S63845MCL1 inhibitor
S63845MCL1 inhibitor
To Order Contact us: caitlyn@ucb-bioproducts.com
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105-350 | GeneOn | 10000 u | EUR 237 |
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SIH-120A | Stressmarq | 1 mg | EUR 179 |
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Description: The substance MAPKII Kinase Inhibitor is a hsp25 kinase inhibitor. It is synthetically produced and has a purity of >95%. The pure substance is white solid which is soluble in DMSO or H20. |
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2084-25 | Biovision | EUR 838 |
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2084-5 | Biovision | EUR 262 |
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2783-25 | Biovision | EUR 457 |
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2783-5 | Biovision | EUR 153 |
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A1035-25 | ApexBio | 25 mg | EUR 90 |
Description: Papain Inhibitor peptide,(C19H29N7O6),a peptide with the sequence H-Gly-Gly-Tyr-Arg-OH,MW= 451.4,this peptide Inhibits the peptidase activity of Papain. |
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1702-1 | Biovision | EUR 180 |
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1716-1 | Biovision | EUR 218 |
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1716-5 | Biovision | EUR 577 |
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1717-1 | Biovision | EUR 218 |
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1717-5 | Biovision | EUR 686 |
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1857-25 | Biovision | EUR 436 |
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1857-5 | Biovision | EUR 147 |
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1922-5 | Biovision | EUR 262 |
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1977-100 | Biovision | EUR 115 |
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1977-500 | Biovision | EUR 240 |
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1983-1 | Biovision | EUR 126 |
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1983-5 | Biovision | EUR 283 |
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5-01416 | CHI Scientific | 4 x 5mg | Ask for price |
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5-01715 | CHI Scientific | 10mg | Ask for price |
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5-01105 | CHI Scientific | 4 x 1mg | Ask for price |
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44R-1107 | Fitzgerald | 50 gram | EUR 3589 |
Description: Trypsin inhibitor enzyme |
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B1869-25 | Biovision | EUR 675 |
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B1869-5 | Biovision | EUR 207 |
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B2593-25 | Biovision | EUR 631 |
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B2593-5 | Biovision | EUR 196 |
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B1233-10 | ApexBio | 10 mg | EUR 469 |
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family. |
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B1233-100 | ApexBio | 100 mg | EUR 1592 |
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family. |
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B1233-25 | ApexBio | 25 mg | EUR 656 |
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family. |
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B1233-5 | ApexBio | 5 mg | EUR 325 |
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family. |
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B1233-50 | ApexBio | 50 mg | EUR 1041 |
Description: CDK4 inhibitor is a selective inhibitor of cyclin-dependent kinase 4 with IC50 value of 10 nM [1].Cyclin-dependent kinase 4 (CDK4) is a Ser/Thr protein kinase and is a member of the cyclin-dependent kinase family. |
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AT160 | Unibiotest | 1mg | EUR 1368 |
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9484-1 | Biovision | EUR 120 |
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9484-5 | Biovision | EUR 327 |
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abx098030-10kU | Abbexa | 10 kU | EUR 537 |
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abx098030-2kU | Abbexa | 2 kU | EUR 425 |
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E1KS1083 | EnoGene | 5 mg | EUR 873 |
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C4439-10 | ApexBio | 10 mg | EUR 206 |
Description: IC50: 186-210 nMPKR Inhibitor is a double-stranded RNA-activated protein kinase (PKR) inhibitor. Initiation of protein synthesis is reported to be regulated by kinase-dependent phosphorylation reactions. |
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C4439-25 | ApexBio | 25 mg | EUR 398 |
Description: IC50: 186-210 nMPKR Inhibitor is a double-stranded RNA-activated protein kinase (PKR) inhibitor. Initiation of protein synthesis is reported to be regulated by kinase-dependent phosphorylation reactions. |
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C4439-5 | ApexBio | 5 mg | EUR 137 |
Description: IC50: 186-210 nMPKR Inhibitor is a double-stranded RNA-activated protein kinase (PKR) inhibitor. Initiation of protein synthesis is reported to be regulated by kinase-dependent phosphorylation reactions. |
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C3327-1 | ApexBio | 1 mg | EUR 154 |
Description: EGFR inhibitor is a cell permeable, pyrimidine compound that selectively inhibits the EGFR kinase with IC50 value of 21 nM [1]. EGFR is a transmembrane protein, and is a receptor for members of epidermal growth factor family. |
