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| Product | Description | |
|---|---|---|
| Tiotropium Bromide Hydrate | Tiotropium Bromide Hydrate. Alternative Names: Tiotropium Bromide Monohydrate; Tiotropium Bromide Xhydrate. CAS No. 139404-48-1. Purity: 95%+. Product ID: ACM139404481. Molecular formula: C19H22NO4S2Br·H2O. Mole weight: 490.43. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Tiotropium bromide monohydrate | Tiotropium bromide monohydrate. Group: Biochemicals. Grades: Highly Purified. CAS No. 139404-48-1. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C19H22NO4S2·H2O·Br. US Biological Life Sciences. |  Worldwide |
| Tiotropium bromide monohydrate | Tiotropium bromide monohydrate (BA-679 BR monohydrate) is a long-acting anticholinergic bronchodilator. Tiotropium bromide monohydrate blocks the action of acetylcholine at muscarinic M1, M2, and M3 receptors, prevents bronchoconstriction, and dilates bronchial airways. Tiotropium bromide monohydrate is applicable to research related to chronic obstructive pulmonary disease and asthma[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BA-679 BR monohydrate. CAS No. 411207-31-3. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg. Product ID: HY-B0460. |  |
| Tiotropium bromide monohydrate | 100mg Pack Size. Group: Analytical Reagents, Biochemicals, Building Blocks, Organics. Formula: C19H22BrNO4S2.H2O. CAS No. 139404-48-1. Prepack ID 90025485-100mg. Molecular Weight 490.43. See USA prepack pricing. |  |
| Tiotropium-[d3] Bromide | Tiotropium-[d3] Bromide is the labelled analogue of Tiotropium bromide. Tiotropium bromide is an anticholinergic bronchodilator used in the management of chronic obstructive pulmonary disease. Synonyms: Tiotropium D3 Bromide; (1α,2β,4β,5α,7β)-7-[(2-Hydroxy-2,2-di-2-thienylacetyl)oxy]-9,9-dimethyl-3-oxa-9-azoniatricyclo[3.3.1.02,4]nonane-d3 Bromide. Grade: 98% by HPLC; 99% atom D. CAS No. 1127226-56-5. Molecular formula: C19H19D3BrNO4S2. Mole weight: 475.43. |  |
| Tiotropium-d3 Bromide | Muscarinic receptor antagonist. Bronchodilator. Group: Biochemicals. Alternative Names: (1α,2 β,4 β,5α,7 β )-7-[(2-Hydroxy-2, 2-di-2-thienylacetyl)oxy]-9, 9-dimethyl-3-oxa-9-azoniatricyclo[3. 3. 1. 02, 4]nonane-d3 Bromide. Grades: Highly Purified. CAS No. 1127226-56-5. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Tiotropium-[d3] Iodide | An isotope labelled derivative of Tiotropium bromide. Tiotropium bromide is an anticholinergic bronchodilator used in the management of chronic obstructive pulmonary disease. Synonyms: (1R,2R,4S,5S,7S)-7-{[2-hydroxy-2,2-bis(thiophen-2-yl)acetyl]oxy}-9-(D3)methyl-9-methyl-3-oxa-9-azatricyclo[3.3.1.0,4]nonan-9-ium iodide. Grade: 95% by HPLC; 98% atom D. CAS No. 412010-61-8. Molecular formula: C19H19D3NO4S2I. Mole weight: 522.44. | |
| Tiotropium impurity 1 | Tiotropium impurity 1. Uses: For analytical and research use. CAS No. 588-63-6. Molecular formula: C9H11BrO. Mole weight: 215.09. Catalog: APB588636. |  |
