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| Product | Description | |
|---|---|---|
| Trastuzumab emtansine | Trastuzumab emtansine (Ado-Trastuzumab emtansine) is an antibody-drug conjugate ( ADC ) that incorporates the HER2-targeted antitumor properties of trastuzumab with the cytotoxic activity of the microtubule-inhibitory agent DM1 (derivative of maytansine). Trastuzumab emtansine can be used for the research of advanced breast cancer [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ado-Trastuzumab emtansine; PRO132365; T-DM 1. CAS No. 1018448-65-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P9921. |  |
| Trastuzumab emtansine | Trastuzumab emtansine is an antibody-drug conjugate (ADC) consisting of the recombinant anti-epidermal growth factor receptor 2 (HER2) monoclonal antibody trastuzumab conjugated to the maytansinoid DM1 via a nonreducible thioether linkage (MCC) with potential antineoplastic activity. The trastuzumab moiety of this ADC binds to HER2 on tumor cell surface surfaces. Upon internalization, the DM1 moiety is released and binds to tubulin, thereby disrupting microtubule assembly/disassembly dynamics and inhibiting cell division and the proliferation of cancer cells that overexpress HER2. Linkage of antibody and drug through a nonreducible linker has been reported to contribute to the improved efficacy and reduced toxicity of this ADC compared to similar ADCs constructed with reducible linkers. Grade: 95%. CAS No. 1018448-65-1. Molecular formula: C6448H9948N1720O2012S44·(C47H62ClN4O13S)n. |  |
| Trastuzumab emtansine (solution) | Trastuzumab emtansine (Ado-Trastuzumab emtansine) is an antibody-drug conjugate (ADC) that incorporates the HER2-targeted antitumor properties of trastuzumab with the cytotoxic activity of the microtubule-inhibitory agent DM1 (derivative of maytansine). Trastuzumab emtansine can be used for the research of advanced breast cancer [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ado-Trastuzumab emtansine (solution) ; PRO132365 (solution) ; T-DM 1 (solution). CAS No. 1018448-65-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P9921A. | |
| Trastuzumab rezetecan | Trastuzumab rezetecan (SHR-A1811) is a HER2 -targeting antibody-drug conjugate (ADC). Trastuzumab rezetecan is composed of a humanized anti-HER2 antibody (HY-P9907), a cleavable linker MC-Gly-Gly-Phe-Gly (HY-44246), and a topoisomerase I inhibitor payload Rezetecán (HY-147408). Trastuzumab rezetecan can be used for research in HER2-positive breast cancer [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SHR-A1811. CAS No. 2924909-11-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-164762. | |
| Trastuzumab vedotin | Trastuzumab vedotin (MRG002) is an anti-human epidermal growth factor receptor 2 (HER2) antibody-drug conjugate (ADC). Trastuzumab vedotin is composed of a humanized anti-HER2 antibody Trastuzumab (HY-P9907), an enzymatically cleavable peptide-linker Valine-citrulline, a tubulin inhibitor Monomethyl auristatin E (MMAE; HY-15162). Trastuzumab vedotin can be used for the research of HER2-positive breast cancer[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MRG002; Trastuzumab MMAE. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-164992. | |
| Traumatic Acid | Traumatic Acid, is the product of a biosynthetic pathway from a physiological role of alpha-ketol fatty acids in plant lipid hydroperoxide lyase metabolism. This compound is also used in would healing as it stimulates cell division to form a protective callus around the wound site. Group: Biochemicals. Grades: Highly Purified. CAS No. 6402-36-4. Pack Sizes: 100mg, 500mg. Molecular Formula: C12H20O4, Molecular Weight: 228.28. US Biological Life Sciences. |  Worldwide |
