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| Product | Description | |
|---|---|---|
| Tebbe reagent solution | Tebbe reagent solution. Uses: For analytical and research use. CAS No. 67719-69-1. Mole weight: 284.58. Catalog: AP67719691. |  |
| Tebentafusp | Tebentafusp (IMCgp100) is a bispecific fusion protein to target gp100 peptide-HLA-A*02:01 (a melanoma-associated antigen). Tebentafusp guides T cells to kill gp100-expressing tumor cells via a high affinity T-cell receptor (TCR) binding domain and an anti-CD3 T-cell engaging domain. Tebentafusp leads to inflammatory cytokines and cytolytic proteins production, resulting in the direct lysis of tumour cells[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: IMCgp100. CAS No. 1874157-95-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99339. |  |
| Tebideutorexant | Tebideutorexant is an OX1R-selective inhibitor with oral bioavailability and blood-brain barrier permeability, with human OX1R pKi 8.17 and rat OX1R pKi 8.13.Tebideutorexant selectively modulates OX1R, with no significant functional effect on OX2R. Tebideutorexant can be used for the research of panic and anxiety disorders[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: JNJ-61393215. CAS No. 1637681-55-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-147403S. | |
| Tebipenem | Tebipenem is an orally available carbapenem antibiotic, shows broad-spectrum activity against Gram-positive and -negative bacteria, except for Pseudomonas aeruginosa. Uses: Scientific research. Category: Signaling pathways. Alternative Names: LJC 11036. CAS No. 161715-21-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0076. | |
| Tebipenem pivoxil | Tebipenem Pivoxil has high intestinal apical membrane permeability due to plural intestinal transport routes, including the uptake transporters such as OATP1A2 and OATP2B1 as well as simple diffusion. Synonyms: L-084; L 084; L084; ME1211; ME-1211; ME 1211; SPR994; SPR-994; SPR 994; TBM-PI; Tebipenem pivoxil. Grade: ≥ 98% by HPLC. CAS No. 161715-24-8. Molecular formula: C22H31N3O6S2. Mole weight: 497.63. |  |
| Tebipenem pivoxil | Tebipenem pivoxil (L084) is an orally active antibiotic against a variety of pathogenic bacteria. Tebipenem pivoxil binds penicillin-binding protein (PBP), thereby inhibiting cell wall synthesis[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: L084. CAS No. 161715-24-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0396. | |
| Tebipenem Pivoxil impurity 1 | Tebipenem Pivoxil impurity 1. Uses: For analytical and research use. Molecular formula: C17H18N2O7. Mole weight: 362.34. Catalog: APB12295. | |
| Tebipenem Pivoxil impurity 10 | Tebipenem Pivoxil impurity 10. Uses: For analytical and research use. Molecular formula: C22H31N3O6S2. Mole weight: 497.63. Catalog: APB12299. | |
| Tebipenem Pivoxil impurity 11 | Tebipenem Pivoxil impurity 11. Uses: For analytical and research use. CAS No. 161715-24-8. Molecular formula: C22H31N3O6S2. Mole weight: 497.63. Catalog: APB161715248. | |
| Tebipenem Pivoxil impurity 12 | Tebipenem Pivoxil impurity 12. Uses: For analytical and research use. Molecular formula: C28H43N3O9S2. Mole weight: 629.78. Catalog: APB12300. | |
| Tebipenem Pivoxil impurity 13 | Tebipenem Pivoxil impurity 13. Uses: For analytical and research use. CAS No. 1595319-80-4. Molecular formula: C28H43N3O9S2. Mole weight: 629.78. Catalog: APB1595319804. | |
| Tebipenem Pivoxil impurity 14 | Tebipenem Pivoxil impurity 14. Uses: For analytical and research use. CAS No. 1391053-29-4. Molecular formula: C23H35N3O7S2. Mole weight: 529.67. Catalog: APB1391053294. | |
