NCBI Taxonomy: 1763

Mycobacterium (ncbi_taxid: 1763)

found 27 associated metabolites at genus taxonomy rank level.

Ancestor: Mycobacteriaceae

Child Taxonomies: Mycobacterium lufu, Mycobacterium lactis, Mycobacterium leprae, Mycobacterium cookii, Mycobacterium gastri, Mycobacterium xenopi, Mycobacterium celatum, Mycobacterium szulgai, Mycobacterium buckleii, Mycobacterium branderi, Mycobacterium kansasii, Mycobacterium gordonae, Mycobacterium hyorhinis, Mycobacterium bohemicum, Mycobacterium shimoidei, Mycobacterium tilburgii, Mycobacterium malmoense, Mycobacterium asiaticum, Mycobacterium novum, Mycobacterium lacus, Mycobacterium album, Mycobacterium gallinarum, Mycobacterium columbarii, Mycobacterium isoniacini, Mycobacterium conspicuum, Mycobacterium uberis, Mycobacterium fragae, Mycobacterium sacrum, Mycobacterium haemophilum, environmental samples, Mycobacterium deserti, Mycobacterium aemonae, Mycobacterium alsense, Mycobacterium paraffinicum, Mycobacterium scrofulaceum, Mycobacterium visibile, Mycobacterium savoniae, Mycobacterium spongiae, Mycobacterium piscinum, Mycobacterium persicum, Mycobacterium eburneum, Mycobacterium simulans, Mycobacterium jacuzzii, Mycobacterium albicans, Mycobacterium adipatum, Mycobacterium uekiense, Mycobacterium innocens, Mycobacterium kuopiense, Mycobacterium lehmannii, Mycobacterium neumannii, Mycobacterium neglectum, Mycobacterium kiyosense, Mycobacterium decipiens, Mycobacterium angelicum, Mycobacterium seoulense, Mycobacterium kyogaense, Mycobacterium aquaticum, Mycobacterium botniense, Mycobacterium talmoniae, Mycobacterium lacticola, Mycobacterium salfingeri, Mycobacterium basiliense, Mycobacterium riyadhense, Mycobacterium helveticum, Mycobacterium kyorinense, Mycobacterium hippophais, Mycobacterium suricattae, Mycobacterium paraterrae, Mycobacterium barrassiae, Mycobacterium attenuatum, Mycobacterium aquiterrae, Mycobacterium chesapeaki, Mycobacterium siernhoferi, Mycobacterium fuerthensis, Mycobacterium nebraskense, Mycobacterium yunnanensis, Mycobacterium bourgelatii, Mycobacterium ostraviense, unclassified Mycobacterium, Mycobacterium noviomagense, Mycobacterium shinjukuense, Mycobacterium brasiliensis, Mycobacterium paragordonae, Mycobacterium lepromatosis, Mycobacterium sydneyiensis, Mycobacterium paraseoulense, Mycobacterium anthracenicum, Mycobacterium hackensackense, Mycobacterium vicinigordonae, Mycobacterium simiae complex, Mycobacterium heckeshornense, Mycobacterium pseudokansasii, Mycobacterium ulcerans group, Mycobacterium syngnathidarum, Mycobacterium petroleophilum, Mycobacterium dioxanotrophicus, Mycobacterium terramassiliense, Mycobacterium rhizamassiliense, Mycobacterium numidiamassiliense, Mycobacterium avium complex (MAC), Mycobacterium tuberculosis complex, Candidatus Mycobacterium wuenschmannii, Candidatus Mycobacterium methanotrophicum, Mycobacterium cf. xenopi 'Hymi_Wue Tb_939/99'

Muramic acid

(2R)-2-{[(2R,3R,4S,5S,6R)-3-amino-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy}propanoic acid

C9H17NO7 (251.1004972)


