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| Product | Description | |
|---|---|---|
| Tedizolid Impurity 54 | Tedizolid Impurity 54. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: benzyl (2-bromo-3-fluorophenyl)carbamate. CAS No. 2295578-89-9. Molecular Formula: C14H11BrFNO2. Mole Weight: 323.00. Catalog: APB2295578899. |  |
| Tedizolid Impurity 6 | Tedizolid Impurity 6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1003-99-2. Molecular Formula: C6H5BrFN. Mole Weight: 190.02. Catalog: APB1003992. | |
| Tedizolid Impurity 6 | One of the impurities of Tedizolid, which has been found to be an antibacterial agent and could be effective in the treatment of bacterial skin infections. Synonyms: (5R)-3-[3-Fluoro-4-[6-(2-methyl-2H-tetrazol-5-yl)-3-pyridinyl]phenyl]-5-[(phosphonooxy)methyl]-2-Oxazolidinone. Grades: > 95%. Molecular formula: C17H16FN6O6P. Mole weight: 450.33. |  |
| Tedizolid Impurity 7 | One of the impurities of Tedizolid, which has been found to be an antibacterial agent and could be effective in the treatment of bacterial skin infections. Synonyms: ent-Tedizolid Phosphate; (5S)-3-[3-Fluoro-4-[6-(2-methyl-2H-tetrazol-5-yl)?-3-pyridinyl]?phenyl]?-5-[(phosphonooxy)?methyl]?-2-oxazolidinone. Grades: > 95%. CAS No. 1835340-19-6. Molecular formula: C17H16FN6O6P. Mole weight: 450.33. | |
| Tedizolid Impurity 7 | Tedizolid Impurity 7. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1000578-04-0. Molecular Formula: C6H4Br2FN. Mole Weight: 268.91. Catalog: APB1000578040. | |
| Tedizolid Impurity 8 Imidazolium Salt | Thd Imidazolium salt form of one impurity of Tedizolid, which has been found to be an antibacterial agent and could be effective in the treatment of bacterial skin infections. Synonyms: P,?P'-bis[[(5R)?-3-[3-Fluoro-4-[6-(2-methyl-2H-tetrazol-5-yl)?-3-pyridinyl]?phenyl]?-2-oxo-5-oxazolidinyl]?methyl]diphosphoric Acid Ester Imidazolium Salt. Grades: > 95%. CAS No. 1256966-04-7. Molecular formula: C34H30F2N12O11P2. 2C3H4N2. Mole weight: 1018.80. | |
| Tedizolid Impurity 9 | One of the impurities of Tedizolid, which has been found to be an antibacterial agent and could be effective in the treatment of bacterial skin infections. Synonyms: (5R)-3-(4-broMo-3-fluorophenyl)-5-(hydroxyMethyl)oxazolidin-2-one. Grades: > 95%. CAS No. 444335-16-4. Molecular formula: C10H9BrFNO3. Mole weight: 290.09. | |
| Tedizolid Impurity 9 | Tedizolid Impurity 9. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (R)-3-(4-bromo-3-fluorophenyl)-5-(hydroxymethyl)oxazolidin-2-one. CAS No. 444335-16-4. Molecular Formula: C10H9BrFNO3. Mole Weight: 290.09. Catalog: APB444335164. | |
| Tedizolid Impurity 9 | Tedizolid Impurity 9. Uses: For analytical and research use. Group: Impurity standards. CAS No. 60456-23-7. Molecular Formula: C3H6O2. Mole Weight: 74.08. Catalog: APB60456237. | |
| Tedizolid phosphate | Tedizolid phosphate (TR-701FA) is a MAO-A and MAO-B inhibitor with activity against Gram-positive bacteria [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TR-701FA. CAS No. 856867-55-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14855B. |  |
| Tedizolid Phosphate | Torezolid phosphate is a novel oxazolidinone for gram-positive infections, with IC50 of 8.7 μM and 5.7 μM for monoamine oxidase (MAO)-A and MAO-B, respectively. It is commonly used for the treatment of acute bacterial skin and skin structure infections (ABSSSI) caused by several Gram-positive bacteria. Uses: The treatment of acute bacterial skin and skin structure infections (absssi). Synonyms: TR-701FA; Torezolid phosphate; Sivextro; Tedizolid (phosphate); UNII-O7DRJ6R4DW. Grades: >98%. CAS No. 856867-55-5. Molecular formula: C17H16FN6O6P. Mole weight: 450.32. | |