| Tebipenem Pivoxil impurity 15 | Tebipenem Pivoxil impurity 15. Uses: For analytical and research use. CAS No. 384330-54-5. Molecular formula: C12H18N4S4. Mole weight: 346.54. Catalog: APB384330545. | |
| Tebipenem Pivoxil impurity 16 | Tebipenem Pivoxil impurity 16. Uses: For analytical and research use. Molecular formula: C35H41N2O10PSi. Mole weight: 708.78. Catalog: APB12302. | |
| Tebipenem Pivoxil impurity 17 | Tebipenem Pivoxil impurity 17. Uses: For analytical and research use. CAS No. 698970-05-7. Molecular formula: C23H32N2O7Si. Mole weight: 476.6. Catalog: APB698970057. | |
| Tebipenem Pivoxil impurity 18 | Tebipenem Pivoxil impurity 18. Uses: For analytical and research use. Molecular formula: C23H33N3O7S2. Mole weight: 527.65. Catalog: APB12301. | |
| Tebipenem Pivoxil impurity 19 | Tebipenem Pivoxil impurity 19. Uses: For analytical and research use. CAS No. 161715-20-4. Molecular formula: C23H26N4O6S2. Mole weight: 518.6. Catalog: APB161715204. | |
| Tebipenem Pivoxil impurity 2 | Tebipenem Pivoxil impurity 2. Uses: For analytical and research use. CAS No. 137049-39-9. Molecular formula: C22H22NO8P. Mole weight: 459.39. Catalog: APB137049399. | |
| Tebipenem Pivoxil impurity 20 | Tebipenem Pivoxil impurity 20. Uses: For analytical and research use. CAS No. 110312-12-4. Molecular formula: C23H32N4O7Si. Mole weight: 504.62. Catalog: APB110312124. | |
| Tebipenem Pivoxil impurity 21 | Tebipenem Pivoxil impurity 21. Uses: For analytical and research use. CAS No. 161715-27-1. Molecular formula: C6H10N2OS. Mole weight: 158.22. Catalog: APB161715271. | |
| Tebipenem Pivoxil impurity 22 | Tebipenem Pivoxil impurity 22. Uses: For analytical and research use. CAS No. 179337-62-3. Molecular formula: C7H12N2O3S2. Mole weight: 236.3. Catalog: APB179337623. | |
| Tebipenem Pivoxil impurity 23 | Tebipenem Pivoxil impurity 23. Uses: For analytical and research use. CAS No. 161715-28-2. Molecular formula: C8H12N2OS2. Mole weight: 216.32. Catalog: APB161715282. | |
| Tebipenem Pivoxil impurity 24 | Tebipenem Pivoxil impurity 24. Uses: For analytical and research use. Molecular formula: C29H29N2O11P. Mole weight: 612.53. Catalog: APB12304. | |
| Tebipenem Pivoxil impurity 25 | Tebipenem Pivoxil impurity 25. Uses: For analytical and research use. Molecular formula: C22H31N3O6S2. Mole weight: 497.63. Catalog: APB12305. | |
| Tebipenem Pivoxil impurity 26 | Tebipenem Pivoxil impurity 26. Uses: For analytical and research use. Molecular formula: C29H27N2O10P. Mole weight: 594.51. Catalog: APB12303. | |
| Tebipenem Pivoxil impurity 3 | Tebipenem Pivoxil impurity 3. Uses: For analytical and research use. Molecular formula: C29H25N2O11P. Mole weight: 608.5. Catalog: APB12297. | |
| Tebipenem Pivoxil impurity 4 | Tebipenem Pivoxil impurity 4. Uses: For analytical and research use. CAS No. 1380688-27-6. Molecular formula: C22H33N3O7S2. Mole weight: 515.64. Catalog: APB1380688276. | |
| Tebipenem Pivoxil impurity 5 | Tebipenem Pivoxil impurity 5. Uses: For analytical and research use. CAS No. 1665289-91-7. Molecular formula: C23H33N3O7S2. Mole weight: 527.65. Catalog: APB1665289917. | |
| Tebipenem Pivoxil impurity 6 | Tebipenem Pivoxil impurity 6. Uses: For analytical and research use. CAS No. 1595319-78-0. Molecular formula: C44H62N6O12S4. Mole weight: 995.25. Catalog: APB1595319780. | |
| Tebipenem Pivoxil impurity 7 | Tebipenem Pivoxil impurity 7. Uses: For analytical and research use. CAS No. 1595319-82-6. Molecular formula: C16H23N3O5S2. Mole weight: 401.5. Catalog: APB1595319826. | |