| Traumatic Acid | Traumatic Acid is a wound healing agent and a cytokinin (phytohormone). Traumatic Acid enhances the biosynthesis of collagen in cultured human skin fibroblasts. Traumatic Acid inhibits MCF-7 breast cancer cells viability and enhances apoptosis and oxidative stress. Traumatic Acid can be used in studies of cancer, circulatory disorders (including arterial hypertension), and skin diseases associated with oxidative stress and impaired collagen biosynthesis [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 6402-36-4. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-119358. | |
| Travaprost | Travaprost. Group: Biochemicals. Grades: Purified. CAS No. 157283-68-6. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Travoprost | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardschiral moleculespharmaceutical toxicology. Alternative Names: AL 6221, Travatanz, Travoprost, Travaprost,7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-[(1E,3R)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]-1-butenyl]cyclopentyl]-(5Z)-5-heptenoic acid 1-methylethyl ester, [1R-[1alpha(Z),2beta(1E,3R*),3alpha,5alpha]]-7-[3,5-dihydroxy-2-[3-hydroxy-4-[3-(trifluoromethyl)phenoxy]-1-butenyl]cyclopentyl]-5-Heptenoic acid 1-methylethyl ester, Travatan. |  |
| Travoprost | Travoprost (Fluprostenol isopropyl ester), an isopropyl ester proagent, is a high affinity, selective FP prostaglandin full receptor agonist. Travoprost has the ocular hypotensive efficacy and has the potential for glaucoma and ocular hypertension [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Fluprostenol isopropyl ester; AL6221; Flu-Ipr. CAS No. 157283-68-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-B0584. | |
| Travoprost | Selective FP prostaglandin receptor agonist. Isopropyl ester of (+)-fluprostenol. Antiglaucoma. Used to treat glaucoma. Group: Biochemicals. Alternative Names: (5Z) -7-[ (1R, 2R, 3R, 5S) -3, 5-Dihydroxy-2-[ (1E, 3R) -3-hydroxy-4-[3- (trifluoromethyl) phenoxy]-1-buten-1-yl]cyclopentyl]-5-heptenoic Acid 1-Methylethyl Ester; AL 6221; Travaprost; Travatan. Grades: Highly Purified. CAS No. 157283-68-6. Pack Sizes: 5mg, 10mg, 25mg. Molecular Formula: C??H??F?O?, Molecular Weight: 500.55. US Biological Life Sciences. | Worldwide |
| Travoprost Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Traxillaside | Traxillaside is purified from the barks of Torreya nucifera Sieb. et Zucc. It has significant neuroprotective activities against glutamate-induced toxicity in primary cultures of rat cortical cells. Synonyms: (3R,4R)-3-[[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl]-4-[(3,4,5-trimethoxyphenyl)methyl]oxolan-2-one. Grade: 97.5%. CAS No. 149415-62-3. Molecular formula: C28H36O12. Mole weight: 564.59. | |
| Traxoprodil | Traxoprodil (CP101,606) is a potent and selective NMDA antagonist and protect hippocampal neurons with an IC 50 of 10 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP101,606. CAS No. 134234-12-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W018061. | |
| Trazodone | Trazodone (AF-1161 free base) is a serotonin receptor antagonist and reuptake inhibitor. Trazodone can be used for the research of major depressive disorder. Trazodone also has potential for sleep disorder research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AF-1161 free base. CAS No. 19794-93-5. Pack Sizes: 10 mM * 1 mL; 25 mg. Product ID: HY-B0478A. | |
