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| Product | Description | |
|---|---|---|
| Trichloropropene Oxide | Trichloropropene Oxide. Group: Biochemicals. Alternative Names: 1,1,1-Trichloro-2,3-epoxypropane; (Trichloromethyl) oxirane; 1,1,1-Trichloro-2,3-epoxypropane; 1,1,1-Trichloro-2-propene Oxide; 1,1,1-Trichloropropane 2,3-Epoxide; 1,1,1-Trichloropropane 2,3-Oxide; 1,1,1-Trichloropropene 2,3-Oxide; 1,1,1-Trichloropropene Oxide; 1,1,1-Trichloropropylene Oxide; 1,2-Epoxy-3,3,3-trichloropropane; 2- (Trichloromethyl) oxirane; 3,3,3-Trichloro-1,2-epoxypropane; 3,3,3-Trichloropropene Oxide; 3,3,3-Trichloropropylene Oxide; NSC 136558; TCPO. Grades: Highly Purified. CAS No. 3083-23-6. Pack Sizes: 10mg. Molecular Formula: C3H3Cl3O, Molecular Weight: 161.41. US Biological Life Sciences. |  Worldwide |
| Trichloro(propyl)silane | Propyltrichlorosilane appears as a colorless liquid with a pungent odor. Corrosive to metals and tissue.;Liquid. Group: Silane coupling agentsself assembly and contact printing materials. Alternative Names: Propyltrichlorosilane. CAS No. 141-57-1. Product ID: trichloro(propyl)silane. Molecular formula: 177.52. Mole weight: C3H7Cl3Si. CCC[Si](Cl)(Cl)Cl. InChI=1S/C3H7Cl3Si/c1-2-3-7(4, 5)6/h2-3H2, 1H3. DOEHJNBEOVLHGL-UHFFFAOYSA-N. >99% (GC). |  |
| Trichloropyranthrene-8,16-dione | Trichloropyranthrene-8,16-dione. Uses: Designed for use in research and industrial production. Additional or Alternative Names: EINECS 215-373-7, Trichloropyranthrene-8,16-dione, 8,16-Pyranthrenedione, trichloro-, CID3037033, 1324-34-1. Product Category: Heterocyclic Organic Compound. CAS No. 1324-34-1. Molecular formula: C30H11Cl3O2. Mole weight: 509.766140 [g/mol]. Purity: 0.96. IUPACName: 1,2,3-trichloropyranthrene-8,16-dione. Canonical SMILES: C1=CC=C2C(=C1)C3=CC4=C5C6=C(C=CC(=C36)C2=O)C=C7C5=C(C=C4)C(=O)C8=C(C(=C(C=C78)Cl)Cl)Cl. Density: 1.651g/cm³. ECNumber: 215-373-7. Product ID: ACM1324341. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Trichloro(pyridine)gold(III) | Trichloro(pyridine)gold(III). Uses: Designed for use in research and industrial production. Additional or Alternative Names: Trichloropyridinegold(III); SC10719; Trichloro(pyridine)gold(III); trichlorogold. Product Category: Gold series of catalysts. CAS No. 14911-01-4. Molecular formula: C5H5AuCl3N. Mole weight: 382.419g/mol. IUPACName: pyridine;trichlorogold. Canonical SMILES: C1=CC=NC=C1.Cl[Au](Cl)Cl. Product ID: ACM14911014. Alfa Chemistry ISO 9001:2015 Certified. | |
| Trichlorosyringol | Trichlorosyringol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3,4,5-Trichloro-2,6-dimethoxyphenol. Product Category: Chlorinated Phenol and Resin Acids Standards. CAS No. 2539-26-6. Molecular formula: C8H7Cl3O3. Mole weight: 257.5. Purity: 99+%. Product ID: ACM2539266. Alfa Chemistry ISO 9001:2015 Certified. | |
| Trichlorotetradecylsilane | Trichlorotetradecylsilane. Group: Silane coupling agentsself assembly and contact printing materials. CAS No. 18402-22-7. Product ID: trichloro(tetradecyl)silane. Molecular formula: 331.8g/mol. Mole weight: C14H29Cl3Si. CCCCCCCCCCCCCC[Si](Cl)(Cl)Cl. InChI=1S / C14H29Cl3Si / c1-2-3-4-5-6-7-8-9-10-11-12-13-14-18 (15, 16) 17 / h2-14H2, 1H3. LPMVYGAHBSNGHP-UHFFFAOYSA-N. | |
| Trichlorovinylsilane | Vinyltrichlorosilane appears as a colorless to pale yellow fuming liquid with a pungent odor. Vapor and liquid may cause burns. More dense than water. Vapors are heavier than air.;Liquid. Group: Self-assembly materials silane coupling agentsself assembly and lithographyposs nanohybrid materials self assembly and contact printing materials. CAS No. 75-94-5. Product ID: trichloro(ethenyl)silane. Molecular formula: 161.48g/mol. Mole weight: C2H3Cl3Si. C=C[Si](Cl)(Cl)Cl. InChI=1S/C2H3Cl3Si/c1-2-6(3, 4)5/h2H, 1H2. GQIUQDDJKHLHTB-UHFFFAOYSA-N. | |
