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| Product | Description | |
|---|---|---|
| Allylamine hydrochloride | Allylamine hydrochloride. Uses: This product is suitable for scientific research. Group: Monomers. Alternative Names: 3-Aminopropene hydrochloride, Mono-allylamine hydrochloride. CAS No. 10017-11-5. Product ID: prop-2-en-1-amine; hydrochloride. Molecular formula: 93.56. Mole weight: C3H8ClN. Cl.NCC=C. 1S/C3H7N.ClH/c1-2-3-4;/h2H, 1, 3-4H2;1H. MLGWTHRHHANFCC-UHFFFAOYSA-N. MP 118-120deg. |  |
| Poly(fluorescein isothiocyanate allylamine hydrochloride) | Poly(fluorescein isothiocyanate allylamine hydrochloride). Group: other materials. | |
| 1-Bromopropyn-3-ol | 1-Bromopropyn-3-ol is an intermediate int he synthesis of Terbinafine Hydrochloride (T107500), which is a synthetic allylamine antifungal. Group: Biochemicals. Grades: Highly Purified. CAS No. 2060-25-5. Pack Sizes: 2.5g, 10g. Molecular Formula: C3H3BrO. US Biological Life Sciences. |  Worldwide |
| (2Z)-1-Chloro-6,6-dimethyl-2-hepten-4-yne | (2Z)-1-Chloro-6,6-dimethyl-2-hepten-4-yne is a byproduct in the synthesis of Terbinafine Hydrochloride (T107500); an orally active, antimycotic allylamine related to Naftifine. It is a specific inhibitor of squalene epoxidase, a key enzyme in fungal ergosterol biosynthesis. Also antifungal. Group: Biochemicals. Grades: Highly Purified. CAS No. 635708-74-6. Pack Sizes: 10mg, 100mg. Molecular Formula: C?H??Cl, Molecular Weight: 156.65. US Biological Life Sciences. | Worldwide |
| Allylamine dihydrogen phosphate | Polyallylamine hydrochloride is a cationic polyelectrolyte prepared by the polymerization of allylamine. Uses: Poly(allylamine hydrochloride) has many biomedical applications. the most prominent use of this polyelectrolyte is in the field of cell encapsulation. a layer by layer method is used by alternating positively and negatively charged polyelectrolytes to build a barrier between the cell and the harsher outside environment. upon cell lysis, the capsule of layered polyelectrolytes maintains its structural integrity and can be used for purposes such as drug delivery. Additional or Alternative Names: phosphoricacid; prop-2-en-1-amine. Product Category: Heterocyclic Organic CompoundAllyl Monomers. CAS No. 121092-93-1. Molecular formula: C3H10NO4P. Mole weight: 155.09 g/mol. Purity: 0.95. IUPACName: phosphoric acid;prop-2-en-1-amine. Canonical SMILES: NCC=C.OP(O)(O)=O. Product ID: ACM-MO-121092931. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Allylamine HCl | Allylamine is an organic compound with the formula C3H5NH2. This colorless liquid is the simplest stable unsaturated amine. Synonyms: Allylamine Hydrochloride; 3-Aminopropene hydrochloride, Mono-allylamine hydrochloride. Grade: > 95%. CAS No. 10017-11-5. Molecular formula: C3H7N. HCl. Mole weight: 93.56. |  |
| Desmethyl Naftifine HCl | 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. Synonyms: 1-Naphthalenemethanami?ne, N-(3-phenyl-2-propenyl)?-, hydrochloride, (E)?- (9CI). Grade: > 95%. CAS No. 98978-52-0. Molecular formula: C20H19N. HCl. Mole weight: 273.38 36.46. | |