| TIP 39, Tuberoinfundibular Neuropeptide | TIP 39, Tuberoinfundibular Neuropeptide is an endogenous PTH2 receptor agonist and antihypertensive agent. TIP 39, Tuberoinfundibular Neuropeptide selectively activates the PTH2 receptor with no activity on the PTH1 receptor, stimulates cAMP production, activates adenylate cyclase, and elevates intracellular calcium levels via mobilization from intracellular stores. TIP 39, Tuberoinfundibular Neuropeptide is highly conserved in humans, mice, and rats. TIP 39, Tuberoinfundibular Neuropeptide is applicable to research related to nociception and inflammation-induced pain[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 277302-47-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P1852. | |
| TIP 39, Tuberoinfundibular Neuropeptide | It is a neuropeptide and parathyroid hormone 2 receptor (PTH2R) agonist. Synonyms: Ser-Leu-Ala-Leu-Ala-Asp-Asp-Ala-Ala-Phe-Arg-Glu-Arg-Ala-Arg-Leu-Leu-Ala-Ala-Leu-Glu-Arg-Arg-His-Trp-Leu-Asn-Ser-Tyr-Met-His-Lys-Leu-Leu-Val-Leu-Asp-Ala-Pro; TIP 39 (39 mer); L-seryl-L-leucyl-L-alanyl-L-leucyl-L-alanyl-L-alpha-aspartyl-L-alpha-aspartyl-L-alanyl-L-alanyl-L-phenylalanyl-L-arginyl-L-alpha-glutamyl-L-arginyl-L-alanyl-L-arginyl-L-leucyl-L-leucyl-L-alanyl-L-alanyl-L-leucyl-L-alpha-glutamyl-L-arginyl-L-arginyl-L-histidyl-L-tryptophyl-L-leucyl-L-asparagyl-L-seryl-L-tyrosyl-L-methionyl-L-histidyl-L-lysyl-L-leucyl-L-leucyl-L-valyl-L-leucyl-L-alpha-aspartyl-L-alanyl-L-proline. Grade: ≥95% by HPLC. CAS No. 277302-47-3. Molecular formula: C202H325N61O54S. Mole weight: 4504.17. | |
| TIP48/49-IN-1 | TIP48/49-IN-1 is an orally active, specific RUVBL1/2 (TIP48/49) ATPase inhibitor with an IC50 of 59 nM against purified RUVBL1/2. TIP48/49-IN-1 inhibits the DNA replication process, leading to S-phase arrest. TIP48/49-IN-1 induces apoptosis. TIP48/49-IN-1 can be used for the research of non-small cell lung cancer (NSCLC) cells[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1807337-58-1. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103702. | |
| Tipelukast-[d6] | Tipelukast-[d6] is the labelled analogue of Tipelukast, which could be used as an oral anti-inflammatory agent and has been found to exhibit potential activities against non-alcoholic fatty liver disease as a leukotriene receptor antagonist. Synonyms: Tipelukast-D6. Molecular formula: C29H32D6O7S. Mole weight: 536.71. | |
| tipepidine Impurity 1 | tipepidine Impurity 1. Uses: For analytical and research use. CAS No. 5169-77-7. Molecular formula: C21H25NO7S2. Mole weight: 467.55. Catalog: APB5169777. | |
| Tiphenylphosphine-3,3',3''-trisulfonic acid trisodium salt | Tiphenylphosphine-3,3',3''-trisulfonic acid trisodium salt. Group: Biochemicals. Grades: Highly Purified. CAS No. 63995-70-0. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C18H12Na3O9PS3. US Biological Life Sciences. | Worldwide |
| Tipifarnib | A farnesyltransferase inhibitor. Sensitizes human multiple myeloma cell to proteasome inhibition by blocking degradation of bortezomib-induced aggresomes. Also shown to inhibit the growth of myeloid leukemia cell lines and primary leukemia cells by inducing apoptosis and cell-cycle blockage when combined with rapamycin(R124000). Group: Biochemicals. Alternative Names: 6-[(R)-Amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl]-4-(3-chlorophenyl)-1-methyl-2(1H)-quinolinone; (R)-(+)-R 115777; Zarnestra. Grades: Highly Purified. CAS No. 192185-72-1. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Tipifarnib | Tipifarnib (IND 58359) binds to and inhibits farnesyltransferase (FTase) with an IC50 of 0.86 nM. Antineoplastic activity and antiparasitic activity[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: IND 58359; R115777. CAS No. 192185-72-1. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10502. | |
