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| Product | Description | |
|---|---|---|
| Tigecycline hydrate | Tigecycline (GAR-936) hydrate is a broad-spectrum glycylcycline antibiotic. The mean inhibitory concentration (MIC) of Tigecycline hydrate for E. coli (MG1655 strain) is approximately 125 ng/mL. MIC50 and MIC90 are 1 and 2 mg/L for Acinetobacter baumannii (A. baumannII), respectively. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Tigecyclin, Tigecycline hydrate, 9-t-Butylglycylamido-minocycline hydrate, 1229002-07-6. Product Category: Inhibitors. CAS No. 1229002-07-6. Molecular formula: C29H41N5O9. Mole weight: 585.65 (anhydrous basis). Purity: 0.96. IUPACName: (4S,4aS,5aR,12aR)-9-[[2-(tert-butylamino)acetyl]amino]-4,7-bis(dimethylamino)-1,10,11,12a-tetrahydroxy-3,12-dioxo-4a,5,5a,6-tetrahydro-4H-tetracene-2-carboxamide;hydrate. Canonical SMILES: O=C(C(C1=O)=C(O)[C@@H](N(C)C)[C@]2([H])C[C@]3([H])CC4=C(C(C3=C(O)[C@@]21O)=O)C(O)=C(NC(CNC(C)(C)C)=O)C=C4N(C)C)N.O.[x]. Product ID: ACM1229002076. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Tigecycline hydrate | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Tigecycline hydrate | Tigecycline (GAR-936) hydrate is a broad-spectrum glycylcycline antibiotic. The mean inhibitory concentration (MIC) of Tigecycline hydrate for E. coli (MG1655 strain) is approximately 125 ng/mL [1]. MIC 50 and MIC 90 are 1 and 2 mg/L for Acinetobacter baumannii ( A. baumannii ), respectively [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GAR-936 hydrate. CAS No. 1229002-07-6. Pack Sizes: 1 mg. Product ID: HY-B0117D. |  |
| Tigecycline hydrochloride | Tigecycline is active against a broad range of gram-negative and gram-positive bacterial species including clinically important multidrug-resistant nosocomial and community-acquired bacterial pathogens. Tigecycline has been shown to inhibit the translation elongation step by binding to the ribosome 30S subunit and preventing aminoacylated tRNAs to accommodate in the ribosomal A site. Tigecycline has also been found to be effective for the treatment of community- as well as hospital-acquired and ventilator-associated pneumonia and bacteremia, sepsis with shock and urinary tract infections. Tigecycline appears to be a valuable treatment option for the management of superbugs, especially where conventional therapy has failed. Synonyms: GAR-936; GAR 936; GAR936; Tygacil. Grades: >98%. CAS No. 197654-04-9. Molecular formula: C29H40ClN5O8. Mole weight: 622.11. |  |
| Tigecycline Impurity 1 | An impurity of Ticlopidine which is a glycylcycline antibiotic and acts by reversibly binding to the 30S ribosomal subunit. Grades: > 95%. Molecular formula: C23H26N4O9. Mole weight: 502.49. | |
| Tigecycline Impurity 2 | An impurity of Ticlopidine which inhibits protein translation by blocking entry of aminoacyl-trna into the ribosome A site; regarded as the first of a new class of glycylcyline antibiotics. Grades: > 95%. Molecular formula: C24H28N4O10. Mole weight: 532.51. | |
| Tigecycline Impurity 3 | An impurity of Ticlopidine which is a first-in-class, broad spectrum antibiotic with activity against antibiotic-resistant organisms. Grades: > 95%. Molecular formula: C20H19N3O9. Mole weight: 445.39. | |
| Tigecycline Impurity 38 | Tigecycline Impurity 38. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1333466-46-8. Molecular formula: C23H26N4O9. Mole weight: 502.48. Catalog: APB1333466468. | |
| Tigecycline Impurity 5 | An impurity of Ticlopidine which has been shown to inhibit the translation elongation step by binding to the ribosome 30S subunit and preventing aminoacylated tRNAs to accommodate in the ribosomal A site. Grades: > 95%. Molecular formula: C24H30N4O8. Mole weight: 502.53. | |
