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| Product | Description | |
|---|---|---|
| Tenofovir Impurity X | Tenofovir Impurity X. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1878175-82-6. Molecular Formula: C11H17N5O2. Mole Weight: 251.29. Catalog: APB1878175826. |  |
| Tenofovir Impurity Z | Tenofovir Impurity Z. Uses: For analytical and research use. Group: Impurity standards. CAS No. 161760-03-8. Molecular Formula: C10H15O6PS. Mole Weight: 294.26. Catalog: APB161760038. | |
| Tenofovir Isopropyl Carbamate | Protected Tenofovir. Acyclic phosphonate nucleotide analogue; reverse transcriptase inhibitor. Used as an anti-HIV agent. Antiviral. Group: Biochemicals. Alternative Names: [ [ (1R) -2 (6-Isopropyl aminocarbamate-9H-purin-9-yl) -1-methylethoxy] methyl] phosphonic Acid. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Tenofovir Isopropyl Ethyl Diester | Tenofovir Isopropyl Ethyl Diester. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 2,4,6,8-Tetraoxa-5-phosphanonanedioic acid, 5-[[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl]-, 1-ethyl 9-(1-methylethyl) ester, 5-oxide. CAS No. 1422284-16-9. IUPAC Name: [[ (2R) -1- (6-aminopurin-9-yl) propan-2-yl]oxymethyl- (ethoxycarbonyloxymethoxy) phosphoryl]oxymethyl propan-2-yl carbonate. Molecular Formula: C18H28N5O10P. Mole Weight: 505.42. Catalog: APS1422284169. SMILES: CCOC (=O)OCOP (=O) (CO[C@H] (C)Cn1cnc2c (N)ncnc12)OCOC (=O)OC (C)C. Format: Neat. | |
| Tenofovir isopropyl monoisoproxil hydrochloride | Tenofovir isopropyl monoisoproxil hydrochloride. Group: Biochemicals. Alternative Names: iPr-POC PMPA hydrochloride; Tenofovir disoproxil related compound G. Grades: Highly Purified. CAS No. 1246812-40-7. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C17H28N5O7P·HCl. US Biological Life Sciences. | Worldwide |
| Tenofovir isoproxil monoester | Tenofovir isoproxil monoester. Group: Biochemicals. Grades: Highly Purified. CAS No. 211364-69-1. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. US Biological Life Sciences. | Worldwide |
| Tenofovir maleate | Tenofovir hydrate reduces the viral cytopathic effect of HIV-1(IIIB), HIV-2(ROD) and HIV(EHO) with EC50 of 1.15 μg/mL, 1.12 μg/mL and 1.05 μg/mL in MT-4 cells. Tenofovir hydrate also reduces the viral cytopathic effect of SIV(mac251) , SIV(B670) ,SHIV(89.6) and SHIV(RTSHIV). Tenofovir hydrate inhibits hepatitis B virus (HBV) activity in HepG2 2.2.15, HepAD38 and HepAD79 cells. Tenofovir hydrate (4 μM) completely inhibits the growth of HIVIIIB in MT-2 cells. Tenofovir hydrate inhibits synthesis of negative strand strong-stop DNA with IC50 of 9 ?M for wild-type RT, 6 ?M for M184V RT and 50 ?M for K65R RT. Tenofovir hydrate (30 mg/kg) completely prevents SIV infection in all macaques without toxicity. Tenofovir hydrate treatment reduces plasma viral RNA levels to undetectable, with parallel decreases in the infectivity of plasma and infectious cells in peripheral blood mononuclear cells and cerebrospinal fluid (CSF) and stabilization of CD4+ T-cell numbers. Tenofovir hydrate (30 mg/kg, s.c.) completely abrogates HIV infection via intravaginal exposure in pig-tailed macaques. Synonyms: Viread maleate; GS 1278 maleate; GS1278 maleate; GS-1278 maleate; PMPA maleate; TDF maleate. Grades: >98%. CAS No. 1236287-04-9. Molecular formula: C13H18N5O8P. Mole weight: 403.28. |  |
| Tenofovir Monoisoproxil Dimer Ammonium Sodium Salt (>85%) | Tenofovir Monoisoproxil Dimer Ammonium Sodium Salt (>85%). Uses: For analytical and research use. Group: Impurity standards. Pack Sizes: 2.5MG. Catalog: APS013126. Format: Neat. Shipping: Dry ice. | |
