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| Product | Description | |
|---|---|---|
| T cells Targeted SM102 LNP-EGFP mRNA (m1Ψ) | This product is a LNP prepared from SM102 as the ionizable lipid and modified with CD3 antibody. It's specifically designed for targeted delivery of EGFP mRNA to CD3+ T cells. EGFP mRNA, a common fluorescence reporter, translates into enhanced green fluorescent protein, which exhibits an excitation wavelength of 488 nm and emission at 507 nm. The loaded EGFP mRNA is modified with N1-methyl-pseudouridine to enhance expression and reduce immunogenicity. It is only for research purposes. Group: Lipid nanoparticle. |  |
| TCEP-d12 Hydrochloride | Biochemical tool for selective reduction of disulfide bridges at low pH; reductant for redox assay. Group: Biochemicals. Alternative Names: 3, 3', 3''-Phosphinidynetri spropanoic Acid-d12; Tris(2-carboxyethyl)phosphine-d12 Hydrochloride; Tris (carboxyethyl) phosphine-d12 Hydrochloride. Grades: Highly Purified. CAS No. 1189959-10-1. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| TCEP-d16 hydrochloride | TCEP-d16 (hydrochloride) is the deuterium labeled TCEP hydrochloride[1]. TCEP hydrochloride (Tris(2-carboxyethyl)phosphine hydrochloride) is a non-thiol reducing agent that is more stable and produces a faster S-S reductive reaction than other chemical reductants. TCEP hydrochloride is a trialkylphosphine, selectively reduces protein disuldes without altering the properties or interacting with thiol-directed agents in the reaction mixture. TCEP hydrochloride is also a commonly used reducing agent in the DNA/AuNP chemistry[2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1174025-33-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-W011500S. |  |
| TCEP hydrochloride | TCEP hydrochloride (Tris(2-carboxyethyl)phosphine hydrochloride) is a non-thiol reducing agent that is more stable and produces a faster S-S reductive reaction than other chemical reductants. TCEP hydrochloride is a trialkylphosphine, selectively reduces protein disuldes without altering the properties or interacting with thiol-directed agents in the reaction mixture. TCEP hydrochloride is also a commonly used reducing agent in the DNA/AuNP chemistry[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Tris(2-carboxyethyl)?phosphine hydrochloride. CAS No. 51805-45-9. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-W011500. | |
| TCEP Hydrochloride | Biochemical tool for selective reduction of disulfide bridges at low pH; reductant for redox assay. Group: Biochemicals. Alternative Names: 3, 3', 3''-Phosphinidynetri spropanoic Acid Hydrochloride; Tris(2-carboxyethyl)phosphine Hydrochloride; Tris (carboxyethyl) phosphine Hydrochloride; TCEP·HCl. Grades: Highly Purified. CAS No. 51805-45-9. Pack Sizes: 1g, 5g, 25g. Molecular Formula: C9H15O6P. US Biological Life Sciences. | Worldwide |
| TCEP Hydrochloride | TCEP Hydrochloride is used for selective reduction of disulfide bridges at low pH. Synonyms: TCEP.HCL; Tris(2-Carboxyethyl)Phosphine Hydrochloride; 3,3',3''-Phosphinetriyltripropanoic acid hydrochloride; TCEP HCl; TCEP; UNII-H49AAM893K; MFCD00145469; TCEP (hydrochloride); Tris(carboxyethyl)phosphine hydrochloride; H49AAM893K; Propanoic acid, 3,3',3''-phosphinidynetris-, hydrochloride. Grade: 98% (AT). CAS No. 51805-45-9. Molecular formula: C9H16ClO6P. Mole weight: 286.65. |  |
| TCF-1 | TCF-1. Purity: 95%+. Product ID: ACMA00064460. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| TC-F 2 | TC-F 2. Group: Biochemicals. Grades: Purified. CAS No. 1304778-15-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCFH | A safe, affordable reagent for ester and difficult amide synthesis. Uses: Peptide Synthesis. Group: Coupling Reagents. Alternative Names: Chloro-N,N,N,N-tetramethylformamidinium hexafluorophosphate. CAS No. 207915-99-9. |  Luxembourg Bio Technologies |
| TC-FPR 43 | TC-FPR 43. Group: Biochemicals. Grades: Purified. CAS No. 903895-98-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-G 1000 | TC-G 1000. Group: Biochemicals. Grades: Purified. CAS No. 245744-18-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-G 1001 | TC-G 1001. Group: Biochemicals. Grades: Purified. CAS No. 494191-73-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-G 1003 | TC-G 1003. Group: Biochemicals. Grades: Purified. CAS No. 1021912-42-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TC-G 1004 | TC-G 1004. Group: Biochemicals. Grades: Purified. CAS No. 1061747-72-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-G 1005 | TC-G 1005 is a potent, selective and orally active agonist of the BA receptor Takeda G protein-coupled receptor 5 (TGR5), with EC50s of 0.72 and 6.2 nM for hTGR5 and mTGR5, respectively. TC-G 1005 can reduce glucose levels in vivo[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1415407-60-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-110173. | |
