NCBI Taxonomy: 128434

Talaromyces diversus (ncbi_taxid: 128434)

found 23 associated metabolites at species taxonomy rank level.

Ancestor: Talaromyces sect. Trachyspermi

Child Taxonomies: none taxonomy data.

Juglone

InChI=1/C10H6O3/c11-7-4-5-9(13)10-6(7)2-1-3-8(10)12/h1-5,12

C10H6O3 (174.0317)


Juglone is a hydroxy-1,4-naphthoquinone that is 1,4-naphthoquinone in which the hydrogen at position 5 has been replaced by a hydroxy group. A plant-derived 1,4-naphthoquinone with confirmed antibacterial and antitumor activities. It has a role as a herbicide, a reactive oxygen species generator and a geroprotector. Juglone is a natural product found in Talaromyces diversus, Carya alba, and other organisms with data available. Occurs in Juglans subspecies and pecan nuts (Carya illinoensis). Juglone is found in many foods, some of which are common walnut, liquor, black walnut, and nuts. Juglone is found in black walnut. Juglone occurs in Juglans species and pecan nuts (Carya illinoensis D000074385 - Food Ingredients > D005503 - Food Additives > D005520 - Food Preservatives D009676 - Noxae > D003603 - Cytotoxins D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors

   

Patulin

(2,4-Dihydroxy-2H-pyran-3(6H)-ylidene)acetic acid, 3,4-lactone

C7H6O4 (154.0266)


Patulin is found in pomes. Mycotoxin, found as a contaminant of foods, e.g. apple juice. Sometimes detd. in apple juice Patulin is a mycotoxin produced by a variety of molds, particularly Aspergillus and Penicillium. It is commonly found in rotting apples, and the amount of patulin in apple products is generally viewed as a measure of the quality of the apples used in production. It is not a particularly potent toxin, but a number of studies have shown that it is genotoxic, which has led to some theories that it may be a carcinogen, though animal studies have remained inconclusive. Patulin is also an antibiotic. Several countries have instituted patulin restrictions in apple products. The World Health Organization recommends a maximum concentration of 50 µg/L in apple juice Mycotoxin, found as a contaminant of foods, e.g. apple juice. Sometimes detd. in apple juice D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D009153 - Mutagens Patulin (Terinin) is a mycotoxin produced by fungi including the Aspergillus, Penicillium, and Byssochlamys species, is suspected to be clastogenic, mutagenic, teratogenic and cytotoxic. Patulin induces autophagy-dependent apoptosis through lysosomal-mitochondrial axis, and causes DNA damage[1][2][3][4].

   

2,4,8-Trihydroxy-1-tetralone

2,4,8-Trihydroxy-1-tetralone

C10H10O4 (194.0579)


   

patulin

patulin

C7H6O4 (154.0266)


D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins CONFIDENCE standard compound; INTERNAL_ID 5971 D009676 - Noxae > D009153 - Mutagens CONFIDENCE Reference Standard (Level 1) Patulin (Terinin) is a mycotoxin produced by fungi including the Aspergillus, Penicillium, and Byssochlamys species, is suspected to be clastogenic, mutagenic, teratogenic and cytotoxic. Patulin induces autophagy-dependent apoptosis through lysosomal-mitochondrial axis, and causes DNA damage[1][2][3][4].

   

Herqueinone

Herqueinone

C20H20O7 (372.1209)


   

Nucin

InChI=1\C10H6O3\c11-7-4-5-9(13)10-6(7)2-1-3-8(10)12\h1-5,12

C10H6O3 (174.0317)


D000074385 - Food Ingredients > D005503 - Food Additives > D005520 - Food Preservatives D009676 - Noxae > D003603 - Cytotoxins D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors

   

(+)-Diversonol

(+)-Diversonol

C15H18O6 (294.1103)


A natural product found in Microdiplodia species.

   

Mycoin

4-Hydroxy-4H-furo[3,2-c]pyran-2(6H)-one

C7H6O4 (154.0266)


A furopyran and lactone that is (2H-pyran-3(6H)-ylidene)acetic acid which is substituted by hydroxy groups at positions 2 and 4 and in which the hydroxy group at position 4 has condensed with the carboxy group to give the corresponding bicyclic lactone. A mycotoxin produced by several species of Aspergillus and Penicillium, it has antibiotic properties but has been shown to be carcinogenic and mutagenic. D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D009153 - Mutagens Patulin (Terinin) is a mycotoxin produced by fungi including the Aspergillus, Penicillium, and Byssochlamys species, is suspected to be clastogenic, mutagenic, teratogenic and cytotoxic. Patulin induces autophagy-dependent apoptosis through lysosomal-mitochondrial axis, and causes DNA damage[1][2][3][4].