| Tigecycline Impurity 6 | An impurity of Ticlopidine which is active against a broad range of gram-negative and gram-positive bacterial species including clinically important multidrug-resistant nosocomial and community-acquired bacterial pathogens. Grades: > 95%. Molecular formula: C20H21N3O7. Mole weight: 415.41. | |
| Tigecycline Impurity 8 | An impurity of Ticlopidine which appears to be a valuable treatment option for the management of superbugs, especially where conventional therapy has failed. Synonyms: 12-oxo-11 hydroxy Tigecycline. Grades: > 95%. Molecular formula: C29H37N5O8. Mole weight: 583.65. | |
| Tigecycline Impurity 9 | An impurity of Ticlopidine which is a glycylcycline antibiotic, used to treat infection by drug resistant bacteria such as Staphylococcus aureus (Staph aureus) and Acinetobacter baumannii. Synonyms: Tigecycline quinone analog. Grades: > 95%. Molecular formula: C26H32N4O8. Mole weight: 528.57. | |
| Tigecycline impurity (ring-open) | | |
| Tigecycline mesylate | Tigecycline mesylate a first-in-class, broad spectrum antibiotic with activity against antibiotic-resistant organisms. Synonyms: Tigecycline mesylate; 1135871-27-0; Tigecycline (mesylate); (4S,4aS,5aR,12aR)-9-[[2-(tert-butylamino)acetyl]amino]-4,7-bis(dimethylamino)-1,10,11,12a-tetrahydroxy-3,12-dioxo-4a,5,5a,6-tetrahydro-4H-tetracene-2-carboxamide; methanesulfonic acid; GAR-936 mesylate; HY-B0117B; AKOS030526271; CS-1878. Grades: >98%. CAS No. 1135871-27-0. Molecular formula: C30H43N5O11S. Mole weight: 681.75. | |
| Tigecycline Mesylate | Tigecycline Mesylate. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1135871-27-0. Molecular formula: C30H43N5O11S. Mole weight: 681.75. Catalog: APB1135871270. | |
| Tigecycline Metabolite M1 | A metabolite of Tigecycline which is a glycylcycline antibiotic and acts by reversibly binding to the 30S ribosomal subunit. Synonyms: t-Butylaminoacetic Acid. Grades: > 95%. Molecular formula: C6H13NO2. Mole weight: 131.18. | |
| Tigecycline Metabolite M2 | A metabolite of Tigecycline which inhibits protein translation by blocking entry of aminoacyl-trna into the ribosome A site; regarded as the first of a new class of glycylcyline antibiotics. Synonyms: Epimer of Tigecycline Glucuronide. Grades: > 95%. Molecular formula: C35H47N5O14. Mole weight: 761.79. | |
| Tigecycline Metabolite M3 | A metabolite of Tigecycline which is a first-in-class, broad spectrum antibiotic with activity against antibiotic-resistant organisms. Synonyms: Tigecycline Glucuronide. Grades: > 95%. Molecular formula: C35H47N5O14. Mole weight: 761.79. | |
| Tigecycline Metabolite M4 | A metabolite of Tigecycline whiche is active against a broad range of gram-negative and gram-positive bacterial species including clinically important multidrug-resistant nosocomial and community-acquired bacterial pathogens. Synonyms: Epimer of N-Acetyl-9-Aminominocycline. Grades: > 95%. Molecular formula: C25H30N4O8. Mole weight: 514.54. | |
| Tigecycline Metabolite M5 | A metabolite of Tigecycline which has been shown to inhibit the translation elongation step by binding to the ribosome 30S subunit and preventing aminoacylated tRNAs to accommodate in the ribosomal A site. Synonyms: N-Acetyl-9-Aminominocycline. Grades: > 95%. Molecular formula: C25H30N4O8. Mole weight: 514.54. | |
| Tigecycline Metabolite M6 | Cas No. 149934-19-0. | |
| Tigecycline Metabolite M7 | A metabolite of Tigecycline which appears to be a valuable treatment option for the management of superbugs, especially where conventional therapy has failed. Synonyms: Epimer of Hydroxy Tigecycline. Grades: > 95%. Molecular formula: C29H39N5O9. Mole weight: 601.66. | |
| Tigecycline Metabolite M8 | A metabolite of Tigecycline which is a glycylcycline antibiotic, used to treat infection by drug resistant bacteria such as Staphylococcus aureus (Staph aureus) and Acinetobacter baumannii. Synonyms: Hydroxyl Tigecycline. Grades: > 95%. Molecular formula: C29H39N5O9. Mole weight: 601.66. | |
