PD-0325901
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EZSolution? PD-0325901, Sterile-Filtered |
1990-1 |
Biovision |
each |
EUR 326.4 |
PD-1/PD-L1 Inhibitor 2 |
B1050-25 |
Biovision |
each |
EUR 679.2 |
PD-1/PD-L1 Inhibitor 2 |
B1050-5 |
Biovision |
each |
EUR 242.4 |
PD-1/PD-L1 Inhibitor 1 |
B1213-25 |
Biovision |
each |
EUR 679.2 |
PD-1/PD-L1 inhibitor 2 |
B6023-25 |
ApexBio |
25 mg |
EUR 525.6 |
Description: PD-1/PD-L1 inhibitor 2 is a PD-1/PD-L1 interaction inhibitor. |
PD-1/PD-L1 inhibitor 2 |
B6023-5 |
ApexBio |
5 mg |
EUR 205.2 |
Description: PD-1/PD-L1 inhibitor 2 is a PD-1/PD-L1 interaction inhibitor. |
PD-1/PD-L1 inhibitor 1 |
B6172-25 |
ApexBio |
25 mg |
EUR 543.6 |
Description: IC50: 0.006-0.10 ?MPD-1/PD-L1 inhibitor 1 is a PD-1/PD-L1 interaction inhibitor.Plenty of studies show that blocking the PD-1/PD-Ll interactions can lead to the restorage and augment of T cell activation in many systems. |
PD-1/PD-L1 inhibitor 1 |
B6172-5 |
ApexBio |
5 mg |
EUR 201.6 |
Description: IC50: 0.006-0.10 ?MPD-1/PD-L1 inhibitor 1 is a PD-1/PD-L1 interaction inhibitor.Plenty of studies show that blocking the PD-1/PD-Ll interactions can lead to the restorage and augment of T cell activation in many systems. |
PD 151746 |
B4791-100 |
ApexBio |
100 mg |
EUR 714 |
Description: PD 151746 is a potent and selective inhibitor of calpain with Ki value of 0.26 ?M for ?-Calpain. Calpain is a calcium-dependent, non-lysosomal cysteine protease that expressed in mammals and many other organisms. |
PD 151746 |
B4791-25 |
ApexBio |
25 mg |
EUR 338.4 |
Description: PD 151746 is a potent and selective inhibitor of calpain with Ki value of 0.26 ?M for ?-Calpain. Calpain is a calcium-dependent, non-lysosomal cysteine protease that expressed in mammals and many other organisms. |
PD 151746 |
B4791-5 |
ApexBio |
5 mg |
EUR 142.8 |
Description: PD 151746 is a potent and selective inhibitor of calpain with Ki value of 0.26 ?M for ?-Calpain. Calpain is a calcium-dependent, non-lysosomal cysteine protease that expressed in mammals and many other organisms. |
PD 151746 |
B4791-5.1 |
ApexBio |
10 mM (in 1mL DMSO) |
EUR 151.2 |
Description: PD 151746 is a potent and selective inhibitor of calpain with Ki value of 0.26 ?M for ?-Calpain. Calpain is a calcium-dependent, non-lysosomal cysteine protease that expressed in mammals and many other organisms. |
PD 334581 |
B5727-10 |
ApexBio |
10 mg |
EUR 583.2 |
PD 334581 |
B5727-50 |
ApexBio |
50 mg |
EUR 2220 |
PD 173074 |
1675-100 |
Biovision |
each |
Ask for price |
PD 173074 |
27056 |
BPS Bioscience |
10 mg |
EUR 125 |
Description: PD 173074 inhibited the kinase activity of FGFR1 with an IC50 of 25 nM in vitro, while inhibiting Src, the receptors for insulin, epidermal growth factor (EGF) and PDGF, and several serine/threonine kinases with 1000-fold or higher IC50 values. PD 173074 was an ATP-competitive inhibitor of FGFR1, with a Ki of around 40 nM. PD 173074 inhibited autophosphorylation of FGFR1 and VEGFR2 in a dose-dependent manner with IC50s in the range of 1-5 nM and 100-200 nM, respectively. |