| Trichlorovinylsilane | Trichlorovinylsilane. Group: Biochemicals. Grades: Reagent Grade. CAS No. 75-94-5. Pack Sizes: 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| Trichodermin | Trichodermin is a terpenoid antibiotic which has anti-fungal and protozoal effects. It is originally isolated from Trichoderma viride. Synonyms: Trichoderonin; NSC 73846; 12,13-Epoxytrichothec-9-en-4-ol acetate; [(2S)-trimethylspiro[[?]-2,2'-oxirane]yl] acetate. Grades: 99%. CAS No. 4682-50-2. Molecular formula: C17H24O4. Mole weight: 292.37. |  |
| Trichodesmine | Trichodesmine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (3R,4R,5R,8a1R,13aR)-4,5-Dihydroxy-3-isopropyl-4,5-dimethyl-4,5,8,8a1,10,12,13,13a-octahydro-2H-[1,6]dioxacycloundecino[2,3,4-gh]pyrrolizine-2,6(3H)-dione. Product Category: Heterocyclic Organic Compound. CAS No. 548-90-3. Molecular formula: C18H27O6N. Mole weight: 353.4. Purity: 95%+. Product ID: ACM548903. Alfa Chemistry ISO 9001:2015 Certified. | |
| trichodiene synthase | This enzyme belongs to the family of lyases, specifically those carbon-oxygen lyases acting on phosphates. This enzyme participates in terpenoid biosynthesis. Group: Enzymes. Synonyms: trichodiene synthetase; sesquiterpene cyclase; trans,trans-farnesyl-diphosphate sesquiterpenoid-lyase. Enzyme Commission Number: EC 4.2.3.6. CAS No. 101915-76-8. 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-5220; trichodiene synthase; EC 4.2.3.6; 101915-76-8; trichodiene synthetase; sesquiterpene cyclase; trans,trans-farnesyl-diphosphate sesquiterpenoid-lyase. Cat No: EXWM-5220. |  |
| Trichodimerol | BMS-182123 is a substance produced by Penicillum chrysogenum V39673 that can inhibit the production of Tumor necrosis factor (TNF-a). The IC50 of inhibiting lipopolysaccharide (LPS) induced TNF-a in murine macrophages and human monocytes were 600 ng/mL and 4.0 μg/mL, respectively. Synonyms: BMS-182123. CAS No. 145174-90-9. Molecular formula: C28H32O8. Mole weight: 496.55. | |
| Trichodion | Trichodion is originally isolated from Trichosporiella sp. It inhibits the expression of secretion alkaline phosphatase (SEAP) Reporter gene mediated by IFN-V with IC50 of 5-10 μg/mL, and it also inhibits the expression of human IFN-α promoter-driven Luciferase Reporter gene with IC50 of 2.5-5μg/mL. Molecular formula: C12H14O5. Mole weight: 238.24. | |
| Tricholine citrate (65% in water) | Tricholine Citrate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 546-63-4. Pack Sizes: 50 mg (1.30 M * 77 μL in Water); 100 mg (1.30 M * 154 μL in Water); 1 g (1.30 M * 1.54 mL in Water). Product ID: HY-W127728. |  |
| Tricholine Citrate(ca. 65% in Water) | Synonyms: Choline Citrate Solution (ca. 65% in Water). Grades: > 95%. CAS No. 546-63-4. Molecular formula: (C5H14NO)3 · C6H5O7. Mole weight: 501.61. | |
| Tricholongin BI | Tricholongin BI is an antimicrobial peptide isolated from Trichoderma longibrachiatum. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Ala-Gly-Phe-Ala-Ala-Gln-Ala-Ala-Ala-Ser-Leu-Ala-Pro-Val-Ala-Ala-Gln-Gln-Leu. Grades: >95%. | |
| Tricholongin BII | Tricholongin BII is an antimicrobial peptide isolated from Trichoderma longibrachiatum. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Ala-Gly-Phe-Ala-Ala-Gln-Ala-Ala-Ala-Ser-Leu-Ala-Pro-Val-Ala-Ile-Gln-Gln-Leu. Grades: >95%. | |
| Tricholorethylene | Tricholorethylene. Category CHLORINATED SOLVENTS. Pack Sizes Bulk/ Drums |  |
