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| Product | Description | |
|---|---|---|
| togavirin | Known from the Sindbis and Semliki forest togaviruses. Once released, the core protein does not retain catalytic activity. Togavirin is the type example of peptidase family S3 and has a similar tertiary structure to chymotrypsin. Group: Enzymes. Synonyms: Sindbis virus protease; Sindbis virus core protein; NsP2 proteinase. Enzyme Commission Number: EC 3.4.21.90. CAS No. 342882-56-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4182; togavirin; EC 3.4.21.90; 342882-56-8; Sindbis virus protease; Sindbis virus core protein; NsP2 proteinase. Cat No: EXWM-4182. |  |
| TokeOni | TokeOni. Molecular formula: C16H19ClN2O2S. Mole weight: 338.9g/mol. IUPAC Name: (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]buta-1,3-dienyl]-4,5-dihydro-1,3-thiazole-4-carboxylic acid;hydrochloride. SMILES: CN(C)C1=CC=C(C=C1)C=CC=CC2=NC(CS2)C(=O)O.Cl. InChI: InChI=1S/C16H18N2O2S.ClH/c1-18(2)13-9-7-12(8-10-13)5-3-4-6-15-17-14(11-21-15)16(19)20;/h3-10,14H,11H2,1-2H3,(H,19,20);1H/b5-3+,6-4+;/t14-;/m1./s1. |  |
| Tokinolide B | Tokinolide B. Group: Biochemicals. Grades: Plant Grade. CAS No. 112966-16-2. Pack Sizes: 10mg. Molecular Formula: C24H28O4, Molecular Weight: 380.48. US Biological Life Sciences. |  Worldwide |
| Tolafentrine | Tolafentrine. Group: Biochemicals. Alternative Names: rel- (-) -N- [4- [ (4aR, 10bS) -1, 2, 3, 4, 4a, 10b-Hexahydro-8, 9-dimethoxy-2-methylbenzo [c] [1, 6] naphthyridin-6-yl] phenyl] -4-methyl Benzene sulfonamide. Grades: Highly Purified. CAS No. 139308-65-9. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C28H31N3O4S. US Biological Life Sciences. | Worldwide |
| Tolazamide | Tolazamide. Group: Biochemicals. Alternative Names: N- [ [ (Hexahydro-1H-azepin-1-yl) amino] carbonyl] -4-methyl Benzene sulfonamide; 1-(4-Methylphenylsulfonyl)-3-(hexahydro-1H-azepin-1-yl)urea; 1-(Hexahydro-1-azepinyl)-3-p-tolylsulfonylurea. Grades: Highly Purified. CAS No. 1156-19-0. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Tolazoline hydrochloride | Tolazoline is a non-selective competitive α-adrenergic receptor antagonist. Grade: >98%. CAS No. 59-97-2. Molecular formula: C10H12N2.HCl. Mole weight: 196.68. |  |
| Tolazoline hydrochloride | Tolazoline hydrochloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 59-97-2. Pack Sizes: 50g, 100g, 250g, 500g, 1kg. US Biological Life Sciences. | Worldwide |
| Tolazoline, Hydrochloride. (2-Benzyl-2-imidazoline) | An a-adrenergic antagonist. A peripheral vasodilator. Group: Biochemicals. Alternative Names: 2-Benzyl-2-imidazoline. Grades: Highly Purified. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| Tolbutamide | Tolbutamide is an orally active KATP inhibitor. Tolbutamide inhibits cell proliferation, stimulates exocytosis of glucagon and reduces fetal lethality of mice. Tolbutamide can be used in the research of diabete[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 64-77-7. Pack Sizes: 10 mM * 1 mL in DMSO; 500 mg; 1 g; 5 g. Product ID: HY-B0401. |  |
