NCBI Taxonomy: 40296

Penicillium italicum (ncbi_taxid: 40296)

found 48 associated metabolites at species taxonomy rank level.

Ancestor: Penicillium

Child Taxonomies: Penicillium italicum var. avellaneum

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].

   

deoxybrevianamide E

L-Prolyl-2-(1,1-dimethylallyl)-L-tryptophan anhydride

C21H25N3O2 (351.194667)


A cyclic dipeptide that is brevianamide F (cyclo-L-Trp-L-Pro) substituted at position 2 on the indole ring by a 1,1-dimethylallyl group.

   
   

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].

   

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].

   

[(2z)-3-hydroxy-4-[(2e)-4-methyloct-2-enoyl]-5-oxofuran-2-ylidene]acetic acid

[(2z)-3-hydroxy-4-[(2e)-4-methyloct-2-enoyl]-5-oxofuran-2-ylidene]acetic acid

C15H18O6 (294.11033280000004)


   

(3s)-1-hydroxy-3-{[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methyl}-3h,6h,7h-pyrrolo[1,2-a]pyrazin-4-one

(3s)-1-hydroxy-3-{[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methyl}-3h,6h,7h-pyrrolo[1,2-a]pyrazin-4-one

C21H23N3O2 (349.1790178)


   

{5-butyl-5-methyl-2',4'-dioxo-3,4-dihydro-[2,3'-bioxolyliden]-5'-ylidene}acetic acid

{5-butyl-5-methyl-2',4'-dioxo-3,4-dihydro-[2,3'-bioxolyliden]-5'-ylidene}acetic acid

C15H18O6 (294.11033280000004)


   

6,7-dihydroxy-4-oxo-3-(3-oxobut-1-en-1-yl)chromene-5-carboxylic acid

6,7-dihydroxy-4-oxo-3-(3-oxobut-1-en-1-yl)chromene-5-carboxylic acid

C14H10O7 (290.042651)


   

6,7-dihydroxy-3-(1-hydroxy-3-oxobutyl)-4-oxochromene-5-carboxylic acid

6,7-dihydroxy-3-(1-hydroxy-3-oxobutyl)-4-oxochromene-5-carboxylic acid

C14H12O8 (308.0532152)


   

methyl 2-[4-(5-butyl-5-methylfuran-2-ylidene)-3,5-dioxooxolan-2-ylidene]acetate

methyl 2-[4-(5-butyl-5-methylfuran-2-ylidene)-3,5-dioxooxolan-2-ylidene]acetate

C16H18O6 (306.11033280000004)


   

(3s,8as)-1-hydroxy-3-{[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one

(3s,8as)-1-hydroxy-3-{[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one

C21H25N3O2 (351.194667)


   

[(2z)-3-hydroxy-4-[(2e,4r)-4-methyloct-2-enoyl]-5-oxofuran-2-ylidene]acetic acid

[(2z)-3-hydroxy-4-[(2e,4r)-4-methyloct-2-enoyl]-5-oxofuran-2-ylidene]acetic acid

C15H18O6 (294.11033280000004)


   

[3-hydroxy-4-(4-methyloct-2-enoyl)-5-oxofuran-2-ylidene]acetic acid

[3-hydroxy-4-(4-methyloct-2-enoyl)-5-oxofuran-2-ylidene]acetic acid

C15H18O6 (294.11033280000004)


   

[(e,5r,5'z)-5-butyl-5-methyl-2',4'-dioxo-3,4-dihydro-[2,3'-bioxolyliden]-5'-ylidene]acetic acid

[(e,5r,5'z)-5-butyl-5-methyl-2',4'-dioxo-3,4-dihydro-[2,3'-bioxolyliden]-5'-ylidene]acetic acid

C15H18O6 (294.11033280000004)


   

6,7-dihydroxy-4-oxo-3-[(1e)-3-oxobut-1-en-1-yl]chromene-5-carboxylic acid

6,7-dihydroxy-4-oxo-3-[(1e)-3-oxobut-1-en-1-yl]chromene-5-carboxylic acid

C14H10O7 (290.042651)


   

[(2z)-5-hydroxy-4-[(2e)-4-methyloct-2-enoyl]-3-oxofuran-2-ylidene]acetic acid

[(2z)-5-hydroxy-4-[(2e)-4-methyloct-2-enoyl]-3-oxofuran-2-ylidene]acetic acid

C15H18O6 (294.11033280000004)


   

[(2z)-4-[(2z)-5-butyl-5-methylfuran-2-ylidene]-3,5-dioxooxolan-2-ylidene]acetic acid

[(2z)-4-[(2z)-5-butyl-5-methylfuran-2-ylidene]-3,5-dioxooxolan-2-ylidene]acetic acid

C15H16O6 (292.0946836)


   

6,7-dihydroxy-3-[(1r)-1-hydroxy-3-oxobutyl]-4-oxochromene-5-carboxylic acid

6,7-dihydroxy-3-[(1r)-1-hydroxy-3-oxobutyl]-4-oxochromene-5-carboxylic acid

C14H12O8 (308.0532152)


   

[(2z)-4-[(2z,5r)-5-butyl-5-methylfuran-2-ylidene]-3,5-dioxooxolan-2-ylidene]acetic acid

[(2z)-4-[(2z,5r)-5-butyl-5-methylfuran-2-ylidene]-3,5-dioxooxolan-2-ylidene]acetic acid

C15H16O6 (292.0946836)


   

methyl 2-[(2z)-4-[(2z,5r)-5-butyl-5-methylfuran-2-ylidene]-3,5-dioxooxolan-2-ylidene]acetate

methyl 2-[(2z)-4-[(2z,5r)-5-butyl-5-methylfuran-2-ylidene]-3,5-dioxooxolan-2-ylidene]acetate

C16H18O6 (306.11033280000004)


   

[4-(5-butyl-5-methylfuran-2-ylidene)-3,5-dioxooxolan-2-ylidene]acetic acid

[4-(5-butyl-5-methylfuran-2-ylidene)-3,5-dioxooxolan-2-ylidene]acetic acid

C15H16O6 (292.0946836)