| Trichostatin a | Trichostatin A (TSA) is a potent and specific inhibitor of HDAC class I/II, with an IC50 value of 1.8 nM for HDAC. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (2E,4E,6R)-7-(4-(DIMETHYLAMINO)PHENYL)-N-HYDROXY-4,6-DIMETHYL-7-OXO-2,4-HEPTADIENAMIDE;7-[4-(DIMETHYLAMINO)PHENYL]-N-HYDROXY-4,6R-DIMETHYL-7-OXO-2E,4E-HEPTADIENAMIDE;4,6-DIMETHYL-7-[P-DIMETHYLAMINOPHENYL]-7-OXAHEPTA-2,4-DIENOHYDROXAMIC ACID;4,6-DIMETHYL-7-[P-DIMETHYLAMINOPHENYL]-7-OXOHEPTA-2,4-DIENOHYDROXAMIC ACID;7-(4-(dimethylamino)phenyl)-n-hydroxy-4,6-dimethyl-7-oxo-4-heptadienamide;TSA;TRICHOSTATIN A;TRICHOSTATIN A, STREPTOMYCES SPECIES. Product Category: Inhibitors. CAS No. 58880-19-6. Molecular formula: C17H22N2O3. Mole weight: 302.37. Purity: 0.9953. Density: 1.139. Product ID: ACM58880196. Alfa Chemistry ISO 9001:2015 Certified. | |
| Trichostatin A | Trichostatin A (TSA) is a potent and specific inhibitor of HDAC class I/II , with an IC 50 value of 1.8 nM for HDAC [1]. Uses: Scientific research. Group: Natural products. Alternative Names: TSA. CAS No. 58880-19-6. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15144. | |
| Trichostatin A | Potent, reversible inhibitor of histone deacetylase. Mediates the activation of O6-methylguanine-DNA methyltransferase (MGMT). May be involved in cell cycle progression of several cell types, induces cell growth arrest at both G1 and G2/M phases. In some cases induces apoptosis. Group: Biochemicals. Grades: Highly Purified. CAS No. 58880-19-6. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Trichostatin A | ?98% (HPLC), from Streptomyces sp. Group: Fluorescence/luminescence spectroscopy. |  |
| Trichostatin A | Trichostatin A, also known as TSA, is an HDAC inhibitor. TSA inhibits the eukaryotic cell cycle during the beginning of the growth stage. TSA can be used to alter gene expression by interfering with the removal of acetyl groups from histones (histone deacetylases, HDAC) and therefore altering the ability of DNA transcription factors to access the DNA molecules inside chromatin. It is a member of a larger class of histone deacetylase inhibitors (HDIs or HDACIs) that have a broad spectrum of epigenetic activities. Uses: Reprogramming. Synonyms: TSA; Antibiotic A-300; 7-(4-(Dimethylamino)phenyl)-N-hydroxy-4,6-dimethyl-7-oxo-2,4-heptadienamide. Grades: 98%. CAS No. 58880-19-6. Molecular formula: C17H22N2O3. Mole weight: 302.37. | |
| Trichostatin A | Trichostatin A Inhibitor. Uses: Scientific use. Product Category: T6270. CAS No. 58880-19-6. |  |
| Trichostatin A, Ready Made Solution | 5 mM in DMSO (0.2 ?m-filtered), from Streptomyces sp. Group: Fluorescence/luminescence spectroscopy. | |
| Trichostatin A, Streptomyces sp. - CAS 58880-19-6 | A potent and reversible, cell-permeable inhibitor of histone deacetylase. Group: Fluorescence/luminescence spectroscopy. | |
| Trichostatin A (TSA, A300, R-(E,E)-7-(4-(dimethylamino)phenyl)-N-hydroxy- 4,6-dimethyl-7-oxo-2,4-heptadienamide) | Antibiotic. Antifungal. Antiprotozoal. Potent and reversible, cell permeable inhibitor of histone deacetylase (HDAC). Immunosuppressive. Anticancer compound. Antifibrogenic. Apoptosis inducer. Induces cell growth arrest at both G1 and G2/M phases. Enhances the efficacy of anticancer agents that target DNA. Inactivates mitotic spindle checkpoint. Smooth muscle cell proliferation inhibitor. Telomerase inhibitor. Downregulates DNA methyltransferase DNMT1 and affects DNA methylation. Anti-inflammatory. Inhibits osteoclastogenesis and bone resorption. Group: Biochemicals. Alternative Names: TSA, A300, R-(E,E)-7-(4-(dimethylamino)phenyl)-N-hydroxy- 4,6-dimethyl-7-oxo-2,4-heptadienamide. Grades: Highly Purified. CAS No. 58880-19-6. Pack Sizes: 1mg, 5mg. Molecular Formula: C17H22N2O3, Molecular Weight: 302.4. US Biological Life Sciences. | Worldwide |
