PD-0325901

PD-0325901

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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-ECGF
PR15044 10 ug
EUR 487

PD 98,059
GK2140-10MG 10 mg
EUR 172

PD 98,059
GK2140-1MG 1 mg
EUR 91

PD 98,059
GK2140-50MG 50 mg
EUR 378

PD 98,059
GK2140-5MG 5 mg
EUR 137

PD 150,606
GL2543-25MG 25 mg
EUR 413

PD 150,606
GL2543-5MG 5 mg
EUR 154

PD-ECGF
GT15181 100 ug
EUR 526

PD 407824
HY-18961 100mg
EUR 1542

PD 151746
HY-19749 50mg
EUR 491

PD 169316
HY-10578 10mM/1mL
EUR 255

PD 90780
HY-110166 5mg
EUR 326

PD 117519
HY-100032 5mg
EUR 119

PD-166866
HY-101296 10mM/1mL
EUR 138

PD-159020
HY-101598 1mg
EUR 1125

PD 123319
HY-10259 5mg
EUR 182

PD 0332991
E1KS1116 5mg
EUR 677

PD 150606
A4413-25 25 mg
EUR 428
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 5 mg
EUR 144
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 10 mg
EUR 242
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 25 mg
EUR 498
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 5 mg
EUR 187
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 173074
A8253-10 10 mg
EUR 108
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 10 mM (in 1mL DMSO)
EUR 119
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 50 mg
EUR 212
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 Evaluation Sample
EUR 81
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 180970
A8606-10 10 mg
EUR 431
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 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 169316
A8689-10 10 mg
EUR 163
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-0325901