PD 184161 |
C4361-10 |
ApexBio |
10 mg |
EUR 339.6 |
Description: IC50: 10-100 nMPD 184161 is a MEK1/2 inhibitor. The intracellular signaling pathway of mitogen-activated protein kinases is involved in the regulation of various cellular functions. |
PD 184161 |
C4361-25 |
ApexBio |
25 mg |
EUR 673.2 |
Description: IC50: 10-100 nMPD 184161 is a MEK1/2 inhibitor. The intracellular signaling pathway of mitogen-activated protein kinases is involved in the regulation of various cellular functions. |
PD 184161 |
C4361-5 |
ApexBio |
5 mg |
EUR 217.2 |
Description: IC50: 10-100 nMPD 184161 is a MEK1/2 inhibitor. The intracellular signaling pathway of mitogen-activated protein kinases is involved in the regulation of various cellular functions. |
PD 166326 |
C3677-1 |
ApexBio |
1 mg |
EUR 193.2 |
Description: IC50: 8 nM for c-abl PD 166326 is a receptor tyrosine kinase inhibitor.Receptor tyrosine kinases are the high-affinity cell surface receptors for many growth factors, cytokines, as well as hormones. |
PD 166326 |
C3677-10 |
ApexBio |
10 mg |
EUR 1128 |
Description: IC50: 8 nM for c-abl PD 166326 is a receptor tyrosine kinase inhibitor.Receptor tyrosine kinases are the high-affinity cell surface receptors for many growth factors, cytokines, as well as hormones. |
PD 166326 |
C3677-5 |
ApexBio |
5 mg |
EUR 661.2 |
Description: IC50: 8 nM for c-abl PD 166326 is a receptor tyrosine kinase inhibitor.Receptor tyrosine kinases are the high-affinity cell surface receptors for many growth factors, cytokines, as well as hormones. |
PD 176252 |
B7122-10 |
ApexBio |
10 mg |
EUR 614.4 |
PD 198306 |
B7124-1 |
ApexBio |
1 mg |
EUR 151.2 |
Description: IC50: 8 nM for MEK [1]PD 198306 is a potent, selective and non-ATP competitive MAPK/ERK-kinase (MEK) inhibitor. MEK is a kinase enzyme which phosphorylates mitogen-activated protein kinase (MAPK). |
PD 198306 |
B7124-10 |
ApexBio |
10 mg |
EUR 634.8 |
Description: IC50: 8 nM for MEK [1]PD 198306 is a potent, selective and non-ATP competitive MAPK/ERK-kinase (MEK) inhibitor. MEK is a kinase enzyme which phosphorylates mitogen-activated protein kinase (MAPK). |
PD 198306 |
B7124-5 |
ApexBio |
5 mg |
EUR 381.6 |
Description: IC50: 8 nM for MEK [1]PD 198306 is a potent, selective and non-ATP competitive MAPK/ERK-kinase (MEK) inhibitor. MEK is a kinase enzyme which phosphorylates mitogen-activated protein kinase (MAPK). |
PD 135158 |
B7127-10 |
ApexBio |
10 mg |
EUR 583.2 |
PD 135158 |
B7127-50 |
ApexBio |
50 mg |
EUR 2220 |
PD 158780 |
B7130-10 |
ApexBio |
10 mg |
EUR 278.4 |
PD 158780 |
B7130-25 |
ApexBio |
25 mg |
EUR 543.6 |
PD 158780 |
B7130-5 |
ApexBio |
5 mg |
EUR 181.2 |
PD 118057 |
B7203-10 |
ApexBio |
10 mg |
EUR 400.8 |
PD 118057 |
B7203-50 |
ApexBio |
50 mg |
EUR 1491.6 |
PD 146176 |
B7208-10 |
ApexBio |
10 mg |
EUR 180 |
PD 146176 |
B7208-25 |
ApexBio |
25 mg |
EUR 344.4 |
PD 146176 |
B7208-50 |
ApexBio |
50 mg |
EUR 567.6 |
