A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
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| Product | Description | |
|---|---|---|
| TCS-OX2-29 | TCS-OX2-29 is a potent, high affinities and selective orexin-2 receptor (OX2R) antagonist with an IC50 value of 40 nM and a pKI value of 7.5. TCS-OX2-29 displays ~250-fold selectivity for OX2 over OX1[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 372523-75-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100452. |  |
| TC-SP 14 | TC-SP 14. Group: Biochemicals. Grades: Purified. CAS No. 1257093-40-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| TCS PIM-1 1 | TCS PIM-1 1. Group: Biochemicals. Grades: Purified. CAS No. 491871-58-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS PIM-1 1 | TCS PIM-1 1 (SC 204330) is a potent, selective and ATP-competitive Pim-1 kianse inhibitor with an IC50 of 50 nM, displays good selectivity over Pim-2 and MEK1/MEK2 (IC50s >20000 nM)[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SC 204330. CAS No. 491871-58-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18086. | |
| TCS PIM-1 4a | TCS PIM-1 4a. Group: Biochemicals. Grades: Purified. CAS No. 438190-29-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS PrP Inhibitor 13 | TCS PrP Inhibitor 13. Group: Biochemicals. Grades: Purified. CAS No. 34320-83-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCTU | TCTU. Group: Biochemicals. Alternative Names: O-(6-Chlorobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N,N,N',N'-Tetramethyl-O-(6-chloro-1H-benzotriazol-1-yl)uronium tetrafluoroborate; 1-[Bis (dimethylamino) methylen]-5-chlorobenzotriazolium 3-oxide tetrafluoroborate. Grades: Highly Purified. CAS No. 330641-16-2. Pack Sizes: 50g, 100g, 250g, 500g, 1kg. Molecular Formula: C11H15BClF4N5O. US Biological Life Sciences. | Worldwide |
| TCTU | Used for peptide solid-phase synthesis. Suitable for automatic multiple peptide synthesizers. Uses: Peptide Synthesis. Group: Coupling Reagents. Alternative Names: O-(6-Chlorobenzotriazol-1-yl)-N,N,N?,N?-tetramethyluronium tetrafluoroborate. CAS No. 330641-16-2. |  Luxembourg Bio Technologies |
| TCV-309 chloride | TCV-309 chloride is a potent and specific platelet activating factor (PAF) antagonist. TCV-309 chloride specifically inhibits PAF-induced aggregation of rabbit and human platelets, and [3H]PAF binding to rabbit platelet microsomes with IC50 values of 33 nM, 58 nM and 27 nM, respectively. TCV-309 chloride has beneficial effects in anaphylactic shock[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 121494-09-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19121A. | |
| tcY-NH2 | tcY-NH2 ((trans-Cinnamoyl)-YPGKF-NH2) is a potent selective PAR4 antagonist peptide. tcY-NH2 inhibits thrombin- and AY-NH2-induced platelet aggregation and endostatin release, and can be used in the research of inflammation, immunology[1][2][6]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (trans-Cinnamoyl)-YPGKF-NH2. CAS No. 327177-34-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P1263. | |
| tcY-NH2 | tcY-NH2. Group: Biochemicals. Grades: Purified. CAS No. 327177-34-4. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| tcY-NH2 TFA | tcY-NH2 TFA is a selective PAR4 antagonist peptide, and it inhibits thrombin- and AY-NH2-induced rat platelet aggregation. Synonyms: N-trans-cinnamoyl-L-tyrosyl-L-prolyl-glycyl-L-lysyl-L-phenylalaninamide trifluoroacetic acid; (trans-Cinnamoyl)-YPGKF-NH2 TFA; L-Phenylalaninamide, N-[(2E)-1-oxo-3-phenyl-2-propenyl]-L-tyrosyl-L-prolylglycyl-L-lysyl-, trifluoroacetate; N-[(2E)-1-Oxo-3-phenyl-2-propen-1-yl]-L-tyrosyl-L-prolylglycyl-L-lysyl-L-phenylalaninamide trifluoroacetate. Grade: 99%. CAS No. 1262750-73-1. Molecular formula: C42H50F3N7O9. Mole weight: 853.88. |  |