| Tenofovir Monomethyl Ester | Acyclic phosphonate nucleotide analogue; reverse transcriptase inhibitor. Used as an anti-HIV agent. Antiviral. Group: Biochemicals. Alternative Names: (±)-[[2-(6-Amino-9H-purin-9-yl)-1-methylethoxy]methyl]-phosphonic Acid Monomethyl Ester. Grades: Highly Purified. CAS No. 123155-85-1. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Tenofovir monophosphate | The monophosphate salt form of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Synonyms: PMPA-monophosphate; [(2r)-1-(6-Aminopurin-9-Yl)propan-2-Yl]oxymethyl-phosphonooxy-phosphinic acid. Grades: > 95%. CAS No. 206646-04-0. Molecular formula: C9H15N5O7P2. Mole weight: 367.19. | |
| Tenofovir Mono POC Dimer | Cas No. 1962114-92-6. | |
| Tenofovir Phosphate | A metabolite of Tenofovir. Contains an undetermined amout of water and phosphoric acid. Group: Biochemicals. Alternative Names: [(1R)-2(6-Amino-9H-purin-9-yl)-1-methylethoxy]methyl]-isohypophosphoric Acid; PMPA-monophosphate. Grades: Highly Purified. CAS No. 206646-04-0. Pack Sizes: 1mg. Molecular Formula: C9H15N5O7P2, Molecular Weight: 367.19. US Biological Life Sciences. | Worldwide |
| Tenofovir Related Compound 1 | One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Synonyms: 9-[ (2R) -2- (diphenoxyphosphorylmethoxy) propyl]purin-6-amine. Grades: > 95%. CAS No. 342631-41-8. Molecular formula: C21H22N5O4P. Mole weight: 439.41. | |
| Tenofovir Related Compound 10 | One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Synonyms: 1-(9H-purin-6-ylamino)propan-2-ol; N-(2-Hydroxypropyl)adenine. Grades: > 95%. CAS No. 16958-60-4. Molecular formula: C8H11N5O. Mole weight: 193.21. | |
| Tenofovir Related Compound 2 | One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Synonyms: (R)-Phenyl hydrogen (((1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphonate. Grades: > 95%. CAS No. 379270-35-6. Molecular formula: C15H18N5O4P. Mole weight: 363.32. | |
| Tenofovir Related Compound 3 | One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Grades: > 95%. CAS No. 52364-31-5. Molecular formula: C13H13O4P. Mole weight: 264.22. | |
| Tenofovir Related Compound 4 | One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Synonyms: Desphenyl Tenofovir Alafenamide; P-((((R)-1-(6-Amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)-N-((S)-1-isopropoxy-1-oxopropan-2-yl)phosphonamidic acid. Grades: > 95%. CAS No. 851456-00-3. Molecular formula: C15H25N6O5P. Mole weight: 400.38. | |
| Tenofovir Related Compound 5 | One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Grades: > 95%. CAS No. 1234081-04-9. Molecular formula: C21H29N6O5P. Mole weight: 476.48. | |
| Tenofovir Related Compound 6 | One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Synonyms: Tenofovir alafenamide; propan-2-yl (2S)-2-[[[(2R)-1-(6-aminopurin-9-yl)propan-2-yl]oxymethyl-phenoxyphosphoryl]amino]propanoate. Grades: > 95%. CAS No. 383365-04-6. Molecular formula: C21H29N6O5P. Mole weight: 476.48. | |
| Tenofovir Related Compound 7 | One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Synonyms: propan-2-yl (2R)-2-aminopropanoate. Grades: > 95%. CAS No. 79487-89-1. Molecular formula: C6H13NO2. Mole weight: 131.18. | |
| Tenofovir Related Compound 8 | One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Synonyms: Tenofovir Bis(L-alanine Isopropyl Ester) Amide. Grades: > 95%. CAS No. 1883563-86-7. Molecular formula: C21H36N7O6P. Mole weight: 513.54. | |
| Tenofovir Related Compound 9 | One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Synonyms: (S)-9-[2-(Hydroxypropyl] Adenine; 9-[(2S)-2-Hydroxypropyl]adenine; L-(+)-9-(2-Hydroxypropyl)adenine; (αS)-6-Amino-α-methyl-9H-purine-9-ethanol. Grades: > 95%. CAS No. 14047-27-9. Molecular formula: C8H11N5O. Mole weight: 193.21. | |
| Tenofovir Trimer Impurity 1 | One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Grades: > 95%. Molecular formula: C55H82N15O27P3. Mole weight: 1478.27. | |