| Tipiracil | Tipiracil is a thymidine phosphorylase (TPase) inhibitor. Uses: Scientific research. Category: Signaling pathways. CAS No. 183204-74-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-A0063A. | |
| Tipiracil hydrochloride | Tipiracil (hydrochloride) is a thymidine phosphorylase inhibitor (TPI), used for cancer research. Uses: Scientific research. Category: Signaling pathways. CAS No. 183204-72-0. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-A0063. | |
| Tiplaxtinin | Tiplaxtinin is a selective and orally efficacious inhibitor of plasminogen activator inhibitor-1 (PAI-1) with IC50 of 2.7 μM[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PAI-039; Tiplasinin. CAS No. 393105-53-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15253. | |
| Tipranavir | Storage and Stability. Group: Biochemicals. Alternative Names: N-[3-[(1R)-1-[(6R)-5,6-Dihydro-4-hydroxy-2-oxo-6-(2-phenylethyl)-6-propyl-2H-pyran-3-yl]propyl]phenyl]-5-(trifluoromethyl)-2-pyridinesulfonamide; PNU-140690; Aptivus. Grades: Highly Purified. CAS No. 174484-41-4. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. US Biological Life Sciences. | Worldwide |
| Tipranavir | Tipranavir (PNU-140690) inhibits the enzymatic activity and dimerization of HIV-1 protease, exerts potent activity against multi-protease inhibitor (PI)-resistant HIV-1 isolates with IC50s of 66-410 nM[1][2]. Tipranavir inhibits SARS-CoV-2 3CLpro activity[3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PNU-140690. CAS No. 174484-41-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15148. | |
| Tipranavir-[d4] | Tipranavir-[d4] is the labelled analogue of Tipranavir, which is a nonpeptidic HIV protease inhibitor and has been found to be effective as an antiviral. Synonyms: Tipranavir D4; N-[3-[(1R)-1-[(6R)-5,6-Dihydro-4-hydroxy-2-oxo-6-(2-phenylethyl)-6-propyl-2H-pyran-3-yl]propyl]phenyl]-5-(trifluoromethyl)-2-pyridinesulfonamide-d4. Grade: 95% by HPLC; 98% atom D. CAS No. 1217819-15-2. Molecular formula: C31H29D4F3N2O5S. Mole weight: 606.69. | |
| Tipranavir-d4 (N-[3-[(1R)-1-[(6R)-5,6-Dihydro-4-hydroxy-2-oxo-6-(2-phenylethyl)-6-propyl-2H-pyran-3-yl]propyl]phenyl]-5-(trifluoromethyl)-2-pyridinesulfonamide-d4,. PNU-140690-d4, Aptivus-d4,. ) | Nonpeptidic HIV protease inhibitor (NPPI). Antiviral. Group: Biochemicals. Alternative Names: N-[3-[(1R)-1-[(6R)-5,6-Dihydro-4-hydroxy-2-oxo-6-(2-phenylethyl)-6-propyl-2H-pyran-3-yl]propyl]phenyl]-5-(trifluoromethyl)-2-pyridinesulfonamide-d4; PNU-140690-d4; Aptivus-d4. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Tipranavir. (N-[3-[(1R)-1-[(6R)-5,6-Dihydro-4-hydroxy-2-oxo-6-(2-phenylethyl)-6-propyl-2H-pyran-3-yl]propyl]phenyl]-5-(trifluoromethyl)-2-pyridinesulfonamide,. PNU-140690, Aptivus,. ) | Nonpeptidic HIV protease inhibitor (NPPI). Antiviral. Group: Biochemicals. Alternative Names: N-[3-[(1R)-1-[(6R)-5,6-Dihydro-4-hydroxy-2-oxo-6-(2-phenylethyl)-6-propyl-2H-pyran-3-yl]propyl]phenyl]-5-(trifluoromethyl)-2-pyridinesulfonamide; PNU-140690; Aptivus. Grades: Highly Purified. CAS No. 174484-41-4. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| TipranavirP | Tipranavir is a protease inhibitor that inhibits HIV-1 resistant to more than 1 protease inhibitor.Tipranavir effectively inhibits HIV-1 protease enzyme activity and dimerisation and has potent activity against multiple protease inhibitor (PI) HIV-1 isolates (IC50 of 66-410 nM). Category: Active pharmaceutical ingredients. CAS No. 174484-41-4. Product ID: API174484414. Molecular formula: C31H33F3N2O5S. Mole weight: 602.66. |  |