| Tebipenem Pivoxil impurity 8 | Tebipenem Pivoxil impurity 8. Uses: For analytical and research use. CAS No. 682747-73-5. Molecular formula: C28H32NO10P. Mole weight: 573.53. Catalog: APB682747735. | |
| Tebipenem Pivoxil impurity 9 | Tebipenem Pivoxil impurity 9. Uses: For analytical and research use. Molecular formula: C27H39N3O7S2. Mole weight: 581.74. Catalog: APB12298. | |
| Tebotelimab | Tebotelimab (MGD-013) is a humanized IgG4κ bispecific PD-1/LAG-3 dual-affinity re-targeting (DART) antibody. Tebotelimab binds cell-surface expressed PD-1 and LAG-3 with EC50s of 1.65 nM and 0.41 nM in NS0 cells, respectively. Tebotelimab blocks PD-1/PD-L1, PD-1/PD-L2 and LAG-3/HLA (MHC-II) interactions and PD-1 signaling. Tebotelimab restores exhausted T-cell responses and and enhances antitumour immunity[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MGD-013. CAS No. 2245725-04-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99573. | |
| Tebuconazol | 1g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C16H22ClN3O. CAS No. 107534-96-3. Prepack ID 89966850-1g. Molecular Weight 307.82. See USA prepack pricing. |  |
| Tebuconazole | Ergosterol biosynthesis inhibitor. Fungicide. Group: Biochemicals. Grades: Highly Purified. CAS No. 107534-96-3. Pack Sizes: 500mg. US Biological Life Sciences. |  Worldwide |
| Tebuconazole-[d9] | One of the labelled form of Tebuconazole, which is a triazole compound and has been found to be an ergosterol biosynthesis inhibitor. Synonyms: Tebuconazole-(tert-butyl-d9); α-[2-(4-Chlorophenyl)ethyl]-α-(1,1-dimethylethyl-d9)-1H-1,2,4-triazole-1-ethanol; (+/-)-Tebuconazole-d9. Grade: >95%. CAS No. 1246818-83-6. Molecular formula: C16H13D9ClN3O. Mole weight: 316.87. | |
| Tebuconazole (Standard) | Tebuconazole (Standard) is the analytical standard of Tebuconazole. This product is intended for research and analytical applications. Tebuconazole is an orally active agricultural azole fungicide which can also inhibit CYP51 with IC50s of 0.9 and 1.3 μM for Candida albicans CYP51 (CaCYP51) and truncated Homo sapiens CYP51 (Δ60HsCYP51), respectively. Tebuconazole induces lipid accumulation and oxidative stress in HepG2 Cells. Tebuconazole decreases MAC-T cells viability and proliferation, induces ER-stress-mediated apoptosis and increases oxidative stress levels in MAC-T cells[1][2][3][4][5][6]. Uses: Scientific research. Category: Signaling pathways. CAS No. 107534-96-3. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0852R. | |
| Tebuconazole-(tert-butyl-d9) | Tebuconazole-(tert-butyl-d9). Uses: For analytical and research use. CAS No. 1246818-83-6. Mole weight: 316.87. Catalog: AP1246818836. | |
| Tebuconazole-(trimethyl-13C3) | Tebuconazole-(trimethyl-13C3). Uses: For analytical and research use. CAS No. 1313734-83-6. Mole weight: 310.80. Catalog: AP1313734836. | |
| Tebufenozide | Tebufenozide is a nonsteroidal ecdysone agonist used to control pest. Tebufenozide has cytotoxic and induces apoptosis in HeLa and insect Tn5B1-4 cells[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 112410-23-8. Pack Sizes: 10 mM * 1 mL in DMSO; 25 mg; 50 mg; 100 mg. Product ID: HY-B2054. | |
| Tebufenozide | Tebufenozide. Group: Biochemicals. Alternative Names: 3,5-Dimethyl-1-(1,1-dimethylethyl)-2-(4-ethylbenzoyl)hydrazide benzoic acid; 1-tert-Butyl-1- (3, 5-dimethylbenzoyl) -2- (4-ethylbenzoyl) hydrazine; 3,5-Dimethylbenzoic acid N-tert-butyl-N- (4-ethylbenzoyl) hydrazide. Grades: Highly Purified. CAS No. 112410-23-8. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C22H28N2O2. US Biological Life Sciences. | Worldwide |
