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| Product | Description | |
|---|---|---|
| Tegaserod maleate | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Tegaserod Maleate | Tegaserod maleate is a partial agonist of the 5-HT4 receptor (Ki = 12 nM) that can treat irritable bowel syndrome (IBS). Uses: A gastroproeinetic used in the treatment of irritable bowel syndrome. a selective serotonin 5ht4-receptor partial agonist. Synonyms: (Z)-but-2-enedioic acid;1-[[(Z)-(5-methoxyindol-3-ylidene)methyl]amino]-2-pentylguanidine5-methoxyindol-3-carboxaldehyde amino(pentylamino)methylenehydrazone hydrogen maleateHTF 919; HTF919; HTF-919SDZ HTF 919SDZ HTF-919tegaserodtegaserod maleateZelmacZelnorm. Grades: ≥99%. CAS No. 189188-57-6. Molecular formula: C20H27N5O5. Mole weight: 417.46. |  |
| Tegaserod, Maleate (SDZ-HTF-919, Zelmac, 2- [ (5-Methoxy-1H-indol-3-yl ) methyl ene ] -N-pentyl hydrazinecarbo ximidamide , Maleate) | A gastroproeinetic used in the treatment of irritable bowel syndrome. A selective serotonin 5HT4-receptor partial agonist. Group: Biochemicals. Alternative Names: SDZ-HTF-919, Zelmac, 2- [ (5-Methoxy-1H-indol-3-yl ) methyl ene ] -N-pentyl hydrazinecarbo ximidamide , Maleate. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| Teglarinad chloride | Teglarinad chloride, also known as GMX1777, is a water-soluble prodrug of a cyanoguanidine compound with potential antineoplastic activity. In vivo, teglarinad chloride is rapidly converted into active drug through hydrolytic cleavage of a carbonate ester bond. Although the exact mechanism of action has yet to be fully elucidated, the active drug appears to antagonize nuclear factor-kappa B (NF-kB) transcription, resulting in the induction of tumor cell apoptosis. Uses: Antitumor agent. Synonyms: apoptosis inducer GMX1777; GMX 1777; GMX-1777; UNII-D6V5QYX9MZ; 1- [ [ [ [2- [2- [2- [2-Methoxyethoxy] ethoxy] ethoxy] ethoxy] carbonyl] oxy] methyl] -4- [N'-cyano-N''- [6- [4-chlorophenoxy] hexyl] guanidino] pyridinium chloride. CAS No. 432037-57-5. Molecular formula: C30H43Cl2N5O8. Mole weight: 672.61. | |
| Tegobuvir | Tegobuvir is a non-nucleoside nonstructural protein (NS)5B polymerase inhibitor. Synonyms: GS-9190; GS 9190; GS9190; GS-333126; GS 333126; GS333126; Tegobuvir. Grades: >98%. CAS No. 1000787-75-6. Molecular formula: C25H14F7N5. Mole weight: 517.4. | |
| Tegoprazan | Tegoprazan (CJ-12420), a potassium-competitive acid blocker, is a reversible, orally active and highly selective inhibitor of gastric H + /K + -ATPase. Tegoprazan inhibits gastric acid secretion and motility against porcine, canine and human H + /K + -ATPase with IC 50 values ranging from 0.29-0.52 μM in vitro. Tegoprazan significantly improves colitis and enhances the intestinal epithelial barrier function in mice. Tegoprazan is promising for research of Inflammatory bowel, gastric acid-related, motilityimpaired diseases [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CJ-12420; RQ-00000004. CAS No. 942195-55-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17623. |  |
| Tegoprubart | Tegoprubart is a monoclonal antibody directed against CD40 ligand (CD40L), a key mediator of costimulation. Inhibition of CD40L reduces cellular and antibody-mediated immunity and creates a more tolerant immune environment. Tegoprubart was demonstrated to have in vivo efficacy in transplantation animal models. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2628092-47-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P990083. | |
