D609 PC-PLC inhibitor
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Syk Inhibitor |
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1983-1 | Biovision | each | EUR 151.2 |
Syk Inhibitor |
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1983-5 | Biovision | each | EUR 339.6 |
PKR Inhibitor |
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C4439-10 | ApexBio | 10 mg | EUR 247.2 |
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. |
PKR Inhibitor |
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C4439-25 | ApexBio | 25 mg | EUR 477.6 |
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. |
PKR Inhibitor |
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C4439-5 | ApexBio | 5 mg | EUR 164.4 |
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. |
ITK inhibitor |
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A3509-10 | ApexBio | 10 mg | EUR 927.6 |
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. |
ITK inhibitor |
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A3509-50 | ApexBio | 50 mg | EUR 2448 |
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. |
Lck Inhibitor |
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A3539-1 | ApexBio | 1 mg | EUR 184.8 |
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. |
Lck Inhibitor |
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A3539-5 | ApexBio | 5 mg | EUR 266.4 |
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. |
MEK inhibitor |
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A3594-10 | ApexBio | 10 mg | EUR 895.2 |
Description: A potent MEK inhibitor, Antitumor agent. |
MEK inhibitor |
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A3594-5 | ApexBio | 5 mg | EUR 656.4 |
Description: A potent MEK inhibitor, Antitumor agent. |
MEK inhibitor |
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A3594-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 717.6 |
Description: A potent MEK inhibitor, Antitumor agent. |
CBF? Inhibitor |
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C3398-10 | ApexBio | 10 mg | EUR 243.6 |
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?. |
CBF? Inhibitor |
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C3398-25 | ApexBio | 25 mg | EUR 471.6 |
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?. |
CBF? Inhibitor |
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C3398-5 | ApexBio | 5 mg | EUR 157.2 |
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?. |
DDR Inhibitor |
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HY-W018931 | MedChemExpress | 10mM/1mL | EUR 1197.6 |
Lck Inhibitor |
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HY-12072 | MedChemExpress | 100mg | EUR 2422.8 |
MEK inhibitor |
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HY-12202 | MedChemExpress | 5mg | EUR 514.8 |
CPA inhibitor |
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HY-70005 | MedChemExpress | 50mg | EUR 1556.4 |
PKM2 Inhibitor |
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B2593-25 | Biovision | each | EUR 757.2 |
PKM2 Inhibitor |
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B2593-5 | Biovision | each | EUR 235.2 |
CDK4 inhibitor |
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B1233-10 | ApexBio | 10 mg | EUR 562.8 |
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. |
CDK4 inhibitor |
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B1233-100 | ApexBio | 100 mg | EUR 1910.4 |
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. |
CDK4 inhibitor |
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B1233-25 | ApexBio | 25 mg | EUR 787.2 |
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. |
CDK4 inhibitor |
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B1233-5 | ApexBio | 5 mg | EUR 390 |
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. |
CDK4 inhibitor |
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B1233-50 | ApexBio | 50 mg | EUR 1249.2 |
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. |
Chk2 Inhibitor |
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1702-1 | Biovision | each | EUR 216 |
SCD1 Inhibitor |
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1716-1 | Biovision | each | EUR 261.6 |
SCD1 Inhibitor |
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1716-5 | Biovision | each | EUR 692.4 |
ACC2 Inhibitor |
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1717-1 | Biovision | each | EUR 261.6 |
ACC2 Inhibitor |
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1717-5 | Biovision | each | EUR 823.2 |
BRAF inhibitor |
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A3263-10 | ApexBio | 10 mg | EUR 459.6 |
Description: BRAF inhibitor is a potent BRAF inhibitor. |
BRAF inhibitor |
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A3263-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 537.6 |
Description: BRAF inhibitor is a potent BRAF inhibitor. |
BRAF inhibitor |
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A3263-50 | ApexBio | 50 mg | EUR 1182 |
Description: BRAF inhibitor is a potent BRAF inhibitor. |
CDK9 inhibitor |
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A3294-10 | ApexBio | 10 mg | EUR 393.6 |
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. |
CDK9 inhibitor |
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A3294-100 | ApexBio | 100 mg | EUR 1796.4 |
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. |
CDK9 inhibitor |
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A3294-5 | ApexBio | 5 mg | EUR 236.4 |
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. |
CDK9 inhibitor |
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A3294-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 254.4 |
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. |
CDK9 inhibitor |
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A3294-50 | ApexBio | 50 mg | EUR 1015.2 |
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. |
PDK1 inhibitor |
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A3706-10 | ApexBio | 10 mg | EUR 594 |
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. |
PDK1 inhibitor |
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A3706-100 | ApexBio | 100 mg | EUR 3099.6 |
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. |
PDK1 inhibitor |
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A3706-5 | ApexBio | 5 mg | EUR 348 |
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. |
PDK1 inhibitor |
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A3706-50 | ApexBio | 50 mg | EUR 2067.6 |
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. |
PI3K-? Inhibitor |
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B1869-25 | Biovision | each | EUR 810 |
PI3K-? Inhibitor |
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B1869-5 | Biovision | each | EUR 248.4 |
EGFR Inhibitor |
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C3327-1 | ApexBio | 1 mg | EUR 184.8 |
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. |
EGFR Inhibitor |
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C3327-25 | ApexBio | 25 mg | EUR 1375.2 |
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. |
EGFR Inhibitor |
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C3327-5 | ApexBio | 5 mg | EUR 435.6 |
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. |
NFAT Inhibitor |
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A4539-1 | ApexBio | 1 mg | EUR 165.6 |
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. |
NFAT Inhibitor |
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A4539-10 | ApexBio | 10 mg | EUR 915.6 |
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. |
NFAT Inhibitor |
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A4539-5 | ApexBio | 5 mg | EUR 540 |
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. |
NFAT Inhibitor |
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H-4874.0500 | Bachem | 0.5mg | EUR 327.6 |
Description: Sum Formula: C75H118N20O22S; CAS# [249537-73-3] net |
NFAT Inhibitor |
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H-4874.1000 | Bachem | 1.0mg | EUR 544.8 |
Description: Sum Formula: C75H118N20O22S; CAS# [249537-73-3] net |
NFAT Inhibitor |
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HY-P1026 | MedChemExpress | 5mg | EUR 523.2 |
BRAF inhibitor |
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HY-10247 | MedChemExpress | 10mM/1mL | EUR 424.8 |
Nav1.7 inhibitor |
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HY-13985 | MedChemExpress | 10mM/1mL | EUR 696 |
Renin Inhibitor |
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2084-25 | Biovision | each | EUR 1005.6 |
Renin Inhibitor |
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2084-5 | Biovision | each | EUR 314.4 |
SIRT2 Inhibitor |
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1857-25 | Biovision | each | EUR 523.2 |
SIRT2 Inhibitor |
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1857-5 | Biovision | each | EUR 176.4 |
STAT5 Inhibitor |
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C4105-10 | ApexBio | 10 mg | EUR 235.2 |
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]. |
STAT5 Inhibitor |
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C4105-25 | ApexBio | 25 mg | EUR 451.2 |
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]. |
STAT5 Inhibitor |
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C4105-5 | ApexBio | 5 mg | EUR 151.2 |
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]. |
Stat5 Inhibitor |
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9484-1 | Biovision | each | EUR 144 |
Stat5 Inhibitor |
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9484-5 | Biovision | each | EUR 392.4 |
miRNA Inhibitor |
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M1265-10 | Biovision | each | EUR 666 |
miRNA Inhibitor |
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M1265-2 | Biovision | each | EUR 424.8 |