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| Product | Description | |
|---|---|---|
| Fusaric acid | Fusaric acid. Group: Biochemicals. Alternative Names: 5-Butyl-2-pyridinecarboxylic acid; 5-Butylpicolinic acid. Grades: Highly Purified. CAS No. 536-69-6. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences. |  Worldwide |
| Fusaric acid | Fusaric acid is a potent dopamine β-hydroxylase inhibitor. Uses: Scientific research. Group: Natural products. CAS No. 536-69-6. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-128483. |  |
| Fusaric acid 99+.9% | Fusaric acid 99+.9%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences. | Worldwide |
| 2-Hydroxy-4,6-dimethoxybenzoic Acid | 2-Hydroxy-4,6-dimethoxybenzoic acid is a reagent used in the synthesis of rac Zearalenone-d6 (Z270502). rac Zearalenone-d6 s an estrogenic mycotoxin produced by Fusarium fungi commonly found in grains. One of a group of compounds known as resorcylic acid lactones. Group: Biochemicals. Grades: Highly Purified. CAS No. 3187-19-7. Pack Sizes: 100mg, 250mg. Molecular Formula: C9H10O5, Molecular Weight: 198.05. US Biological Life Sciences. | Worldwide |
| alpha-Zearalenol-[d5] | α-Zearalenol-[d5] is a labelled impurity of Zearalenol. Zearalenol, a resorcylic acid lactones derivative, could be produced by Fusarium fungi in grains and has been found to be an environmental contaminant. Synonyms: α-Zearalenol-d5; (E)-(7S,11R)-2,4,11-Trihydroxy-7-methyl-7,8,9,10,11,12,13,14-octahydro-10,10,11,12,12-D5-6-oxa-benzocyclotetradecen-5-one; (-)-α-Zearalenol-d5; Zearalenol-d5; trans-Zearalenol-d5; (3S,7R,11E)-3,4,5,6,7,8,9,10-Octahydro-7,14,16-trihydroxy-3-methyl-1H-2-benzoxacyclotetradecin-1-one-d5. Grades: 95% by HPLC; 98% atom D. CAS No. 36455-72-8. Molecular formula: C18H19D5O5. Mole weight: 325.41. |  |
| Aquastatin A | Aquastatin A is an adenosine triphosphatase inhibitor produced by Fusariumaquaeductuum. Synonyms: 4-{[4-(Hexopyranosyloxy)-2-hydroxy-6-pentadecylbenzoyl]oxy}-2-hydroxy-6-methylbenzoic acid. CAS No. 153821-50-2. Molecular formula: C36H52O12. Mole weight: 676.79. | |
| Beta-Zearalanol | Beta-Zearalenol is an mycotoxin produced by Fusarium spp, which causes apoptosis and oxidative stress in mammalian reproductive cells [1]. Beta-Zearalenol is the derivative of zearalenone (ZEA) which can conjugate with glucuronic acid [2]. Uses: Scientific research. Group: Natural products. CAS No. 42422-68-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-N6740. | |
| DL-Pantolactone | DL-Pantolactone can be hydrolyzed to Pantoic acid by the lactonohydrolase of Fusarium oxysporum. DL-Pantolactone also can be used in the preparation of 3,5-dinitrobenzoyl-DL-pantolactone [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 79-50-5. Pack Sizes: 10 mM * 1 mL; 5 g; 10 g. Product ID: HY-W053519. | |
| Equisetin | The tetramic acid equisetin, is produced by a number of species of Fusarium. Interest in equisetin emerged with reports of its inhibitory activity against human immunodeficiency virus type 1 (HIV-1) integrase in vitro that was mechanistically distinct from previously described inhibitors. Equisetin inhibits 3' end-processing and strand transfer as well as disintegration catalysed by either the full-length enzyme or the truncated integrase core. Group: Biochemicals. Grades: Highly Purified. CAS No. 57749-43-6. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Fosfonochlorin | It is produced by the strain of Talaromyces flavus SANK 15680 and Fusarium oxysporum SANK 10182. Chloroacetylphosphoric acid only has the activity of anti-proteus bacteria, but in the presence of glucose-6-phosphate (G-6-P), it is also effective against Staphylococcus aureus, Escherichia coli, Haemophilus haemophilus, some Shigella and Salmonella bacteria. The mechanism of antibacterial action is to inhibit cell wall biosynthesis and affect the formation of plasmoglobin. Synonyms: (chloroacetyl)phosphonic acid; Chloroacetylphosphonate. Grades: 98%. CAS No. 89699-33-2. Molecular formula: C2H4ClO4P. Mole weight: 158.48. | |