| Tolbutamide | An antidiabetic, used as a hypoglycemic agent in veterinary medicine. Group: Biochemicals. Alternative Names: N-[(Butylamino)carbonyl]-4-methyl-benzenesulfonamide; 1-Butyl-3-(p-tolylsulfonyl)urea; Tolyl sulfonyl butyl urea; 3-(p-Tolyl-4-sulfonyl)-1-butylurea; N-Butyl-N'-(4-methyl-phenylsulfonyl)urea; Artosin; Artozin; Mobenol; Diabetol; Orabet; Oralin; Orezan; Orinase; Orinaz; Oterben; Pramidex; Rastinon; NSC 23813; NSC 87833. Grades: Highly Purified. CAS No. 64-77-7. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Tolbutamide-d9 | Labeled Tolbutamide. An antidiabetic, used as a hypoglycemic agent in veterinary medicine. Group: Biochemicals. Alternative Names: N- [ (Butylamino-d9) carbonyl] -4-methyl Benzene sulfonamide; 1-(Butyl-3-(p-tolyl-sulfonyl)urea-d9; Tolylsulfonylbutylurea-d9; 3-(p-Tolyl-4-sulfonyl)-1-butylurea-d9; N-Butyl-N'- (4-methylphenylsulfonyl) urea-d9; Artosin-d9; Artozin-d9; Mobenol-d9; Diabetol-d9; Orabet-d9; Oralin-d9; Orezan-d9; Orinase-d9; Orinaz-d9; Oterben-d9; Pramidex-d9; Rastinon-d9; NSC 23813-d9; NSC 87833-d9. Grades: Highly Purified. CAS No. 1219794-57-6. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Tolbutamide-[d9] | Tolbutamide-[d9] is the labelled analogue of Tolbutamide. Tolbutamide is an inhibitor of potassium channel, used for type II diabetes. Synonyms: Tolbutamide D9; 4-Methyl-N-{[2-(2H3)methyl(2H6)propan-2-yl]carbamoyl}benzene-1-sulfonamide. Grade: 95% by HPLC; 98% atom D. CAS No. 1219794-57-6. Molecular formula: C12H9D9N2O3S. Mole weight: 279.40. | |
| Tolcapone | Tolcapone (Ro 40-7592) is a selective, potent and orally active COMT inhibitor with an IC50of 773 nM. Tolcapone can inhibits α-syn and Aβ42 oligomerization and fibrillogenesis. Tolcapone can cause oxidative stress and induce cancer cells apoptosis and ROS production. Tolcapone can be used for the researches of cancer and neurological disease, such as Parkinson disease and neuroblastoma[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ro 40-7592. CAS No. 134308-13-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-17406. | |
| Tolcapone ( (3, 4-Dihydroxy-5-nitro-phenyl) (4-methylphenyl) methanone, Ro-40-7592, Tasmar) | Orally active inhibitor of central and peripheral catechol-O-methyltransferase (COMT). Antiparkinsonian. Group: Biochemicals. Alternative Names: (3, 4-Dihydroxy-5-nitro-phenyl) (4-methylphenyl) methanone; Ro-40-7592; Tasmar. Grades: Highly Purified. CAS No. 134308-13-7. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Tolcapone-d4 | Orally active inhibitor of central and peripheral catechol-O-methyltransferase (COMT). Antiparkinsonian. Group: Biochemicals. Alternative Names: (3,4-Dihydroxy-5-nitrophenyl)(4-methylphenyl-d4)methanone; Ro-40-7592-d4; Tasmar-d4. Grades: Highly Purified. CAS No. 1246816-93-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Tolcapone-[d4] | Tolcapone-[d4] is the labelled analogue of Tolcapone. Tolcapone is a nitrocatechol-type inhibitor of the enzyme catechol-O-methyltransferase. It can be used to treat Parkinson's disease. Synonyms: Tolcapone D4; (3,4-Dihydroxy-5-nitrophenyl)(4-methylphenyl-d4)methanone. Grade: 95% by HPLC; 98% atom D. CAS No. 1246816-93-2. Molecular formula: C14H7D4NO5. Mole weight: 277.27. | |
| Tolcapone-[d7] | An isotope labelled form of Tolcapone. Tolcapone is a nitrocatechol-type inhibitor of the enzyme catechol-O-methyltransferase. It can be used to treat Parkinson's disease. Synonyms: Tolcapone-d7; 5-[4-(D3)methyl(D4)benzoyl]-3-nitrobenzene-1,2-diol. Grade: 95% by HPLC; 98% atom D. CAS No. 2749285-04-7. Molecular formula: C14H4D7NO5. Mole weight: 280.28. | |
| Tolcapone Related Compound A | Tolcapone Related Compound A. Uses: For analytical and research use. CAS No. 1391053-03-4. Mole weight: 228.24. Catalog: AP1391053034. |  |