| Trazodone 1,4-Di-N-Oxide | A possible metabolite of Trazodone-HCl. Group: Biochemicals. Alternative Names: 2-[3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl]-. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Trazodone-d6 (2-[3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl-d6]-1,2,4-triazolo[4,3-a]pyridin-3(2H)-one) | Trazodone was originally discovered and developed in Italy in the 1960s by Angelini research laboratories as a second-generation antidepressant. It was developed according to the mental pain hypothesis, which was postulated from studying patients and which proposes that major depression is associated with a decreased pain threshold. Trazodone also has anxiolytic, and hypnotic effects (1). Trazodone was patented and marketed in many countries all over the world. It was approved by the Food and Drug Administration (FDA) at the end of 1981. Group: Biochemicals. Alternative Names: 2-[3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl-d6]-1,2,4-triazolo[4,3-a]pyridin-3(2H)-one. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Trazodone-d6 hydrochloride | Trazodone-d 6 (hydrochloride) is the deuterium labeled Trazodone hydrochloride[1]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: AF-1161-d6. CAS No. 1181578-71-1. Pack Sizes: 1 mg; 5 mg. Product ID: HY-B0478AS. | |
| Trazodone-D6 hydrochloride solution | 100 ?g/mL in methanol (as free base), ampule of 1 mL, certified reference material. Group: Certified reference materials (crms). | |
| Trazodone hydrochloride | Trazodone hydrochloride (AF-1161) is a serotonin receptor antagonist and reuptake inhibitor with anti-neuroinflammatory effects. Trazodone hydrochloride can be used for research in major depressive disorder and also holds potential for studies related to sleep disorders [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AF-1161. CAS No. 25332-39-2. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0478. | |
| Trazodone Hydrochloride | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardsbritish pharmacopoeiapharmaceutical toxicologypharmacopoeial standards. Alternative Names: Trazodone hydrochloride, Trittico, Pragmazone, Mesyrel, Bimaran, Tombran, AF 1161, Molipaxin, Trazolan, KB 831, Desyrel, Thombran, 1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one, 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-, monohydrochloride (9CI),1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one, 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-, hydrochloride (1:1), s-Triazolo[4,3-a]pyridin-3(2H)-one, 2-[3-[4-(m-chlorophenyl)-1-piperazinyl]propyl]-, monohydrochloride (8CI). | |
| Trazodone Hydrochloride | Antidepressant. Group: Biochemicals. Alternative Names: 2-[3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl]-1,2,4-triazolo[4,3-a]pyridin-3(2H)-one Hydrochloride; Bimaran; Desyrel; KB 831; Mesyrel; Molipaxin; Pragmazone; Thombran; Tombran; Trazodone hydrochloride; Trazolan; Trittico. Grades: Highly Purified. CAS No. 25332-39-2. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Trazodone (hydrochloride) (Standard) | Trazodone (hydrochloride) (Standard) is the analytical standard of Trazodone (hydrochloride). This product is intended for research and analytical applications. Trazodone (hydrochloride) (AF-1161) is an antidepressant belonging to the class of serotonin receptor antagonists and reuptake inhibitors for treatment of anxiety disorders. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AF-1161 (Standard). CAS No. 25332-39-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0478R. | |
| Trazodone N-Oxide | Trazodone N-Oxide. Group: Biochemicals. Alternative Names: 2-[3-[4-(3-Chlorophenyl)-1-oxido-1-piperazinyl]propyl]-. Grades: Highly Purified. CAS No. 55290-68-1. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Trazodone Related Compound C | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Trazodone Related Compound D | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Trazodone Related Compound F | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| TRC051384 | TRC051384 is a potent inducer of heat shock protein 70 (HSP70). TRC051384 exhibits protective effects against neuronal trauma via inhibition of necroptosis. TRC051384 can be used for the research of ischemic stroke[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 867164-40-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101712. | |