| Tedizolid Phosphate N-Oxide | One of the impurities of Tedizolid, which has been found to be an antibacterial agent and could be effective in the treatment of bacterial skin infections. Grades: > 95%. Molecular formula: C17H16FN6O7P. Mole weight: 466.33. | |
| Teduglutide | Teduglutide is a glucagon-like peptide-2 (GLP-2) analogue that made of 33 amino acid. Teduglutide differs from GLP-2 by an amino acid (an alanine is replaced with a glycine). Teduglutide is superior to GLP-2 on its longer acting. It was approved by FDA named Gattex® on December 21, 2012 as an orphan drug for the treatment of short bowel syndrome (SBS). Uses: A glucagon-like peptide-2 (glp-2) analogue for the treatment of short bowel syndrome(sbs). Synonyms: Teduglutide; Gattex; (Gly2)GLP-2; ALX-0600; Gly(2)-GLP-2; ALX 0600; ALX0600. Grades: 98%. CAS No. 197922-42-2. Molecular formula: C164H252N44O55S. Mole weight: 3752.07. | |
| Teduglutide | Teduglutide (ALX-0600) is an analog of human glucagon like peptide-2 (GLP-2). Teduglutide can activate the expression of nuclear receptor subfamily 4 group a member 1 (NR4a1)/nur77 and intestinal FXR signaling in human hepatic stellate cells, thereby improving liver inflammation and fibrosis in mice with sclerosing cholangitis. Teduglutide can alleviate intestinal dysfunction in mice, improve lung injury, alleviate obesity related neuroinflammation and cell apoptosis [1] [2] [3] [4]. Uses: Scientific research. Group: Peptides. Alternative Names: ALX-0600. CAS No. 197922-42-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1624. | |
| Tefazoline | Heterocyclic Organic Compound. Alternative Names: Tefazoline;2-[(5,6,7,8-Tetrahydronaphthalen-1-yl)methyl]-2-imidazoline;2-(5,6,7,8-tetrahydronaphthalen-1-ylmethyl)-4,5-dihydro-1H-imidazole;2-(tetralin-5-ylmethyl)-4,5-dihydro-1H-imidazole. CAS No. 1082-56-0. Molecular formula: C14H18N2. Catalog: ACM1082560. |  |
| Tefibazumab | Tefibazumab is a humanized IgG1κ monoclonal antibody that binds to the surface-expressed adhesion protein clumping factor A. Tefibazumab can be used for the research of serious Staphylococcus aureus infections [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: INH-H 2002. CAS No. 521079-87-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99571. | |
| Teflubenzuron | Teflubenzuron. Group: Biochemicals. Alternative Names: Tefluron; AC 291898; CME 134; CME 134-01; CME 13406; Calicide; Ektobann; HOE 522; MK 139; Nomolt; Nomolt agro; OMS 3009; N-[[ (3, 5-Dichloro-2, 4-difluorophenyl) amino]carbonyl]-2, 6-difluorobenzamide. Grades: Highly Purified. CAS No. 83121-18-0. Pack Sizes: 1g. Molecular Formula: C14H6Cl2F4N2O2, Molecular Weight: 381.11. US Biological Life Sciences. |  Worldwide |
| Tegafur | Tegafur (FT 207; NSC 148958) is a chemotherapeutic 5-FU proagent used in the treatment of cancers; is a component of tegafur-uracil. Uses: Scientific research. Group: Signaling pathways. Alternative Names: FT 207; NSC 148958. CAS No. 17902-23-7. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-17400. | |
| Tegafur-13c,15n2 | Heterocyclic Organic Compound. Alternative Names: 5-Fluoro-1-(tetrahydro-2-furanyl)-2,4(1H,3H)-pyrimidinedione-13C,15N2; 1-(2-Tetrahydrofuryl)-5-fluorouracil-13C,15N2; 5-Fluoro-1-(tetrahydro-2'-furyl)uracil-13C,15N2; Citofur; Coparogin-13C,15N2; Exonal-13C,15N2; FT 207-13C,15N2; Fental-13C,15N2; Fluaid-13C,15N2; Fluorafur-13C,15N2; Fluorofur-13C,15N2; Franrose-13C,15N2; Ftorafur-13C,15N2; Fulaid-13C,15N2; Fulfeel-13C,15N2. CAS No. 1189456-27-6. Molecular formula: C713CH9F15N2O3. Mole weight: 203.15. Appearance: White Solid. Purity: 0.96. IUPACName: 5-fluoro-1-(oxolan-2-yl)pyrimidine-2,4-dione. Canonical SMILES: C1CC(OC1)N2C=C(C(=O)NC2=O)F. Catalog: ACM1189456276. | |
