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| Product | Description | |
|---|---|---|
| Tofatinib Impurity A | Tofatinib Impurity A. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1092578-46-5. Molecular formula: C16H20N6O. Mole weight: 312.38. Catalog: APB1092578465. |  |
| Tofatinib Impurity D | Tofatinib Impurity D. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1252883-90-1. Molecular formula: C20H25N5. Mole weight: 335.45. Catalog: APB1252883901. | |
| Tofatinib Impurity Q | Tofatinib Impurity Q. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1675248-19-7. Molecular formula: C16H22N6O2. Mole weight: 330.39. Catalog: APB1675248197. | |
| Tofatinib Impurity T | Tofatinib Impurity T. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1092578-43-2. Molecular formula: C16H20N6O. Mole weight: 312.38. Catalog: APB1092578432. | |
| Tofenacin | A metabolite of Orphenadrine. An antidepressant prodrug. Group: Biochemicals. Alternative Names: N-Methyl-2- [ (2-methylphenyl) phenylmethoxy] ethanamine; N-Methyl-2- [ (o-methyl-α -phenylbenzyl) oxy] ethylamine; Demethylorphenadrine; N-Demethylorphenadrine; N-Desmethylorphenadrine; Tofenacine. Grades: Highly Purified. CAS No. 15301-93-6. Pack Sizes: 2.5mg. US Biological Life Sciences. |  Worldwide |
| Tofenacin Hydrochloride | Tofenacin Hydrochloride. Group: Biochemicals. Alternative Names: ORPHENADRINE RELATED COMPOUND C. Grades: Highly Purified. CAS No. 10488-36-5. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C17H21NOClH. US Biological Life Sciences. | Worldwide |
| Tofersen | Tofersen (BIIB067) is an antisense oligonucleotide that mediates RNase H-dependent degradation of superoxide dismutase 1 (SOD1) mRNA to reduce the synthesis of SOD1 protein. Tofersen can be used for the research of amyotrophic lateral sclerosis (ALS)[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BIIB067; ISIS-SOD1Rx. CAS No. 2088232-70-4. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-132580. |  |
| Tofersen sodium | Tofersen sodium is an antisense oligonucleotide that mediates RNase H-dependent degradation of superoxide dismutase 1 (SOD1) mRNA to reduce the synthesis of SOD1 protein. Tofersen sodium can be used for the research of amyotrophic lateral sclerosis (ALS)[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BIIB067 sodium; ISIS-SOD1Rx sodium. CAS No. 1898254-60-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-132580A. | |
| Tofisopam | Tofisopam, a 2,3-benzodiazepine compound, is an orally active anxiolytic agent. Tofisopam can inhibit phosphodiesterase PDE isoenzyme activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 22345-47-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0165. | |
| Tofogliflozin | Tofogliflozin. Group: Biochemicals. Alternative Names: (1S, 3'R, 4'S, 5'S, 6'R) -6-[ (4-Ethylphenyl) methyl]-3', 4', 5', 6'-tetrahydro-6'- (hydroxymethyl) spiro[isobenzofuran-1 (3H) , 2'-[2H]pyran]-3', 4', 5'-triol; CSG 452. Grades: Highly Purified. CAS No. 903565-83-3. Pack Sizes: 25mg. Molecular Formula: C22H26O6. US Biological Life Sciences. | Worldwide |
| Tofogliflozin hydrate | Tofogliflozin hydrate (CSG-452 hydrate) is a potent and highly specific sodium/glucose cotransporter 2 (SGLT2) inhibitor with an IC 50 of 2.9 nM and K i values of 2.9 nM, 14.9 nM, and 6.4 nM for human, rat, and mouse SGLT2 [1]. Tofogliflozin partially inhibits high glucose-induced reactive oxyen species (ROS) generation in tubular cells [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CSG-452 hydrate. CAS No. 1201913-82-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-13413. | |
| 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. |  |
| Togni Reagent II | Togni Reagent II. Group: Biochemicals. Alternative Names: 1-(Trifluoromethyl)-1,2-benziodoxol-3(1H)-one. Grades: Highly Purified. CAS No. 887144-94-7. Pack Sizes: 1g. Molecular Formula: C8H4F3IO2, Molecular Weight: 316.02. US Biological Life Sciences. | Worldwide |
| Tognis Reagent | Tognis Reagent. Group: Biochemicals. Alternative Names: 3,3-Dimethyl-1-(trifluoromethyl)-2-benziodoxole. Grades: Highly Purified. CAS No. 887144-97-0. Pack Sizes: 1g. Molecular Formula: C10H10F3IO, Molecular Weight: 330.09. US Biological Life Sciences. | Worldwide |
| TokeOni | TokeOni. Group: other materials. Product ID: (4S)-2-[(1E,3E)-4-[4-(dimethylamino)phenyl]buta-1,3-dienyl]-4,5-dihydro-1,3-thiazole-4-carboxylic acid; hydrochloride. Molecular formula: 338.9g/mol. Mole weight: C16H19ClN2O2S. CN (C)C1=CC=C (C=C1)C=CC=CC2=NC (CS2)C (=O)O. Cl. 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. PZCNKVAGZCXXHX-SSRSOBHISA-N. |  |
| 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 |