| TRC 051384 | TRC 051384. Group: Biochemicals. Grades: Purified. CAS No. 867164-40-7. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Trebananib | Trebananib (2xCon4C; AMG 386) is an Fc fusion peptibody that prevents Tie2 receptor activation through binding of both angiopoietin 1 (Ang1) and Ang2. Trebananib has anti-angiogenesis activity [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: 2xCon4C; AMG 386. CAS No. 894356-79-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99546. | |
| Trecovirsen sodium | Trecovirsen sodium is a 25-mer antisense phosphorothioate oligonucleotide targeted at the gag site of the HIV gene. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GEM91 sodium. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-149906C. | |
| Tree moss extract | Tree moss extract. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Treemossabsolute(Pseudeverniafurfuracea);Oils, tree moss;TREEMOSSCONCRETE;treemoss oil. Product Category: Heterocyclic Organic Compound. CAS No. 68648-41-9. Product ID: ACM68648419. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Treemoss Extract (technical grade) | Treemoss Extract (technical grade). Uses: Designed for use in research and industrial production. Additional or Alternative Names: Evernia furfuracea, ext. Product Category: Promotional Products. CAS No. 90028-67-4. Purity: Tech. Product ID: ACM90028674-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tree Peony Root Bark Extract | Tree peony root bark extract is extracted from China’ s national flower peony, the active ingredient of tree peony root bark extract is paeonol, which appear in white or light yellow crystallize powder with special smell and taste spicy. Paeonol can easily soluble in ethanol, methanol and hot water, insoluble in normal temperature water. Peony bark extract has composure, antipyretic, analgesia effects. It also has central inhibition effect. Group: Others. Mole weight: 166.18. Tree Peony Root Bark Extract; Paeonia suffruticosa Andr. Cat No: EXTC-055. |  |
| Tregalizumab | Tregalizumab is a humanized anti-human CD4 monoclonal antibody (IgG1 type) that selectively activates the suppressive properties of regulatory T cells (Tregs) in vitro. Tregalizumab can be used in the research of autoimmune diseases (resulting from insufficient Treg activity) and allergies [1] [2] [3]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: BT-061. CAS No. 1207446-68-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99327. | |
| Trehalase | Trehalase is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Signaling pathways. CAS No. 9025-52-9. Pack Sizes: 1 U. Product ID: HY-P2766. | |
| Trehalosamine | Trehalosamine is a carbohydrate antibiotic originally isolated from Str. sp. It has anti-gram-positive bacteria and Pseudomonas aeruginosa and mycobacterium action. Synonyms: 2-Trehalosamine; 2-amino-2-deoxy-alpha-D-glucopyranosyl alpha-D-glucopyranoside; alpha-D-Glucopyranosyl 2-amino-2-deoxy-alpha-D-glucopyranoside. CAS No. 27208-79-3. Molecular formula: C12H23NO10. Mole weight: 341.31. | |
| Trehalose | Trehalose. Categories: trehalose; 99-20-7. |  CA, FL & NJ |