| Tolcapone Related Compound B | Tolcapone Related Compound B. Uses: For analytical and research use. CAS No. 134612-80-9. Mole weight: 287.27. Catalog: AP134612809. | |
| Toldimfos sodium | Toldimfos sodium. Alternative Names: sodium [4-(dimethylamino)-2-methylphenyl]phosphinate;TodlimfosSodium;4-Dimethylamino-o-tolyl phosphonous acid, sodium salt;Phosphinic acid, 4-(dimethylamino)-2-methylphenyl-, sodium salt;TOLDIMPHOSSODIUM;TONOPHOSPHAN;[2-Methyl-4-(dimethylamino)phenyl]phosphinic acid sodium salt;[4-(Dimethylamino)-2-methylphenyl]phosphinic acid sodium salt. CAS No. 575-75-7. Purity: 95%+. Product ID: ACM575757. Molecular formula: C9H13NNaO2P. Mole weight: 221.17. IUPAC Name: sodium;[4-(dimethylamino)-2-methylphenyl]-oxido-oxophosphanium. Canonical SMILES: CC1=C(C=CC(=C1)N(C)C)[P+](=O)[O-].[Na+]. ECNumber: 209-391-4. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Tolebrutinib | Tolebrutinib (SAR442168) is a potent, selective, orally active and brain-penetrant inhibitor of Bruton tyrosine kinase (BTK), with IC50s of 0.4 and 0.7 nM in Ramos B cells and in HMC microglia cells, respectively. Tolebrutinib exhibits efficacy in central nervous system immunity. Tolebrutinib can be used for the research of multiple sclerosis (MS)[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SAR442168; PRN2246. CAS No. 1971920-73-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109192. | |
| Tolfenamic Acid | Tolfenamic Acid (GEA 6414) is a CNS-penetrant non-steroidal anti-inflammatory and anti-cancer agent, selectively inhibits COX-2, with an IC50 of 13.49 μM (3.53 μg/mL) in LPS-treated (COX-2) canine DH82 monocyte/macrophage cells, but shows no effect on COX-1. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GEA 6414. CAS No. 13710-19-5. Pack Sizes: 10 mM * 1 mL in DMSO; 500 mg; 5 g; 10 g. Product ID: HY-B0335. | |
| Tolfenamic Acid | Non-steroidal anti-inflammatory drugs (NSAIDs). Group: Biochemicals. Alternative Names: 2-[ (3-Chloro-2-methylphenyl) amino]benzoic Acid. Grades: Highly Purified. CAS No. 13710-19-5. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Tolfenamic acid-[13C6] | Tolfenamic acid-[13C6] is the labelled analogue of Tolfenamic acid, which is a non-steroidal anti-inflammatory drug (NSAID). It is a derivative of anthranilic acid, related structurally to Mefenamic and Flufenamic acids. Synonyms: 2-(3-Chloro-2-methyl-phenylamino)-13C6-benzoic acid; Tolfenamic acid-13C6; Tolfenamic Acid-(Benzoic ring-13C6); N-(3-Chloro-o-tolyl)anthranilic Acid-13C6; Clotam-13C6; Migea-13C6; N-(2-Methyl-3-chlorophenyl)anthranilic Acid-13C6; Tolfedine-13C6; Tolfine-13C6. Grade: 95% by HPLC; 98% atom 13C. CAS No. 1420043-61-3. Molecular formula: C8[13C]6H12ClNO2. Mole weight: 267.66. | |
| Tolfenamic Acid Acyl- β-D-Glucuronide Benzyl Ester | Protected Tolfenamic Acid Acyl- β-D-Glucuronide (T535310), a metabolite of Tolfenamic acid (T535300). Group: Biochemicals. Alternative Names: 1-[2-[ (3-Chloro-2-methylphenyl) amino]benzoate] β-D-Glucopyranuronic Acid Benzyl Ester. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Tolfenamic Acid-[d4] | Tolfenamic Acid-[d4] is the labelled analogue of Tolfenamic Acid, which is a non-steroidal anti-inflammatory drug (NSAID). It is a derivative of anthranilic acid, related structurally to Mefenamic and Flufenamic acids. Synonyms: Tolfenamic Acid D4; 2-[(3-Chloro-2-methylphenyl)amino]benzoic Acid-d4; N-(3-Chloro-o-tolyl)anthranilic Acid-d4; Clotam-d4; Migea-d4; N-(2-Methyl-3-chlorophenyl)anthranilic Acid-d4; Tolfedine-d4; Tolfine-d4. Grade: 98% by HPLC; 99% atom D. CAS No. 1246820-82-5. Molecular formula: C14H3D4ClNO2. Mole weight: 265.73. | |