| TC-G 1006 | TC-G 1006. Group: Biochemicals. Grades: Purified. CAS No. 1324003-64-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-G 1008 | TC-G 1008. Group: Biochemicals. Grades: Purified. CAS No. 1621175-65-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-G-1008 | TC-G-1008 (GPR39-C3) is a potent and orally available GPR39 agonist with EC50 values of 0.4 and 0.8 nM for rat and human receptors respectively. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GPR39-C3. CAS No. 1621175-65-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103007. | |
| TC-G 24 | TC-G 24. Group: Biochemicals. Grades: Purified. CAS No. 1257256-44-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-H 106 | TC-H 106. Group: Biochemicals. Grades: Purified. CAS No. 937039-45-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCH-165 | TCH-165 is a small molecule modulator of proteasome assembly, which increases 20S levels and facilitates 20S-mediated protein degradation[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1446350-60-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-120722. | |
| TC HSD 21 | TC HSD 21. Group: Biochemicals. Grades: Purified. CAS No. 330203-01-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC HSD 21 | TC HSD 21 is a selective inhibitor of 17β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) against related 17β-HSD isozymes, with an IC50 of 14 nM in HeLa cells. TC HSD 21 can be used in the research of prostate cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 330203-01-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103394. | |
| TC HSD 21 (5-[ (3-Bromo-4-hydroxyphenyl) methylene]-3- (4-methoxyphenyl) -2-thioxo-4-thiazolidinone) | Potent 17beta-hydroxysteroid dehydrogenase type 3 (17beta-HSD3) inhibitor (IC50 values are 6 and 40nm at human and mouse 17beta-HSD3 respectively). Displays no activity at 17beta-HSD1, 17beta-HSD2, ERalpha, androgen receptors or glucocorticoid receptors. Group: Biochemicals. Grades: Highly Purified. CAS No. 330203-01-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TC-I 15 | TC-I 15 (TC-I-15) is a type of allosteric collagen-binding integrin α2β1 inhibitor, and it also inhibits α1β1 and α11β1. TC-I 15 inhibits platelet adhesion to collagen and thrombus deposition. TC-I 15 prevents the formation of a pre-metastatic microenvironment by inhibiting the uptake of cancer-associated fibroblast (CAF) extracellular vesicles (EVs) by lung fibroblasts, which reduces the metastasis of salivary gland adenocystic carcinoma (SACC) to the lungs in mouse models, [1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 916734-43-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-107588. | |
| TC-I 2000 | TC-I 2000. Group: Biochemicals. Grades: Purified. CAS No. 1159996-20-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-I 2014 | TC-I 2014. Group: Biochemicals. Grades: Purified. CAS No. 1221349-53-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-I 2014 | TC-I 2014 (compound 5) is a potent and orally active Benzimidazole-containing transient receptor potential melastatin 8 (TRPM8) antagonist, with IC50 values of 0.8 nM, 3.0 nM and 4.4 nM for canine, human and rat channels respectively. TC-I 2014 exhibits antiallodynic properties in pain models[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1221349-53-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-110199. | |
| TCID | TCID. Group: Biochemicals. Grades: Purified. CAS No. 30675-13-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCID | TCID (4,5,6,7-Tetrachloroindan-1,3-dione) is a potent and selective neuronal ubiquitin C-terminal hydrolase (UCH-L3) inhibitor with an IC50 of 0.6 μM[1]. TCID diminishes glycine transporter GlyT2 ubiquitination in brainstem and spinal cord primary neurons[2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 4,5,6,7-Tetrachloroindan-1,3-dione. CAS No. 30675-13-9. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-18638. | |
| TCIP3 | TCIP3 is a bivalent molecular glue with with dual binding to p300/CBP and BCL6. TCIP3 redirects p300 and CBP to activate programmed cell death genes normally repressed by the oncogenic driver, BCL6. TCIP3 can be used for the study of diffuse large B cell lymphomas (DLBCLs). TCIP3 exhibits no toxicity in non-transformed tonsillar lymphocytes or fibroblasts[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3067681-36-8. Pack Sizes: 10 mM * 1 mL in DMSO; 500 μg; 1 mg; 5 mg; 10 mg. Product ID: HY-173552. | |
| TCJL37 | TCJL37 is a potent, selective, and orally bioavailable TYK2 inhibitor with a Ki of 1.6 nM. TCJL37 can be used for the research of inflammatory bowel diseases (IBD)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1258294-34-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-16640. | |
