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| Product | Description | |
|---|---|---|
| Tryptophanase (Crude Enzyme) | This enzyme belongs to the family of lyases, specifically in the "catch-all" class of carbon-carbon lyases. This enzyme participates in tryptophan metabolism and nitrogen metabolism. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Drug development; food industry; medicine; synthesis; biotechnology. Group: Enzymes. Synonyms: L-tryptophanase; L-tryptophan indole-lyase (deaminating); TNase. Enzyme Commission Number: EC 4.1.99.1. CAS No. 9024-00-4. TNase. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. L-tryptophanase; L-tryptophan indole-lyase (deaminating); TNase. Pack: 100ml. Cat No: NATE-1851. |  |
| Tryptophan-cholic acid | Tryptophan-cholic acid (Trp-CA) is a microbial amino acid-conjugated bile acid that acts as an endogenous ligand and agonist (EC50=9.6 μM) for the orphan G protein-coupled receptor (GPCR) MRGPRE (Mas-related G protein-coupled receptor family member E). Tryptophan-cholic acid is orally effective but has poor oral absorption and does not cross the blood-brain barrier. Tryptophan-cholic acid promotes the secretion of glucagon-like peptide GLP-1, thereby improving glucose tolerance in diabetic mice. Tryptophan-cholic acid improves glucose tolerance, promotes insulin secretion, and alleviates high-fat diet-induced hepatic steatosis without causing pruritus side effects. Tryptophan-cholic acid is primarily used in research on type 2 diabetes (T2D)[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Trp-CA. CAS No. 1630745-39-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N15721. |  |
| tryptophan dehydrogenase | Activated by Ca2+. Group: Enzymes. Synonyms: NAD(P)+-L-tryptophan dehydrogenase; L-tryptophan dehydrogenase; L-Trp-dehydrogenase; TDH. Enzyme Commission Number: EC 1.4.1.19. CAS No. 94047-13-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1452; tryptophan dehydrogenase; EC 1.4.1.19; 94047-13-9; NAD(P)+-L-tryptophan dehydrogenase; L-tryptophan dehydrogenase; L-Trp-dehydrogenase; TDH. Cat No: EXWM-1452. | |
| Tryptophan EP Impurity A (Tadalafil Impurity 50) | Tryptophan EP Impurity A (Tadalafil Impurity 50). Uses: For analytical and research use. CAS No. 132685-02-0. Molecular formula: C24H26N4O4. Mole weight: 434.5. Catalog: APB132685020. |  |
| Tryptophan EP Impurity B | Tryptophan EP Impurity B. Uses: For analytical and research use. CAS No. 184955-21-3. Molecular formula: C11H12N2O4. Mole weight: 236.23. Catalog: APB184955213. | |
| Tryptophan EP Impurity C | Tryptophan EP Impurity C. Uses: For analytical and research use. CAS No. 2922-83-0. Molecular formula: C10H12N2O3. Mole weight: 208.22. Catalog: APB2922830. | |
| Tryptophan EP Impurity D | Tryptophan EP Impurity D. Uses: For analytical and research use. CAS No. 4350-9-8. Molecular formula: C11H12N2O3. Mole weight: 220.23. Catalog: APB4350098. | |
| Tryptophan EP Impurity E | Tryptophan EP Impurity E. Uses: For analytical and research use. CAS No. 3978-11-8. Molecular formula: C11H12N2O4. Mole weight: 236.23. Catalog: APB3978118. | |
| Tryptophan EP Impurity F | Tryptophan EP Impurity F. Uses: For analytical and research use. CAS No. 145545-23-9. Molecular formula: C9H12N2O2. Mole weight: 180.21. Catalog: APB145545239. | |
| Tryptophan EP Impurity G | Tryptophan EP Impurity G. Uses: For analytical and research use. CAS No. 21704-80-3. Molecular formula: C11H12N2O3. Mole weight: 220.23. Catalog: APB21704803. | |
| Tryptophan EP Impurity H | Tryptophan EP Impurity H. Uses: For analytical and research use. CAS No. 6052-68-2. Molecular formula: C12H12N2O2. Mole weight: 216.24. Catalog: APB6052682. | |
| Tryptophan EP Impurity I | Tryptophan EP Impurity I. Uses: For analytical and research use. CAS No. 5470-37-1. Molecular formula: C13H14N2O2. Mole weight: 230.27. Catalog: APB5470371. | |
