PD-0325901

PD-0325901

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EZSolution? PD-0325901, Sterile-Filtered
1990-1
EUR 272

PD-1/PD-L1 Inhibitor 2
B1050-25
EUR 566

PD-1/PD-L1 Inhibitor 2
B1050-5
EUR 202

PD-1/PD-L1 Inhibitor 1
B1213-25
EUR 566

PD-1/PD-L1 inhibitor 2
B6023-25 25 mg
EUR 438
Description: PD-1/PD-L1 inhibitor 2 is a PD-1/PD-L1 interaction inhibitor.

PD-1/PD-L1 inhibitor 2
B6023-5 5 mg
EUR 171
Description: PD-1/PD-L1 inhibitor 2 is a PD-1/PD-L1 interaction inhibitor.

PD-1/PD-L1 inhibitor 1
B6172-25 25 mg
EUR 453
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 5 mg
EUR 168
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 98059
1666-5
EUR 158

PD 173074
1675-1
EUR 137

PD 173074
1675-100 Ask for price

PD 150,606
1906-25
EUR 370

PD 150,606
1906-5
EUR 137

PD 169316
B1703-25
EUR 544

PD 169316
B1703-5
EUR 175

PD-166866
B2223-25
EUR 675

PD-166866
B2223-5
EUR 207

PD-146176
B2313-25
EUR 675

PD-146176
B2313-5
EUR 207

PD-168393
B2352-25
EUR 414

PD-168393
B2352-5
EUR 142

PD 151746
B4791-100 100 mg
EUR 595
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 25 mg
EUR 282
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 5 mg
EUR 119
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 10 mM (in 1mL DMSO)
EUR 126
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 10 mg
EUR 486

PD 334581
B5727-50 50 mg
EUR 1850

PD 0332991
E1KS1116 5mg
EUR 677

PD 145305
C5830-10 10 mg
EUR 428
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 5 mg
EUR 263
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 184161
C4361-10 10 mg
EUR 283
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 25 mg
EUR 561
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 5 mg
EUR 181
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 1 mg
EUR 161
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 10 mg
EUR 940
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 5 mg
EUR 551
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 81723
B6705-10 10 mg
EUR 284

PD 81723
B6705-50 50 mg
EUR 1038

PD 102807
B6821-10 10 mg
EUR 389

PD 102807
B6821-50 50 mg
EUR 1476

PD 160170
B6972-10 10 mg
EUR 340

PD 176252
B7122-10 10 mg
EUR 512

PD 198306
B7124-1 1 mg
EUR 126
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 10 mg
EUR 529
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 5 mg
EUR 318
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 10 mg
EUR 486

PD 135158
B7127-50 50 mg
EUR 1850

PD 158780
B7130-10 10 mg
EUR 232

PD-0325901