A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
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
Tipranovir b-D-glucuronide
Tipranovir b-D-glucuronide is a metabolite of the anti-HIV drug Tipranavir. It is a glucuronide conjugate that is formed in the liver and excreted in bile. This metabolite has no known pharmacological activity but can be used as a biomarker to monitor Tipranavir therapy. CAS No. 947408-14-2. Molecular formula: C37H41F3N2O11S. Mole weight: 778.79.
Tiprolisant
Tiprolisant is potent and selective nonimidazole inverse agonist at the histamine H3 receptor. (Ki=0.16 nM). Uses: The histamine h3 receptor. Synonyms: Pitolisant; 1-[3-[3- (4-chlorophenyl) propoxy]propyl]piperidine. Grades: ≥95%. CAS No. 362665-56-3. Molecular formula: C17H26ClNO. Mole weight: 295.85.
Tiq-a
TIQ-A is a potent TNKS (poly-ART, PARP) inhibitor, with an IC50 of 24 nM for TNKS2. TIQ-A is a potential anti-ischemic agent. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TIQ-A, 4H-Thieno[2,3-c]isoquinolin-5-one, PARP Inhibitor X, TIQ-A, Thieno[2,3-c]isoquinolin-5-one, 420849-22-5, SureCN422013, T2825_SIGMA, CTK1C8658, ZINC00003266, AG-F-49683, Thieno[2,3-c]isoquinolin-5(4H)-one, NCGC00165904-01, FT-0675250, G18. Product Category: Inhibitors. CAS No. 420849-22-5. Molecular formula: C11H7NOS. Mole weight: 201.24. Purity: ≥98%. IUPACName: 4H-thieno[2,3-c]isoquinolin-5-one. Canonical SMILES: C1=CC=C2C(=C1)C3=C(NC2=O)SC=C3. Density: 1.359g/cm³. Product ID: ACM420849225. Alfa Chemistry ISO 9001:2015 Certified. Categories: TiQal.
TIQ-A
TIQ-A is a PARP1 inhibitor with IC50 value of 450 nM. It exhibits neuroprotective effects in cultured mouse cortical neurons injured by oxygen-glucose deprivation (IC50 = 0.15 μM). Uses: Poly(adp-ribose) polymerase inhibitors. Synonyms: 4H-Thieno[2,3-c]isoquinolin-5-one; Thieno[2,3-c]isoquinolin-5(4H)-one; 4H,5H-thieno[2,3-c]isoquinolin-5-one. Grades: ≥98%. CAS No. 420849-22-5. Molecular formula: C11H7NOS. Mole weight: 201.2.
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
Tirabrutinib
Tirabrutinib (ONO-4059) is an orally active Brutons Tyrosine Kinase ( BTK ) inhibitor (can cross the blood-brain barrier (BBB)), with an IC 50 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. Group: Signaling pathways. Alternative Names: ONO-4059; GS-4059. CAS No. 1351636-18-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15771.
Tirabrutinib hydrochloride
Tirabrutinib (ONO-4059) hydrochloride is an orally active Brutons Tyrosine Kinase ( BTK ) inhibitor (can cross the blood-brain barrier (BBB)), with an IC 50 of 6.8 nM. Tirabrutinib hydrochloride irreversibly and covalently binds to BTK and inhibits aberrant B cell receptor signaling. Tirabrutinib hydrochloride can be used in studies of autoimmune diseases and hematological malignancies [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ONO-4059 hydrochloride; GS-4059 hydrochloride. CAS No. 1439901-97-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15771A.
Tiragolumab
Tiragolumab is a humanized monoclonal antibody and immune checkpoint inhibitor that selectively binds to TIGIT, which suppresses the immune response to cancer. Synonyms: anti-TIGIT; RG6058; MTIG7192A. CAS No. 1918185-84-8.
