NCBI Taxonomy: 5523

Fusarium lateritium (ncbi_taxid: 5523)

found 43 associated metabolites at species taxonomy rank level.

Ancestor: Fusarium lateritium species complex

Child Taxonomies: Fusarium lateritium f. mori, Fusarium lateritium var. buxi, Fusarium lateritium var. majus, Fusarium lateritium var. longum, Fusarium lateritium f. sp. celosiae, Fusarium lateritium var. lateritium

Picolinic acid

5-Aminopyridine-2-carboxylic acid

C6H5NO2 (123.032027)


Picolinic acid is a metabolite of the tryptophan catabolism. Picolinic acid is produced under inflammatory conditions and a costimulus with interferon-gamma (IFNgamma) of macrophage (Mphi) effector functions, is a selective inducer of the Mphi inflammatory protein-1alpha (MIP-1alpha) and -1beta (MIPs), two chemokines/cytokines involved in the elicitation of the inflammatory reactions and in the development of the Th1 responses. IFNgamma and picolinic acid have reciprocal effects on the production of MIPs chemokines and the expression of their receptor. The concerted action of IFNgamma and picolinic acid on MIP-1alpha/beta chemokine/receptor system is likely to be of pathophysiological significance and to represent an important regulatory mechanism for leukocyte recruitment and distribution into damaged tissues during inflammatory responses. Picolinic acid has an effect on the production of L-arginine-derived reactive nitrogen intermediates in macrophages, by augmenting IFN-gamma-induced NO2- production, and acts synergistically with IFN-gamma in activating macrophages. Children with acrodermatitis enteropathica (AE) are treated with oral zinc dipicolinate (zinc-PA). The concentration of picolinic acid in the plasma of asymptomatic children with AE was significantly less than that of normal children. However, oral treatment with PA alone is ineffective. The results support the hypothesis that the genetic defect in AE is in the tryptophan pathway, although the role of PA in zinc metabolism remains to be defined. (PMID:15206716, 8473748, 1701787, 6694049). Picolinic acid is a metabolite of the tryptophan catabolism. Picolinic acid is produced under inflammatory conditions and a costimulus with interferon-gamma (IFNgamma) of macrophage (Mphi) effector functions, is a selective inducer of the Mphi inflammatory protein-1alpha (MIP-1alpha) and -1beta (MIPs), two chemokines/cytokines involved in the elicitation of the inflammatory reactions and in the development of the Th1 responses. IFNgamma and picolinic acid have reciprocal effects on the production of MIPs chemokines and the expression of their receptor. The concerted action of IFNgamma and picolinic acid on MIP-1alpha/beta chemokine/receptor system is likely to be of pathophysiological significance and to represent an important regulatory mechanism for leukocyte recruitment and distribution into damaged tissues during inflammatory responses. Picolinic acid has an effect on the production of L-arginine-derived reactive nitrogen intermediates in macrophages, by augmenting IFN-gamma-induced NO2- production, and acts synergistically with IFN-gamma in activating macrophages. D064449 - Sequestering Agents > D002614 - Chelating Agents > D007502 - Iron Chelating Agents [Raw Data] CBA16_Picolinic-acid_pos_10eV_1-8_01_816.txt [Raw Data] CBA16_Picolinic-acid_pos_20eV_1-8_01_817.txt KEIO_ID P045 Picolinic acid (PCL 016) is a topical antiviral agent, which inhibits adenovirus replication in rabbits.

   

Enniatin B

Enniatin B

C33H57N3O9 (639.4094592)


An enniatin obtained from formal cyclocondensation of three N-[(2R)-2-hydroxy-3-methylbutanoyl]-N-methyl-L-valine units. D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents CONFIDENCE Reference Standard (Level 1)

   

Enniatin B

4,10,16-trimethyl-3,6,9,12,15,18-hexakis(propan-2-yl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

C33H57N3O9 (639.4094592)


   

Bassiatin

(3S-trans)-4-Methyl-6-(1-methylethyl)-3-(phenylmethyl)-2,5-morpholinedione

C15H19NO3 (261.13648639999997)


A member of the class of morpholines that is morpholine-2,5-dione substituted by a benzyl, isopropyl and a methyl group at positions 3, 6 and 4 respectively. It is isolated from the culture broth of the fungus Beauveria bassiana and acts as a platelet aggregation inhibitor.

   

picolinic acid

2-Pyridinecarboxylic acid

C6H5NO2 (123.032027)


A pyridinemonocarboxylic acid in which the carboxy group is located at position 2. It is an intermediate in the metabolism of tryptophan. D064449 - Sequestering Agents > D002614 - Chelating Agents > D007502 - Iron Chelating Agents Picolinic acid (PCL 016) is a topical antiviral agent, which inhibits adenovirus replication in rabbits.

   

1-(4-hydroxyquinazolin-2-yl)ethanone

1-(4-hydroxyquinazolin-2-yl)ethanone

C10H8N2O2 (188.0585748)


   

(3r,6r,9s,12r,15s,18r)-3-[(2r)-butan-2-yl]-9-[(2s)-butan-2-yl]-6,12,15,18-tetraisopropyl-4,10,16-trimethyl-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

(3r,6r,9s,12r,15s,18r)-3-[(2r)-butan-2-yl]-9-[(2s)-butan-2-yl]-6,12,15,18-tetraisopropyl-4,10,16-trimethyl-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

C35H61N3O9 (667.4407576)


   

3,6,12,18-tetraisopropyl-4,10,16-trimethyl-9,15-bis(sec-butyl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

3,6,12,18-tetraisopropyl-4,10,16-trimethyl-9,15-bis(sec-butyl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

C35H61N3O9 (667.4407576)


   
   

3,6,9,12,18-pentaisopropyl-4,10,16-trimethyl-15-(sec-butyl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

3,6,9,12,18-pentaisopropyl-4,10,16-trimethyl-15-(sec-butyl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

C34H59N3O9 (653.4251084)


   

5-hydroxy-9-methoxy-2-methyl-4,6-dioxopyrano[3,4-g]chromene-8-carboxylic acid

5-hydroxy-9-methoxy-2-methyl-4,6-dioxopyrano[3,4-g]chromene-8-carboxylic acid

C15H10O8 (318.037566)


   

(3r,6r,9s,12r,15s,18r)-3,6,9,12,15,18-hexaisopropyl-4,10,16-trimethyl-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

(3r,6r,9s,12r,15s,18r)-3,6,9,12,15,18-hexaisopropyl-4,10,16-trimethyl-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

C33H57N3O9 (639.4094592)


   

(3s,6r,9s,12r,15r,18r)-3-[(2s)-butan-2-yl]-6,9,12,15,18-pentaisopropyl-4,10,16-trimethyl-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

(3s,6r,9s,12r,15r,18r)-3-[(2s)-butan-2-yl]-6,9,12,15,18-pentaisopropyl-4,10,16-trimethyl-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

C34H59N3O9 (653.4251084)


   

(3r,6r)-3-benzyl-6-isopropyl-4-methylmorpholine-2,5-dione

(3r,6r)-3-benzyl-6-isopropyl-4-methylmorpholine-2,5-dione

C15H19NO3 (261.13648639999997)


   

3-benzyl-6-isopropyl-4-methylmorpholine-2,5-dione

3-benzyl-6-isopropyl-4-methylmorpholine-2,5-dione

C15H19NO3 (261.13648639999997)