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| Product | Description | |
|---|---|---|
| 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. Synonyms: 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. Grade: ≥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. | |
| 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. Synonyms: 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. Grade: >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. Synonyms: 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). Synonyms: 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 |
| 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 |
| TSU-68 | TSU-68 is a inhibitor that targets vascular endothelial growth factor receptor 2, platelet-derived growth factor receptor β, and fibroblast growth factor receptor 1. The inhibitory effects of TSU-68 towards these growth factors lead to substantial antitumor activity and showed potential in its development in therapeutic uses. Group: Biochemicals. Alternative Names: (Z)-3-(2,4-dimethyl-5-((2-oxoindolin-3-ylidene)methyl)-1H-pyrrol-3-yl)propanoic Acid; 3-[2,4-Dimethyl-5-[(2-oxo-1,2-dihydro-3H-indol-3-ylidene)methyl]-1H-pyrrol-3-yl]propionic Acid; 3-[4-(2-Carboxyethyl)-3,5-dimethylpyrrol-2-methylidenyl]-2-indolinone; 5-[(1,2-Dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-propanoic acid; NSC 702827; Orantinib; SU 6668. Grades: Highly Purified. CAS No. 252916-29-3. Pack Sizes: 10mg. 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. Synonyms: 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. Synonyms: 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. Grade: ≥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. |  |
| Tth111 I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA (HindIII-digest) in 1 hour at 65°C in a total reaction volume of 50 μl. Applications: After 2-fold overdigestion with enzyme 10% of the dna fragments can be ligated. Group: Restriction Enzymes. Purity: 400U; 2000U. GACN↑NNGTC CTGNN↓NCAG. Activity: 5000u.a./ml. Appearance: 10 X SE-buffer Y. Storage: -20°C. Form: Liquid. Source: An E.coli strain, that carries the cloned gene Tth111I from Thermus Thermophilus 111. Pack: 10 mM Tris-HCl (pH 7.5); 500 mM NaCl; 0,1 mM EDTA; 1 mM DTT; 50% glycerol. Cat No: ET-1185RE. | |
| TTK21 | TTK21 is an activator of the histone acetyltransferases CBP/p300. TTK21 passes the blood-brain barrier, induces no toxicity, and reaches different parts of the brain when conjugated to glucose-based carbon nanosphere (CSP). TTK21 has beneficial implications for the brain functions of neurogenesis and long-term memory[1].CSP-TTK21 can ameliorate Aβ-impaired long-term potentiation (LTP). CSP-TTK21 may enhance the transcription of genes that promote synaptic health and cognitive function[2]. CSP-TTK21 is orally effective and leads to improvements in motor functions, histone acetylation dynamics in a spinal injury rat model[3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 709676-56-2. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-116673. | |
| TTMPP | TTMPP. Group: Biochemicals. Grades: Highly Purified. CAS No. 91608-15-0. Pack Sizes: 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| TTNPB | TTNPB is a retinoic acid analog that selectively and potently activates the retinoic acid receptors. It is reported to increase the efficiency of induced pluripotent stem cell (iPSC) chemical reprogramming. Group: Biochemicals. Alternative Names: AGN-191183, Arotinoid acid, Arotinoic acid, Ro 13-7410; 4-[(E)-2-(5,5,8,8-tetramethyl-6,7-dihydronaphthalen-2-yl)prop-1-enyl]benzoic acid. Grades: Purified. CAS No. 71441-28-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TTNPB | TTNPB is a highly potent RAR agonist. Competitive binding assays using human RARs yield IC50s of α=5.1 nM, β= 4.5 nM, and γ=9.3 nM, respectively. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ro 13-7410; Arotinoid acid; AGN191183. CAS No. 71441-28-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15682. | |