| Trehalose | Trehalose occurs as virtually odorless, white or almost white crystals with a sweet taste (approximately 45% of the sweetness of sucrose). Synonyms: Ascend; α-D-glucopyranosyl-α-D-glucopyranoside; (α-D-glucosido)-α-D-glucoside; mycose; natural trehalose; α, α-trehalose; Treha; trehalose dihydrate. Product ID: PE-0116. Category: Color adjuvant; Flavor enhancer; freeze-drying Agents; Humectant; Stabilizing Agents; Sweetening Agents; Diluent; Thickening Agents. Product Keywords: Flavoring Agents; Stabilizers; Lyophilization Reagents; ; PE-0116; Trehalose; Color adjuvant; Flavor enhancer; freeze-drying Agents; Humectant; Stabilizing Agents; Sweetening Agents; Diluent; Thickening Agents;. UNII: NA. Chemical Name: (2R, 3R, 4S, 5R, 6R)-2-(Hydroxymethyl)-6-[(2R, 3R, 4S, 5R, 6R)- 3, 4, 5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-oxane-3, 4, 5- triol anhydrous [99-20-7] (2R, 3R, 4S, 5R, 6R)-2-(Hydroxymethyl)-6-[(2R, 3R, 4S, 5R, 6R)- 3, 4, 5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-oxane-3, 4, 5- triol dihydrate [6138-23-4]. Grade: Pharmceutical Excipients. Administration route: Injection. Dosage Form: Injections. Stability and Storage Conditions: Trehalose is a relatively stable material. At 60°C for 5 hours it loses not more than 1.5% w/w of water (the dihydrate water of crystallization is retained). Open stored powder may liquefy at high relative humidity (≥90%). Trehalose should be stored |  |
| Trehalose | 25g Pack Size. Group: Carbohydrates, Sugars. Formula: C12H22O11. CAS No. 99-20-7. Prepack ID 74350211-25g. Molecular Weight 342.3. See USA prepack pricing. |  |
| Trehalose | Trehalose. Group: Sweeteners. |  |
| trehalose 2-sulfotransferase | The sulfation of trehalose in the bacterium Mycobacterium tuberculosis is required for the biosynthesis of sulfolipid-1. Group: Enzymes. Synonyms: Stf0 sulfotransferase. Enzyme Commission Number: EC 2.8.2.37. 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-3397; trehalose 2-sulfotransferase; EC 2.8.2.37; Stf0 sulfotransferase. Cat No: EXWM-3397. | |
| Trehalose-6,6'-dibehenate | Trehalose-6,6'-dibehenate is an orally active glycolipid. Trehalose-6,6'-dibehenate activates Mincle and inflammasome , inducing IL-1β secretion in a caspase activity-dependent manner. Trehalose-6,6'-dibehenate exerts a Myd88 -dependent adjuvant activity. Trehalose-6,6'-dibehenate induces Th-1/Th-17 immune responses [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. CAS No. 66758-35-8. Pack Sizes: 5 mg; 10 mg. Product ID: HY-112137. | |
| Trehalose 6,6-dimycolate | Trehalose 6,6'-dimycolate (Cord Factor) is trehalose 6,6'-dimycolate, a cell wall glycolipid of Mycobacterium tuberculosis, which can be used to simulate inflammation and granuloma induced by Mycobacterium tuberculosis (MTB) form. Trehalose 6,6-dimycolate also protects Mycobacterium tuberculosis from macrophage-mediated killing, inhibits efficient antigen presentation, and reduces the development of protective T cell responses [1] [2]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Cord Factor. CAS No. 61512-20-7. Pack Sizes: 1 mg. Product ID: HY-W145657. | |
| Trehalose 6-phosphate dipotassium salt | Trehalose 6-phosphate dipotassium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TREHALOSE 6-PHOSPHATE DIPOTASSIUM SALT;trehalose-6-phosphate dipotassium;TREHALOSE 6-PHOSPHATE DIPOTASSIUM SALT(SALTDATA: dipotassium salt);Trehalose 6-phosphate (potassium salt). Product Category: Heterocyclic Organic Compound. CAS No. 136632-28-5. Molecular formula: C12H21K2O14P. Mole weight: 498.46. Product ID: ACM136632285. Alfa Chemistry ISO 9001:2015 Certified. | |