| Trichostatin A (TSA) (Histone Deacetylase Inhibitor)89/1/20 | Trichostatin A is an antifungal antibiotic that is a reversible, potent and specific inhibitor of mammalian histone deacetylase (HDAC) both in vivo and in vitro. Histone deacetylase inhibition causes chromatin relaxation and gene expression modulation. May induce apoptosis. TSA inhibits the eukaryotic cell cycle and induces morphological reversion of transformed cells. It blocks cell cycle progression at G1 phase in Hela Cells. TSA causes accumulation of highly acetylated histones in vivo, while inhibiting the activity of partially purified histone deacetylase in vitro. Group: Biochemicals. Alternative Names: 4,6-Dimethyl-7-[p-dimethylaminophenyl]- 7-oxohepta-2, 4-dienohydroxamic acid). Grades: Highly Purified. CAS No. 58880-19-6. Pack Sizes: 1mg, 5mg. US Biological Life Sciences. | Worldwide |
| Trichostatin C | Trichostatin C can protect the more unstable N-OH group of trichostatin A. It has anti-fungal, protozoan and anti-tumor activity. Synonyms: 145-A. Grades: >95% by HPLC. CAS No. 68676-88-0. Molecular formula: C23H32N2O8. Mole weight: 464.51. | |
| Trichostatin C (Antibiotic 145-A) | Trichostatin C is the first example of a glucopyranosyl hydroxamate from nature. The conjugation may act to protect the less stable N-OH group of Trichostatin A. Trichostatin C displays antifungal, antiprotozoan and antitumor activity, albeit less active than trichostatin A. Group: Biochemicals. Alternative Names: Antibiotic 145-A. Grades: Highly Purified. CAS No. 68676-88-0. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Trichostatin D | Trichostatin D is a metamorphosis cell phenotype recovery inducer produced by the strain of Streptomyces violaceusniger. Synonyms: 1-O-({(2E,4E,6R)-7-[4-(dimethylamino)phenyl]-4,6-dimethyl-7-oxohepta-2,4-dienoyl}amino)-alpha-D-glucopyranose. CAS No. 157479-37-3. Molecular formula: C23H32N2O8. Mole weight: 464.51. | |
| Trichostatin RK | Trichostatin RK is a trigustatine derivative produced by the strain of Streptomyces sp. RK98-A74. It can induce luciferase, but its activity is lower than that of trigustatin. Molecular formula: C18H24N2O2. Mole weight: 300.39. | |
| Trichothecin | Trichothecin has anti-fungal and protozoal effects and it's produced by the strain of Trichothecium roseum. Synonyms: NSC 92492; 12,13-Epoxy-4-hydroxytrichothec-9-en-8-one crotonate. CAS No. 6379-69-7. Molecular formula: C19H24O5. Mole weight: 332.39. | |
| Trichoviridin | It is originally isolated from Trichoderma viride. Trichoviridin has anti-bacterial and fungal effects. Synonyms: Isonitrin C; Trichoviridine. CAS No. 56283-32-0. Molecular formula: C8H9NO4. Mole weight: 183.16. | |
| Tricin | Tricin is a natural flavonoid present in large amounts in Triticum aestivum. Tricin can inhibit human cytomegalovirus (HCMV) replication by inhibiting CDK9. Tricin inhibits the proliferation and invasion of C6 glioma cells via the upregulation of focal-adhesion-finase (FAK)-targeting microRNA-7. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Solid. CAS No. 520-32-1. Molecular formula: C17H14O7. Mole weight: 330.29. Purity: 0.99. Canonical SMILES: O=C1C=C(C2=CC(OC)=C(O)C(OC)=C2)OC3=CC(O)=CC(O)=C13. Product ID: ACM520321-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tricin | Tricin is a natural flavonoid found in large amounts in wheat. Tricin inhibits HCMV replication by inhibiting CDK9. Tricin inhibits the proliferation and invasion of C6 glioma cells by upregulating the expression of FAK-targeting microRNA-7 [1] [2] [3] [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. CAS No. 520-32-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N1127. | |