| Tenofovir Trimer Impurity 2 | One impurity of Tenofovir, which is an acyclic phosphonate nucleotide derivative, could be used in antiviral treatment as an everse transcriptase inhibitor. Grades: > 95%. Molecular formula: C50H74N15O24P3. Mole weight: 1362.15. | |
| Tenovin-1 | Tenovin-1, a p53 activator, protects p53 from MDM2-mediated degradation. Tenovin-1 acts through inhibition of the protein-deacetylating activities of SirT1 and SirT2. Tenovin-1 is also a dihydroorotate dehydrogenase (DHODH) inhibitor [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 380315-80-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-13423. |  |
| Tenovin-1 | Tenovin-1. Group: Biochemicals. Grades: Purified. CAS No. 380315-80-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Tenovin-1 | Tenovin-1 is a small molecule activator of p53 transcriptional activity. At 10 μM, it elevates p53 expression in MCF-7 cells within two hours of treatment and longer-term exposure that significantly decreases the growth of BL2 Burkitt's lymphoma and ARN8 melanoma cells. Synonyms: Tenovin-1; Tenovin 1; Tenovin1. CAS No. 380315-80-0. Molecular formula: C20H23N3O2S. Mole weight: 369.48052. | |
| Tenovin-2 | Tenovin-2, a diminutive compound inhibitor, offers promise as a therapeutic agent for a range of malignancies, including but not limited to breast cancer and leukemia. Its mechanism of action is attributed to the activation of p53, a multifunctional protein responsible for regulating cellular growth and division. Synonyms: 4-Tert-butyl-N-[[4- (2-methylpropanoylamino) phenyl]carbamothioyl]benzamide; N-[4- ({[ (4-tert-butylbenzoyl) amino]carbothioyl}amino) phenyl]-2-methylpropanamide. CAS No. 666211-30-9. Molecular formula: C22H27N3O2S. Mole weight: 397.537. | |
| Tenovin-3 | Tenovin-3 is a p53 transcription activator that is able to increase p53 levels, determined in MCF-7 cells treated for 6 hr at 10 μM. Synonyms: Tenovin-3; Tenovin 3; Tenovin3. CAS No. 1011301-27-1. Molecular formula: C18H21N3OS. Mole weight: 327.446. | |
| Tenovin-6 | Tenovin-6, also known as Tnv-6, is a bioactive small molecule SIRT2 inhibitor with anti-neoplastic activity. Inhibition of the Sirtuin class of protein deacetylases with activation of p53 function is associated with the pro-apoptotic effects of Tnv-6 in many tumors. Synonyms: Tenovin-6; Tenovin 6; Tenovin6. CAS No. 1011557-82-6. Molecular formula: C25H34N4O2S. Mole weight: 454.63. | |
| Tenovin-6 | Tenovin-6, an analog of Tenovin-1 (HY-13423), is an activator of p53 transcriptional activity. Tenovin-6 inhibits the protein deacetylase activities of purified human SIRT1, SIRT2, and SIRT3 with IC 50 s of 21 μM, 10 μM, and 67 μM, respectively. Tenovin-6 also inhibits dihydroorotate dehydrogenase (DHODH) [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1011557-82-6. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15510. | |
| Tenovin 6 Hydrochloride | Tenovin-6 is the water soluble analog of Tenovin-1 (HY-13423) and acts as a potent SIRT1 (IC50=21 μM) and SIRT2 (IC50=10 μM) inhibitor as well as p53 activator. Synonyms: Tenovin 6 Hydrochloride; Tenovin6 Hydrochloride; Tenovin-6 Hydrochloride. Grades: >98%. CAS No. 1011301-29-3. Molecular formula: C25H35ClN4O2S. Mole weight: 491.09. | |
| Tenovin-6 Hydrochloride | Tenovin-6 Hydrochloride, an analog of Tenovin-1 (HY-13423), is an activator of p53 transcriptional activity. Tenovin-6 Hydrochloride inhibits the protein deacetylase activities of purified human SIRT1, SIRT2, and SIRT3 with IC 50 s of 21 μM, 10 μM, and 67 μM, respectively. Tenovin-6 Hydrochloride also inhibits dihydroorotate dehydrogenase (DHODH) [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1011301-29-3. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15510B. | |