| Tolfenamic Acid EP Impurity B | Tolfenamic Acid EP Impurity B. Uses: For analytical and research use. CAS No. 87-60-5. Molecular formula: C7H8ClN. Mole weight: 141.6. Catalog: APB87605. | |
| Tolimidone | Tolimidone is a potent and selective allosteric activator of Lyn kinase with an EC50 of 63 nM. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MLR-1023. CAS No. 41964-07-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-59047. | |
| Tolinapant | Tolinapant (ASTX660) is an orally bioavailable dual antagonist of cellular inhibitor of apoptosis protein (cIAP) and X-linked inhibitor of apoptosis protein (XIAP). Uses: Scientific research. Category: Signaling pathways. Alternative Names: ASTX660. CAS No. 1799328-86-1. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109565. | |
| Tolmetin-d3 | Anti-inflammatory. Group: Biochemicals. Alternative Names: 1-Methyl-d3-5-(4-methylbenzoyl)-1H-pyrrole-2-acetic Acid; 1-Methyl-d3-5-p-toluoylpyrrole-2-acetic Acid; 5-[(p-Tolyl)carbonyl]-1-methyl-d3-pyrrole-2-acetic Acid; McN 2559-d3; Tolmetine-d3. Grades: Highly Purified. CAS No. 1184998-16-0. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Tolmetin-d3 Ethyl Ester | Intermediate for the preparation of Isotope Labeled Tolmetin. Group: Biochemicals. Alternative Names: 1-Methyl-d3-5-(4-methylbenzoyl)-1H-pyrrole-2-acetic Acid Ethyl Ester. Grades: Highly Purified. CAS No. 1215579-60-4. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Tolmetin Sodium | Tolmetin Sodium is the sodium salt of tolmetin, a nonsteroidal anti-inflammatory drug (NSAID) of the pyrrole acetic acid class. It is structurally distinguished from most NSAIDs by its aromatic pyrrolyl acetic acid core, with a para-methylbenzoyl substituent at the N-1 position. Applications: Indicated for the treatment of rheumatoid arthritis, osteoarthritis, and juvenile rheumatoid arthritis. tolmetin sodium is a pyrrole acetic acid class nsaid that provides anti-inflammatory, analgesic, and antipyretic effects through cyclooxygenase inhibition, with a structurally unique pyrrolyl ring system. Category: Active pharmaceutical ingredients. Synonyms: sodium 1-methyl-5-(4-methylbenzoyl)-1H-pyrrole-2-acetate;1-Methyl-5-(p-toluoyl)-1H-pyrrole-2-acetic acid sodium salt. CAS No. 35711-34-3. Product ID: API35711343. Molecular formula: C15H14NNaO3. Mole weight: 279.27. EINECS: 252-687-3. InChIKey: QGUALMNFRILWRA-UHFFFAOYSA-M. |  |
| Tolmetin Sodium Salt Dihydrate | Anti-inflammatory. Group: Biochemicals. Alternative Names: 1-Methyl-5-(4-methylbenzoyl)-1H-pyrrole-2-acetic Acid Sodium Dihydrate; 1-Methyl-5-p-toluoylpyrrole-2-acetic Acid Sodium Dihydrate; 5-[(p-Tolyl)carbonyl]-1-methylpyrrole-2-acetic Acid Sodium Dihydrate; McN 2559-21-98; Tolectin; Tolmene. Grades: Highly Purified. CAS No. 64490-92-2. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Tolnaftate | Antifungal. Group: Biochemicals. Alternative Names: N-Methyl-N- (3-methylphenyl) carbamothioic Acid O-2-Naphthalenyl Ester; Methyl (3-methylphenyl) carbamothioic Acid O-2-Naphthalenyl Ester; 2-Naphthyl N-Methyl-N-(3-tolyl)thiocarbamate. Grades: Highly Purified. CAS No. 2398-96-1. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| TOLNAFTATE (>98%) | TOLNAFTATE (>98%). CAS No. 2398-96-1. Product ID: ALC-FP-2398961. Molecular formula: C19H17NOS. Mole weight: 307.41 g/mol. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Tolnaftate-[d7] | Tolnaftate-[d7] is the labelled analogue of Tolnaftate, which could be used as an Antifungal agent. Synonyms: Tolnaftate D7; N-Methyl-N-(3-methylphenyl)carbamothioic Acid O-2-Naphthalenyl-d7 Ester. Grade: 95% by HPLC; 95% atom D. CAS No. 1329835-64-4. Molecular formula: C19H10D7NOS. Mole weight: 314.45. | |
