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| Product | Description | |
|---|---|---|
| Tenuigenin | Tenuigenin is a major active component isolated from the root of the Chinese herb Polygala tenuifolia. Tenuigenin protects against S.aureus-induced pneumonia by inhibiting NF-κB activation. Tenuigenin has anti-inflammatory effect[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Senegenin. CAS No. 2469-34-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 20 mg; 50 mg; 100 mg. Product ID: HY-N0802. |  |
| Tenuiorin | Tenuiorin. Alternative Names: 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. |  |
| Tephrosin | Tephrosin is a flavonoid compound found in the herbs of Derris robusta. Tephrosin shows potent antitumor activity. Uses: Antitumor. Alternative Names: 13,13a-Dihydro-7a-hydroxy-9,10-dimethoxy-3,3-dimethyl-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one;Hydroxydeguelin;Deguelinol I. Grades: >97%. CAS No. 76-80-2. Molecular formula: C23H22O7. Mole weight: 410.43. | |
| Tepilamide fumarate | Tepilamide fumarate (XP-23829; PPC-06) is an oral fumaric acid ester, acts as a proagent ofMonomethyl fumarate (HY-103252), and is used in the research of moderate to severe chronic plaque psoriasis. Tepilamide fumarate can enhance the effectiveness of oncolytic viruses[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: XP-23829; PPC-06. CAS No. 1208229-58-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109105. | |
| Teplizumab | Teplizumab (MGA-031) is a Fc receptor non-binding anti-human CD3 monoclonal antibody. Teplizumab reduces the loss of beta-cell function. Teplizumab can be used in the research of type 1 diabetes[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MGA-031; PRV-031. CAS No. 876387-05-2. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P99222. | |
| Teplizumab | Teplizumab is a humanized anti-CD3 monoclonal antibody indicated to delay the onset of Stage 3 type 1 diabetes in patients with Stage 2 type 1 diabetes. Alternative Names: MGA-031; PRV-031; Tzield. CAS No. 876387-05-2. | |
| Teplow's Amyloid β-Protein (1-40) (scrambled II) | Teplow's Amyloid β-Protein (1-40) (scrambled II) is a specially designed negative control in the Abeta40 study. Teplow's Amyloid β-Protein (1-40) does not exhibit some of the phenomena regularly observed by Abeta40 (fiber formation, oligomerization, toxicity to neurons), and has a relatively flat hydropathy profile, which may have been an advantage in some studies, for example, to avoid nonspecific interactions with cell membranes. ''Scrambled'' means that it contains the same amino acids as Abeta40, but in a different order. Alternative Names: β-Amyloid (1-40) (scrambled II); H-Tyr-His-Ala-Gly-Val-Asp-Lys-Glu-Val-Val-Phe-Asp-Glu-Gly-Gly-Ala-Glu-His-Gly-Leu-Ala-Gln-Lys-Ile-Val-Arg-Gly-Phe-Gly-Val-Ser-Asp-Val-Ser-Met-Ile-His-Asn-Leu-Phe-OH. Grades: ≥95%. CAS No. 1987844-71-2. Molecular formula: C194H295N53O58S. Mole weight: 4329.86. | |
| Teplow's Amyloid β-Protein (1-42) (scrambled II) | Teplow's Amyloid β-Protein (1-42) (scrambled II) is a specially designed negative control in the Abeta42 study. Teplow's Amyloid β-Protein (1-42) does not exhibit some of the phenomena regularly observed by Abeta42 (fiber formation, oligomerization, toxicity to neurons), and has a relatively flat hydropathy profile, which may have been an advantage in some studies, for example, to avoid nonspecific interactions with cell membranes. ''Scrambled'' means that it contains the same amino acids as Abeta42, but in a different order. Alternative Names: β-Amyloid (1-42) (scrambled II); H-Tyr-His-Ala-Gly-Val-Asp-Lys-Glu-Val-Val-Phe-Asp-Glu-Gly-Ala-Gly-Ala-Glu-His-Gly-Leu-Ala-Gln-Lys-Ile-Val-Arg-Gly-Phe-Gly-Val-Ser-Asp-Val-Ser-Met-Ile-His-Ile-Asn-Leu-Phe-OH. Grades: ≥95%. CAS No. 1987844-92-7. Molecular formula: C203H311N55O60S. Mole weight: 4514.03. | |