| Tebufenpyrad | Tebufenpyrad. Group: Biochemicals. Alternative Names: 4-Chloro-N-[[4- (1, 1-dimethylethyl) phenyl]methyl]-3-ethyl-1-methyl-1H-pyrazole-5-carboxamide; AC 801757; Fenpyrad. Grades: Highly Purified. CAS No. 119168-77-3. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C18H24ClN3O. US Biological Life Sciences. | Worldwide |
| TE buffer (100X) pH 8.0 | 1lt Pack Size. Group: Biochemicals, Buffers. Prepack ID 11225962-1lt. See USA prepack pricing. | |
| Tecaginlimab | Tecaginlimab (BNT-312) is a Fc-inert bispecific antibody for dual targeting and conditional stimulation of CD40 and 4-1BB. Tecaginlimab can enhance priming and reactivation of tumor-specific immunity[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BNT-312; DuoBody-CD40x-4-1BB; GEN1042. CAS No. 2253891-70-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99572. | |
| Tecalcet Hydrochloride | Tecalcet Hydrochloride (R 568 Hydrochloride), an orally active calcimimetic compound, allosterically and positively modulates the calcium-sensing receptor (CaSR). Tecalcet Hydrochloride (R 568 Hydrochloride) increases the sensitivity to activation by extracellular Ca2+[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: R-568 hydrochloride; NPS R-568. CAS No. 177172-49-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-10167A. | |
| Tecarfarin | Tecarfarin (ATI-5923) is an orally active and non-competitive vitamin K epoxide reductase (VKOR) antagonist, and impairs the activation of the vitamin K-dependent clotting factors II, VII, IX and X[1]. Tecarfarin has the antithrombotic activity [2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ATI-5923. CAS No. 867257-26-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14854. | |
| Tecarfarin-[13C,d3] | An isotope labelled of Tecarfarin. Tecarfarin is a vitamin K antagonist that can be used as an anticoagulant. Synonyms: 1,1,1,3,3,3-hexafluoro-2-(13C,D3)methylpropan-2-yl 4-[(4-hydroxy-2-oxo-2H-chromen-3-yl)methyl]benzoate. Grade: 95% by HPLC; 98% atom D; 98% atom 13C. Molecular formula: C20[13C]H11D3F6O5. Mole weight: 464.34. | |
| Tecastemizole | Tecastemizole (R 43512) is a selective antagonist of H1 receptor and a major metabolite of astemizole with anti-inflammatory effects. Category: Active pharmaceutical ingredients. CAS No. 75970-99-9. Product ID: API75970999. Molecular formula: C19H21FN4. Mole weight: 324.4. |  |
| Tecastemizole | Tecastemizole (Norastemizole), a major metabolite of Astemizole, is a potent and selective H1 receptor antagonist. Tecastemizole shows anti-inflammatory activities[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Norastemizole. CAS No. 75970-99-9. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-105014. | |
| Technetium tc 99m Apcitide | Technetium Tc-99m Apcitide is a radiopharmaceutical. Synonyms: Acutect (TN). CAS No. 178959-14-3. Molecular formula: C51H73N17NaO20S5Tc. Mole weight: 1526.45. | |
| Teclistamab | Teclistamab is a human bispecific antibody to BCMA and CD3 that recognizes BCMA on target cells and CD3 on T cells and induces T cell-mediated cytotoxicity leading to T cell activation and subsequent target cell lysis. Teclistamab can be used in studies of diseases related to multiple myeloma (MM)[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: JNJ-7957; JNJ-64007957; Tecvayli. CAS No. 2119595-80-9. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P99392. | |
| Tecotabart | HY-P990946 is an CLDN18-targeting IgG1κ type humanized antibody, the recommed isotype control is Human IgG1 kappa, Isotype Control (HY-P99001)[1]. Uses: Scientific research. Category: Inhibitory antibodies. Alternative Names: LM-102. CAS No. 2823329-10-6. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-P990946. | |