| Tegosept (Drosophila anti-fungal agent) (p-Hydroxybenzoic acid methyl ester, Methyl 4-hydroxybenzoate, Nipagine) | Drosophila anti-fungal agent or mold inhibitor used in conjunction with Drosophila Insect Diet (Caltech). Used as a fly food preservative. Odorless, tasteless and non-toxic (sanctioned for food use), Tegosept is active at low concentrations against a broad spectrum of microorganisms. Drosophila Diet Medium:1. Dissolve 226.53 grams Drosophila Diet Medium (Powder) D9600-07 per liter of distilled/ deionized water, heating to boiling with stirring until completely solubilized. 2. Allow to cool to 80°C.3. Add in while stirring antifungal agents: Tegosept (0.07-2%/L) or Propionic Acid Mix (11.7ml/L). Note: both can be added for additional fungal protection or to eliminate sporadic mold problems.4. Dispense into appropriate containers, store at 4ºC in the dark. Group: Biochemicals. Alternative Names: p-hydroxybenzoic acid, methyl ester; methyl paraben; nipagen; Lexgard M. Grades: Molecular Biology Grade. CAS No. 99-76-3. Pack Sizes: 250g, 1Kg, 2.5Kg, 5Kg. Molecular Formula: C8H8O3 , Molecular Weight: US Biological Life Sciences. | Worldwide |
| teichoic-acid-transporting ATPase | ABC-type (ATP-binding cassette-type) ATPase, characterized by the presence of two similar ATP-binding domains. Does not undergo phosphorylation during the transport process. An enzyme found in Gram-positive bacteria that exports teichoic acid. Group: Enzymes. Enzyme Commission Number: EC 7.5.2.4 (Formerly EC 3.6.3.40). 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-4679; teichoic-acid-transporting ATPase; EC 3.6.3.40. Cat No: EXWM-4679. |  |
| Teichuronic acid | Cas No. 37251-79-9. | |
| Teicoplanin | 100mg Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C89H99Cl2N9O29. CAS No. 61036-62-2. Prepack ID 63289624-100mg. Molecular Weight 1829.69. See USA prepack pricing. |  |
| Teicoplanin | Teicoplanin. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g, 5g. US Biological Life Sciences. | Worldwide |
| Teicoplanin | Teicoplanin is a glycopeptide antibiotic produced by the fermentation of actinomycetes. Teicoplanin is a new generation of glycopeptide antibiotics developed after vancomycin. Synonyms: Tagocid; TEIC; Teicoplaninsterile; lyophilisedteicoplanin; TazobactuMSodiuM+PiperacillinSodiuM; TeichoMycin, TeChemicalbookcoplanin, Targocid, TeicoMid, 8327A, DL507IT, L12507, MDL507, MW1900; TeicoplanincoMplex; TEICOPLANIN[A(2-1)shown]. CAS No. 61036-62-2. Product ID: PAP-0059. Molecular formula: C78H77Cl2N8O32R. Category: Anti-Infectives. Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; Teicoplanin; PAP-0059; Anti-Infectives; C78H77Cl2N8O32R; 61036-62-2. Appearance: White to faint yellow. Standard: EP/USP/IP/JP. Chemical Name: Tagocid. Grade: Pharmaceutical Grade. Solubility: H2O: soluble10mg/mL. Storage: 2-8°C. Applications: Clinical mainly used penicillin, cephalosporin resistant gram-positive bacteria infection, such as endocarditis, osteomyelitis, sepsis and respiratory tract, urinary tract, skin infection. Product Description: Teicoplanin is a glycopeptide antibiotic produced by the fermentation of actinomycetes. Teicoplanin is a new generation of glycopeptide antibiotics developed after vancomycin. |  |
| Teicoplanin | Teicoplanin is a glycopeptide antibiotic indicated for use in serious infections caused by Gram-positive bacteria, including Methicillin-resistant Staphylococcus aureus and Enterococcus aureus.Teicoplanin shows antiviral activity for HIV-1, SARS-CoV1 and SARS-CoV2. Teicoplanin sodium shows anti-MRSA activity [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Antibiotic MDL-507; MDL-507. CAS No. 61036-62-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0097. | |
| Teicoplanin | Teichomycin is a glycopeptide antibiotic produced by Actinoplanes teichomyceticus nov. sp. (ATTCC 31121). Activity against gram-positive bacteria. Uses: Anti-bacterial agents. Synonyms: Targocid; Teichomycin; Teichomycin A2; Teicoplanin. Grades: Assay: 900 IU/mg (anhydrous and sodium-free substance). CAS No. 61036-62-2. Molecular formula: C88H97Cl2N9O33. Mole weight: 1879.65. | |