Muramic acid is an amino sugar acid. In terms of chemical composition, it is the ether of lactic acid and glucosamine. It occurs naturally as N-acetylmuramic acid in peptidoglycan, whose primary function is a structural component of many typical bacterial cell walls. Muramic acid, also known as muramate or murexide, belongs to the class of organic compounds known as sugar acids and derivatives. Sugar acids and derivatives are compounds containing a saccharide unit which bears a carboxylic acid group. Muramic acid is an amino sugar acid. It occurs naturally as N-acetylmuramic acid in peptidoglycan, whose primary function is a structural component of many typical bacterial cell walls. In terms of chemical composition, it is the ether of lactic acid and glucosamine. Muramic acid is a marker of bacterial peptidoglycan, in environmental and clinical specimens. (PMID: 10778926) [HMDB] Muramic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=1114-41-6 (retrieved 2024-07-01) (CAS RN: 1114-41-6). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

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.

   

6-Methylsalicylic acid

2-HYDROXY-6-METHYLBENZOIC ACID

C8H8O3 (152.0473418)


A monohydroxybenzoic acid that is salicylic acid in which the hydrogen ortho to the carboxylic acid group is substituted by a methyl group. D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates

   

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

   

2-(3,7,12,16,20,24-Hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaenyl)-1,3,3-trimethylcyclohexene

2-(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)


   

zeta-Carotene

7,8,7,8-Tetrahydro-psi-psi-carotene

C40H60 (540.469476)


D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids 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. Window width to select the precursor ion was 3 Da.; CONE_VOLTAGE is 5 V.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 19HP8024 to the Mass Spectrometry Society of Japan.

   
   

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.

   

Neurosporene

Neurosporene

C40H58 (538.4538268)


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

   

(8z)-9-{hydroxy[(5s)-6-{[(1r,2s)-1-{[(3s)-1-hydroxy-2-oxoazepan-3-yl]-c-hydroxycarbonimidoyl}-1-methylbutan-2-yl]oxy}-5-({hydroxy[(4r,5r)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]methylidene}amino)-6-oxohexyl]carbamoyl}non-8-enoic acid

(8z)-9-{hydroxy[(5s)-6-{[(1r,2s)-1-{[(3s)-1-hydroxy-2-oxoazepan-3-yl]-c-hydroxycarbonimidoyl}-1-methylbutan-2-yl]oxy}-5-({hydroxy[(4r,5r)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]methylidene}amino)-6-oxohexyl]carbamoyl}non-8-enoic acid

C39H57N5O12 (787.4003521999999)


   

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

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

C40H54O (550.4174434)


   

11-{hydroxy[6-({1-[(1-hydroxy-2-oxoazepan-3-yl)-c-hydroxycarbonimidoyl]-1-methylbutan-2-yl}oxy)-5-({hydroxy[2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]methylidene}amino)-6-oxohexyl]carbamoyl}undec-10-enoic acid

11-{hydroxy[6-({1-[(1-hydroxy-2-oxoazepan-3-yl)-c-hydroxycarbonimidoyl]-1-methylbutan-2-yl}oxy)-5-({hydroxy[2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]methylidene}amino)-6-oxohexyl]carbamoyl}undec-10-enoic acid

C41H61N5O12 (815.4316506)


   

3,4,5-trihydroxy-6-{[1,3,4,5-tetrahydroxy-1-(4-hydroxy-2-imino-1h-pteridin-6-yl)pentan-2-yl]oxy}oxane-2-carboxylic acid

3,4,5-trihydroxy-6-{[1,3,4,5-tetrahydroxy-1-(4-hydroxy-2-imino-1h-pteridin-6-yl)pentan-2-yl]oxy}oxane-2-carboxylic acid

C17H23N5O12 (489.1343158)


   

(4r,6s)-6-decyl-3-methylidene-2-oxooxane-4-carboxylic acid

(4r,6s)-6-decyl-3-methylidene-2-oxooxane-4-carboxylic acid

C17H28O4 (296.19874880000003)


   

3-(4-hydroxy-2-imino-6-oxo-1,5-dihydropteridin-7-yl)-2-oxopropanoic acid

3-(4-hydroxy-2-imino-6-oxo-1,5-dihydropteridin-7-yl)-2-oxopropanoic acid

C9H7N5O5 (265.04471720000004)