| Tepoditamab | Tepoditamab (MCLA-117) is a full-length human IgG1 bispecific monoclonal antibody that binds to CLEC12A of myeloid cells and CD3 of cytotoxic T cells. Among others, CLEC12A is a myeloid differentiation antigen. Tepoditamab kills AML leukaemia mother cells and AML leukaemia stem cells, induces T cell-mediated proliferative lysis of AML cells. Tepoditamab induces upto 30-fold T-cell expansion. Tepoditamab results in moderate to strong cytokine (IFNγ, IL-6, IL-8, IL-10, and TNFα) and IFNγ release in human whole blood and PBMC, respectively. Tepoditamab can be used in acute myeloid leukaemia (AML) research[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MCLA 117. CAS No. 2044679-53-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P99390. | |
| Tepotinib | Tepotinib (EMD-1214063) is an orally active and highly selective, reversible, ATP-competitive c-Met inhibitor with an IC50 of 3 nM, >200-fold selective for c-Met than IRAK4, TrkA, Axl, IRAK1, and Mer. Tepotinib inhibits c-Met phosphorylation and induces autophagy. Tepotinib has antitumor effects[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: EMD-1214063. CAS No. 1100598-32-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14721. | |
| Tepotinib | Tepotinib, also known as EMD 1214063 and MSC2156119, is an inhibitor of MET tyrosine kinase with potential antineoplastic activity. Tepotinib selectively binds to MET tyrosine kinase and disrupts MET signal transduction pathways, which may induce apoptosis in tumor cells overexpressing this kinase. The receptor tyrosine kinase MET (also known as hepatocyte growth factor receptor or HGFR), is the product of the proto-oncogene c-Met and is overexpressed or mutated in many tumor cell types. This protein plays key roles in tumor cell proliferation, survival, invasion, and metastasis, and tumor angiogenesis. Alternative Names: EMD-1214063; EMD1214063; EMD 1214063; MSC-2156119; MSC2156119; MSC-2156119. CAS No. 1100598-32-0. Molecular formula: C29H28N6O2. Mole weight: 492.583. | |
| Tepotinib (EMD-1214063) | Tepotinib is a potent and selective c-Met inhibitor with IC50 of 4 nM, >200-fold selective for c-Met than IRAK4, TrkA, Axl, IRAK1, and Mer. Tepotinib (EMD 1214063) induces autophagy. Phase 1. Group: Inhibitors. Alternative Names: EMD 1214063, MSC2156119. CAS No. 1100598-32-0. Pack Sizes: 5mg. Product ID: S7067. Formula: C29H28N6O2. Smiles: CN1CCC(CC1)COC2=CN=C(N=C2)C3=CC=CC(=C3)CN4C(=O)C=CC(=N4)C5=CC=CC(=C5)C#N. Storage Conditions: 2 years -80 in solvent. |  United States; Europe |
| Tepoxalin | Tepoxalin is an orally active dual inhibitor of Cyclooxygenase/Lipoxygenase, with IC50 values of 4.6 μM (sheep cyclooxygenase), 2.85 μM (rat cyclooxygenase), 0.15 μM (rat 5-lipoxygenase), and 3.0 μM (h12-lipoxygenase), respectively. Tepoxalin inhibits ROS production and NF-κB activation. Tepoxalin suppresses the production of thromboxane B2, leukotriene B4, prostaglandins and cytokines, and blocks platelet aggregation. Tepoxalin exhibits potent anti-inflammatory activity in rats with adjuvant-induced arthritis. Tepoxalin possesses analgesic activity. Tepoxalin shows no ulcerogenic activity within the anti-inflammatory dose range. Tepoxalin can be used in studies related to adjuvant-induced arthritis, skin inflammation and Alzheimer's disease[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. CAS No. 103475-41-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13219. | |
