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| Product | Description | |
|---|---|---|
| TCS-1102 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| TCS 1105 | TCS 1105. Group: Biochemicals. Grades: Purified. CAS No. 185391-33-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| TCS 1105 | TCS 1105 is a GABAA benzodiazepine receptor (BZR) ligand that acts as an agonist at α2 and antagonist at α1 benzodiazepine receptors (Ki = 118 and 245 nM, respectively). Synonyms: TCS 1105; TCS1105; TCS-1105; N-[(-4-Fluorophenyl)methyl]-α-oxo-1H-indole-3-acetamide. Grades: ≥99% by HPLC. CAS No. 185391-33-7. Molecular formula: C17H13FN2O2. Mole weight: 296.3. |  |
| TCS 1205 | TCS 1205 is a GABAA α2 benzodiazepine receptor agonist and GABAA α1 partial agonist in vitro (Ki = 14 and 121 nM, respectively). It displays non-sedative anxiolytic activity in vivo. Synonyms: TCS 1205; TCS1205; TCS-1205; 5-Nitro-α-oxo-N-(1R)-phenylethyl]-1H-indole-3-acetamide; 2-(5-nitro-1H-indol-3-yl)-2-oxo-N-[(1R)-1-phenylethyl]acetamide. Grades: ≥99% by HPLC. CAS No. 355022-97-8. Molecular formula: C18H15N3O4. Mole weight: 337.33. | |
| TCS 1205 | TCS 1205. Group: Biochemicals. Grades: Purified. CAS No. 355022-97-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS 183 | TCS 183. Group: Biochemicals. Grades: Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| TCS 183 | TCS 183 is a fragment 1-13 of human and mouse GSK-3β sequence. TCS 183 is potentially used as a competitive inhibitor of GSK-3β (Ser9) phosphorylation. Synonyms: TCS 183; TCS183; TCS-183. Molecular formula: C58H96N20O20S. Mole weight: 1425.58. | |
| TCS 184 | TCS 184 is a scrambled control peptide for use with TCS 183. Synonyms: TCS 184; TCS184; TCS-184. CAS No. 1315378-71-2. Molecular formula: C58H96N20O20S. Mole weight: 1425.58. | |
| TCS 184 | TCS 184. Group: Biochemicals. Grades: Purified. CAS No. 1315378-71-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| TCS 2002 | TCS 2002. Group: Biochemicals. Grades: Purified. CAS No. 1005201-24-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS 2002 | TCS 2002 is a potent and cell-permeable inhibitor of GSK-3β (IC50 = 35 nM). Oral adminstration of TCS 2002 inhibits cold water stress-induced tau hyperphosphorylation in the mouse brain. Synonyms: TCS-2002; TCS 2002; TCS2002; 2-Methyl-5-[3-[4-(methylsulfinyl)phenyl]-5-benzofuranyl]-1,3,4-oxadiazole. Grades: ≥99% by HPLC. CAS No. 1005201-24-0. Molecular formula: C18H14N2O3S. Mole weight: 338.38. | |
| TCS 21311 | TCS 21311 is a potent JAK3 inhibitor (IC50 = 8 nM) with selectivity for JAK3 over JAK1, JAK2 and TYK2 (IC50 = 1017, 2550 and 8055 nM, respectively). It also inhibits GSK-3β, PKCα and PKCθ (IC50 = 3, 13 and 68 nM, respectively). Synonyms: NIBR3049; NIBR-3049; NIBR 3049; TCS-21311; TCS 21311; TCS21311; 3-[5-[4-(2-Hydroxy-2-methyl-1-oxopropyl)-1-piperazinyl]-2-(trifluoromethyl)phenyl]-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione. Grades: ≥98% by HPLC. CAS No. 1260181-14-3. Molecular formula: C27H25F3N4O4. Mole weight: 526.51. | |