| Tigecycline (open C-ring D-ring) Quinone Trifluoroacetic Acid Salt | Tigecycline (open C-ring D-ring) quinone Trifluoroacetic Acid Salt is a salt of Tigecycline (open C-ring D-ring) quinone, an impurity of Tigecycline (T440015). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C26H32N4O8 · x(C2HF3O2). US Biological Life Sciences. |  Worldwide |
| Tigecycline Pentacyclic Analog, Technical Grade | Tigecycline Pentacyclic Analog, Technical Grade. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: Tigecycline Pentacyclic Analog,,(1S,4aR,4bR,10aR,11aS)-9-(Dimethylamino)-7-[[2-[(1,1-dimethylethyl)amino]acetyl]amino]-1,2,4a,5,10,10a,11,11a-octahydro-1,4,4a,6-tetrahydroxy-2,5,12-trioxo-1,4b-methano-4bH-benzo[b]fluorene-3-carboxamide. CAS No. 1268494-40-1. Molecular formula: C27H32N4O9. Mole weight: 556.56. Catalog: APS1268494401. SMILES: CN(C)c1cc(NC(=O)CNC(C)(C)C)c(O)c2C(=O)C34C(CC5C(O)(C(=O)C(=C(O)C35O)C(=O)N)C4=O)Cc12. Format: Neat. | |
| Tigecycline Powder | (4s,4as,5ar,12as)-4,7-Bis(dimethylamino)-9-((tert-butylamino)acetamido)-3,10,12,12a-tetrahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracen-2-carboxamide. immunosuppressant. CAS No. 220620-09-7. Product ID: 8-04293. |  |
| Tigecycline Related Compound B | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Tigecycline Tricyclic Analog | An impurity of Tigecycline, which is a glycylcycline antibiotic used to treat infection by drug resistant bacteria such as Staphylococcus aureus (Staph aureus) and Acinetobacter baumannii. Grades: > 95%. CAS No. 1268494-40-1. Molecular formula: C27H32N4O9. Mole weight: 556.56. | |
| Tigemonam | Tigemonam, also known as SQ 30836, a monobactam, inhibited 90% of strains tested of Escherichia coli, Klebsiella spp., Proteus spp., Salmonella spp., Haemophilus influenzae and Branhamella catarrhalis at concentrations of 0.25 mg/l or below. Synonyms: 2-[(Z)-[1-(2-amino-1,3-thiazol-4-yl)-2-[[(3S)-2,2-dimethyl-4-oxo-1-sulfooxyazetidin-3-yl]amino]-2-oxoethylidene]amino]oxyacetic acid; SQ 30836; SQ-30836; tigemonam. CAS No. 102507-71-1. Molecular formula: C12H15N5O9S2. Mole weight: 437.41. | |
| Tigilanol tiglate | Tigilanol tiglate (EBC-46) is a protein kinase C ( PKC )/ C1 domain activator. Tigilanol tiglate is associated with mitochondrial/endoplasmic reticulum (ER) dysfunction, leading to activation of the unfolded protein response (UPRmt/ER) and subsequent induction of ATP depletion, organelles expansion, Caspase activation, gasdermin E cleavage, and terminal necrosis. Tigilanol tiglate, as a small anti-tumor molecule with immunomodulatory effects, can be used in the study of head and neck squamous cell carcinoma and soft tissue sarcoma [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EBC-46. CAS No. 943001-56-7. Pack Sizes: 1 mg. Product ID: HY-109076. | |
| Tiglic acid | Tiglic acid is a monocarboxylic unsaturated organic acid found in croton oil and in several other natural products. Tiglic aci has a role as a plant metabolite [1]. Uses: Scientific research. Group: Natural products. CAS No. 80-59-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 1 g. Product ID: HY-W012999. | |
