NCBI Taxonomy: 69790

Penicillium vinaceum (ncbi_taxid: 69790)

found 14 associated metabolites at species taxonomy rank level.

Ancestor: Penicillium

Child Taxonomies: none taxonomy data.

Indole-3-carboxaldehyde

1H-indole-3-carbaldehyde

C9H7NO (145.0528)


Indole-3-carboxaldehyde (IAld or I3A), also known as 3-formylindole or 3-indolealdehyde, belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of a pyrrole ring fused to benzene to form 2,3-benzopyrrole. In humans, I3A is a biologically active metabolite which acts as a receptor agonist at the aryl hydrocarbon receptor in intestinal immune cells. It stimulates the production of interleukin-22 which facilitates mucosal reactivity (PMID:27102537). I3A is a microbially derived tryptophan metabolite produced by Clostridium and Lactobacillus (PMID:30120222, 27102537). I3A has also been found in the urine of patients with untreated phenylketonuria (PMID:5073866). I3A has been detected, but not quantified, in several different foods, such as beans, Brussels sprouts, cucumbers, cereals and cereal products, and white cabbages. This could make I3A a potential biomarker for the consumption of these foods. Indole-3-carbaldehyde is a heteroarenecarbaldehyde that is indole in which the hydrogen at position 3 has been replaced by a formyl group. It has a role as a plant metabolite, a human xenobiotic metabolite, a bacterial metabolite and a marine metabolite. It is a heteroarenecarbaldehyde, an indole alkaloid and a member of indoles. Indole-3-carboxaldehyde is a natural product found in Euphorbia hirsuta, Derris ovalifolia, and other organisms with data available. A heteroarenecarbaldehyde that is indole in which the hydrogen at position 3 has been replaced by a formyl group. Found in barley and tomato seedlings and cotton Indole-3-carboxaldehyde. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=487-89-8 (retrieved 2024-07-02) (CAS RN: 487-89-8). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Indole-3-carboxaldehyde (3-Formylindole), a banlangen extract, is the product of the oxidative degradation of indole-3-acetic acid (IAA) by crude enzyme preparations from etiolated pea seedlings. Indole-3-carboxaldehyde (3-Formylindole) is a biochemical used to prepare analogs of the indole phytoalexin cyclobrassinin[1]. Indole-3-carboxaldehyde (3-Formylindole), a banlangen extract, is the product of the oxidative degradation of indole-3-acetic acid (IAA) by crude enzyme preparations from etiolated pea seedlings. Indole-3-carboxaldehyde (3-Formylindole) is a biochemical used to prepare analogs of the indole phytoalexin cyclobrassinin[1].

   

CYCLOPIAZONIC ACID

.alpha.-Cyclopiazonic acid

C20H20N2O3 (336.1474)


D002317 - Cardiovascular Agents > D000889 - Anti-Arrhythmia Agents D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents D004791 - Enzyme Inhibitors Cyclopiazonic acid (CPA), a neurotoxic secondary metabolite (SM) made by Aspergillus flavus, is an inhibitor of endoplasmic reticulum calcium ATPase (Ca2+ATPase; SERCA) and a potent inducer of cell death in plants[1].

   

Indole-3-carboxaldehyde

INDOLE-3-CARBOXYALDEHYDE

C9H7NO (145.0528)


Indole-3-carboxaldehyde (3-Formylindole), a banlangen extract, is the product of the oxidative degradation of indole-3-acetic acid (IAA) by crude enzyme preparations from etiolated pea seedlings. Indole-3-carboxaldehyde (3-Formylindole) is a biochemical used to prepare analogs of the indole phytoalexin cyclobrassinin[1]. Indole-3-carboxaldehyde (3-Formylindole), a banlangen extract, is the product of the oxidative degradation of indole-3-acetic acid (IAA) by crude enzyme preparations from etiolated pea seedlings. Indole-3-carboxaldehyde (3-Formylindole) is a biochemical used to prepare analogs of the indole phytoalexin cyclobrassinin[1].

   

AI3-52407

5-21-08-00246 (Beilstein Handbook Reference)

C9H7NO (145.0528)


Indole-3-carboxaldehyde (3-Formylindole), a banlangen extract, is the product of the oxidative degradation of indole-3-acetic acid (IAA) by crude enzyme preparations from etiolated pea seedlings. Indole-3-carboxaldehyde (3-Formylindole) is a biochemical used to prepare analogs of the indole phytoalexin cyclobrassinin[1]. Indole-3-carboxaldehyde (3-Formylindole), a banlangen extract, is the product of the oxidative degradation of indole-3-acetic acid (IAA) by crude enzyme preparations from etiolated pea seedlings. Indole-3-carboxaldehyde (3-Formylindole) is a biochemical used to prepare analogs of the indole phytoalexin cyclobrassinin[1].

