NCBI Taxonomy: 49546

Flavobacteriaceae (ncbi_taxid: 49546)

found 28 associated metabolites at family taxonomy rank level.

Ancestor: Flavobacteriales

Child Taxonomies: Saonia, Kordia, Zhouia, Olleya, Pricia, Jejuia, Cerina, Taeania, Tamlana, Formosa, Mesonia, Hoppeia, Wocania, Snuella, Gelidibacter, Polaribacter, Yeosuana, Myroides, Rasiella, Bizionia, Zobellia, Dokdonia, Eudoraea, Gillisia, Coenonia, Jejudonia, Muriicola, Lutimonas, Pukyongia, Pibocella, Vaginella, Algitalea, Daejeonia, Nonlabens, Avrilella, Kriegella, Joostella, Gangjinia, Psychroserpens, Flavobacterium, Capnocytophaga, Aureitalea, Imtechella, Geojedonia, Abyssalbus, Hwangdonia, Flavicella, Aquibacter, Lutaonella, Lacinutrix, Aquimarina, Ulvibacter, Aureivirga, Lutibacter, Actibacter, Haloanella, Algibacter, Maribacter, Ilumomonas, Ochrovirga, Euzebyella, Flavivirga, Arenibacter, Costertonia, Amoebinatus, Namhaeicola, Fulvibacter, Spongitalea, Paramesonia, Aureicoccus, Siansivirga, Flavococcus, Aureimarina, Croceitalea, Aequorivita, Croceivirga, Galbibacter, Gilvibacter, Flavimarina, Cochleicola, Marinitalea, Citreitalea, Citreibacter, Aureibaculum, Ascidiimonas, Poritiphilus, Luteirhabdus, Aureisphaera, Xanthomarina, Urechidicola, Cellulophaga, Neptunitalea, Robertkochia, Spodiobacter, Orabacterium, Zunongwangia, Aurantivirga, Sediminicola, Spongiivirga, Croceibacter, Coraliitalea, Endobryopsis, Coccinimonas, Frondibacter, Croceimarina, Oceanistipes, Postechiella, Feifantangia, Hanstruepera, Flaviramulus, Prasinibacter, Marinirhabdus, Spongiiferula, Aurantibacter, Flagellimonas, Maritimimonas, Pareuzebyella, Tenacibaculum, Mariniflexile, Sediminitalea, Paenimyroides, Subsaxibacter, Allomuricauda, Robiginitalea, Coccinistipes, Aquaticitalea, Psychroflexus, Mangrovimonas, Ulvibacterium, Sinomicrobium, Corallibacter, Litoribaculum, Patiriisocius, Pontimicrobium, Prosiliicoccus, Pseudozobellia, Sufflavibacter, Seonamhaeicola, Sungkyunkwania, Gelatiniphilus, Hyunsoonleella, Pelagihabitans, Gaetbulibacter, Aestuariimonas, Sediminibacter, Mesohalobacter, Xanthobacillum, Oceanihabitans, Planktosalinus, Leptobacterium, Aggregatimonas, Wenyingzhuangia, Marixanthomonas, Christiangramia, Pseudalgibacter, Paucihalobacter, Antarcticimonas, Thermobacterium, Aestuariivivens, Ascidianibacter, Salegentibacter, Marixanthotalea, Haloflavibacter, Aurantiacicella, Mesoflavibacter, Winogradskyella, Salinimicrobium, Changchengzhania, Ascidiaceibacter, Pustulibacterium, Leeuwenhoekiella, Subsaximicrobium, Aestuariibaculum, Maripseudobacter, Spongiimicrobium, Confluentibacter, Neoflavobacterium, Aegicerativicinus, Zeaxanthinibacter, Amniculibacterium, Pseudofulvibacter, Lentiprolixibacter, Halomarinibacterium, Pseudotenacibaculum, Meridianimaribacter, Antarcticibacterium, Ichthyenterobacterium, environmental samples, Candidatus Hemobacterium, Candidatus Marivariicella, unclassified Flavobacteriaceae, Candidatus Maricapacicella, Candidatus Arcticimaribacter, Flavobacteriaceae incertae sedis, Altibacter/Constantimarinum group

