NCBI Taxonomy: 70113

Penicillium parvum (ncbi_taxid: 70113)

found 36 associated metabolites at species taxonomy rank level.

Ancestor: Penicillium

Child Taxonomies: none taxonomy data.

Mycophenolic acid

(4E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-2-benzofuran-5-yl)-4-methylhex-4-enoic acid

C17H20O6 (320.125982)


Mycophenolic acid is an an immunosuppresant drug and potent anti-proliferative, and can be used in place of the older anti-proliferative azathioprine. It is usually used as part of triple therapy including a calcineurin inhibitor (ciclosporin or tacrolimus) and prednisolone. It is also useful in research for the selection of animal cells that express the E. coli gene coding for XGPRT (xanthine guanine phosphoribosyltransferase). L - Antineoplastic and immunomodulating agents > L04 - Immunosuppressants > L04A - Immunosuppressants > L04AA - Selective immunosuppressants D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D000995 - Antitubercular Agents C471 - Enzyme Inhibitor > C2087 - Inosine Monophosphate Dehydrogenase Inhibitor C308 - Immunotherapeutic Agent > C574 - Immunosuppressant CONFIDENCE standard compound; INTERNAL_ID 8577 CONFIDENCE standard compound; INTERNAL_ID 2698 CONFIDENCE standard compound; INTERNAL_ID 4128 COVID info from COVID-19 Disease Map D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Mycophenolic acid is a potent uncompetitive inosine monophosphate dehydrogenase (IMPDH) inhibitor with an EC50 of 0.24 μM.?Mycophenolic acid demonstrates antiviral effects against a wide range of RNA viruses including influenza. Mycophenolic acid is an immunosuppressive agent. Antiangiogenic and antitumor effects[1][2].

   

6-(4-Hydroxy-6-methoxy-7-methyl-3-oxo-1H-isobenzofuran-5-yl)-4-methyl-4-hexenoic acid

6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-2-benzofuran-5-yl)-4-methylhex-4-enoic acid

C17H20O6 (320.125982)


   

Euparvic acid

(-)-Euparvic acid

C14H16O6 (280.0946836)


   

Mycophenolic acid

Mycophenolic (Mycophenolate)

C17H20O6 (320.125982)


A member of the class of 2-benzofurans that is 2-benzofuran-1(3H)-one which is substituted at positions 4, 5, 6, and 7 by methyl, methoxy, (2E)-5-carboxy-3-methylpent-2-en-1-yl, and hydroxy groups, respectively. It is an antibiotic produced by Penicillium brevi-compactum, P. stoloniferum, P. echinulatum and related species. An immunosuppressant, it is widely used (partiularly as its sodium salt and as the 2-(morpholin-4-yl)ethyl ester prodrug, mycophenolate mofetil) to prevent tissue rejection following organ transplants and for the treatment of certain autoimmune diseases. L - Antineoplastic and immunomodulating agents > L04 - Immunosuppressants > L04A - Immunosuppressants > L04AA - Selective immunosuppressants D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D000995 - Antitubercular Agents C471 - Enzyme Inhibitor > C2087 - Inosine Monophosphate Dehydrogenase Inhibitor C308 - Immunotherapeutic Agent > C574 - Immunosuppressant COVID info from COVID-19 Disease Map D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS CONFIDENCE isolated standard relative retention time with respect to 9-anthracene Carboxylic Acid is 1.096 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.098 CONFIDENCE standard compound; EAWAG_UCHEM_ID 2808 Mycophenolic acid is a potent uncompetitive inosine monophosphate dehydrogenase (IMPDH) inhibitor with an EC50 of 0.24 μM.?Mycophenolic acid demonstrates antiviral effects against a wide range of RNA viruses including influenza. Mycophenolic acid is an immunosuppressive agent. Antiangiogenic and antitumor effects[1][2].

   

3-Hydroxy-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1H-2-benzofuran-5-yl)-4-methylhex-4-enoic acid

3-Hydroxy-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1H-2-benzofuran-5-yl)-4-methylhex-4-enoic acid

C17H20O7 (336.120897)


   

(2s)-4-(6-hydroxy-4-methoxy-7-methyl-3-oxo-1h-2-benzofuran-5-yl)-2-methylbutanoic acid

(2s)-4-(6-hydroxy-4-methoxy-7-methyl-3-oxo-1h-2-benzofuran-5-yl)-2-methylbutanoic acid

C15H18O6 (294.11033280000004)


   

5,7-dihydroxy-4-methyl-3h-2-benzofuran-1-one

5,7-dihydroxy-4-methyl-3h-2-benzofuran-1-one

C9H8O4 (180.0422568)


   

7,9-dihydroxy-6-methoxy-3-methyl-1h-pyrano[4,3-b]chromen-10-one

7,9-dihydroxy-6-methoxy-3-methyl-1h-pyrano[4,3-b]chromen-10-one

C14H12O6 (276.06338519999997)


   

7-hydroxy-6-{2-[(2s,3r)-3-hydroxy-2-methyl-5-oxooxolan-2-yl]ethyl}-5-methoxy-4-methyl-3h-2-benzofuran-1-one

7-hydroxy-6-{2-[(2s,3r)-3-hydroxy-2-methyl-5-oxooxolan-2-yl]ethyl}-5-methoxy-4-methyl-3h-2-benzofuran-1-one

C17H20O7 (336.120897)


   

(3s,4e)-3-hydroxy-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1h-2-benzofuran-5-yl)-4-methylhex-4-enoic acid

(3s,4e)-3-hydroxy-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1h-2-benzofuran-5-yl)-4-methylhex-4-enoic acid

C17H20O7 (336.120897)


   

7-hydroxy-6-[2-(3-hydroxy-2-methyl-5-oxooxolan-2-yl)ethyl]-5-methoxy-4-methyl-3h-2-benzofuran-1-one

7-hydroxy-6-[2-(3-hydroxy-2-methyl-5-oxooxolan-2-yl)ethyl]-5-methoxy-4-methyl-3h-2-benzofuran-1-one

C17H20O7 (336.120897)


   

4-(4,6-dihydroxy-7-methyl-3-oxo-1h-2-benzofuran-5-yl)-2-methylbutanoic acid

4-(4,6-dihydroxy-7-methyl-3-oxo-1h-2-benzofuran-5-yl)-2-methylbutanoic acid

C14H16O6 (280.0946836)


   

4-(6-hydroxy-4-methoxy-7-methyl-3-oxo-1h-2-benzofuran-5-yl)-2-methylbutanoic acid

4-(6-hydroxy-4-methoxy-7-methyl-3-oxo-1h-2-benzofuran-5-yl)-2-methylbutanoic acid

C15H18O6 (294.11033280000004)