 24, no12, pp. 1443-1445, {{INIST|13400364}}, {{doi|10.1248/bpb.24.1443}}</ref> in '']'',<ref>5A-Reductase inhibitory tannin-related compounds isolated from Shorea laevifolia. Yoshio Hirano, Ryuichiro Kondo and Kokki Sakai, Journal of wood science, Volume 49, Number 4, pp. 339-343, {{doi|10.1007/s10086-002-0481-y}}</ref> in '']'' and '']''.<ref>The use of microfluorometric method for activity-guided isolation of antiplasmodial compound from plant extracts. M. N. Shuaibu, P. A. Wuyep, T. Yanagi, K. Hirayama, T. Tanaka and I. Kouno, Parasitol Res (2008) 102, pp. 1119–1127, {{doi|10.1007/s00436-008-0879-6}}</ref>


==See also== == See also ==
* ] * ]


==References== == References ==
{{reflist}} {{reflist}}


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{{Natural-phenol-stub}} {{aromatic-stub}}
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