beauvericin
chemical compound
Press Enter · cited answer in seconds
0 sources
beauvericin
Summary
beauvericin is a type of chemical entity[1]. beauvericin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (40 views/month).[2]
Key Facts
- beauvericin's instance of is recorded as type of chemical entity[3].
- beauvericin's canonical SMILES is recorded as O=C1OC(C(=O)N(C)C(C(=O)OC(C(=O)N(C)C(C(=O)OC(C(=O)N(C)C1CC=2C=CC=CC2)C(C)C)CC=3C=CC=CC3)C(C)C)CC=4C=CC=CC4)C(C)C[4].
- beauvericin's chemical formula is recorded as C₄₅H₅₇N₃O₉[5].
- beauvericin is a type of Beauvericin[6].
- beauvericin's found in taxon is recorded as Fusarium oxysporum[7].
- beauvericin's found in taxon is recorded as Beauveria bassiana[8].
- beauvericin's found in taxon is recorded as Fusarium proliferatum[9].
- beauvericin's found in taxon is recorded as Fusarium sporotrichioides[10].
- beauvericin's found in taxon is recorded as Fusarium equiseti[11].
- beauvericin's found in taxon is recorded as Fusarium poae[12].
- beauvericin's found in taxon is recorded as Fusarium avenaceum[13].
- beauvericin's found in taxon is recorded as Cordyceps tenuipes[14].
- beauvericin's found in taxon is recorded as Isaria tenuipes[15].
- beauvericin's found in taxon is recorded as Fusarium fujikuroi[16].
- beauvericin's found in taxon is recorded as Fusarium subglutinans[17].
- beauvericin's found in taxon is recorded as Paecilomyces tenuipes[18].
- beauvericin's found in taxon is recorded as Fusarium incarnatum[19].
- beauvericin's found in taxon is recorded as Cordyceps fumosorosea[20].
- beauvericin's found in taxon is recorded as Isaria cicadae[21].
- beauvericin's found in taxon is recorded as Cordyceps cicadae (Miq.) Massee[22].
- beauvericin's found in taxon is recorded as Guignardia[23].
- beauvericin's isomeric SMILES is recorded as O=C1N(C)C@HCc4ccccc4C@HCc4ccccc4">[24].
- beauvericin's mass is recorded as {'unit': 'Q483261', 'amount': '+783.409480404'}[25].
- beauvericin's stereoisomer of is recorded as cyclo[D-OVal-N(Me)Phe-D-OVal-N(Me)Phe-OVal-D-N(Me)Phe][26].
- beauvericin's stereoisomer of is recorded as cyclo[D-OVal-N(Me)Phe-D-OVal-N(Me)Phe-OVal-N(Me)Phe][27].
Why It Matters
beauvericin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (40 views/month).[2] beauvericin has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28]