| Tiglic Acid | Tiglic acid is the stable isomer of angelic acid. Tiglic acid was found as glyceride in croton oil, as butyl ester in the oil of the Roman camomile, and as geranyl tiglate in oil of geranium. Tiglic acid is formed during the charcoaling of maple wood. Group: Biochemicals. Alternative Names: (2E)-2-Methyl-2-butenoic Acid; (E)-2-Methylcrotonic Acid; (E)-2,3-Dimethylacrylic Acid; (E)-2-Methyl-2-butenoic acid; (E)-α-Methylcrotonic acid; Cevadic Acid; NSC 44235; NSC 8999; Tiglinic Acid; trans-2,3-Dimethylacrylic Acid; trans-2-Methyl-2-butenoic Acid; trans-2-Methylcrotonic Acid; trans-α, β-Dimethylacrylic Acid. Grades: Highly Purified. CAS No. 80-59-1. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| Tiglic Acid Benzyl Ester | Tiglic Acid Benzyl Ester. Group: Biochemicals. Alternative Names: (2E)-2-Methyl-2-butenoic Acid Phenylmethyl Ester; Benzyl Tiglate; NSC 69098. Grades: Highly Purified. CAS No. 37526-88-8. Pack Sizes: 10g. Molecular Formula: C12H14O2, Molecular Weight: 190.24. US Biological Life Sciences. | Worldwide |
| Tiglic Acid-d3 | Tiglic Acid-d3. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| Tiglic aldehyde | Tiglic aldehyde. Uses: Designed for use in research and industrial production. Additional or Alternative Names: methyl-2-butenal,2-methyl-2-butenal;2,3-DIMETHYLACROLEIN;2-Methylcrotonaldehyde;Tiglic aldehyde;trans-2,3-Dimethylacrolein;trans-2-Methyl-2-butenal;2,3-Dimethyl-2-propenal;2,3-Dimethylacrylaldehyde. Product Category: Heterocyclic Organic Compound. CAS No. 1115-11-3. Molecular formula: C5H8O. Mole weight: 84.12. Purity: 0.98. Density: 0.871. Product ID: ACM1115113. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tiglic aldehyde - Trans-2-methyl-2-butenal | 5g Pack Size. Group: Analytical Reagents, Aroma Chemicals, Biochemicals, Building Blocks, Flavours and Fragrance Materials, Organics. Formula: CH3CH=C(CH3)CHO. CAS No. 497-03-0. Prepack ID 90028589-5g. Molecular Weight 84.12. See USA prepack pricing. |  |
| Tigloyl Chloride | Tigoloyl Chloride is used in the polymerization of propylene as well as through a Freidel-Crafts reaction for the preparation of permethylindenyl complexes of transition metals. As well, it is primarily used as a reagent in the enantioselective synthesis of dihydropyrans. Group: Biochemicals. Alternative Names: (2E)-2-Methyl-2-butenoyl Chloride; (E)-2-Methyl-2-butenoyl Chloride; Tiglic Acid Chloride. Grades: Highly Purified. CAS No. 35660-94-7. Pack Sizes: 1g, 5g, 10g. US Biological Life Sciences. | Worldwide |
| Tigloylgomisin P | Tigloylgomisin P, a lignin, has anti-HIV activity with an EC50 of 37 μM. Tigloylgomisin P has anticancer effect. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (5R)-6β,7β-Dimethyl-1,2,3,12-tetramethoxy-10,11-methylenedioxy(5,6,7,8-tetrahydrodibenzo[a,c]cyclooctene)-5β,6α-diol 5-[(E)-2-methyl-2-butenoate]. Product Category: Inhibitors. Appearance: Powder. CAS No. 69176-51-8. Molecular formula: C28H34O9. Mole weight: 514.56. Purity: 0.98. IUPACName: [(8R,9R,10S)-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] (E)-2-methylbut-2-enoate. Canonical SMILES: CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC. Product ID: ACM69176518-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tiglyl Glycine | A metabolite a Isoleucine. Group: Biochemicals. Alternative Names: N-[(2E)-2-Methyl-1-oxo-2-buten-1-yl]glycine. Grades: Highly Purified. CAS No. 35842-45-6. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Tiglyl Glycine Methyl Ester | Protected Tiglyl Glycine. Group: Biochemicals. Alternative Names: N-[(2E)-2-Methyl-1-oxo-2-buten-1-yl]glycine Methyl Ester. Grades: Highly Purified. CAS No. 55649-53-1. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| Tigogenin | 25R,3ß-OH. CAS No. 77-60-1. Product ID: 1-01559. Molecular formula: C27H44O3. Mole weight: 416.64. Purity: ≥92% (HPLC). Properties: mp 196-208C° LOD ≤0.5%. Reference: | |
| Tigogenin | Tigogenin. Group: Biochemicals. Alternative Names: 22-Isoallospirostan-3 β-ol. Grades: Plant Grade. CAS No. 77-60-1. Pack Sizes: 20mg. Molecular Formula: C27H44O3, Molecular Weight: 416.636. US Biological Life Sciences. | Worldwide |
