NCBI Taxonomy: 66431

Streptomyces thioluteus (ncbi_taxid: 66431)

found 76 associated metabolites at species taxonomy rank level.

Ancestor: Streptomyces

Child Taxonomies: none taxonomy data.

4-Aminobenzoic acid

4-aminobenzoic acid

C7H7NO2 (137.0476762)


p-Aminobenzoic acid, also known as 4-aminobenzoic acid or PABA, is an organic compound with molecular formula C7H7NO2. PABA is a white crystalline substance that is only slightly soluble in water. It consists of a benzene ring substituted with an amino group and a carboxylic acid. PABA is an essential nutrient for some bacteria and is sometimes called vitamin Bx. However, PABA is not essential for humans and it varies in its activity from other B vitamins. PABA is sometimes marketed as an essential nutrient under the premise that it can stimulate intestinal bacteria. Certain bacteria in the human intestinal tract such as E. coli generate PABA from chorismate. Humans lack the enzymes to convert PABA into folate, and therefore require folate from dietary sources such as green leafy vegetables. Although some intestinal bacteria can synthesize folate from PABA and some E. coli can synthesize folate this requires six enzymatic activities in folate synthesis which are not all done in the same bacteria. PABA used to be a common sunscreen agent until it was found to also be a sensitizer. The potassium salt of PABA is used therapeutically in fibrotic skin disorders. PABA can also be found in Acetobacter (DOI: 10.3181/00379727-52-14147). CONFIDENCE standard compound; INTERNAL_ID 1139; DATASET 20200303_ENTACT_RP_MIX499; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2913; ORIGINAL_PRECURSOR_SCAN_NO 2910 CONFIDENCE standard compound; INTERNAL_ID 1139; DATASET 20200303_ENTACT_RP_MIX499; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2878; ORIGINAL_PRECURSOR_SCAN_NO 2876 CONFIDENCE standard compound; INTERNAL_ID 1139; DATASET 20200303_ENTACT_RP_MIX499; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3022; ORIGINAL_PRECURSOR_SCAN_NO 3020 CONFIDENCE standard compound; INTERNAL_ID 1139; DATASET 20200303_ENTACT_RP_MIX499; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2902; ORIGINAL_PRECURSOR_SCAN_NO 2899 CONFIDENCE standard compound; INTERNAL_ID 1139; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3034; ORIGINAL_PRECURSOR_SCAN_NO 3032 CONFIDENCE standard compound; INTERNAL_ID 1139; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3039; ORIGINAL_PRECURSOR_SCAN_NO 3037 D - Dermatologicals > D02 - Emollients and protectives > D02B - Protectives against uv-radiation > D02BA - Protectives against uv-radiation for topical use Acquisition and generation of the data is financially supported in part by CREST/JST. Listed in the EAFUS Food Additive Database (Jan. 2001) but with no reported use KEIO_ID A043 4-Aminobenzoic acid is an intermediate in the synthesis of folic acid by bacteria, plants and fungi. 4-Aminobenzoic acid is an intermediate in the synthesis of folic acid by bacteria, plants and fungi.

   

Aureothin

2-Methoxy-3,5-dimethyl-6-[(2R,4Z)-4-[(2E)-2-methyl-3-(4-nitrophenyl)prop-2-en-1-ylidene]oxolan-2-yl]-4H-pyran-4-one

C22H23NO6 (397.1525298)


A C-nitro compound that is (3Z)-3-[(2E)-2-methyl-3-(4-nitrophenyl)prop-2-en-1-ylidene]tetrahydrofuran which is substituted by a 6-methoxy-3,5-dimethyl-4-oxo-4H-pyran-2-yl group at position 5. It is isolated from the soil bacterium, Streptomyces thioluteus and exhibits antitumor, antifungal, and insecticidal activities.

   

Hemipyocyanine

1-Hydroxyphenanzine

C12H8N2O (196.06365979999998)


CONFIDENCE standard compound; INTERNAL_ID 186

   

Questiomycin A

2-Acetylamino-(3H)-phenoxazin-3-one

C12H8N2O2 (212.0585748)


Questiomycin A, also known as 2-aminophenoxazin-3-one (APO), is found in mushrooms such as Calocybe gambosa (St Georges mushroom). 2-Aminophenoxazin-3-one is a benzoxazinoid metabolite. It was found excreted in the feces of rats that were fed a rye bread-based diet which makes this compound a potential fecal biomarker of whole grain intake (PMID: 23113707).