| TCL053 | TCL053 is an ionizable lipid carrier and used to introduce active components, in particular nucleic acids, into cells with excellent efriciency. TCL053, together with DPPC (Dipalmitoylphosphatidylcholine), PEG-DMG (Polyethylene glycoldimyristoyl glycerol), and cholesterol, forms lipid nanoparticle (LNP) which is able to deliver Cas9 mRNA and sgRNA into skeletal muscle[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2361162-70-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-147332. | |
| TC LPA5 4 | TC LPA5 4 is a LPA5 (GPR92)-specific non-lipid antagonist. TC LPA5 4 inhibits LPA-induced aggregation of isolated human platelet (LPA5-RH7777 cell line) with an IC50 of 800 nM. TC LPA5 4 displays selectivity for LPA5 over 80 other screened agent targets[1]. TC LPA5 4 inhibits cell proliferation and migration of thyroid cancer cells[2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1393814-38-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107615. | |
| TC LPA5 4 | TC LPA5 4. Group: Biochemicals. Grades: Purified. CAS No. 1393814-38-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCMCB07 | TCMCB07, a cyclic nonapeptide peptide, is an orally active and brain-penetrant melanocortin receptor 4 (MC4R) antagonist. TCMCB07 plays an important role in cachexia. TCMCB07 has potential transport capabilities[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Mifomelatide. CAS No. 1456699-27-6. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P5971. | |
| TC-MCH 7c | TC-MCH 7c. Group: Biochemicals. Grades: Purified. CAS No. 864756-35-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TC Mps1 12 | TC Mps1 12. Group: Biochemicals. Grades: Purified. CAS No. 1206170-62-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-N 1752 | TC-N 1752. Group: Biochemicals. Grades: Purified. CAS No. 1211866-85-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-N 1752 | TC-N 1752 is a potent and orally active inhibitor of Nav1.7, with IC50s of 0.17 μM, 0.3 μM, 0.4 μM, 1.1 μM and 2.2 μM at hNav1.7, hNav1.3, hNav1.4, hNaV1.5 and rNav1.8, respectively. TC-N 1752 also inhibits tetrodotoxin-sensitive sodium channels. TC-N 1752 shows analgesic efficacy in the Formalin model of pain[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1211866-85-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107405. | |
| TCN 201 | TCN 201. Group: Biochemicals. Grades: Purified. CAS No. 852918-02-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCN-201 (3-Chloro-4-fluoro-N- [ (4-{ [2- (phenylcarbonyl) hydrazino] carbonyl}phenyl) methyl] benzenesulfonamide, NMDA Antagonist X) | A negative allosteric modulator selective for NR2A containingnMDA receptors (pIC50 = 6.8 and <4.3uM for NR2A and NR2B, respectively). No effect on NR2B-containingnMDA receptors with concentrations less than 50 mM. Inhibition on NR2A containingnMDA receptors is glycine (or D-serine)-binding, but not glutamate-binding, dependent. Group: Biochemicals. Grades: Highly Purified. CAS No. 852918-02-6. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| TCN 213 | TCN 213. Group: Biochemicals. Alternative Names: N-(Cyclohexylmethyl)-2-[[5-[(phenylmethyl)amino]-1,3,4-thiadiazol-2-yl]thio]-acetamide. Grades: Highly Purified. CAS No. 556803-08-8. Pack Sizes: 10mg. Molecular Formula: C18H24N4OS2, Molecular Weight: 376.54. US Biological Life Sciences. | Worldwide |
| TC-N 22A | TC-N 22A. Group: Biochemicals. Grades: Purified. CAS No. 1314140-00-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCN 237 dihydrochloride | TCN 237 dihydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 700878-19-9. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TCN 238 | TCN 238. Group: Biochemicals. Grades: Purified. CAS No. 125404-04-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC NTR1 17 | TC NTR1 17. Group: Biochemicals. Grades: Purified. CAS No. 1146757-96-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCNT Type 1- Carbon Nanotubes Thin Walled | TCNT Type 1- Carbon Nanotubes Thin Walled. CAS No. 308068-56-6. |  |
| TC-O 9311 | TC-O 9311 is a potent orphan G protein-coupled receptor 139 (GPR139) agonist with an EC50 of 39 nM[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 444932-31-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-101777. | |
| TC-O 9311 | TC-O 9311. Group: Biochemicals. Grades: Purified. CAS No. 444932-31-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCO-NHS ester | TCO-NHS ester is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs[1]. TCO-NHS ester is a click chemistry reagent, it contains a TCO group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing Tetrazine groups. Uses: Scientific research. Category: Signaling pathways. CAS No. 1191901-33-3. Pack Sizes: 50 mg; 100 mg; 250 mg; 1 g. Product ID: HY-141165. | |