| Tigogenin | Tigogenin, one of steroidal sapogenins, is widely used for synthesizing steroid agents. Tigogenin inhibits adipocytic differentiation and induces osteoblastic differentiation in mouse bone marrow stromal cells [1]. Uses: Scientific research. Group: Natural products. CAS No. 77-60-1. Pack Sizes: 5 mg; 10 mg; 20 mg. Product ID: HY-N1403. | |
| Tigolaner | Tigolaner (BAY-1272858) acts on γ-aminobutyric acid ( GABA ) and glutamate-gated chloride channels. Tigolaner has antiparasitic activity [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY-1272858. CAS No. 1621436-41-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109077. | |
| Tigonenin acetate | Tigonenin acetate. Product ID: 1-01109. Molecular formula: C29H46O4. Mole weight: 458.68. Purity: >95%. Source : | |
| Tigulixostat | Tigulixostat (LC350189) is an orally active, non-purine selective xanthine oxidase inhibitor. Tigulixostat lowers the production of uric acid. Tigulixostat can be used for gout and hyperuricemia study [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LC350189. CAS No. 1287766-55-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139585. | |
| Tilarginine | Synonyms: N-Monomethyl-L-arginine; L-Monomethylarginine. Grades: > 98.0% (TLC). CAS No. 17035-90-4. Molecular formula: C7H16N4O2. Mole weight: 188.23. | |
| Tilavonemab | Tilavonemab (ABBV-8E12) is a humanized anti- tau antibody that targets the extracellular form of pathological tau protein aggregates by binding to the N-terminal 25-30 amino acid residues of tau protein. Tilavonemab blocks the ability of human and mouse neurons to take up tau aggregates, reduces the loss of brain volume, slows the progression of tau pathology, and improves cognitive abilities in transgenic mice expressing mutant human tau. Tilavonemab is used in Alzheimer's disease research [1] [2] [3]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: ABBV-8E12; C2N-8E12. CAS No. 2096513-89-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99163. | |
| Tilbroquinol | Tilbroquinol. Group: Biochemicals. Alternative Names: 5-Methyl-7-bromo-8-hydroxyquinoline; 5-Methyl-7-bromooxine; 8-Hydroxy-7-bromo-5-methylquinoline; Tilbroquinol. Grades: Highly Purified. CAS No. 7175-9-9. Pack Sizes: 50mg. Molecular Formula: C10H8BrNO, Molecular Weight: 238.08. US Biological Life Sciences. | Worldwide |
| Tilbroquinol | Tilbroquinol is an antiprotozoal agent effective against amoebiasis. It has been used against Vibrio cholerae. Grades: >98%. CAS No. 7175-9-9. Molecular formula: C10H8BrNO. Mole weight: 238.08. | |
| Tildacerfont | Tildacerfont is a potent and orally active corticotrophin-releasing factor type 1 (CRF1) receptort antagonis. Tildacerfont effectively reduces adrenocorticotropic hormone (ACTH) and adrenal androgen levels. Tildacerfont has favourable safety profile. Tildacerfont can be used for researching congenital adrenal hyperplasia [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SPR001; LY2371712. CAS No. 1014983-00-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113603. | |
| Tildipirosin | Tildipirosin, a long-acting macrolide, has antibiotic activity. Uses: Scientific research. Group: Signaling pathways. CAS No. 328898-40-4. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-A0071. | |
| Tildrakizumab | Tildrakizumab (SCH 900222) is a humanized anti- IL-23 (p19 subunit) monoclonal antibody. IL-23 is a critical cytokine to maintain the Th17 cell phenotype. Tildrakizumab has high-affinity for single-chain IL-23 ( K d : 136 pM). Tildrakizumab is effective against moderate to severe plaque psoriasis [1] [2] [3]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: SCH 900222; MK 3222; Anti-Human IL23 Recombinant Antibody. CAS No. 1326244-10-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99256. | |
