Metabolites

Displaying 451 - 500 of 855

Search Library articles
Drupal spam blocked by CleanTalk.
Metabolite Produced by (Species) Molecular weightsort ascending References Structure image
aflatoxin G1 A. arachidicola 328.28
  1. http://pubchem.ncbi.nlm.nih.gov/compound/14421
  2. http://www.ncbi.nlm.nih.gov/pubmed/6778015
  3. http://download.springer.com/static/pdf/301/art%253A10.1007%252FBF01087128.pdf
aflatoxin G1 A. flavus 328.28
  1. http://pubchem.ncbi.nlm.nih.gov/compound/14421
  2. http://www.ncbi.nlm.nih.gov/pubmed/6778015
  3. http://download.springer.com/static/pdf/301/art%253A10.1007%252FBF01087128.pdf
aflatoxin Q1 A. flavus 328
  1. http://pubchem.ncbi.nlm.nih.gov/compound/104757
  2. http://ci.nii.ac.jp/openurl/query
  3. http://www.sciencedirect.com/science/article/pii/S0040402001827216
Gliotoxin Aspergillus sp. HT-2 326.39
  1. Pubchem
  2. The nature of the antibiotic substances produced by Aspergillus fumigatus.
  3. A preliminary note on the antibacterial substance from Aspergillus flavus
  4. Gliotoxin from Aspergillus chevalieri.
  5. Aspergillin PZ, a Novel Isoindole-alkaloid from Aspergillus awamori
  6. Production of mycotoxins by Aspergillus lentulus and other medically important and closely related species in section Fumigati.
  7. Determination of optimum growth conditions for gliotoxin production by Aspergillus fumigatus and development of a novel method f
Gliotoxin A. sydowii 326.39
  1. Pubchem
  2. The nature of the antibiotic substances produced by Aspergillus fumigatus.
  3. A preliminary note on the antibacterial substance from Aspergillus flavus
  4. Gliotoxin from Aspergillus chevalieri.
  5. Aspergillin PZ, a Novel Isoindole-alkaloid from Aspergillus awamori
  6. Production of mycotoxins by Aspergillus lentulus and other medically important and closely related species in section Fumigati.
  7. Determination of optimum growth conditions for gliotoxin production by Aspergillus fumigatus and development of a novel method f
Gliotoxin A. niger 326.39
  1. Pubchem
  2. The nature of the antibiotic substances produced by Aspergillus fumigatus.
  3. A preliminary note on the antibacterial substance from Aspergillus flavus
  4. Gliotoxin from Aspergillus chevalieri.
  5. Aspergillin PZ, a Novel Isoindole-alkaloid from Aspergillus awamori
  6. Production of mycotoxins by Aspergillus lentulus and other medically important and closely related species in section Fumigati.
  7. Determination of optimum growth conditions for gliotoxin production by Aspergillus fumigatus and development of a novel method f
Gliotoxin A. fumigatus 326.39
  1. Pubchem
  2. The nature of the antibiotic substances produced by Aspergillus fumigatus.
  3. A preliminary note on the antibacterial substance from Aspergillus flavus
  4. Gliotoxin from Aspergillus chevalieri.
  5. Aspergillin PZ, a Novel Isoindole-alkaloid from Aspergillus awamori
  6. Production of mycotoxins by Aspergillus lentulus and other medically important and closely related species in section Fumigati.
  7. Determination of optimum growth conditions for gliotoxin production by Aspergillus fumigatus and development of a novel method f
Gliotoxin A. flavus 326.39
  1. Pubchem
  2. The nature of the antibiotic substances produced by Aspergillus fumigatus.
  3. A preliminary note on the antibacterial substance from Aspergillus flavus
  4. Gliotoxin from Aspergillus chevalieri.
  5. Aspergillin PZ, a Novel Isoindole-alkaloid from Aspergillus awamori
  6. Production of mycotoxins by Aspergillus lentulus and other medically important and closely related species in section Fumigati.
