A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Tauroisolithocholanoic acid. Alternative Names: 5β-cholanic acid-3β-ol-N-(2-sulphoethyl)-amide, sodium salt. CAS No. 2707415-30-1. Purity: >99%. Product ID: ALCFA2707415301. Molecular formula: C26H44NNaO5S. Mole weight: 505.69. Alfa Chemistry - ISO 9001:32057 Certified.
Taurolidine
Taurolidine is a derivative of the amino acid Taurine. Taurolidine exhibits antiendotoxin and antimicrobial activity, and has also been shown to exhibit antitumour activity in vitro and in vivo. Taurolidine is used for the treatment of sepsis and is utilized in hospitals to prevent catheter-related bloodstream infections. Group: Biochemicals. Grades: Highly Purified. CAS No. 19388-87-5. Pack Sizes: 1g, 5g, 10g. Molecular Formula: C?H??N?O?S?, Molecular Weight: 284.36. US Biological Life Sciences.
Worldwide
Taurolidine
Taurolidine is a potent antimicrobial and anticancer agent. Taurolidine inhibits cell proliferation. Taurolidine induces apoptosis and autophagy. Taurolidine rescues mice from sepsis-associated lethality[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 19388-87-5. Pack Sizes: 10 mM * 1 mL in DMSO; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-W011522.
Taurolithocholic acid
Taurolithocholic acid is an orally active bile acid and antiviral agent. Taurolithocholic acid upregulates FADS2 by activating the TGR5-PI3K/AKT-SREBP2 signaling axis, inhibits SFTSV-induced ferroptosis (Ferroptosis), viral replication and viral entry of HBV/HDV, while reducing the release of IL-1β, lipid ROS and LDH. While exerting antiviral protective effects, Taurolithocholic acid also stimulates the recycling of hepatocellular membrane transporters, impairs canalicular bile acid secretion function, and induces hepatocyte cholestasis, apoptosis and acute hepatocellular injury. Taurolithocholic acid serves as an experimental model compound for hepatocellular cholestasis. At concentrations ≤200 μM, Taurolithocholic acid shows no cytotoxicity and does not activate the interferon pathway. Taurolithocholic acid not only protects mice from lethal SFTSV infection but also is suitable for studies related to severe fever with thrombocytopenia syndrome and cholestasis[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 516-90-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-113308.
Taurolithocholic acid 3-sulfate disodium
Taurolithocholic acid 3-sulfate disodium is a GPR39 agonist with EC50s of 71.6 ?and 69.4 (absence of Zn2+) and 9 and 9.6 μM (presence of Zn2+) in M39-20 and hGPR39-2 cells, respectively. Taurolithocholic acid 3-sulfate disodium stimulates GPR39 receptors to initiate intracellular calcium signaling, independent of Zn2+ binding sites H17 and H19. Taurolithocholic acid 3-sulfate disodium can be used for the research of gallbladder disease[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 3-Sulfotaurolithocholic acid disodium. CAS No. 64936-83-0. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg. Product ID: HY-137255.
Taurolithocholic acid sodium salt is an orally active bile acid and antiviral agent. Taurolithocholic acid sodium salt upregulates FADS2 by activating the TGR5-PI3K/AKT-SREBP2 signaling axis, inhibits SFTSV-induced ferroptosis, viral replication and viral entry of HBV/HDV, while reducing the release of IL-1β, lipid ROS and LDH. While exerting antiviral protective effects, Taurolithocholic acid sodium salt also stimulates the recycling of hepatocellular membrane transporters, impairs canalicular bile acid secretion function, and induces hepatocyte cholestasis, apoptosis and acute hepatocellular injury. Taurolithocholic acid sodium salt serves as an experimental model compound for hepatocellular cholestasis. At concentrations ≤200 μM, Taurolithocholic acid sodium salt shows no cytotoxicity and does not activate the interferon pathway. Taurolithocholic acid sodium salt not only protects mice from lethal SFTSV infection but also is suitable for studies related to severe fever with thrombocytopenia syndrome and cholestasis[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 6042-32-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113308A.