| Trehalose-6-phosphate hydrolase from Bacillus subtilis, Recombinant | In enzymology, an alpha,alpha-phosphotrehalase (EC 3.2.1.93) is an enzyme that catalyzes the chemical reaction: alpha,alpha-trehalose 6-phosphate + H2O <-> D-glucose + D-glucose 6-phosphate. Thus, the two substrates of this enzyme are alpha,alpha'-trehalose 6-phosphate and H2O, whereas its two products are D-glucose and D-glucose 6-phosphate. This enzyme belongs to the family of hydrolases, specifically those glycosidases that hydrolyse O- and S-glycosyl compounds. This enzyme participates in starch and sucrose metabolism. Group: Enzymes. Synonyms: α,α-Trehalose-6-phosphate phosphoglucohydrolase; α,α-phosphotrehalase; phosphotrehalase; alpha,alpha-trehalose-6-phosphate phosphoglucohydrolase; alpha,alpha-phosph. Enzyme Commission Number: EC 3.2.1.93. CAS No. 54576-93-1. Purity: >95 % as judged by SDS-PAGE. α,α-phosphotrehalase. Mole weight: 68727.7 Da. Activity: 78.3 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Bacillus subtilis subsp. subtilis str. 168. α,α-Trehalose-6-phosphate phosphoglucohydrolase; α,α-phosphotrehalase; phosphotrehalase; alpha,alpha-trehalose-6-phosphate phosphoglucohydrolase; alpha,alpha-phosphotrehalase; EC 3.2.1.93; Trehalose-6-phosphate hydrolase. Cat No: NATE-1230. | |
| Trehalose-6-phosphate hydrolase from Escherichia coli, Recombinant | In enzymology, an alpha,alpha-phosphotrehalase (EC 3.2.1.93) is an enzyme that catalyzes the chemical reaction: alpha,alpha-trehalose 6-phosphate + H2O <-> D-glucose + D-glucose 6-phosphate. Thus, the two substrates of this enzyme are alpha,alpha'-trehalose 6-phosphate and H2O, whereas its two products are D-glucose and D-glucose 6-phosphate. This enzyme belongs to the family of hydrolases, specifically those glycosidases that hydrolyse O- and S-glycosyl compounds. This enzyme participates in starch and sucrose metabolism. Group: Enzymes. Synonyms: α,α-Trehalose-6-phosphate phosphoglucohydrolase; α,α-phosphotrehalase; phosphotrehalase; alpha,alpha-trehalose-6-phosphate phosphoglucohydrolase; alpha,alpha-phosphot. Enzyme Commission Number: EC 3.2.1.93. CAS No. 54576-93-1. Purity: >95 % as judged by SDS-PAGE. α,α-phosphotrehalase. Mole weight: 67657.8 Da. Activity: 252.4 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Escherichia coli str. K-12 substr. W3110. α,α-Trehalose-6-phosphate phosphoglucohydrolase; α,α-phosphotrehalase; phosphotrehalase; alpha,alpha-trehalose-6-phosphate phosphoglucohydrolase; alpha,alpha-phosphotrehalase; EC 3.2.1.93; Trehalose-6-phosphate hydrolase. Cat No: NATE-1231. | |
| trehalose 6-phosphate phosphorylase | The enzyme from Lactococcus lactis is specific for trehalose 6-phosphate. Differs from EC 2.4.1.64, α,α-trehalose phosphorylase, in that trehalose is not a substrate. Group: Enzymes. Synonyms: trehalose 6-phosphate:phosphate β-D-glucosyltransferase. Enzyme Commission Number: EC 2.4.1.216. CAS No. 403512-51-6. 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-2444; trehalose 6-phosphate phosphorylase; EC 2.4.1.216; 403512-51-6; trehalose 6-phosphate:phosphate β-D-glucosyltransferase. Cat No: EXWM-2444. | |
| Trehalose octaacetate | Trehalose octaacetate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,3,4,6,2',3',4',6'-Octa-O-acetyl-a,a-trehalose. CAS No. 25018-27-3. Molecular formula: C28H38O19. Mole weight: 678.59. Product ID: ACM25018273. Alfa Chemistry ISO 9001:2015 Certified. | |
| trehalose O-mycolyltransferase | Catalyses the exchange of mycolic acid between trehalose, trehalose mycolate and trehalose bismycolate. Trehalose 6-palmitate can also act as donor. Group: Enzymes. Synonyms: α,α'-trehalose 6-monomycolate:α,α'-trehalose mycolyltransferase; α,α'-trehalose-6-mycolate:α,α'-trehalose-6-mycolate 6'-mycolyltransferase. Enzyme Commission Number: EC 2.3.1.122. CAS No. 111694-11-2. 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-2060; trehalose O-mycolyltransferase; EC 2.3.1.122; 111694-11-2; α,α'-trehalose 6-monomycolate:α,α'-trehalose mycolyltransferase; α,α'-trehalose-6-mycolate:α,α'-trehalose-6-mycolate 6'-mycolyltransferase. Cat No: EXWM-2060. | |