   

12-(7,9-dihydroxy-4,6-dimethyldec-4-en-2-yl)-7,9-dimethyl-2-oxo-1-oxacyclododec-9-en-6-yl 12,13,15-trihydroxy-2,4,6,10-tetramethylhexadeca-2,4,6,8,10-pentaenoate

12-(7,9-dihydroxy-4,6-dimethyldec-4-en-2-yl)-7,9-dimethyl-2-oxo-1-oxacyclododec-9-en-6-yl 12,13,15-trihydroxy-2,4,6,10-tetramethylhexadeca-2,4,6,8,10-pentaenoate

C45H72O9 (756.5176062)


   

(10z)-11-{hydroxy[6-({1-[(1-hydroxy-2-oxoazepan-3-yl)-c-hydroxycarbonimidoyl]-1-methylbutan-2-yl}oxy)-5-({hydroxy[2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]methylidene}amino)-6-oxohexyl]carbamoyl}undec-10-enoic acid

(10z)-11-{hydroxy[6-({1-[(1-hydroxy-2-oxoazepan-3-yl)-c-hydroxycarbonimidoyl]-1-methylbutan-2-yl}oxy)-5-({hydroxy[2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]methylidene}amino)-6-oxohexyl]carbamoyl}undec-10-enoic acid

C41H61N5O12 (815.4316506)


   

9-({5-[(1,3-dihydroxy-2-{[hydroxy(2-hydroxyphenyl)methylidene]amino}butylidene)amino]-6-({1-[(1-hydroxy-2-oxoazepan-3-yl)-c-hydroxycarbonimidoyl]-1-methylbutan-2-yl}oxy)-6-oxohexyl}(hydroxy)carbamoyl)non-8-enoic acid

9-({5-[(1,3-dihydroxy-2-{[hydroxy(2-hydroxyphenyl)methylidene]amino}butylidene)amino]-6-({1-[(1-hydroxy-2-oxoazepan-3-yl)-c-hydroxycarbonimidoyl]-1-methylbutan-2-yl}oxy)-6-oxohexyl}(hydroxy)carbamoyl)non-8-enoic acid

C39H59N5O13 (805.4109164)


   

(2r)-n-[(2r,3r,4r,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[(1s,2r,3r,4r,5s,6s)-2,3,4,5,6-pentahydroxycyclohexyl]oxy}oxan-3-yl]-2-[(1-hydroxyethylidene)amino]-3-sulfanylpropanimidic acid

(2r)-n-[(2r,3r,4r,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[(1s,2r,3r,4r,5s,6s)-2,3,4,5,6-pentahydroxycyclohexyl]oxy}oxan-3-yl]-2-[(1-hydroxyethylidene)amino]-3-sulfanylpropanimidic acid

C17H30N2O12S (486.15193800000003)


   

1-{4-[(4-{[5-hydroxy-4-({5-hydroxy-4-[(4-hydroxy-5-methoxy-6-methyloxan-2-yl)oxy]-3-methoxy-6-methyloxan-2-yl}oxy)-3-methoxy-6-methyloxan-2-yl]oxy}-3,5-dimethoxy-6-methyloxan-2-yl)oxy]phenyl}-10-methoxy-9-methyl-2-[(2-methylpentanoyl)oxy]dodecan-4-yl 2-methylpentanoate

1-{4-[(4-{[5-hydroxy-4-({5-hydroxy-4-[(4-hydroxy-5-methoxy-6-methyloxan-2-yl)oxy]-3-methoxy-6-methyloxan-2-yl}oxy)-3-methoxy-6-methyloxan-2-yl]oxy}-3,5-dimethoxy-6-methyloxan-2-yl)oxy]phenyl}-10-methoxy-9-methyl-2-[(2-methylpentanoyl)oxy]dodecan-4-yl 2-methylpentanoate

C61H104O21 (1172.7069734)


   