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C3327-25 | ApexBio | 25 mg | EUR 1146 |
Description: EGFR inhibitor is a cell permeable, pyrimidine compound that selectively inhibits the EGFR kinase with IC50 value of 21 nM [1]. EGFR is a transmembrane protein, and is a receptor for members of epidermal growth factor family. |
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C3327-5 | ApexBio | 5 mg | EUR 363 |
Description: EGFR inhibitor is a cell permeable, pyrimidine compound that selectively inhibits the EGFR kinase with IC50 value of 21 nM [1]. EGFR is a transmembrane protein, and is a receptor for members of epidermal growth factor family. |
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C3398-10 | ApexBio | 10 mg | EUR 203 |
Description: CBF? inhibitor is a small molecule which binds to CBF? and inhibits its association with Runx1 [1].Core binding factors (CBFs) are heterodimeric transcription factors containing a DNA-binding CBF? component (a RUNX protein) and an enhancer of binding, CBF?. |
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C3398-25 | ApexBio | 25 mg | EUR 393 |
Description: CBF? inhibitor is a small molecule which binds to CBF? and inhibits its association with Runx1 [1].Core binding factors (CBFs) are heterodimeric transcription factors containing a DNA-binding CBF? component (a RUNX protein) and an enhancer of binding, CBF?. |
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C3398-5 | ApexBio | 5 mg | EUR 131 |
Description: CBF? inhibitor is a small molecule which binds to CBF? and inhibits its association with Runx1 [1].Core binding factors (CBFs) are heterodimeric transcription factors containing a DNA-binding CBF? component (a RUNX protein) and an enhancer of binding, CBF?. |
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C4105-10 | ApexBio | 10 mg | EUR 196 |
Description: STAT5 Inhibitor is a cell-permeable inhibitor of STAT5 with IC50 value of 47 ?M against STAT5? SH2 domain EPO peptide binding activity [1]. |
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C4105-25 | ApexBio | 25 mg | EUR 376 |
Description: STAT5 Inhibitor is a cell-permeable inhibitor of STAT5 with IC50 value of 47 ?M against STAT5? SH2 domain EPO peptide binding activity [1]. |
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C4105-5 | ApexBio | 5 mg | EUR 126 |
Description: STAT5 Inhibitor is a cell-permeable inhibitor of STAT5 with IC50 value of 47 ?M against STAT5? SH2 domain EPO peptide binding activity [1]. |
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AG160 | Unibiotest | 1 mg | EUR 523 |
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A3263-10 | ApexBio | 10 mg | EUR 383 |
Description: BRAF inhibitor is a potent BRAF inhibitor. |
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A3263-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 448 |
Description: BRAF inhibitor is a potent BRAF inhibitor. |
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A3263-50 | ApexBio | 50 mg | EUR 985 |
Description: BRAF inhibitor is a potent BRAF inhibitor. |
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A3294-10 | ApexBio | 10 mg | EUR 328 |
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes. |
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A3294-100 | ApexBio | 100 mg | EUR 1497 |
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes. |
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A3294-5 | ApexBio | 5 mg | EUR 197 |
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes. |
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A3294-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 212 |
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes. |
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A3294-50 | ApexBio | 50 mg | EUR 846 |
Description: CDK9 inhibitor is a small-molecule selective inhibitor of CDK9 (cyclin dependent kinase 9) with IC50 value of 39 nM [1].CDKs are a group of serine/threonine kinases and are widely spread in all known eukaryotes. |
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A3509-10 | ApexBio | 10 mg | EUR 773 |
Description: Interleukin-2-inducible T cell kinase (ITK) is a non-receptor tyrosine kinase expressed in T cells, NKT cells and mast cells which plays a crucial role in regulating the T cell receptor (TCR), CD28, CD2, chemokine receptor CXCR4, and FcepsilonR-mediated signaling pathways. |
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A3509-50 | ApexBio | 50 mg | EUR 2040 |
Description: Interleukin-2-inducible T cell kinase (ITK) is a non-receptor tyrosine kinase expressed in T cells, NKT cells and mast cells which plays a crucial role in regulating the T cell receptor (TCR), CD28, CD2, chemokine receptor CXCR4, and FcepsilonR-mediated signaling pathways. |
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A3539-1 | ApexBio | 1 mg | EUR 154 |
Description: Lck Inhibitor is a small-molecule inhibitor of with IC50 value of 7 nM [1].The lymphocyte specific kinase which expressed in NK cells and T-cells is a member of the Src kinase family. |
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A3539-5 | ApexBio | 5 mg | EUR 222 |
Description: Lck Inhibitor is a small-molecule inhibitor of with IC50 value of 7 nM [1].The lymphocyte specific kinase which expressed in NK cells and T-cells is a member of the Src kinase family. |
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A3594-10 | ApexBio | 10 mg | EUR 746 |
Description: A potent MEK inhibitor, Antitumor agent. |