| tcY-NH2 TFA | tcY-NH2 ((trans-Cinnamoyl)-YPGKF-NH2) TFA is a potent selective PAR4 antagonist peptide. tcY-NH2 TFA inhibits thrombin- and AY-NH2-induced platelet aggregation and endostatin release, and can be used in the research of inflammation, immunology[1][2][6]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (trans-Cinnamoyl)-YPGKF-NH2 TFA. CAS No. 1262750-73-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P1263A. | |
| TD034 | TD034 is a selective, reversible and noncovalent HDAC11 inhibitor with an IC50 of 5.1 nM and a Ki of 1.5 nM. TD034 does not inhibit other HDACs or sirtuins. TD034 inhibits the defatty acylation of SHMT2 (HDAC11 substrate). TD034 decreases the YAP1 level via HDAC11 inhibition. TD034 can be used for the study of lung cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3030718-42-1. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-176542. | |
| TD1092 | TD1092 is a pan-IAP degrader, degrades cIAP1, cIAP2, and XIAP. TD1092 activates Caspase 3/7, and promotes cancer cells apoptosis via IAP degradation. TD1092 inhibits TNFα mediated NF-κB pathway and reduces the phosphorylation of IKK, IkBα, p65, and p38. TD1092 can act as PROTAC, and is used for cancer research[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3037417-26-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-151966. | |
| TD-165 | TD-165 is a PROTAC-based cereblon (CRBN) degrader. TD-165 comprises a?cereblon (CRBN)?ligand binding group, a linker and an?von Hippel-Landau (VHL)?binding group[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2305936-56-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-130714. | |
| TD-198946 | TD-198946, a thienoindazole derivative, is a potent chondrogenic agent. Uses: Scientific research. Category: Signaling pathways. CAS No. 364762-86-7. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15642. | |
| TD-428 | TD-428 is a PROTAC connected by ligands for Cereblon and BRD4. TD-428 is a highly specific BRD4 degrader with a DC50 of 0.32 nM[1]. TD-428 is a BET PROTAC, which comprises TD-106 (a CRBN ligand) linked to JQ1 (a BET inhibitor). TD-428 efficiently induce BET protein degradation[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2334525-50-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114407. | |
| TD52 | TD52, an Erlotinib (HY-50896) derivative, is an orally active, potent cancerous inhibitor of protein phosphatase 2A (CIP2A) inhibitor. TD52 mediates the apoptotic effect in triple-negative breast cancer (TNBC) cells via regulating the CIP2A/PP2A/p-Akt signalling pathway. TD52 indirectly reduced CIP2A by disturbing Elk1 binding to the CIP2A promoter. TD52 has less p-EGFR inhibition and has potent anti-cancer activity[1]. TD52 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Category: Signaling pathways. CAS No. 1798328-24-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-135699. | |
| TDA Reagent | 10ml Pack Size. Group: Inorganic Chemicals, Salts. Formula: FeCl3 ,HCl , H2O. CAS No. 7647-01-0. Prepack ID 90005084-10ml. See USA prepack pricing. |  |
| TDCPP | Tris(1,3-dichloro-2-propyl)phosphate is a clear colorless viscous liquid. Generally a super-cooled liquid at room temperature but may occasionally solidify when held at low temperatures for prolonged periods. (NTP, 1992);Liquid. CAS No. 13674-87-8. Molecular formula: C9H15Cl6O4P. Mole weight: 430.9g/mol. IUPAC Name: tris(1,3-dichloropropan-2-yl) phosphate. SMILES: C(C(CCl)OP(=O)(OC(CCl)CCl)OC(CCl)CCl)Cl. InChI: InChI=1S/C9H15Cl6O4P/c10-1-7(2-11)17-20(16,18-8(3-12)4-13)19-9(5-14)6-15/h7-9H,1-6H2. |  |