| Tiletamine Hydrochloride | Tiletamine is a receptor antagonist, an anesthetic. Group: Biochemicals. Alternative Names: 2-(Ethylamino)-2-(2-thienyl)cyclohexanone Hydrochloride; CI 634; CL 399; CN 54521-2; NSC 167740; Tiletamin Hydrochloride. Grades: Highly Purified. CAS No. 14176-50-2. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Tilfrinib | Tilfrinib, a pyridoindol derivative, has been found to be a breast tumor kinase (Brk) inhibitor that could probably restrain the proliferation of breast cancer cells. IC50: 3.15 nM. Synonyms: CHEMBL3133821; MolPort-042-624-535; BDBM50001733; AKOS027470214; 3-(1H-Pyrido[2,3-b]indole-4-ylamino)phenol; Tilfrinib|3-(9H-Pyrido[2,3-b]indol-4-ylamino)phenol. Grades: 98%. CAS No. 1600515-49-8. Molecular formula: C17H13N3O. Mole weight: 275.31. | |
| Tilidine-D6 hydrochloride solution | 100 ?g/mL in methanol (as free base), ampule of 1 mL, certified reference material. Group: Certified reference materials (crms). | |
| Tiliquinol | Tiliquinol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Tiliquinol, Tiliquinolum, 5-Methyl-8-quinolinol, 5-Methylquinolin-8-ol, Tiliquinolum [INN-Latin], UNII-813OG1OGVG, 5-Methyl-8-hydroxyquinoline, Oprea1_613347, AIDS020545, AIDS-020545, CID71208, EINECS 226-905-2, NSC130828, ZINC00002171, NSC 130828, NCGC00164506-01, LT00013759, 5541-67-3. Product Category: Heterocyclic Organic Compound. CAS No. 5541-67-3. Molecular formula: C10H9NO. Mole weight: 159.184560 [g/mol]. Purity: 0.96. IUPACName: 5-methylquinolin-8-ol. Canonical SMILES: CC1=C2C=CC=NC2=C(C=C1)O. Density: 1.21g/cm³. ECNumber: 226-905-2. Product ID: ACM5541673. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tiliroside | Tiliroside, a glycosidic flavonoid, possesses anti-diabetic activities. Tiliroside is a noncompetitive inhibitor of α-amylase with a K i value of 84.2 μM. Tiliroside inhibits carbohydrate digestion and glucose absorption in the gastrointestinal tract [1]. Uses: Scientific research. Group: Natural products. CAS No. 20316-62-5. Pack Sizes: 5 mg; 10 mg; 20 mg. Product ID: HY-N1425. | |
| Tiliroside | Tiliroside. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 6''-O-trans-p-coumaroylastragalin. Product Category: Heterocyclic Organic Compound. Appearance: Yellow powder. CAS No. 20316-62-5. Molecular formula: C30H26O13. Mole weight: 594.52. Purity: 0.98. IUPACName: [(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate. Canonical SMILES: C1=CC(=CC=C1/C=C/C(=O)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O. Density: 1.68±0.1 g/ml. Product ID: ACM20316625. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tiliroside | A naturally occurring flavonoid that shows anti-complement, anti-inflammatory and free radical scavenger activity. Inhibits the production of the inflammatory mediators nitric oxide (NO), TNF-a and IL-12 in activated macrophages. Also inhibits human Low Density Lipoprotein (LDL) oxidation. Group: Biochemicals. Grades: Highly Purified. CAS No. 10238-21-8. Pack Sizes: 1mg, 5mg. US Biological Life Sciences. | Worldwide |
| Tilivapram | Tilivapram, a pyridine derivative, has been found to be a phosphodiesterase IV inhibitor that could probably be used in studying its bioactivities in sorts of areas. Synonyms: Tilivapram; UNII-B5983P6VWM; Tilivapram [INN]; B5983P6VWM; SCHEMBL1433277; 4-(cyclopropylmethoxy)-N-(3,5-dichloro-1-hydroxypyridin-4-ylidene)-5-methoxypyridine-2-carboxamide. Grades: 98%. CAS No. 166741-91-9. Molecular formula: C16H15Cl2N3O4. Mole weight: 384.21. | |
| Tilmicosin | 100mg Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C46H80N2O13. CAS No. 108050-54-0. Prepack ID 81409792-100mg. Molecular Weight 869.13. See USA prepack pricing. | |