| Tenoxicam | Tenoxicam. Group: Biochemicals. Alternative Names: 4-Hydroxy-2-methyl-N-2-pyridinyl-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide 1,1-dioxide; Alganex; Dolmen. Grades: Highly Purified. CAS No. 59804-37-4. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C13H11N3O4S2. US Biological Life Sciences. | Worldwide |
| Tenoxicam | Tenoxicam (Ro-12-0068), an antiinflammatory agent with analgesic and antipyretic properties. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro-12-0068. CAS No. 59804-37-4. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-B0440. | |
| Tenoxicam | Tenoxicam is a non-steroidal anti-inflammatory drug (NSAID).Tenoxicam is a good HO. radicals scavenger with an IC50 of 56.7 μM. Synonyms: BRN-0572193; BRN0572193; BRN 0572193; Tenoxicam; Liman; Octiveran. Grades: >98%. CAS No. 59804-37-4. Molecular formula: C13H11N3O4S2. Mole weight: 337.37832. | |
| Tenoxicam (4-Hydroxy-2-methyl-N-2-pyridinyl-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide- 1,1-dioxide, Ro-12-0068, Alganex, Dolmen, Liman, Mobiflex, Rexalgan, Tilatil, Tilcotil,. ) | Nonsteroidal anti-inflamatory agent. Group: Biochemicals. Alternative Names: 4-Hydroxy-2-methyl-N-2-pyridinyl-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide- 1,1-dioxide; Ro-12-0068; Alganex; Dolmen; Liman; Mobiflex; Rexalgan; Tilatil; Tilcotil. Grades: Highly Purified. CAS No. 59804-37-4. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Tenoxicam Impurity 1 | Tenoxicam Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 16817-89-3. Molecular Formula: C7H8N2O3. Mole Weight: 168.15. Catalog: APB16817893. | |
| Tenoxicam Impurity C | One impurity of Tenoxicam, which is a phenothiazine derivative and could be used as a nonsteroidal anti-inflamatory drug. Synonyms: N-Methylthiophene-2-carboxamide; N-Methyl-2-(aminocarbonyl)thiophene. Grades: > 95%. CAS No. 39880-77-8. Molecular formula: C6H7NOS. Mole weight: 141.19. | |
| Tenoxicam Impurity D | One impurity of Tenoxicam, which is a phenothiazine derivative and could be used as a nonsteroidal anti-inflamatory drug. Synonyms: N-Methyl-N'-(2-pyridyl)oxamide. Grades: > 95%. CAS No. 52781-01-8. Molecular formula: C8H9N3O2. Mole weight: 179.18. | |
| Tenoxicam Impurity E | One impurity of Tenoxicam, which is a phenothiazine derivative and could be used as a nonsteroidal anti-inflamatory drug. Synonyms: 2-Methylthieno[2,3-d]isothiazol-3(2H)-one 1,1-Dioxide. Grades: > 95%. CAS No. 94040-09-2. Molecular formula: C6H5NO3S2. Mole weight: 203.24. | |
| Tenoxicam Impurity H | One impurity of Tenoxicam, which is a phenothiazine derivative and could be used as a nonsteroidal anti-inflamatory drug. Synonyms: 3-[(Methylamino)sulfonyl]-2-thiophenecarboxylic Acid; 3-(N-Methylsulfamoyl)-2-thiophenecarboxylic Acid. Grades: > 95%. CAS No. 64527-92-0. Molecular formula: C6H7NO4S2. Mole weight: 221.25. | |
| TentaGel HL NH2 | TentaGel HL NH2. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| TentaGel S-Br | TentaGel S-Br. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Tentagel S-CH(OEt)2 | Tentagel S-CH(OEt)2. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| TentaGel S-COOH | TentaGel S-COOH. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Tentagel S HMBA | Tentagel S HMBA. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 10g. US Biological Life Sciences. | Worldwide |
| TentaGel S NH2 | TentaGel S NH2. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| TentaGel S-OH | TentaGel S-OH. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| TentaGel S PHB | TentaGel S PHB. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| TentaGel S PHB-L-Thr(tBu)Fmoc | TentaGel S PHB-L-Thr(tBu)Fmoc. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 2.5g. US Biological Life Sciences. | Worldwide |
