Revision as of 22:32, 9 August 2011 editZéroBot (talk | contribs)704,777 editsm r2.7.1) (robot Adding: fi:Proamanulliini← Previous edit |
Latest revision as of 07:35, 16 March 2023 edit undoInternetArchiveBot (talk | contribs)Bots, Pending changes reviewers5,382,344 edits Rescuing 1 sources and tagging 0 as dead.) #IABot (v2.0.9.3) (Whoop whoop pull up - 12776 |
(14 intermediate revisions by 12 users not shown) |
Line 1: |
Line 1: |
|
{{chembox |
|
{{chembox |
|
|
| Verifiedfields = changed |
⚫ |
| verifiedrevid = 385631746 |
|
|
|
| Watchedfields = changed |
|
|ImageFile=Proamanullin structure.png |
|
|
⚫ |
| verifiedrevid = 443950451 |
|
|ImageSize=200px |
|
|
|ImageFile1=Proamanullin 3d chemical structure.png |
|
| ImageFile=Proamanullin structure.png |
|
|ImageSize1=200px |
|
| ImageSize=200px |
|
|
| ImageFile1= |
⚫ |
|IUPACName= |
|
|
|
| ImageSize1= |
⚫ |
|OtherNames=2-L-Proline-3-isoleucine-alpha-amanitin |
|
|
⚫ |
| IUPACName= |
⚫ |
|Section1= {{Chembox Identifiers |
|
|
⚫ |
| OtherNames=2-L-Proline-3-isoleucine-alpha-amanitin |
⚫ |
| CASNo=54532-46-6 |
|
|
⚫ |
|Section1={{Chembox Identifiers |
⚫ |
| PubChem=171350 |
|
|
|
| CASNo_Ref = {{cascite|correct|??}} |
⚫ |
| SMILES=O=C(NCC(N(C(NCC(N(C3)C(N(CC(N)=O)C(N54CCC5)=O)=O)=O)=O)()(C)CC)=O)(CC1=C(S3=O)NC2=C1C=CC(O)=C2)NC(((C)CC)()N4=O)=O |
|
|
⚫ |
| CASNo=54532-46-6 |
|
⚫ |
| PubChem=171350 |
|
|
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} |
|
|
| ChemSpiderID = 48308194 |
|
⚫ |
| SMILES=O=C(NCC(N(C(NCC(N(C3)C(N(CC(N)=O)C(N54CCC5)=O)=O)=O)=O)()(C)CC)=O)(CC1=C(S3=O)NC2=C1C=CC(O)=C2)NC(((C)CC)()N4=O)=O |
|
|
| InChI = 1/C39H54N10O11S/c1-5-18(3)31-36(57)42-15-29(52)43-26-17-61(60)38-22(21-10-9-20(50)12-23(21)46-38)13-24(33(54)41-16-30(53)47-31)44-37(58)32(19(4)6-2)48-35(56)27-8-7-11-49(27)39(59)25(14-28(40)51)45-34(26)55/h9-10,12,18-19,24-27,31-32,46,50H,5-8,11,13-17H2,1-4H3,(H2,40,51)(H,41,54)(H,42,57)(H,43,52)(H,44,58)(H,45,55)(H,47,53)(H,48,56)/t18-,19-,24-,25-,26-,27-,31-,32-,61?/m0/s1 |
|
|
| InChIKey = CTYHFRWAIRSHQT-YRDOMICZBU |
|
|
| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
|
|
| StdInChI = 1S/C39H54N10O11S/c1-5-18(3)31-36(57)42-15-29(52)43-26-17-61(60)38-22(21-10-9-20(50)12-23(21)46-38)13-24(33(54)41-16-30(53)47-31)44-37(58)32(19(4)6-2)48-35(56)27-8-7-11-49(27)39(59)25(14-28(40)51)45-34(26)55/h9-10,12,18-19,24-27,31-32,46,50H,5-8,11,13-17H2,1-4H3,(H2,40,51)(H,41,54)(H,42,57)(H,43,52)(H,44,58)(H,45,55)(H,47,53)(H,48,56)/t18-,19-,24-,25-,26-,27-,31-,32-,61?/m0/s1 |
|
|
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
|
|