| trehalose-phosphatase | This enzyme belongs to the family of hydrolases, specifically those acting on phosphoric monoester bonds. The systematic name of this enzyme class is alpha,alpha-trehalose-6-phosphate phosphohydrolase. Other names in common use include trehalose 6-phosphatase, trehalose 6-phosphate phosphatase, and trehalose-6-phosphate phosphohydrolase. This enzyme participates in starch and sucrose metabolism. Group: Enzymes. Synonyms: trehalose 6-phosphatase; trehalose 6-phosphate phosphatase; trehalose-6-phosphate phosphohydrolase. Enzyme Commission Number: EC 3.1.3.12. CAS No. 9025-72-3. T6PP. 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-3615; trehalose-phosphatase; EC 3.1.3.12; 9025-72-3; trehalose 6-phosphatase; trehalose 6-phosphate phosphatase; trehalose-6-phosphate phosphohydrolase. Cat No: EXWM-3615. | |
| Trehalose-phosphatase from Mycobacterium tuberculosis, Recombinant | In enzymology, a trehalose-phosphatase (EC 3.1.3.12) is an enzyme that catalyzes the chemical reaction: alpha,alpha-trehalose 6-phosphate + H2O <-> alpha,alpha-trehalose + phosphate. Thus, the two substrates of this enzyme are alpha,alpha'-trehalose 6-phosphate and H2O, whereas its two products are alpha,alpha-trehalose and phosphate. This enzyme belongs to the family of hydrolases, specifically those acting on phosphoric monoester bonds. Group: Enzymes. Synonyms: Trehalose 6-phosphatase; trehalose 6-phosphate phosphatase; trehalose-6-phosphate phosphohydrolase; TPP; T6PP. Enzyme Commission Number: EC 3.1.3.12. CAS No. 9025-72-3. Purity: >95 % as judged by SDS-PAGE. T6PP. Mole weight: 61948.7 Da. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Mycobacterium tuberculosis H37Rv. Trehalose 6-phosphatase; trehalose 6-phosphate phosphatase; trehalose-6-phosphate phosphohydrolase; TPP; T6PP. Cat No: NATE-1232. | |
| Trehalose-phosphatase from Thermus thermophilus, Recombinant | In enzymology, a trehalose-phosphatase (EC 3.1.3.12) is an enzyme that catalyzes the chemical reaction: alpha,alpha-trehalose 6-phosphate + H2O <-> alpha,alpha-trehalose + phosphate. Thus, the two substrates of this enzyme are alpha,alpha'-trehalose 6-phosphate and H2O, whereas its two products are alpha,alpha-trehalose and phosphate. This enzyme belongs to the family of hydrolases, specifically those acting on phosphoric monoester bonds. Group: Enzymes. Synonyms: Trehalose 6-phosphatase; trehalose 6-phosphate phosphatase; trehalose-6-phosphate phosphohydrolase; TPP; T6PP. Enzyme Commission Number: EC 3.1.3.12. CAS No. 9025-72-3. Purity: >95 % as judged by SDS-PAGE. T6PP. Mole weight: 27788.9 Da. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Thermus thermophilus HB8. Trehalose 6-phosphatase; trehalose 6-phosphate phosphatase; trehalose-6-phosphate phosphohydrolase; TPP; T6PP. Cat No: NATE-1233. | |
| Trehalose USP | Trehalose USP. CAS No. 99-20-7. Molecular formula: C12H22O11. |  |
| Treiethanolamine 85% 102-71-6 | Treiethanolamine 85% - Surface Coatings. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. |  North America & APAC |
| Trelagliptin | Trelagliptin (SYR-472) is a potent, orally active and highly selective DPP-4 inhibitor with an IC 50 of 4 nM. Trelagliptin succinate improves glycemic control in vivo and can be used for the study of type 2 diabetes mellitus (T2DM) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SYR-472. CAS No. 865759-25-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15408. | |
| Trelagliptin | Trelagliptin is a highly selective, long-acting dipeptidyl peptidase IV (DPP-4) inhibitor. This inhibitor provides sustained reduction of plasma DPP-4 activity and lowering of blood glucose in animal models of diabetes. Group: Biochemicals. Grades: Highly Purified. CAS No. 865759-25-7. Pack Sizes: 5mg, 10mg. Molecular Formula: C18H20FN5O2, Molecular Weight: 357.38. US Biological Life Sciences. | Worldwide |