| Toladryl | A diphenylhydramine analog classified as an antihistaminic. Group: Biochemicals. Alternative Names: N, N-Dimethyl-2- [ (4-methylphenyl) phenylmethoxy] ethanamine; 4-Methyldiphenhydramine; p-Methyldiphenhydramine; N, N-Dimethyl-N-[2- (p-methyl-α -phenylbenzyloxy) ethyl]amine; p-Methylbenzhydryl 2-Dimethylaminoethyl Ether. Grades: Highly Purified. CAS No. 19804-27-4. Pack Sizes: 50mg. 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 |
| Tolazamide | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metabolitesapi standardspharmaceutical toxicology. Alternative Names: Tolinase, 1-(Hexahydro-1H-azepin-1-yl)-3-(p-tolylsulfonyl)urea, 1-(Hexahydro-1-azepinyl)-3-p-tolylsulfonylurea, Diabewas, Tolazamide, NSC 70762, 1-(4-Methylphenylsulfonyl)-3-(hexahydro-1H-azepin-1-yl)urea, Urea, 1-(hexahydro-1H-azepin-1-yl)-3-(p-tolylsulfonyl)- (6CI,7CI,8CI), Tolanase, U 17835, Norglycin,Benzenesulfonamide, N-[[(hexahydro-1H-azepin-1-yl)amino]carbonyl]-4-methyl-, N-(p-Toluenesulfonyl)-N'-hexamethyleniminourea. | |
| Tolazamide | Tolazamide is an oral hypoglycemic agent used in the study of type 2 diabetes. Uses: Scientific research. Group: Signaling pathways. Alternative Names: U-17835. CAS No. 1156-19-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0920. | |
| Tolazoline | Tolazoline(Imidaline) is a non-selective competitive α-adrenergic receptor antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Imidaline; NSC35110. CAS No. 59-98-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-A0066. | |
| 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 (Imidaline) hydrochloride is an alpha-adrenergic receptor inhibitor. Uses: Scientific research. Group: Natural products. Alternative Names: Imidaline hydrochloride; NSC35110 hydrochloride. CAS No. 59-97-2. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-A0066A. | |
| 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 | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardspharmaceutical toxicology. Alternative Names: 2-Benzyl-2-imidazoline hydrochloride, Benzazoline hydrochloride,Tolazoline Hydrochloride, 4,5-Dihydro-2-(phenylmethyl)-1H-imidazole hydrochloride, Phenylmethylimidazolin hydrochloride, 2-Benzyl-2-iminazoline hydrochloride, 2-Benzyl-4,5-imidazoline hydrochloride. | |
| 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 K ATP 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. Group: Signaling pathways. CAS No. 64-77-7. Pack Sizes: 10 mM * 1 mL; 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 | analytical standard. Group: Additional drugs. | |
| Tolbutamide | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metabolitesapi standardseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: Tolbutamide. | |
| 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. | |
| Tolbutamide (Standard) | Tolbutamide (Standard) is the analytical standard of Tolbutamide. This product is intended for research and analytical applications. Tolbutamide is an orally active K ATP 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. Group: Signaling pathways. CAS No. 64-77-7. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B0401R. | |
| Tolcapone | Tolcapone (Ro 40-7592) is a selective, orally active and powerful mixed (peripheral and central) COMT inhibitor with an IC 50 of 773?nM in the liver [1]. Tolcapone is also a potent inhibitor of α-syn and Aβ42 oligomerization and fibrillogenesis [2]. Tolcapone induces oxidative stress leading to apoptosis and inhibition of tumor growth in neuroblastoma [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 40-7592. CAS No. 134308-13-7. Pack Sizes: 10 mM * 1 mL; 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 | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Tolcapone Related Compound B | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Tolcide 2230 | Antimicrobial agent used as a substitute for chlorophenols in industrial applications. Group: Biochemicals. Alternative Names: Thiocyanic Acid (2-Benzothiazolylthio) methyl Ester; 2- (Thiocyanato methyl thio) benzo [d] thiazole. Grades: Highly Purified. CAS No. 21564-17-0. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Tolclofos-methyl | Tolclofos-methyl is a broad-spectrum aromatic hydrocarbon fungicide that is used as a see treatment for protection against soil-borne and seed borne fungal pathogens that caused seed decay and seedling blights. Uses: Scientific research. Group: Signaling pathways. CAS No. 57018-04-9. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-B2053. | |
| Tolclofos-methyl | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. | |
| Tolclofos-methyl (Standard) | Tolclofos-methyl (Standard) is the analytical standard of Tolclofos-methyl. This product is intended for research and analytical applications. Uses: Scientific research. Group: Signaling pathways. CAS No. 57018-04-9. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B2053R. | |