The major human metabolite, a bile acid which inhibits radioligand binding to muscarinic M1, but not to M2 or M3 receptors. Group: Biochemicals. Alternative Names: 2-[[(3α,5 β ) -3-Hydroxy-24-oxocholan-24-yl] amino] ethanesulfonic Acid. Grades: Highly Purified. CAS No. 6042-32-6. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Taurolithocholic Acid Sulfate
Taurolithocholic Acid Sulfate is a metabolite of bile acids. Sulfation is a major metabolic pathway involved in the elimination and detoxification of bile acids (BAs). Group: Biochemicals. Alternative Names: 2-[[(3α,5 β ) -24-Oxo-3- (sulfooxy) cholan-24-yl] amino] ethanesulfonic Acid; N-(3α-Hydroxy-5 β-cholan-24-oyl)taurine Hydrogen Sulfate (Ester); 3α-Hydroxy-5 β-cholanoyltaurine 3-Sulfate; Sulfolithocholyl taurine; Sulfotaurolithocholic Acid; Taurolithocholic Acid 3-Sulfate; Taurolithocholic Acid 3α-Sulfate; Taurosulfolithocholic Acid. Grades: Highly Purified. CAS No. 64936-83-0. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Tauro-ω-muricholic acid sodium
Tauro-ω-muricholic acid sodium (TωMCA sodium) is a bile acid released by the liver and an analog of tauro-α-muricholic acid. Tauro-ω-muricholic acid sodium is investigated as a potential marker in plasma for early-onset neonatal sepsis (EOS) and cholestasis studies[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: TωMCA sodium. CAS No. 2456348-84-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-136066.
In the reverse reaction, alanine can act instead of taurine, but more slowly, and 2-oxobutanoate and 2-oxopentanoate can act instead of pyruvate. Group: Enzymes. Synonyms: 2-N-(D-1-carboxyethyl)taurine:NAD+ oxidoreductase (taurine-forming). Enzyme Commission Number: EC 1.5.1.23. CAS No. 104645-74-1. 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-1505; tauropine dehydrogenase; EC 1.5.1.23; 104645-74-1; 2-N-(D-1-carboxyethyl)taurine:NAD+ oxidoreductase (taurine-forming). Cat No: EXWM-1505.
Tauroursodeoxycholate
Tauroursodeoxycholate (Tauroursodeoxycholic acid) is an orally active endoplasmic reticulum (ER) stress inhibitor. Tauroursodeoxycholate significantly reduces expression of apoptosis molecules, such as caspase-3 and caspase-12. Tauroursodeoxycholate also inhibits ERK[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Tauroursodeoxycholic acid; TUDCA; UR 906. CAS No. 14605-22-2. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 500 mg. Product ID: HY-19696.
Tauroursodeoxycholate-d4
Tauroursodeoxycholate-d4 is deuterium labeled Tauroursodeoxycholate. Tauroursodeoxycholate (Tauroursodeoxycholic acid) is an endoplasmic reticulum (ER) stress inhibitor. Tauroursodeoxycholate significantly reduces expression of apoptosis molecules, such as caspase-3 and caspase-12. Tauroursodeoxycholate also inhibits ERK. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Tauroursodeoxycholic acid-d4; TUDCA-d4; UR 906-d4. CAS No. 2410279-94-4. Pack Sizes: 100 μg (198.52 μM * 1 mL in Methanol); 1 mg; 5 mg. Product ID: HY-19696S1.
Tauroursodeoxycholate dihydrate
Tauroursodeoxycholate dehydrate is an orally active taurine conjugate of Ursodeoxycholic acid (HY-13771). Tauroursodeoxycholate dehydrate inhibits caspase-3/7, Apoptosis, IRE1α/TRAF2/NF-κB, prevents JNK phosphorylation, inhibits ROS generation, and activates Akt signaling. Tauroursodeoxycholate dehydrate prevents cataract formation, reduces renal tubular damage in type 2 diabetic mice, reduces I/R injury in liver, and inhibits intestinal inflammation and barrier disruption in nonalcoholic fatty liver disease[1][2][3][4][5][6][7][8][9][10]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Tauroursodeoxycholic acid dihydrate; TUDCA dihydrate; UR 906 dihydrate. CAS No. 117609-50-4. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 500 mg. Product ID: HY-19696B.
Tauroursodeoxycholate sodium
Tauroursodeoxycholate (Tauroursodeoxycholic acid; TUDCA) sodium is an endoplasmic reticulum (ER) stress inhibitor. Tauroursodeoxycholate significantly reduces expression of apoptosis molecules, such as caspase-3 and caspase-12. Tauroursodeoxycholate also inhibits ERK. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Tauroursodeoxycholic acid sodium; TUDCA sodium; UR 906 sodium. CAS No. 35807-85-3. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg. Product ID: HY-19696A.
