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| Product | Description | |
|---|---|---|
| TC-DAPK 6 | TC-DAPK 6. Group: Biochemicals. Grades: Purified. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| TCDDMDA | TCDDMDA. |  |
| TC-E3 5032 | TC-E3 5032 is a linker used in PROTAC technology that can be used in the synthesis of HDAC6 and anaplastic lymphoma kinase (ALK) degraders. Alternative Names: E3 ligase Ligand 4; 1H-Isoindole-1,3(2H)-dione, 2-(2,6-dioxo-3-piperidinyl)-4-fluoro-; Thalidomide 4-fluoride; Thalidomide fluoride; 4-Fluoro-thalidomide; Cereblon ligand 4;E3 ligase Ligand 4; 2-(2,6-Dioxo-3-piperidinyl)-4-fluoro-1H-isoindole-1,3(2H)-dione. Grades: ≥ 98%. CAS No. 835616-60-9. Molecular formula: C13H9FN2O4. Mole weight: 276.22. |  |
| TC-E 5001 | TC-E 5001. Group: Biochemicals. Grades: Purified. CAS No. 865565-29-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-E 5002 | TC-E 5002. Group: Biochemicals. Grades: Purified. CAS No. 1453071-47-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-E 5003 | TC-E 5003. Group: Biochemicals. Grades: Purified. CAS No. 17328-16-4. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| TC-E 5003 | TC-E 5003 is a selective protein arginine methyltransferase 1 (PRMT1) inhibitor with an IC50 of 1.5 μM against hPRMT1. TC-E 5003 modulates the lipopolysaccharide (LPS) (HY-D1056)-induced AP-1 and NF-κB signaling pathways with anti-inflammatory properties. TC-E 5003 also upregulates the expression of Ucp1 and Fgf21, activates protein kinase A signaling and lipolysis in primary subcutaneous adipocytes from both mouse and humans. TC-E 5003 is promising for research of obesity and associated metabolic disorders, oxidative stress, inflammation and cancers[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 17328-16-4. Pack Sizes: 10 mM * 1 mL in DMSO; 25 mg; 50 mg; 100 mg. Product ID: HY-107574. |  |
| TC-E 5005 | TC-E 5005. Group: Biochemicals. Grades: Purified. CAS No. 959705-64-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-E 5006 | TC-E 5006. Group: Biochemicals. Grades: Purified. CAS No. 1257395-14-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-E 5007 | TC-E 5007. Group: Biochemicals. Grades: Purified. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| 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-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 | TCEP Hydrochloride is used for selective reduction of disulfide bridges at low pH. Alternative Names: 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. Grades: 98% (AT). CAS No. 51805-45-9. Molecular formula: C9H16ClO6P. Mole weight: 286.65. | |
| 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 |
| 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-1008 | TC-G-1008, also known as GPR39-C3, is a potent and orally available GPR39 agonist (EC50= 0.4 and 0.8 nM for rat and human receptors respectively) with great selectivity for GPR39 over a panel of kinases (IC50s > 10 μM) and displays minimal binding affinity for ghrelin and neurotensin-1 receptors (IC50s > 30 μM). Alternative Names: GPR39-C3, GPR39C3, GPR39 C3, TC-G-1008, TC-G1008, TC-G 1008, TCG-1008, TCG1008, TCG 1008; N-[3-chloro-4-[[[2-(methylamino)-6-pyridin-2-ylpyrimidin-4-yl]amino]methyl]phenyl]methanesulfonamide; GPR39-C3; N-(3-chloro-4-(((2-(methylamino)-6-(2-pyridinyl)-4-pyrimidinyl)amino)methyl)phenyl)methanesulfonamide; TC-G 1008. CAS No. 1621175-65-2. Molecular formula: C18H19ClN6O2S. Mole weight: 418.9. | |
| 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) methyle-ne]-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 is a DUB inhibitor for ubiquitin C-terminal hydrolase L3 with IC50 of 0.6 μM, 125-fold selective to L1. Alternative Names: 4,5,6,7-Tetrachloroindan-1,3-dione; UCH-L3 Inhibitor. Grades: >98%. CAS No. 30675-13-9. Molecular formula: C9H2Cl4O2. Mole weight: 283.92. | |
| 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. Group: Biochemicals. Grades: Purified. CAS No. 1393814-38-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| 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. | |
| 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 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. | |
| TC-N 1752 | TC-N 1752. Group: Biochemicals. Grades: Purified. CAS No. 1211866-85-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCN 201 | TCN 201. Group: Biochemicals. Grades: Purified. CAS No. 852918-02-6. Pack Sizes: 10mg, 50mg. 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 |
| tCnitro-CE Phosphoramidite | tCnitro-CE Phosphoramidite, a reagent vital for the synthesis of oligonucleotides, features a promising nitro group situated at the 5'-end capable of introducing a modification or label. Its applications in nucleic acid-based technologies like gene editing and diagnostics research remain unparalleled. Alternative Names: 5'-O-(4,4'-Dimethoxytrityl)-1'-(7-nitro-1,3-diaza-2-oxophenothiazin-1-yl)-2'-deoxy-ß-D-ribofuranosyl-3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite. Molecular formula: C45H49N6O9PS. Mole weight: 880.94. | |
| tCnitroNucleoside | tCnitroNucleoside is a multifaceted biomedical compound used to study cancer, viral infections and genetically rooted ailments. Grades: ≥ 95%. CAS No. 1139889-25-0. Molecular formula: C15H14N4O6S. Mole weight: 378.36. | |
| 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 Nucleoside | tC Nucleoside, an exceptional fluorescent analogue of thymidine intended for DNA synthesis and detection, has proven to be instrumental in numerous DNA studies. Its use in DNA hybridization, polymerase chain reaction (PCR), and DNA sequencing is scientifically deemed significant. Additionally, its exclusive fluorescent properties have contributed significantly to drug discovery research as it enables accurate detection of interactions with DNA. Grades: ≥ 97%. CAS No. 162902-04-7. Molecular formula: C15H15N3O4S. Mole weight: 333.36. | |
| 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-DBCO | TCO-PEG12-DBCO is a long chain PEGreagent containing a TCO and a DBCO moiety. TCO group specifically and efficiently reacts with terrahydrazine under mild condition. DBCO is very reactive toward Azide through click chemistry, the PEG spacer increases the aqueous solubility of the reagent. Grades: 95%. CAS No. 2055022-06-3. Molecular formula: C54H81N3O16. Mole weight: 1028.3. | |
| 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-PEG2-Sulfo-NHS ester | TCO-PEG2-Sulfo-NHS ester is a polyethylene glycol (PEG)-based PROTAC linker. TCO-PEG2-Sulfo-NHS ester can be used in the synthesis of a series of PROTACs. Alternative Names: TCO-PEG2-Sulfo-NHS ester-EDC Urea; 1-(3-(Dimethylamino)propyl)-3-ethylurea 1-((3-(2-(2-(((cyclooct-4-en-1-yloxy)carbonyl)amino)ethoxy)ethoxy)propanoyl)oxy)-2,5-dioxopyrrolidine-3-sulfonate; 1-[(3-{2-[2-({[(4Z)-cyclooct-4-en-1-yloxy]carbonyl}amino)ethoxy]ethoxy}propanoyl)oxy]-2,5-dioxopyrrolidine-3-sulfonic acid; 1-[3-(dimethylamino)propyl]-3-ethylurea. Grades: 95%. CAS No. 2353409-48-8. Molecular formula: C28H49N5O12S. Mole weight: 679.78. | |
| 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. | |
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