| TentaGel S RAM | TentaGel S RAM. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Tentagel S SH | Tentagel S SH. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| TentaGel S Trt-L-Ala-Fmoc | TentaGel S Trt-L-Ala-Fmoc. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| tentoxilysin | Zinc enzyme produced by Clostridium tetani. Proenzyme of 150 kDa is processed to disulfide-linked subunits of 100 and 50 kDa, the latter being responsible for the endopeptidase activity. Weakly inhibited by captopril, and phosphoramidon. The clostridial neurotoxins disable the neuroexocytosis apparatus, and have been described as the most toxic substances known. Tentoxilysin acts at the spinal inhibitory interneurons, blocking the release of various neurotransmitters to produce spastic paralysis. Type example of peptidase family M27 (tentoxilysin family). Group: Enzymes. Synonyms: tetanus neurotoxin. Enzyme Commission Number: EC 3.4.24.68. CAS No. 107231-12-9. 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-4351; tentoxilysin; EC 3.4.24.68; 107231-12-9; tetanus neurotoxin. Cat No: EXWM-4351. |  |
| Tentoxin | Tentoxin, a cyclic tetrapeptide isolated from the plant pathogen A. alternata, has been found to restrain chloroplast development so that could be used as a natural herbicide. It is a selectively phytotoxic compound and used to eliminate polyphenol oxidase (PPO) activity from seedlings of higher plants. Synonyms: Cycloleucyl-N-methylalanylglycyl-N-methyl dehydrophenylalanine; (3S,6S,12Z)-12-benzylidene-1,6,7-trimethyl-3-(2-methylpropyl)-1,4,7,10-tetrazacyclododecane-2,5,8,11-tetrone; Cyclo(N-methyl-L-alanyl-L-leucyl-α,β-didehydro-N-methylphenylalanylglycyl); (Z)-Cyclic(N-methyl-L-alanyl-L-leucyl-α,β-didehydro-N-methylphenylalanylglycyl). Grades: ≥98%. CAS No. 28540-82-1. Molecular formula: C22H30N4O4. Mole weight: 414.50. | |
| Tentoxin | Tentoxin is a cyclic tetrapeptide isolated from Alternaria tenuis , acts as a herbicide, causes seedling chlorosis, inhibits cyclic photophosphorylation and functions as an energy transfer inhibitor [1]. Uses: Scientific research. Group: Natural products. CAS No. 28540-82-1. Pack Sizes: 500 μg. Product ID: HY-N6717. | |
| Tentoxin | Tentoxin. Group: Biochemicals. Alternative Names: Cyclo(N-methyl-L-alanyl-L-leucyl-α, β -didehydro-N- methyl phenylalanylglycyl) ; 1,4,7,10-Tetraazacyclododecane Cyclic Peptide Deriv.; (Z)-Cyclic(N-methyl-L-alanyl-L-leucyl-α, β -didehydro-N- methyl phenylalanylglycyl) . Grades: Highly Purified. CAS No. 28540-82-1. Pack Sizes: 1mg. Molecular Formula: C22H30N4O4, Molecular Weight: 414.5. US Biological Life Sciences. | Worldwide |
| Tentoxin-d3 | Tentoxin-d3. Group: Biochemicals. Alternative Names: Cyclo(N-methyl-L-alanyl-L-leucyl-α, β -didehydro-N- methyl phenylalanylglycyl) -d3; 1,4,7,10-Tetraazacyclododecane Cyclic Peptide Deriv.-d3; (Z)-Cyclic(N-methyl-L-alanyl-L-leucyl-α, β -didehydro-N- methyl phenylalanylglycyl) -d3. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C22H27D3N4O4, Molecular Weight: 417.52. US Biological Life Sciences. | Worldwide |
| Tenuazonic acid | Tenuazonic acid is a nitrogen-containing heterocyclic antibiotic produced by Alternaria tenuis Auct 430 and Asp. sp. 1404. It has inhibitory effect on enterovirus, respiratory virus, vaccinia virus and herpes simplex virus. It can inhibit KB cells and amoeba in dysentery. Synonyms: 3-acetyl-5-(butan-2-yl)-4-hydroxy-2,5-dihydro-1H-pyrrol-2-one. Grades: >98%. CAS No. 610-88-8. Molecular formula: C10H15NO3. Mole weight: 197.23. | |
| Tenuazonic acid | Tenuazonic acid is a nonhost-selective mycotoxin belonging to the tetramic acids family. Tenuazonic acid inhibits protein biosynthesis on ribosomes by suppressing the release of new protein. Tenuazonic acid is acutely toxic, and oral LD 50 is set between 81-186 mg/kg in rats and mice. Tenuazonic acid blocks electron transport beyond the primary quinone receptor (QA) by interacting with the D1 protein and is a photosystem II (PSII) inhibitor. In addition, Tenuazonic acid has antiviral effects on measles virus, enterovirus, respiratory virus and so on. Tenuazonic acid has an inhibitory effect on skin cancer [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Natural products. CAS No. 610-88-8. Pack Sizes: 5 mg. Product ID: HY-N6715. | |
