NCBI Taxonomy: 33

Myxococcus fulvus (ncbi_taxid: 33)

found 35 associated metabolites at species taxonomy rank level.

Ancestor: Myxococcus

Child Taxonomies: Myxococcus fulvus HW-1, Myxococcus fulvus 124B02, Myxococcus fulvus Mx f65

Myxothiazol

Myxothiazol A

C25H33N3O3S2 (487.1963228)


A 2,4-bi-1,3-thiazole substituted at the 4-position with a (1E,3S,4R,5E)-7-amino-3,5-dimethoxy-4-methyl-7-oxohepta-1,5-dien-1-yl] group and at the 2-position with a (2S,3E,5E)-7-methylocta-3,5-dien-2-yl group. It is an inhibitor of coenzyme Q - cytochrome c reductase. D000890 - Anti-Infective Agents > D000935 - Antifungal Agents D004791 - Enzyme Inhibitors

   

Carotenoid B

1-Hydroxy-γ-carotene/ 1-OH-γ-Carotene/ (Carotenoid B)

C40H58O (554.4487418)


A carotenol that is 1,2-dihydro-beta,psi-carotene which carries a hydroxy group at position 1.

   

Myxocoxanthin

3,4-Didehydro-1,2-dihydro-1-hydroxy-beta,psi-carotene

C40H56O (552.4330926)


A carotenol that is (3E)-3,4-didehydro-1,2-dihydro-beta,psi-carotene which carries a hydroxy group at position 1.

   

4-Ketomyxol

Ketomyxol/ 2-Hydroxyflexixanthin

C40H54O4 (598.4021884)


   

1'-hydroxy-gamma-carotene

2,6,10,14,19,23-hexamethyl-25-(2,6,6-trimethylcyclohex-1-en-1-yl)pentacosa-6,8,10,12,14,16,18,20,22,24-decaen-2-ol

C40H58O (554.4487418)


1-hydroxy-gamma-carotene is a member of the class of compounds known as xanthophylls. Xanthophylls are carotenoids containing an oxygenated carotene backbone. Carotenes 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. Xanthophylls arise by oxygenation of the carotene backbone. 1-hydroxy-gamma-carotene is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 1-hydroxy-gamma-carotene can be found in a number of food items such as red bell pepper, elderberry, jute, and plains prickly pear, which makes 1-hydroxy-gamma-carotene a potential biomarker for the consumption of these food products.

   

Ketomyxol

(3S,2S)-3,1,2-Trihydroxy-3,4-didehydro-1,2-dihydro-beta,psi-caroten-4-one

C40H54O4 (598.4021884)


   

1'-hydroxy-gamma-carotene

2,6,10,14,19,23-hexamethyl-25-(2,6,6-trimethylcyclohex-1-en-1-yl)pentacosa-6,8,10,12,14,16,18,20,22,24-decaen-2-ol

C40H58O (554.4487418)


1-hydroxy-gamma-carotene is a member of the class of compounds known as xanthophylls. Xanthophylls are carotenoids containing an oxygenated carotene backbone. Carotenes 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. Xanthophylls arise by oxygenation of the carotene backbone. 1-hydroxy-gamma-carotene is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 1-hydroxy-gamma-carotene can be found in a number of food items such as red bell pepper, elderberry, jute, and plains prickly pear, which makes 1-hydroxy-gamma-carotene a potential biomarker for the consumption of these food products. 1-hydroxy-γ-carotene is a member of the class of compounds known as xanthophylls. Xanthophylls are carotenoids containing an oxygenated carotene backbone. Carotenes 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. Xanthophylls arise by oxygenation of the carotene backbone. 1-hydroxy-γ-carotene is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 1-hydroxy-γ-carotene can be found in a number of food items such as red bell pepper, elderberry, jute, and plains prickly pear, which makes 1-hydroxy-γ-carotene a potential biomarker for the consumption of these food products.

   

(2e,4s,5r,6e)-3,5-dimethoxy-4-methyl-7-(2-{2-[(2r,3z,5e)-7-methylocta-3,5-dien-2-yl]-1,3-thiazol-4-yl}-1,3-thiazol-4-yl)hepta-2,6-dienimidic acid

(2e,4s,5r,6e)-3,5-dimethoxy-4-methyl-7-(2-{2-[(2r,3z,5e)-7-methylocta-3,5-dien-2-yl]-1,3-thiazol-4-yl}-1,3-thiazol-4-yl)hepta-2,6-dienimidic acid

C25H33N3O3S2 (487.1963228)


   

3-[(1e,3e,5e,7e,9e,11e,13e,15e,17e,19e,21e)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,21,23-dodecaen-1-yl]-2,4,4-trimethylcyclohex-2-en-1-one

3-[(1e,3e,5e,7e,9e,11e,13e,15e,17e,19e,21e)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,21,23-dodecaen-1-yl]-2,4,4-trimethylcyclohex-2-en-1-one

C40H52O (548.4017942)


   

n-[(1e,5r)-5-{5-[(2e,4e)-2,5-dimethylocta-2,4-dienoyl]-4-hydroxy-6-oxopyran-2-yl}hex-1-en-1-yl]methoxycarboximidic acid

n-[(1e,5r)-5-{5-[(2e,4e)-2,5-dimethylocta-2,4-dienoyl]-4-hydroxy-6-oxopyran-2-yl}hex-1-en-1-yl]methoxycarboximidic acid

C23H31NO6 (417.2151266)


   

(2e,4r,5s,6e)-3,5-dimethoxy-4-methyl-7-(2-{2-[(2s,3e,5e)-7-methylocta-3,5-dien-2-yl]-1,3-thiazol-4-yl}-1,3-thiazol-4-yl)hepta-2,6-dienimidic acid

(2e,4r,5s,6e)-3,5-dimethoxy-4-methyl-7-(2-{2-[(2s,3e,5e)-7-methylocta-3,5-dien-2-yl]-1,3-thiazol-4-yl}-1,3-thiazol-4-yl)hepta-2,6-dienimidic acid

C25H33N3O3S2 (487.1963228)