  7. Determination of optimum growth conditions for gliotoxin production by Aspergillus fumigatus and development of a novel method f
Gliotoxin A. chevalieri 326.39
  1. Pubchem
  2. The nature of the antibiotic substances produced by Aspergillus fumigatus.
  3. A preliminary note on the antibacterial substance from Aspergillus flavus
  4. Gliotoxin from Aspergillus chevalieri.
  5. Aspergillin PZ, a Novel Isoindole-alkaloid from Aspergillus awamori
  6. Production of mycotoxins by Aspergillus lentulus and other medically important and closely related species in section Fumigati.
  7. Determination of optimum growth conditions for gliotoxin production by Aspergillus fumigatus and development of a novel method f
Gliotoxin A. awamori 326.39
  1. Pubchem
  2. The nature of the antibiotic substances produced by Aspergillus fumigatus.
  3. A preliminary note on the antibacterial substance from Aspergillus flavus
  4. Gliotoxin from Aspergillus chevalieri.
  5. Aspergillin PZ, a Novel Isoindole-alkaloid from Aspergillus awamori
  6. Production of mycotoxins by Aspergillus lentulus and other medically important and closely related species in section Fumigati.
  7. Determination of optimum growth conditions for gliotoxin production by Aspergillus fumigatus and development of a novel method f
Gliotoxin Neosartorya pseudofischeri 326.39
  1. Pubchem
  2. The nature of the antibiotic substances produced by Aspergillus fumigatus.
  3. A preliminary note on the antibacterial substance from Aspergillus flavus
  4. Gliotoxin from Aspergillus chevalieri.
  5. Aspergillin PZ, a Novel Isoindole-alkaloid from Aspergillus awamori
  6. Production of mycotoxins by Aspergillus lentulus and other medically important and closely related species in section Fumigati.
  7. Determination of optimum growth conditions for gliotoxin production by Aspergillus fumigatus and development of a novel method f