| TCS 21311 | TCS 21311. Group: Biochemicals. Grades: Purified. CAS No. 1260181-14-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS 21311 | TCS 21311 (NIBR3049) is a potent, highly selective JAK3 inhibitor with an IC50 of 8 nM, it displays >100-fold selectivity over JAK1, JAK2 and TYK2. TCS 21311 (NIBR3049) inhibits PKC?, PKC?, and GSK3? with IC50s of 13, 68, and 3 nM, respectively[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NIBR3049. CAS No. 1260181-14-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-108264. |  |
| TCS-21311 | A potent JAK3 inhibitor; selective for JAK3 over JAK1, JAK2 and TYK2. It also inhibits GSK-3 β, PKCα and PKC?. Group: Biochemicals. Alternative Names: 3-[5-[4- (2-Hydroxy-2-methyl-1-oxopropyl) -1-piperazinyl]-2- (trifluoromethyl) phenyl]-4- (1H-indol-3-yl) -1H-pyrrole-2, 5-dione; TCS 21311. Grades: Highly Purified. CAS No. 1260181-14-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TCS 2210 | TCS 2210. Group: Biochemicals. Grades: Purified. CAS No. 1201916-31-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS-2210 | TCS 2210 is a small molecule inducer of neuronal differentiation. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TCS-2210; TCS 2210; TCS2210. Product Category: Others. Appearance: To be determined. CAS No. 1201916-31-5. Molecular formula: C18H17N3O3. Mole weight: 323.35. Purity: >98%. IUPACName: 1,2-dihydro-N-hydroxy-2-oxo-3-(3-phenylpropyl)-6-quinoxalinecarboxamide. Canonical SMILES: O=C(C1=CC2=C(NC(C(CCCC3=CC=CC=C3)=N2)=O)C=C1)NO. Product ID: ACM1201916315. Alfa Chemistry ISO 9001:2015 Certified. |  |
| TCS 2312 | TCS 2312 is a potent checkpoint kinase 1 (chk1) inhibitor (Ki = 0.38 nM, EC50 = 60 nM). TCS 2312 potentiates the cell killing activity of Gemcitabine in breast and prostate cancer cell lines, and exhibits antiproliferative effects in vitro. Synonyms: TCS 2312; TCS2312; TCS-2312; 4'-[5-[[3-[ (Cyclopropylamino) methyl]phenyl]amino]-1H-pyrazol-3-yl]-[1, 1'-biphenyl]-2, 4-diol. Grades: ≥97% by HPLC. CAS No. 838823-31-7. Molecular formula: C25H24N4O2. Mole weight: 412.48. | |
| TCS 2312 | TCS 2312. Group: Biochemicals. Grades: Purified. CAS No. 838823-31-7. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| TCS 2314 | TCS 2314. Group: Biochemicals. Grades: Purified. CAS No. 317353-73-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS 2314 | TCS 2314 is an integrin very late antigen-4 (VLA-4; α4β1) antagonist (IC50 = 4.4 nM) that inhibits the activation of inflammatory cells. Synonyms: TCS2314, TCS 2314, TCS-2314; 1-[[ (3S) -4-[2-[4-[[[ (2-Methylphenyl) amino]carbonyl]amino]phenyl]acety]l-3-morpholinyl]carbonyl]-4-piperidinediacetic acid. Grades: ≥99% by HPLC. CAS No. 317353-73-4. Molecular formula: C28H34N4O6. Mole weight: 522.59. | |
| TCS 2510 | TCS 2510. Group: Biochemicals. Grades: Purified. CAS No. 346673-06-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| TCS 2510 | TCS 2510 is a selective EP4 agonist (EC50 = 2.5 nM; Ki = 1.2 nM) that displays no significant binding at other prostaglandin receptors at concentrations up to 14 μM. EP4 agonist improves bone healing, provides cardio- and neuroprotection, and reduces inflammation and renal dysfunction. Synonyms: TCS 2510, TCS-2510, TCS2510; (5R)-5-[(3S)-3-Hydroxy-4-phenyl-1-buten-1-yl]-1-[6-(2H-tetrazol-5-yl)hexyl]-2-pyrrolidinone; 5-(3-hydroxy-4-phenylbut-1-enyl)-1-[6-(2H-tetrazol-5-yl)hexyl]pyrrolidin-2-one. Grades: ≥98% by HPLC. CAS No. 346673-06-1. Molecular formula: C21H29N5O2. Mole weight: 383.49. | |