Tauroursodeoxycholate sodium (Standard)
Tauroursodeoxycholate (sodium) (Standard) is the analytical standard of Tauroursodeoxycholate (sodium). This product is intended for research and analytical applications. Tauroursodeoxycholate (Tauroursodeoxycholic acid; TUDCA) sodium is an endoplasmic reticulum (ER) stress inhibitor. Tauroursodeoxycholate significantly reduces expression of apoptosis molecules, such as caspase-3 and caspase-12. Tauroursodeoxycholate also inhibits ERK. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Tauroursodeoxycholic acid sodium (Standard); TUDCA sodium (Standard); UR 906 sodium (Standard). CAS No. 35807-85-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19696AR.
Tauroursodeoxycholic acid, sodium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100mg, 250mg, 500mg, 1g. US Biological Life Sciences.
Worldwide
Tauroursodeoxycholic Acid Sodium Salt
Tauroursodeoxycholate inhibits human cholangiocarcinoma growth via Ca2+-, PKC-, and MAPK-dependent pathways. Group: Biochemicals. Alternative Names: 2-[[(3α,5 β,7 β ) -3, 7-Dihydroxy-24-oxocholan-24-yl] amino] ethanesulfonic Acid. Grades: Highly Purified. CAS No. 35807-85-3. Pack Sizes: 50mg, 100mg, 250mg. US Biological Life Sciences.
Worldwide
Tauroursodeoxycholic acid sodium salt (90%)
Tauroursodeoxycholic acid sodium salt (90%). Group: Biochemicals. Alternative Names: 2- [ [ (3a, 5b, 7b) -3, 7-Dihydroxy-24-oxocholan-24-yl] amino] ethanesulfonic acid. Grades: Highly Purified. CAS No. 35807-85-3. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C26H44NNaO6S. US Biological Life Sciences.
Worldwide
Tauroursodeoxycholic Acid (TUDCA)
Tauroursodeoxycholic Acid (TUDCA).
CA, FL & NJ
Tauroursodeoxycholic Acid (TUDCA)
Tauroursodeoxycholic acid (TUDCA) is the taurine conjugate of ursodeoxycholic acid (UDCA) and acts as a mitochondrial stabilizer and anti-apoptotic agent in several models of neurodegenerative diseases, including AD, Parkinson's diseases (PD), and Huntington's diseases (HD). Group: Inhibitors. CAS No. 14605-22-2. Pack Sizes: 25mg. Product ID: S3654. Formula: C26H45NO6S. Storage Conditions: 2 years -80 in solvent.
United States; Europe
Taurultam Impurity7
Taurultam Impurity7. Uses: For analytical and research use. CAS No. 19388-88-6. Molecular formula: C16H32N8O8S4. Mole weight: 592.72. Catalog: APB19388886.
Taurultam Impurity8
Taurultam Impurity8. Uses: For analytical and research use. CAS No. 78723-71-4. Molecular formula: C4H11NO3S. Mole weight: 135.2. Catalog: APB78723714.
Tautomycetin
Tautomycetin. Group: Biochemicals. Grades: Purified. CAS No. 119757-73-2. Pack Sizes: 50ug. US Biological Life Sciences.
Worldwide
Tau tracer 2
Tau tracer 2 (PI-2620) is a Tau tracer used for imaging Tau protein aggregates. Tau tracer 2 can be used to diagnose neurodegenerative diseases[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PI-2620. CAS No. 2173361-80-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-134880.
Tavaborole
Tavaborole (AN-2690) is an antifungal agent with activity against Trichophyton species, in a topical solution formulation for the potential treatment of onychomycosis. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AN-2690. CAS No. 174671-46-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10980.
Tavaborole
Tavaborole (Kerydin) is a boron-containing small molecule antifungal agent with broad-spectrum activity against filamentous fungi, including both mold and yeast. Category: Active pharmaceutical ingredients. CAS No. 174671-46-6. Product ID: API174671466. Molecular formula: C7H6BFO2. Mole weight: 151.93.
