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词条 Amanin
释义

  1. Toxicology

  2. See also

  3. References

{{About|the toxin|the fictional beings with the same name|Amanin (Star Wars)}}{{Chembox
| Verifiedfields = changed
| verifiedrevid = 443949523
| ImageFile = Amanin.png
| ImageSize = 200px
| IUPACName =
| OtherNames =
|Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 28316
| InChI = 1/C39H53N9O14S/c1-5-16(2)31-36(59)41-12-28(52)42-26-15-63(62)38-22(21-7-6-19(50)8-23(21)45-38)10-24(33(56)40-13-29(53)46-31)43-37(60)32(17(3)18(4)49)47-35(58)27-9-20(51)14-48(27)39(61)25(11-30(54)55)44-34(26)57/h6-8,16-18,20,24-27,31-32,45,49-51H,5,9-15H2,1-4H3,(H,40,56)(H,41,59)(H,42,52)(H,43,60)(H,44,57)(H,46,53)(H,47,58)(H,54,55)
| InChIKey = OFILNAORONITPV-UHFFFAOYAZ
| SMILES = CC[C@H](C)[C@H]1C(=O)NCC(=O)N[C@H]2CS(=O)C3=C(C[C@@H](C(=O)NCC(=O)N1)NC(=O)[C@@H](NC(=O)[C@@H]4C[C@H](CN4C(=O)[C@@H](NC2=O)CC(=O)O)O)[C@@H](C)[C@H](CO)O)C5=CC=CC=C5N3
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C39H53N9O14S/c1-5-16(2)31-36(59)41-12-28(52)42-26-15-63(62)38-22(21-7-6-19(50)8-23(21)45-38)10-24(33(56)40-13-29(53)46-31)43-37(60)32(17(3)18(4)49)47-35(58)27-9-20(51)14-48(27)39(61)25(11-30(54)55)44-34(26)57/h6-8,16-18,20,24-27,31-32,45,49-51H,5,9-15H2,1-4H3,(H,40,56)(H,41,59)(H,42,52)(H,43,60)(H,44,57)(H,46,53)(H,47,58)(H,54,55)
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = OFILNAORONITPV-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 21150-21-0
| PubChem = 30508
}}
|Section2={{Chembox Properties
| Appearance = | C=39 | H=53 | N=9 | O=14 | S=1
| Density =
| MeltingPt =
| BoilingPt =
| Solubility = }}
|Section3={{Chembox Hazards
| MainHazards =
| FlashPt =
| AutoignitionPt = }}
}}

Amanin is a cyclic peptide. It is one of the amatoxins, all of which are found in several members of the mushroom genus Amanita.

Toxicology

Like other amatoxins, amanin is an inhibitor of RNA polymerase II. Upon ingestion, it binds to the RNA polymerase II enzyme which completely prevents mRNA synthesis, effectively causing cytolysis of hepatocytes (liver cells) and kidney cells.[1]

See also

  • Mushroom poisoning

References

1. ^{{cite journal |author1 = M. Cochet-Meillhac |author2 =Chambon P. | journal = Biochim Biophys Acta | volume = 353 | pages = 160–184 | year = 1974 | url = http://toxnet.nlm.nih.gov/cgi-bin/sis/search/f?./temp/~ZI8h7t:1 | doi = 10.1016/0005-2787(74)90182-8|pmid = 4601749 | title = Animal DNA-dependent RNA polymerases. 11. Mechanism of the inhibition of RNA polymerases B by amatoxins | issue = 2}}
{{Poisonous Amanitas}}{{Toxins}}

4 : Peptides|Amatoxins|Hepatotoxins|Indoles

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