| Tepoxalin | Non-steroidal anti-inflammatory drug (NSAID) with potent anti-inflammatory and analgesic properties approved for veterinary use. It has inhibitory effect on cyclooxygenase and 5-lipxygenase activity as well as inhibiting the production of cytokines in peripheral cells outside the CNS. Tepoxalin, also known as ORF-20485; RWJ-20485; is a 5-lipoxygenase inhibitor potentially for the treatment of asthma, osteoarthritis (OA). Tepoxalin has in vivo inhibitory activity against COX-1, COX-2, and 5-LOX in dogs at the current approved recommended dosage.Tepoxalin inhibits inflammation and microvascular dysfunction induced by abdominal irradiation in rats. Tepoxalin enhances the activity of an antioxidant, pyrrolidine dithiocarbamate, in attenuating tumor necrosis factor alpha-induced apoptosis in WEHI 164 cells. Group: Biochemicals. Alternative Names: 5-(4-Chlorophenyl)-N-hydroxy-1-(4-methoxyphenyl)-N-methyl-1H-pyrazole-3-propanamide; ORF 20485; RWJ 20485. Grades: Highly Purified. CAS No. 103475-41-8. Pack Sizes: 10mg. Molecular Formula: C??H??ClN?O?, Molecular Weight: 385.84. US Biological Life Sciences. |  Worldwide |
| TEPP-46 | TEPP-46 (ML-265) is a potent and selective pyruvate kinase M2 (PKM2) activator with an AC50 of 92 nM, showing little or no effect on PKM1, PKL and PKR[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ML-265. CAS No. 1221186-53-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg. Product ID: HY-18657. | |
| TEPP-46 (ML265) | TEPP-46 (ML265, CID-44246499, NCGC00186528) is a potent activator of PKM2 in both biochemical (AC50 = 92 nM) and cell-based assays with high selectivity over PKM1, PKR and PKL. Group: Inhibitors. Alternative Names: CID-44246499, NCGC00186528. CAS No. 1221186-53-3. Pack Sizes: 5mg. Product ID: S7302. Formula: C17H16N4O2S2. Smiles: CN1C2=C(C3=C1C(=O)N(N=C3)CC4=CC(=CC=C4)N)SC(=C2)S(=O)C. Storage Conditions: 2 years -80 in solvent. | United States; Europe |
| Teprenone | Teprenone. Group: Biochemicals. Alternative Names: 6,10,14,18-Tetramethyl-5,9,13,17-nonadecatetraen-2-one. Grades: Highly Purified. CAS No. 6809-52-5. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C23H38O. US Biological Life Sciences. | Worldwide |
| Teprenone | Teprenone is an anti-ulcer agent, and works as an inducer of heat shock proteins (HSPs). Uses: Scientific research. Category: Signaling pathways. Alternative Names: Geranylgeranylacetone. CAS No. 6809-52-5. Pack Sizes: 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-B0779. | |
| Teprenone impurity 14 | Teprenone impurity 14. Uses: For analytical and research use. CAS No. 3879-23-0. Molecular formula: C23H38O. Mole weight: 330.56. Catalog: APB3879230. |  |
| Teprenone impurity 16 (Farnesylaceton) | Teprenone impurity 16 (Farnesylaceton). Uses: For analytical and research use. CAS No. 1117-52-8. Molecular formula: C18H30O. Mole weight: 262.44. Catalog: APB1117528. | |
| Teprenone Impurity 19 (Trans-Nerolidol) | Teprenone Impurity 19 (Trans-Nerolidol). Uses: For analytical and research use. CAS No. 40716-66-3. Molecular formula: C15H26O. Mole weight: 222.37. Catalog: APB40716663. | |
| Teprenone impurity 20 | Teprenone impurity 20. Uses: For analytical and research use. CAS No. 1117-51-7. Molecular formula: C18H30O. Mole weight: 262.44. Catalog: APB1117517. | |
| Teprenone Impurity 21 (Cis-Nerolidol) | Teprenone Impurity 21 (Cis-Nerolidol). Uses: For analytical and research use. CAS No. 3790-78-1. Molecular formula: C15H26O. Mole weight: 222.37. Catalog: APB3790781. | |
| Teprenone impurity 22 | Teprenone impurity 22. Uses: For analytical and research use. CAS No. 109826-68-8. Molecular formula: C23H40O. Mole weight: 332.57. Catalog: APB109826688. | |
| Teprenone impurity 24 | Teprenone impurity 24. Uses: For analytical and research use. CAS No. 70901-63-2. Molecular formula: C20H32. Mole weight: 272.48. Catalog: APB70901632. | |
| Teprenone Impurity 26 (Geranylgeraniol) | Teprenone Impurity 26 (Geranylgeraniol). Uses: For analytical and research use. CAS No. 24034-73-9. Molecular formula: C20H34O. Mole weight: 290.49. Catalog: APB24034739. | |
