about
Characterization of a polyketide synthase in Aspergillus niger whose product is a precursor for both dihydroxynaphthalene (DHN) melanin and naphtho-γ-pyroneFungal naphtho-γ-pyrones: Potent antibiotics for drug-resistant microbial pathogens.Endophytic naphthopyrone metabolites are co-inhibitors of xanthine oxidase, SW1116 cell and some microbial growths.Antifungal and antibacterial metabolites from an endophytic Aspergillus sp. associated with Melia azedarach.Structural revision of aspernigrin A, reisolated from Cladosporium herbarum IFB-E002.New dimeric naphthopyrones from Aspergillus niger.Complete 1H and 13C NMR assignments of aurasperone A and fonsecinone A, two bis-naphthopyrones produced by Aspergillus aculeatus
P921
Q35055799-039962B3-D3FB-4562-815E-9FBB4A98B4B9Q36785081-51B195BE-B233-4BDF-B5BE-909D76C2582FQ40489532-4754F960-6F63-4BF6-B4AA-89E94A5F5EA3Q43739089-4FD91844-2CB5-448B-B509-1BA452DC390DQ46614169-B238FB14-72C8-40CC-B819-5E227FEEF6D3Q46945743-9560DB3A-359C-4872-A859-CAE92A6C3826Q81198787-C271D311-D265-417A-8095-5875B7F06A21
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
fonsecinone a
@en
type
label
fonsecinone a
@en
prefLabel
fonsecinone a
@en
P592
P662
P683
P231
95152-75-3
P233
CC1=CC(=O)C2=C(C=C3C=C(C(=C(C3 ...... C64)OC)OC)O)C(=O)C=C(O5)C)OC)O
P234
1S/C32H26O10/c1-13-7-18(33)26- ...... 42-32(25)27/h7-12,35-36H,1-6H3
P235
FFNPXDMNZBCNMN-UHFFFAOYSA-N
P274
P592
CHEMBL451678
P652
4422E9639H