| TTNPB (Arotinoid acid) | TTNPB is a potent RAR agonist, and inhibits binding of [3H]tRA with IC50 of 5.1 nM, 4.5 nM, and 9.3 nM for human RARα, β, and γ, respectively. Group: Inhibitors. Alternative Names: Arotinoid Acid, Ro 13-7410, AGN-191183. CAS No. 71441-28-6. Pack Sizes: 10mg. Product ID: S4627. Formula: C24H28O2. Smiles: CC(=CC1=CC=C(C=C1)C(=O)O)C2=CC3=C(C=C2)C(CCC3(C)C)(C)C. Storage Conditions: 2 years -80 in solvent. | United States; Europe |
| TTP 22 | TTP 22. Group: Biochemicals. Grades: Purified. CAS No. 329907-28-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TTP-6171 | TTP-6171 is a non-covalent inhibitor of Monkeypox virus I7L protease, and it can be used for research on poxvirus infections[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 825647-78-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-147036. | |
| TTRAP Control Peptide (TRAF and TNF Receptor Associated Protein) | TTRAP Control Peptide (TRAF and TNF Receptor Associated Protein). Group: Molecular Biology. Pack Sizes: 100ug. US Biological Life Sciences. | Worldwide |
| TTT-28 | TTT-28 is a synthesized thiazole-valine peptidomimetic, a novel selective inhibitor of ABCB1 (P-gp/MDR1) with high efficacy and low toxicity, which reverses the ATP-binding cassette sub-family B member 1 (ABCB1)-mediated multidrug resistance (MDR) by selectively blocking the efflux function of ABCB1[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1609138-51-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101511. | |
| TTX-030 | TTX-030 is a humanized antibody expressed in CHO cells, targeting ENTPD1/CD39. TTX-030 contains huIgG4SP heavy chain and huκ light chain, with a predicted molecular weight (MW) of 150 kDa. The isotype control for TTX-030 can refer to Human IgG4 kappa, Isotype Control (HY-P99003). Uses: Scientific research. Category: Inhibitory antibodies. Alternative Names: Eltivutabart. CAS No. 2935496-38-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990670. | |
| Tu-AMP 1 | Tu-AMP 1 is an antimicrobial peptide isolated from Tulipa gesneriana L. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Lys-Ser-Cys-Cys-Arg-Asn-Thr-Thr-Ala-Arg-Asn-Cys-Tyr-Asn-Val-Cys-Arg-Ile-Pro-Gly-Thr-Pro-Arg-Pro-Val-Cys-Ala-Ala-Thr-Cys-Asp-Cys-Lys-Leu-Ile-Thr-Gly-Thr-Lys-Cys-Pro-Pro-Gly-Tyr-Glu-Lys. | |
| Tu-AMP 2 | Tu-AMP 2 is an antimicrobial peptide isolated from Tulipa gesneriana L. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Lys-Ser-Cys-Cys-Arg-Asn-Thr-Thr-Ala-Arg-Asn-Cys-Tyr-Asn-Val-Cys-Arg-Ile-Pro-Gly. | |
| Tubacin | Tubacin (Tubulin acetylation inducer) is a highly potent, selective, reversible, and cell-permeable inhibitor of histone deacetylase 6 (HDAC6, IC50=4nm). Displays 1000-fold more selectivity for HDAC6 over other HDACs. It inhibits a-tubulin deacetylation in mammalian cells. Unlike trichostatin A (TSA), which is a broad spectrum HDAC inhibitor, tubacin is specific for the tubulin deacetylase activity of HDAC6. Tubacin causes increased acetylation of a-tubulin, accumulation of polyubiquitinated proteins, and apoptosis. It does not affect global histone deacetylation, gene-expression profiling, or cell cycle progression mediated a-tubulin deacetylation in mammalian cells. Group: Biochemicals. Alternative Names: (N-[4-[(2R,4R,6S)-4-[[(4,5-Diphenyl- 2-oxazolyl)thio]methyl]-6-[4-(hydroxymethyl)phenyl]-1,3- dioxan-2-yl]phenyl]-N'-hydroxyoctanediamide). Grades: Highly Purified. CAS No. 537049-40-4. Pack Sizes: 500ug, 1mg, 2.5mg. Molecular Formula: C??H??N?O?S, Molecular Weight: 721.86. US Biological Life Sciences. | Worldwide |
| Tubacin | Tubacin is a potent and selective inhibitor of HDAC6, with an IC50 value of 4 nM and approximately 350-fold selectivity over HDAC1. Tubacin also inhibits metallo-β-lactamase domain-containing protein 2 (MBLAC2). Uses: Scientific research. Category: Signaling pathways. CAS No. 537049-40-4. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13428. | |
| Tubastatin A | Tubastatin A is a potent and selective HDAC6 inhibitor with an IC50 of 15 nM in a cell-free assay, and is selective (1000-fold more) against all other isozymes except HDAC8 (57-fold more). Tubastatin A also inhibits HDAC10 and metallo-β-lactamase domain-containing protein 2 (MBLAC2). Uses: Scientific research. Category: Signaling pathways. CAS No. 1252003-15-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-13271A. | |
