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Wikipedia:WikiProject Chemicals/Chembox validation/VerifiedDataSandbox and Α-Viniferin: Difference between pages

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Saving copy of the {{chembox}} taken from revid 471316836 of page Alpha-Viniferin for the Chem/Drugbox validation project (updated: 'ChemSpiderID', 'StdInChI', 'StdInChIKey', 'CASNo').
 
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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid [{{fullurl:Alpha-Viniferin|oldid=471316836}} 471316836] of page [[Alpha-Viniferin]] with values updated to verified values.}}
{{chembox
{{chembox
| Verifiedfields = changed
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 457807065
| verifiedrevid = 477319821
| Name = α-Viniferin
| Name = α-Viniferin
| Reference = <!-- <ref>http://www.</ref> -->
| ImageFile = Alpha-viniferin.svg
| Reference =
| ImageFile = Alpha-viniferin.svg
| ImageSize = 200px
| ImageSize = 200px
| PIN = (1''R'',5b''R'',6''R'',10b''S'',11''S'',15b''R'')-1,6,11-Tris(4-hydroxyphenyl)-1,5b,6,10b,11,15b-hexahydrocyclonona[1,2,3-''cd'':4,5,6-''c''′''d''′:7,8,9-''c''′′''d''′′]tris([1]benzofuran)-4,9,14-triol
| IUPACName =
| OtherNames = α-Viniferin; (+)-α-Viniferin
| OtherNames = α-Viniferin; (+)-α-Viniferin
|Section1= {{Chembox Identifiers
|Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 170167
| ChemSpiderID = 333272
| InChI = 1/C42H30O9/c43-22-7-1-19(2-8-22)40-37-28-13-25(46)17-32-35(28)39(42(50-32)21-5-11-24(45)12-6-21)30-15-27(48)18-33-36(30)38(29-14-26(47)16-31(49-40)34(29)37)41(51-33)20-3-9-23(44)10-4-20/h1-18,37-48H
| InChI = 1/C42H30O9/c43-22-7-1-19(2-8-22)40-37-28-13-25(46)17-32-35(28)39(42(50-32)21-5-11-24(45)12-6-21)30-15-27(48)18-33-36(30)38(29-14-26(47)16-31(49-40)34(29)37)41(51-33)20-3-9-23(44)10-4-20/h1-18,37-48H
| InChIKey = KUTVNHOAKHJJFL-UHFFFAOYAE
| InChIKey = KUTVNHOAKHJJFL-UHFFFAOYAE
| SMILES1 = Oc1ccc(cc1)C%10Oc2cc(O)cc7c2C%10c8cc(O)cc9OC(c3ccc(O)cc3)C(c5cc(O)cc6OC(c4ccc(O)cc4)C7c56)c89
| SMILES1 = Oc1ccc(cc1)C%10Oc2cc(O)cc7c2C%10c8cc(O)cc9OC(c3ccc(O)cc3)C(c5cc(O)cc6OC(c4ccc(O)cc4)C7c56)c89
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C42H30O9/c43-22-7-1-19(2-8-22)40-37-28-13-25(46)17-32-35(28)39(42(50-32)21-5-11-24(45)12-6-21)30-15-27(48)18-33-36(30)38(29-14-26(47)16-31(49-40)34(29)37)41(51-33)20-3-9-23(44)10-4-20/h1-18,37-48H/t37-,38-,39+,40+,41+,42-/m1/s1
| StdInChI = 1S/C42H30O9/c43-22-7-1-19(2-8-22)40-37-28-13-25(46)17-32-35(28)39(42(50-32)21-5-11-24(45)12-6-21)30-15-27(48)18-33-36(30)38(29-14-26(47)16-31(49-40)34(29)37)41(51-33)20-3-9-23(44)10-4-20/h1-18,37-48H
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = KUTVNHOAKHJJFL-ZSIJVUTGSA-N
| StdInChIKey = KUTVNHOAKHJJFL-UHFFFAOYSA-N
| CASNo = <!-- blanked - oldvalue: 62218-13-7 -->
| CASNo = 62218-13-7
| CASNo_Ref = {{cascite|changed|??}}
| CASNo_Ref = {{cascite|correct|CAS}}
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 53XER6FHLX
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 66359
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 443463
| ChEMBL = 443463
| PubChem = 196402
| PubChem = 196402
| SMILES = OC(C=C1)=CC=C1[C@@H]2[C@@H](C3=C4C(O[C@@H](C5=CC=C(O)C=C5)[C@@H]4C6=C([C@@H]7[C@H](C8=CC=C(O)C=C8)O9)C9=CC(O)=C6)=CC(O)=C3)C%10=C7C=C(O)C=C%10O2