| TIQ-A | TIQ-A. Group: Biochemicals. Alternative Names: Thieno[2,3-C]isoquinolin-5-one. Grades: Highly Purified. CAS No. 420849-22-5. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C11H7NOS. US Biological Life Sciences. | Worldwide |
| TIQ-A (Thieno[2,3-C]isoquinolin-5-one) | TIQ-A (Thieno[2,3-C]isoquinolin-5-one). Group: Biochemicals. Alternative Names: Thieno[2,3-C]isoquinolin-5-one. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Tiquizium Bromide | Tiquizium Bromide is a antimuscarinic agent that was used on airway smooth muscle in vitro and in patients with chronic obstructive pulmonary disease. Group: Biochemicals. Alternative Names: HS 902; HSR 902; Thiaton; (5R, 9aR) -rel-3- (Di-2-thienylmethylene) octahydro-5-methyl-2H-quinolizinium Bromide; trans-3- (Di-2-thienylmethylene) octahydro-5-methyl-2H-quinolizinium Bromide. Grades: Highly Purified. CAS No. 71731-58-3. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Tiquizium Bromide Impurity 2 | Tiquizium Bromide Impurity 2. Uses: For analytical and research use. Molecular formula: C10H19N. Mole weight: 153.27. Catalog: APB09973. | |
| Tirabrutinib | Tirabrutinib (ONO-4059) is an orally active Brutons Tyrosine Kinase (BTK) inhibitor (can cross the blood-brain barrier (BBB)), with an IC50 of 6.8 nM. Tirabrutinib irreversibly and covalently binds to BTK and inhibits aberrant B cell receptor signaling. Tirabrutinib can be used in studies of autoimmune diseases and hematological malignancies[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ONO-4059; GS-4059. CAS No. 1351636-18-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15771. | |
| Tiragolumab | Tiragolumab is an immune checkpoint inhibitor binding to the T-cell immunoglobulin and ITIM domain (TIGIT). Tiragolumab in combination with Atezolizumab (HY-P9904) and Bevacizumab (HY-P9906) has benefit in unresectable hepatocellular carcinoma. Tiragolumab can be used to study non-small cell lung cancer (NSCLC) and melanoma[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MTIG-7192A; RG-6058. CAS No. 1918185-84-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P9986. | |
| Tirandamycin A | Tirandamycin A is originally isolated from Str. tirandis var. tirandis NRRL 3689, and it has anti-gram-positive bacteria effect. Synonyms: NSC 107067; 3-Pyrrolin-2-one, 4-hydroxy-3-(4-methyl-6-(1,2,7-trimethyl-5-oxo-3,9,10-trioxatricyclo(4.3.1.0(sup 2,4))dec-8-yl)-2,4-heptadienoyl)-, (E,E)-. Grade: 95% by HPLC. CAS No. 34429-70-4. Molecular formula: C22H27NO7. Mole weight: 417.45. | |
| Tirapazamine | Tirapazamine (SR259075) is an anticancer agent that shows selective cytotoxicity for hypoxic cells in solid tumors, thereby inducing single-and double-strand breaks in DNA, base damage, and cell death. Tirapazamine is an anticancer and bioreductive agent.Tirapazamine (SR259075) can enhance the cytotoxic effects of ionizing radiation in hypoxic cells[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SR259075; SR4233; Win59075; SML 0552; SR 259075; Tirazone. CAS No. 27314-97-2. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 200 mg. Product ID: HY-13767. | |