(6z)-7-{hydroxy[6-({1-[(1-hydroxy-2-oxoazepan-3-yl)-c-hydroxycarbonimidoyl]-1-methylbutan-2-yl}oxy)-5-({hydroxy[2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]methylidene}amino)-6-oxohexyl]carbamoyl}hept-6-enoic acid

(6z)-7-{hydroxy[6-({1-[(1-hydroxy-2-oxoazepan-3-yl)-c-hydroxycarbonimidoyl]-1-methylbutan-2-yl}oxy)-5-({hydroxy[2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]methylidene}amino)-6-oxohexyl]carbamoyl}hept-6-enoic acid

C37H53N5O12 (759.3690538)


   

(6s,7s,9e,12r)-12-[(2s,4e,6r,7r,9r)-7,9-dihydroxy-4,6-dimethyldec-4-en-2-yl]-7,9-dimethyl-2-oxo-1-oxacyclododec-9-en-6-yl (2e,4e,6e,8e,11r)-11-hydroxy-4,6,8-trimethyl-13-oxopentadeca-2,4,6,8-tetraenoate

(6s,7s,9e,12r)-12-[(2s,4e,6r,7r,9r)-7,9-dihydroxy-4,6-dimethyldec-4-en-2-yl]-7,9-dimethyl-2-oxo-1-oxacyclododec-9-en-6-yl (2e,4e,6e,8e,11r)-11-hydroxy-4,6,8-trimethyl-13-oxopentadeca-2,4,6,8-tetraenoate

C43H68O8 (712.4913928000001)


   

1-methyl-4-(6,10,14,18,22-pentamethyltricosa-1,5,9,13-tetraen-2-yl)cyclohex-1-ene

1-methyl-4-(6,10,14,18,22-pentamethyltricosa-1,5,9,13-tetraen-2-yl)cyclohex-1-ene

C35H60 (480.469476)


   

2-methyl-3-(3,7,10,14,18,22,26,30,34-nonamethylhexatriaconta-2,9,13,17,21,25,29,33-octaen-1-yl)naphthalene-1,4-dione

2-methyl-3-(3,7,10,14,18,22,26,30,34-nonamethylhexatriaconta-2,9,13,17,21,25,29,33-octaen-1-yl)naphthalene-1,4-dione

C56H82O2 (786.6314472)


   

10-({5-[(1,3-dihydroxy-2-{[hydroxy(2-hydroxyphenyl)methylidene]amino}butylidene)amino]-6-({1-[(1-hydroxy-2-oxoazepan-3-yl)-c-hydroxycarbonimidoyl]-1-methylbutan-2-yl}oxy)-6-oxohexyl}(hydroxy)carbamoyl)dec-9-enoic acid

10-({5-[(1,3-dihydroxy-2-{[hydroxy(2-hydroxyphenyl)methylidene]amino}butylidene)amino]-6-({1-[(1-hydroxy-2-oxoazepan-3-yl)-c-hydroxycarbonimidoyl]-1-methylbutan-2-yl}oxy)-6-oxohexyl}(hydroxy)carbamoyl)dec-9-enoic acid

C40H61N5O13 (819.4265656)


   

(2s,3r)-n-[(3s)-1-hydroxy-2-oxoazepan-3-yl]-3-{[(2s)-2-({hydroxy[(4s,5r)-5-methyl-2-[(1z)-6-oxocyclohexa-2,4-dien-1-ylidene]-1,3-oxazolidin-4-yl]methylidene}amino)-6-[(2z)-n-hydroxyhexadec-2-enamido]hexanoyl]oxy}-2-methylpentanimidic acid

(2s,3r)-n-[(3s)-1-hydroxy-2-oxoazepan-3-yl]-3-{[(2s)-2-({hydroxy[(4s,5r)-5-methyl-2-[(1z)-6-oxocyclohexa-2,4-dien-1-ylidene]-1,3-oxazolidin-4-yl]methylidene}amino)-6-[(2z)-n-hydroxyhexadec-2-enamido]hexanoyl]oxy}-2-methylpentanimidic acid

C45H71N5O10 (841.5200666)