Tiragolumab
Tiragolumab is an immune checkpoint inhibitor binding to T-cell immunoglobulin and ITIM domain ( TIGIT ). Tiragolumab, alone or in combination with the PD-L1 inhibitor Atezolizumab (HY-P9904), may be effective against multiple solid malignancies-most notably non-small cell lung cancer (NSCLC) [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. 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)-. Grades: 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. Group: Signaling pathways. Alternative Names: SR259075; SR4233; Win59075; SML 0552; SR 259075; Tirazone. CAS No. 27314-97-2. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg. Product ID: HY-13767.
Tirapazamine
Tirapazamine is a benzotriazine di-N-oxide with potential antineoplastic activity. Tirapazamine is selectively activated by multiple reductases to form free radicals in hypoxic cells, thereby inducing single-and double-strand breaks in DNA, base damage, and cell death. This agent also sensitizes hypoxic cells to ionizing radiation and inhibits the repair of radiation-induced DNA strand breaks via inhibition of topoisomerase II. Check for active clinical trials or closed clinical trials using this agent. Synonyms: US brand name: Tirazone. Code names: SR 4233. WIN 59075. SR-259075, NSC-130181, Win-59075, SR-4233. Grades: 0.98. CAS No. 27314-97-2. Molecular formula: C7H6N4O2. Mole weight: 178.15.
Tirasemtiv
Tirasemtiv is an activator of the fast skeletal muscle troponin complex. Tirasemtiv is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CK-2017357. CAS No. 1005491-05-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15964.
Tirasemtiv
Tirasemtiv is a a small-molecule fast-skeletal-troponin activator, which is being developed as a potential treatment for diseases and conditions associated with aging, muscle weakness and wasting or neuromuscular dysfunction. Synonyms: CK2017357; CK-2017357; CK 2017357; Tirasemtiv. Grades: >98%. CAS No. 1005491-05-3. Molecular formula: C12H14N4O. Mole weight: 230.27.
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 IC 50 s 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. Group: Signaling pathways. Alternative Names: 3,3',5-Triiodothyroacetic acid. CAS No. 51-24-1. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B1201.
Tirbanibulin
Tirbanibulin (KX2-391) is an inhibitor of Src that targets the peptide substrate site of Src, with GI 50 of 9-60 nM in cancer cell lines. Uses: Scientific research. Group: Signaling pathways. Alternative Names: KX2-391; KX-01. CAS No. 897016-82-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 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 GI 50 of 9-60 nM in cancer cell lines. Uses: Scientific research. Group: Signaling pathways. Alternative Names: KX2-391 dihydrochloride; KX-01 dihydrochloride. CAS No. 1038395-65-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10340A.
Tirbanibulin Mesylate
Tirbanibulin Mesylate (KX2-391 Mesylate) is an inhibitor of Src that targets the peptide substrate site of Src, with GI 50 of 9-60 nM in cancer cell lines. Uses: Scientific research. Group: Signaling pathways. Alternative Names: KX2-391 Mesylate; KX01 Mesylate. CAS No. 1080645-95-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10340B.
Tirenzepine dihydrochloride
Tirenzepine dihydrochloride. Uses: For analytical and research use. Group: Impurity standards. CAS No. 147416-96-4. Molecular Formula: C19H24Cl2N4O2S. Mole Weight: 443.39. Catalog: APB147416964.
Tirilazad
Tirilazad is a nonglucocorticoid, 21-aminosteroid that inhibits lipid peroxidation. Tirilazad can attenuate brain or spinal cord injury caused by trauma, stroke, ischemia and reperfusion injury. Tirilazad has antiviral activities against nCoV. Tirilazad is neuroprotective for ischaemic stroke, can be used for subarachnoid hemorrhage research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: U 74006F free base. CAS No. 110101-66-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-132280.
Tirnovetmab
Tirnovetmab (KIND-016) is an antibody. Tirnovetmab can be used for experiment research. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: KIND-016. CAS No. 2364504-80-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99557.
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. Group: Signaling pathways. Alternative Names: L700462; MK383. CAS No. 144494-65-5. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-17369B.
Tirofiban
Tirofiban (MK-383, Aggrastat) is a nonpeptide derivative of tyrosine that selectively inhibits the GP-IIb/IIIa receptor, with minimal effects on the ?vβ3 vitronectin receptor. Uses: Antithrombotic; in treatment of unstable angina. Synonyms: Tirofiban; MK383; MK-383; MK 383. Grades: >98%. CAS No. 144494-65-5. Molecular formula: C22H36N2O5S. Mole weight: 440.6.