| SMILES = OC(C=C1)=CC=C1[C@@H]2[C@@H](C3=C4C(O[C@@H](C5=CC=C(O)C=C5)[C@@H]4C6=C([C@@H]7[C@H](C8=CC=C(O)C=C8)O9)C9=CC(O)=C6)=CC(O)=C3)C%10=C7C=C(O)C=C%10O2
}}
}}
|Section2= {{Chembox Properties
|Section2={{Chembox Properties
| C=42|H=30|O=9
| C=42 | H=30 | O=9
| Appearance =
| ExactMass = 678.188983 u
| Appearance =
| Density =
| Density =
| MeltingPt =
| MeltingPt =
| BoilingPt =
| BoilingPt =
| Solubility =
| Solubility =
}}
}}
|Section3= {{Chembox Hazards
|Section3={{Chembox Hazards
| MainHazards =
| MainHazards =
| FlashPt =
| FlashPt =
| Autoignition =
| AutoignitionPt =
}}
}}
}}
}}
'''α-Viniferin''' is a stilbene [[trimer (chemistry)|trimer]]. It can be isolated from ''[[Caragana chamlagu]]''<ref name="Sang">{{cite journal | doi = 10.1248/bpb.25.125 | title = (+)-α-Viniferin, a Stilbene Trimer from Caragana chamlague, Inhibits Acetylcholinesterase | year = 2002 | last1 = Sung | first1 = Sang Hyun | last2 = Kang | first2 = So Young | last3 = Lee | first3 = Ki Yong | last4 = Park | first4 = Mi Jung | last5 = Kim | first5 = Jeong Hun | last6 = Park | first6 = Jong Hee | last7 = Kim | first7 = Young Chul | last8 = Kim | first8 = Jinwoong | last9 = Kim | first9 = Young Choong | journal = Biological & Pharmaceutical Bulletin | volume = 25 | issue = 1 | pages = 125–127| pmid = 11824541 | doi-access = free }}</ref> and from ''[[Caragana sinica]]''<ref name="Shu">{{cite journal | pmid = 16595888 | year = 2006 | last1 = Shu | first1 = N | last2 = Zhou | first2 = H | last3 = Hu | first3 = C | title = Simultaneous determination of the contents of three stilbene oligomers in Caragana sinica collected in different seasons using an improved HPLC method | volume = 29 | issue = 4 | pages = 608–12 | journal = Biological & Pharmaceutical Bulletin | doi=10.1248/bpb.29.608| doi-access = free }}</ref> and from the stem bark of ''[[Dryobalanops aromatica]]''.<ref>{{Cite journal|pmid=21338657|doi=10.1016/j.fitote.2011.02.006|title=Malaysianol A, a new trimer resveratrol oligomer from the stem bark of Dryobalanops aromatica|year=2011|last1=Wibowo|first1=A.|last2=Ahmat|first2=N.|last3=Hamzah|first3=A.S.|last4=Sufian|first4=A.S.|last5=Ismail|first5=N.H.|last6=Ahmad|first6=R.|last7=Jaafar|first7=F.M.|last8=Takayama|first8=H.|journal=Fitoterapia|volume=82|issue=4|pages=676–81}}</ref> It is also present in relation to resistance to ''[[Botrytis cinerea]]'' and ''[[Plasmopara viticola]]'' in ''[[Vitis vinifera]]'' and ''[[Vitis riparia]]''.<ref>Disease resistance of Vitis spp. and the production of the stress metabolites resveratrol, epsilon -viniferin, alpha -viniferin and pterostilbene. Langcake P, Physiological Plant Pathology, 1981, Vol. 18, No. 2, pages 213-226 ([http://www.cabdirect.org/abstracts/19811698041.html;jsessionid=53F909297760080793211FD6C4B32445 abstract] {{Webarchive|url=https://web.archive.org/web/20141210021426/http://www.cabdirect.org/abstracts/19811698041.html;jsessionid=53F909297760080793211FD6C4B32445 |date=2014-12-10 }})</ref> It has been shown to inhibit [[acetylcholinesterase]].<ref name="Sang"/>

== References ==
{{reflist}}

{{Acetylcholine metabolism and transport modulators}}
{{Oligostilbenoid}}

{{DEFAULTSORT:Viniferin, alpha-}}
[[Category:Resveratrol oligomers]]
[[Category:Acetylcholinesterase inhibitors]]


{{Aromatic-stub}}