| Teprenone impurity 27 | Teprenone impurity 27. Uses: For analytical and research use. Molecular formula: C23H38O2. Mole weight: 346.56. Catalog: APB10905. | |
| Teprenone Impurity 27 (Geranylnerol) | Teprenone Impurity 27 (Geranylnerol). Uses: For analytical and research use. CAS No. 57784-25-5. Molecular formula: C20H34O. Mole weight: 290.49. Catalog: APB57784255. | |
| Teprenone impurity 28 | Teprenone impurity 28. Uses: For analytical and research use. Molecular formula: C23H38O2. Mole weight: 346.56. Catalog: APB10906. | |
| Teprenone impurity 29 | Teprenone impurity 29. Uses: For analytical and research use. Molecular formula: C23H38O2. Mole weight: 346.56. Catalog: APB10909. | |
| Teprenone impurity 3 | Teprenone impurity 3. Uses: For analytical and research use. CAS No. 3796-69-8. Molecular formula: C18H30O. Mole weight: 262.44. Catalog: APB3796698. | |
| Teprenone impurity 30 | Teprenone impurity 30. Uses: For analytical and research use. CAS No. 3796-64-3. Molecular formula: C23H38O. Mole weight: 330.56. Catalog: APB3796643. | |
| Teprenone impurity 31 | Teprenone impurity 31. Uses: For analytical and research use. CAS No. 3879-24-1. Molecular formula: C23H38O. Mole weight: 330.56. Catalog: APB3879241. | |
| Teprenone impurity 32 | Teprenone impurity 32. Uses: For analytical and research use. CAS No. 3796-67-6. Molecular formula: C23H38O. Mole weight: 330.56. Catalog: APB3796676. | |
| Teprenone impurity 33 | Teprenone impurity 33. Uses: For analytical and research use. Molecular formula: C23H38O. Mole weight: 330.56. Catalog: APB10911. | |
| Teprenone impurity 35 | Teprenone impurity 35. Uses: For analytical and research use. Molecular formula: C23H38O. Mole weight: 330.56. Catalog: APB10910. | |
| Teprenone impurity 36 | Teprenone impurity 36. Uses: For analytical and research use. Molecular formula: C23H38O. Mole weight: 330.56. Catalog: APB10912. | |
| Teprenone impurity 37 | Teprenone impurity 37. Uses: For analytical and research use. Molecular formula: C23H40O. Mole weight: 332.57. Catalog: APB10907. | |
| Teprenone impurity 38 | Teprenone impurity 38. Uses: For analytical and research use. Molecular formula: C92H152O8. Mole weight: 1386.22. Catalog: APB10908. | |
| Teprenone impurity 39 | Teprenone impurity 39. Uses: For analytical and research use. CAS No. 3796-63-2. Molecular formula: C23H38O. Mole weight: 330.56. Catalog: APB3796632. | |
| Teprenone impurity 4 | Teprenone impurity 4. Uses: For analytical and research use. CAS No. 3953-35-3. Molecular formula: C18H30O. Mole weight: 262.44. Catalog: APB3953353. | |
| Teprenone impurity 41 | Teprenone impurity 41. Uses: For analytical and research use. CAS No. 3796-66-5. Molecular formula: C23H38O. Mole weight: 330.56. Catalog: APB3796665. | |
| Teprenone impurity 42 | Teprenone impurity 42. Uses: For analytical and research use. CAS No. 3879-25-2. Molecular formula: C23H38O. Mole weight: 330.56. Catalog: APB3879252. | |
| Teprotide | Teprotide, a nonapeptide isolated from the snake Bothrops jararaca, is an angiotensin converting enzyme (ACE) inhibitor that inhibits the conversion of angiotensin I to angiotensin II and may potentiate some of the pharmacological actions of bradykinin. It used as an antihypertension agent. Alternative Names: SQ20881; H-Pyr-Trp-Pro-Arg-Pro-Gln-Ile-Pro-Pro-OH; L-pyroglutamyl-L-tryptophyl-L-prolyl-L-arginyl-L-prolyl-L-glutaminyl-L-isoleucyl-L-prolyl-L-proline; Teprotide; Bradykinin Potentiating Peptide 9a; BPP 9a; 5-Oxo-L-prolyl-L-tryptophyl-L-prolyl-L-arginyl-L-prolyl-L-glutaminyl-L-isoleucyl-L-prolyl-L-proline; Angiotensin Converting Enzyme Inhibitor. Grades: ≥95%. CAS No. 35115-60-7. Molecular formula: C53H76N14O12. Mole weight: 1101.26. | |
| Teprotumumab | Teprotumumab is an IGF-1 receptor (IGF-1R) blocking human monoclonal antibody. Teprotumumab has been approved for the treatment of thyroid eye disease. Alternative Names: Tepezza. CAS No. 1036734-93-6. | |