| Micro particles based on polystyrene, magnetic ( std dev <0.1 μm) | 1 μm particle size, std dev <0.1 μm. Uses: Micro particles based on polystyrene, magnetic has been used to deposit polyelectrolytes (pe), poly(allylamine hydrochloride), and poly(sodium 4-styrenesulfonate) (pah/pss) onto negatively charged magnetic polystyrene (ps) microparticles, to prepare pe-functionalized microparticles, for the fabrication of a biohybrid algal microswimmer toward biomedical applications. Group: Polystyrene (ps). Alternative Names: Latex beads from PS, magnetic. | |
| Naftifine-[d3] Hydrochloride | Naftifine-[d3] Hydrochloride is the labelled salt of Naftifine. Naftifine is a topical, synthetic, broad spectrum allylamine derivate. It has antifungal, antibacterial and anti-inflammatory activity and is used for the treatment of tinea pedis, tinea cruris, and tinea corporis. Synonyms: Naftifine D3 HCl; (E)-N-(Methyl-d3)-N-(3-phenyl-2-propen-1-yl)-1-naphthalenemethanamine Hydrochloride; (E)-N-Cinnamyl-N-(methyl-d3)-1-naphthalenemethanamine Hydrochloride; Exoderil-d3; Naftifungin-d3; Naftin-d3. Grade: 98%; ≥99% atom D. CAS No. 1246833-81-7. Molecular formula: C21H18D3N.HCl. Mole weight: 326.86. | |
| Naftifine hydrochloride | Naftifine 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. Synonyms: AW 105843; AW105843; AW-105843; AW 105-843; SN 105843; SN105843; SN-105843; Naftifine hydrochloride. Grade: >98%. CAS No. 65473-14-5. Molecular formula: C21H21N.HCl. Mole weight: 323.86. | |
| Poly(allylamine) solution | Polyallylamine hydrochloride is a cationic polyelectrolyte prepared by the polymerization of allylamine. Uses: Soluble in water, lower alcohols, ethylene glycol and formamide. Group: Hydrophilic polymers. Alternative Names: PAH. CAS No. 30551-89-4. Pack Sizes: Packaging 1, 5, 25 g in poly bottle. Product ID: prop-2-en-1-amine. Molecular formula: average Mw ~15,000. Mole weight: [CH2CH(CH2NH2)]n. NCC=C. 1S/C3H7N/c1-2-3-4/h2H,1,3-4H2. VVJKKWFAADXIJK-UHFFFAOYSA-N. | |
| Terbinafine hydrochloride | Terbinafine HCl is a hydrochloride salt of terbinafine that is a synthetic allylamine antifungal and a squalene epoxidase inhibitor with an IC50 of 30 nM for Candida albicans. Synonyms: OKY-046 HCl; OKY 046 HCl; OKY046 HCl. Grade: >98%. CAS No. 78628-80-5. Molecular formula: C21H26ClN. Mole weight: 327.89. | |
| 17-AAG hydrochloride | 17-AAG hydrochloride is a potent HSP90 inhibitor with IC50 value of 5 nM, which is a 100-fold higher binding affinity for HSP90 derived from tumour cells than that from normal cells. It is less toxic by binding to Hsp90 and altering its function. It causes the degradation of HER2, HER3, Akt, and both mutant and wild-type androgen receptor (AR), leading to the RB-dependent G1 growth arrest of prostate cancer cells. It has the ability to induce apoptosis of cells transformed with imatinib mesylate-resistant T315I and E255K BCR-ABL mutants with IC50 values of 2.3 μM and 1.0 μM, respectively. It displays significantly higher binding affinity for Hsp90 from 3T3-src, B16 or CT26 xenografts in nude mice compared with that from the normal tissues in vivo. Uses: 17-aag hydrochloride has the ability to induce apoptosis of cells transformed with imatinib mesylate-resistant t315i