| Tecovirimat | Tecovirimat Inhibitor. Uses: Scientific use. Product Category: T17026. CAS No. 869572-92-9. |  |
| Tecovirimat | Tecovirimat (ST-246) is an orally bioavailable and selective compound against orthopoxviruses including vaccinia, monkeypox, camelpox, cowpox, ectromelia (mousepox), smallpox and variola viruses. Tecovirimat is evaluated against vaccinia, cowpox virus, ectromelia virus with EC50 values of 0.01 μM, 0.48 μM and 0.05 μM, respectively. Tecovirimat targets the orthopoxvirus protein VP37 which is necessary for membrane envelopment of intracellular mature virus particles to form enveloped virus. Tecovirimat exerts antiviral activity on the target of the cowpox virus V061 gene, which is homologous to vaccinia virus F13L, encoding a major envelope protein (p37) required for production of extracellular virus[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ST-246. CAS No. 869572-92-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14805. | |
| Tecovirimat monohydrate | Tecovirimat (ST-246) monohydrate is the monohydrate form of Tecovirimat (HY-14805). Tecovirimat monohydrate is an orally bioavailable and selective compound against orthopoxviruses [including vaccinia, monkeypox, camelpox, cowpox, ectromelia (mousepox), smallpox and variola viruses]. Tecovirimat monohydrate is evaluated against vaccinia, cowpox virus, ectromelia virus with EC50 values of 0.01 μM, 0.48 μM and 0.05 μM, respectively. Tecovirimat monohydrate targets the orthopoxvirus protein VP37 which is necessary for membrane envelopment of intracellular mature virus particles to form enveloped virus. Tecovirimat monohydrate exerts antiviral activity on the target of the cowpox virus V061 gene, which is homologous to vaccinia virus F13L, encoding a major envelope protein (p37) required for production of extracellular virus. Tecovirimat monohydrate could be used in the study for orthopoxvirus-induced diseases[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ST-246 monohydrate. CAS No. 1162664-19-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14805A. | |
| Tectochrysin | Tectochrysin is a flavonoid isolated from the heartwood of Pinus strobus L. It leads to apoptotic cell death in NSCLC cells through activating of DR3 and Fas expression. Uses: Antioxidant. Synonyms: 5-hydroxy-7-methoxyflavone; 5-Hydroxy-7-methoxy-2-phenyl-4H-chromen-4-one. Grade: 99%. CAS No. 520-28-5. Molecular formula: C16H12O4. Mole weight: 268.3. | |
| Tectol | Tectol, isolated from Lippia sidoides, exhibits significant activity against human leukemia cell lines HL60 and CEM[1]. Tectol is a farnesyltransferase (FTase) inhibitor with IC50s of 2.09 and 1.73 μM for human and T. brucei FTase, respectively. Tectol inhibits drug-resistant strain of P. falciparum (FcB1) with an IC50 of 3.44 μM[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 24449-39-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N7634. | |
| Tectol | Tectol. Alternative Names: 2, 2, 2', 2'- Tetramethyl-[5, 5'- Bi- 2H- naphtho[1, 2- b] pyran] - 6, 6'- diol. CAS No. 24449-39-6. Product ID: ACM24449396. Molecular formula: C30H26O4. Mole weight: 450.52. IUPAC Name: 5-(6-hydroxy-2,2-dimethylbenzo[h]chromen-5-yl)-2,2-dimethylbenzo[h]chromen-6-ol. Canonical SMILES: CC1(C=CC2=C(O1)C3=CC=CC=C3C(=C2C4=C(C5=CC=CC=C5C6=C4C=CC(O6)(C)C)O)O)C. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Tectomer 2-Tailed (C8H16(CH2NHGLY4)2.2HCl), 90% | Tectomer 2-Tailed (C8H16(CH2NHGLY4)2.2HCl), 90%. |  |
| Tectomer 3-Tailed (CH3C(CH2-NH-Gly7)3.3CF3CO2H), 90% | Tectomer 3-Tailed (CH3C(CH2-NH-Gly7)3.3CF3CO2H), 90%. | |