| Tricine | Tricine is a biological buffer (zwitterionic) designed by Good, et al., and typically referred to as Goods buffer useful in cell culture media formulations. Selection of biological buffer systems should include the following criteria: exclusion by biological membranes, low absorption between 240 and 700nm, chemically stable, and stable to temperature and concentration changes. Group: Biochemicals. Alternative Names: N-Tris (Hydroxymethyl) methylglycine; N-[2-Hydroxy-1, 1-bis (hydroxymethyl) ethyl]glycine. Grades: Molecular Biology Grade. CAS No. 5704-4-1. Pack Sizes: 250g, 500g, 1Kg. Molecular Formula: C6H13NO5, Molecular Weight: 179.2. US Biological Life Sciences. | Worldwide |
| Tricine | Tricine is widely used as a buffer in protein electrophoresis, nucleic acid analysis, and immunology, which can help adjust pH and stabilize chemical reactions. In addition, the compound can also be used in research in certain medical fields, such as in antibody detection and drug screening. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 5704-4-1. Pack Sizes: 10 mM * 1 mL; 5 g; 10 g; 25 g. Product ID: HY-D0860. | |
| Tricine Ultrapure (N-(Tris(hydroxymethyl)methyl)glycine) | 1kg Pack Size. Group: Biochemicals, Buffers. Formula: (HOCH2)3CNHCH2CO2H. CAS No. 5704-4-1. Prepack ID 16725607-1kg. Molecular Weight 179.17. See USA prepack pricing. |  |
| Tricine Ultrapure (N-(Tris(hydroxymethyl)methyl)glycine) | 100g Pack Size. Group: Biochemicals, Buffers. Formula: (HOCH2)3CNHCH2CO2H. CAS No. 5704-4-1. Prepack ID 16725607-100g. Molecular Weight 179.17. See USA prepack pricing. | |
| Tricine Ultrapure (N-(Tris(hydroxymethyl)methyl)glycine) | 500g Pack Size. Group: Biochemicals, Buffers. Formula: (HOCH2)3CNHCH2CO2H. CAS No. 5704-4-1. Prepack ID 16725607-500g. Molecular Weight 179.17. See USA prepack pricing. | |
| tricin synthase | The enzymes from Oryza sativa (ROMT-15 and ROMT-17) catalyses the stepwise methylation of tricetin to its 3'-mono- and 3',5'-dimethyl ethers. In contrast with the wheat enzyme (EC 2.1.1.169, tricetin 3',4',5'-O-trimethyltransferase), tricetin dimethyl ether is not converted to its 3',4',5'-trimethylated ether derivative. The enzymes from Hordeum vulgare (HvOMT1) and from Zea mays (ZmOMT1) form the 3',5'-dimethyl derivative as the major product. Group: Enzymes. Synonyms: ROMT-17; ROMT-15; HvOMT1; ZmOMT1. Enzyme Commission Number: EC 2.1.1.175. 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-1773; tricin synthase; EC 2.1.1.175; ROMT-17; ROMT-15; HvOMT1; ZmOMT1. Cat No: EXWM-1773. | |
| Tricirbine | Triciribine is a potent AKT inhibitor and a cell-permeable tricyclic nucleoside molecule with potential antineoplastic activity. Akt-1, -2, and -3 are serine/threonine protein kinases in the phosphatidylinositol (PI3)-kinase signalling pathway that play a critical role in the regulation of cell proliferation and survival. Following recruitment of Akt to the plasma membrane, phosphorylation at threonine 308 and serine 473 (Akt-1 numbering) by phosphoinositide-dependent kinases (PDK) 1 and 2 results in full activation of the enzyme. Triciribine is a cell-permeable tricyclic nucleoside that inhibits the phosphorylation, activation, and signalling of Akt-1, -2, and -3. It does not inhibit phosphatidylinositol 3 (PI3)-Kinase or PDK1, the direct upstream activators of Akt, nor does it