PD 173212 |
B7424-10 |
ApexBio |
10 mg |
EUR 634.8 |
PD 173212 |
B7424-5 |
ApexBio |
5 mg |
EUR 451.2 |
PD 173212 |
B7424-5.1 |
ApexBio |
10 mM (in 1mL DMSO) |
EUR 574.8 |
PD 161570 |
B7486-10 |
ApexBio |
10 mg |
EUR 544.8 |
PD 161570 |
B7486-50 |
ApexBio |
50 mg |
EUR 2056.8 |
PD 150606 |
A4413-25 |
ApexBio |
25 mg |
EUR 513.6 |
Description: PD 150606 is a specific inhibitor of calpain with Ki value of 0.21 ?M and 0.37 ?M for mu- and m- calpains, respectively [1]. |
PD 150606 |
A4413-5 |
ApexBio |
5 mg |
EUR 172.8 |
Description: PD 150606 is a specific inhibitor of calpain with Ki value of 0.21 ?M and 0.37 ?M for mu- and m- calpains, respectively [1]. |
PD 166793 |
A4438-10 |
ApexBio |
10 mg |
EUR 290.4 |
Description: Broad spectrum MMP inhibitor. Displays high affinity for MMP-2, -3 and -13 (IC50 values are 4, 7 and 8 nM respectively) and exhibits > 750-fold selectivity over MMP-1, -7 and -9. Attenuates left ventricular remodelling and dysfunction in rat model of heart failure. |
PD 166793 |
A4438-25 |
ApexBio |
25 mg |
EUR 597.6 |
Description: Broad spectrum MMP inhibitor. Displays high affinity for MMP-2, -3 and -13 (IC50 values are 4, 7 and 8 nM respectively) and exhibits > 750-fold selectivity over MMP-1, -7 and -9. Attenuates left ventricular remodelling and dysfunction in rat model of heart failure. |
PD 166793 |
A4438-5 |
ApexBio |
5 mg |
EUR 224.4 |
Description: Broad spectrum MMP inhibitor. Displays high affinity for MMP-2, -3 and -13 (IC50 values are 4, 7 and 8 nM respectively) and exhibits > 750-fold selectivity over MMP-1, -7 and -9. Attenuates left ventricular remodelling and dysfunction in rat model of heart failure. |
PD 81723 |
B6705-10 |
ApexBio |
10 mg |
EUR 340.8 |
PD 81723 |
B6705-50 |
ApexBio |
50 mg |
EUR 1245.6 |
PD 102807 |
B6821-10 |
ApexBio |
10 mg |
EUR 466.8 |
PD 102807 |
B6821-50 |
ApexBio |
50 mg |
EUR 1771.2 |
PD 160170 |
B6972-10 |
ApexBio |
10 mg |
EUR 408 |
PD 180970 |
A8606-10 |
ApexBio |
10 mg |
EUR 517.2 |
Description: ATP-competitive inhibitor of p210bcr/abl tyrosine kinase; selectively induces apoptosis in chronic myeloid leukemia (CML) K562 cells. Inhibits in vivo tyrosine phosphorylation of Gab2, CrkL and p210bcr/abl (IC50 values are 80, 80 and 170 nM respectively). |
PD 169316 |
A8689-10 |
ApexBio |
10 mg |
EUR 195.6 |
Description: IC50: A potent, selective and cell-permeable suppressor of p38 MAP kinase, with the IC50 value of 89 nM.PD169316, a specific p38 MAPK inhibitor, blocks signal transduction mediated by both TGF-? and Activin A, but not bone morphogenetic protein (BMP) 4. |
PD 169316 |
A8689-5.1 |
ApexBio |
10 mM (in 1mL DMSO) |
EUR 268.8 |
Description: IC50: A potent, selective and cell-permeable suppressor of p38 MAP kinase, with the IC50 value of 89 nM.PD169316, a specific p38 MAPK inhibitor, blocks signal transduction mediated by both TGF-? and Activin A, but not bone morphogenetic protein (BMP) 4. |
PD 169316 |
A8689-50 |
ApexBio |
50 mg |
EUR 595.2 |