| TCS 3035 | TCS 3035. Group: Biochemicals. Grades: Purified. CAS No. 871085-49-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS 3035 | TCS 3035 is a GPR35 agonist (pEC50 = 5.13 and 5.86 for rat and human GPR35 orthologs, respectively). Synonyms: TCS-3035; TCS 3035; TCS3035; 2-[4-[ (Z) - (2, 4-Dioxo-5-thiazolidinylidene) methyl]phenoxyacetic acid; GPR35 Agonist, Compound 10. Grades: ≥98% by HPLC. CAS No. 871085-49-3. Molecular formula: C12H9NO5S. Mole weight: 279.27. | |
| TCS 359 | TCS 359. Group: Biochemicals. Alternative Names: 2- [ (3, 4-Dimethoxybenzoyl) amino]-4, 5, 6, 7-tetrahydrobenzo [b]thiophene-3-carboxamide. Grades: Highly Purified. CAS No. 301305-73-7. Pack Sizes: 10mg. Molecular Formula: C18H20N2O4S, Molecular Weight: 360.43. US Biological Life Sciences. | Worldwide |
| TCS-359 | TCS-359 is a potent inhibitor of FLT3 with IC50 of 42 nM. Synonyms: TCS359, TCS 359, TCS-359. Grades: 0.98. CAS No. 301305-73-7. Molecular formula: C18H20N2O4S. Mole weight: 360.428. | |
| TCS 401 | TCS 401 is a selective inhibitor of protein-tyrosine phosphatase 1B (PTP1B) (Ki = 0.29, 59, 560, 1100, > 2000, > 2000 and > 2000 μM for PTP1B, CD45 D1D2, PTPβ, PTPε D1, SHP-1, PTPα D1 and LAR D1D2, respectively). Several PTPs have been proposed to act as negative regulators of insulin signaling, suggesting PTP as a potential drug target in diabetes. Synonyms: Thieno[2,3-c]pyridine-3-carboxylic acid, 2-[(carboxycarbonyl)amino]-4,5,6,7-tetrahydro-, hydrochloride (1:1); Thieno[2,3-c]pyridine-3-carboxylic acid, 2-[(carboxycarbonyl)amino]-4,5,6,7-tetrahydro-, monohydrochloride; 2-(Carboxyformamido)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylic acid hydrochloride; TCS401; TCS-401; 2-[(Carboxycarbonyl)amino]-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylic acid hydrochloride. Grades: ≥98% by HPLC. CAS No. 243966-09-8. Molecular formula: C10H10N2O5S.HCl. Mole weight: 306.72. | |
| TCS 401 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| TCS 401 | TCS 401. Group: Biochemicals. Grades: Purified. CAS No. 243966-09-8. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TCS 46b | TCS 46b. Group: Biochemicals. Grades: Purified. CAS No. 302799-86-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS 46b | TCS 46b is a subtype-selective NR1A/NR2B NMDA receptor antagonist (IC50 = 5.3, 35000 and > 100000 nM for NR1A/2B, NR1A/2A and NR1A/2C receptor subtypes, respectively). TCS 46b potentiates the effect of L-DOPA in 6-OHDA-lesioned rats following oral administration. Synonyms: 2H-Benzimidazol-2-one, 1,3-dihydro-5-[3-[4-(phenylmethyl)-1-piperidinyl]-1-propyn-1-yl]-; 1,3-Dihydro-5-[3-[4-(phenylmethyl)-1-piperidinyl]-1-propyn-1-yl]-2H-benzimidazol-2-one; 2H-Benzimidazol-2-one, 1,3-dihydro-5-[3-[4-(phenylmethyl)-1-piperidinyl]-1-propynyl]-; 5-(3-(4-benzylpiperidin-1-yl)prop-1-yn-1-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one; TCS 46B. Grades: ≥98% by HPLC. CAS No. 302799-86-6. Molecular formula: C22H23N3O. Mole weight: 345.44. | |