   

methyl 1,2,8-trihydroxy-6-methyl-9-oxo-3,4-dihydro-2h-xanthene-1-carboxylate

methyl 1,2,8-trihydroxy-6-methyl-9-oxo-3,4-dihydro-2h-xanthene-1-carboxylate

C16H16O7 (320.0896)


   

2,4,5-trihydroxy-3,4-dihydro-2h-naphthalen-1-one

2,4,5-trihydroxy-3,4-dihydro-2h-naphthalen-1-one

C10H10O4 (194.0579)


   

3,4,5-trihydroxy-3,4-dihydro-2h-naphthalen-1-one

3,4,5-trihydroxy-3,4-dihydro-2h-naphthalen-1-one

C10H10O4 (194.0579)


   

(7ar,9r)-4,6,7a-trihydroxy-5-methoxy-1,8,8,9-tetramethyl-9h-phenaleno[1,2-b]furan-3,7-dione

(7ar,9r)-4,6,7a-trihydroxy-5-methoxy-1,8,8,9-tetramethyl-9h-phenaleno[1,2-b]furan-3,7-dione

C20H20O7 (372.1209)


   

(3r,4r)-3,4,5-trihydroxy-3,4-dihydro-2h-naphthalen-1-one

(3r,4r)-3,4,5-trihydroxy-3,4-dihydro-2h-naphthalen-1-one

C10H10O4 (194.0579)


   

(1's,2'r,3s,4's,9's,12's,13's)-12'-hydroxy-2,2,2',6',9',13'-hexamethyl-16'-methylidene-6,11',15'-trioxo-10',14'-dioxaspiro[pyran-3,5'-tetracyclo[7.6.1.0¹,¹².0²,⁷]hexadecan]-6'-en-4'-yl acetate

(1's,2'r,3s,4's,9's,12's,13's)-12'-hydroxy-2,2,2',6',9',13'-hexamethyl-16'-methylidene-6,11',15'-trioxo-10',14'-dioxaspiro[pyran-3,5'-tetracyclo[7.6.1.0¹,¹².0²,⁷]hexadecan]-6'-en-4'-yl acetate

C27H32O9 (500.2046)


   
   

4,5-dihydroxy-3,4-dihydro-2h-naphthalen-1-one

4,5-dihydroxy-3,4-dihydro-2h-naphthalen-1-one

C10H10O3 (178.063)


   

12'-hydroxy-2,2,2',6',9',13'-hexamethyl-16'-methylidene-6,11',15'-trioxo-10',14'-dioxaspiro[pyran-3,5'-tetracyclo[7.6.1.0¹,¹².0²,⁷]hexadecan]-6'-en-4'-yl acetate

12'-hydroxy-2,2,2',6',9',13'-hexamethyl-16'-methylidene-6,11',15'-trioxo-10',14'-dioxaspiro[pyran-3,5'-tetracyclo[7.6.1.0¹,¹².0²,⁷]hexadecan]-6'-en-4'-yl acetate

C27H32O9 (500.2046)


   

(4s)-4,8-dihydroxy-3,4-dihydro-2h-naphthalen-1-one

(4s)-4,8-dihydroxy-3,4-dihydro-2h-naphthalen-1-one

C10H10O3 (178.063)


   

methyl (1r,2r)-1,2,8-trihydroxy-6-methyl-9-oxo-3,4-dihydro-2h-xanthene-1-carboxylate

methyl (1r,2r)-1,2,8-trihydroxy-6-methyl-9-oxo-3,4-dihydro-2h-xanthene-1-carboxylate

C16H16O7 (320.0896)


   

(4s)-4,5-dihydroxy-3,4-dihydro-2h-naphthalen-1-one

(4s)-4,5-dihydroxy-3,4-dihydro-2h-naphthalen-1-one

C10H10O3 (178.063)


   

(2r,4s)-2,4,5-trihydroxy-3,4-dihydro-2h-naphthalen-1-one

(2r,4s)-2,4,5-trihydroxy-3,4-dihydro-2h-naphthalen-1-one

C10H10O4 (194.0579)


   

4,6,7a-trihydroxy-5-methoxy-1,8,8,9-tetramethyl-9h-phenaleno[1,2-b]furan-3,7-dione

4,6,7a-trihydroxy-5-methoxy-1,8,8,9-tetramethyl-9h-phenaleno[1,2-b]furan-3,7-dione

C20H20O7 (372.1209)


   

(2r,4s)-2,4,8-trihydroxy-3,4-dihydro-2h-naphthalen-1-one

(2r,4s)-2,4,8-trihydroxy-3,4-dihydro-2h-naphthalen-1-one

C10H10O4 (194.0579)