| Tenuazonic Acid | An alternaria mycotoxin, found in common edible crops. It inhibits protein synthesis in fibroblasts. Group: Biochemicals. Alternative Names: L-3-Acetyl-5-sec-butyl-4-hydroxy-3-pyrrolin-2-one; (5S)-3-Acetyl-1,5-dihydro-4-hydroxy-5-[(1S)-1-methylpropyl]-2H-pyrrol-2-one; AAC-toxin; L-Tenuazonic Acid. Grades: Highly Purified. CAS No. 610-88-8. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Tenuazonic acid Copper Salt | Tenuazonic Acid Copper Salt is an alternaria mycotoxin, found in common edible crops. It inhibits protein synthesis in fibroblasts. Synonyms: 3-Pyrrolin-2-one, 3-acetyl-5-sec-butyl-4-hydroxy-, L-, Copper Salt; L-3-Acetyl-5-sec-butyl-4-hydroxy-3-pyrrolin-2-one Copper Salt; (5S)-3-Acetyl-1,5-dihydro-4-hydroxy-5-[(1S)-1-methylpropyl]-2H-pyrrol-2-one Copper Salt; AAC-toxin Copper Salt; L-Tenuazonic Acid Copper Salt. Grades: ≥98%. CAS No. 12427-40-6. Molecular formula: C20H28CuN2O6. Mole weight: 455.99. | |
| Tenuifgenin | Tenuifgenin is a Chinese herbal extract with anti-oxidative and anti-inflammatory effects involving toxin induced cell models of ParkinsonÂs disease. Group: Biochemicals. Grades: Highly Purified. CAS No. 2469-34-3. Pack Sizes: 5mg, 25mg. Molecular Formula: C30H45ClO6, Molecular Weight: 537.13. US Biological Life Sciences. | Worldwide |
| Tenuifolin | Tenuifolin is effective and has a protective action. Tenuifolin inhibits β-secretase decreases Aβ protein secretion, suppresses Aβ25-35 secretion, and subsequently caspase-3 and caspase-9 become active. Tenuifolin's ability to lower AChE activity, increase at the same time, increase the ability of the upper glands, and improve the ability to read and remember. Research on tenuifolin's potential for use in urinary disease (AD) [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 20183-47-5. Pack Sizes: 1 mg; 5 mg; 10 mg; 20 mg. Product ID: HY-N0702. | |
| Tenuifolin | Tenuifolin. Group: Biochemicals. Grades: Plant Grade. CAS No. 20183-47-5. Pack Sizes: 20mg. Molecular Formula: C36H56O12, Molecular Weight: 680.82. US Biological Life Sciences. | Worldwide |
| Tenuifoliside A | Tenuifoliside A. Group: Biochemicals. Grades: Plant Grade. CAS No. 139726-35-5. Pack Sizes: 10mg. Molecular Formula: C31H38O17, Molecular Weight: 682.62. US Biological Life Sciences. | Worldwide |
| Tenuifoliside B | Tenuifoliside B is one of the acylated oligosaccharides in the roots of P. tenuifolia, showed the cerebral protective effect on potassium cyanide. It has been shown to have neuroprotective and cognitive-enhancing effects. Synonyms: 3-O-[(2E)-3-(4-Hydroxy-3,5-dimethoxyphenyl)-1-oxo-2-propen-1-yl]-beta-D-fructofuranosyl alpha-D-glucopyranoside 6-(4-hydroxybenzoate). Grades: >98%. CAS No. 139726-36-6. Molecular formula: C30H36O17. | |
| Tenuifoliside B | Formula: Group: Biochemicals. Grades: Plant Grade. CAS No. 139726-36-6. Pack Sizes: 5mg, 10mg. US Biological Life Sciences. | Worldwide |
| Tenuiorin | Synonyms: 2-Hydroxy-4-[(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy]-6-methylbenzoic acid 3-hydroxy-4-methoxycarbonyl-5-methylphenyl ester; Peltigerin; Methyl 2-hydroxy-4-({2-hydroxy-4-[(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy]-6-methylbenzoyl}oxy)-6-methylbenzoate; Benzoic acid, 2-hydroxy-4-[(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy]-6-methyl-, 3-hydroxy-4-(methoxycarbonyl)-5-methylphenyl ester. CAS No. 570-07-0. Molecular formula: C26H24O10. Mole weight: 496.46. | |
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