| Tiratricol | Tiratricol is an orally available thyroid hormone analog that inhibits pituitary thyroid-stimulating hormone secretion. Tiratricol is an intracellular toxin neutralizer that inhibits LPS and lipid A cytotoxicity with IC50s of 20 μM and 32 μM, respectively. Tiratricol reduces TNF production in lipopolysaccharide-stimulated macrophages. Tiratricol also has antiviral activity and is an inhibitor of yellow fever virus (Flavivirus). It can bind to the RdRp domain of the viral NS5 protein to hinder YFV replication.[2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 3,3',5-Triiodothyroacetic acid. CAS No. 51-24-1. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 500 mg. Product ID: HY-B1201. | |
| Tirbanibulin | Tirbanibulin (KX2-391) is an inhibitor of Src that targets the peptide substrate site of Src, with GI50 of 9-60 nM in cancer cell lines. Uses: Scientific research. Category: Signaling pathways. Alternative Names: KX2-391; KX-01. CAS No. 897016-82-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10340. | |
| Tirbanibulin dihydrochloride | Tirbanibulin (dihydrochloride) (KX2-391 (dihydrochloride)) is an inhibitor of Src that targets the peptide substrate site of Src, with GI50 of 9-60 nM in cancer cell lines. Uses: Scientific research. Category: Signaling pathways. Alternative Names: KX2-391 dihydrochloride; KX-01 dihydrochloride. CAS No. 1038395-65-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10340A. | |
| Tirnovetmab | Tirnovetmab (KIND-016) is a fully caninized, high-affinity monoclonal antibody that targets IL-31. Tirnovetmab can be used in research related to atopic dermatitis in dogs. Uses: Scientific research. Category: Signaling pathways. Alternative Names: KIND-016. CAS No. 2364504-80-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99557. | |
| Tirofiban | Tirofiban. Alternative Names: TIROFIBAN;(2s)-2-(butylsulfonylamino)-3-[4-[4-(4-piperidyl)butoxy]phenyl]propanoic acid;Aggrastat;MK-383;N-(Butylsulfonyl)-O-[4-(4-piperidinyl)butyl]-L-tyrosine;C07965;Tirofiban/Tirofiban HCl;irofiban. CAS No. 144494-65-5. Purity: 98+%. Product ID: ACM144494655. Molecular formula: C22H36N2O5S. Mole weight: 440.6. IUPAC Name: (2S)-2-(butylsulfonylamino)-3-[4-(4-piperidin-4-ylbutoxy)phenyl]propanoicacid. Canonical SMILES: CCCCS(=O)(=O)NC(CC1=CC=C(C=C1)OCCCCC2CCNCC2)C(=O)O. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Tirofiban | Tirofiban (L700462) is a selective and reversible platelet integrin receptor (Gp IIb/IIIa) antagonist that inhibits fibrinogen binding to this receptor and has antithrombotic activity. Tirofiban induces proliferation and migration on endothelial cell by inducing production of VEGF. Tirofiban can significantly reduces myocardial no-reflow and ischemia-reperfusion injury by alleviating myocardial microvascular structural and endothelial dysfunction in the ischemic area[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: L700462; MK383. CAS No. 144494-65-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17369B. | |
