NCBI Taxonomy: 469
Acinetobacter (ncbi_taxid: 469)
found 6 associated metabolites at genus taxonomy rank level.
Ancestor: Moraxellaceae
Child Taxonomies: Acinetobacter junii, Acinetobacter lwoffii, Acinetobacter equi, Acinetobacter apis, Acinetobacter soli, Acinetobacter johnsonii, Acinetobacter lanii, Acinetobacter rudis, Acinetobacter venetianus, Acinetobacter larvae, Acinetobacter oryzae, Acinetobacter kookii, Acinetobacter ihumii, Acinetobacter parvus, Acinetobacter populi, Acinetobacter baylyi, Acinetobacter amyesii, Acinetobacter marinus, Acinetobacter thutiue, environmental samples, Acinetobacter indicus, Acinetobacter guerrae, Acinetobacter gerneri, Acinetobacter tandoii, Acinetobacter towneri, Acinetobacter pecorum, Acinetobacter haemolyticus, Acinetobacter defluvii, Acinetobacter Taxon 24, Acinetobacter brisouii, Acinetobacter nectaris, Acinetobacter baretiae, Acinetobacter modestus, Acinetobacter vivianii, Acinetobacter cumulans, Acinetobacter septicus, Acinetobacter albensis, Acinetobacter celticus, Acinetobacter ursingii, Acinetobacter bouvetii, Acinetobacter faecalis, Acinetobacter pollinis, Acinetobacter wanghuae, Acinetobacter pragensis, Acinetobacter plantarum, Acinetobacter boissieri, Acinetobacter piscicola, Acinetobacter gandensis, Acinetobacter stercoris, Acinetobacter entericus, Acinetobacter bohemicus, Acinetobacter portensis, Acinetobacter chinensis, Acinetobacter geminorum, Acinetobacter higginsii, Acinetobacter dispersus, Acinetobacter rathckeae, Acinetobacter sedimenti, Acinetobacter radioresistens, Acinetobacter tibetensis, Acinetobacter wuhouensis, Acinetobacter silvestris, Acinetobacter seohaensis, Acinetobacter bereziniae, Acinetobacter guillouiae, Acinetobacter schindleri, Acinetobacter variabilis, Acinetobacter kanungonis, Acinetobacter oleivorans, Acinetobacter genospecies, Acinetobacter puyangensis, Acinetobacter courvalinii, Acinetobacter xiamenensis, Acinetobacter tianfuensis, Acinetobacter genomosp. 6, Acinetobacter antiviralis, Acinetobacter pullicarnis, Acinetobacter harbinensis, Acinetobacter idrijaensis, Acinetobacter genomosp. C1, Acinetobacter beijerinckii, Acinetobacter halotolerans, Acinetobacter shaoyimingii, Acinetobacter genomosp. 23, Acinetobacter sichuanensis, Acinetobacter gyllenbergii, Acinetobacter chengduensis, Acinetobacter tjernbergiae, unclassified Acinetobacter, Acinetobacter nematophilus, Acinetobacter kyonggiensis, Acinetobacter glutaminasificans, Acinetobacter proteolyticus, Acinetobacter genomosp. NB4, Acinetobacter pseudolwoffii, Acinetobacter rhizosphaerae, Acinetobacter qingfengensis, Acinetobacter genomosp. 33YU, Acinetobacter genomosp. 15TU, Acinetobacter genomosp. NB21, Acinetobacter genomosp. NB28, Acinetobacter genomosp. NB33, Acinetobacter genomosp. NB53, Acinetobacter genomosp. NB54, Acinetobacter rongchengensis, Acinetobacter genomosp. 15BJ, Acinetobacter refrigeratoris, Acinetobacter movanagherensis, Acinetobacter psychrotolerans, Acinetobacter colistiniresistens, Candidatus Acinetobacter avistercoris, Acinetobacter calcoaceticus/baumannii complex
Indole-3-carboxaldehyde
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].
AI3-52407
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].