S63845MCL1 inhibitor
S63845MCL1 inhibitor
To Order Contact us: caitlyn@ucb-bioproducts.com
 Ribunuclease Inhibitor / RNase Inhibitor |
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| 105-350 | GeneOn | 10000 u | EUR 237 |
) MAPKII Kinase Inhibitor (Hsp25 Kinase Inhibitor) |
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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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 Renin Inhibitor |
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| 2084-25 | Biovision | EUR 838 | |
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Renin Inhibitor |
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| 2084-5 | Biovision | EUR 262 | |
 Apoptosis inhibitor |
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| 2783-25 | Biovision | EUR 457 | |
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Apoptosis inhibitor |
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| 2783-5 | Biovision | EUR 153 | |
 Papain Inhibitor |
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| A1035-25 | ApexBio | 25 mg | EUR 90 |
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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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 Chk2 Inhibitor |
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| 1702-1 | Biovision | EUR 180 | |
 SCD1 Inhibitor |
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| 1716-1 | Biovision | EUR 218 | |
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SCD1 Inhibitor |
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| 1716-5 | Biovision | EUR 577 | |
 ACC2 Inhibitor |
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| 1717-1 | Biovision | EUR 218 | |
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ACC2 Inhibitor |
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| 1717-5 | Biovision | EUR 686 | |
 SIRT2 Inhibitor |
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| 1857-25 | Biovision | EUR 436 | |
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SIRT2 Inhibitor |
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| 1857-5 | Biovision | EUR 147 | |
 Elastase Inhibitor |
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| 1922-5 | Biovision | EUR 262 | |
 Myeloperoxidase Inhibitor |
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| 1977-100 | Biovision | EUR 115 | |
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Myeloperoxidase Inhibitor |
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| 1977-500 | Biovision | EUR 240 | |
 Syk Inhibitor |
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| 1983-1 | Biovision | EUR 126 | |
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Syk Inhibitor |
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| 1983-5 | Biovision | EUR 283 | |
 Kallikrein Inhibitor |
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| 5-01416 | CHI Scientific | 4 x 5mg | Ask for price |
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Papain Inhibitor |
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| 5-01715 | CHI Scientific | 10mg | Ask for price |
 Endotoxin Inhibitor |
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| 5-01105 | CHI Scientific | 4 x 1mg | Ask for price |
 Trypsin inhibitor |
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| 44R-1107 | Fitzgerald | 50 gram | EUR 3589 |
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Description: Trypsin inhibitor enzyme |
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 PI3K-? Inhibitor |
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| B1869-25 | Biovision | EUR 675 | |
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PI3K-? Inhibitor |
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| B1869-5 | Biovision | EUR 207 | |
 PKM2 Inhibitor |
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| B2593-25 | Biovision | EUR 631 | |
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PKM2 Inhibitor |
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| B2593-5 | Biovision | EUR 196 | |
 CDK4 inhibitor |
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| B1233-10 | ApexBio | 10 mg | EUR 469 |
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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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CDK4 inhibitor |
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| B1233-100 | ApexBio | 100 mg | EUR 1592 |
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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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CDK4 inhibitor |
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| B1233-25 | ApexBio | 25 mg | EUR 656 |
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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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CDK4 inhibitor |
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| B1233-5 | ApexBio | 5 mg | EUR 325 |
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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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CDK4 inhibitor |
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| B1233-50 | ApexBio | 50 mg | EUR 1041 |
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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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Trypsin inhibitor |
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| AT160 | Unibiotest | 1mg | EUR 1368 |
 Stat5 Inhibitor |
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| 9484-1 | Biovision | EUR 120 | |
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Stat5 Inhibitor |
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| 9484-5 | Biovision | EUR 327 | |
 Rinbonuclease Inhibitor |
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| abx098030-10kU | Abbexa | 10 kU | EUR 537 |
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Rinbonuclease Inhibitor |
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| abx098030-2kU | Abbexa | 2 kU | EUR 425 |
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 XL647Kinase Inhibitor |
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| E1KS1083 | EnoGene | 5 mg | EUR 873 |
 PKR Inhibitor |
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| C4439-10 | ApexBio | 10 mg | EUR 206 |
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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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PKR Inhibitor |
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| C4439-25 | ApexBio | 25 mg | EUR 398 |
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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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PKR Inhibitor |
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| C4439-5 | ApexBio | 5 mg | EUR 137 |
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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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 EGFR Inhibitor |
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| C3327-1 | ApexBio | 1 mg | EUR 154 |
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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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EGFR Inhibitor |
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| C3327-25 | ApexBio | 25 mg | EUR 1146 |
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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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EGFR Inhibitor |
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| C3327-5 | ApexBio | 5 mg | EUR 363 |
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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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 CBF? Inhibitor |
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| C3398-10 | ApexBio | 10 mg | EUR 203 |
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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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CBF? Inhibitor |
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| C3398-25 | ApexBio | 25 mg | EUR 393 |
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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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CBF? Inhibitor |
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| C3398-5 | ApexBio | 5 mg | EUR 131 |
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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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 STAT5 Inhibitor |
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| C4105-10 | ApexBio | 10 mg | EUR 196 |
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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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STAT5 Inhibitor |
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| C4105-25 | ApexBio | 25 mg | EUR 376 |
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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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STAT5 Inhibitor |
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| C4105-5 | ApexBio | 5 mg | EUR 126 |
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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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Trypsin inhibitor |
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| AG160 | Unibiotest | 1 mg | EUR 523 |
 BRAF inhibitor |
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| A3263-10 | ApexBio | 10 mg | EUR 383 |
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Description: BRAF inhibitor is a potent BRAF inhibitor. |
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BRAF inhibitor |
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| A3263-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 448 |