   

Deoxyaureothin

Deoxyaureothin

C22H25NO5 (383.173264)


A 4-pyranone that is 2-methoxy-3,5-dimethyl-4H-pyran-4-one which is substituted at position 6 by a 2,4-dimethyl-1-(p-nitrophenyl)hexa-1,3-dien-6-yl group (the E,E isomer).

   

3,6-dibenzylidenepiperazine-2,5-dione

3,6-dibenzylidenepiperazine-2,5-dione

C18H14N2O2 (290.1055224)


   

1,6-Dimethoxyphenazine

1,6-Dimethoxyphenazine

C14H12N2O2 (240.0898732)


A member of the class of phenazines that is phenazine substituted by methoxy groups at positions 1 and 6. It is a bacterial metabolite found in Streptomyces thioluteus.

   
   
   

4-Aminobenzoate

4-Aminobenzoic acid

C7H7NO2 (137.0476762)


4-Aminobenzoic acid is an intermediate in the synthesis of folic acid by bacteria, plants and fungi. 4-Aminobenzoic acid is an intermediate in the synthesis of folic acid by bacteria, plants and fungi.

   

4-Aminobenzoic acid

4-Aminobenzoic acid

C7H7NO2 (137.0476762)


D - Dermatologicals > D02 - Emollients and protectives > D02B - Protectives against uv-radiation > D02BA - Protectives against uv-radiation for topical use An aminobenzoic acid in which the amino group is para to the carboxy group. 4-Aminobenzoic acid is an intermediate in the synthesis of folic acid by bacteria, plants and fungi. 4-Aminobenzoic acid is an intermediate in the synthesis of folic acid by bacteria, plants and fungi.

   

4-Aminobenzoic acid

4-Aminobenzoic acid

C7H6NO2 (136.0398516)


   
   
   

2-Amino-3H-phenoxazin-3-one

2-Amino-3H-phenoxazin-3-one

C12H8N2O2 (212.0585748)


   

(3r)-n-{[(2s,5s,6r)-6-hydroxy-5-{[(3r)-1-hydroxy-3-isocyanobutylidene]amino}oxan-2-yl]methyl}-3-isocyanobutanimidic acid

(3r)-n-{[(2s,5s,6r)-6-hydroxy-5-{[(3r)-1-hydroxy-3-isocyanobutylidene]amino}oxan-2-yl]methyl}-3-isocyanobutanimidic acid

C16H24N4O4 (336.1797464)


   

n-{4-methyl-5-oxo-[1,2]dithiolo[4,3-b]pyrrol-6-yl}propanimidic acid

n-{4-methyl-5-oxo-[1,2]dithiolo[4,3-b]pyrrol-6-yl}propanimidic acid

C9H10N2O2S2 (242.018368)


   

2-amino-3-oxophenoxazine-1-carboxylic acid

2-amino-3-oxophenoxazine-1-carboxylic acid

C13H8N2O4 (256.0484048)


   

(3z,6z)-bis(phenylmethylidene)pyrazine-2,5-diol

(3z,6z)-bis(phenylmethylidene)pyrazine-2,5-diol

C18H14N2O2 (290.1055224)


   

(3r)-n-[(2s)-1-(acetyloxy)-6-{[(3r)-1-hydroxy-3-isocyanobutylidene]amino}hexan-2-yl]-3-isocyanobutanimidic acid

(3r)-n-[(2s)-1-(acetyloxy)-6-{[(3r)-1-hydroxy-3-isocyanobutylidene]amino}hexan-2-yl]-3-isocyanobutanimidic acid

C18H28N4O4 (364.2110448)


   

5-hydroxy-3-[(4-methoxyphenyl)methylidene]-6-(phenylmethylidene)-1h-pyrazin-2-one

5-hydroxy-3-[(4-methoxyphenyl)methylidene]-6-(phenylmethylidene)-1h-pyrazin-2-one

C19H16N2O3 (320.1160866)


   

5-hydroxy-3,6-bis[(4-methoxyphenyl)methylidene]-1h-pyrazin-2-one

5-hydroxy-3,6-bis[(4-methoxyphenyl)methylidene]-1h-pyrazin-2-one

C20H18N2O4 (350.1266508)