| Tirofiban-butyl-d9, Hydrochloride (N-(Butyl-d9-sulfonyl)-O-[4-(4-piperidynyl)butyl]-L-tyrosine, Hydrochloride) | Labeled Tirofiban, a specific nonpeptide platelet fibrinogen receptor (GPIIb/IIIa) antagonist. An antithrombotic used in the treatment of unstable angina. Group: Biochemicals. Alternative Names: N-(Butyl-d9-sulfonyl)-O-[4-(4-piperidynyl)butyl]-L-tyrosine, Hydrochloride. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Tirofiban hydrochloride | Tirofiban hydrochloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 142373-60-2. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. Molecular Formula: C22H36N2O5S·HCl. US Biological Life Sciences. | Worldwide |
| Tirofiban hydrochloride hydrate | Tirofiban hydrochloride hydrate. Group: Biochemicals. Alternative Names: N-(Butylsulfonyl)-O-[4-(4-piperidynyl)butyl]-L-tyrosine, hydrochloride hydrate. Grades: Highly Purified. CAS No. 150915-40-5. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C22H39ClN2O6S. US Biological Life Sciences. | Worldwide |
| Tirofiban, Hydrochloride Hydrate (N-(Butylsulfonyl)-O-[4-(4-piperidynyl)butyl]-L-tyrosine, Hydrochloride Hydrate) | A specific nonpeptide platelet fibrinogen receptor (GPIIb/IIIa) antagonist. An antithrombotic used in the treatment of unstable angina. Group: Biochemicals. Alternative Names: N-(Butylsulfonyl)-O-[4-(4-piperidynyl)butyl]-L-tyrosine, Hydrochloride Hydrate. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Tirofiban hydrochloride monohydrate | Tirofiban hydrochloride monohydrate. Alternative Names: Tirofiban Hydrochloride;TirofibanhydrochlorideHCl;N-(Butylsulfonyl)-O-[4-(4-piperidinyl)butyl]-L-tyrosine hydrochloride;L 700462;L-Tyrosine, N-(butylsulfonyl)-o-(4-(4-piperidinyl)butyl)-, monohydrochloride;N-(Butylsulfonyl)-o-(4-(4-piperidinyl)butyl)-L-t. CAS No. 142373-60-2. Purity: 98%. Product ID: ACM142373602. Molecular formula: C22H36N2O5S.HCl. Mole weight: 477.06. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Tirofiban Impurity 19 | Tirofiban Impurity 19. Uses: For analytical and research use. CAS No. 158808-75-4. Molecular formula: C18H28N2O3. Mole weight: 320.43. Catalog: APB158808754. | |
| Tirofiban Impurity 2 | Tirofiban Impurity 2. Uses: For analytical and research use. Molecular formula: C22H35ClN2O5S. Mole weight: 475.04. Catalog: APB09925. | |
| Tirofiban Impurity 25 | Tirofiban Impurity 25. Uses: For analytical and research use. Alternative Names: N,N-diethylpentane-1-sulfonamide. CAS No. 14674-02-3. Molecular formula: C9H21NO2S. Mole weight: 207.33. Catalog: APB14674023. | |
| Tirofiban Impurity 3 | Tirofiban Impurity 3. Uses: For analytical and research use. CAS No. 2683065-73-6. Molecular formula: C22H35ClN2O5S. Mole weight: 475.04. Catalog: APB2683065736. | |
| Tirofiban Impurity 4 | Tirofiban Impurity 4. Uses: For analytical and research use. Molecular formula: C22H35N3O6S. Mole weight: 469.6. Catalog: APB09926. | |
| Tirofiban Impurity 5 | Tirofiban Impurity 5. Uses: For analytical and research use. Molecular formula: C22H35N3O6S. Mole weight: 469.6. Catalog: APB09928. | |
| Tirofiban Impurity 6 | Tirofiban Impurity 6. Uses: For analytical and research use. Molecular formula: C22H34N4O7S. Mole weight: 498.6. Catalog: APB09927. | |
| Tirofiban Impurity 7 | Tirofiban Impurity 7. Uses: For analytical and research use. Molecular formula: C13H18N2O6S. Mole weight: 330.36. Catalog: APB09929. | |
| Tirofiban Impurity 8 | Tirofiban Impurity 8. Uses: For analytical and research use. Molecular formula: C22H36Cl2N2O5S. Mole weight: 511.5. Catalog: APB09930. | |