   

6-benzyl-1,4-dimethyl-3-(2-methylpropyl)-1,4-diazepane-2,5,7-trione

6-benzyl-1,4-dimethyl-3-(2-methylpropyl)-1,4-diazepane-2,5,7-trione

C18H24N2O3 (316.1787)


   

(3r,8as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one

(3r,8as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one

C16H17N3O2 (283.1321)


   

5,7-diacetyl-6-[(3r)-5-carboxy-6,7-dihydroxy-4-oxo-2,3-dihydro-1-benzopyran-3-yl]-2,3-dihydroxy-9-oxoxanthene-1-carboxylic acid

5,7-diacetyl-6-[(3r)-5-carboxy-6,7-dihydroxy-4-oxo-2,3-dihydro-1-benzopyran-3-yl]-2,3-dihydroxy-9-oxoxanthene-1-carboxylic acid

C28H18O14 (578.0697)


   

5,7-diacetyl-6-(5-carboxy-6,7-dihydroxy-4-oxo-2,3-dihydro-1-benzopyran-3-yl)-2,3-dihydroxy-9-oxoxanthene-1-carboxylic acid

5,7-diacetyl-6-(5-carboxy-6,7-dihydroxy-4-oxo-2,3-dihydro-1-benzopyran-3-yl)-2,3-dihydroxy-9-oxoxanthene-1-carboxylic acid

C28H18O14 (578.0697)


   

6,8-dihydroxy-3-(2-hydroxy-4-oxopentyl)isochromen-1-one

6,8-dihydroxy-3-(2-hydroxy-4-oxopentyl)isochromen-1-one

C14H14O6 (278.079)


   

5,7-diacetyl-6-(5-carboxy-6,7-dihydroxy-2-methoxy-4-oxochromen-3-yl)-2,3-dihydroxy-9-oxoxanthene-1-carboxylic acid

5,7-diacetyl-6-(5-carboxy-6,7-dihydroxy-2-methoxy-4-oxochromen-3-yl)-2,3-dihydroxy-9-oxoxanthene-1-carboxylic acid

C29H18O15 (606.0646)


   

(2s,3r,7r,8s,10s,13z)-10,11-dihydroxy-3-methyl-13-(phenylmethylidene)-8-[(1e)-prop-1-en-1-yl]-9-oxa-1,12-diazatricyclo[8.4.0.0²,⁷]tetradec-11-en-14-one

(2s,3r,7r,8s,10s,13z)-10,11-dihydroxy-3-methyl-13-(phenylmethylidene)-8-[(1e)-prop-1-en-1-yl]-9-oxa-1,12-diazatricyclo[8.4.0.0²,⁷]tetradec-11-en-14-one

C22H26N2O4 (382.1892)


   

(2r,3s,7s,8r)-10,11-dihydroxy-3-methyl-13-(phenylmethylidene)-8-(prop-1-en-1-yl)-9-oxa-1,12-diazatricyclo[8.4.0.0²,⁷]tetradec-11-en-14-one

(2r,3s,7s,8r)-10,11-dihydroxy-3-methyl-13-(phenylmethylidene)-8-(prop-1-en-1-yl)-9-oxa-1,12-diazatricyclo[8.4.0.0²,⁷]tetradec-11-en-14-one

C22H26N2O4 (382.1892)


   

10,11-dihydroxy-3-methyl-13-(phenylmethylidene)-8-(prop-1-en-1-yl)-9-oxa-1,12-diazatricyclo[8.4.0.0²,⁷]tetradec-11-en-14-one

10,11-dihydroxy-3-methyl-13-(phenylmethylidene)-8-(prop-1-en-1-yl)-9-oxa-1,12-diazatricyclo[8.4.0.0²,⁷]tetradec-11-en-14-one

C22H26N2O4 (382.1892)


   

5,7-diacetyl-6-(5-carboxy-6,7-dihydroxy-4-oxochromen-3-yl)-2,3-dihydroxy-9-oxoxanthene-1-carboxylic acid

5,7-diacetyl-6-(5-carboxy-6,7-dihydroxy-4-oxochromen-3-yl)-2,3-dihydroxy-9-oxoxanthene-1-carboxylic acid

C28H16O14 (576.054)