and e255k bcr-abl mutants. Synonyms: 17-AAG hydrochloride; 17 AAG hydrochloride; 17AAG hydrochloride; [(3R,5S,6R,7S,8E,10S,11S,12Z,14E)-6-hydroxy-5,11-dimethoxy-3,7,9,15-tetramethyl-16,20,22-trioxo-21-(prop-2-enylamino)-17-azabicyclo[16.3.1]docosa-1(21),8,12,14,18-pentaen-10-yl] carbamate hydrochloride; Tanespimycin Hydrochloride; NSC 330507 Hydrochloride; CP 127374 Hydrochloride; 17-(Allylamino)-17-desmethylgeldanamycin hydrochloride. Grade: >98%. CAS No. 911710-03-7. Molecular formula: C31H44ClN3O8. Mole weight: 622.15. | |
| 17-N- (2-Di methyl aminoethylamino) -17-demethoxy Geldanamycin Hydrochloride | 17-DMAG is an analogue of Gelamycin and 17- (Allylamino) geldanamycin. 17-DMAG acts as a Hsp90 inhibitor and displays more potent antitumor activity than 17-AAG. Group: Biochemicals. Alternative Names: 17-Demethoxy-17- [ [2- (dimethylamino) ethyl] amino] geldanamycin Hydrochloride; 17-N- (2-Di methyl aminoethylamino) -17-demethoxygeldanamycin Hydrochloride; 17-[2- (Dimethylamino) ethylamino]-17-desmethylgeldanamycin Hydrochloride; Alvespimycin Hydrochloride; DMAG Hydrochloride; NSC 707545 Hydrochloride; 17-DMAG Hydrochloride. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| (8-Chloro-2,3,4,5-tetrahydro-1-benzoxepin-5-yl)-methyl-prop-2-enylazanium chloride | (8-Chloro-2,3,4,5-tetrahydro-1-benzoxepin-5-yl)-methyl-prop-2-enylazanium chloride. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-Benzoxepin-5-amine, 2,3,4,5-tetrahydro-8-chloro-N-methyl-N-2-propenyl-, hydrochloride, 2,3,4,5-Tetrahydro-8-chloro-N-methyl-N-2-propenyl-1-benzoxepin-5-amine hydrochloride, 5-(N-Methyl-N-allylamino)-8-chloro-2,3,4,5-tetrahydro-1-benzoxepin hydrochloride, 37483-78-6, AC1L1YDN, LS-42465, (8-chloro-2,3,4,5-tetrahydro-1-benzoxepin-5-yl)-methyl-prop-2-enylazanium chloride, 8-chloro-N-methyl-N-(prop-2-en-1-yl)-2,3,4,5-tetrahydro-1-benzoxepin-5-aminium chloride. Product Category: Heterocyclic Organic Compound. CAS No. 37483-78-6. Molecular formula: C14H19Cl2NO. Mole weight: 288.213 g/mol. Purity: 0.96. IUPACName: (8-chloro-2,3,4,5-tetrahydro-1-benzoxepin-5-yl)-methyl-prop-2-enylazanium;chloride. Product ID: ACM37483786. Alfa Chemistry ISO 9001:2015 Certified. | |
| N-2-Propen-1-yl-9H-purin-6-amine Hydrobromide | N-2-Propen-1-yl-9H-purin-6-amine is an N-substituted purine and is structurally related to 9-Propenyladenine (P768800), an impurity of Tenofovir (T018500). Group: Biochemicals. Alternative Names: N-Allyladenine Hydrochloride; N6-Allyladenine Hydrochloride; 6-Allylaminopurine Hydrobromide; N-Allyladenine Hydrobromide; N6-Allyladenine Hydrobromide; NSC 17212 Hydrobromide. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Terbinafine, Hydrochloride (Lamisil, N- [ (2E) -6, 6-Di methyl -2-hepten-4-ynyl] -N- methyl -1-naphthalene methanamine) | An orally active, antimycotic allylamine related to naftifine. A specfic inhibitor of squalene epoxidase, a key enzyme in fungal ergosterol biosynthesis. Group: Biochemicals. Alternative Names: Lamisil, N- [ (2E) -6, 6-Di methyl -2-hepten-4-ynyl] -N- methyl -1-naphthalene methanamine. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
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