| Teicoplanin | Teicoplanin is a glycopeptide antibiotic used in the prophylaxis and treatment of serious infections caused by Gram-positive bacteria, including Methicillin-resistant Staphylococcus aureus and Enterococcus faecalis. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TEICOPLANIN;8327a;antibiotic8327a;teichomycin;Teocoplanin ;Telicoplanin;TEICOPLANIN, JP;TeicoplaninSodium. Product Category: Inhibitors. CAS No. 61036-62-2. Molecular formula: C78H77Cl2N8O32R. Mole weight: 1709.39. Purity: ≥98.0%. Product ID: ACM61036622. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Teicoplanin A2 | Teichomycin A2. Grades: JP. CAS No. 61036-64-4. Product ID: 8-01437. Molecular formula: C90H99Cl2N9O34. Mole weight: 1921.69. |  |
| Teicoplanin Complex | Teicoplanin complex is family of closely related metabolites produced by Actinoplanes teichomyceticus which possesses potent broad spectrum antibiotic activity against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus and Enterococcus faecalis. The metabolites share a common glycopeptide core (teicoplanin A3) on which a family of fatty acids varying in length, degree of saturation and branching are linked as amides through one of the aminoglycoside moieties. The major component of the complex is teicoplanin A2 which comprises five major components (teicoplanin A2-1 to A2-5), teicoplanin A3 and four minor components (named teicoplanin RS-1 to RS-4). Group: Biochemicals. Alternative Names: Teichomycin, Tecoplanin, Targocid, Teicomid, Antibiotic 8327A, DL 507IT, L12507, MDL 507, MW 1900. Grades: Highly Purified. CAS No. 61036-62-2. Pack Sizes: 25mg. Molecular Formula: C??H??Cl?N?O??, Molecular Weight: 1829.69. US Biological Life Sciences. | Worldwide |
| Teijin compound 1 | Teijin compound 1 is a potent CCR2b antagonist. Synonyms: (S)-N-(2-((1-(4-chlorobenzyl)pyrrolidin-3-yl)amino)-2-oxoethyl)-3-(trifluoromethyl)benzamide hydrochloride. CAS No. 1313730-14-1. Molecular formula: C21H21ClF3N3O2.HCl. Mole weight: 476.32. | |
| Teijin compound 1 | Teijin compound 1. Group: Biochemicals. Grades: Purified. CAS No. 1313730-14-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Teijin compound 1 hydrochloride | ?98% (HPLC), powder. Group: Fluorescence/luminescence spectroscopy. | |
| Telacebec | Telacebec (Q203) is a midazopyridine amide compound. Telacebec is active against Mycobacterium tuberculosis H37Rv with an MIC 50 of 2.7 nM in culture broth medium. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Q203; IAP6. CAS No. 1334719-95-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101040. | |
| Telacebec free base | Telacebec, also known as Q-203, is an antituberculosis agent and a potent inhibitor of mycobacterium tuberculosis protein potentially for the treatment of tuberculosis. Telacebec targets Mycobacterium tuberculosis cellular energy production through inhibition of the mycobacterial cytochrome bc1 complex. Q203 inhibited the growth of MDR and XDR M. tuberculosis clinical isolates in culture broth medium in the low nanomolar range and was efficacious in a mouse model of tuberculosis at a dose less than 1 mg per kg body weight, which highlights the potency of this compound. In addition, Q203 displays pharmacokinetic and safety profiles compatible with once-daily dosing. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Telacebec free base; Q-203 free base; Q 203; Q203. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 1334719-95-7. Molecular formula: C29H28ClF3N4O2. Mole weight: 557.01. Purity: >98%. IUPACName: 6-chloro-2-ethyl-N-(4-(4-(4-(trifluoromethoxy)phenyl)piperidin-1-yl)benzyl)imidazo[1,2-a]pyridine-3-carboxamide. Canonical SMILES: O=C(C1=C(CC)N=C2C=CC(Cl)=CN21)NCC3=CC=C(N4CCC(C5=CC=C(OC(F)(F)F)C=C5)CC4)C=C3. Product ID: ACM1334719957. Alfa Chemistry ISO 9001:2015 Certified. | |
| Telaglenastat | Telaglenastat (CB-839) is a first-in-class, selective, reversible and orally active glutaminase 1 (GLS1) inhibitor. Telaglenastat selectively inhibits GLS1 splice variants KGA (kidney-type glutaminase) and GAC (glutaminase C) compared to GLS2. The IC 50 s are 23 nM and 28 nM for endogenous glutaminase in mouse kidney and brain, respectively. Telaglenastat inuduces autophagy and has antitumor activity [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CB-839. CAS No. 1439399-58-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-12248. | |