| Tryptophan EP Impurity J | Tryptophan EP Impurity J. Uses: For analytical and research use. CAS No. 164068-19-3. Molecular formula: C22H23N3O4. Mole weight: 393.44. Catalog: APB164068193. | |
| Tryptophan EP Impurity K | Tryptophan EP Impurity K. Uses: For analytical and research use. CAS No. 149724-31-2. Molecular formula: C20H19N3O2. Mole weight: 333.39. Catalog: APB149724312. | |
| Tryptophan EP Impurity L | Tryptophan EP Impurity L. Uses: For analytical and research use. CAS No. 287170-99-4. Molecular formula: C21H19N3O2. Mole weight: 345.4. Catalog: APB287170994. | |
| Tryptophan Feed Grade | Tryptophan Feed Grade. Group: Food ingredients. Pack Sizes: 10Kgs Bags. |  |
| Tryptophan Impurity 1 | Tryptophan Impurity 1. Uses: For analytical and research use. CAS No. 29702-35-0. Molecular formula: C16H20N2O2. Mole weight: 272.35. Catalog: APB29702350. | |
| Tryptophan Impurity 10 | Tryptophan Impurity 10. Uses: For analytical and research use. CAS No. 881025-90-7. Molecular formula: C11H13ClN2O3. Mole weight: 256.69. Catalog: APB881025907. | |
| Tryptophan Impurity 11 | Tryptophan Impurity 11. Uses: For analytical and research use. CAS No. 68807-89-6. Molecular formula: C11H11N3O3. Mole weight: 233.23. Catalog: APB68807896. | |
| Tryptophan Impurity 12 | Tryptophan Impurity 12. Uses: For analytical and research use. Molecular formula: C12H10N4O3. Mole weight: 258.24. Catalog: APB09910. | |
| Tryptophan Impurity 13 | Tryptophan Impurity 13. Uses: For analytical and research use. Molecular formula: C26H30N4O4. Mole weight: 462.55. Catalog: APB09911. | |
| Tryptophan Impurity 14 | Tryptophan Impurity 14. Uses: For analytical and research use. CAS No. 40856-80-2. Molecular formula: C12H11N3O2. Mole weight: 229.24. Catalog: APB40856802. | |
| Tryptophan Impurity 2 | Tryptophan Impurity 2. Uses: For analytical and research use. CAS No. 75917-16-7. Molecular formula: C17H22N2O2. Mole weight: 286.38. Catalog: APB75917167. | |
| Tryptophan Impurity 3 | Tryptophan Impurity 3. Uses: For analytical and research use. Molecular formula: C17H20N2O2. Mole weight: 284.36. Catalog: APB09909. | |
| Tryptophan Impurity 4 | Tryptophan Impurity 4. Uses: For analytical and research use. CAS No. 2390-99-0. Molecular formula: C16H20N2O. Mole weight: 256.35. Catalog: APB2390990. | |
| Tryptophan Impurity 5 | Tryptophan Impurity 5. Uses: For analytical and research use. CAS No. 25800-42-4. Molecular formula: C16H18N2O. Mole weight: 254.33. Catalog: APB25800424. | |
| Tryptophan Impurity 6 | Tryptophan Impurity 6. Uses: For analytical and research use. CAS No. 548-42-5. Molecular formula: C16H18N2. Mole weight: 238.33. Catalog: APB548425. | |
| Tryptophan Impurity 7 | Tryptophan Impurity 7. Uses: For analytical and research use. CAS No. 548-43-6. Molecular formula: C16H18N2O. Mole weight: 254.33. Catalog: APB548436. | |
| Tryptophan Impurity 9 | Tryptophan Impurity 9. Uses: For analytical and research use. CAS No. 36060-94-3. Molecular formula: C14H16N2O3. Mole weight: 260.29. Catalog: APB36060943. | |
| tryptophan N-monooxygenase | A heme-thiolate protein (P-450). This enzyme catalyses two successive N-hydroxylations of L-tryptophan, the first steps in the biosynthesis of both auxin and the indole alkaloid phytoalexin camalexin. The product of the two hydroxylations, N,N-dihydroxy-L-tryptophan, is extremely labile and dehydrates spontaneously. The dehydrated product is then subject to a decarboxylation that produces an oxime. It is still not known whether the decarboxylation is spontaneous or catalysed by the enzyme. Group: Enzymes. Synonyms: tryptophan N-hydroxylase; CYP79B1; CYP79B2; CYP79B3. Enzyme Commission Number: EC 1.14.13.125. 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-0726; tryptophan N-monooxygenase; EC 1.14.13.125; tryptophan N-hydroxylase; CYP79B1; CYP79B2; CYP79B3. Cat No: EXWM-0726. | |