| TCS 5861528 | TCS 5861528 is a selective TRPA1 blocker with IC50 values are 14.3 and 18.7μM respectively), attenuates diabetes mellitus hypersensitivity and displays antinociceptive properties. Uses: A potent and selective trpa1 (trp ankyrin 1) channel antagonist. Synonyms: Chembridge-5861528;TCS5861528, TCS-5861528, TCS 5861528, N-(4-butan-2-ylphenyl)-2-(1,3-dimethyl-2,6-dioxopurin-7-yl)acetamide. Grades: >98 %. CAS No. 332117-28-9. Molecular formula: C19H23N5O3. Mole weight: 369.42. | |
| TCS 5861528 | TCS 5861528. Group: Biochemicals. Grades: Purified. CAS No. 332117-28-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-S 7001 | TC-S 7001 is a potent and highly selective ROCK inhibitor. Its IC50 values are 0.6 and 1.1 nM for ROCK1 and ROCK2, respectively. It exhibits >200-fold selectivity over TRK and FLT3 receptors, and >900-fold selectivity over a panel of other kinases and cardiovascular relevent enzymes and receptors. It reduces blood pressure in normotensive and hypertensive rats. Synonyms: TC-S 7001; TC S 7001; TCS 7001; TC-S-7001; TCS7001; Azaindole-1; Azaindole 1; 6-Chloro-N4-{3,5-difluoro-4-[(3-methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]phenyl}pyrimidine-2,4-diamine;Rho Kinase Inhibitor;ROCK inhibitor;ROCK. Grades: >98 %. CAS No. 867017-68-3. Molecular formula: C18H13ClF2N6O. Mole weight: 402.79. | |
| TC-S 7003 | TC-S 7003. Group: Biochemicals. Grades: Purified. CAS No. 847950-09-8. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TC-S 7005 | TC-S 7005. Group: Biochemicals. Grades: Purified. CAS No. 1082739-92-1. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TC-S 7005 | TC-S 7005 is a potent and selective polo-like kinase 2 (PLK2) inhibitor (IC50 = 4 nM) with selectivity over PLK3 and PLK1 (IC50 = 24 and 214 nM, respectively). TC-S 7005 has been shown to induce mitotic arrest and cell death in HCT 116 colorectal cells. Synonyms: TC-S 7005; TC S 7005; TCS 7005; TCS-7005; TCS7005; 3-(1,3-Benzodioxol-5-yl)-N-[(1S)-1-phenylethyl]-isoxazolo[5,4-c]pyridin-5-amine; 2-amino-isoxazolopyridine. Grades: ≥98% by HPLC. CAS No. 1082739-92-1. Molecular formula: C21H17N3O3. Mole weight: 359.38. | |
| TC-S 7006 | TC-S 7006 is a potent, selective and reversible Tpl2 (Cot; MAP3K8) inhibitor (IC50 = 50 nM) with selectivity for Tpl2 over MEK, p38, Src, MK2, PKC and EGFR. TC-S 7006 was shown to inhibit LPS-induced TNF-α secretion from primary human monocytes and attenuate acute myeloid leukemia (AML) cell proliferation in vitro. TC-S 7006 also suppresses cytolytic activity of human CD8+ cytotoxic T lymphocytes. Synonyms: 4-[(3-Chloro-4-fluorophenyl)amino]-6-[(3-pyridinylmethyl)amino]-1,7-naphthyridine-3-carbonitrile; TC-S 7006; TC S 7006; TCS 7006; Tpl2 Kinase Inhibitor. Grades: ≥99% by HPLC. CAS No. 871307-18-5. Molecular formula: C21H14ClFN6. Mole weight: 404.83. | |
