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Revision as of 14:36, 28 July 2011 edit139.127.253.7 (talk)No edit summary← Previous edit Latest revision as of 08:22, 23 December 2022 edit undoCyrej (talk | contribs)Extended confirmed users1,718 editsm top: commaTags: Mobile edit Mobile app edit Android app edit 
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{{chembox {{chembox
| Verifiedfields = changed | Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 399529379 | verifiedrevid = 441877939
|ImageFile=Aphidicolin structure.png | ImageFile=Aphidicolin structure.png
|ImageSize=200px | ImageSize=200px
|IUPACName= (3''R'',4''R'',4a''R'',6a''S'',8''R'',9''R'',11a''S'',11b''S'')-4,9-bis(hydroxymethyl)-4,11b-dimethyltetradecahydro-8,11a-methanocycloheptanaphthalene-3,9-diol | IUPACName= (3''R'',4''R'',4a''R'',6a''S'',8''R'',9''R'',11a''S'',11b''S'')-4,9-bis(hydroxymethyl)-4,11b-dimethyltetradecahydro-8,11a-methanocycloheptanaphthalene-3,9-diol
|OtherNames= | OtherNames=
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 10280269 | ChemSpiderID = 10280269
| ChEMBL_Ref = {{ebicite|changed|EBI}} | ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 2766
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 29711 | ChEMBL = 29711
| InChI = 1/C20H34O4/c1-17(11-21)15-4-3-13-9-14-10-19(13,7-8-20(14,24)12-22)18(15,2)6-5-16(17)23/h13-16,21-24H,3-12H2,1-2H3/t13-,14+,15-,16+,17-,18-,19-,20-/m0/s1 | InChI = 1/C20H34O4/c1-17(11-21)15-4-3-13-9-14-10-19(13,7-8-20(14,24)12-22)18(15,2)6-5-16(17)23/h13-16,21-24H,3-12H2,1-2H3/t13-,14+,15-,16+,17-,18-,19-,20-/m0/s1
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = NOFOAYPPHIUXJR-APNQCZIXSA-N | StdInChIKey = NOFOAYPPHIUXJR-APNQCZIXSA-N
| CASNo_Ref = {{cascite|correct|??}}
| CASNo=38966-21-1 | CASNo=38966-21-1
| UNII_Ref = {{fdacite|correct|FDA}}
| PubChem=457964
| UNII = 192TJ6PP19
| SMILES = OC4(O)CC31C4C3CC2(C)(CO)(O)CC12C
| PubChem=457964
| SMILES = OC4(O)CC31C4C3CC2(C)(CO)(O)CC12C
}} }}
|Section2={{Chembox Properties |Section2={{Chembox Properties
|C=20|H=34|O=4 | C=20 | H=34 | O=4
| MolarMass=338.48 g/mol | MolarMass=338.48 g/mol
| Appearance= | Appearance=
| Density= | Density=
| MeltingPt= | MeltingPt=
| BoilingPt= | BoilingPt=
| Solubility= | Solubility=
}} }}
|Section3={{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards= | MainHazards=
| FlashPt= | FlashPt=
| AutoignitionPt =
| Autoignition=
}} }}
}} }}


'''Aphidicolin''' is defined as a tetracyclic ] ] with antiviral and antimitotical properties. Aphidicolin is a reversible ] of ] nuclear ] replication. It blocks the cell cycle at early ]. It is a specific inhibitor of ] B,D in eukaryotic cells and in some viruses and an ] inducer in ] cells. '''Aphidicolin''' is a tetracyclic ] ] isolated from the fungus '']'' with antiviral and antimitotic properties. Aphidicolin is a reversible ] of ] nuclear ] replication. It blocks the cell cycle at early ]. It is a specific inhibitor of ] and ] in eukaryotic cells and in some viruses (]<ref>{{cite journal|last1=DeFilippes|first1=FM|title=Effect of aphidicolin on vaccinia virus: isolation of an aphidicolin-resistant mutant.|journal=Journal of Virology|date=Nov 1984|volume=52|issue=2|pages=474–82|doi=10.1128/JVI.52.2.474-482.1984|pmid=6436508|pmc=254548}}</ref><ref>{{cite journal|last1=Bucknall|first1=R. A.|last2=Moores|first2=H.|last3=Simms|first3=R.|last4=Hesp|first4=B.|title=Antiviral Effects of Aphidicolin, a New Antibiotic Produced by Cephalosporium aphidicola|journal=Antimicrobial Agents and Chemotherapy|date=1 September 1973|volume=4|issue=3|pages=294–298|doi=10.1128/AAC.4.3.294|pmc=444544|pmid=4357181}}</ref> and ]) and an ] inducer in ] cells. Natural aphidicolin is a secondary metabolite of the fungus '']''.<ref> {{webarchive |url=https://web.archive.org/web/20060626051436/http://www.fermentek.co.il/aphidicolin.htm |date=June 26, 2006 }} from ]</ref>
<br>Natural aphidicolin is a secondary metabolite of the fungus '']''<ref> from ]</ref>.


==References== == Bibliography ==
* {{cite journal |author=Dhillon VS, Husain SA, Ray GN |title=Expression of aphidicolin-induced fragile sites and their relationship between genetic susceptibility in breast cancer, ovarian cancer, and non-small-cell lung cancer patients |journal=Teratog., Carcinog. Mutagen. |volume=Suppl 1 |issue= |pages=35–45 |year=2003 |pmid=12616595 |doi=10.1002/tcm.10068 |url=}} * {{cite journal |vauthors=Dhillon VS, Husain SA, Ray GN |title=Expression of aphidicolin-induced fragile sites and their relationship between genetic susceptibility in breast cancer, ovarian cancer, and non-small-cell lung cancer patients |journal=Teratogenesis, Carcinogenesis, and Mutagenesis |volume=Suppl 1 |pages=35–45 |year=2003 |pmid=12616595 |doi=10.1002/tcm.10068 }}
* {{cite book|last1=Mahy|first1=Brian W J|title=A dictionary of virology|url=https://archive.org/details/dictionaryofviro0000mahy|url-access=registration|date=2001|publisher=Academic Press|location=San Diego, Calif. |isbn=978-0-12-465327-6|page=|edition=3.}}


== References ==
<references/>
{{reflist|2}}


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