| Tirofiban Impurity A | Tirofiban Impurity A. Uses: For analytical and research use. CAS No. 149490-60-8. Molecular formula: C13H19NO5S. Mole weight: 301.36. Catalog: APB149490608. | |
| Tirofiban Impurity B | Tirofiban Impurity B. Uses: For analytical and research use. CAS No. 149463-65-0. Molecular formula: C9H13Cl2N. Mole weight: 206.11. Catalog: APB149463650. | |
| Tiron | Tiron is a non-toxic chelator of a variety of metals. Tiron is cell permeable analog of vitamin E and function as hydroxyl radical and superoxide scavenger. Tiron is an orally active antioxidant. Tiron can be used to alleviate acute metal overload in animals[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 149-45-1. Pack Sizes: 10 mM * 1 mL in DMSO; 10 g; 25 g; 50 g; 100 g. Product ID: HY-D0261. | |
| Tiron | Tiron. CAS No. 149-45-1. |  Pennsylvania PA |
| Tiron (1,2-Dihydroxybenzene-3,5-disulfonic acid disodium salt) C6H6Na2O9S2 | 25g Pack Size. Group: Analytical Reagents, Building Blocks, Organics, Stains & Indicators. Formula: C6H6Na2O9S2. CAS No. 149-45-1. Prepack ID 58661995-25g. Molecular Weight 332.22. See USA prepack pricing. | |
| Tiropramide Hydrochloride | Tiropramide is an antispasmodic agent. Studies sugges that Tiropramide has a pure musculotropic smooth muscle relaxant activity. Tiropramide is considered to be useful to inhibit the contractile response of the urinary bladder. Group: Biochemicals. Alternative Names: (±) - α - (Benzoylamino) -4- [2- (diethylamino) ethoxy] -N, N-dipropyl benzenepropanamide Hydrochloride; Alfospas; Maiorad; Tiromid. Grades: Highly Purified. CAS No. 53567-47-8. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| tirucalladienol synthase | The product from Arabidopsis thaliana is 85% tirucalla-7,24-dien-3β-ol with trace amounts of other triterpenoids. Group: Enzymes. Synonyms: PEN3. Enzyme Commission Number: EC 5.4.99.56. 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-5599; tirucalladienol synthase; EC 5.4.99.56; PEN3. Cat No: EXWM-5599. |  |
| Tirzepatide | Tirzepatide Inhibitor. Uses: Scientific use. Product Category: TP1111L. CAS No.: |  |
| Tirzepatide | Tirzepatide is a dual GIP and GLP-1 receptor agonist and a drug candidate for the treatment of type 2 diabetes. Uses: Treating type 2 diabetes is one of the main conditions where tirzepatide shows promise. millions of people worldwide suffer with this chronic illness, which is characterized by poor glucose metabolism and insulin resistance. targeting several receptors, such as the glucose-dependent insulinotropic polypeptide (gip) and glucagon-like peptide-1 (glp-1) receptors, is part of tirzepatide's distinct mo. Synonyms: L-Tyrosyl-2-methylalanyl-L-α-glutamylglycyl-L-threonyl-L-phenylalanyl-L-threonyl-L-seryl-L-α-aspartyl-L-tyrosyl-L-seryl-L-isoleucyl-2-methylalanyl-L-leucyl-L-α-aspartyl-L-lysyl-L-isoleucyl-L-alanyl-L-glutaminyl-N6-[(22S)-22,42-dicarboxy-1,10,19,24-tetraoxo-3,6,12,15-tetraoxa-9,18,23-triazadotetracont-1-yl]-L-lysyl-L-alanyl-L-phenylalanyl-L-valyl-L-glutaminyl-L-tryptophyl-L-leucyl-L-isoleucyl-L-ala. Grade: ≥95%. CAS No. 2023788-19-2. Molecular formula: C225H348N48O68. Mole weight: 4813.45. | |
| Tirzepatide | Tirzepatide. Categories: tirzepatide; 2023788-19-2. |  CA, FL & NJ |