| TC-S 7006 | TC-S 7006. Group: Biochemicals. Grades: Purified. CAS No. 871307-18-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-S 7009 | TC-S 7009. Group: Biochemicals. Grades: Purified. CAS No. 1422955-31-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-S 7009 | TC-S 7009 is a high affinity and selective HIF-2α inhibitor (Kd = 81 nM) that displays >60-fold selectivity for HIF-2α over HIF-1&alpha. TC-S 7009 binds to the HIF-2α PAS-B domain to disrupt HIF-2α-ARNT heterodimerization, decrease HIF-2α DNA-binding and suppress expression of HIF-2α target genes in vitro. Synonyms: TCS 7009; TC S 7009; TC-S 7009; N-(3-Chloro-5-fluorophenyl)-4-nitro-2,1,3-benzoxadiazol-5-amine. Grades: ≥99% by HPLC. CAS No. 1422955-31-4. Molecular formula: C12H6ClFN4O3. Mole weight: 308.65. | |
| TC-S 7010 | TC-S 7010. Group: Biochemicals. Grades: Purified. CAS No. 1158838-45-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS ERK 11e | Potent and selective extracellular signal-related kinase 2 (ERK2) inhibitor (Ki values are <2, 395, 540 and 852 nM for ERK2, GSK-3, Aurora Kinase A and Cdk2 respectively). Potently blocks proliferation of HT29 cells (IC50 = 48 nM). Orally bioavailable. Group: Biochemicals. Grades: Highly Purified. CAS No. 896720-20-0. Pack Sizes: 10mg. Molecular Formula: C24H20Cl2FN5O2. US Biological Life Sciences. | Worldwide |
| TCS ERK 11e (Potent and Selective ERK2 Inhibitor, 4-[2-[(2-Chloro-4-fluorophenyl)amino]-5-methyl-4-pyrimidinyl]-N-[(1S)-1-(3-chlorophenyl)-2-hydroxyethyl]-1H-pyrrole-2-carboxamide) | Potent and selective extracellular signal-related kinase 2 (ERK2) inhibitor (Ki values are <2, 395, 540 and 852nm for ERK2, GSK-3, Aurora Kinase A and Cdk2 respectively). Potently blocks proliferation of HT29 cells (IC50 = 48nm). Orally bioavailable. Group: Biochemicals. Grades: Highly Purified. CAS No. 896720-20-0. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TCS HDAC6 20b | TCS HDAC6 20b. Group: Biochemicals. Grades: Purified. CAS No. 956154-63-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TCS HDAC6 20b | TCS HDAC6 20b is a histone deacetylase 6 (HDAC6) inhibitor. TCS HDAC6 20b inhibits HCT116 growth at a concentration of 5 μM in combination with taxol. It also inhibits growth of MCF-7 cells stimulated by estrogen. Synonyms: NCT-14b; NCT 14b; NCT14b; 2-Methylpropanethioic acid-S-[(6S)-6-[[(1,1-dimethylethoxy)carbonyl]amino]-7-oxo-7-(tricyclo[3.3.1.13,7]dec-1-ylamino)heptyl] ester. Grades: ≥98% by HPLC. CAS No. 956154-63-5. Molecular formula: C26H44N2O4S. Mole weight: 480.7. | |
| TCS JNK 5a | TCS JNK 5a. Group: Biochemicals. Grades: Purified. CAS No. 312917-14-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS JNK 6o | TCS JNK 6o. Group: Biochemicals. Grades: Purified. CAS No. 894804-07-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS JNK 6o | TCS JNK 6o is an ATP-competitive c-Jun N-terminal kinase (JNK) inhibitor with Kis of 2, 4 and 52 nM for JNK1, JNK2 and JNK3, respectively, and IC50s of 45 and 160 nM for JNK1 and JNK2, respectively. It shows >1000-fold selectivity over other kinases, including ERK2 and p38. It can inhibit apoptosis, caspase cleavage and cytochrome C release. Synonyms: JNK Inhibitor VIII; N-(4-Amino-5-cyano-6-ethoxy-2-pyridinyl)-2,5-dimethoxybenzeneacetamide; Benzeneacetamide, N-(4-amino-5-cyano-6-ethoxy-2-pyridinyl)-2,5-dimethoxy-. Grades: ≥98% by HPLC. CAS No. 894804-07-0. Molecular formula: C18H20N4O4. Mole weight: 356.38. | |