| Toldimfos sodium | Toldimfos sodium. Uses: Designed for use in research and industrial production. Additional or 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. Molecular formula: C9H13NNaO2P. Mole weight: 221.17. Purity: 95%+. IUPACName: 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. Product ID: ACM575757. Alfa Chemistry ISO 9001:2015 Certified. Categories: Sodium (4-(dimethylamino)-2-methylphenyl)phosphinate. |  |
| Tolebrutinib | Tolebrutinib (SAR442168) is a potent, selective, orally active and brain-penetrant inhibitor of Bruton tyrosine kinase (BTK) , with IC 50 s 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. Group: Signaling pathways. Alternative Names: SAR442168; PRN2246. CAS No. 1971920-73-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109192. | |
| 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 | Tolfenamic Acid (GEA 6414) is a non-steroidal anti-inflammatory and anti-cancer agent, selectively inhibits COX-2 , with an IC 50 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. Group: Signaling pathways. Alternative Names: GEA 6414. CAS No. 13710-19-5. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-B0335. | |
| 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-(benzoic ring-13C6) | analytical standard. Group: Opiates / synthetic analgesic drug standards. | |
| 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 (Standard) | Tolfenamic Acid (Standard) is the analytical standard of Tolfenamic Acid. This product is intended for research and analytical applications. Tolfenamic Acid (GEA 6414) is a non-steroidal anti-inflammatory and anti-cancer agent, selectively inhibits COX-2 , with an IC 50 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. Group: Signaling pathways. Alternative Names: GEA 6414 (Standard). CAS No. 13710-19-5. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0335R. | |
| Tolfenpyrad | Tolfenpyrad is an insecticide approved for marketing in Japan in 2002. Uses: Scientific research. Group: Signaling pathways. CAS No. 129558-76-5. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-17516. | |
| 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. Group: Signaling pathways. Alternative Names: ASTX660. CAS No. 1799328-86-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109565. | |
| Toll Like Receptor 2, Positive Control (TLR2, TIL4, CD282) | Toll Like Receptor 2, Positive Control (TLR2, TIL4, CD282). Group: Molecular Biology. Pack Sizes: 15ul. US Biological Life Sciences. | Worldwide |
| Tolmetin | Tolmetin is an orally active and potent COX inhibitor with IC 50 s of 0.35 μM and 0.82 μM human COX-1 and COX-2, respectively. Tolmetin is a non-steroidal anti-inflammatory drug (NSAID) [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 26171-23-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-B1799. | |
| 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 | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Tolmetin sodium dihydrate | Tolmetin sodium dihydrate is an orally active and potent COX inhibitor with IC 50 s of 0.35 μM and 0.82 μM human COX-1 and COX-2, respectively. Tolmetin sodium dihydrate is a non-steroidal anti-inflammatory drug (NSAID) [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 64490-92-2. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1489. | |
| 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 | Tolnaftate (NP-27) is a synthetic thiocarbamate used as an anti-fungal agent. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Carbamothioic acid, N-methyl-N-(3-methylphenyl)-, O-2-naphthalenyl ester. Product Category: Inhibitors. Appearance: White powder. CAS No. 2398-96-1. Molecular formula: C19H17NOS. Mole weight: 307.41. Purity: 0.9994. Canonical SMILES: S=C(OC1=CC=C2C=CC=CC2=C1)N(C)C3=CC=CC(C)=C3. Density: 1.223 g/cm³. Product ID: ACM2398961. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tolnaftate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metabolitesapi standardseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: O-Naphthalen-2-yl methyl(3-methylphenyl)carbamothioate,Tolnaftate. | |
| Tolnaftate | Tolnaftate (NP-27) is a synthetic thiocarbamate used as an anti-fungal agent. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NP-27. CAS No. 2398-96-1. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0370. | |
| Tolnaftate-d7 | Tolnaftate-d7. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1329835-64-4. Molecular formula: C19H10D7NOS. Mole weight: 314.45. Catalog: APB1329835644. | |
| 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 Impurity 1 | Tolnaftate Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 10506-37-3. Molecular formula: C11H7ClOS. Mole weight: 222.69. Catalog: APB10506373. | |
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