Classification Term: 170889
Thiazole alkaloids (ontology term: 97094574b7febcb3e2e1ba8070fbb064)
found 43 associated metabolites at sub_class
metabolite taxonomy ontology rank level.
Ancestor: Serine alkaloids
Child Taxonomies: There is no child term of current ontology term.
Pyochelin
A member of the class of thiazolidines that is (4R)-3-methyl-1,3-thiazolidine-4-carboxylic acid which is substituted at position 2 by a (4R)-2-(2-hydroxyphenyl)-4,5-dihydro-1,3-thiazol-4-yl group. A siderophore that is produced by Pseudomonas aeruginosa (via condensation of salicylic acid and two molecules of cysteine) as a mixture of two easily interconvertible diastereoisomers, pyochelin I (major) and pyochelin II (minor). The enantiomeric compounds, enant-pyochelin, are produced by Pseudomonas fluorescens. D064449 - Sequestering Agents > D002614 - Chelating Agents > D007502 - Iron Chelating Agents D000890 - Anti-Infective Agents > D000935 - Antifungal Agents
Pyochelin
D064449 - Sequestering Agents > D002614 - Chelating Agents > D007502 - Iron Chelating Agents D000890 - Anti-Infective Agents > D000935 - Antifungal Agents
4-Methylaeruginoic acid
A 1,3-thiazole that is 4,5-dihydro-1,3-thiazole-4-carboxylic acid substituted by a 2-hydroxyphenyl group at position 2 and a methyl group at position 4 (the 4S stereoisomer). It is isolated from the culture broth of Streptomyces sp.KCTC9303 and exhibits potent cytotoxic activites against number of tumour cell lines.
(2r,4r)-2-[(4r)-2-(2-Hydroxyphenyl)-4,5-Dihydro-1,3-Thiazol-4-Yl]-3-Methyl-1,3-Thiazolidine-4-Carboxylic Acid
D064449 - Sequestering Agents > D002614 - Chelating Agents > D007502 - Iron Chelating Agents D000890 - Anti-Infective Agents > D000935 - Antifungal Agents
Pulicatin A
C11H13NO2S (223.06669580000002)
A natural product found in Streptomyces speciesCP32 and Streptomyces species.
Pulicatin B
C11H13NO2S (223.06669580000002)
A natural product found in Streptomyces speciesCP32.
pyochelin I
A pyochelin that has R-stereochemistry at the thioaminal centre; the diastereoisomer with S-stereochemistry at this centre is pyochelin II. Pseudomonas aeruginosa produces a mixture of pyochelin I (major) and pyochelin II (minor) via condensation of salicylic acid and two molecules of cysteine. The enantiomeric compounds, enant-pyochelin I and II, are produced by Pseudomonas fluorescens.
6,6-dichloro-3-methoxy-n,5-dimethyl-n-[2-phenyl-1-(1,3-thiazol-2-yl)ethyl]hex-2-enamide
4,4,4-trichloro-n,3-dimethyl-n-[4,4,4-trichloro-3-methyl-1-(1,3-thiazol-2-yl)butyl]butanamide
8,8,8-trichloro-2,7-dimethyl-n-[2-methyl-1-(1,3-thiazol-2-yl)propyl]octa-2,4-dienimidic acid
2-[2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-thiazol-4-yl]-3,4-dimethyl-1,3-thiazolidine-4-carboxylic acid
2-[2-(2-hydroxyphenyl)-4,5-dihydro-1,3-thiazol-4-yl]-3,4-dimethyl-1,3-thiazolidine-4-carboxylic acid
(2s,4r)-2-[(4s,5s)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-thiazol-4-yl]-3,4-dimethyl-1,3-thiazolidine-4-carboxylic acid
(2e,5s)-6,6-dichloro-3-methoxy-n,5-dimethyl-n-[(1s)-2-phenyl-1-(1,3-thiazol-2-yl)ethyl]hex-2-enamide
(4s)-2-(2-hydroxyphenyl)-4,5-dihydro-1,3-thiazole-4-carboxylic acid
C10H9NO3S (223.03031239999999)
2-[4-(hydroxymethyl)-4,5-dihydro-1,3-thiazol-2-yl]phenol
2-(2-hydroxyphenyl)-1,3-thiazole-4-carboxylic acid
(2r,4s)-2-[(4s)-2-(2-hydroxyphenyl)-4,5-dihydro-1,3-thiazol-4-yl]-3,4-dimethyl-1,3-thiazolidine-4-carboxylic acid
(7s)-8,8,8-trichloro-2,7-dimethyl-n-[(1s)-2-methyl-1-(1,3-thiazol-2-yl)propyl]octa-2,4-dienimidic acid
(4s)-2-[(4s)-2-(2-hydroxyphenyl)-4,5-dihydro-1,3-thiazol-4-yl]-3-methyl-1,3-thiazolidine-4-carboxylic acid
(2e,5s)-6,6,6-trichloro-3-methoxy-5-methyl-n-[(1s,3s)-4,4,4-trichloro-3-methyl-1-(1,3-thiazol-2-yl)butyl]hex-2-enimidic acid
4,4,4-trichloro-3-methyl-n-[4,4,4-trichloro-3-methyl-1-(1,3-thiazol-2-yl)butyl]butanimidic acid
C13H16Cl6N2OS (457.91144660000003)
(2z)-6,6,6-trichloro-3-methoxy-5-methyl-n-[4,4,4-trichloro-3-methyl-1-(1,3-thiazol-2-yl)butyl]hex-2-enimidic acid
(2e,4e)-8,8,8-trichloro-2,7-dimethyl-n-[(1s)-2-methyl-1-(1,3-thiazol-2-yl)propyl]octa-2,4-dienimidic acid
2-(2-hydroxyphenyl)-4-methyl-5h-1,3-thiazole-4-carboxylic acid
(2e,4e,7s)-8,8,8-trichloro-2,7-dimethyl-n-[(1s)-2-methyl-1-(1,3-thiazol-2-yl)propyl]octa-2,4-dienimidic acid
(2r,4r)-2-[(4s,5s)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-thiazol-4-yl]-3,4-dimethyl-1,3-thiazolidine-4-carboxylic acid
(4r)-2-(6-hydroxy-1,3-benzothiazol-2-yl)-4,5-dihydro-1,3-thiazole-4-carboxylic acid
(2e,5s)-6,6-dichloro-3-methoxy-n,5-dimethyl-n-[2-phenyl-1-(1,3-thiazol-2-yl)ethyl]hex-2-enamide
(3s)-4,4-dichloro-3-methyl-n-[(1s,3s)-4,4,4-trichloro-3-methyl-1-(1,3-thiazol-2-yl)butyl]butanimidic acid
(3s)-4,4,4-trichloro-n,3-dimethyl-n-[(1s,3s)-4,4,4-trichloro-3-methyl-1-(1,3-thiazol-2-yl)butyl]butanamide
4,4-dichloro-3-methyl-n-[4,4,4-trichloro-3-methyl-1-(1,3-thiazol-2-yl)butyl]butanimidic acid
(3s)-4,4,4-trichloro-3-methyl-n-[(1s,3s)-4,4,4-trichloro-3-methyl-1-(1,3-thiazol-2-yl)butyl]butanimidic acid
C13H16Cl6N2OS (457.91144660000003)