inhibit PKC, PKA, ERK1/2, serum- and glucocorticoid-inducible kinase, p38, STAT3, or JNK signalling pathways. Triciribine effectively inhibits growth of Akt-overexpressing human cancer cell lines in vitro with 50% inhibition at ~5-10 μM. It also inhibit growth of tumor xenografts in mice by greater than 80% at a dose of 1 mg/kg/day. Synonyms: VQD-002; VQD 002; VQD002; NSC-154020; NSC 154020; NSC154020; Triciribine; TCN-P; triciribine; Tricyclic nucleoside; Pentaazacentopthylene; API-2; Akt Inhibitor V. Grades: 99.81%. CAS No. 35943-35-2. Molecular formula: C13H16N6O4. Mole weight: 320.309. | |
| Tricirbine Phosphate | Tricirbine Phosphate is the phosphate salt of Tricirbine. Triciribine is a tricyclic nucleoside that inhibits the phosphorylation, activation, and signalling of Akt - Akt-1, Akt-2 and Akt-3. Triciribine is currently under studies of breast cancer and ovarian cancer as an antineoplastic. Synonyms: TCN-P; UNII-5L5GE3DV88; NSC-280594; C13H17N6O7P. CAS No. 61966-08-3. Molecular formula: C13H17N6O7P. Mole weight: 400.29. | |
| Triciribine | Cell-permeable. A synthetic tricyclic nucleoside which acts as a specific inhibitor of the Akt signaling pathway. It selectively inhibits the phosphorylation and activation of Akt1, -2 and -3 but does not inhibit Akt kinase activity nor known upstream Akt activators such as PI 3-Kinase and PDK1. Group: Biochemicals. Alternative Names: 1,5-Dihydro-5-methyl-1-b-D-ribofuranosyl-1,2,5,6,8-pentaazanaphthylen-3-amine, NSC 154020. Grades: Highly Purified. CAS No. 35943-35-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Triciribine | Triciribine is a DNA synthesis inhibitor, also inhibits Akt and HIV-1/2 with IC 50 of 130 nM, and 0.02-0.46 μM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: API-2; NSC 154020; TCN. CAS No. 35943-35-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15457. | |
| Triciribine hydrate | ?97% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Triclabendazole | analytical standard. Group: Application areaspharma & vet compounds & metabolitesstandards for environmental regulatory methodspharma & vet compounds & metabolitesapi standardseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: Triclabendazole. | |
| Triclabendazole | Triclabendazole is a benzimidazole, and it binds to tubulin impairing intracellular transport mechanisms and interferes with protein synthesis. It is a new type of imidazole anthelmintic. It is effective for Fasciola hepatica in ruminants such as cattle, sheep, goats, and Fasciola hepatica, Fasciola deer, Fasciola hepatica, Fasciola hepatica, etc. Synonyms: 5-Chloro-6-(2,3-dichlorophenoxy)-2-methylthiobenzimidazole; CGA-89317, Egaten; Fasinex. Grades: >98%. CAS No. 68786-66-3. Molecular formula: C14H9Cl3N2OS. Mole weight: 359.66. | |
| Triclabendazole | Triclabendazole is an orally active parasite inhibitor. Triclabendazole has anti- Leishmania activity and induces gasdermin E (GSDME)-dependent pyroptosis by caspase-3 activation. Triclabendazole can be used for the research of fasciola hepatica [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CGA89317. CAS No. 68786-66-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0621. | |