| Telaglenastat | Telaglenastat Inhibitor. Uses: Scientific use. Product Category: T6797. CAS No. 1439399-58-2. |  |
| Telaprevir | Telaprevir is a peptidomimetic inhibitor of hepatitis C virus protease. Group: Biochemicals. Alternative Names: (1S, 3aR, 6aS) - (2S) -2-Cyclohexyl-N- (2-pyrazinylcarbonyl) glycyl-3-methyl-L-valyl-N- [ (1S) -1- [2- (cyclopropylamino) -2-oxoacetyl] butyl] octahydrocyclopenta [c] pyrrole-1-carboxamide. Grades: Highly Purified. CAS No. 402957-28-2. Pack Sizes: 1mg, 2mg, 5mg. US Biological Life Sciences. | Worldwide |
| Telaprevir | Telaprevir is a potent, selective, peptidomimetic inhibitor of the hepatitis C virus (HCV) NS3-4A serine protease, and it demonstrated excellent antiviral activity both in genotype 1b HCV replicon cells (50% inhibitory concentration [IC50] = 354 nM) and in human fetal hepatocytes infected with genotype 1a HCV-positive patient sera (IC50 = 280 nM). Telaprevir forms a covalent but reversible complex with the genotype 1a HCV NS3-4A protease in a slow-on, slow-off process with a steady-state inhibition constant (K(I)*) of 7 nM. Dissociation of the covalent enzyme-inhibitor complex of Telaprevir and genotype 1a HCV protease has a half-life of almost an hour. A >4-log10 reduction in the HCV RNA levels was observed after a 2-week incubation of replicon cells with Telaprevir, with no rebound of viral RNA observed after withdrawal of the inhibitor. In several animal species, Telaprevir exhibits a favorable pharmacokinetic profile with high exposure in the liver. In a recently developed HCV protease mouse model, Telaprevir showed excellent inhibition of HCV NS3-4A protease activity in the liver. Uses: Oligopeptides. Synonyms: Telavic; VRT 111950; VX 950; Incivek; Incivo; LY 570310; MP 424; S-Telaprevir; (1S, 3aR, 6aS) - (2S) -2-Cyclohexyl-N- (2-pyrazinylcarbonyl) glycyl-3-methyl-L-valyl-N- [ (1S) -1- [2- (cyclopropylamino) -2-oxoacetyl]butyl]octahydrocyclopenta [c]pyrrole-1-carboxamide. Grades: ≥98% (HPLC). CAS No. 402957-28-2. Molecular formula: C36H53N7O6. Mole weight: 679.85. | |
| Telaprevir | Telaprevir (VX-950) is a highly selective, reversible, and potent peptidomimetic inhibitor of the HCV NS3-4A protease , the steady-state inhibitory constant ( K i ) of Telaprevir is 7 nM against a genotype 1 (H strain) NS3 protease domain plus a NS4A cofactor peptide [1] [2] [3]. Telaprevir inhibits SARS-CoV-2 3CL pro activity [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: VX-950. CAS No. 402957-28-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10235. | |
| Telaprevir-d4 | A labeled peptidomimetic inhibitor of hepatitis C virus protease. Group: Biochemicals. Alternative Names: (1S, 3aR, 6aS) - (2S) -2-Cyclohexyl-N- (2-pyrazinylcarbonyl) glycyl-3-methyl-L-valyl-N- [ (1S) -1- [2- [ (cyclopropyl-d4) amino] -2-oxoacetyl] butyl] octahydrocyclopenta [c] pyrrole-1-carboxamide. Grades: Highly Purified. Pack Sizes: 250ug. US Biological Life Sciences. | Worldwide |
| Telaprevir impurity 6 | Telaprevir impurity 6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1033882-31-3. Molecular formula: C19H28N4O4. Mole weight: 376.46. Catalog: APB1033882313. | |
| Telapristone | Telapristone, the active metabolite of telapristone acetate (also known as CDB-4124), is a selective progesterone antagonist developed for the long-term treatment of symptoms associated with endometriosis and uterine fibroids. Synonyms: (8S,11R,13S,14S,17R)-11-[4-(dimethylamino)phenyl]-17-hydroxy-17-(2-methoxyacetyl)-13-methyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one; Telapristone; metabolite of telapristone acetate (CDB-4124); 198414-31-2 (Telapristone acetate). Grades: >98%. CAS No. 198414-30-1. Molecular formula: C29H37NO4. Mole weight: 463.618. | |
