NCBI Taxonomy: 28572

Talaromyces funiculosus (ncbi_taxid: 28572)

found 25 associated metabolites at species taxonomy rank level.

Ancestor: Talaromyces sect. Talaromyces

Child Taxonomies: none taxonomy data.

Patulin

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

C7H6O4 (154.0266076)


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].

   
   
   

patulin

patulin

C7H6O4 (154.0266076)


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].

   

(1S,5R,6R,14R,15S,17R,22S)-5,10,15-trihydroxy-6,14,18,18,22-pentamethyl-7,13-dioxapentacyclo[12.8.0.03,12.04,9.017,22]docosa-3(12),4(9),10,20-tetraene-8,19-dione

(1S,5R,6R,14R,15S,17R,22S)-5,10,15-trihydroxy-6,14,18,18,22-pentamethyl-7,13-dioxapentacyclo[12.8.0.03,12.04,9.017,22]docosa-3(12),4(9),10,20-tetraene-8,19-dione

C25H30O7 (442.199143)


   
   
   
   

Mycoin

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

C7H6O4 (154.0266076)


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].

   

6-[(acetyloxy)(phenyl)methyl]-1-(2-hydroxyethyl)-4-oxopyridine-3-carboximidic acid

6-[(acetyloxy)(phenyl)methyl]-1-(2-hydroxyethyl)-4-oxopyridine-3-carboximidic acid

C17H18N2O5 (330.1215658)


   

6-[(s)-hydroxy(phenyl)methyl]-4-oxo-1h-pyridine-3-carboximidic acid

6-[(s)-hydroxy(phenyl)methyl]-4-oxo-1h-pyridine-3-carboximidic acid

C13H12N2O3 (244.0847882)


   

16,20-dihydroxy-4,8,8,12-tetramethyl-13-oxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁷,²²]docosa-1(14),15,17(22)-triene-7,18-dione

16,20-dihydroxy-4,8,8,12-tetramethyl-13-oxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁷,²²]docosa-1(14),15,17(22)-triene-7,18-dione

C25H32O5 (412.2249622)


   

n-{2,2,12,15,15-pentamethyl-12-nonyl-6,7,8,11-tetrakis[(trimethylsilyl)oxy]-3,13-dioxa-2,15-disilahexadecan-5-yl}ethanimidic acid

n-{2,2,12,15,15-pentamethyl-12-nonyl-6,7,8,11-tetrakis[(trimethylsilyl)oxy]-3,13-dioxa-2,15-disilahexadecan-5-yl}ethanimidic acid

C40H93NO7Si6 (867.5567348)


   

(3s,4s,9r,12s,20r)-16,20-dihydroxy-4,8,8,12-tetramethyl-13-oxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁷,²²]docosa-1(14),15,17(22)-triene-7,18-dione

(3s,4s,9r,12s,20r)-16,20-dihydroxy-4,8,8,12-tetramethyl-13-oxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁷,²²]docosa-1(14),15,17(22)-triene-7,18-dione

C25H32O5 (412.2249622)


   

n-{6-[hydroxy(phenyl)methyl]-1-(2-hydroxyethyl)-4-oxopyridine-3-carbonyl}-3-methylbutanimidic acid

n-{6-[hydroxy(phenyl)methyl]-1-(2-hydroxyethyl)-4-oxopyridine-3-carbonyl}-3-methylbutanimidic acid

C20H24N2O5 (372.1685134)