Tavaborole Impurity 1
Tavaborole Impurity 1. Uses: For analytical and research use. CAS No. 1061223-45-7. Molecular formula: C7H8BFO3. Mole weight: 169.95. Catalog: APB1061223457.
Tavaborole Impurity 2
Tavaborole Impurity 2. Uses: For analytical and research use. CAS No. 874290-63-8. Molecular formula: C7H6BFO4. Mole weight: 183.93. Catalog: APB874290638.
Tavapadon
Tavapadon (PF-06649751) is an orally active and highly selective dopamine D1/D5 receptor partial agonist. Tavapadon is effective in enabling movement and reducing disability and has the potential for Parkinson's disease[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PF-06649751; CVL-751. CAS No. 1643489-24-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-119486.
Tavilermide
Tavilermide is a selective, partial agonist of TrkA, or a nerve growth factor (NGF) mimetic. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MIM-D3. CAS No. 263251-78-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17622.
Taxachitriene B
Taxachitriene B is extracted from the needles of the Chinese yew Taxus chinensis. Synonyms: (2R,3E,5S,7S,8E,10S,11R,13S)-10-hydroxy-8-(hydroxymethyl)-4,14,15,15-tetramethylbicyclo[9.3.1]pentadeca-1(14),3,8-triene-2,3,5,7,13-pentayl pentaacetate; Bicyclo[9.3.1]pentadeca-3,8,14-triene-2,3,5,7,10,13-hexol, 8-(hydroxymethyl)-4,14,15,15-tetramethyl-, 2,3,5,7,13-pentaacetate, (2R,3E,5S,7S,8E,10S,11R,13S)-. Grade: 98.0%. CAS No. 167906-75-4. Molecular formula: C30H42O12. Mole weight: 594.65.
Taxacin
Taxacin is a natural diterpenoid compound found in several plants. Synonyms: (1S,3aR,4R,5R,5aR,7S,9S,9aR,10R,11S,11aR)-9a-((benzoyloxy)methyl)-7-(cinnamoyloxy)-11a-hydroxy-1,3a-dimethyl-6-methylene-13-oxotetradecahydro-1,4-ethanobenzo[5,6]cycloocta[1,2-c]furan-5,9,10,11-tetrayl tetraacetate. Grade: >97%. CAS No. 117229-54-6. Molecular formula: C44H48O15. Mole weight: 816.84.
taxadien-5α-ol O-acetyltransferase
This is the third enzyme in the biosynthesis of the diterpenoid antineoplastic drug taxol (paclitaxel), which is widely used in the treatment of carcinomas, sarcomas and melanomas. Group: Enzymes. Synonyms: acetyl coenzyme A:taxa-4(20),11(12)-dien-5α-ol O-acetyl transferase. Enzyme Commission Number: EC 2.3.1.162. CAS No. 229032-29-5. 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-2102; taxadien-5α-ol O-acetyltransferase; EC 2.3.1.162; 229032-29-5; acetyl coenzyme A:taxa-4(20),11(12)-dien-5α-ol O-acetyl transferase. Cat No: EXWM-2102.
taxadiene 5α-hydroxylase
This microsomal cytochrome-P-450-dependent enzyme is involved in the biosynthesis of the diterpenoid antineoplastic drug Taxol (paclitaxel). The reaction includes rearrangement of the 4(5)-double bond to a 4(20)-double bond, possibly through allylic oxidation. Group: Enzymes. Enzyme Commission Number: EC 1.14.99.37. CAS No. 9035-51-2. 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-1048; taxadiene 5α-hydroxylase; EC 1.14.99.37; 9035-51-2. Cat No: EXWM-1048.
taxadiene synthase
This is the committed step in the biosynthesis of the diterpenoid antineoplastic drug Taxol (paclitaxel). The cyclization involves a 1,5-hydride shift. Group: Enzymes. Synonyms: geranylgeranyl-diphosphate diphosphate-lyase (cyclizing, taxadiene-forming). Enzyme Commission Number: EC 4.2.3.17. CAS No. 169277-52-5. 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-5173; taxadiene synthase; EC 4.2.3.17; 169277-52-5; geranylgeranyl-diphosphate diphosphate-lyase (cyclizing, taxadiene-forming). Cat No: EXWM-5173.