| tryptophan-phenylpyruvate transaminase | Valine, leucine and isoleucine can replace tryptophan as amino donor. Group: Enzymes. Synonyms: L-tryptophan-α-ketoisocaproate aminotransferase. Enzyme Commission Number: EC 2.6.1.28. CAS No. 37277-87-5. 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-2867; tryptophan-phenylpyruvate transaminase; EC 2.6.1.28; 37277-87-5; L-tryptophan-α-ketoisocaproate aminotransferase. Cat No: EXWM-2867. | |
| Tryptophan Related Compound A | Tryptophan Related Compound A. Uses: For analytical and research use. CAS No. 132685-02-0. Mole weight: 434.49. Catalog: AP132685020. | |
| Tryptophan Related Compound B | Tryptophan Related Compound B. Uses: For analytical and research use. CAS No. 1218-34-4. Mole weight: 246.26. EC Number: 214-935-9. Catalog: AP1218344. | |
| tryptophan synthase | A pyridoxal-phosphate protein. The α-subunit catalyses the conversion of 1-C-(indol-3-yl)glycerol 3-phosphate to indole and D-glyceraldehyde 3-phosphate (this reaction was included formerly under EC 4.1.2.8). The indole migrates to the β-subunit where, in the presence of pyridoxal 5'-phosphate, it is combined with L-serine to form L-tryptophan. In some organisms this enzyme is part of a multifunctional protein that also includes one or more of the enzymes EC 2.4.2.18 (anthranilate phosphoribosyltransferase), EC 4.1.1.48 (indole-3-glycerol-phosphate synthase), EC 4.1.3.27 (anthranilate synthase) and EC 5.3.1.24 (phosphoribosylanthranilate isomerase). In thermophilic organ.indoleglycerol-phosphate); L-serine hydro-lyase [adding 1-C-(indol-3-yl)glycerol 3-phosphate, L-tryptophan and glyceraldehyde-3-phosphate-forming]. Enzyme Commission Number: EC 4.2.1.20. CAS No. 9014-52-2. 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-5014; tryptophan synthase; EC 4.2.1.20; 9014-52-2; L-tryptophan synthetase; indoleglycerol phosphate aldolase; tryptophan desmolase; tryptophan synthetase; L-serine hydro-lyase (adding indoleglycerol-phosphate); L-serine hydro-lyase [adding 1-C-(indol-3-yl)glycerol 3-phosphate, L-tryptophan and glyceraldehyde-3-phosphate-forming]. Cat No: EXWM-5014. | |
| tryptophan synthase (indole-salvaging) | Most mesophilic bacteria have a multimeric tryptophan synthase complex (EC 4.2.1.20) that forms L-tryptophan from L-serine and 1-C-(indol-3-yl)glycerol 3-phosphate via an indole intermediate. This intermediate, which is formed by the α subunits, is transferred in an internal tunnel to the β units, which convert it to tryptophan. In thermophilic organisms the high temperature enhances diffusion and causes the loss of indole. This enzyme, which does not combine with the α unit to form a complex, salvages the lost indole back to L-tryptophan. It has a much lower Km for indole than the β subunit of EC 4.2.1.20. Group: Enzymes. Synonyms: tryptophan synthase β2. Enzyme Commission Number: EC 4.2.1.122. 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-4963; tryptophan synthase (indole-salvaging); EC 4.2.1.122; tryptophan synthase β2. Cat No: EXWM-4963. | |
| tryptophan transaminase | A pyridoxal-phosphate protein. Also acts on 5-hydroxytryptophan and, to a lesser extent, on the phenyl amino acids. Group: Enzymes. Synonyms: L-phenylalanine-2-oxoglutarate aminotransferase; tryptophan aminotransferase; 5-hydroxytryptophan-ketoglutaric transaminase; hydroxytryptophan aminotransferase; L-tryptophan aminotransferase; L-tryptophan transaminase. Enzyme Commission Number: EC 2.6.1.27. CAS No. 9022-98-4. 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-2866; tryptophan transaminase; EC 2.6.1.27; 9022-98-4; L-phenylalanine-2-oxoglutarate aminotransferase; tryptophan aminotransferase; 5-hydroxytryptophan-ketoglutaric transaminase; hydroxytryptophan aminotransferase; L-tryptophan aminotransferase; L-tryptophan transaminase. Cat No: EXWM-2866. | |