Farnesyl pyrophosphate

{[hydroxy({[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy})phosphoryl]oxy}phosphonic acid

C15H28O7P2 (382.1310198)


Farnesyl pyrophosphate is an intermediate in the HMG-CoA reductase pathway used by organisms in the biosynthesis of terpenes and terpenoids. -- Wikipedia [HMDB]. Farnesyl pyrophosphate is found in many foods, some of which are kumquat, macadamia nut, sweet bay, and agave. Farnesyl pyrophosphate is an intermediate in the HMG-CoA reductase pathway used by organisms in the biosynthesis of terpenes and terpenoids. -- Wikipedia.

   

gamma-Carotene

2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E,19E)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaen-1-yl]-1,3,3-trimethylcyclohex-1-ene

C40H56 (536.4381776)


gamma-Carotene is a cyclic carotene obtained by the cyclization of lycopene. It is found in human serum and breast milk (PMID: 9164160). Carotenoids are isoprenoid molecules that are widespread in nature and are typically seen as pigments in fruits, flowers, birds, and crustacea. Animals are unable to synthesize carotenoids de novo and rely upon the diet as a source of these compounds. Over recent years there has been considerable interest in dietary carotenoids with respect to their potential in alleviating age-related diseases in humans. This attention has been mirrored by significant advances in cloning most of the carotenoid genes and in the genetic manipulation of crop plants with the intention of increasing levels in the diet. Studies have shown an inverse relationship between the consumption of certain fruits and vegetables and the risk of epithelial cancer. Since carotenoids are among the micronutrients found in cancer-preventive foods, detailed qualitative and quantitative determination of these compounds, particularly in fruits and vegetables and in human plasma, have recently become increasingly important (PMID: 1416048, 15003396). Gamma-carotene, also known as γ-carotene, is a member of the class of compounds known as carotenes. Carotenes are a type of unsaturated hydrocarbons containing eight consecutive isoprene units. They are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Gamma-carotene can be found in a number of food items such as corn, yellow bell pepper, fig, and papaya, which makes gamma-carotene a potential biomarker for the consumption of these food products.

   

Rubixanthin

(1R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E,19E)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaen-1-yl]-3,5,5-trimethylcyclohex-3-en-1-ol

C40H56O (552.4330926)


Rubixanthin is found in apricot. Rubixanthin, or natural yellow 27, is a natural xanthophyll pigment with a red-orange color found in rose hips. As a food additive it used under the E number E161d as a food coloring. (Wikipedia Rubixanthin, or natural yellow 27, is a natural xanthophyll pigment with a red-orange color found in rose hips. As a food additive it used under the E number E161d as a food coloring.

   

Geranyl-PP

[({[(2E)-3,7-dimethylocta-2,6-dien-1-yl]oxy}(hydroxy)phosphoryl)oxy]phosphonic acid

C10H20O7P2 (314.068423)