Tirofiban
Tirofiban. Uses: For analytical and research use. Group: Impurity standards. CAS No. 144494-65-5. Molecular Formula: C22H36N2O5S. Mole Weight: 440.6. Catalog: APB144494655.
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 Chloro Impurity
One of the impurities of Tirofiban, which has been found to be a glycoprotein IIb/IIIa inhibitor and could be used as an antiplatelet agent. Molecular formula: C22H35ClN2O5S. Mole weight: 475.05.
Tirofiban Cyclohexyl Impurity
One of the impurities of Tirofiban, which has been found to be a glycoprotein IIb/IIIa inhibitor and could be used as an antiplatelet agent. Molecular formula: C22H42N2O5S. Mole weight: 446.65.
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
Tirofiban hydrochloride is the hydrochloride salt form of Tirofiban. Tirofiban is a nonpeptide tyrosine derivative. It is used as an antiplatelet drug in the class of glycoprotein IIb/IIIa inhibitors. Uses: Fibrinolytic agents. Synonyms: Tirofiban HCl; (2S)-2-(butylsulfonylamino)-3-[4-(4-piperidin-4-ylbutoxy)phenyl]propanoic acid hydrochloride. CAS No. 142373-60-2. Molecular formula: C22H36N2O5S.HCl. Mole weight: 477.057.
Tirofiban Hydrochloride
Tirofiban Hydrochloride. Uses: For analytical and research use. Group: Impurity standards. CAS No. 150915-40-5. Molecular Formula: C22H39ClN2O6S. Mole Weight: 495.07. Catalog: APB150915405.
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.
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 (L700462) hydrochloride monohydrate is a selective and reversible platelet integrin receptor ( Gp IIb/IIIa ) antagonist that inhibits fibrinogen binding to this receptor and has antithrombotic activity. Tirofiban hydrochloride monohydrate induces proliferation and migration on endothelial cell by inducing production of VEGF. Tirofiban hydrochloride monohydrate 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. Group: Signaling pathways. Alternative Names: L700462 hydrochloride monohydrate; MK383 hydrochloride monohydrate. CAS No. 150915-40-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-17369.
Tirofiban Hydrochloride Monohydrate
Tirofiban is a specific nonpeptide platelet fibrinogen receptor (GPIIb/IIIa) antagonist. Tirofiban is an antithrombotic used in the treatment of unstable angina. Uses: The treatment of unstable angina. Synonyms: N-(Butylsulfonyl)-4-(4-(4-piperidyl)butoxy)-L-phenylalanine monohydrochloride monohydrate; Aggrastat; L 700462; L700462; L-700,462; MK-383; MK 383; MK383; Tirofiban; Tirofiban hydrochloride monohydrate. Grades: >98%. CAS No. 150915-40-5. Molecular formula: C22H39ClN2O6S. Mole weight: 495.07.
Tirofiban Impurity
One of the impurities of Tirofiban, which has been found to be a glycoprotein IIb/IIIa inhibitor and could be used as an antiplatelet agent. Synonyms: 4-(4-Pyridyl)butanoic Acid. Molecular formula: C9H11NO2. Mole weight: 165.19.
Tirofiban Impurity 19
Tirofiban Impurity 19. Uses: For analytical and research use. Group: Impurity standards. CAS No. 158808-75-4. Molecular Formula: C18H28N2O3. Mole Weight: 320.43. Catalog: APB158808754.
Tirofiban Impurity 1 Dihydrochloride
One of the impurities of Tirofiban, which has been found to be a glycoprotein IIb/IIIa inhibitor and could be used as an antiplatelet agent. Molecular formula: C31H41N3O5S. 2 HCl. Mole weight: 640.67.
Tirofiban Impurity 25
Tirofiban Impurity 25. Uses: For analytical and research use. Group: Impurity standards. 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. Group: Impurity standards. CAS No. 2683065-73-6. Molecular Formula: C22H35ClN2O5S. Mole Weight: 475.04. Catalog: APB2683065736.