| Telapristone acetate | Telapristone acetate, also known as CDB-4124, acts as an investigational selective progesterone receptor modulator (SPRM) tested for treatment of progesterone sensitive myomata. Synonyms: CDB4124; CDB-4124; CDB 4124; [(8S,11R,13S,14S,17R)-11-[4-(dimethylamino)phenyl]-17-(2-methoxyacetyl)-13-methyl-3-oxo-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-yl] acetate; 198414-30-1 (Telapristone); CDB4124; CDB-4124; CDB 4124; Telapristone acetate; brand name : Proellex Progenta. Grades: >98%. CAS No. 198414-31-2. Molecular formula: C31H39NO5. Mole weight: 505.64. | |
| Telapristone Acetate | Telapristone Acetate are inhibitors, targeted towards breast cancer research. Also, acts as an investigational selective progesterone receptor modulator (SPRM) being studied for the treatment of certain progesterone-sensitive conditions. Group: Biochemicals. Grades: Highly Purified. CAS No. 198414-31-2. Pack Sizes: 1mg, 10mg. Molecular Formula: C31H39NO5, Molecular Weight: 505.65. US Biological Life Sciences. | Worldwide |
| Telatinib | Telatinib is a potent inhibitor of VEGFR2/3, c-Kit and PDGFRα with IC50 of 6 nM/4 nM, 1 nM and 15 nM, respectively. Synonyms: BAY 57-9352; BAY579352; BAY-57-9352. Grades: >98%. CAS No. 332012-40-5. Molecular formula: C20H16ClN5O3. Mole weight: 409.83. | |
| Telatinib | Telatinib (Bay 57-9352) is an orally active, small molecule inhibitor of VEGFR2 , VEGFR3 , PDGFα , and c-Kit with IC 50 s of 6, 4, 15 and 1 nM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Bay 57-9352. CAS No. 332012-40-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10527. | |
| Telatinib mesylate | Telatinib mesylate (Bay 57-9352 mesylate) is a potent and orally active VEGFR2 , VEGFR3 , PDGFα , and c-Kit inhibitor with IC 50 s of 6 nM, 4 nM, 15 nM and 1 nM, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Bay 57-9352 mesylate. CAS No. 332013-26-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10527C. | |
| Telavancin hydrochloride | Telavancin hydrochloride is the hydrochloride form of Telavancin (HY-112959). Telavancin hydrochloride is a semisynthetic derivative of vancomycin, and exhibits antibacterial efficacy through inhibition of cell wall synthesis and disruption of cell membrane barrier function. Telavancin hydrochloride is efficient against antibiotic resistant S. aureus strains MRSA, VISA, and hVISA. Telavancin hydrochloride attenuates gram positive bacteria induced complicated skin and skin structure infections (cSSSI) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TD-6424 hydrochloride. CAS No. 560130-42-9. Pack Sizes: 1 mg. Product ID: HY-16485. | |
| Telavancin hydrochloride | Telavancin hydrochloride, a derivative of vancomycin, is a potent medication used to combat an array of bacterial infections. These infections include, but are not limited to, skin and soft tissue infections, bloodstream infections caused by Staphylococcus aureus, and Streptococcus pyogenes. Its mode of action is to repress the synthesis of bacterial cell walls. Its efficacy against methicillin-resistant organisms makes it a highly effective option against bacterial infections in clinical settings. Synonyms: Telavancin Hydrochloride; 560130-42-9; Telavancin HCl; Vibativ; UNII-0701472ZG0. CAS No. 560130-42-9. Molecular formula: C80H106Cl2N11O27P·HCl. Mole weight: 1792.096. | |
| Telazorlimab | Telazorlimab (GBR-830) is a humanized monoclonal antibody against OX40 costimulatory receptor on activated T cells. Telazorlimab can be used for the research of autoimmune diseases [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: GBR-830. CAS No. 2126777-87-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99570. | |