| Tddefensin | Tddefensin is an antibacterial peptide isolated from Tityus discrepans. | |
| TDFA | TDFA is a protein arginine deiminase 4 (PAD4) inhibitor (IC50 = 2.3, 8.5, 26 and 71 μM for PAD4, PAD1, PAD3 and PAD2, respectively) used for the treatment of autoimmune disorders. Synonyms: (3S)-3-[[(2S,3R)-2-acetamido-3-hydroxybutanoyl]amino]-4-[[(2S)-1-amino-5-[(1-amino-2-fluoroethylidene)amino]-1-oxopentan-2-yl]amino]-4-oxobutanoic acid. CAS No. 1345019-64-8. Molecular formula: C17H29FN6O7. Mole weight: 448.45. | |
| TDI-011536 | TDI-011536 is a potent Lats kinase inhibitor, interrupts Hippo-Yap signaling and initiates the proliferation of lesioned heartmuscle cells. TDI-011536 can be used in studies of organ conservation and regeneration[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2687970-96-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-150042. | |
| TDI-011536 | TDI-011536 is a potent Lats kinase inhibitor that interrupts Hippo-Yap signaling and promotes proliferation of lesioned cardiac muscle cells. Group: Inhibitors. CAS No. 2687970-96-1. Pack Sizes: 5mg. Product ID: E1314. Formula: C19H16N4O2S. Storage Conditions: 3 years -20°C powder. |  United States; Europe |
| TDI-10229 | TDI-10229 is a potent and orally bioavailable inhibitor of soluble adenylyl cyclase (sAC, ADCY10). TDI-10229 displays nanomolar inhibition of sAC in both biochemical and cellular assays (IC50 of 195 nM) and exhibits mouse pharmacokinetic properties sufficient to warrant its use as an in vivo tool compound[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2810887-45-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-132298. | |
| TDI-11055 | TDI-11055 is a selective and orally active eleven-nineteen leukemia (ENL) inhibitor, which displaces ENL from chromatin by blocking its YEATS domain interaction with acylated histones. TDI-11055 inhibits ENL and AF9 YEATS domains with IC50 values of 50 nM and 70 nM, respectively, and no activity against GAS41 or YEATS2. TDI-11055 decreases chromatin occupancy of ENL-associated complexes, impairs transcription elongation, suppresses key oncogenic gene expression programs, and induces differentiation. TDI-11055 can be used for the research of acute myeloid leukemia[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3057216-63-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-162350. | |
| TDI-11861 | TDI-11861 is an orally active soluble sAC inhibitor optimized and designed based on TDI-10229 (HY-132298), with an IC50 of 3.3 nM and a KD of 1.4 nM. TDI-11861 has advantages such as high affinity, slow dissociation, and good pharmacokinetics. TDI-11861 can be used for research on male contraception and related sAC pharmacology[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2857049-72-8. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-151798. | |
| TDI-2760 | TDI-2760 is an Aβ aggregation inhibitor with an IC50 of 1.67 μM. TDI-2760 can inhibit the Aβ-fibrinogen interaction and Aβ aggregation, and also modulate the contact system activation induced by Aβ42. TDI-2760 can be used in research related to vascular abnormalities and Aβ aggregation in Alzheimer's disease[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 956128-08-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-121815. | |
| TDI-6118 | TDI-6118 (Compound 5) is a potent brain-penetrant inhibitor of EZH2. EZH2-IN-12 has the potential for the research of central nervous system malignancies[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3056015-28-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-144330. | |