| Tolnaftate EP Impurity B | Tolnaftate EP Impurity B. Uses: For analytical and research use. CAS No. 127084-74-6. Molecular formula: C21H14O2S. Mole weight: 330.4. Catalog: APB127084746. | |
| Tolnaftate EP Impurity D | Tolnaftate EP Impurity D. Uses: For analytical and research use. CAS No. 696-44-6. Molecular formula: C8H11N. Mole weight: 121.18. Catalog: APB696446. | |
| Tolnaftate Impurity 1 | Tolnaftate Impurity 1. Uses: For analytical and research use. CAS No. 10506-37-3. Molecular formula: C11H7ClOS. Mole weight: 222.69. Catalog: APB10506373. | |
| Tolnaftate Impurity 2 | Tolnaftate Impurity 2. Uses: For analytical and research use. Molecular formula: C13H13NOS. Mole weight: 231.31. Catalog: APB12154. | |
| Tolnaftate Impurity 3 | Tolnaftate Impurity 3. Uses: For analytical and research use. Molecular formula: C11H8O2S. Mole weight: 204.24. Catalog: APB12153. | |
| Tolnaftate Impurity 4 (2,2'-dinaphthyl ether) | Tolnaftate Impurity 4 (2,2'-dinaphthyl ether). Uses: For analytical and research use. CAS No. 613-80-9. Molecular formula: C20H14O. Mole weight: 270.33. Catalog: APB613809. | |
| Tolnaftate Impurity 5 | Tolnaftate Impurity 5. Uses: For analytical and research use. CAS No. 128726-56-7. Molecular formula: C18H20N2S4. Mole weight: 392.61. Catalog: APB128726567. | |
| Tolnaftate Impurity 6 | Tolnaftate Impurity 6. Uses: For analytical and research use. CAS No. 10103-06-7. Molecular formula: C12H12O2. Mole weight: 188.23. Catalog: APB10103067. | |
| Tolnaftate (Standard) | Tolnaftate (Standard) is the analytical standard of Tolnaftate. This product is intended for research and analytical applications. Tolnaftate (NP-27) is a synthetic thiocarbamate used as an anti-fungal agent. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NP-27 (Standard). CAS No. 2398-96-1. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0370R. | |
| Tolperisone 4-carboxylic acid hydrochloride hydrate | Tolperisone 4-carboxylic acid hydrochloride hydrate. Group: Biochemicals. Alternative Names: 4-[2-Methyl-1-oxo-3- (1-piperidinyl) propyl]benzoic acid hydrochloride hydrate. Grades: Highly Purified. CAS No. 446063-44-1. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C16H26ClNO5. US Biological Life Sciences. | Worldwide |
| Tolperisone-d10 hydrochloride | Tolperisone-d10 hydrochloride. Alternative Names: 2-Methyl-1-(4-methylphenyl)-3-(1-piperidinyl-d10)-1-propanone Hydrochloride. CAS No. 1185160-65-9. Product ID: ACM1185160659. Molecular formula: C16H14D10ClNO. Mole weight: 291.88. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Tolperisone-[d10] Hydrochloride | Tolperisone-[d10] Hydrochloride is the labelled analogue of Tolperisone, which is an ion channel blocker and centrally-acting muscle relaxant. Synonyms: Tolperisone D10 Hydrochloride; 2-Methyl-1-(4-methylphenyl)-3-(1-piperidinyl-d10)-1-propanone Hydrochloride. Grade: 95% by HPLC; 98% atom D. CAS No. 1185160-65-9. Molecular formula: C16H13D10NOHCl. Mole weight: 291.88. | |