| Telbivudine | Nucleoside analog; specific inhibitor of hepatitis B virus (HBV) replication. Antiviral. Group: Biochemicals. Grades: Highly Purified. CAS No. 3424-98-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Telbivudine | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopycarbohydrates. Alternative Names: L-Deoxythymidine, 1-(2-Deoxy-?-L-erythro-pentofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione, NV 02B, Thymine, 1-(2-deoxy-?-L-erythro-pentofuranosyl)- (7CI,8CI), Telbivudine, Epavudine, ?-L-Thymidine, 2'-Deoxy-L-thymidine, Sebivo, L-Thymidine,2,4(1H,3H)-Pyrimidinedione, 1-(2-deoxy-?-L-erythro-pentofuranosyl)-5-methyl-, Tyzeka. | |
| Telbivudine | Telbivudine (Epavudine), an orally active thymidine nucleoside analog, is a potent antiviral inhibitor of hepatitis B virus (HBV) replication [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Epavudine; L-Thymidine; NV 02B. CAS No. 3424-98-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0017. | |
| Telbivudine | Telbivudine is an antiviral drug used in the treatment of hepatitis B infection. It is marketed by Swiss pharmaceutical company Novartis under the trade names Sebivo (Europe) and Tyzeka (United States). Clinical trials have shown it to be significantly more effective than lamivudine or adefovir, and less likely to cause resistance. Uses: Antiviral agents. Synonyms: LDT 600; LD-T600; LDT600; Telbivudine; Tyzeka; Epavudine. Grades: 98%. CAS No. 3424-98-4. Molecular formula: C10H14N2O5. Mole weight: 242.23. | |
| Telbivudine | 2'-deoxy-L-thymidine;1-((2s,4r,5s)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)-5-methylpyrimidine-2,4-dione. 5-HT3 receptor antagonist prevents acute nausea and vomiting associated with emetogenic cancer chemotherapy. CAS No. 3424-98-4. Product ID: 8-04316. Molecular formula: C10H14N2O5. Mole weight: 242.23. Purity: 0.98. Properties: yellow crystal mp 115 ~ 117°C. | |
| Telbivudine-d3 | Labeled nucleoside analog; specific inhibitor of hepatitis B virus (HBV) replication. Antiviral. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Telcagepant | Telcagepant (MK-0974) is an orally active calcitonin gene-related peptide (CGRP) receptor antagonist with K i s of 0.77 nM and 1.2 nM for human and rhesus CGRP receptors, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-0974. CAS No. 781649-09-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-32709. | |
| Telcagepant | Telcagepant is a calcitonin gene-related peptide(CGRP) receptor antagonist under development for the acute treatment and prevention of migraine. It is a highly potent, selective, and orally bioavailable antagonist of the human (K(I) = 0.77 nM) and rhesus (K(I) = 1.2 nM) CGRP receptors, which displays 1500-fold lower affinity for the canine and rat receptors as determined via (125)I-human CGRP competition binding assays in vitro. It displayed moderate clearance (14-20 ml min(-1) kg(-1)) in monkeys, while oral bioavailability was 6%. It was developed by Merck & Co. It was found to have equal potency to rizatriptan and zolmitriptan in two Phase III clinical trials in the acute treatment of migraine. But the company has now terminated development of the drug. Uses: Telcagepant is used to acute treatment and prevention of migraine. Synonyms: MK 0974; MK0974; MK-0974; N-[(3R,6S)-6-(2,3-Difluorophenyl)hexahydro-2-oxo-1-(2,2,2-trifluoroethyl)-1H-azepin-3-yl]-4-(2,3-dihydro-2-oxo-1H-imidazo[4,5-b]pyridin-1-yl)-1-piperidinecarboxamide;N-(6-(2,3-Difluorophenyl)-2-oxo-1-(2,2,2-trifluoroethyl)azepan-3-yl)-4-(2-oxo-2,3-dihydro-1H-imidazo(4,5-B)pyridin-1-yl)piperidine-1-carboxamide. Grades: 95%. CAS No. 781649-09-0. Molecular formula: C26H27F5N6O3. Mole weight: 566.53. | |
| Telenzepine dihydrochloride | Telenzepine dihydrochloride is a selective and orally active muscarinic M1 receptor antagonist with a K i of 0.94 nM. Telenzepine dihydrochloride inhibits gastric acid secretion and has antiulcer effects [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 147416-96-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1789A. | |