| Tegafur-13C,15N2 | A labeled form of Tefafur, a drug used as an antineoplastic. Group: Biochemicals. Grades: Highly Purified. CAS No. 17902-23-7. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Tegafur (5-Fluoro-1-(tetrahydro-2-fuanyl)-2,4-(1H,3H)-pyrimidinedione, Citofur, Exonal, Fental) | Used as an antineoplastic. Group: Biochemicals. Alternative Names: 5-Fluoro-1-(tetrahydro-2-fuanyl)-2,4-(1H,3H)-pyrimidinedione, Citofur, Exonal, Fental. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Tegafur-Uracil | Tegafur-Uracil (UFT; BMS-200604) is an effective oral chemotherapy drug based on fluoropyrimidine. Tegafur-Uracil inhibits thymidylate synthase. Tegafur-Uracil can be used in combination with leucovorin (LV) and polysaccharide K (PSK) for research on solid tumors [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: UFT; BMS-200604. CAS No. 74578-38-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16110. | |
| Tegaserod | Tegaserod is an orally active serotonin receptor 4 ( HTR4 ; 5-HT 4 R ) agonist and a 5-HT 2B receptor antagonist. Tegaserod has pK i s of 7.5, 8.4 and 7.0 for human recombinant 5-HT 2A , 5-HT 2B and 5-HT 2C receptors, respectively. Tegaserod causes tumor cell apoptosis , blunts PI3K/Akt/mTOR signaling and decreases S6 phosphorylation. Tegaserod has anti-tumor activity and has the potential for irritable bowel syndrome (IBS) research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 145158-71-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14153. | |
| Tegaserod maleate | Tegaserod maleate (SDZ-HTF-919) is an orally active serotonin receptor 4 ( HTR4 ; 5-HT 4 R ) agonist and a 5-HT 2B receptor antagonist. Tegaserod maleate has pK i s of 7.5, 8.4 and 7.0 for human recombinant 5-HT 2A , 5-HT 2B and 5-HT 2C receptors, respectively. Tegaserod maleate causes tumor cell apoptosis , blunts PI3K/Akt/mTOR signaling and decreases S6 phosphorylation. Tegaserod maleate has anti-tumor activity and has the potential for irritable bowel syndrome (IBS) research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SDZ-HTF-919; HTF-919. CAS No. 189188-57-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14153A. | |
| Tegaserod maleate | Tegaserod maleate. Group: Biochemicals. Grades: Purified. CAS No. 189188-57-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| 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. | |
| Tegoprazan | Tegoprazan. Uses: For analytical and research use. Group: Impurity standards. CAS No. 942195-55-3. Molecular Formula: C20H19F2N3O3. Mole Weight: 387.39. Catalog: APB942195553. | |
| Tegoprazan Impurity 1 | Tegoprazan Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1640981-19-6. Molecular Formula: C16H14N2O3. Mole Weight: 282.3. Catalog: APB1640981196. | |
| Tegoprazan Impurity 10 | Tegoprazan Impurity 10. Uses: For analytical and research use. Group: Impurity standards. CAS No. 844648-22-2. Molecular Formula: C9H6F2O2. Mole Weight: 184.14. Catalog: APB844648222. | |
| Tegoprazan Impurity 12 | Tegoprazan Impurity 12. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1640981-20-9. Molecular Formula: C18H19N3O2. Mole Weight: 309.37. Catalog: APB1640981209. | |
| Tegoprazan Impurity 15 | Tegoprazan Impurity 15. Uses: For analytical and research use. Group: Impurity standards. CAS No. 942195-56-4. Molecular Formula: C20H19F2N3O3. Mole Weight: 387.39. Catalog: APB942195564. | |
| Tegoprazan Impurity 18 | Tegoprazan Impurity 18. Uses: For analytical and research use. Group: Impurity standards. CAS No. 362525-67-5. Molecular Formula: C16H15BrN2O. Mole Weight: 331.21. Catalog: APB362525675. | |
| Tegoprazan Impurity 19 | Tegoprazan Impurity 19. Uses: For analytical and research use. Group: Impurity standards. CAS No. 774582-60-4. Molecular Formula: C15H15BrN2O. Mole Weight: 319.2. Catalog: APB774582604. | |