| tryptophan-tRNA ligase | This enzyme belongs to the family of ligases, to be specific those forming carbon-oxygen bonds in aminoacyl-tRNA and related compounds. This enzyme participates in tryptophan metabolism and aminoacyl-trna biosynthesis. Group: Enzymes. Synonyms: tryptophanyl-tRNA synthetase; L-tryptophan-tRNATrp ligase (AMP-forming); tryptophanyl-transfer ribonucleate synthetase; tryptophanyl-transfer ribonucleic acid synthetase; tryptophanyl-transfer RNA synthetase; tryptophanyl ribonucleic synthetase; tryptophanyl-transfer ribonucleic synthetase; tryptophanyl-tRNA synthase; tryptophan translase; TrpRS. Enzyme Commission Number: EC 6.1.1.2. CAS No. 9023-44-3. 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-5651; tryptophan-tRNA ligase; EC 6.1.1.2; 9023-44-3; tryptophanyl-tRNA synthetase; L-tryptophan-tRNATrp ligase (AMP-forming); tryptophanyl-transfer ribonucleate synthetase; tryptophanyl-transfer ribonucleic acid synthetase; tryptophanyl-transfer RNA synthetase; tryptophanyl ribonucleic synthetase; tryptophanyl-transfer ribonucleic synthetase; tryptophanyl-tRNA synthase; tryptophan translase; TrpRS. Cat No: EXWM-5651. | |
| tryptophanyl aminopeptidase | From Trichosporon cutaneum. Also acts on L-tryptophanamide. Requires Mn2+. Group: Enzymes. Synonyms: tryptophan aminopeptidase; L-tryptophan aminopeptidase. Enzyme Commission Number: EC 3.4.11.17. CAS No. 76689-19-5. 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-4013; tryptophanyl aminopeptidase; EC 3.4.11.17; 76689-19-5; tryptophan aminopeptidase; L-tryptophan aminopeptidase. Cat No: EXWM-4013. | |
| Tryptophanyl-phenylalanine | Tryptophanyl-phenylalanine is a dipeptide composed of tryptophan and phenylalanine. It is an incomplete breakdown product of protein digestion or protein catabolism. Alternative Names: H-WF-OH; L-tryptophyl-L-phenylalanine; Trp-Phe; (S)-2-((S)-2-Amino-3-(1H-indol-3-yl)propanamido)-3-phenylpropanoic acid; L-Phenylalanine, L-tryptophyl-; L-Trp-L-Phe; L-Trp-L-Phe-OH. Grades: ≥95%. CAS No. 6686-2-8. Molecular formula: C20H21N3O3. Mole weight: 351.40. |  |
| Tryptophol | Tryptophol. Group: Biochemicals. Alternative Names: 3-(2-hydroxyethyl)indole, indole-3-ethanol. Grades: Highly Purified. CAS No. 526-55-6. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C10H11NO. US Biological Life Sciences. |  Worldwide |
| Tryptophol | Tryptophol is an aromatic alcohol and secondary metabolite produced by microorganisms. Tryptophol induces apoptosis and cleavage of caspase-8. Tryptophol inhibits Cunninghamella blakesleeana biofilm. Tryptophol has anti-phage infection, biofilm formation regulation, anti-inflammatory, hemolytic, sleep induction, temperature change, seizure susceptibility and immune regulation activities. Tryptophol is used in the research of African trypanosomiasis, sleep disorders, epilepsy[1][2][3][4][5][6][7][8][9][10][11][12]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Indole-3-ethanol. CAS No. 526-55-6. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg. Product ID: HY-W010155. | |
| Tryptophol (Standard) | Tryptophol (Standard) (Indole-3-ethanol (Standard)) is an analytical standard of Tryptophol (HY-W010155). This product is intended for use in research and analytical applications.Tryptophol is an aromatic alcohol and secondary metabolite produced by microorganisms. Tryptophol induces Apoptosis and cleavage of caspase-8. Tryptophol inhibits Cunninghamella blakesleeana biofilm. Tryptophol has anti-phage infection, biofilm formation regulation, anti-inflammatory, hemolytic, sleep induction, temperature change, seizure susceptibility and immune regulation activities. Tryptophol is used in the research of African trypanosomiasis, sleep disorders, epilepsy. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Indole-3-ethanol (Standard). CAS No. 526-55-6. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W010155R. | |
