A-1155463 (BCL-XL Inhibitor)
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R(-)-Gossypol (Bcl-2 inhibitor) |
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SIH-223-50MG | Stressmarq | 50 mg | EUR 763.2 |
Description: The substance R(-)-Gossypol is a bcl-2 inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is dark yellow solid which is soluble to 25 mM in ethanol and in DMSO.. |
Aurora A Inhibitor I |
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A4126-10 | ApexBio | 10 mg | EUR 240 |
Description: IC50: 3.4 nM.Aurora A Inhibitor I is a novel, potent, and selective inhibitor of Aurora A . Aurora kinases are reported to be required for mitosis and to complete cell division. |
Aurora A Inhibitor I |
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A4126-5 | ApexBio | 5 mg | EUR 164.4 |
Description: IC50: 3.4 nM.Aurora A Inhibitor I is a novel, potent, and selective inhibitor of Aurora A . Aurora kinases are reported to be required for mitosis and to complete cell division. |
Aurora A Inhibitor I |
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A4126-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 199.2 |
Description: IC50: 3.4 nM.Aurora A Inhibitor I is a novel, potent, and selective inhibitor of Aurora A . Aurora kinases are reported to be required for mitosis and to complete cell division. |
Aurora A Inhibitor I |
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A4126-50 | ApexBio | 50 mg | EUR 630 |
Description: IC50: 3.4 nM.Aurora A Inhibitor I is a novel, potent, and selective inhibitor of Aurora A . Aurora kinases are reported to be required for mitosis and to complete cell division. |
Aurora A Inhibitor I |
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M75000 | EpiGentek | 5 mg | EUR 1137.06 |
Brefeldin A (GEF inhibitor) |
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SIH-225-25MG | Stressmarq | 25 mg | EUR 346.8 |
Description: The substance Brefeldin A is a gef inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is white crystalline solid which is soluble to 10 mM in ethanol and to 50 mM in DMSO. |
Brefeldin A (GEF inhibitor) |
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SIH-225-5MG | Stressmarq | 5 mg | EUR 145.2 |
Description: The substance Brefeldin A is a gef inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is white crystalline solid which is soluble to 10 mM in ethanol and to 50 mM in DMSO. |
Huperzine A (ACH inhibitor) |
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SIH-365-1MG | Stressmarq | 1 mg | EUR 168 |
Description: The substance Huperzine A is a ach inhibitor. It is synthetically produced and has a purity of >95%. The pure substance is off-white solid which is soluble in DMSO, methanol or ethanol. . |
Huperzine A (ACH inhibitor) |
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SIH-365-5MG | Stressmarq | 5 mg | EUR 444 |
Description: The substance Huperzine A is a ach inhibitor. It is synthetically produced and has a purity of >95%. The pure substance is off-white solid which is soluble in DMSO, methanol or ethanol. . |
Herbimycin A (Hsp90 inhibitor) |
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SIH-116A | Stressmarq | 100 µg | EUR 277.2 |
Description: The substance Herbimycin A is a hsp90 inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is yellow solid which is soluble in DMSO (>25 mg/ml) and ethanol (10 mg/ml). |
Herbimycin A (Hsp90 inhibitor) |
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SIH-116B | Stressmarq | 1 mg | EUR 1183.2 |
Description: The substance Herbimycin A is a hsp90 inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is yellow solid which is soluble in DMSO (>25 mg/ml) and ethanol (10 mg/ml). |
Trichostatin A (HDAC inhibitor) |
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SIH-254-1MG | Stressmarq | 1 mg | EUR 247.2 |
Description: The substance Trichostatin A is a hdac inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is beige solid which is soluble to 10 mM in ethanol and to 50 mM in DMSO. |
Trichostatin A (HDAC inhibitor) |
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SIH-254-5MG | Stressmarq | 5 mg | EUR 735.6 |
Description: The substance Trichostatin A is a hdac inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is beige solid which is soluble to 10 mM in ethanol and to 50 mM in DMSO. |
CCK-A receptor inhibitor 1 |
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HY-U00387 | MedChemExpress | 10mg | EUR 16242 |
Pepstatin A (Aspartic protease inhibitor) |
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SIH-533-25MG | Stressmarq | 25 mg | EUR 319.2 |
Description: The substance Pepstatin A is a aspartic protease inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is off white powder which is soluble in DMSO (5 mg/ml) or ethanol (1 mg/ml). |
Pepstatin A (Aspartic protease inhibitor) |
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SIH-533-5MG | Stressmarq | 5 mg | EUR 158.4 |
Description: The substance Pepstatin A is a aspartic protease inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is off white powder which is soluble in DMSO (5 mg/ml) or ethanol (1 mg/ml). |
DiscoveryPak? HMG Co-A Inhibitor Set |
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S242-5 | Biovision | each | EUR 516 |
Ribunuclease Inhibitor / RNase Inhibitor |
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105-310 | GeneOn | 2000 u | EUR 91.2 |
Ribunuclease Inhibitor / RNase Inhibitor |
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105-350 | GeneOn | 10000 u | EUR 284.4 |
Neurite Outgrowth Inhibitor (Nogo A) Antibody |
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20-abx218403 | Abbexa |
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MAPKII Kinase Inhibitor (Hsp25 Kinase Inhibitor) |
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SIH-120A | Stressmarq | 1 mg | EUR 214.8 |
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. |
GST Inhibitor-1 (Cibacron Blue 3G-A, Sodium Salt) |
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1555R-1000 | Biovision | each | EUR 248.4 |
Antizyme Inhibitor 1 (Antizyme inhibitor 1) Antibody |
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abx230450-100ug | Abbexa | 100 ug | EUR 577.2 |
Antizyme Inhibitor 1 (Antizyme Inhibitor 1) Antibody |
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20-abx111016 | Abbexa |
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Monoamine Oxidase A (MAO-A) Inhibitor Screening Kit (Fluorometric) |
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K796-100 | Biovision | each | EUR 770.4 |
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 |
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?. |
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. |
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 |
DDR Inhibitor |
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HY-W018931 | MedChemExpress | 10mM/1mL | EUR 1197.6 |
CPA inhibitor |
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HY-70005 | MedChemExpress | 50mg | EUR 1556.4 |
Plasminogen activator inhibitor 2 type A Antibody |
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20-abx109400 | Abbexa |
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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. |
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. |
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. |
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 |
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 |
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. |