| Tirzepatide acetate | Tirzepatide acetate is a dual GIP and GLP-1 receptor agonist used as a drug candidate for the treatment of type 2 diabetes. Synonyms: L-Tyrosyl-2-methylalanyl-L-α-glutamylglycyl-L-threonyl-L-phenylalanyl-L-threonyl-L-seryl-L-α-aspartyl-L-tyrosyl-L-seryl-L-isoleucyl-2-methylalanyl-L-leucyl-L-α-aspartyl-L-lysyl-L-isoleucyl-L-alanyl-L-glutaminyl-N6-[(22S)-22,42-dicarboxy-1,10,19,24-tetraoxo-3,6,12,15-tetraoxa-9,18,23-triazadotetracont-1-yl]-L-lysyl-L-alanyl-L-phenylalanyl-L-valyl-L-glutaminyl-L-tryptophyl-L-leucyl-L-isoleucyl-L-ala. CAS No. 2931515-08-9. Molecular formula: C227H352N48O70. Mole weight: 4873.58. | |
| Tirzepatide (LY3298176) sodium | Tirzepatide (LY3298176, GIP/GLP-1 RA, TZP) sodium is a dual GIP/GLP-1 receptor agonist. Tirzepatide differentially induces internalization of the GIP and GLP-1 receptors with EC50 values of 18.2 nM and 18.1 nM, respectively. Group: Peptides. CAS No. 2023788-19-2 (free base). Pack Sizes: 1mg. Product ID: P1206. Formula: C225H348N48O68• XNa. Storage Conditions: 3 years-20°C powder. |  United States; Europe |
| Tirzepatide (sodium salt) | Tirzepatide (sodium salt). CAS No. 2023788-19-2. Purity: ≥98.0% (HPLC). Product ID: ALC-FP-2023788192. Molecular formula: C225H348N48O68. Mole weight: 4813.45. Alfa Chemistry - ISO 9001:32057 Certified. | |
| TIS108 | TIS108 is a triazole-type strigolactone biosynthesis inhibitor. TIS108 inhibits Arabidopsis embryogenesis and root hair growth, and promotes shoot branching. TIS108 can also increase the gibberellin content in Gastrodia elata. TIS108 can be used in the research of plant growth and development as well as plant responses to the environment[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1315459-30-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-136403. | |
| Tislelizumab | Tislelizumab is a monoclonal antibody that specifically binds to programmed cell death receptor 1 (PD-1), blocking its interaction with programmed death ligand 1 (PD-L1) and programmed death ligand 2 (PD-L2). Tislelizumab can reactivate immune cells such as T lymphocytes and enhance anti-tumor activity. Tislelizumab can be used for the research of a variety of tumors including typical Hodgkin's lymphoma, urothelial carcinoma, non-small cell lung cancer and hepatocellular carcinoma[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BGB-A317. CAS No. 1858168-59-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99052. | |
| Tisolagiline | Tisolagiline (KDS2010) is the selective, reversible and orally active inhibitor for MAO-B with an IC50 of 8 nM. Tisolagiline exhibits neuroprotective and anti-neuroinflammatory activities[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: KDS2010. CAS No. 1894207-44-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-127109. | |
| Tisotumab | Tisotumab (Anti-Human F3 Recombinant Antibody) is a human IgG1 monoclonal antibody and ADC antibody. Tisotumab targets tissue factor (TF). Tisotumab can be used to synthesize antibody-drug conjugates (ADCs) targeting tissue factor (TF), Tisotumab vedotin (HY-152963). Tisotumab can be used for the research of solid tumors[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Anti-Human F3 Recombinant Antibody. CAS No. 1418628-81-5. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P99271. | |
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