| Triclabendazole | Triclabendazole(CGA89317) is a benzimidazole, it binds to tubulin impairing intracellular transport mechanisms and interferes with protein synthesis.Target: Microtubule/TubulinTriclabendazole treatment produces percentage decreases of the fluke egg output by 15.3%, 4.3% and 36.6%, respectively, in sheep, dairy cows and heifers, these results indicate the presence of TCBZ-resistant Fasciola hepatica in sheep and cattle on this farm. Triclabendazole sulphoxide (50 mg/mL) results in extensive damage to the tegument of triclabendazole-susceptible F. hepatica, whereas triclabendazole-resistant flukes shows only localized and relatively minor disruption of the tegument covering the spines.Triclabendazole is metabolized into a number of compounds, depending on the route of administration, plasma levels peak at 18-24 hours (Triclabendazole sulphoxide) and 36-48 hours (Triclabendazole sulphone), neither Triclabendazole nor any toher metabolites can be detected in plasma. Triclabendazole sulphoxide blocks the transport of secretory bodies from the cell body to the tegumental surface, the block occurs at the site of their formation by the Golgi complex in the cell body, in their movement through the cytoplasmic connections to the syncytium, and in their movement from the base to the apex of the syncytium. Triclabendazole binds to the colchicine binding site on the β-tubulin molecule and this has been used at the basis for evalu | |
| Triclabendazole | 5g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C14H9Cl3N2OS. CAS No. 68786-66-3. Prepack ID 65631957-5g. Molecular Weight 359.66. See USA prepack pricing. | |
| Triclabendazole (5-Chloro-6-(2,3-dichlorophenoxy)-2-methylthio-1H-benzimidazole, CGA-89317, Fasinex) | An anthelmintic (fasciola). Group: Biochemicals. Alternative Names: 5-Chloro-6-(2,3-dichlorophenoxy)-2-methylthio-1H-benzimidazole, CGA-89317, Fasinex. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Triclabendazole-(methyl-d3) | analytical standard. Group: Application areas. | |
| Triclabendazole S-Oxide | Triclabendazole S-Oxide is an impurity of Triclabendazole. Triclabendazole is an anthelmintic used for liver fiukes. Molecular formula: C14H9Cl3N2O2S. Mole weight: 375.66. | |
| Triclabendazole (Standard) | Triclabendazole (Standard) is the analytical standard of Triclabendazole. This product is intended for research and analytical applications. Triclabendazole is an orally active parasite inhibitor. Triclabendazole has anti- Leishmania activity and induces gasdermin E (GSDME)-dependent pyroptosis by caspase-3 activation. Triclabendazole can be used for the research of fasciola hepatica [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 68786-66-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0621R. | |
| Triclabendazole sulfone | Triclabendazole sulfone is an impurity of Triclabendazole. Triclabendazole is an anthelmintic used for liver fiukes. Synonyms: 5-Chloro-6-(2,3-dichlorophenoxy)-2-methylsulfonyl-1H-benzoimidazole. CAS No. 106791-37-1. Molecular formula: C14H9Cl3N2O3S. Mole weight: 391.647. | |
| Triclabendazole Sulfone | analytical standard. Group: Application areaspesticides & metabolitespesticides & metabolitespharma & vet compounds & metabolitesimpurity standardspharmaceutical toxicology. Alternative Names: 6-Chloro-5-(2,3-dichlorophenoxy)-2-(methylsulfonyl)-1H-benzimidazole, CGA 110753, 6-Chloro-5-(2,3-dichlorophenoxy)-2-(methylsulfonyl)-1H-benzimidazole, 1H-Benzimidazole, 5-chloro-6-(2,3-dichlorophenoxy)-2-(methylsulfonyl)- (9CI), Triclabendazole Sulfone. | |
| Triclabendazole Sulfone | Triclabendazole Sulfone. Group: Biochemicals. Alternative Names: 6-Chloro-5-(2,3-dichlorophenoxy)-2-(methylsulfonyl)-1H-benzimidazol. Grades: Highly Purified. CAS No. 106791-37-1. Pack Sizes: 25mg. Molecular Formula: C14H9Cl3N2O3S, Molecular Weight: 391.66. US Biological Life Sciences. | Worldwide |
| Triclabendazole sulfoxide | analytical standard. Group: Application areas. | |