| Tegoprazan Impurity 22 | Tegoprazan Impurity 22. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2168520-25-8. Molecular Formula: C11H13N3O2. Mole Weight: 219.24. Catalog: APB2168520258. | |
| Tegoprazan Impurity 3 | Tegoprazan Impurity 3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1640981-16-3. Molecular Formula: C18H18N2O3. Mole Weight: 310.35. Catalog: APB1640981163. | |
| Tegoprazan Impurity 4 | Tegoprazan Impurity 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1640981-02-7. Molecular Formula: C18H20N2O4. Mole Weight: 328.37. Catalog: APB1640981027. | |
| Tegoprazan Impurity 5 | Tegoprazan Impurity 5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 39269-74-4. Molecular Formula: C12H12N2O. Mole Weight: 200.24. Catalog: APB39269744. | |
| Tegoprazan Impurity 7 | Tegoprazan Impurity 7. Uses: For analytical and research use. Group: Impurity standards. CAS No. 942195-91-7. Molecular Formula: C9H8F2O2. Mole Weight: 186.16. Catalog: APB942195917. | |
| Tegoprazan Impurity 8 | Tegoprazan Impurity 8. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2713-34-0. Molecular Formula: C6H4F2O. Mole Weight: 130.09. Catalog: APB2713340. | |
| 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 |
| TEGRELLO impurity TAG-05 reference substance | TEGRELLO impurity TAG-05 reference substance. Uses: For analytical and research use. Group: Impurity standards. CAS No. 220241-60-1. Molecular Formula: C15H23ClN4O3S. Mole Weight: 374.88. Catalog: APB220241601. | |
| Tegretol hydrobromide | Tegretol hydrobromide. Uses: For analytical and research use. Group: Impurity standards. CAS No. 906093-29-6. Molecular Formula: C22H31BrN6OS. Mole Weight: 507.5. Catalog: APB906093296. | |
| 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 | 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. Group: Inhibitors. Alternative Names: TEICOPLANIN; 8327a; antibiotic8327a; teichomycin; Teocoplanin ;Telicoplanin;TEICOPLANIN, JP;TeicoplaninSodium. CAS No. 61036-62-2. Molecular formula: C78H77Cl2N8O32R. Mole weight: 1709.39. Purity: ≥98.0%. Catalog: ACM61036622. | |
| 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. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g, 5g. US Biological Life Sciences. | Worldwide |
| 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 | 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 A2-2 | Teicoplanin A2-2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 91032-26-7. Molecular Formula: C88H97Cl2N9O33. Mole Weight: 1879.67. Catalog: APB91032267. | |
| Teicoplanin A2-4 | Teicoplanin A2-4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 91032-37-0. Molecular Formula: C89H99Cl2N9O33. Mole Weight: 1893.7. Catalog: APB91032370. | |
| Teicoplanin A2-5 | Teicoplanin A2-5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 91032-38-1. Molecular Formula: C89H99Cl2N9O33. Mole Weight: 1893.7. Catalog: APB91032381. | |
| 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 |
| 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. Group: Inhibitors. Alternative Names: Telacebec free base; Q-203 free base; Q 203; Q203. CAS No. 1334719-95-7. Molecular formula: C29H28ClF3N4O2. Mole weight: 557.01. Appearance: Solid powder. 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. Catalog: ACM1334719957. | |
| 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. |  |
| Telamycin impurity 1 | Telamycin impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 217649-77-9. Molecular Formula: C46H76N2O14. Mole Weight: 881.11. Catalog: APB217649779. | |
| 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 |
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