NCBI Taxonomy: 87284

Umbilicaria spodochroa (ncbi_taxid: 87284)

found 16 associated metabolites at species taxonomy rank level.

Ancestor: Umbilicaria

Child Taxonomies: none taxonomy data.

Lecanoricacid

4-(2,4-dihydroxy-6-methylbenzoyl)oxy-2-hydroxy-6-methylbenzoic acid

C16H14O7 (318.0739494)


D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates Lecanoric acid is a histidine-decarboxylase inhibitor isolated from fungus. The inhibition by lecanoric acid is competitive with histidineand noncompetitive with pyridoxal phosphate. Lecanoric acid did not inhibit aromatic amino acid decarboxylase[1].

   

Gyrophoric acid

4-[4-(2,4-dihydroxy-6-methylbenzoyl)oxy-2-hydroxy-6-methylbenzoyl]oxy-2-hydroxy-6-methylbenzoic acid

C24H20O10 (468.105642)


Origin: Microbe, Carboxylic acids

   
   
   

Atranorin

methyl 1-(3-formyl-2,4-dihydroxy-6-methylphenylcarbonyloxy)-3-hydroxy-2,5-dimethyl-4-benzenecarboxylate

C19H18O8 (374.1001628)


Atranorin is a carbonyl compound. Atranorin is a natural product found in Candelaria concolor, Loxospora elatina, and other organisms with data available. Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity[1][2]. Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity[1][2]. Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity[1][2].

   
   

2-hydroxy-4-[2-hydroxy-4-(4-hydroxy-2-methoxy-6-methylbenzoyloxy)-6-methylbenzoyloxy]-6-methylbenzoic acid

2-hydroxy-4-[2-hydroxy-4-(4-hydroxy-2-methoxy-6-methylbenzoyloxy)-6-methylbenzoyloxy]-6-methylbenzoic acid

C25H22O10 (482.1212912)


   

2-hydroxy-4-[2-hydroxy-6-methyl-4-(3,4,6-trihydroxy-2-methylbenzoyloxy)benzoyloxy]-6-methylbenzoic acid

2-hydroxy-4-[2-hydroxy-6-methyl-4-(3,4,6-trihydroxy-2-methylbenzoyloxy)benzoyloxy]-6-methylbenzoic acid

C24H20O11 (484.100557)


   

3-[4-(2,4-dihydroxy-6-methylbenzoyloxy)-2-hydroxy-6-methylbenzoyloxy]-4,6-dihydroxy-2-methylbenzoic acid

3-[4-(2,4-dihydroxy-6-methylbenzoyloxy)-2-hydroxy-6-methylbenzoyloxy]-4,6-dihydroxy-2-methylbenzoic acid

C24H20O11 (484.100557)