| Tectomer 4-Tailed (C(CH2-NH-Gly7)4.4HCl), 90% | Tectomer 4-Tailed (C(CH2-NH-Gly7)4.4HCl), 90%. CAS No. 318286-59-8. | |
| Tectoridin | Tectoridin is a isoflavone isolated from Maackia amurensis. Tectoridin is a phytoestrogen and activates estrogen and thyroid hormone receptors. Tectoridin exerts the estrogenic effects via ER-dependent genomic pathway and GPR30-dependent nongenomic pathway[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 611-40-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0791. | |
| Tectoridin | Tectoridin. Group: Biochemicals. Alternative Names: Tectorigenin 7-glucoside; Shekanin; Shekkanin. Grades: Plant Grade. CAS No. 611-40-5. Pack Sizes: 20mg. Molecular Formula: C22H22O11, Molecular Weight: 462.403. US Biological Life Sciences. | Worldwide |
| Tectorigenin | Tectorigenin. Group: Biochemicals. Grades: Plant Grade. CAS No. 548-77-6. Pack Sizes: 20mg. Molecular Formula: C16H12O6, Molecular Weight: 300.26. US Biological Life Sciences. | Worldwide |
| Tectorigenin | Tectorigenin induced differentiation of human promyelocytic leukemia HL-60 cells to granulocytes and monocytes/macrophages, and caused apoptotic changes of DNA in the cells, as did genistein. Tectorigenin also inhibited autophosphorylation of epidermal growth factor (EGF) receptor by EGF and decreased the expression of Bcl-2 protein, with less activity than genistein. From these results, tectorigenin may be a possible therapeutic agent for leukemia. Uses: Antioxidant. Synonyms: 5,7-Dihydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one; 6-Methoxy-5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-chromen-4-one; 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-6-methoxy-; Isoflavone, 4',5,7-trihydroxy-6-methoxy-; 5,7,4'-Trihydroxy-6-methoxyisoflavone; K 251T; Tectrigenin. Grade: >98%. CAS No. 548-77-6. Molecular formula: C16H12O6. Mole weight: 300.26. | |
| Tectorigenin | Tectorigenin is a plant isoflavonoid originally isolated from the dried flower of Pueraria lobate Benth. Uses: Scientific research. Category: Natural products. CAS No. 548-77-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0792. | |
| Tectorigenin 7-O-xylosylglucoside | Tectorigenin 7-O-xylosylglucoside. Group: Biochemicals. CAS No. 231288-19-0. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Tectoroside | Tectoroside is a natural sesquiterpene compound found in several plants. Synonyms: (3aR,4R,6aR,8S,9aR,9bR)-3,6,9-trimethylene-2-oxo-8-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)dodecahydroazuleno[4,5-b]furan-4-yl 2-hydroxy-3-(4-hydroxyphenyl)propanoate. Grade: >98%. CAS No. 124960-89-0. Molecular formula: C30H36O12. Mole weight: 588.6. | |
| TED-347 | TED-347 is a potent, irreversible, covalent and allosteric inhibitor at YAP-TEAD protein-protein interaction with an EC50 of 5.9 μM for TEAD4?Yap1 protein-protein interaction. TED-347 specifically and covalently bonds with Cys-367 within the central pocket of TEAD4 with a Ki of 10.3 μM. TED-347 blocks TEAD transcriptional activity and has antitumor activity[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2378626-29-8. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-125269. | |
| Tedizolid | Tedizolid. Group: Biochemicals. Alternative Names: 3-[3-Fluoro-4-[6-(2-methyl-2H-tetrazol-5-yl)-3-pyridinyl]phenyl]-5-(hydroxymethyl)-2-oxazolidinone, DA 7157; TR 700. Grades: Highly Purified. CAS No. 856866-72-3. Pack Sizes: 5mg. Molecular Formula: C17H15FN6O3, Molecular Weight: 370.34. US Biological Life Sciences. | Worldwide |
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