Dihydrosterigmatocystin A. versicolor 326.30
  1. Pubchem
  2. Mycological chemistry. VII. Sterigmatocystin, a metabolite of Aspergillus versicolor (Vuillemin) Tiraboschi.
Dihydrosterigmatocystin Emericella corrugata 326.30
  1. Pubchem
  2. Mycological chemistry. VII. Sterigmatocystin, a metabolite of Aspergillus versicolor (Vuillemin) Tiraboschi.
Dihydrosterigmatocystin Emericella quadrilineata 326.30
  1. Pubchem
  2. Mycological chemistry. VII. Sterigmatocystin, a metabolite of Aspergillus versicolor (Vuillemin) Tiraboschi.
Dihydrosterigmatocystin Emericella rugulosa 326.30
  1. Pubchem
  2. Mycological chemistry. VII. Sterigmatocystin, a metabolite of Aspergillus versicolor (Vuillemin) Tiraboschi.
Dihydrosterigmatocystin Emericella striata 326.30
  1. Pubchem
  2. Mycological chemistry. VII. Sterigmatocystin, a metabolite of Aspergillus versicolor (Vuillemin) Tiraboschi.
9-deacetylfumigaclavine C A. fumigatus 324.45982
  1. http://pubs.acs.org/doi/abs/10.1021/np800700e
  2. http://pubchem.ncbi.nlm.nih.gov/compound/42640472
  3. http://www.ncbi.nlm.nih.gov/pubmed/19256529
Phthalide or chromanol (7) A. duricaulis 324.33
  1. Highly substituted chromanols from cultures of Aspergillus duricaulis.
sterigmatocystin sterigmatocystin 324.284
  1. http://pubchem.ncbi.nlm.nih.gov/compound/5280389
Asperxanthone Aspergillus sp. (MF-93) 324.28
  1. http://onlinelibrary.wiley.com/doi/10.1002/ps.1645/abstract
Sterigmatocystin A. versicolor 324.28
  1. Link
Cryptoechinuline C A. amstelodami 323.35
  1. Stereochemical course of the α,​β-​desaturation of L-​tryptophan in the biosynthesis of cryptoechinuline A in Aspergillus amstel
Monacolin L β-hydroxy acid A. terreus 323.2245
  1. Culture-based and sequence-based insights into biosynthesis of secondary metabolites by Aspergillus terreus ATCC 20542
asnipyrone A A. niger 322.397
  1. http://pubchem.ncbi.nlm.nih.gov/compound/53483955
  2. http://pubs.acs.org/doi/pdf/10.1021/np200381u
  3. http://www.heterocycles.jp/newlibrary/downloads/PDF/03580/28/2
6-Deoxyversicolorin A A. versicolor 322
  1. https://www.jstage.jst.go.jp/article/bcsj1926/52/3/52_3_677/_article
  2. http://pubchem.ncbi.nlm.nih.gov/compound/147356
brevianamide M A. versicolor 321.33
  1. Brevianamide J, A New Indole Alkaloid Dimer from Fungus Aspergillus versicolor
  2. Secondary metabolites from an algicolous Aspergillus versicolor strain
Dibenzo[1,4]dioxin 1 Compound 2 A. versicolor 321.1462
  1. PubMed
  2. Wiley
13-O-Methylviriditin A. viridinutans 321
  1. http://www.ncbi.nlm.nih.gov/pubmed/10924177
  2. http://pubchem.ncbi.nlm.nih.gov/compound/10591878
Nigerapyrone B A. niger 320.38
  1. Pubchem
  2. Nigerapyrones A-​H, α-​pyrone derivatives from the marine mangrove-​derived endophytic fungus Aspergillus niger MA-​132.
Bianthrone and secoanthraquinone secondary metabolite 1 A. wentii 318.28
  1. Natural products from fungi. 26. Secoanthraquinone from emodin.
  2. Secondary mold metabolites. IX. Structure of a new bianthrone and of three new secoanthraquinones from Aspergillus wentii Wehm
Asperthecin A. nidulans 318.24
  1. http://www.biochemj.org/
  2. http://www.biochemj.org/
Asperthecin A. quadrilineatus 318.24
  1. http://www.biochemj.org/
  2. http://www.biochemj.org/
Emerin A. nidulans 316.35
  1. Pubchem
  2. New metabolite from Aspergillus nidulans.
  3. Isolation and structures of dicyanide derivatives, epurpurins A to C, from Emericella purpurea.
Emerin Emericella purpurea 316.35
  1. Pubchem
  2. New metabolite from Aspergillus nidulans.
  3. Isolation and structures of dicyanide derivatives, epurpurins A to C, from Emericella purpurea.
Dibenzo[1,4]dioxin 1 Compound 3 A. versicolor 315.1587
  1. PubMed
  2. Wiley
Isosulochrin dehydrate A. wentii 314.29
