NCBI Taxonomy: 1497626

Chondria atropurpurea (ncbi_taxid: 1497626)

found 30 associated metabolites at species taxonomy rank level.

Ancestor: Chondria

Child Taxonomies: none taxonomy data.

1204-06-4

3-Indoleacrylic acid

C11H9NO2 (187.0633254)


trans-3-Indoleacrylic acid is an endogenous metabolite.

   

Indoleacrylic acid

(2E)-3-(1H-indol-3-yl)prop-2-enoic acid

C11H9NO2 (187.0633254)


Indoleacrylic acid (CAS: 1204-06-4), also known as indoleacrylate, IA, and IAcrA, is a member of the class of compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. Indoleacrylic acid is practically insoluble (in water) and a weak acidic compound (based on its pKa). Within the cell, indoleacrylic acid is primarily located in the membrane (predicted from logP). Indoleacrylic acid is best known as a plant growth hormone (a natural auxin), whereas its biological role in animals is still unknown. A two-stage production of this compound is likely: intestinal microorganisms catabolize tryptophan to indole derivatives which are then absorbed and converted into indoleacrylic acid and its glycine conjugate, indolylacryloylglycine (IAcrGly). Indolylacryloylglycine excretion in urine is especially pronounced in some myopathies, namely in boys with Duchenne muscular dystrophy (PMID: 10707769). It has been recently found that indoleacrylic acid promotes intestinal epithelial barrier function and mitigates inflammatory responses. Stimulating indoleacrylic acid production could promote anti-inflammatory responses and have therapeutic benefits (PMID: 28704649). Urinary Indole-3-acrylate is produced by Clostridium sporogenes (PMID: 29168502). Indoleacrylic acid is also a metabolite of Peptostreptococcus (PMID: 28704649, 29168502). trans-3-Indoleacrylic acid is an endogenous metabolite.

   

3-Indoleacrylic acid

Indole-3-acrylic acid

C11H9NO2 (187.0633254)


trans-3-Indoleacrylic acid is an endogenous metabolite.

   

(2e)-3-(1h-indol-3-yl)prop-2-enimidic acid

(2e)-3-(1h-indol-3-yl)prop-2-enimidic acid

C11H10N2O (186.079309)


   

(e,2e)-3-(7-methoxy-1-methylindol-3-yl)-n-[(1e)-2-(1-methylindol-3-yl)ethenyl]prop-2-enimidic acid

(e,2e)-3-(7-methoxy-1-methylindol-3-yl)-n-[(1e)-2-(1-methylindol-3-yl)ethenyl]prop-2-enimidic acid

C24H23N3O2 (385.1790178)


   

(e,2e)-3-(1h-indol-3-yl)-n-[(1e)-2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

(e,2e)-3-(1h-indol-3-yl)-n-[(1e)-2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

C21H17N3O (327.1371552)


   

3-(1h-indol-3-yl)prop-2-enimidic acid

3-(1h-indol-3-yl)prop-2-enimidic acid

C11H10N2O (186.079309)


   

(2e)-3-(1h-indol-3-yl)-n-[2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

(2e)-3-(1h-indol-3-yl)-n-[2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

C21H17N3O (327.1371552)


   

(e,2e)-3-(7-hydroxy-1h-indol-3-yl)-n-[(1e)-2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

(e,2e)-3-(7-hydroxy-1h-indol-3-yl)-n-[(1e)-2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

C21H17N3O2 (343.1320702)


   

(z,2e)-3-(1h-indol-3-yl)-n-[(1z)-2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

(z,2e)-3-(1h-indol-3-yl)-n-[(1z)-2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

C21H17N3O (327.1371552)


   

3-(1h-indol-3-yl)-n-[2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

3-(1h-indol-3-yl)-n-[2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

C21H17N3O (327.1371552)


   

3-(7-hydroxy-1h-indol-3-yl)-n-[2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

3-(7-hydroxy-1h-indol-3-yl)-n-[2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

C21H17N3O2 (343.1320702)