| TRYPTOSE,BR | TRYPTOSE,BR. CAS No. 84843-69-6. | |
| TS-002266 | TS-002266 is a small molecule TUT4/7 inhibitor with anti-leukemic effects. TS-002266 is promising for research of cancers[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2702325-64-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-169091. | |
| TS 155-2 | A macrocyclic lactone related to hygrolidin but produced by a different streptomyces species. TS155-2 is an inhibitor of calcium entry into the cell induced by thrombin stimulation. It has antihypertensive, antiplatelet, antiischemia and anti-inflammatory activities. Alternative Names: Antibiotic TS 155-2; 2E-butenedioic acid-1-[(2R,4R,5S,6R)-tetrahydro-2-hydroxy-2-[(1S,2R,3S)-2-hydroxy-3-[(2R,3S,4E,6E,9S,10S,11R,12E,14E)-10-hydroxy-3-methoxy-7,9,11,13,15-pentamethyl-16-oxooxacyclohexadeca-4,6,12,14-tetraen-2-yl]-1-methylbutyl]-5-methyl-6-(1-methylethyl)-2H-pyran-4-yl] ester; JBIR 100. Grades: >95% by HPLC. CAS No. 303009-07-6. Molecular formula: C39H60O11. Mole weight: 704.89. | |
| TSA- 1003 | TSA- 1003. |  |
| TsAP-1 | TsAP-1 is a scorpion venom peptide isolated from the venom of the Brazilian yellow scorpion, Tityus serrulatus. It has broad-spectrum antibacterial and anti-cancer activity, and its effectiveness can be significantly enhanced by increasing its cationicity. Alternative Names: Phe-Leu-Ser-Leu-Ile-Pro-Ser-Leu-Val-Gly-Gly-Ser-Ile-Ser-Ala-Phe-Lys. Molecular formula: C83H134N18O22. Mole weight: 1736.09. | |
| TSE-424) | TSE-424) Inhibitor. Uses: Scientific use. Product Category: T2544. CAS No. 198481-33-3. |  |
| TseF I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 65°C in a total reaction volume of 50 μl. Applications: After 10-fold overdigestion with enzyme more than 95% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 200U; 1000U. ↑GTSAC CASTG&darr. Activity: 5000u.a./ml. Appearance: 10 X SE-buffer B. Storage: -20°C. Form: Liquid. Source: An E.coli strain, that carries the cloned gene TseFI from Thermus species F35. Pack: 10 mM Tris-HCl (pH 7.6); 50 mM NaCl; 0,1 mM EDTA; 1 mM DTT; 200 μg/ml BSA; 50% glycerol. Cat No: ET-1184RE. | |
| T-Select H-2Ld P815 (66-74) | T-Select H-2Ld P815 (66-74). Alternative Names: V-erb-b2 avian erythroblastic leukemia viral oncoprotein 2 isoform C (66-74). | |
| TSG101 Antibody [B19D18] | tsg 101,TSG101. Group: Antibodies. Alternative Names: Tumor susceptibility gene 101 protein, ESCRT-I complex subunit TSG101. CAS No. Pack Sizes: 20uL. Product ID: F1543. Storage Conditions: -20°C (avoid freeze-thaw cycles), 2 years. |  United States; Europe |
| T-(S)-GNA phosphoramidite | T-(S)-GNA phosphoramidite is a crucial building block in the synthesis of oligonucleotides used to treat various diseases such as cancer, viral infections, and genetic disorders. It is used to specifically modify the nucleotides of the oligonucleotide, enhancing its therapeutic potential and specificity. By utilizing this product, researchers can improve the efficacy and selectivity of their oligonucleotide-based therapies. Alternative Names: (S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-3-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)propan-2-yl (2-cyanoethyl) diisopropylphosphoramidite; 1-[(S)-2-[[(Diisopropylamino)(2-cyanoethoxy)phosphino]oxy]-3-[(4,4'-dimethoxytrityl)oxy]propyl]thymine. Grades: ≥98%. CAS No. 168332-13-6. Molecular formula: C38H47N4O7P. Mole weight: 702.78. | |
