PD-0325901

PD-0325901

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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-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 1
B1213-5
EUR 185

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 169316
HY-10578 10mM/1mL
EUR 255

PD 90780
HY-110166 5mg
EUR 326

PD 407824
HY-18961 100mg
EUR 1542

PD 151746
HY-19749 50mg
EUR 491

PD 0332991
E1KS1116 5mg
EUR 677

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

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

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 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 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 158780
B7130-10 10 mg
EUR 232

PD 158780
B7130-25 25 mg
EUR 453

PD 158780
B7130-5 5 mg
EUR 151

PD 118057
B7203-10 10 mg
EUR 334

PD 118057
B7203-50 50 mg
EUR 1243

PD 146176
B7208-10 10 mg
EUR 150

PD 146176
B7208-25 25 mg
EUR 287

PD 146176
B7208-50 50 mg
EUR 473

PD 173212
B7424-10 10 mg
EUR 529

PD 173212
B7424-5 5 mg
EUR 376

PD 173212
B7424-5.1 10 mM (in 1mL DMSO)
EUR 479

PD 161570
B7486-10 10 mg
EUR 454

PD 161570
B7486-50 50 mg
EUR 1714

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-ECGF
PR15044 10 ug
EUR 487

PD-ECGF
GT15181 100 ug
EUR 526

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 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 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 169316
A8689-5.1 10 mM (in 1mL DMSO)
EUR 224
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 50 mg
EUR 496
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 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 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 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 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

Ribosome-inactivating protein PD-L1 / PD-L2 Antibody
20-abx319445
  • EUR 411.00
  • EUR 1845.00
  • EUR 599.00
  • EUR 182.00
  • EUR 300.00
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug

Ribosome-inactivating protein PD-L1/PD-L2 Antibody
1-CSB-PA306294LA01PJJ
  • EUR 317.00
  • EUR 335.00
  • 100ug
  • 50ug
Description: A polyclonal antibody against Ribosome-inactivating protein PD-L1/PD-L2. Recognizes Ribosome-inactivating protein PD-L1/PD-L2 from Phytolacca dioica. This antibody is Unconjugated. Tested in the following application: ELISA

PD 123319 (ditrifluoroacetate)
HY-10259A 10mg
EUR 215

(+)-PD 128907 hydrochloride
HY-110000 50mg
EUR 751

PD-168077 maleate
HY-21098A 10mM/1mL
EUR 176

PD-1,CD279
E6TA00107 0.1mg
EUR 343

PD-L1, CD274
E6TA00108 0.1mg
EUR 343

PD-L1 Protein
20-abx261703
  • EUR 3418.00
  • EUR 328.00
  • EUR 230.00
  • 1 mg
  • 20 ug
  • 5 ug

PD-L1 Protein
20-abx263458
  • EUR 1609.00
  • EUR 328.00
  • EUR 230.00
  • 100 ug
  • 10 ug
  • 2 µg

PD-ECGF Antibody
abx236264-100ug 100 ug
EUR 551

PD 98059, >99%
BC064-010 10mg
EUR 232

PD 98059, >99%
BC064-025 25mg
EUR 300

PD 98059, >99%
BC064-050 50mg
EUR 448

PD-1 Antibody
24505-100ul 100ul
EUR 390

PD-1 Antibody
24506-100ul 100ul
EUR 390

PD 168077 maleate
B6578-10 10 mg
EUR 302

PD 168077 maleate
B6578-50 50 mg
EUR 1096

PD 123319 ditrifluoroacetate
A3704-10 10 mg
EUR 209
Description: Description:IC50 Value: 1.2 ±0.4 mM (Inhibition of adenylyl cyclase elicited by 0.1 microM Ang II) [2]PD 123319 ditrifluoroacetate is a potent, selective, non-peptide angiotensin AT2 receptor antagonist.

PD 123319 ditrifluoroacetate
A3704-25 25 mg
EUR 408
Description: Description:IC50 Value: 1.2 ±0.4 mM (Inhibition of adenylyl cyclase elicited by 0.1 microM Ang II) [2]PD 123319 ditrifluoroacetate is a potent, selective, non-peptide angiotensin AT2 receptor antagonist.

PD 123319 ditrifluoroacetate
A3704-5 5 mg
EUR 171
Description: Description:IC50 Value: 1.2 ±0.4 mM (Inhibition of adenylyl cyclase elicited by 0.1 microM Ang II) [2]PD 123319 ditrifluoroacetate is a potent, selective, non-peptide angiotensin AT2 receptor antagonist.

PD 123319 ditrifluoroacetate
A3704-50 50 mg
EUR 656
Description: Description:IC50 Value: 1.2 ±0.4 mM (Inhibition of adenylyl cyclase elicited by 0.1 microM Ang II) [2]PD 123319 ditrifluoroacetate is a potent, selective, non-peptide angiotensin AT2 receptor antagonist.

PD 168568 dihydrochloride
B7420-10 10 mg
EUR 308

PD 168568 dihydrochloride
B7420-50 50 mg
EUR 1136

PD 0332991 (Palbociclib)
B7798-25 25 mg
EUR 154
Description: PD-0332991 is selective and oral inhibitor of cyclin-dependent kinase 4/6 with IC50 values of 11nM and 16nM, respectively for CDK4 and CDK6 [1].PD-0332991 is a highly specific inhibitor of CDK4/6.

PD 0332991 (Palbociclib)
B7798-5 5 mg
EUR 108
Description: PD-0332991 is selective and oral inhibitor of cyclin-dependent kinase 4/6 with IC50 values of 11nM and 16nM, respectively for CDK4 and CDK6 [1].PD-0332991 is a highly specific inhibitor of CDK4/6.

PD 0332991 (Palbociclib)
B7798-S Evaluation Sample
EUR 81
Description: PD-0332991 is selective and oral inhibitor of cyclin-dependent kinase 4/6 with IC50 values of 11nM and 16nM, respectively for CDK4 and CDK6 [1].PD-0332991 is a highly specific inhibitor of CDK4/6.

PD-1 Antibody
P1001-01m 0.1m
EUR 165

PD-L1 Antibody
P1013-1ml 1ml
EUR 673

PD-1 Antibody
P1001-1ml 1ml
EUR 376

PD-L1 Antibody
P1013-01m 0.1m
EUR 187

PD-L1 Antibody
49251-100ul 100ul
EUR 333

PD-0325901