| Teprotumumab | Teprotumumab is an IGF-1 receptor (IGF-1R) blocking human monoclonal antibody. Teprotumumab binds to the ligand binding extracellular α-subunit domain of IGF-1R. Teprotumumab inhibits TSH and IGF-1 action in fibrocytes. Teprotumumab attenuates TSH-dependent IL-6 and IL-8 expression and Akt phosphorylation. Teprotumumab can be used for thyroid-associated ophthalmopathy research[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1036734-93-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99165. | |
| TEP (Triethyl Phosphate) | Phosphate ester used as flame retardant and plasticizer. Clear colorless liquid, low viscosity, miscible with most organic solvents, high purity >99.5%. Uses: Pu foams, pvc, coatings, lubricants. Group: Flame retardant / additive. Alternative Names: TEP. Grades: Industrial Grade. Approvals: REACH Compliant, RoHS. CAS No. 78-40-0. Pack Sizes: 200 kg Steel Drums / 1,000 kg IBCs / 18 MT ISO Tank. Product ID: FG-TEP. |  United States (serving international markets) |
| Terameprocol | Terameprocol is an inhibitor targeting the Sp1 transcription factor, which can selectively inhibit the transcription of Sp1-dependent genes. Terameprocol exerts its effects by inhibiting Sp1-mediated gene transcription, such as reducing the expression of genes like CDC2, survivin and HMGB1, thereby arresting the cell cycle, inducing apoptosis, and suppressing the inflammatory response. Terameprocol exhibits anti-proliferative, pro-apoptotic, and anti-inflammatory activities and is currently mainly used in the research of diseases such as cancer and pulmonary arterial hypertension[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: EM-1421. CAS No. 24150-24-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10447. | |
| Terazosin | Terazosin is a quinazoline derivative and a competitive and orally active α1-adrenoceptor antagonist. Terazosin works by relaxing blood vessels and the opening of the bladder. Terazosin has the potential for benign prostatic hyperplasia (BPH) and high blood pressure treatment[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 63590-64-7. Pack Sizes: 10 mM * 1 mL in DMSO; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0371. | |
| Terazosin-[d8] | Labelled Terazosin. Terazosin, works by blocking the action of adrenaline on smooth muscle of the bladder and the blood vessel walls, is a selective alpha1-antagonist used for treatment of symptoms of benign prostatic hyperplasia (BPH). Alternative Names: (4-(4-Amino-6,7-dimethoxyquinazolin-2-yl)piperazin-1-yl-2,2,3,3,5,5,6,6-d8)(tetrahydrofuran-2-yl)methanone; 6,7-dimethoxy-2-[4-(oxolane-2-carbonyl)(D8)piperazin-1-yl]quinazolin-4-amine. Grades: >98%. CAS No. 1006718-20-2. Molecular formula: C19H17D8N5O4. Mole weight: 395.48. | |
| Terazosin EP impurity B | Terazosin EP impurity B. Uses: For analytical and research use. CAS No. 1177261-73-2. Molecular formula: C19H24N4O5. Mole weight: 388.42. Catalog: APB1177261732. | |
| Terazosin EP impurity D | Terazosin EP impurity D. Uses: For analytical and research use. CAS No. 102714-74-9. Molecular formula: C15H19N5O3. Mole weight: 317.35. Catalog: APB102714749. | |
| Terazosin EP impurity F | Terazosin EP impurity F. Uses: For analytical and research use. CAS No. 109678-71-9. Molecular formula: C19H27N5O4. Mole weight: 389.46. Catalog: APB109678719. | |
| Terazosin EP impurity G | Terazosin EP impurity G. Uses: For analytical and research use. CAS No. 105356-89-6. Molecular formula: C18H23N5O4. Mole weight: 371.41. Catalog: APB105356896. | |
| Terazosin EP impurity H | Terazosin EP impurity H. Uses: For analytical and research use. CAS No. 105356-90-9. Molecular formula: C18H23N5O4. Mole weight: 373.41. Catalog: APB105356909. | |