| Triclabendazole sulfoxide | Triclabendazole sulfoxide (TCBZ-SO) is the main plasma metabolite of Triclabendazole, and exhibits anti-parasite effects. Triclabendazole sulfoxide can inhibit membrane transporter ABCG2/BCRP [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TCBZ-SO. CAS No. 100648-13-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-136450. | |
| Triclabendazole Sulfoxide | Triclabendazole Sulfoxide. Group: Biochemicals. Alternative Names: 6-Chloro-5-(2,3-dichlorophenoxy)-2-(methylsulfinyl)-1H-benzimidazole. Grades: Highly Purified. CAS No. 100648-13-3. Pack Sizes: 25mg. Molecular Formula: C14H9Cl3N2O2S, Molecular Weight: 375.66. US Biological Life Sciences. | Worldwide |
| Triclocarban | Used as bacteriostat and antiseptic in soaps and other cleansing compositions. Antiseptic, disinfectant. Group: Biochemicals. Alternative Names: N-(4-Chlorophenyl)-N'-(3,4-dichlorophenyl)urea. Grades: Highly Purified. CAS No. 101-20-2. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Triclocarban | Triclocarban. CAS No. 101-20-2. Pack Sizes: 5, 100 g in glass bottle. Product ID: CDC10-0350. Molecular formula: C13H9Cl3N2O. Category: Cosmetic Preservatives. Product Keywords: Cosmetic Ingredients; Cosmetic Preservatives; Triclocarban; CDC10-0350; 101-20-2; C13H9Cl3N2O; MFCD00013254; 101-20-2. Purity: 0.99. Color: White. Physical State: Powder. Quality Level: 100. Storage: Keep in a cool, dry, dark location in a tightly sealed container or cylinder. Keep away from incompatible materials, ignition sources and untrained individuals. Secure and label area. Protect containers/cylinders from physical damage. Boiling Point: 344.2°C at 760 mmHg. Melting Point: 250-260°C. Density: 1.534 g/cm3. Product Description: 3,4,4'-Trichlorocarbanilide(TCC) is employed as bacteriostat and antimicrobial agent in bar soaps, cosmetics and other personal care prducts.TCC is a toxic, persistent and potentially bioaccumulative polychlorinated binuclear aromatic urea pesticide. |  |
| Triclocarban-13C6 | Labeled Triclocarban. Group: Biochemicals. Alternative Names: N-(4-Chlorophenyl)-N'-(3,4-dichlorophenyl)urea. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Triclocarban Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Triclocarban Related Compound C | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Triclocarban Related Compound D Mixture | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Triclocarban (Standard) | Triclocarban (Standard) (3,4,4-Trichlorocarbanilide (Standard)) is the analytical standard of Triclocarban (HY-B1805). This product is intended for research and analytical applications. Triclocarban, a broad spectrum antibacterial compound, is widely used in a broad range of applications such as the production of soaps, skin creams, toothpastes and deodorants. Triclocarban is a potential endocrine-disrupting chemical with the capacity to modulate androgen and estrogen activities as well as other hormone-mediated biological processes [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 3,4,4-Trichlorocarbanilide (Standard). CAS No. 101-20-2. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B1805R. | |
| Triclofenol Piperazine | Triclofenol piperazine is used for the treatment of patients infected with parasite such as hookworms. Uses: Triclofenol piperazine is used for the treatment of patients infected with parasite such as hookworms. Synonyms: CI-416; CI416; CI 416; Triclofenol piperazate; Triclofenol piperazina; Piperazin-2-one compound with 2,4,5-trichlorophenol. Grades: 98%. CAS No. 5714-82-9. Molecular formula: C16H16Cl6N2O2. Mole weight: 481.03. | |
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