| TSHR antagonist S37a | TSHR antagonist S37a is a highly selective thyrotropin receptor (TSHR) antagonist, with potential for the treatment of Graves' orbitopathy[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2143452-20-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-129995A. | |
| TSI-01 | TSI-01 is a pro-inflammatory phospholipid mediator that is rapidly synthesized by lyso-PAF acetyltransferase (lyso-PAFAT) in response to extracellular stimuli. Two types of lyso-PAFAT have been identified: lysophosphatidylcholine acyltransferase (LPCAT)1, which is mostly expressed in the lungs, and LPCAT2, which is expressed in inflammatory cells. TSI-01 is a selective inhibitor of LPCAT2 (IC50s=0.47 versus 3.02 μM for human LPCAT2 and LPCAT1, respectively). 60 μM it is shown to suppress PAF biosynthesis in mouse peritoneal macrophages stimulated with a calcium ionophore. Uses: Scientific research. Category: Signaling pathways. CAS No. 704878-75-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112825. | |
| TSLP-IN-1 | TSLP-IN-1 is a potent thymic stromal lymphopoietin (TSLP) inhibitor. TSLP-IN-1 disrupts TSLP-TSLPR protein-protein interaction, and downregulates IL-4 and IL-13. TSLP-IN-1 can be used for the research of inflammation diseases, such as skin disease, asthma, and allergies[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 512837-95-5. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-207120. | |
| TSPO1 | TSPO1 is an electon transfer layer (ETL) or hole blocking layer (HBL) in OLED devices. Alternative Names: Diphenyl[4-(triphenylsilyl)phenyl]phosphineoxide. CAS No. 1286708-86-8. Molecular formula: C36H29OPSi. Mole weight: 536.67. Purity: 95%+. IUPAC Name: (4-diphenylphosphorylphenyl)-triphenylsilane. SMILES: C1=CC=C(C=C1)[Si](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=C(C=C4)P(=O)(C5=CC=CC=C5)C6=CC=CC=C6. InChI: InChI=1S/C36H29OPSi/c37-38(30-16-6-1-7-17-30,31-18-8-2-9-19-31)32-26-28-36(29-27-32)39(33-20-10-3-11-21-33,34-22-12-4-13-23-34)35-24-14-5-15-25-35/h1-29H. | |
| TSQ | TSQ is a cytosolic zinc ion fluorescence probe that is membrane permeable and can be used for intracellular imaging of zinc proteins (λmax ~470 nm). TSQ can combine with Zn2+ in the presence of Ca2+ and Mg2+ to produce blue fluorescence (Ex/Em = 334/495 nm)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 109628-27-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-119287. | |
| TSTU | TSTU is a peptide coupling reagent converts carboxylates to N-succinimidyl active esters. Uses: Peptide Synthesis. Group: Coupling Reagents. Alternative Names: N,N,N?,N?-Tetramethyl-O-(N-succinimidyl)uronium tetrafluoroborate. CAS No. 105832-38-0. |  Luxembourg Bio Technologies |
| TSTU | TSTU. Group: Biochemicals. Alternative Names: N,N,N',N'-Tetramethyl-O-(N-succinimidyl)uronium tetrafluoroborate; O-(N-Succinimidyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate. Grades: Highly Purified. CAS No. 105832-38-0. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C9H16BF4N3O3. US Biological Life Sciences. | Worldwide |
| Tsugaric acid A | Tsugaric acid A. Group: Biochemicals. Grades: Plant Grade. CAS No. 174391-64-1. Pack Sizes: 10mg. Molecular Formula: C32H50O4, Molecular Weight: 498.74. US Biological Life Sciences. | Worldwide |
| TT-012 | TT-012 is a MITF inhibitor with a human MITF C50 of 13.1 nM and a human MITF Kd value of 15.5 nM. TT-012 reduces mRNA levels of MITF downstream genes linked to melanosome biogenesis, cell survival, and proliferation, and upregulates cell cycle-inhibiting genes. TT-012 can be used for the research of melanoma[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1164471-33-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-156483. | |