| TC SL C5 | TC SL C5 is a metastasis-associated lung adenocarcinoma transcript 1 (Malat1) RNA inhibitor. Synonyms: 5-(4-Methoxyphenyl)-N-[(3-methoxyphenyl)methyl]-1-methyl-1H-Imidazol-2-amine. Grades: ≥98% by HPLC. CAS No. 827327-28-6. Molecular formula: C19H21N3O2. Mole weight: 323.4. | |
| TCS OX2 29 | TCS OX2 29. Group: Biochemicals. Grades: Purified. CAS No. 372523-75-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS OX2 29 | TCS OX2 29 is a potent and selective OX2 receptor antagonist (IC50 = 40 nM) displaying >250-fold selectivity for OX2 over OX1 and a range of receptors, ion channels and transporters. Orexin is a neuropeptide produced in the lateral hypothalamus (LH) regulates arousal, pain and appetite. Synonyms: (2S)-1-(3,4-Dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)-3,3-dimethyl-2-[(4-pyridinylmethyl)amino]-1-butanone hydrochloride. Grades: ≥98% by HPLC. CAS No. 372523-75-6. Molecular formula: C23H31N3O3.HCl. Mole weight: 433.97. | |
| TCS-OX2-29 | TCS-OX2-29 is a potent, high affinities and selective orexin-2 receptor (OX 2 R) antagonist with an IC 50 value of 40 nM and a pK I value of 7.5. TCS-OX2-29 displays ~250-fold selectivity for OX 2 over OX 1 [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 372523-75-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100452. | |
| TCS-OX2-29 HCl | TCS-OX2-29, also known as TCSOX229, is a selective OX2 receptor antagonist (IC50 = 40 nM, pKi=7.5) with >250-fold selectivity for hOX2R compared with hOX1R (IC50s = 40 nM and >10,000 nM, respectively) and a range of receptors, ion channels and transporters. Synonyms: (2S)-1-(3,4-Dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)-3,3-dimethyl-2-[(4-pyridinylmethyl)amino]-1-butanone hydrochloride; TCSOX229, TCSOX-229, TCSOX 229, TCS-OX229; TCS OX2 29; TCS OX229; TCS-OX2-29; TCS OX-229; TCS OX2 29 HCl; TCS OX2 29 hydrochloride. CAS No. 1610882-30-8. Molecular formula: C23H32ClN3O3. Mole weight: 433.97. | |
| TC-SP 14 | TC-SP 14 is a potent and selective S1P1 agonist (EC50 = 0.042 and 3.47 μM for human S1P1 and S1P3, respectively). TC-SP 14 attenuates immune response to antigen challenge and reduces circulating blood lymphocyte counts in a rodent model of delayed-type hypersensitivity. Synonyms: 1-[[3-Fluoro-4-[5-[(2-fluorophenyl)methyl]-2-benzothiazolyl]phenyl]methyl]-3-azetidinecarboxylic acid. Grades: ≥98% by HPLC. CAS No. 1257093-40-5. Molecular formula: C25H20F2N2O2S. Mole weight: 450.5. | |
| 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(sc-204330) is a potent and selective ATP-competitive Pim-1 kianse inhibitor with IC50 of 50 nM, displaying good selectivity over Pim-2 and MEK1/MEK2(IC50s >20,000 nM). Synonyms: TCS PIM-1 1; 491871-58-0; 6-(5-bromo-2-hydroxyphenyl)-2-oxo-4-phenyl-1,2-dihydropyridine-3-carbonitrile; 6-(5-bromo-2-hydroxyphenyl)-2-oxo-4-phenyl-1H-pyridine-3-carbonitrile; CHEMBL391586; CHEBI:86453; 3-Cyano-4-phenyl-6-(3-bromo-6-hydroxy)phenyl-2(1H)-pyridone; C18H11BrN2O2; 2obj; MFCD00276275; PIM1i; pyridone-based