| TDI-6570 | TDI-6570 (TDI-006570) is a blood-brain barrier-permeable, orally active cGAS inhibitor with an IC50 of 1.64 μM. TDI-6570 exhibits high gastrointestinal absorption and a long brain half-life in mice, and shows no toxicity to primary neurons. By inhibiting the cGAS-STING-IFN signaling pathway, TDI-6570 reduces STING levels and the activation of TBK1, blocks double-stranded DNA-induced cGAS activation and downstream interferon-stimulated gene expression, thereby reducing tau protein spread and improving synaptic loss. TDI-6570 reverses memory deficits, increases the amplitude of long-term potentiation, enhances the MEF2C transcriptional network, restores PSD-95 and vGAT punctate structures, and significantly improves cognitive resilience. TDI-6570 can be applied to the research of Alzheimer's disease, Parkinson's disease, systemic lupus erythematosus, as well as various central nervous system and autoimmune diseases[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: TDI-006570. CAS No. 2287331-29-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-164288. | |
| TDI (Toluene Diisocyanate) | Aromatic diisocyanate used for producing flexible PU foams. Pale yellow liquid. Sensitive to moisture. Used with polyether polyols (FlexiFoam Series). Uses: Furniture, bedding, automotive, and coatings. Group: Isocyanate (flamiguard / flexifoam). Alternative Names: TDI 80/20 Grade. Grades: TDI 80/20 Grade. Approvals: ASTM D1638, ISO 9001 Certified Supply. CAS No. 26471-62-5. Pack Sizes: 250 kg steel drums / 1,000 kg IBCs / 20 MT ISO tank. Product ID: FG-TDI. |  United States (serving international markets) |
| TDO-IN-1 | TDO-IN-1 is an orally active and selective inhibitor of tryptophan 2,3-dioxygenase (TDO), shows excellent selectivity over indoleamine-2,3-dioxygenase (IDO), with an IC50 value of 0.62 μM (IDO). TDO-IN-1 reverse the local immune tolerance of tumor tissue to inhibit tumor growth in vivo[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2490672-92-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-151425. | |
| TDP1 Inhibitor-1 | TDP1 Inhibitor-1 is a potent Tyrosyl-DNA Phosphodiesterase 1 (TDP1) inhibitor with an IC50 of 7 μM. TDP1 Inhibitor-1 shows cytotoxicity against multiple cancer cells. TDP1 Inhibitor-1 can be used for the research of cancer, such as breast cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2248702-80-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-119372. | |
| TDP1 Inhibitor-2 | TDP1 Inhibitor-2 (compound 5) is a potent inhibitor for TDP1 (tyrosyl-DNA phosphodiesterase 1), with an IC50 of 99 nM. TDP1 Inhibitor-2 also can inhibit SCAN1 (spinocerebellar ataxia syndrome with axonal neuropathy), with an IC50 of 3.5 μM[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 859142-95-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-147750. | |
| TDP1 Inhibitor-3 | TDP1 Inhibitor-3 (Compound 4E) is a (TDP1) inhibitor with an IC50 value of 0.63 μM[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3074962-67-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-157886. | |
| TDP-4-oxo-6-deoxy-α-D-glucose-3,4-oxoisomerase (dTDP-3-dehydro-6-deoxy-α-D-galactopyranose-forming) | The enzyme is involved in the biosynthesis of dTDP-3-acetamido-3,6-dideoxy-α-D-galactose. Four moieties of α-D-rhamnose and two moities of 3-acetamido-3,6-dideoxy-α-D-galactose form the repeating unit of the glycan chain in the S-layer of the bacterium Aneurinibacillus thermoaerophilus. |  |
