Fungal Enzyme Suppliers UK
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Product | Description | |
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Desmethyl Naftifine HCl Quick enquiry Where to buy Suppliers range | An impurity of Naftifine, which is an allylamine antifungal drug for the topical treatment of tinea pedis, tinea cruris, and tinea corporis, probably involves selectively blocking sterol biosynthesis via inhibition of the squalene 2,4-epoxidase enzyme. Group: Pharmaceuticals. Alternative Names: 1-Naphthalenemethanami?ne, N-(3-phenyl-2-propenyl)?-, hydrochloride, (E)?- (9CI). CAS No. 98978-52-0. Pack Sizes: 1mg; 1g; 10g. Product ID: 98978-52-0. Custom synthesis is available. Send your inquiries for more information. | London |
Naftifine cis-Isomer Quick enquiry Where to buy Suppliers range | An impurity of Naftifine, which is an allylamine antifungal drug for the topical treatment of tinea pedis, tinea cruris, and tinea corporis, probably involves selectively blocking sterol biosynthesis via inhibition of the squalene 2,5-epoxidase enzyme. Group: Pharmaceuticals. Alternative Names: (Z)-N-Methyl-N-(3-phenyl-2-propen-1-yl)-1-naphthalenemethanamine Hydrochloride;(Z)-N-Cinnamyl-N-methyl-1-naphthalenemethanamine Hydrochloride. CAS No. 65473-08-7. Pack Sizes: 1mg; 1g; 10g. Product ID: 65473-08-7. Custom synthesis is available. Send your inquiries for more information. | London |
Naftifine Impurity 1 Quick enquiry Where to buy Suppliers range | An impurity of Naftifine, which is an allylamine antifungal drug for the topical treatment of tinea pedis, tinea cruris, and tinea corporis, probably involves selectively blocking sterol biosynthesis via inhibition of the squalene 2,3-epoxidase enzyme. Group: Pharmaceuticals. Alternative Names: 1-(4-(Aminomethyl)naphthalen-1-yl)-N,N-dimethylmethanamine. Pack Sizes: 1mg; 1g; 10g. Product ID: N0001-008958. Custom synthesis is available. Send your inquiries for more information. | London |
Posaconazole Impurity 33 Quick enquiry Where to buy Suppliers range | Posaconazole Impurity 33 is an impurity of Posaconazole. Posaconazole is a broad-spectrum triazole compound that is active against fungi by inhibiting the lanosterol 14α-demethylase enzyme. Uses: Posaconazole intermediate. Antifungal agent. Group: Pharmaceuticals. Alternative Names: [S- (R*, R*) ]-2-[1-Ethyl-2- (phenylmethoxy) propyl]hydrazinecarboxaldehyde; 2-[ (1S, 2S) -1-Ethyl-2- (phenylmethoxy) propyl]hydrazinecarboxaldehyde. CAS No. 170985-85-0. Pack Sizes: 1mg; 1g; 10g. Product ID: 170985-85-0. Custom synthesis is available. Send your inquiries for more information. | London |
Sorbic Acid Quick enquiry Where to buy Suppliers range | Sorbic acid can be used to inhibit bacterial, yeast and fungal sulfhydryl enzymes by inhibiting amino acid uptake. Uses: Synthesis. Group: Pharmaceutical Ingredients. Intermediates & Reagents. Sorbic Acid. CAS No. 110-44-1. Product ID: PIM000006740. | DKSH Great Britain |
Talaromycesone A Quick enquiry Where to buy Suppliers range | Talaromycesone A is a fungal metabolite originally isolated from Talaromyces. It is active against S. epidermidis and methicillin-resistant S. aureus (MRSA) bacteria (IC50s = 3.70 and 5.48 μM, respectively). Talaromycesone A inhibits acetylcholinesterase (AChE) in a cell-free assay (IC50 = 7.49 μM for the human enzyme). Group: Pharmaceuticals. CAS No. 1658474-60-2. Pack Sizes: 1mg; 1g; 10g. Product ID: 1658474-60-2. Custom synthesis is available. Send your inquiries for more information. | London |
Tavaborole Quick enquiry Where to buy Suppliers range | Tavaborole (AN2690) is a potent antifungal that targets the post-transfer editing site of leucyl-tRNA synthetase (LeuRS). Tavaborole forms a covalent adduct with the 3' adenosine of tRNA(leu) at the editing site of fungal, but not bacterial LeuRS, locking the enzyme in an inactive conformation. Tavaborole was recently approved for the treatment of onychomycosis of the toenail in adults. Group: Pharmaceuticals. Alternative Names: Tavaborole; AN2690; AN 2690. CAS No. 174671-46-6. Pack Sizes: 1mg; 1g; 10g. Product ID: 174671-46-6. Custom synthesis is available. Send your inquiries for more information. | London |
Terpendole I Quick enquiry Where to buy Suppliers range | Terpendole I is a fungal metabolite originally isolated from A. yamanashiensis. It is a weak inhibitor of acyl-coenzyme A:cholesterol acyltransferase (ACAT; IC50=145 μM) and is active against the bacteria B. cereus and B. subtilis (MICs = 100 μg/ml for both) but not S. aureus, P. aeruginosa, or K. pneumoniae (MICs = >200 μg/ml for all) or the fungus C. albicans (MIC = 200 μg/ml). It is also cytotoxic to HeLa cells with an IC50 value of 52.6 μM. Group: Pharmaceuticals. Alternative Names: Terpendole I; 167612-17-1; (1S, 2R, 5S, 7S, 8R, 9R, 11S, 12S, 15S)-7-(2-hydroxypropan-2-yl)-1, 2-dimethyl-6, 10-dioxa-24-azaheptacyclo[13.10.0.02, 12.05, 11.09, 11.017, 25.018, 23]pentacosa-17(25), 18, 20, 22-tetraene-8, 12-diol; (2S, 3R, 3aR, 4aS, 4bS, 6aS, 12bS, 12cR, 14aS)-3, 3a, 5, 6, 6a, 7, 12, 12b, 12c, 13, 14, 14a-dodecahydro-2-(1-hydroxy-1-methylethyl)-12b, 12c-dimethyl-2H, 4bH-oxireno[4', 4'a]-1-benzopyrano[5', 6':6, 7]indeno[1, 2-b]indole-3, 4b-diol; SCHEMBL20869892. CAS No. 167612-17-1. Pack Sizes: 1mg; 1g; 10g. Product ID: 167612-17-1. Custom synthesis is available. Send your inquiries for more information. | London |