| Terazosin EP impurity I | Terazosin EP impurity I. Uses: For analytical and research use. CAS No. 1177261-85-6. Molecular formula: C20H27N5O4. Mole weight: 401.47. Catalog: APB1177261856. | |
| Terazosin EP impurity J | Terazosin EP impurity J. Uses: For analytical and research use. CAS No. 152551-75-2. Molecular formula: C19H27N5O4. Mole weight: 389.46. Catalog: APB152551752. | |
| Terazosin EP impurity K | Terazosin EP impurity K. Uses: For analytical and research use. CAS No. 19216-56-9. Molecular formula: C19H21N5O4. Mole weight: 383.41. Catalog: APB19216569. | |
| Terazosin EP impurity L | Terazosin EP impurity L. Uses: For analytical and research use. CAS No. 40172-95-0. Molecular formula: C9H12N2O2. Mole weight: 180.21. Catalog: APB40172950. | |
| Terazosin EP impurity M | Terazosin EP impurity M. Uses: For analytical and research use. CAS No. 31350-27-3. Molecular formula: C14H14N2O4. Mole weight: 274.28. Catalog: APB31350273. | |
| Terazosin EP impurity N | Terazosin EP impurity N. Uses: For analytical and research use. CAS No. 63074-07-7. Molecular formula: C9H16N2O2. Mole weight: 184.24. Catalog: APB63074077. | |
| Terazosin EP impurity O | Terazosin EP impurity O. Uses: For analytical and research use. CAS No. 547730-06-3. Molecular formula: C14H22N2O4. Mole weight: 282.34. Catalog: APB547730063. | |
| Terazosin EP Impurity O-RR | One impurity of Terazosin, which is a piperazine derivative and has been found to be an α-1-adrenergic blocker. Alternative Names: Terazosin impurity 11-RR. Grades: 95%. Molecular formula: C14H22N2O4. Mole weight: 282.33. | |
| Terazosin HCl dihydrate | Terazosin HCl dihydrate. Group: Biochemicals. Grades: Highly Purified. CAS No. 70024-40-7. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C19H25N5O4·ClH·2H2O. US Biological Life Sciences. | Worldwide |
| Terazosin hydrochloride | Terazosin hydrochloride. Uses: For analytical and research use. CAS No. 70024-40-7. Mole weight: 459.92. Catalog: AP70024407. | |
| Terazosin hydrochloride | Terazosin hydrochloride. Uses: For analytical and research use. CAS No. 63590-64-7. Mole weight: 423.89. Catalog: AP63590647. | |
| Terazosin, Hydrochloride | An a-1-adrenergicblocker related to prazosin. Group: Biochemicals. Alternative Names: 1- (4-Amino-6, 7-dimethoxy-2-quinazolinyl) -4-[ (tetrahydro-2-furanyl) carbonxyl]piperazine, Hydrochloride. Grades: Highly Purified. CAS No. 63074-08-8. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| Terazosin Hydrochloride Dihydrate EP Impurity E | Terazosin Hydrochloride Dihydrate EP Impurity E. CAS No. 102839-00-9. | |
| Terazosin hydrochloride,pharma | Terazosin hydrochloride,pharma. Alternative Names: Terazosin hydrochloride, Terazosin HCl, Vasocard, 63074-08-8, Abbott-45975, Terazosin hydrochloride anhydrous, 1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-4-[(tetrahydro-2-furanyl)carbonyl]piperazine hydrochloride, DSSTox_CID_25493, DSSTox_RID_80913, DSSTox_GSID_45493, MLS001305722, Piperazine, 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-((tetrahydro-2-furanyl)carbonyl)-, monohydrochloride, SMR000044015, CAS-63074-08-8, 63590-64-7 (Parent), Prestwick_146, terazosinhydrochloride, terazosine hydrochloride, Tetrazosin hydrochloride, AC1L2BPY. CAS No. 141269-45-6. Purity: 96%. Product ID: ACM141269456. Molecular formula: C19H26ClN5O4. Mole weight: 423.893840 [g/mol]. IUPAC Name: [4-(4-amino-6,7-dimethoxyquinazolin-2-yl)piperazin-1-yl]-(oxolan-2-yl)methanone;hydrochloride. ECNumber: 613-138-7. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Terazosin impurity 1 | Terazosin impurity 1. Uses: For analytical and research use. CAS No. 1486464-41-8. Molecular formula: C24H30Cl2N8O4. Mole weight: 565.46. Catalog: APB1486464418. | |
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