| Trelagliptin-[13C,d3] | Trelagliptin-[13C,d3] is a labelled form of Trelagliptin, a medication for the treatment of type 2 diabetes. Synonyms: 2-({6-[(3R)-3-aminopiperidin-1-yl]-3-(13C,D3)methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl}methyl)-4-fluorobenzonitrile; (R)-2-((6-(3-aminopiperidin-1-yl)-3-(methyl-13C-d3)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)methyl)-4-fluorobenzonitrile. Grade: ≥99% atom D. Molecular formula: C17[13C]H17D3FN5O2. Mole weight: 361.40. | |
| Trelagliptin Succinat | Trelagliptin Succinat. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1029877-94-8. Molecular formula: C22H26FN5O6. Mole weight: 475.48. Catalog: APB1029877948. | |
| Trelagliptin succinate | Trelagliptin (SYR-472) succinate is a potent, orally active and highly selective DPP-4 inhibitor with an IC 50 of 4 nM. Trelagliptin succinate improves glycemic control in vivo and can be used for the study of type 2 diabetes mellitus (T2DM) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SYR-472 succinate. CAS No. 1029877-94-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15408A. | |
| TREM2-IN-1 | TREM2-IN-1 (OPA) is a TREM2 inhibitor derived from oxaliplatin and artesunate. TREM2-IN-1 can relieves immunosuppressive tumor microenvironment and enhancing chemical anticancer efficiency. TREM2-IN-1 deters the tumor growth in mice models bearing MC38 colorectal tumor by reducing the number of CD206 + and CX 3 CR1 + immunosuppressive macrophages. TREM2-IN-1 also promotes the expansion and infiltration of immunostimulatory dendritic, cytotoxic T and natural killer cells [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2000236-36-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-160421. | |
| Tremelimumab | Tremelimumab (Ticilimumab) is a fully human monoclonal antibody specific for cytotoxic T-lymphocyte antigen-4 ( CTLA-4 ) and can be used for metastatic melanoma research [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Ticilimumab; CP-675206. CAS No. 745013-59-6. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P9918. | |
| Tremin 283 Wollastonite | Tremin 283 Wollastonite. Group: Polymers. |  |
| Trenbolone 17, 17b- (HRP) | Trenbolone 17, 17b- (HRP). Group: Biochemicals. Grades: Purified. Pack Sizes: 500ul. US Biological Life Sciences. | Worldwide |
| Trenbolone 17-acetate | Trenbolone 17-acetate. Group: Biochemicals. Grades: Reagent Grade. CAS No. 10161-34-9. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| Trenbolone 3, 17b- (HRP) | Trenbolone 3, 17b- (HRP). Group: Biochemicals. Grades: Purified. Pack Sizes: 500ul. US Biological Life Sciences. | Worldwide |
| Trenbolone Acetate System Suitability Mixture | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Trenbolone enanthate | 1g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C18H22O2. CAS No. 10161-33-8. Prepack ID 32690521-1g. Molecular Weight 270.37. See USA prepack pricing. | |
| Trenizine | Trenizine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Trenizine, Trenizine [INN], UNII-1WPQ720NCK, AC1MJ5O1, CHEMBL2104897, 4-(4-benzhydrylpiperazin-1-yl)-1-(4-tert-butylphenyl)butan-1-ol, (+-)-alpha-(p-tert-Butylphenyl)-4-(diphenylmethyl)-1-piperazinebutanol, 82190-93-0. Product Category: Heterocyclic Organic Compound. CAS No. 82190-93-0. Molecular formula: C31H40N2O. Mole weight: 456.67. Purity: 0.96. IUPACName: 4-(4-benzhydrylpiperazin-1-yl)-1-(4-tert-butylphenyl)butan-1-ol. Canonical SMILES: CC(C)(C)C1=CC=C(C=C1)C(CCCN2CCN(CC2)C(C3=CC=CC=C3)C4=CC=CC=C4)O. Density: 1.069g/cm³. Product ID: ACM82190930. Alfa Chemistry ISO 9001:2015 Certified. | |
| Treosulfan | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
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