  1. Isolation and structures of four new metabolites from Aspergillus wentii
aflatoxin B2 A. flavus 314.29
  1. http://pubchem.ncbi.nlm.nih.gov/substance/386492
  2. http://www.sciencemag.org/content/142/3596/1191.abstract
  3. http://www.sciencemag.org/content/142/3596/1191.full.pdf
  4. http://onlinelibrary.wiley.com/doi/10.1002/bit.260050303/abstract
aflatoxin B2 A. parasiticus 314.29
  1. http://pubchem.ncbi.nlm.nih.gov/substance/386492
  2. http://www.sciencemag.org/content/142/3596/1191.abstract
  3. http://www.sciencemag.org/content/142/3596/1191.full.pdf
  4. http://onlinelibrary.wiley.com/doi/10.1002/bit.260050303/abstract
aflatoxin B2 A. nomius 314.29
  1. http://pubchem.ncbi.nlm.nih.gov/substance/386492
  2. http://www.sciencemag.org/content/142/3596/1191.abstract
  3. http://www.sciencemag.org/content/142/3596/1191.full.pdf
  4. http://onlinelibrary.wiley.com/doi/10.1002/bit.260050303/abstract
aflatoxicol (Aflatoxin Ro) A. flavus 314.289
  1. http://pubchem.ncbi.nlm.nih.gov/substance/49857167
  2. http://aem.asm.org/content/56/5/1465
  3. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC184431/
aflatoxicol (Aflatoxin Ro) A. niger 314.289
  1. http://pubchem.ncbi.nlm.nih.gov/substance/49857167
  2. http://aem.asm.org/content/56/5/1465
  3. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC184431/
aflatoxicol B A. flavus 314
  1. http://pubchem.ncbi.nlm.nih.gov/substance/135258706
  2. https://www.jstage.jst.go.jp/article/shokueishi1960/26/4/26_4_380/_article
  3. http://ci.nii.ac.jp/openurl/query
aflatoxicol B A. parasiticus 314
  1. http://pubchem.ncbi.nlm.nih.gov/substance/135258706
  2. https://www.jstage.jst.go.jp/article/shokueishi1960/26/4/26_4_380/_article
  3. http://ci.nii.ac.jp/openurl/query
aflatoxin B1 A. flavus 312.28
  1. http://pubchem.ncbi.nlm.nih.gov/compound/14403
  2. http://onlinelibrary.wiley.com/doi/10.1002/bit.260050303/abstract
  3. http://www.ncbi.nlm.nih.gov/pubmed/14098440
  4. http://www.nature.com/nature/journal/v198/n4885/abs/1981056a0.html
aflatoxin B1 A. parasiticus 312.28
  1. http://pubchem.ncbi.nlm.nih.gov/compound/14403
  2. http://onlinelibrary.wiley.com/doi/10.1002/bit.260050303/abstract
  3. http://www.ncbi.nlm.nih.gov/pubmed/14098440
  4. http://www.nature.com/nature/journal/v198/n4885/abs/1981056a0.html
aflatoxin B1 A. ochraceoroseus 312.28
  1. http://pubchem.ncbi.nlm.nih.gov/compound/14403
  2. http://onlinelibrary.wiley.com/doi/10.1002/bit.260050303/abstract
  3. http://www.ncbi.nlm.nih.gov/pubmed/14098440
  4. http://www.nature.com/nature/journal/v198/n4885/abs/1981056a0.html
aflatoxin B1 A. pseudotamarii 312.28
  1. http://pubchem.ncbi.nlm.nih.gov/compound/14403
  2. http://onlinelibrary.wiley.com/doi/10.1002/bit.260050303/abstract
  3. http://www.ncbi.nlm.nih.gov/pubmed/14098440
  4. http://www.nature.com/nature/journal/v198/n4885/abs/1981056a0.html
aflatoxin B1 Emericella venezuelensis 312.28
  1. http://pubchem.ncbi.nlm.nih.gov/compound/14403
  2. http://onlinelibrary.wiley.com/doi/10.1002/bit.260050303/abstract
  3. http://www.ncbi.nlm.nih.gov/pubmed/14098440
  4. http://www.nature.com/nature/journal/v198/n4885/abs/1981056a0.html
aflatoxin B1 A. bombycis 312.28
  1. http://pubchem.ncbi.nlm.nih.gov/compound/14403
  2. http://onlinelibrary.wiley.com/doi/10.1002/bit.260050303/abstract
  3. http://www.ncbi.nlm.nih.gov/pubmed/14098440
  4. http://www.nature.com/nature/journal/v198/n4885/abs/1981056a0.html
aflatoxin B1 A. nomius 312.28
  1. http://pubchem.ncbi.nlm.nih.gov/compound/14403
  2. http://onlinelibrary.wiley.com/doi/10.1002/bit.260050303/abstract
  3. http://www.ncbi.nlm.nih.gov/pubmed/14098440
  4. http://www.nature.com/nature/journal/v198/n4885/abs/1981056a0.html

Pages