taxane 10β-hydroxylase
This microsomal cytochrome-P-450-dependent enzyme is involved in the biosynthesis of the diterpenoid antineoplastic drug taxol (paclitaxel). Group: Enzymes. Enzyme Commission Number: EC 1.14.13.76. CAS No. 337514-75-7. 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-0883; taxane 10β-hydroxylase; EC 1.14.13.76; 337514-75-7. Cat No: EXWM-0883.
taxane 13α-hydroxylase
This cytochrome-P-450-dependent enzyme is involved in the biosynthesis of the diterpenoid antineoplastic drug taxol (paclitaxel). Group: Enzymes. Enzyme Commission Number: EC 1.14.13.77. CAS No. 399030-58-1. 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-0884; taxane 13α-hydroxylase; EC 1.14.13.77; 399030-58-1. Cat No: EXWM-0884.
Taxayunnansin A
Taxayunnansin A is isolated from the barks of Taxus chinensis. Synonyms: (2aR,4S,4aS,5R,6R,8S,9aS,10S,10aR,10bS)-6-(benzoyloxy)-8-hydroxy-9a-(2-hydroxypropan-2-yl)-4a,7-dimethyl-3,4,4a,5,6,8,9,9a,10,10a-decahydro-1H-azuleno[5',6':3,4]benzo[1,2-b]oxete-4,5,10,10b(2aH)-tetrayl tetraacetate. Grade: > 95%. CAS No. 153229-31-3. Molecular formula: C35H44O13. Mole weight: 672.7.
Taxcultine
Taxol D is an impurity of Paclitaxel, an antineoplastic. It is used in the study of structure and function of microtubles into tubulin. Paclitaxel is now used to treat patients with lung, ovarian, breast cancer, head and neck cancer, and advanced forms of Kaposi's sarcoma. Paclitaxel is a mitotic inhibitor used in cancer chemotherapy. Synonyms: Baccatin III 13-ester with (2R,3S)-3-butanoylamino-2-hydroxy-3-phenylpropanoic acid; Paclitaxel Propyl analog; Benzenepropanoic acid, α-hydroxy-β-[(1-oxobutyl)amino]-, (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl ester, (αR,βS)-; B. Grade: 98%. CAS No. 153415-46-4. Molecular formula: C44H53NO14. Mole weight: 819.89.
Taxifolin
Taxifolin is a flavonoid in many plants such as Taxus chinensis, Siberian larch, Cedrus deodara and so on. Taxifolin has shown to inhibit the ovarian cancer cell growth in a dose-dependent manner. Uses: Anti-tumor; anti-cancer; anti-inflammatory; antifungal; antioxidant ability. Synonyms: 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-, (2R,3R)-; (2R,3R)-2-(3,4-Dihydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-4H-1-benzopyran-4-one; 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-, (2R-trans)-; Flavanone, 3,3',4',5,7-pentahydroxy-; (+)-(2R,3R)-Dihydroquercetin; (+)-Dihydroquercetin; (+)-Taxifolin; (+)-trans-Taxifolin; (2R,3R)-(+)-Taxifolin; (2R,3R)-3,3',4',5,7-Pentahydroxyflavanone; (2R,3R)-Dihydroquercetin; 2,3-Dihydroquercetin; 3,5,7,3',4'-Pentahydroxyflavanone; Dihydroquercetin; Diquertin; Distylin; Flamena; Flamena D; Flavomix; HSA 8432; Jikuberuchin; Lariksin; Lavitol; Taxifoliol. Grade: >98%. CAS No. 480-18-2. Molecular formula: C15H12O7. Mole weight: 304.25.
Taxifolin
Taxifolin exhibits important anti-tyrosinase activity. Taxifolin exhibits significant inhibitory activity against collagenase with an IC50 value of 193.3 μM. Category: Active pharmaceutical ingredients. CAS No. 480-18-2. Product ID: API480182. Molecular formula: C15H12O7. Mole weight: 304.252. Appearance: Powder.
Taxifolin
Taxifolin ((+)-Dihydroquercetin) exhibits important anti-tyrosinase activity. Taxifolin exhibits significant inhibitory activity against collagenase with an IC50 value of 193.3 μM. Taxifolin is an important natural compound with antifibrotic activity. Taxifolin is a free radical scavenger with antioxidant capacity[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (+)-Dihydroquercetin; (+)-Taxifolin. CAS No. 480-18-2. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 500 mg. Product ID: HY-N0136.