| Tolperisone hydrochloride | 25g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C16H23NO · HCl. CAS No. 3644-61-9. Prepack ID 23755666-25g. Molecular Weight 281.82. See USA prepack pricing. |  |
| Tolperisone hydrochloride | Tolperisone hydrochloride. Group: Biochemicals. Alternative Names: 2-Methyl-1-(4-methylphenyl)-3-(1-piperidinyl)-1-propanone hydrochloride; 2,4'-Dimethyl-3-piperidino-propiophenone hydrochloride; 2, 4'-Di methyl -3-piperidinopropiophenon e hydrochloride. Grades: Highly Purified. CAS No. 3644-61-9. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: C16H24ClNO. US Biological Life Sciences. | Worldwide |
| Tolperisone Hydrochloride (2-Methyl-1-(4-methylphenyl)-3-(1-piperidinyl)-1-propanone) | Used as a muscle relaxant. Group: Biochemicals. Alternative Names: 2-Methyl-1-(4-methylphenyl)-3-(1-piperidinyl)-1-propanone. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Tolprocarb | Tolprocarb is an oomyces fungicide, which has a strong inhibitory effect on rice blast fungus Magnaporthe grisea by inhibiting polyketide synthase in melanin synthesis pathway [1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 911499-62-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W775186. | |
| Tolrestat | Tolrestat is a potent, orally active aldose reductase inhibitor with IC50 of 35 nM. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AY-27773. CAS No. 82964-04-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16500. | |
| Tolrestat | Tolrestat (AY-27773) is a potent inhibitor of aldose reductase (IC50 = 35 nM). Category: Active pharmaceutical ingredients. Synonyms: AY-27773. CAS No. 82964-04-3. Product ID: API82964043. Molecular formula: C16H14F3NO3S. Mole weight: 357.35. | |
| Tolrestat (Standard) | Tolrestat (Standard) is the analytical standard of Tolrestat. This product is intended for research and analytical applications. Tolrestat is a potent, orally active aldose reductase inhibitor with IC50 of 35 nM. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AY-27773 (Standard). CAS No. 82964-04-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16500R. | |
| Tolterodine | Tolterodine ((R)-(+)-Tolterodine) is a mAChR inhibitor and substrate for cytochrome P450 enzymes. Tolterodine competitively binds acetylcholine, reduces sympathetic excitation, and inhibits involuntary bladder muscle contraction. Tolterodine restores the Nrf2/NF-κB signaling pathway, mediates protection against inflammatory response and ferroptosis. Tolterodine ameliorates LPS (HY-D1056)-induced reactive oxygen species production and lipid oxidation. Tolterodine can be used for the research of urinary tract infections and overactive bladder[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (R)-(+)-Tolterodine; (+)-Tolterodine; (R)-Tolterodine; PNU-200583. CAS No. 124937-51-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0024. | |
| Tolterodine Fumarate | One of the impurities of Tolterodine, which is a muscarinic receptor antagonist and has been found to be effective against urinary incontinence. Category: Other apis. Synonyms: UNII-HH7RXJ4PW1. HH7RXJ4PW1. Phenol, 2-((1R)-3-(bis(1-methylethyl)amino)-1-phenylpropyl)-4-methyl-, (2E)-2-butenedioate (1:1) (salt). CAS No. 615254-93-8. Product ID: API615254938. Molecular formula: C26H35NO5. Mole weight: 441.6. SMILES: CC1=CC(=C(C=C1)O)C(CCN(C(C)C)C(C)C)C2=CC=CC=C2.C(=CC(=O)O)C(=O)O. Appearance: Solid. | |