| Telenzepine dihydrochloride | Telenzepine dihydrochloride is a selective and high affinity muscarinic M1 receptor antagonist (Ki = 0.94 nM). Telenzepine was demonstrated ability to inhibit gastric acid secretion. Synonyms: 4,9-Dihydro-3-methyl-4-[(4-methyl-1-piperazinyl)acetyl]-10H-thieno[3,4-b][1,5]benzodiazepin-10-one dihydrochloride; Telenzepine hydrochloride; SR-01000075349. CAS No. 147416-96-4. Molecular formula: C19H22N4O2S.2HCl. Mole weight: 443.39. | |
| Telenzepine dihydrochloride | Telenzepine dihydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 147416-96-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Telenzepine dihydrochloride hydrate | solid, ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Teleocidin A1 | Teleocidin A1 is a powerful nematicide and acaricide produced by Streptomyces, which acts as an effective activator of protein kinase C, a tumor promoter, an inducer of colony stimulating factors, and regulator of expression of several genes. Synonyms: Lyngbyatoxin; Lyngbyatoxin-A. Grades: >98% by HPLC. CAS No. 70497-14-2. Molecular formula: C27H39N3O2. Mole weight: 437.62. | |
| Teleprevir | Teleprevir. Group: Biochemicals. Grades: Highly Purified. CAS No. 402957-28-2. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C36H53N7O6. US Biological Life Sciences. | Worldwide |
| Telisotuzumab | Telisotuzumab (ABT-700) is a human recombinant bivalent antibody, a therapeutic antibody against the hepatocyte growth factor receptor (MET) that binds c-Met with high affinity and inhibits c-Met signaling. Telisotuzumab has antitumor activity [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: ABT-700. CAS No. 1781223-80-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99391. | |
| Telisotuzumab vedotin | Telisotuzumab vedotin (ABBV-399) is an antibody-drug conjugate ( ADCs ) targeting c-Met. Telisotuzumab vedotin consists of Monomethyl Auristatin E (MMAE), Telisotuzumab antibody and a cleavable mc-val-cit-PABC type linker. Telisotuzumab vedotin can be used to study non-small cell lung cancer expressing c-Met protein [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABBV-399. CAS No. 1714088-51-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-141601. | |
| Telitacicept | Telitacicept (RC18) is a fully human TACI-Fc fusion protein. Telitacicept is a dual B lymphocyte stimulator (BLyS)/APRIL (a proliferation-inducing ligand) inhibitor that effectively blocks proliferation of B lymphocytes. Telitacicept can be used in research of B-cell autoimmune disease [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: RC18. CAS No. 2136630-26-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99568. | |
| Telithromycin | ?90% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Telithromycin | 25mg Pack Size. Group: Antibiotics, Biochemicals, Research Organics & Inorganics. Formula: C43H65N5O10. CAS No. 191114-48-4. Prepack ID 83145464-25mg. Molecular Weight 812. See USA prepack pricing. | |
| Telithromycin | Telithromycin (HMR3647) is a novel ketolide antibiotic that structurally resembles macrolides. Telithromycin belongs to the ketolide family that is characterized by a keto group at position 3 of the macrolide ring and is active against bacteria causing community-acquired pneumonia, acute exacerbation of chronic bronchitis, and acute sinusitis. Telithromycin also has similar immunomodulatory effects as macrolides. Telithromycin can be used for the research of respiratory infections including bronchial asthma [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: HMR3647; RU66647. CAS No. 191114-48-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-A0062. | |
| Telithromycin | A ketolide antibiotic, used to treat respiratory infections. Group: Biochemicals. Alternative Names: (3aS, 4R, 7R, 9R, 10R, 11R, 13R, 15R, 15aR)-4-Ethyloctahydro-11-methoxy-3a, 7, 9, 11, 13, 15-hexamethyl-1-[4-[4-(3-pyridinyl)-1H-imidazol-1-yl]butyl]-10-[[3, 4, 6-trideoxy-3-(dimethylamino)-b-D-xylo-hexopyranosyl]oxy]-2H-oxacyclotetradecino[4, 3-d]oxazole-2, 6, 8, 14(1H, 7H, 9H)tetrone; Ketek. Grades: Highly Purified. CAS No. 191114-48-4. Pack Sizes: 2mg, 5mg, 10mg, 25mg. Molecular Formula: C??H??N?O??, Molecular Weight: 812. US Biological Life Sciences. | Worldwide |
