ε-amanitin
Cyclic peptide part of a group of toxins present in Amanita mushrooms
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ε-amanitin
Summary
ε-amanitin is a type of chemical entity[1]. ε-amanitin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (1 views/month).[2]
Key Facts
- ε-amanitin's instance of is recorded as type of chemical entity[3].
- ε-amanitin's chemical structure is recorded as Epsilon-amanitin structure.png[4].
- ε-amanitin's CAS Registry Number is recorded as 21705-02-2[5].
- ε-amanitin's canonical SMILES is recorded as CCC(C)C1NC(=O)CNC(=O)C2Cc3c([nH]c4cc(O)ccc34)S+CC(NC(=O)CNC1=O)C(=O)NC(CC(=O)O)C(=O)N1CC(O)CC1C(=O)NC(C(C)C(C)O)C(=O)N2S+CC(NC(=O)CNC1=O)C(=O)NC(CC(=O)O)C(=O)N1CC(O)CC1C(=O)NC(C(C)C(C)O)C(=O)N2">[6].
- ε-amanitin's InChI is recorded as InChI=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)/t16-,17-,18-,20+,24-,25-,26-,27-,31-,32-,63?/m0/s1[7].
- ε-amanitin's InChIKey is recorded as OFILNAORONITPV-UHFFFAOYSA-N[8].
- ε-amanitin's chemical formula is recorded as C₃₉H₅₃N₉O₁₄S[9].
- ε-amanitin's subclass of is recorded as amanitins[10].
- ε-amanitin's subclass of is recorded as biogenic cyclopeptide[11].
- ε-amanitin's Freebase ID is recorded as /m/05241ry[12].
- ε-amanitin's ChemSpider ID is recorded as 26234941[13].
- ε-amanitin's PubChem CID is recorded as 30508[14].
- ε-amanitin's found in taxon is recorded as Acanthochlamys bracteata[15].
- ε-amanitin's isomeric SMILES is recorded as O=C(NCC(NC@@([H])C@@HCC)=O)C@HNC(C@@([H])N[C@@]4=O)=OC@@([H])C@@HCC)=O)C@HNC([C@@](C@@H[C@@H">[16].
- ε-amanitin's mass is recorded as {'unit': 'Q483261', 'amount': '+903.343268376'}[17].
- ε-amanitin's SureChEMBL ID is recorded as 29365556[18].
- ε-amanitin's DSSTox substance ID is recorded as DTXSID201028142[19].
- ε-amanitin's stereoisomer of is recorded as Amanin[20].
Why It Matters
ε-amanitin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (1 views/month).[2] ε-amanitin has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[21] ε-amanitin is known by 5 alternative names across languages and contexts.[22]