| TT-10 | TT-10 (TAZ-K) is an activator of YES-associated protein (YAP)-transcriptional enhancer factor domain (TEAD) activity. TT-10 can be used for the research of heart diseases accompanied by cardiomyocyte loss[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: TAZ-K. CAS No. 2230640-94-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-125016. | |
| TT 232 | TT 232. Group: Biochemicals. Grades: Purified. CAS No. 147159-51-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| TT-232 | TT 232 is a somatostatin analog that acts as a peptide agonist for sst1/sst4 somatostatin receptors. TT 232 inhibits tyrosine kinase activity in human colon tumor cell lines. TT 232 was shown to suppress proliferation and induce apoptosis in a pancreatic tumor cell line. Alternative Names: TT2-32; TT2 32; TT232; TT-232; TT 232; CAP 232; CAP-232; CAP232. CAS No. 147159-51-1. Molecular formula: C45H58N10O9S2. Mole weight: 947.13. | |
| TT-232 TFA | TT-232 TFA is a somatostatin analog that acts as a peptide agonist for sst1/sst4 somatostatin receptors. TT-232 TFA inhibits tyrosine kinase activity in human colon tumor cell lines. TT-232 TFA was shown to suppress proliferation and induce apoptosis in a pancreatic tumor cell line. Alternative Names: H-D-Phe-Cys-Tyr-D-Trp-Lys-Cys-Thr-NH2.TFA (Disulfide bridge: Cys2-Cys6); D-phenylalanyl-L-cysteinyl-L-tyrosyl-D-tryptophyl-L-lysyl-L-cysteinyl-L-threoninamide (2->6)-disulfide trifluoroacetic acid; CAP 232 TFA; TLN 232 TFA; TT 2-32 TFA. Grades: ≥95%. CAS No. 2703745-48-4. Molecular formula: C45H58N10O9S2.C2HF3O2. Mole weight: 1061.16. | |
| TT3 | TT3 is an ionizable lipid-like material and a lipid nanoparticle (LLNs)-based mRNA delivery vector. TT3 exhibits liver and spleen specificity and excellent delivery efficiency[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1821214-50-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148049. | |
| TTA-A2 | TTA-A2 is a potent, selective and orally active t-type voltage gated calcium channel antagonist with reduced pregnane X receptor (PXR) activation. TTA-A2 is equally potent against the Cav3.1 (a1G) and Cav3.2 (a1H) channels with IC50 values of 89 nM and 92 nM, respectively, at -80 and -100 mV holding potentials. TTA-A2 can be used for the research of a variety of human neurological diseases, including sleep disorders and epilepsy[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 953778-63-7. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111828. | |
| TTA-P2 | TTA-P2 (T-Type calcium channel inhibitor) is a selective, orally active, and BBB-penetrant T-type calcium channel blocker (IC50 = 22 nM). TTA-P2 reduces mechanical hypersensitivity and alleviates acute as well as chronic pain. TTA-P2 significantly reduces firing rates in temporal lobe epilepsy (TLE) neurons to control levels and suppresses synaptically evoked burst firing. TTA-P2 can be studied in research for neurological diseases such as tremor and absence epilepsy[1][2][3]< sup>[4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: T-Type calcium channel inhibitor. CAS No. 1072018-68-8. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-10035. | |
| TTBK1-IN-2 | TTBK1-IN-2 (compound 29) is a potent Tau-Tubulin kinase (TTBK1) inhibitor with IC50s of 0.24 and 4.22 μM, respectively. TTBK1-IN-2 reveals good brain penetration in vivo and is able to reduce TDP-43 phosphorylation not only in cell cultures but also in the spinal cord of transgenic TDP-43 mice[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2765453-51-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145313. | |
| TTCP | TTCP. Alternative Names: Tetracalcium diphosphorus nonaoxide. CAS No. 1306-01-0. Purity: 95+%. Product ID: ACM1306010-3. Molecular formula: Ca4H6O9P2-16. Mole weight: 372.3. Alfa Chemistry - ISO 9001:32057 Certified. |  |
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