| Telithromycin intermediate(7a) | Telithromycin intermediate(7a). Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2'-OBEZOYL-3-O-DE[(2,6-DIDEOXY-3-C-METHYL-3-O-METHYL-ALPHA-L-RIBOHEXOPYRANOSYL)OXY]-11-DEOXY-10,11-DIDEHYDRO-12-O-[(1H-IMIDAZOL-1-YL)CARBONYL]-6-O-METHYL-3-OXO-ERYTHROMYCIN;2'-OBEZOYL-3-O-DE[(2,6-DIDEOXY-3-C-METHYL-3-O-METHYL-Α-L-RIBOHEXOPYRANOSYL)OXY]-1. Product Category: Heterocyclic Organic Compound. CAS No. 160145-83-5. Molecular formula: C41H57N3O11. Mole weight: 767.9. Product ID: ACM160145835. Alfa Chemistry ISO 9001:2015 Certified. Categories: Telithromycin intermediate (7A). | |
| Telluracyclopentadiene | Telluracyclopentadiene. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Tellurophene. Appearance: Solid. CAS No. 288-08-4. Molecular formula: C4H4Te. Mole weight: 179.67. Purity: 0.95. Product ID: ACM288084. Alfa Chemistry ISO 9001:2015 Certified. | |
| Telluric acid | Telluric acids exist in both cubic and monoclinic crystalline forms.1 It may be prepared by treating tellurium and tellurous acid with strong oxidants. Group: Electronic materials. Alternative Names: orthotelluricacid; tellurate; telluric; telluric(vi)acid; telluricacid(h6teo6); telluriumhydroxide; TELLURATE HYDROGEN; TELLURIC ACID. CAS No. 7803-68-1. Pack Sizes: 25, 100 g in poly bottle. Molecular formula: 229.64. Mole weight: H6TeO6. O[Te](O)(O)(O)(O)O. 1S/H6O6Te/c1-7(2, 3, 4, 5)6/h1-6H, FXADMRZICBQPQY-UHFFFAOYSA-N. FXADMRZICBQPQY-UHFFFAOYSA-N. |  |
| Telluric acid, 98% | Telluric acid, 98%. Group: Electronic chemicals. CAS No. 7803-68-1. Molecular formula: 229.6g/mol. Mole weight: H6TeO6;H6O6Te. O[Te](O)(O)(O)(O)O. InChI=1S/H6O6Te/c1-7(2,3,4,5)6/h1-6H. FXADMRZICBQPQY-UHFFFAOYSA-N. | |
| tellurite methyltransferase | The enzyme is involved in the detoxification of tellurite. It can also methylate selenite and selenium dioxide. Group: Enzymes. Synonyms: TehB. Enzyme Commission Number: EC 2.1.1.265. 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-1870; tellurite methyltransferase; EC 2.1.1.265; TehB. Cat No: EXWM-1870. | |
| Tellurium | Tellurium. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TELLURIUM PLASMA EMISSION SPECTROSCOPY STANDARD;TELLURIUM PLASMA EMISSION STANDARD;TELLURIUM, PLASMA STANDARD SOLUTION;TELLURIUM SINGLE ELEMENT PLASMA STANDARD;TELLURIUM SINGLE ELEMENT STANDARD;TELLURIUM SINGLE ELEMENT STANDARD ICP-AES;TELLURIUM STANDARD. Product Category: Micro/NanoElectronics. Appearance: solid. CAS No. 13494-80-9. Molecular formula: Te. Mole weight: 127.6. Purity: metal, 99.5%. IUPACName: tellurium. Canonical SMILES: [Te]. Density: 6.24 g/cm³. ECNumber: 236-813-4. Product ID: ACM13494809-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tellurium Acid | Tellurium Acid. Group: other nano materials. CAS No. 7803-68-1. Molecular formula: 229.64 g/mol. Mole weight: H6O6Te. 99.5%. | |
| Tellurium Chloride | TELLURIUM CHLORIDE, 99.9% pure, -8 mesh, (Synonym: Tellurium Tetrachloride), Formula: TeCl4. CAS No. 10026-07-0. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Tellurium dibromide | Tellurium dibromide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TELLURIUM DIBROMIDE;tellurium(II) bromide;Dibromo telluride;Tellurium(II) dibromide. Product Category: Heterocyclic Organic Compound. CAS No. 7789-54-0. Molecular formula: Br2Te. Mole weight: 287.41. Purity: 0.99. IUPACName: bromo tellurohypobromite. Product ID: ACM7789540. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tellurium Dioxide | Solid. Group: Teo2. Product ID: tellurium dioxide. Molecular formula: 159.6g/mol. Mole weight: TeO2. InChI=1S/O2Te/c1-3-2. LAJZODKXOMJMPK-UHFFFAOYSA-N. | |
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