| Tilmicosin | Tilmicosin (LY-177370) is an orally active calcium channel antagonist and macrolide antibiotic with antimicrobial activity. Tilmicosin mainly acts on the 50S subunit of bacterial ribosomes, inhibiting protein synthesis. Tilmicosin is effective in the treatment of respiratory diseases in livestock such as cattle, sheep and pigs. In addition, Tilmicosin has immunomodulatory and anti-inflammatory effects [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY-177370; EL-870. CAS No. 108050-54-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0905. | |
| Tilmicosin | Macrolide antibiotic structurally related to tylosin. Antibacterial. Group: Biochemicals. Alternative Names: 4A-O-De(2,6-dideoxy-3-C-methyl-α-L-ribo-hexopyranosyl)-20-deoxo-20-[(3R,5S)-3,5-dimethyl-1-piperidinyl]tylosin; Antibiotic EL 870; EL 870; LY 177370; Micotil; Micotil 300; Pulmotil. Grades: Highly Purified. CAS No. 108050-54-0. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Tilmicosin phosphate | Tilmicosin phosphate. Group: Biochemicals. Alternative Names: Micotil; 20-Deoxy-20-(3,5-dimethylpiperidin-1-yl)-desmycosin. Grades: Highly Purified. CAS No. 137330-13-3. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C46H80N2O13·H3PO4. US Biological Life Sciences. | Worldwide |
| Tilmicosin phosphate | Tilmicosin (LY-177370) phosphate is an orally active calcium channel antagonist and macrolide antibiotic with antimicrobial activity. Tilmicosin phosphate mainly acts on the 50S subunit of bacterial ribosomes, inhibiting protein synthesis. Tilmicosin phosphate is effective in the treatment of respiratory diseases in livestock such as cattle, sheep and pigs. In addition, Tilmicosin phosphate has immunomodulatory and anti-inflammatory effects [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY-177370 phosphate; EL-870 phosphate. CAS No. 137330-13-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0905A. | |
| Tilmicosin Phosphate | Tilmicosin phosphate, an antibiotic, has been commonly used as a veterinary drug against ovine respiratory disease for bovine and ovine. Synonyms: Tilmicosin (phosphate); UNII-SMH7U1S683; SMH7U1S683; Tilmicosin phosphate (USAN). Grades: 98%. CAS No. 137330-13-3. Molecular formula: C46H83N2O17P. Mole weight: 967.13. | |
| Tilorone | Tilorone is an orally active antiviral agent and interferon inducer that also has potential antineoplastic, immunomodulatory, and metabolic modulating effects. Tilorone induces an abnormally delayed interferon response and primarily stimulates interferon production in lymphoid tissue. Thus, Tilorone exerts antiviral effects and can be used as a chemotherapeutic agent. Tilorone has the potential to inhibit type 2 diabetes by increasing glucose uptake in vivo and in skeletal muscle cells by enhancing Akt2/AS160 signaling and glucose transporter levels [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. CAS No. 27591-97-5. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1080A. | |
| Tilorone dihydrochloride | Tilorone dihydrochloride is an orally active interferon (IFN) inducer with broad-spectrum antiviral activities. Tilorone dihydrochloride possesses robust anti-Severe fever with thrombocytopenia syndrome virus (SFTSV) activity in vitro and in vivo through stimulation of host innate immunity. Tilorone dihydrochloride can penetrate the blood-brain barrier to activate HIF in the CNS [1] [2] [3].Tilorone dihydrochloride exhibits an inhibitory activity with EC 50 of 230 nM against Ebola virus (EBOV) [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 27591-69-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1080. | |
| Tilorone dihydrochloride | Tilorone dihydrochloride, as a broad-spectrum, orally active antiviral agent, is an orally active interferon inducer. Synonyms: 2,7-bis[2-(diethylamino)ethoxy]fluoren-9-one;dihydrochloride. Grades: ≥ 98 %. CAS No. 27591-69-1. Molecular formula: C25H34N2O3 · 2HCl. Mole weight: 483.47. | |
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