| TCO-NHS Ester (axial) | TCO-NHS Ester axial is a click chemistry reagent that can be used as a building block in amine reactions. TCO-NHS Ester axial contains TCO groups, which can undergo inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing Tetrazine groups. Uses: Scientific research. Category: Signaling pathways. CAS No. 1610931-22-0. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-151698. | |
| TCO-OH | TCO-OH is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 85081-69-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg. Product ID: HY-141186. | |
| TCO-PEG12-NHS ester | TCO-PEG12-NHS ester is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. TCO-PEG12-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2185016-39-9. Pack Sizes: 5 mg; 10 mg. Product ID: HY-141170. | |
| TCO-PEG3-amine | TCO-PEG3-amine is a PEG-based PROTAC linker can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1800507-93-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-141178. | |
| TCO-PEG3-Biotin | TCO-PEG3-Biotin is a cleavable 3 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. TCO-PEG3-Biotin is a click chemistry reagent, it contains a TCO group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing Tetrazine groups. Uses: Scientific research. Category: Signaling pathways. CAS No. 2098630-62-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-136050. | |
| TCO-PEG3-Biotin | TCO-PEG3-Biotin. Grade: >98.0%. Molecular formula: C31H29N3O4S2. Mole weight: 571.71. | |
| TCO-PEG3-maleimide | TCO-PEG3-maleimide (TCO-PEG3-NEM) is a click chemistry reagent. TCO-PEG3-maleimide efficiently binds TCO (trans-cyclooctene) moiety to thiol-containing molecules (such as antibodies, cysteine-containing peptides)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1809356-72-6. Pack Sizes: 5 mg. Product ID: HY-151696. | |
| TCO-PEG4-biotin | TCO-PEG4-biotin is a polyethylene glycol (PEG)-based PROTAC linker. TCO-PEG4-biotin can be used in the synthesis of a series of PROTACs. Grade: 95%. CAS No. 2183440-30-2. Molecular formula: C29H50N4O8S. Mole weight: 614.79. | |
| TCO-PEG4-NHS ester | TCO-PEG4-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. TCO-PEG4-NHS ester is a click chemistry reagent, it contains a TCO group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing Tetrazine groups. Uses: Scientific research. Category: Signaling pathways. CAS No. 1621096-79-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-141167A. | |
| TCO-PEG4-VC-PAB-MMAE | TCO-PEG4-VC-PAB-MMAE is a agent-linker conjugate for ADC. TCO-PEG4-VC-PAB-MMAE contains a cleavable ADC linker (TCO-PEG4-VC-PA) and a potent tubulin inhibitor MMAE (HY-15162)[1]. TCO-PEG4-VC-PAB-MMAE is a click chemistry reagent, it contains a TCO group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing Tetrazine groups. Uses: Scientific research. Category: Signaling pathways. CAS No. 2758671-45-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-148057. | |
| TCO-PEG5-C2-Mal | TCO-PEG5-maleimide is a PEG linker with TCO and maleimide groups, specifically enabling tetrazine click chemistry and thiol conjugation for bioconjugation, probe design, and drug delivery. Uses: Scientific research. Category: Signaling pathways. CAS No. 2748951-17-7. Pack Sizes: 1 mg (195.09 mM * 10 μL in DMSO); 5 mg (195.09 mM * 50 μL in DMSO). Product ID: HY-164785. | |
| TCO-PEG8-NHS ester | TCO-PEG8-NHS ester is a PEG-based PROTAC linker can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2353409-95-5. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-141169. | |
| TCO-PEG8-TFP ester | TCO-PEG8-TFP ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2353410-06-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-141173. | |
| TCO-PEG9-maleimide | TCO-PEG9-maleimide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2183440-37-9. Pack Sizes: 10 mg; 25 mg. Product ID: HY-141184. | |
| TC OT 39 | TC OT 39. Group: Biochemicals. Grades: Purified. CAS No. 479232-57-0. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TC-P 262 | TC-P 262. Group: Biochemicals. Grades: Purified. CAS No. 873398-67-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCPOBOP | TCPOBOP. Group: Biochemicals. Grades: Purified. CAS No. 76150-91-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCPOBOP | TCPOBOP is a constitutive androstane receptor (CAR) agonist that induces robust hepatocyte proliferation and hepatomegaly without any liver injury or tissue loss[1]. TCPOBOP attenuates Fas-induced murine liver injury by altering Bcl-2 proteins[2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 76150-91-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103243. | |
| TCPP-Cd(2+) | TCPP-Cd(2+). Alternative Names: cadmium(2+);hydron;4-[10,15,20-tris(4-carboxylatophenyl)porphyrin-22,24-diid-5-yl]benzoate. CAS No. 82404-76-0. Molecular formula: C48H24N4O8Cd-4·H+. Mole weight: 898.14. Purity: 95%. | |
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