Geranyl diphosphate is the precursor of monoterpenes, a large family of natural occurring C10 compounds predominately found in plants and animals. Geranyl diphosphate is regarded as a key intermediate in the steroid, isoprene and terpene biosynthesis pathways and is used by organisms in the biosynthesis of farnesyl pyrophosphate, geranylgeranyl pyrophosphate, cholesterol, terpenes and terpenoids. (wikipedia). In humans, geranyl diphosphate synthase (GPPS) catalyzes the condensation of dimethylallyl diphosphate (DMAPP) and isopentenyl diphosphate (IPP) to form geranyl diphosphate. Animals produce IPP through the mevalonate (MVA) pathway. Isoprenoid compounds have been implicated in several human disease states including coronary heart disease, blindness, infectious hepatitis and cancer.; ; Geranyl pyrophosphate is an intermediate in the HMG-CoA reductase pathway used by organisms in the biosynthesis of terpenes and terpenoids. -- Wikipedia; Geranyl pyrophosphate is an intermediate in the HMG-CoA reductase pathway used by organisms in the biosynthesis of farnesyl pyrophosphate, geranylgeranyl pyrophosphate, cholesterol, terpenes and terpenoids. Geranyl diphosphate is the precursor of monoterpenes, a large family of natural occurring C10 compounds predominately found in plants and animals. Geranyl diphosphate is regarded as a key intermediate in the steroid, isoprene and terpene biosynthesis pathways and is used by organisms in the biosynthesis of farnesyl pyrophosphate, geranylgeranyl pyrophosphate, cholesterol, terpenes and terpenoids. (wikipedia). In humans, geranyl diphosphate synthase (GPPS) catalyzes the condensation of dimethylallyl diphosphate (DMAPP) and isopentenyl diphosphate (IPP) to form geranyl diphosphate. Animals produce IPP through the mevalonate (MVA) pathway. Isoprenoid compounds have been implicated in several human disease states including coronary heart disease, blindness, infectious hepatitis and cancer. Geranyl pyrophosphate is an intermediate in the HMG-CoA reductase pathway used by organisms in the biosynthesis of terpenes and terpenoids. -- Wikipedia.

   

Neurosporene

(6E,8E,10E,12E,14E,16E,18E,20E,22E,26E)-2,6,10,14,19,23,27,31-Octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,26,30-dodecaene

C40H58 (538.4538268)


Neurosporene, also known as all-trans-neurosporene or 7,8-dihydro-ψ,ψ-carotene, is a member of the class of compounds known as carotenes. Carotenes are a type of unsaturated hydrocarbons containing eight consecutive isoprene units. They are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Thus, neurosporene is considered to be an isoprenoid lipid molecule. Neurosporene can be found in a number of food items such as chicory, poppy, silver linden, and towel gourd, which makes neurosporene a potential biomarker for the consumption of these food products. Neurosporene can be found primarily in blood and breast milk. Neurosporene is a carotenoid pigment. It is an intermediate in the biosynthesis of lycopene and a variety of bacterial carotenoids . Neurosporene is a triterpenoid carotenoid identified in human plasma, (PMID: 1416048), serum (PMID: 1416048), milk (PMID: 9164160), and tissues of the human eye (PMID: 11180970). D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids

   

isopentenyl phosphate

isopentenyl phosphate

C5H11O4P (166.0394936)


   

2,6-Diethyl-3,5-dimethylpyrazine

2,6-Diethyl-3,5-dimethylpyrazine

C10H16N2 (164.13134159999998)


2,6-Diethyl-3,5-dimethylpyrazine is found in coffee and coffee products. 2,6-Diethyl-3,5-dimethylpyrazine is a constituent of roast coffee aroma. 2,6-Diethyl-3,5-dimethylpyrazine is a maillard product. Constituent of roast coffee aroma. Maillard product. 2,6-Diethyl-3,5-dimethylpyrazine is found in coffee and coffee products.

   

gamma-Carotene

beta,psi-Carotene

C40H56 (536.4381776)


A cyclic carotene obtained by the cyclisation of lycopene. Window width to select the precursor ion was 3 Da.; CONE_VOLTAGE is 10 V.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 19HP8024 to the Mass Spectrometry Society of Japan.

   

2,6-Diethyl-3,5-dimethylpyrazine

2,6-Diethyl-3,5-dimethylpyrazine

C10H16N2 (164.13134159999998)


   
   

Geranyl diphosphate

GERANYL PYROPHOSPHATE AMMONIUM 200

C10H20O7P2 (314.068423)


The diphosphate of the polyprenol compound geraniol.