Tirofiban Impurity A
Tirofiban Impurity A. Uses: For analytical and research use. Group: Impurity standards. CAS No. 149490-60-8. Molecular Formula: C13H19NO5S. Mole Weight: 301.36. Catalog: APB149490608.
Tirofiban Impurity A
One of the impurities of Tirofiban, which has been found to be a glycoprotein IIb/IIIa inhibitor and could be used as an antiplatelet agent. Synonyms: Debutylpiperidine Tirofiban; (S)-2-(Butylsulfonamido)-3-(4-hydroxyphenyl)propanoic Acid; N-(Butylsulfonyl)-L-tyrosine. CAS No. 149490-60-8. Molecular formula: C13H19NO5S. Mole weight: 301.36.
Tirofiban Impurity B
Tirofiban Impurity B. Uses: For analytical and research use. Group: Impurity standards. CAS No. 149463-65-0. Molecular Formula: C9H13Cl2N. Mole Weight: 206.11. Catalog: APB149463650.
Tirofiban Impurity C
One of the impurities of Tirofiban, which has been found to be a glycoprotein IIb/IIIa inhibitor and could be used as an antiplatelet agent. Synonyms: N-(n-Butanesulfonyl)-O-[4-(4-pyridinyl)-butyl]-(S)-tyrosine; 2-(Butane-1-sulfonylamino)-3-[4-(4-pyridin-4-yl-butoxy)-phenyl]-popionic Acid. CAS No. 149490-61-9. Molecular formula: C22H30N2O5S. Mole weight: 434.56.
Tirofiban Impurity DiHCl
One of the impurities of Tirofiban, which has been found to be a glycoprotein IIb/IIIa inhibitor and could be used as an antiplatelet agent. Synonyms: 4,4'-Dipyridyl-1,5-Pentane DiHCl. Molecular formula: C15H18N2. 2 HCl. Mole weight: 299.24.
Tiron
Tiron. CAS No. 149-45-1.
Pennsylvania PA
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. Group: Signaling pathways. CAS No. 149-45-1. Pack Sizes: 10 mM * 1 mL; 10 g; 25 g. Product ID: HY-D0261.
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
Tiropramide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Tiropramide;N-[1-[4-(2-diethylaminoethyloxy)benzyl]-2-(dipropylamino)-2-keto-ethyl]benzamide;N-[3-[4-(2-diethylaminoethyloxy)phenyl]-1-(dipropylamino)-1-oxo-propan-2-yl]benzamide;N-[3-[4-(2-diethylaminoethyloxy)phenyl]-1-(dipropylamino)-1-oxopropan-2-yl]. Product Category: Heterocyclic Organic Compound. CAS No. 55837-29-1. Molecular formula: C28H41N3O3. Mole weight: 467.65. Product ID: ACM55837291. Alfa Chemistry ISO 9001:2015 Certified.
Tiropramide Hydrochloride
Tiropramide, a benzoylamino derivative, has been found to be an antispasmodic agent. Synonyms: (±)-α-(Benzoylamino)-4-[2-(diethylamino)ethoxy]-N,N-dipropylbenzenepropanamide Hydrochloride. CAS No. 53567-47-8. Molecular formula: C28H41N3O3. Mole weight: 467.66.
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
Tiropramide Impurity A
One of the impurities of Tiropramide whici has been found to be an antispasmodic agent. Synonyms: N,O-Dibenzoyl-L-tyrosine; N-Benzoyl-L-Tyrosine Benzoate (Ester); L-N-Benzoyltyrosine Benzoate (Ester). CAS No. 14325-35-0. Molecular formula: C23H19NO5. Mole weight: 389.41.
Tiropramide Impurity B
One of the impurities of Tiropramide whici has been found to be an antispasmodic agent. Synonyms: N,O-Dibenzoyl-DL-tyrosyl-N',N'-dipropylamide; α-(Benzoylamino)-4-(benzoyloxy)-N,N-dipropylbenzenepropanamide; (±)-α-(Benzoylamino)-4-(benzoyloxy)-N,N-dipropylbenzenepropanamide. CAS No. 57227-08-4. Molecular formula: C29H32N2O4. Mole weight: 472.59.