   

2-[(1e,3e,5e)-3,5-dimethyl-6-(4-nitrophenyl)hexa-1,3,5-trien-1-yl]-6-methoxy-3,5-dimethylpyran-4-one

2-[(1e,3e,5e)-3,5-dimethyl-6-(4-nitrophenyl)hexa-1,3,5-trien-1-yl]-6-methoxy-3,5-dimethylpyran-4-one

C22H23NO5 (381.15761480000003)


   

2-[(2-hydroxyethyl)amino]phenoxazin-3-one

2-[(2-hydroxyethyl)amino]phenoxazin-3-one

C14H12N2O3 (256.0847882)


   

2-methoxy-3,5-dimethyl-6-[(2r,5z)-5-[(2e)-2-methyl-3-(4-nitrophenyl)prop-2-en-1-ylidene]oxolan-2-yl]pyran-4-one

2-methoxy-3,5-dimethyl-6-[(2r,5z)-5-[(2e)-2-methyl-3-(4-nitrophenyl)prop-2-en-1-ylidene]oxolan-2-yl]pyran-4-one

C22H23NO6 (397.1525298)


   

(3z,6z)-3-[(4-methoxyphenyl)methylidene]-6-(phenylmethylidene)pyrazine-2,5-diol

(3z,6z)-3-[(4-methoxyphenyl)methylidene]-6-(phenylmethylidene)pyrazine-2,5-diol

C19H16N2O3 (320.1160866)


   

2-methoxy-3,5-dimethyl-6-{5-[2-methyl-3-(4-nitrophenyl)prop-2-en-1-ylidene]oxolan-2-yl}pyran-4-one

2-methoxy-3,5-dimethyl-6-{5-[2-methyl-3-(4-nitrophenyl)prop-2-en-1-ylidene]oxolan-2-yl}pyran-4-one

C22H23NO6 (397.1525298)


   

bis(phenylmethylidene)pyrazine-2,5-diol

bis(phenylmethylidene)pyrazine-2,5-diol

C18H14N2O2 (290.1055224)


   

(3z,6z)-bis[(4-methoxyphenyl)methylidene]pyrazine-2,5-diol

(3z,6z)-bis[(4-methoxyphenyl)methylidene]pyrazine-2,5-diol

C20H18N2O4 (350.1266508)


   

(3r)-n-[(2s)-1-hydroxy-6-{[(3r)-1-hydroxy-3-isocyanobutylidene]amino}hexan-2-yl]-3-isocyanobutanimidic acid

(3r)-n-[(2s)-1-hydroxy-6-{[(3r)-1-hydroxy-3-isocyanobutylidene]amino}hexan-2-yl]-3-isocyanobutanimidic acid

C16H26N4O3 (322.2004806)


   

2-[(3e,5e)-3,5-dimethyl-6-(4-nitrophenyl)hexa-3,5-dien-1-yl]-6-methoxy-3,5-dimethylpyran-4-one

2-[(3e,5e)-3,5-dimethyl-6-(4-nitrophenyl)hexa-3,5-dien-1-yl]-6-methoxy-3,5-dimethylpyran-4-one

C22H25NO5 (383.173264)


   

(2e)-3-{8,11-dihydroxy-12-methyl-2-oxo-3,9-diazatricyclo[8.4.0.0³,⁷]tetradeca-1(10),5,11,13-tetraen-5-yl}-n-methylprop-2-enimidic acid

(2e)-3-{8,11-dihydroxy-12-methyl-2-oxo-3,9-diazatricyclo[8.4.0.0³,⁷]tetradeca-1(10),5,11,13-tetraen-5-yl}-n-methylprop-2-enimidic acid

C17H19N3O4 (329.1375494)


   

(3r)-n-[(2s)-6-{[(3r)-1-hydroxy-3-isocyanobutylidene]amino}-1-oxohexan-2-yl]-3-isocyanobutanimidic acid

(3r)-n-[(2s)-6-{[(3r)-1-hydroxy-3-isocyanobutylidene]amino}-1-oxohexan-2-yl]-3-isocyanobutanimidic acid

C16H24N4O3 (320.1848314)


   

6-hydroxy-5h-phenazin-1-one

6-hydroxy-5h-phenazin-1-one

C12H8N2O2 (212.0585748)