| Tubastatin A | Tubastatin A is a potent and selective HDAC6 inhibitor with IC50 of 15 nM in a cell-free assay. It is selective against all the other isozymes (1000-fold) except HDAC8 (57-fold). Tubastatin A promotes autophagy and increases apoptosis. Group: Inhibitors. CAS No. 1252003-15-8. Pack Sizes: 50mg. Product ID: S8049. Formula: C20H21N3O2. Smiles: CN1CCC2=C(C1)C3=CC=CC=C3N2CC4=CC=C(C=C4)C(=O)NO. Storage Conditions: 2 years -80 in solvent. | United States; Europe |
| Tubastatin A Hydrochloride | Tubastatin A Hydrochloride (Tubastatin A HCl) is a potent and selective HDAC6 inhibitor with IC50 of 15 nM in a cell-free assay, and is selective (1000-fold more) against all other isozymes except HDAC8 (57-fold more). Tubastatin A Hydrochloride also inhibits HDAC10 and metallo-β-lactamase domain-containing protein 2 (MBLAC2). Uses: Scientific research. Category: Signaling pathways. Alternative Names: Tubastatin A HCl; TSA HCl. CAS No. 1310693-92-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-13271. | |
| Tubastatin A Hydrochloride | Tubastatin A Hydrochloride. Group: Biochemicals. Alternative Names: N-Hydroxy-4-[(1,2,3,4-tetrahydro-2-methyl-5H-pyrido[4,3-b]indol-5-yl)methyl]benzamide Hydrochloride. Grades: Highly Purified. CAS No. 1310693-92-5. Pack Sizes: 10mg, 50mg, 100mg. Molecular Formula: C20H22ClN3O2, Molecular Weight: 371.86. US Biological Life Sciences. | Worldwide |
| Tubastatin A trifluoroacetate | Tubastatin A trifluoroacetate. Group: Biochemicals. Alternative Names: N-Hydroxy-4-[(1,2,3,4-tetrahydro-2-methyl-5H-pyrido[4,3-b]indol-5-yl)methyl]benzamide 2,2,2-trifluoroacetate. Grades: Highly Purified. CAS No. 1239262-52-2. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C22H22F3N3O4. US Biological Life Sciences. | Worldwide |
| Tubeimoside I | Tubeimoside I. Group: Biochemicals. CAS No. 102040-03-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Tubeimoside I | Tubeimoside I is an orally active HSPD1 inhibitor. Tubeimoside I inhibits NF-κB, MAPK, as well as regulates eNOS-VEGF. Tubeimoside I induces cytoprotective Autophagy via an Akt-mediated pathway. Tubeimoside I inhibits proinflammatory cytokine (IL-6 and IL-1β) production. Tubeimoside I exhibits anti-inflammatory activities. Tubeimoside I promotes angiogenesis and improves sepsis symptoms. Tubeimoside I is used in the research of inflammatory diseases, various cancers, sepsis and ischemic diseases[1][2][3][4][5][6][7][8][9][10][11]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Tubeimoside-1; Lobatoside-H. CAS No. 102040-03-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0890. | |
| Tubeimoside II | Tubeimoside II. Group: Biochemicals. CAS No. 115810-12-3. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Tubeimoside II | Tubeimoside II. Group: Biochemicals. Grades: Plant Grade. CAS No. 115810-12-3. Pack Sizes: 20mg. Molecular Formula: C63H98O30, Molecular Weight: 1335.43. US Biological Life Sciences. | Worldwide |
| Tubeimoside III | Tubeimoside III. Group: Biochemicals. Grades: Plant Grade. CAS No. 115810-13-4. Pack Sizes: 20mg. Molecular Formula: C64H100O31, Molecular Weight: 1365.46. US Biological Life Sciences. | Worldwide |
| Tubeimoside I (Lobatoside H) | Tubeimoside I (Lobatoside H). Group: Biochemicals. Alternative Names: 3-[[2-O-[4-O- (4-Carboxy-3-hydroxy-3-methyl-1-oxobutyl-) -a-L-arabinopyranosyl]-b-D-glucopyranosyl]oxy]-2, 23-dihydroxy-28- (O-b-D-xylopyranosyl- (1-3) -O-6-deoxy-a-L-mannopyranosyl- (1-2) -a-L-arabinopyranosyl) ester; Lobatoside H. Grades: Plant Grade. CAS No. 102040-03-9. Pack Sizes: 20mg. Molecular Formula: C63H98O29, Molecular Weight: 1319.43. US Biological Life Sciences. | Worldwide |
| Tuberactinomycin A | Tuberactinomycin A is produced by the strain of Streptoverticillium griseoverticillatus var. tuberacticus B-386. It is effective against mycobacteria, but less effective against gram-positive and gram-negative bacteria. CAS No. 33103-21-8. Molecular formula: C25H43N13O11. Mole weight: 701.69. | |
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