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A3594-5 | ApexBio | 5 mg | EUR 547 |
Description: A potent MEK inhibitor, Antitumor agent. |
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A3594-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 598 |
Description: A potent MEK inhibitor, Antitumor agent. |
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A3706-10 | ApexBio | 10 mg | EUR 495 |
Description: PDK1 inhibitor is an potent and selective inhibitor of PDK1 with potential as anticancer agent. GSK 2334470,a inhibitor of PDK1, has IC50 value of 0.00251µM and CHEMBL1172241 with IC50 value of 0.085µM. |
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A3706-100 | ApexBio | 100 mg | EUR 2583 |
Description: PDK1 inhibitor is an potent and selective inhibitor of PDK1 with potential as anticancer agent. GSK 2334470,a inhibitor of PDK1, has IC50 value of 0.00251µM and CHEMBL1172241 with IC50 value of 0.085µM. |
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A3706-5 | ApexBio | 5 mg | EUR 290 |
Description: PDK1 inhibitor is an potent and selective inhibitor of PDK1 with potential as anticancer agent. GSK 2334470,a inhibitor of PDK1, has IC50 value of 0.00251µM and CHEMBL1172241 with IC50 value of 0.085µM. |
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A3706-50 | ApexBio | 50 mg | EUR 1723 |
Description: PDK1 inhibitor is an potent and selective inhibitor of PDK1 with potential as anticancer agent. GSK 2334470,a inhibitor of PDK1, has IC50 value of 0.00251µM and CHEMBL1172241 with IC50 value of 0.085µM. |
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A1930-10 | ApexBio | 10 mg | EUR 142 |
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay. |
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A1930-100 | ApexBio | 100 mg | EUR 456 |
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay. |
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A1930-25 | ApexBio | 25 mg | EUR 235 |
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay. |
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A1930-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 108 |
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay. |
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A1930-S | ApexBio | Evaluation Sample | EUR 81 |
Description: M50054, 2,2'-methylenebis (1,3-cyclohexanedione), is a novel inhibitor of apoptosis. [1] In human Fas-expressing WC8 cells, M50054 inhibited apoptosis by soluble human Fas ligand in vitro cell death assay. |
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A2579-5 | ApexBio | 5 mg | EUR 166 |
Description: A potent, irreversible inhibitor of human neutrophil elastase (HNE). The structure of the enzyme-inhibitor complex reveals crosslinking of the catalytic residues His-57 and Ser-195 by the peptidyl chloromethylketone. |
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A4539-1 | ApexBio | 1 mg | EUR 138 |
Description: Selective inhibitor of calcineurin-mediated dephosphorylation of nuclear factor of activated T cells (NFAT). Does not disrupt other calcineurin-dependent pathways. Inhibits NFAT activation and NFAT-dependent expression of endogenous cytokine genes in T cells. |
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A4539-10 | ApexBio | 10 mg | EUR 763 |
Description: Selective inhibitor of calcineurin-mediated dephosphorylation of nuclear factor of activated T cells (NFAT). Does not disrupt other calcineurin-dependent pathways. Inhibits NFAT activation and NFAT-dependent expression of endogenous cytokine genes in T cells. |
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A4539-5 | ApexBio | 5 mg | EUR 450 |
Description: Selective inhibitor of calcineurin-mediated dephosphorylation of nuclear factor of activated T cells (NFAT). Does not disrupt other calcineurin-dependent pathways. Inhibits NFAT activation and NFAT-dependent expression of endogenous cytokine genes in T cells. |
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HY-112722 | MedChemExpress | 10mM/1mL | EUR 744 |
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HY-12072 | MedChemExpress | 100mg | EUR 2019 |
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HY-12202 | MedChemExpress | 5mg | EUR 429 |
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HY-13985 | MedChemExpress | 10mM/1mL | EUR 580 |
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HY-17542 | MedChemExpress | 5mg | EUR 533 |
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HY-70005 | MedChemExpress | 50mg | EUR 1297 |
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HY-P1026 | MedChemExpress | 5mg | EUR 436 |
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HY-10247 | MedChemExpress | 10mM/1mL | EUR 354 |
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H-1382.0001 | Bachem | 1.0mg | EUR 113 |
Description: Sum Formula: C55H97N15O12S2; CAS# [147396-10-9] |
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H-1382.0005 | Bachem | 5.0mg | EUR 318 |
Description: Sum Formula: C55H97N15O12S2; CAS# [147396-10-9] |
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H-4874.0500 | Bachem | 0.5mg | EUR 273 |
Description: Sum Formula: C75H118N20O22S; CAS# [249537-73-3] net |
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H-4874.1000 | Bachem | 1.0mg | EUR 454 |
Description: Sum Formula: C75H118N20O22S; CAS# [249537-73-3] net |
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HY-W018931 | MedChemExpress | 10mM/1mL | EUR 998 |
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M1265-10 | Biovision | EUR 555 |
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M1265-2 | Biovision | EUR 354 |