NCBI Taxonomy: 469

Acinetobacter (ncbi_taxid: 469)

found 76 associated metabolites at genus taxonomy rank level.

Indole-3-carboxaldehyde

1H-indole-3-carbaldehyde

C9H7NO (145.0527612)

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 Indole-3-carbaldehyde is a heteroarenecarbaldehyde that is indole in which the hydrogen at position 3 has been replaced by a formyl group.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 A heteroarenecarbaldehyde that is indole in which the hydrogen at position 3 has been replaced by a formyl group.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].

Pyrrolnitrin

Pyrrolnitrin;3-Chloro-4-(3-chloro-2-nitrophenyl)pyrrole_HCD50

C10H6Cl2N2O2 (255.9806316)

A member of the class of pyrroles carrying chloro and 3-chloro-2-nitrophenyl substituents at positions 3 and 4 respectively. D - Dermatologicals > D01 - Antifungals for dermatological use > D01A - Antifungals for topical use > D01AA - Antibiotics D000890 - Anti-Infective Agents > D000935 - Antifungal Agents C254 - Anti-Infective Agent > C514 - Antifungal Agent Same as: D01094

Indole-3-carboxaldehyde

INDOLE-3-CARBOXYALDEHYDE

C9H7NO (145.0527612)

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].

3-Hydroxybutanoic acid

C4H8O3 (104.0473418)

AI3-52407

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

C9H7NO (145.0527612)

Acinetoferrin

C28H48N4O9 (584.3421118)

(2s)-2-({[(4s)-2-(2,3-dihydroxyphenyl)-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-3-hydroxy-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid

C19H26N4O8 (438.1750556)

(3r,7r)-7,12,14-trihydroxy-3-methyl-3,4,5,6,7,8,9,10-octahydro-2-benzoxacyclododecin-1-one

C16H22O5 (294.1467162)

7,12,14-trihydroxy-3-methyl-3,4,5,6,7,8,9,10-octahydro-2-benzoxacyclododecin-1-one

C16H22O5 (294.1467162)

(2s)-3-(2,3-dihydroxybenzoyloxy)-2-({[(4s)-2-(2,3-dihydroxyphenyl)-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid

C26H30N4O11 (574.191099)

2-({[2-(2,3-dihydroxyphenyl)-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-3-hydroxy-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid

C19H26N4O8 (438.1750556)

(3r)-12,14-dihydroxy-3-methyl-4,6,7,8,9,10-hexahydro-3h-2-benzoxacyclododecine-1,5-dione

C16H20O5 (292.13106700000003)

12,14-dihydroxy-3-methyl-4,5,6,8,9,10-hexahydro-3h-2-benzoxacyclododecine-1,7-dione

C16H20O5 (292.13106700000003)

6-bromo-1h-indole-3-carbaldehyde

C9H6BrNO (222.96327259999998)

2-(2,3-dihydroxyphenyl)-n-hydroxy-n-[2-(3h-imidazol-4-yl)ethyl]-5-methyl-4,5-dihydro-1,3-oxazole-4-carboxamide

C16H18N4O5 (346.12771380000004)

3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)propanoic acid

C20H18N2O10 (446.09614079999994)

(2s)-3-(2,3-dihydroxybenzoyloxy)-2-({[(4s,5r)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid

C27H32N4O11 (588.2067482)

2,3-dihydroxy-n-[(4s,5s)-2-[2-(3h-imidazol-4-yl)ethyl]-5-methyl-3-oxo-1,2-oxazolidin-4-yl]benzenecarboximidic acid

C16H18N4O5 (346.12771380000004)

1-{1-carboxy-3-[(3-carboxy-1-hydroxy-3-{[3-(n-hydroxydecanamido)propyl]-c-hydroxycarbonimidoyl}propylidene)amino]propyl}-2-hydroxy-5-oxopyrrolidine-2-carboxylic acid

C27H44N4O12 (616.2955584)

(3s,3ar,4ar,5r,9as)-3a,9a-dihydroxy-3,4a,5-trimethyl-2h,3h,4h,5h-naphtho[2,3-b]furan-6-one

C15H20O4 (264.13615200000004)

3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]butanimidic acid

C28H34N4O11 (602.2223974)

4,4a,11,12a-tetrahydroxy-3-methoxy-10-methyl-8-{[(2s,3s,4s,5r,6r)-3,4,5-trimethoxy-6-methyloxan-2-yl]oxy}-4h-tetracene-1,5,12-trione

C29H32O13 (588.1842822)

4-{[2-({2-[(2-{[2-({[20-(4-aminobutyl)-6-benzyl-1,4,7,12,15,18,21-heptahydroxy-24-oxo-3-(sec-butyl)-3h,6h,9h,10h,11h,14h,17h,20h,23h,26h,27h,28h,28ah-pyrrolo[2,1-i]1,4,7,10,13,16,19,22-octaazacyclohexacosan-9-yl](hydroxy)methylidene}amino)-1,3-dihydroxybutylidene]amino}-1-hydroxy-3-(1h-indol-3-yl)propylidene)amino]-1-hydroxy-3-methylbutylidene}amino)-1,3-dihydroxybutylidene]amino}-4-{[({1-[(1-{[1-(carboxymethyl-c-hydroxycarbonimidoyl)-2-(4-hydroxyphenyl)ethyl]-c-hydroxycarbonimidoyl}-2-(4-hydroxyphenyl)ethyl)-c-hydroxycarbonimidoyl]-2-(c-hydroxycarbonimidoyl)ethyl}-c-hydroxycarbonimidoyl)methyl]-c-hydroxycarbonimidoyl}butanoic acid

4-{[2-({2-[(2-{[2-({[20-(4-aminobutyl)-6-benzyl-1,4,7,12,15,18,21-heptahydroxy-24-oxo-3-(sec-butyl)-3h,6h,9h,10h,11h,14h,17h,20h,23h,26h,27h,28h,28ah-pyrrolo[2,1-i]1,4,7,10,13,16,19,22-octaazacyclohexacosan-9-yl](hydroxy)methylidene}amino)-1,3-dihydroxybutylidene]amino}-1-hydroxy-3-(1h-indol-3-yl)propylidene)amino]-1-hydroxy-3-methylbutylidene}amino)-1,3-dihydroxybutylidene]amino}-4-{[({1-[(1-{[1-(carboxymethyl-c-hydroxycarbonimidoyl)-2-(4-hydroxyphenyl)ethyl]-c-hydroxycarbonimidoyl}-2-(4-hydroxyphenyl)ethyl)-c-hydroxycarbonimidoyl]-2-(c-hydroxycarbonimidoyl)ethyl}-c-hydroxycarbonimidoyl)methyl]-c-hydroxycarbonimidoyl}butanoic acid

C92H125N21O27 (1955.905334)