| StdInChIKey = CTYHFRWAIRSHQT-YRDOMICZSA-N |
|
}} |
|
}} |
|
|Section2= {{Chembox Properties |
|
|Section2={{Chembox Properties |
|
| Formula=C<sub>39</sub>H<sub>54</sub>N<sub>10</sub>O<sub>11</sub>S |
|
| Formula=C<sub>39</sub>H<sub>54</sub>N<sub>10</sub>O<sub>11</sub>S |
|
| MolarMass=870.97 g/mol |
|
| MolarMass=870.97 g/mol |
|
| Appearance=Colorless, odorless |
|
| Appearance=Colorless, odorless |
|
| Density= |
|
| Density= |
|
| MeltingPt= |
|
| MeltingPt= |
|
| BoilingPt= |
|
| BoilingPt= |
|
| Solubility= |
|
| Solubility= |
|
}} |
|
}} |
|
|Section3= {{Chembox Hazards |
|
|Section3={{Chembox Hazards |
|
| MainHazards= |
|
| MainHazards= |
|
| FlashPt= |
|
| FlashPt= |
|
|
| AutoignitionPt = |
|
| Autoignition= |
|
|
}} |
|
}} |
|
}} |
|
}} |
|
|
|
|
|
'''Promanullin''' is a ] ]. It is an ], all of which are found in several members of the '']'' genus of ]s. |
|
'''Promanullin''' is a ] ]. It is an ], all of which are found in the ] genus '']''. |
|
|
|
|
|
==Toxicology== |
|
==Toxicology== |
|
|
|
|
|
Like other ], proamanullin is an inhibitor of ]. Promanullin has a specific attraction to the enzyme RNA polymerase II. Upon ingestion, it binds to the RNA polymerase II enzyme, effectively causing ] of ]s (liver cells).<ref>{{cite journal |author=Cochet-Meilhac M, Chambon P |title=Animal DNA-dependent RNA polymerases. 11. Mechanism of the inhibition of RNA polymerases B by amatoxins |journal=Biochim. Biophys. Acta |volume=353 |issue=2 |pages=160–84 |year=1974 |month=June |pmid=4601749 |doi= |url=}}</ref> |
|
Like other ], proamanullin is an inhibitor of ]. Promanullin has a specific attraction to the enzyme RNA polymerase II. Upon ingestion, it binds to the RNA polymerase II enzyme, effectively causing ] of ]s (liver cells).<ref>{{cite journal |vauthors=Cochet-Meilhac M, Chambon P |title=Animal DNA-dependent RNA polymerases. 11. Mechanism of the inhibition of RNA polymerases B by amatoxins |journal=Biochim. Biophys. Acta |volume=353 |issue=2 |pages=160–84 |date=June 1974 |pmid=4601749 |doi= 10.1016/0005-2787(74)90182-8}}</ref> |
|
|
|
|
⚫ |
==See also== |
|
⚫ |
*] |
|
|
|
|
|
==References== |
|
==References== |
|
{{reflist}} |
|
{{reflist}} |
|
|
|
⚫ |
==See also== |
|
⚫ |
*] |
|
|
|
|
|
|
==External links== |
|
==External links== |
|
* |
|
* {{Webarchive|url=https://web.archive.org/web/20090113180522/http://dohs.ors.od.nih.gov/pdf/Amatoxins%20REVISED.pdf |date=2009-01-13 }} |
|
|
|
|
|
{{Poisonous Amanitas}} |
|
{{Poisonous Amanitas}} |
Line 48: |
Line 59: |
|
] |
|
] |
|
] |
|
] |
|
] |
|
] |
|
] |
|
] |
|
|
|
|
] |
|