| TDP-4-oxo-6-deoxy-α-D-glucose-3,4-oxoisomerase (dTDP-3-dehydro-6-deoxy-α-D-galactopyranose-forming) | The enzyme is involved in the biosynthesis of dTDP-3-acetamido-3,6-dideoxy-α-D-galactose. Four moieties of α-D-rhamnose and two moities of 3-acetamido-3,6-dideoxy-α-D-galactose form the repeating unit of the glycan chain in the S-layer of the bacterium Aneurinibacillus thermoaerophilus. Group: Enzymes. Synonyms: dTDP-6-deoxy-hex-4-ulose isomerase; TDP-6-deoxy-hex-4-ulose isomerase; FdtA. Enzyme Commission Number: EC 5.3.2.3. 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-5483; TDP-4-oxo-6-deoxy-α-D-glucose-3,4-oxoisomerase (dTDP-3-dehydro-6-deoxy-α-D-galactopyranose-forming); EC 5.3.2.3; dTDP-6-deoxy-hex-4-ulose isomerase; TDP-6-deoxy-hex-4-ulose isomerase; FdtA. Cat No: EXWM-5483. | |
| TDP-4-oxo-6-deoxy-α-D-glucose-3,4-oxoisomerase (dTDP-3-dehydro-6-deoxy-α-D-glucopyranose-forming) | The enzyme is involved in biosynthesis of D-mycaminose. Group: Enzymes. Synonyms: TDP-4-keto-6-deoxy-D-glucose-3,4-ketoisomerase (ambiguous); Tyl1a; dTDP-4-keto-6-deoxy-D-glucose-3,4-ketoisomerase (ambiguous). Enzyme Commission Number: EC 5.3.2.4. 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-5484; TDP-4-oxo-6-deoxy-α-D-glucose-3,4-oxoisomerase (dTDP-3-dehydro-6-deoxy-α-D-glucopyranose-forming); EC 5.3.2.4; TDP-4-keto-6-deoxy-D-glucose-3,4-ketoisomerase (ambiguous); Tyl1a; dTDP-4-keto-6-deoxy-D-glucose-3,4-ketoisomerase (ambiguous). Cat No: EXWM-5484. | |
| TDP-4-oxo-6-deoxy-α-D-glucose-3,4-oxoisomerase (dTDP-3-dehydro-6-deoxy-α-D-glucopyranose-forming) | The enzyme is involved in biosynthesis of D-mycaminose. | |
| TDP-N-acetylfucosamine:lipid II N-acetylfucosaminyltransferase | Involved in the enterobacterial common antigen (ECA) biosynthesis in the bacterium Escherichia coli. The trisaccharide of the product (lipid III) is the repeat unit of ECA. Group: Enzymes. Synonyms: TDP-Fuc4NAc:lipid II Fuc4NAc-transferase; TDP-Fuc4NAc:lipid II Fuc4NAc transferase; wecF (gene name). Enzyme Commission Number: EC 2.4.1.325. 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-2562; TDP-N-acetylfucosamine:lipid II N-acetylfucosaminyltransferase; EC 2.4.1.325; TDP-Fuc4NAc:lipid II Fuc4NAc-transferase; TDP-Fuc4NAc:lipid II Fuc4NAc transferase; wecF (gene name). Cat No: EXWM-2562. | |
| TDRL-551 | TDRL-551 is a potent replication protein A (RPA) inhibitor (IC50 = 18 μM). TDRL-551 inhibits RPA-DNA interaction and increases the anti-cancer efficacy of Platinum (Pt)-based chemotherapy. TDRL-551 can be used for the research of cancer, such as non-small cell lung cancer (NSCLC)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1644626-43-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114842. | |
| TDRL-X80 | TDRL-X80 is a potent inhibitor of xeroderma pigmentosum group A (XPA) protein. TDRL-X80 inhibits XPAs DNA binding activity. TDRL-X80 exhibits activity against single, double, and Cisplatin-damaged DNA with IC50s of 18, 20, and 29 μM in fluorescence polarization (FP) analyses , and with IC50s of 21, 39, and 28 in ELISA Analysis[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 292065-64-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-139038. | |
| TDSP5 | TDSP5, a low molecular weight protamine as a nontoxic heparin/low molecular weight heparin antidote, is a homogeneous 1880-d peptide fragment derived directly from protamine by enzymatic digestion of protamine with thermolysin. TDSP5 neutralizes the anticoagulant effects of heparin and commercial low molecular-weight heparin preparations. TDSP5 shows significantly reduced crossreactivity toward mouse sera containing antiprotamine antibodies. TDSP5 exhibits a decrease in its potential in activating the complement system. Synonyms: LMWP-TDSP5; Low molecular weight protamine-TDSP5. | |
| TDSRCVIGLYHPPLQVY | TDSRCVIGLYHPPLQVY is a disordered control peptide. TDSRCVIGLYHPPLQVY is a peptide containing the same amino acids as LP17 (HY-P3400) but in a different sequence order[1][2]. Uses: Scientific research. Category: Peptides. CAS No. 887973-01-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P3460. | |