Description: IC50: A potent, selective and cell-permeable suppressor of p38 MAP kinase, with the IC50 value of 89 nM.PD169316, a specific p38 MAPK inhibitor, blocks signal transduction mediated by both TGF-? and Activin A, but not bone morphogenetic protein (BMP) 4. |
PD 173074 |
A8253-10 |
ApexBio |
10 mg |
EUR 129.6 |
Description: PD173074 is a poten and selective fibroblast growth factor receptor (FGFR) inhibitor. Fibroblast growth factor-2 is reported to be able to induce proliferation and chemoresistance in Small cell lung cancer (SCLC) cells. |
PD 173074 |
A8253-5.1 |
ApexBio |
10 mM (in 1mL DMSO) |
EUR 142.8 |
Description: PD173074 is a poten and selective fibroblast growth factor receptor (FGFR) inhibitor. Fibroblast growth factor-2 is reported to be able to induce proliferation and chemoresistance in Small cell lung cancer (SCLC) cells. |
PD 173074 |
A8253-50 |
ApexBio |
50 mg |
EUR 254.4 |
Description: PD173074 is a poten and selective fibroblast growth factor receptor (FGFR) inhibitor. Fibroblast growth factor-2 is reported to be able to induce proliferation and chemoresistance in Small cell lung cancer (SCLC) cells. |
PD 173074 |
A8253-S |
ApexBio |
Evaluation Sample |
EUR 97.2 |
Description: PD173074 is a poten and selective fibroblast growth factor receptor (FGFR) inhibitor. Fibroblast growth factor-2 is reported to be able to induce proliferation and chemoresistance in Small cell lung cancer (SCLC) cells. |
PD 145305 |
C5830-10 |
ApexBio |
10 mg |
EUR 513.6 |
Description: PD 145305 is an inactive analog of PD 150606, a potent and selective calpains inhibitor [1]. Calpain is a class of cytosolic cysteine protease that is activated by elevated intracellular calcium. |
PD 145305 |
C5830-5 |
ApexBio |
5 mg |
EUR 315.6 |
Description: PD 145305 is an inactive analog of PD 150606, a potent and selective calpains inhibitor [1]. Calpain is a class of cytosolic cysteine protease that is activated by elevated intracellular calcium. |
PD 0332991 |
E1KS1116 |
EnoGene |
5mg |
EUR 812.4 |
PD-1:PD-L1 Homogeneous Assay Kit |
72014 |
BPS Bioscience |
384 rxns. |
EUR 1070 |
Description: The PD-1:PD-L1 Homogeneous Assay Kit is designed to measure the_x000D_inhibition of PD-1 binding to PD-L1. With this kit, only three simple steps on a microtiter_x000D_plate are required. First, a sample containing PD-1 and an inhibitor of choice is incubated with_x000D_the biotinylated PD-L1 for 60 minutes. Next, acceptor beads are added, then donor beads,_x000D_followed by reading the Alpha-counts. |
PD-1:PD-L2 Homogeneous Assay Kit |
72015 |
BPS Bioscience |
384 rxns. |
EUR 1070 |
Description: The PD-1:PD-L2 Homogeneous Assay Kit is designed to measure the_x000D_inhibition of PD-1 binding to PD-L2. With this kit, only three simple steps on a microtiter_x000D_plate are required. First, a sample containing PD-1 and an inhibitor of choice is incubated with_x000D_the biotinylated PD-L2 for 60 minutes. Next, acceptor beads are added, then donor beads,_x000D_followed by reading the Alpha-counts. |
PD-0325901