Taxifolin 3'-O-glucoside
Taxifolin 3'-O-glucoside is isolated from the leaves of Chamaecyparis obtuse. Synonyms: 4H-1-Benzopyran-4-one, 2-(3-(beta-D-glucopyranosyloxy)-4-hydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-, (2R,3R)-. Grade: 98.0%. CAS No. 31106-05-5. Molecular formula: C21H22O12. Mole weight: 342.29.
taxifolin 8-monooxygenase
A flavoprotein, converting a flavanol into a flavanone. Also acts on fustin, but not on catechin, quercetin or mollisacidin. Group: Enzymes. Synonyms: taxifolin hydroxylase. Enzyme Commission Number: EC 1.14.13.19. CAS No. 39307-19-2. 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-0789; taxifolin 8-monooxygenase; EC 1.14.13.19; 39307-19-2; taxifolin hydroxylase. Cat No: EXWM-0789.
Taxifolin (Standard)
Taxifolin (Standard) is the analytical standard of Taxifolin. This product is intended for research and analytical applications. Taxifolin ((+)-Dihydroquercetin) exhibits important anti-tyrosinase activity. Taxifolin exhibits significant inhibitory activity against collagenase with an IC50 value of 193.3 μM[1]. Taxifolin is an important natural compound with antifibrotic activity. Taxifolin is a free radical scavenger with antioxidant capacity[2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (+)-Dihydroquercetin (Standard); (+)-Taxifolin (Standard). CAS No. 480-18-2. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0136R.
Taxin B
Taxin B is extracted from the seeds of Taxus mairei. It has toxic effects. Synonyms: Tricyclo(9.3.1.14,8)hexadeca-4,10-dien-2-one, 3,6,9,14-tetrakis(acetyloxy)-12-hydroxy-1,5,16,16-tetramethyl-, (1S,3R,6S,8R,9S,10E,12S,14S)-. Grade: 98.0%. CAS No. 168109-52-2. Molecular formula: C28H38O10. Mole weight: 534.60.
Taxinine B
Taxinine B is isolated from the barks of Taxus chinensis, and it has strong inhibitory effects against AA-induced aggregation. Synonyms: 2-Propenoic acid, 3-phenyl-, (1S,3S,4aR,5R,6R,11R,12R,12aS)-1,5,11,12-tetrakis(acetyloxy)-1,2,3,4,4a,5,6,7,8,11,12,12a-dodecahydro-9,12a,13,13-tetramethyl-4-methylene-8-oxo-6,10-methanolobenzocyclodecen-3-yl ester, (2E)-. Grade: > 95%. CAS No. 18457-44-8. Molecular formula: C37H44O11. Mole weight: 664.8.
Taxinine M
Taxinine M is extracted from the seeds of Chinese yew Taxus chinensis. Synonyms: 1,4-Ethanobenzo[5,6]cycloocta[1,2-c]furan-13-one, 5,9,10,11-tetrakis(acetyloxy)-9a-[(benzoyloxy)methyl]tetradecahydro-7,11a-dihydroxy-1,3a-dimethyl-6-methylene-, (1S,3aR,4R,5R,5aR,7S,9S,9aR,10R,11S,11aR)-; (2α,5α,7β,9α,10β,12α)-2,7,9,10-Tetraacetoxy-5,11-dihydroxy-13-oxo-12,17-epoxytax-4(20)-en-19-yl benzoate. Grade: 98.0%. CAS No. 135730-55-1. Molecular formula: C35H42O14. Mole weight: 686.70.
Taxiphyllin
Taxiphyllin isolated from the herbs of Pleioblastus amarus (Keng) Keng f. It can inhibit tyrosinase activity in vitro significantly, so it is a potent tyrosinase inhibitor. Uses: Antibacterial activity. Synonyms: (R)-4-hydroxymandelonitrile β-D-glucoside; (2R)-Taxiphyllin. Grade: 98%. CAS No. 21401-21-8. Molecular formula: C14H17NO7. Mole weight: 311.3.
taxoid 14β-hydroxylase
Requires cytochrome P450. From the yew Taxus cuspidata. Also acts on taxa-4(20),11-dien-5α-yl acetate. Group: Enzymes. Enzyme Commission Number: EC 1.14.13.146. 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-0746; taxoid 14β-hydroxylase; EC 1.14.13.146. Cat No: EXWM-0746.