| Fumonisin B1 | Fumonisin is a group of toxins (B1 or FB1, B2 or FB2, which are equally toxic, and B3 or FB3, which is relatively nontoxic) which are produced by fungi (Fusarium moniliforme and F. proliferatum) that causes equine leukoencephalomalacia, a disease of the central nervous system of equines and is associated with the feeding of moldy corn. Swine may develop porcine pulmonary edema. Group: Biochemicals. Alternative Names: FB; FB1; (2R,2'R)-1,2,3-Propanetricarboxylic Acid 1,1'-[(1S,2R)-1-[(2S,4R,9R,11S,12S)-12-Amino-4,9,11-trihydroxy-2-methyltridecyl]-2-[(1R)-1-methylpentyl]-1,2-ethanediyl] Ester; Macrofusine. Grades: Highly Purified. CAS No. 116355-83-0. Pack Sizes: 1mg, 5mg. Molecular Formula: C??H??NO??, Molecular Weight: 721.83. US Biological Life Sciences. | Worldwide |
| Fumonisin B3 | Fumonisin B3 is a mycotoxin produced by Fusarium moniliforme which is the most commonly reported fungal species infecting maize. Fumonisins acts as an inhibitor of ceramide synthase (sphingosine N-acyltransferase). Synonyms: FB3; (2R,2'R)-2,2'-((((5R,6R,7S,9S,11R,18S,19S)-19-Amino-11,18-dihydroxy-5,9-dimethylicosane-6,7-diyl)bis(oxy))bis(2-oxoethane-2,1-diyl))disuccinic Acid. Grades: ≥98%. CAS No. 1422359-85-0. Molecular formula: C34H59NO14. Mole weight: 705.83. | |
| Fusarin C | Fusarin C is produced by the strain of Fusarium moniliforrme which has mutagenicity. Synonyms: CCRIS 4320; HSDB 7078; (2E,3E,5E,7E,9E)-2-Ethylidene-11-[(1R,5a)-4a-hydroxy-4-(2-hydroxyethyl)-2-oxo-6-oxa-3-azabicyclo[3.1.0]hexan-1a-yl]-4,6,10-trimethyl-11-oxo-3,5,7,9-undecatetraenoic acid methyl ester. CAS No. 79748-81-5. Molecular formula: C23H29NO7. Mole weight: 431.48. | |
| Halymecin B | It is produced by the strain of Fusarium sp. FE-71-1. Synonyms: Decanoic acid, 3-(acetyloxy)-5-[[3-hydroxy-5-[[5-hydroxy-3-(b-D-mannopyranosyloxy)-1-oxodecyl]oxy]-1-oxodecyl]oxy]-, 1-(3-carboxy-2-hydroxypropyl)hexyl ester, [3R-[1[R*(R*)], 3R*, 5R*[3R*, 5R*(3R*, 5R*)]]]-. CAS No. 167173-81-1. Molecular formula: C48H86O19. Mole weight: 967.18. | |
| Halymecin C | It is produced by the strain of Fusarium sp. FE-71-1. Synonyms: Decanoic acid, 3-(acetyloxy)-5-[(3,5-dihydroxy-1-oxodecyl)oxy]-, 1-(3-carboxy-2-hydroxypropyl)hexyl ester, [3R-[1[R*(R*)],3R*,5R*(3R*,5R*)]]-. CAS No. 167173-82-2. Molecular formula: C32H58O11. Mole weight: 618.79. | |
| Moniliformin potassium salt | It is a potent, water-soluble mycotoxin produced by several species of fusarium. It selectively inhibits mitochondrial oxidization of pyruvate and α-ketoglutarate. Synonyms: Semisquaric acid potassium salt; 3-Cyclobutene-1,2-dione, 3-hydroxy-, potassium salt; 1-Hydroxycyclobut-1-ene-3,4-dione potassium salt. Grades: >99% by HPLC. CAS No. 52591-22-7. Molecular formula: C4HKO3. Mole weight: 136.15. | |
| rac Zearalenone-d6 | Estrogenic mycotoxin produced by Fusarium fungi commonly found in grains. One of a group of compounds known as resorcylic acid lactones. Group: Biochemicals. Alternative Names: (+/-)-3,4,5,6,9,10-Hexahydro-14,16-dihydroxy-3-methyl-. Grades: Highly Purified. CAS No. 1185236-04-7. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Zearalenone-14-O-β-glucoside | Zearalenone-14-O-β-glucoside is an impurity of Zearalenol. Zearalenol, a resorcylic acid lactones derivative, could be produced by Fusarium fungi in grains and has been found to be an environmental contaminant. Synonyms: (3S)-16-Hydroxy-3-methyl-3,4,5,6,7,8,9,10-octahydro-1H-2-benzoxacyclotetradecine-1,7-dione-14-O-β-D-glucopyranoside. Molecular formula: C24H32O10. Mole weight: 480.5. | |
| Zearalenone (Zearalanol, Zearanol, Mycotoxin F2, Toxin F2, RAL) | Zearalenone is a phenolic resorcyclic acid lactone and can be produced by a number of species of Fusarium known to colonize cereals. Zearalenone (6-[10-hydroxy-6-oxo-trans-1-undecenyl]-b-resorcyclic acid lactone), also known as F-2 toxin, is an estrogenic mycotoxin that is produced by Fusarium graminearum. This fungus can infect cereal grains and can elaborate large quantities of zearalenone. Zearalenone is a naturally occurring estrogen, recognized as causing hormonal effects in animal species such as the pig. The association between zearalenone exposure and human diseases remains speculative at present; it has been considered as a possible causative agent in outbreaks of precocious pubertal changes in young children and has been suggested to have a possible involvement in human cervical cancer. Group: Biochemicals. Alternative Names: Zearalanol; Zearanol; Mycotoxin F2; Toxin F2; RAL. Grades: Highly Purified. CAS No. 17924-92-4. Pack Sizes: 10mg, 25mg. Molecular Formula: C18H22O5, Molecular Weight: 318.4. US Biological Life Sciences. | Worldwide |
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