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Description: BRAF inhibitor is a potent BRAF inhibitor. |
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BRAF inhibitor |
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| A3263-50 | ApexBio | 50 mg | EUR 985 |
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Description: BRAF inhibitor is a potent BRAF inhibitor. |
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 CDK9 inhibitor |
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| A3294-10 | ApexBio | 10 mg | EUR 328 |
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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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CDK9 inhibitor |
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| A3294-100 | ApexBio | 100 mg | EUR 1497 |
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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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CDK9 inhibitor |
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| A3294-5 | ApexBio | 5 mg | EUR 197 |
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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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CDK9 inhibitor |
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| A3294-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 212 |
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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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CDK9 inhibitor |
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| A3294-50 | ApexBio | 50 mg | EUR 846 |
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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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 ITK inhibitor |
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| A3509-10 | ApexBio | 10 mg | EUR 773 |
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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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ITK inhibitor |
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| A3509-50 | ApexBio | 50 mg | EUR 2040 |
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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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 Lck Inhibitor |
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| A3539-1 | ApexBio | 1 mg | EUR 154 |
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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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Lck Inhibitor |
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| A3539-5 | ApexBio | 5 mg | EUR 222 |
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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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 MEK inhibitor |
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| A3594-10 | ApexBio | 10 mg | EUR 746 |
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Description: A potent MEK inhibitor, Antitumor agent. |
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MEK inhibitor |
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| A3594-5 | ApexBio | 5 mg | EUR 547 |
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Description: A potent MEK inhibitor, Antitumor agent. |
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MEK inhibitor |
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| A3594-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 598 |
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Description: A potent MEK inhibitor, Antitumor agent. |
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 PDK1 inhibitor |
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| A3706-10 | ApexBio | 10 mg | EUR 495 |
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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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PDK1 inhibitor |
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| A3706-100 | ApexBio | 100 mg | EUR 2583 |
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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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PDK1 inhibitor |
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| A3706-5 | ApexBio | 5 mg | EUR 290 |
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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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PDK1 inhibitor |
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| A3706-50 | ApexBio | 50 mg | EUR 1723 |
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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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 Apoptosis Inhibitor |
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| A1930-10 | ApexBio | 10 mg | EUR 142 |
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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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Apoptosis Inhibitor |
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| A1930-100 | ApexBio | 100 mg | EUR 456 |
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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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Apoptosis Inhibitor |
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| A1930-25 | ApexBio | 25 mg | EUR 235 |
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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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Apoptosis Inhibitor |
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| A1930-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 108 |
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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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Apoptosis Inhibitor |
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| A1930-S | ApexBio | Evaluation Sample | EUR 81 |
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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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Elastase Inhibitor |
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| A2579-5 | ApexBio | 5 mg | EUR 166 |
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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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 NFAT Inhibitor |
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| A4539-1 | ApexBio | 1 mg | EUR 138 |
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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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NFAT Inhibitor |
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| A4539-10 | ApexBio | 10 mg | EUR 763 |
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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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NFAT Inhibitor |
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| A4539-5 | ApexBio | 5 mg | EUR 450 |
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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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 Neurotoxin Inhibitor |
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| HY-112722 | MedChemExpress | 10mM/1mL | EUR 744 |
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Lck Inhibitor |
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| HY-12072 | MedChemExpress | 100mg | EUR 2019 |
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MEK inhibitor |
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| HY-12202 | MedChemExpress | 5mg | EUR 429 |
 Nav1.7 inhibitor |
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| HY-13985 | MedChemExpress | 10mM/1mL | EUR 580 |
 PLpro inhibitor |
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| HY-17542 | MedChemExpress | 5mg | EUR 533 |
 CPA inhibitor |
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| HY-70005 | MedChemExpress | 50mg | EUR 1297 |
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NFAT Inhibitor |
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| HY-P1026 | MedChemExpress | 5mg | EUR 436 |
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BRAF inhibitor |
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| HY-10247 | MedChemExpress | 10mM/1mL | EUR 354 |
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Endotoxin Inhibitor |
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| H-1382.0001 | Bachem | 1.0mg | EUR 113 |
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Description: Sum Formula: C55H97N15O12S2; CAS# [147396-10-9] |
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Endotoxin Inhibitor |
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| H-1382.0005 | Bachem | 5.0mg | EUR 318 |
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Description: Sum Formula: C55H97N15O12S2; CAS# [147396-10-9] |
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NFAT Inhibitor |
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| H-4874.0500 | Bachem | 0.5mg | EUR 273 |
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Description: Sum Formula: C75H118N20O22S; CAS# [249537-73-3] net |
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NFAT Inhibitor |
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| H-4874.1000 | Bachem | 1.0mg | EUR 454 |
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Description: Sum Formula: C75H118N20O22S; CAS# [249537-73-3] net |
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 DDR Inhibitor |
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| HY-W018931 | MedChemExpress | 10mM/1mL | EUR 998 |
 miRNA Inhibitor |
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| M1265-10 | Biovision | EUR 555 | |
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miRNA Inhibitor |
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| M1265-2 | Biovision | EUR 354 | |