compound, 1; TCS PIM-11; TCS-PIM-1-1; SCHEMBL15129618; BDBM26673; EX-A308; HMS3229J17; HMS3742G19; BCP15861; 6-(5-bromo-2-hydroxy-phenyl)-2-oxo-4-phenyl-1H-pyridine-3-carbonitrile; AKOS024457365; CCG-101294; CS-2043; DB08705; AC-35434; AS-16824; HY-18086; FT-0700318; S1050; A871835; Q27097891; SC 204330; SC-204330; SC204330; 3-cyano-4-phenyl-6-(3-bromo-6-hydroxyphenyl)-2-pyridone; 6-(5-bromo-2-hydroxyphenyl)-2-oxo-4-phenyl-1,2-dihydro-pyridine-3-carbonitrile; VRV. CAS No. 491871-58-0. Molecular formula: C18H11BrN2O2. Mole weight: 367.202. | |
| 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 is an ATP-competitive Pim-1 kinase inhibitor. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TCS PIM-1 1; SC204330; SC-204330; SC 204330. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 491871-58-0. Molecular formula: C18H11BrN2O2. Mole weight: 367.2. Purity: >98%. IUPACName: 3-Cyano-4-phenyl-6-(3-bromo-6-hydroxy)phenyl-2(1H)-pyridone. Canonical SMILES: O=C1C(C#N)=C(C2=CC=CC=C2)C=C(C3=C(O)C=CC(Br)=C3)N1. Product ID: ACM491871580. Alfa Chemistry ISO 9001:2015 Certified. Categories: 6-(5-bromo-2-hydroxyphenyl)-2-oxo-4-phenyl-1,2-dihydropyridine-3-carbonitrile. | |
| 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 is an antiprion agent that inhibits protease-resistant prion protein (PrP-res) accumulation in two types of prion-infected mouse neuroblastoma (N2a) cell lines (IC50 = 3 nM). It was also shown to cause the inhibition of PrP expression and a decrease of proliferation and survival in schwannoma cell lines. Synonyms: 2,4-Dihydro-5-(4-nitrophenyl)-2-phenyl-3H-pyrazol-3-one; 5-(4-nitrophenyl)-2-phenyl-4H-pyrazol-3-one. Grades: ≥98% by HPLC. CAS No. 34320-83-7. Molecular formula: C15H11N3O3. Mole weight: 281.27. | |
| 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 |
| TC-T 6000 | TC-T 6000 is a potent equilibrative nucleoside transporter 4 (ENT4) inhibitor (IC50 = 74.4 nM), displaying 20-fold and 80-fold selectivity for ENT4 over ENT2 and ENT1, respectively. Synonyms: TCT6000; TCT 6000; TC-T6000. 2,2'-[[4,8-Bis[bis(2-methylpropyl)amino]pyrimido[5,4-d]pyrimidine-2,6-diyl]diimino]bis-ethanol; Dipyridamole Analogue, 30. Grades: ≥98% by HPLC. CAS No. 949467-71-4. Molecular formula: C26H48N8O2. Mole weight: 504.71. | |
| TcTa | TcTa. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4,4',4-Tris(carbazol-9-yl)triphenylamine. Product Category: Organic Light Emitting Diode (OLED). CAS No. 139092-78-7. Molecular formula: C54H36N4. Mole weight: 740.89 g/mol. Product ID: ACM139092787. Alfa Chemistry ISO 9001:2015 Certified. Categories: Tris(4-carbazoyl-9-ylphenyl)amine, T. C. Taylor. | |
| TCTDSTNCYKAT | TCTDSTNCYKAT is an engineered-variant peptide of antifreeze protein (AFP) [1]. Uses: Scientific research. Group: Peptides. CAS No. 1621188-94-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P3158. | |
| 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 |
| 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. Grades: 99%. CAS No. 1262750-73-1. Molecular formula: C42H50F3N7O9. Mole weight: 853.88. | |
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