| TDZD-8 | TDZD-8 is an inhibitor of GSK-3β, with an IC50 of 2 μM; TDZD-8 shows less potent activities against Cdk-1/cyclin B, CK-II, PKA, and PKC, with all IC50s of >100 μM. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GSK-3β Inhibitor I; NP 01139. CAS No. 327036-89-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-11012. | |
| Teaalcohol | Teaalcohol. CAS No. 14203-59-9. Product ID: ACM14203599. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Tea CO2 Extract | Tea CO2 Extract (Jasmin Type). CAS No. 84650-60-2. Kosher: Y. VIGON Item # 503654. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Tea CO2 Extract | Tea CO2 Extract (Green Type). CAS No. 84650-60-2. Kosher: Y. VIGON Item # 503653. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Tea CO2 Extract | Tea CO2 Extract (Pai Mu Tan Type). CAS No. 84650-60-2. Kosher: Y. VIGON Item # 503650. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Tea CO2 Extract | Tea CO2 Extract (Keemun Type). CAS No. 84650-60-2. Kosher: Y. VIGON Item # 503655. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Tea CO2 Extract Organic | Tea CO2 Extract Organic (Green Type). CAS No. MIXTURE. Kosher: Y. VIGON Item # 503652. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Tea CO2 Extract WONF | Tea CO2 Extract WONF (Black Type). CAS No. 84650-60-2. Kosher: Y. VIGON Item # 503651. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| TEAD1/3/4-IN-1 | TEAD1/3/4-IN-1 is an orally active inhibitor of TEAD1/3/4. TEAD1/3/4-IN-1 inhibits the YAP/TAZ-TEAD interaction, with its EC50 being 2 nM. TEAD1/3/4-IN-1 has anti-proliferative activity against NCI-H226 cells. TEAD1/3/4-IN-1 can be used in the research of lung squamous cell carcinoma[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2762619-63-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-174275. | |
| TEAD-IN-1 | TEAD-IN-1 (Compound 2) is potent TEAD autopalmitoylation inhibitor, with an IC50 of 603 nM. TEAD-IN-1 increases the interaction of TEAD and VGLL4. TEAD-IN-1 decreases the interaction of YAP and TEAD. TEAD-IN-1 can be used for the research of cancer[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2412761-57-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-137479. | |
| TEAD-IN-11 | TEAD-IN-11 (compound 38) has a good inhibitory effect on TEAD1 (IC50=8.7 nM), TEAD2 (IC50=3.4 nM), TEAD3 (IC50=5.6 nnM). TEAD-IN-11 has good selective activity against TEAD1-3 as a covalent inhibitor. TEAD-IN-11 can be used for cancer research[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3032196-88-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-161569. | |
| Tea-dodecyl benzene sulfonate | Tea-dodecyl benzene sulfonate. CAS No. 27323-41-7. Pack Sizes: 1 kg. Product ID: CDC10-0414. Molecular formula: C24H45NO6S. Category: Cosmetic Surfactants. Product Keywords: Cosmetic Ingredients; Cosmetic Surfactants; Tea-dodecyl benzene sulfonate; CDC10-0414; 27323-41-7; C24H45NO6S; 248-406-9; 27323-41-7. Purity: 0.99. EC Number: 248-406-9. Physical State: Solid. |  |
| Tea Polyphenol | Tea Polyphenol. Alternative Names: 5,7-Dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate. CAS No. 84650-60-2. Product ID: CI-OT-0139. Molecular formula: C17H19N3O. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Tea Polyphenol Liposome | Tea polyphenol (TP) is a polyphenolic compound extracted from tea leaves, known for their antioxidant, antimicrobial, anticancer, and lipid-lowering effects. This product is a pre-formulated liposome encapsulating Tea Polyphenol. It is only for research purposes. Group: Drug-loaded liposome. |  |