   

farnesyl diphosphate

2-trans,6-trans-Farnesyl diphosphate

C15H28O7P2 (382.1310198)


The trans,trans-stereoisomer of farnesyl diphosphate.

   

Neurosporene

Neurosporene

C40H58 (538.4538268)


D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids

   

Rubixanthin

Rubixanthin

C40H56O (552.4330926)


A carotenol that is a natural xanthophyll pigment. It was formerly used as a food colourant (E161d), but approval for this purpose has been withdrawn throughout the European Union.

   

(4-hydroxy-3,5-dinitrophenyl)acetic acid

(4-hydroxy-3,5-dinitrophenyl)acetic acid

C8H6N2O7 (242.0175006)


A member of the class of phenylacetic acids that is phenylacetic acid in which the phenyl group is substituted by nitro, hydroxy and nitro groups at positions 3, 4 and 5 respectively.

   

methyl 3-(4-hydroxy-3,5-dinitrophenyl)propanoate

methyl 3-(4-hydroxy-3,5-dinitrophenyl)propanoate

C10H10N2O7 (270.04879900000003)


   

4-(2-hydroxyethyl)-2,6-dinitrophenol

4-(2-hydroxyethyl)-2,6-dinitrophenol

C8H8N2O6 (228.0382348)


   

(2r)-4-(methylsulfanyl)butan-2-ol

(2r)-4-(methylsulfanyl)butan-2-ol

C5H12OS (120.0608822)


   
   

(8z)-13-methyltetradec-8-en-2-one

(8z)-13-methyltetradec-8-en-2-one

C15H28O (224.2140038)


   

3,4-bis(4-hydroxyphenyl)-1-(2-phenylethyl)pyrrole-2,5-dione

3,4-bis(4-hydroxyphenyl)-1-(2-phenylethyl)pyrrole-2,5-dione

C24H19NO4 (385.1314014000001)


   

n-(2-methoxy-2-oxoethyl)-15-methyl-3-[(13-methyltetradec-4-enoyl)oxy]hexadecanimidic acid

n-(2-methoxy-2-oxoethyl)-15-methyl-3-[(13-methyltetradec-4-enoyl)oxy]hexadecanimidic acid

C35H65NO5 (579.486248)


   
   

(2s)-2-[(4s)-4-[(1-hydroxyethylidene)amino]-3-oxo-1,2-oxazolidin-2-yl]-5-oxooxolane-2-carboxylic acid

(2s)-2-[(4s)-4-[(1-hydroxyethylidene)amino]-3-oxo-1,2-oxazolidin-2-yl]-5-oxooxolane-2-carboxylic acid

C10H12N2O7 (272.0644482)


   

14-methylpentadec-10-en-2-one

14-methylpentadec-10-en-2-one

C16H30O (238.22965299999998)


   

n-[5-(n-hydroxy-3-methylbutanamido)pentyl]-4-methoxy-4-oxobutanimidic acid

n-[5-(n-hydroxy-3-methylbutanamido)pentyl]-4-methoxy-4-oxobutanimidic acid

C15H28N2O5 (316.1998118)


   

3-[(2s,5s)-5-benzyl-3,6-dihydroxy-2,5-dihydropyrazin-2-yl]-n-(2-phenylethyl)propanimidic acid

3-[(2s,5s)-5-benzyl-3,6-dihydroxy-2,5-dihydropyrazin-2-yl]-n-(2-phenylethyl)propanimidic acid

C22H25N3O3 (379.189582)


   

3-{[5-(n-hydroxy-3-{[5-(n-hydroxy-3-methylbutanamido)pentyl]-c-hydroxycarbonimidoyl}propanamido)pentyl]-c-hydroxycarbonimidoyl}propanoic acid

3-{[5-(n-hydroxy-3-{[5-(n-hydroxy-3-methylbutanamido)pentyl]-c-hydroxycarbonimidoyl}propanamido)pentyl]-c-hydroxycarbonimidoyl}propanoic acid

C23H42N4O8 (502.3002492)