Tiropramide Impurity C
One of the impurities of Tiropramide whici has been found to be an antispasmodic agent. Synonyms: N-Benzoyl-DL-tyrosyl-N',N'-dipropylamide; (±)-α-(Benzoylamino)-4-hydroxy-N,N-dipropylbenzenepropanamide. CAS No. 57227-09-5. Molecular formula: C22H28N2O3. Mole weight: 368.48.
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 is a dual GIP and GLP-1 receptor agonist and a drug candidate for the treatment of type 2 diabetes. Synonyms: LY3298176; Tyr-Aib-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Ile-Aib-Leu-Asp-Lys-Ile-Ala-Gln-Lys-diacid-gamma-Glu-(AEEA)2-Lys-Ala-Phe-Val-Gln-Trp-Leu-Ile-Ala-Gly-Gly-Pro-Ser-Ser-Gly-Ala-Pro-Pro-Pro-Ser-NH2; GIP\GLP-1. Grades: ≥95%. CAS No. 2023788-19-2. Molecular formula: C225H348N48O68. Mole weight: 4813.45.
Tirzepatide
Tirzepatide Inhibitor. Uses: Scientific use. Product Category: TP1111L. CAS No.:
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-alanylglycylglycyl-L-prolyl-L-seryl-L-serylglycyl-L-alanyl-L-prolyl-L-prolyl-L-prolyl-L-serinamide acetate salt; LY 3298176 acetate salt; LY3298176 acetate salt; Tyr-Aib-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Ile-Aib-Leu-Asp-Lys-Ile-Ala-Gln-Lys-diacid-gamma-Glu-(AEEA)2-Lys-Ala-Phe-Val-Gln-Trp-Leu-Ile-Ala-Gly-Gly-Pro-Ser-Ser-Gly-Ala-Pro-Pro-Pro-Ser-NH2 acetate salt. Molecular formula: C227H352N48O70. Mole weight: 4873.58.
tislelizumab
Tislelizumab is a humanized monoclonal antibody (MAb) that targets PD-1 to prevent it binding to PD-L1 and PD-L2. Tislelizumab is developed for the treatment of solid tumor. Uses: Potential treatment of solid tumor. Synonyms: BGB-A317; BGB A317; BGBA317. CAS No. 1858168-59-8.
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. Group: Inhibitory antibodies. CAS No. 1858168-59-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99052.
Tisolagiline
Tisolagiline (KDS2010) is a reversible MAO-B inhibitor used in Parkinson's disease research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: KDS2010. CAS No. 1894207-44-3. Pack Sizes: 10 mM * 1 mL; 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 for the research of solid tumors [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Anti-Human F3 Recombinant Antibody. CAS No. 1418628-81-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99271.
Tisotumab vedotin
Tisotumab vedotin is an antibody drug conjugate (ADC) targeting tissue factor (TF), formed by covalently linking a fully human monoclonal antibody (TF-011) against TF with the microtubule disruptor Monomethyll Auristatin E (MMAE) (HY-15162). Tisotumab vedotin has immunomodulatory and anti-tumor activities, and can be used in the study of advanced or metastatic solid tumors such as cervical cancer [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1418731-10-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-152963.
Tissue, Acetone Powder, Bovine Brain HisTek
Tissue, Acetone Powder, Bovine Brain HisTek. Group: Biologicals. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
Tissue, Acetone Powder, Bovine Heart HisTek
Tissue, Acetone Powder, Bovine Heart HisTek. Group: Biologicals. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
Tissue, Acetone Powder, Chicken Liver HisTek
Tissue, Acetone Powder, Chicken Liver HisTek. Group: Biologicals. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
Tissue, Acetone Powder, Horseradish HisTek
Tissue, Acetone Powder, Horseradish HisTek. Group: Biologicals. Pack Sizes: 1g. US Biological Life Sciences.