| Tolterodine impurity 1 | Tolterodine impurity 1. Uses: For analytical and research use. CAS No. 124936-82-9. Molecular formula: C22H31NO. Mole weight: 325.5. Catalog: APB124936829. | |
| Tolterodine impurity 2 | Tolterodine impurity 2. Uses: For analytical and research use. CAS No. 851789-43-0. Molecular formula: C16H20O2. Mole weight: 244.33. Catalog: APB851789430. | |
| Tolterodine impurity 3 | Tolterodine impurity 3. Uses: For analytical and research use. CAS No. 200801-70-3. Molecular formula: C22H31NO2. Mole weight: 341.5. Catalog: APB200801703. | |
| Tolterodine tartrate | 1g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C22H31NO · C4H6O6. CAS No. 124937-52-6. Prepack ID 51586860-1g. Molecular Weight 475.57448. See USA prepack pricing. | |
| Tolterodine tartrate | Tolterodine tartrate (Kabi-2234) is a mAChR inhibitor and substrate for cytochrome P450 enzymes. Tolterodine tartrate competitively binds acetylcholine, reduces sympathetic excitation, and inhibits involuntary bladder muscle contraction. Tolterodine tartrate restores the Nrf2/NF-κB signaling pathway, mediates protection against inflammatory response and ferroptosis. Tolterodine tartrate ameliorates LPS (HY-D1056)-induced reactive oxygen species production and lipid oxidation. Tolterodine tartrate can be used for the research of urinary tract infections and overactive bladder[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Kabi-2234; PNU-200583E. CAS No. 124937-52-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-90010. | |
| Tolterodine tartrate | Tolterodine tartrate. Group: Biochemicals. Grades: Highly Purified. CAS No. 124937-52-6. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. US Biological Life Sciences. | Worldwide |
| Tolterodine Tartrate | Tolterodine Tartrate is a potent muscarinic receptor antagonists that show selectivity for the urinary bladder over salivary glands in vivo. Category: Active pharmaceutical ingredients. CAS No. 124937-52-6. Product ID: API124937526. Molecular formula: C26H37NO7. Mole weight: 475.574. | |
| Tolterodine Tartrate EP Impurity A | Tolterodine Tartrate EP Impurity A. Uses: For analytical and research use. CAS No. 124937-73-1. Molecular formula: C17H20O2. Mole weight: 256.35. Catalog: APB124937731. | |
| Tolterodine Tartrate EP Impurity C | Tolterodine Tartrate EP Impurity C. Uses: For analytical and research use. Molecular formula: C23H33NO. Mole weight: 339.52. Catalog: APB10859. | |
| Tolterodine Tartrate EP Impurity D | Tolterodine Tartrate EP Impurity D. Uses: For analytical and research use. CAS No. 1391053-65-8. Molecular formula: C20H27NO. Mole weight: 297.44. Catalog: APB1391053658. | |
| Tolterodine Tartrate EP Impurity E | Tolterodine Tartrate EP Impurity E. Uses: For analytical and research use. CAS No. 480432-14-2. Molecular formula: C19H25NO. Mole weight: 283.42. Catalog: APB480432142. | |
| Tolterodine Tartrate EP Impurity F | Tolterodine Tartrate EP Impurity F. Uses: For analytical and research use. CAS No. 124937-53-7. Molecular formula: C22H31NO. Mole weight: 325.5. Catalog: APB124937537. | |
| Tolterodine, Tartrate (PNU-20058E, Detrol, Detrusitol) | A muscarinic receptor antagonist. Used in the treatment of urinary incontinence. Group: Biochemicals. Alternative Names: PNU-20058E, Detrol, Detrusitol. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
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