Substance | Relationship Strength | Studies | Trials | Classes | Roles |
orsellinic acid orsellinic acid: from the Sonoran desert endophytic fungus Chaetomium globosum; structure in first source. o-orsellinic acid : A dihydroxybenzoic acid that is 2,4-dihydroxybenzoic acid in which the hydrogen at position 6 is replaced by a methyl group. | 2.6 | 1 | 0 | dihydroxybenzoic acid; resorcinols | fungal metabolite; marine metabolite; metabolite |
o-methylsterigmatocystin [no description available] | 1.99 | 1 | 0 | sterigmatocystins | |
aflatoxin b1 Aflatoxin B1: A potent hepatotoxic and hepatocarcinogenic mycotoxin produced by the Aspergillus flavus group of fungi. It is also mutagenic, teratogenic, and causes immunosuppression in animals. It is found as a contaminant in peanuts, cottonseed meal, corn, and other grains. The mycotoxin requires epoxidation to aflatoxin B1 2,3-oxide for activation. Microsomal monooxygenases biotransform the toxin to the less toxic metabolites aflatoxin M1 and Q1.. aflatoxin B1 : An aflatoxin having a tetrahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h]chromene skeleton with oxygen functionality at positions 1, 4 and 11. | 6.97 | 1 | 0 | aflatoxin; aromatic ether; aromatic ketone | carcinogenic agent; human metabolite |
averufin averufin: isolated from Aspergillus sp.; has antifungal activity | 7.38 | 2 | 0 | cyclic ketal; organic heteropentacyclic compound; polyketide; polyphenol | fungal metabolite |
sterigmatocystin [no description available] | 1.99 | 1 | 0 | sterigmatocystins | metabolite |
averantin averantin: aflatoxin B(1) precursor; structure in first source. averantin : A tetrahydroxyanthraquinone that is 1,3,6,8-tetrahydroxy-9,10-anthraquinone bearing a 1-hydroxyhexyl substituent at position 2.. (S)-averantin : An optically active form of averantin having S-configuration. | 7.41 | 2 | 0 | averantin | |
ribose ribopyranose : The pyranose form of ribose. | 2.6 | 1 | 0 | D-ribose; ribopyranose | |