| Tea polyphenol reduced graphene oxide | Carbon black oil appears as a dark colored liquid with a petroleum-like odor. Less dense than water and insoluble in water. Vapors heavier than air.;Carbon, activated is a black grains that have been treated to improve absorptive ability. May heat spontaneously if not properly cooled after manufacture.;Carbon, animal or vegetable origin appears as a black powder or granular mixed with a tar or starch and water binder pressed into regular lumps or briquettes. Heats slowly and ignites in air especially if wet.;Graphite (natural) appears as a mineral form of the element carbon. Hexagonal crystals or thin leaf-like layers. Steel-gray to black with a metallic luster and a greasy feel. An electrical conductor. Used for high-temperature crucibles, as a lubricant and in "lead" pencils.;DryPowder; DryPowder, Liquid; DryPowder, PelletsLargeCrystals; DryPowder, PelletsLargeCrystals, WetSolid, OtherSolid, Liquid; DryPowder, WetSolid, Liquid; Liquid; OtherSolid; OtherSolid, GasVapor, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid, Liquid; WetSolid; WetSolid, Liquid;OtherSolid; PelletsLargeCrystals;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; DryPowder, WetSolid; Liquid; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSoli | |
| TEATFB | TEATFB. CAS No. 429-06-1. Molecular formula: C8H20BF4N. Mole weight: 217.06g/mol. IUPAC Name: tetraethylazanium;tetrafluoroborate. SMILES: [B-](F)(F)(F)F.CC[N+](CC)(CC)CC. InChI: InChI=1S/C8H20N.BF4/c1-5-9(6-2,7-3)8-4;2-1(3,4)5/h5-8H2,1-4H3;/q+1;-1. | |
| Tea Tree | Tea Tree features a pleasant tea tree and honeysuckle fragrance, instead of harsh alcohol fumes common in most acne products. Pack Sizes: 1 kg. Product ID: CDC10-0557. Category: Anti-Acne Ingredients. Product Keywords: Cosmetic Ingredients; Active Ingredients; Anti-Acne Ingredients; Tea Tree; CDC10-0557. | |
| Tea Tree Essential Oil | Organic tea tree oil (Melaleuca alternifolia); pure essential oil from Australian leaves and twigs. CAS No. 68647-73-4. Product ID: CI-SC-0442. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Tea tree oil | Tea tree oil. Alternative Names: Melasol. CAS No. 68647-73-4. Purity: 96%. Product ID: ACM68647734. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Tea tree oil | Tea tree oil. Market: Agriculture. PK Chem Industries: We supply chemicals related to Cosmetic, Personal Care, Food, Pharmaceutical, Feed, Agriculture and Mining Industries. |  |
| Tea Tree Oil | Tea Tree Oil. CAS No. 68647-73-4. FEMA No. 3902. Kosher: Y. VIGON Item # 507659. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers, Cosmetics, Aromatherapy, Essetial Oils. | America & Internationally |
| Tea Tree Oil Australian 100% Pure | Tea Tree Oil Australian 100% Pure. CAS No. 68647-73-4. FEMA No. 3902. Kosher: Y. VIGON Item # 507522. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers, Cosmetics, Aromatherapy, Essetial Oils. | America & Internationally |
| Tea Tree Oil EP/BP | Tea Tree Oil EP/BP. CAS No. 68647-73-4. |  |
| Tebanicline dihydrochloride | Tebanicline dihydrochloride (Ebanicline dihydrochloride) is a nAChR modulator with potent, orally effective analgesic activity. It inhibits the binding of cytisine to α4β2 neuronal nAChRs with a Ki of 37 pM[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ebanicline dihydrochloride; ABT-594 dihydrochloride. CAS No. 209326-19-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14316A. | |
| Tebapivat | Tebapivat (PKR activator 2) is a potent pyruvate kinase-R (PKR) activator extracted from patent WO2019035863A1, compound 385[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AG-946; PKR activator 2. CAS No. 2283422-04-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-135884. | |
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