PD-0325901

PD-0325901

Contact us: [email protected]

PD-0325901

1643-5 each
EUR 444

PD 0325901

GL5463 1mg
EUR 208.84

PD 0325901

GL5463-1 1
EUR 68.9

PD 0325901

GL5463-25 25
EUR 228.1

PD 0325901

GL5463-5 5
EUR 98.4

PD 0325901

MBS132263-100mg 100mg
EUR 1065

PD 0325901

MBS132263-500mg 500mg
EUR 2775

PD 0325901

MBS696352-10mg 10mg
EUR 215

PD 0325901

MBS696352-25mg 25mg
EUR 325

PD 0325901

MBS696352-5x25mg 5x25mg
EUR 1410

EZSolution? PD-0325901, Sterile-Filtered

1990-1 each
EUR 326.4

PD-325901, Free Base (PD 0325901, MEK1/2 Inhibitor III)

MBS6061791-10mg 10(mg
EUR 255

PD-325901, Free Base (PD 0325901, MEK1/2 Inhibitor III)

MBS6061791-25mg 25mg
EUR 450

PD-325901, Free Base (PD 0325901, MEK1/2 Inhibitor III)

MBS6061791-5x25mg 5x25mg
EUR 1865

PD150606 (PD 150606; PD-150606)

MBS131512-100mg 100mg
EUR 1495

PD 312236, PD 312237 Mixture

P217850 10mg
EUR 230

PD-1/PD-L1 Inhibitor 2

B1050-25 each
EUR 679.2

PD-1/PD-L1 Inhibitor 2

B1050-5 each
EUR 242.4

PD-1/PD-L1 Inhibitor 1

B1213-25 each
EUR 679.2

PD-1/PD-L1 inhibitor 2

B6023-25 25 mg
EUR 268
Description: Apoptosis|PD-1/PD-L1 interaction#Apoptosis

PD-1/PD-L1 inhibitor 2

B6023-5 5 mg
EUR 84
Description: Apoptosis|PD-1/PD-L1 interaction#Apoptosis

PD-1/PD-L1 inhibitor 1

B6172-25 25 mg
EUR 278.4
Description: Apoptosis|PD-1/PD-L1 interaction

PD-1/PD-L1 inhibitor 1

B6172-5 5 mg
EUR 82.4
Description: Apoptosis|PD-1/PD-L1 interaction

PD-1/PD-L1 Inhibitor 3

B6191-1 1 mg
EUR 248.8
Description: Apoptosis|PD-1/PD-L1 interaction

PD-1/PD-L1 Inhibitor 3

B6191-5 5 mg
EUR 837.6
Description: Apoptosis|PD-1/PD-L1 interaction

PD-1/PD-L1-IN-29

HY-152240 1 mg
EUR 919.93
Description: PD-1/PD-L1-IN-29 (S4-1) is a potent PD-1/PD-L1 inhibitor with an IC50 value of 6.1 nM. PD-1/PD-L1-IN-29 binds PD-L1 and disrupts PD-1/PD-L1 interactions, induces PD-L1 dimerization and internalization, improves its localization to the endoplasmic reticulum, and promotes PD-L1 entry into the endoplasmic reticulum. PD-1/PD-L1-IN-29 has anticancer activity[1].

PD-1/PD-L1-IN-31

HY-149356 Get quote Ask for price
Description: PD-1/PD-L1-IN-31 is a PD-1/PD-L1 inhibitor (IC50=2.2 nM). PD-1/PD-L1-IN-31 promotes secretion of the IFN-γ, and induces immune activity of peripheral blood mononuclear cells (PBMCs) to inhibits tumor cells[1].

PD-1/PD-L1-IN 3

HY-103048 Get quote Ask for price
Description: PD-1/PD-L1-IN 3, a macrocyclic peptide, is a potent and selective inhibitor of the PD-1/PD-L1 and CD80/PD-L1 interactions extracted from patent WO2014151634A1, compound No.1. PD-1/PD-L1-IN 3 interferes with PD-L1 binding to PD-1 and CD80 by binding to PD-L1, with IC50s of 5.60 nM and 7.04 nM, respectively. PD-1/PD-L1-IN 3 can be used for the research of various diseases, including cancer and infectious diseases[1].

PD-1/PD-L1-IN-34

HY-154869 Get quote Ask for price
Description: PD-1/PD-L1-IN-34 (Compound (1S,2S)-A25) inhibits PD-1/PD-L1 interaction (IC50=0.029 μM), with a selected binding affinity with PD-L1 (KD=0.1554 μM). PD-1/PD-L1-IN-34 inhibits tumor growth by activating the immune microenvironment[1].

PD-1/PD-L1-IN-32

HY-155740 Get quote Ask for price
Description: PD-1/PD-L1-IN-32 (compound A56) is a potent PD-1/PD-L1 inhibitor (IC50=2.4 nM), with anticancer activity. PD-1/PD-L1-IN-32 significantly inhibits tumor growth in hPD-L1 MC38 humanized mouse model, without obvious toxicity against mouse normal ability[1].

PD-1/PD-L1-IN-33

HY-155959 10 mg
EUR 1623.4
Description: PD-1/PD-L1-IN-33 (Compound N11) is a PD-1/PD-L1 inhibitor. PD-1/PD-L1-IN-33 inhibits PD-1 and PD-L1 interaction with an IC50: 6.3 nM. PD-1/PD-L1-IN-33 promotes T-cell proliferation, activation, and infiltration into tumor spheres. PD-1/PD-L1-IN-33 has immunomodulatory and anticancer activity[1].

PD-1/PD-L1-IN-36

HY-163041 Get quote Ask for price
Description: PD-1/PD-L1-IN-36 (Compound 2k) is a PD-1/PD-L1 complex inhibitor (IC50: 15 nM). PD-1/PD-L1-IN-36 can be used for research of cancer immunotherapy[1].

PD-1/PD-L1-IN 5

HY-129172A Get quote Ask for price
Description: PD-1/PD-L1-IN 5 is a PD-1/PD-L1 protein/protein interaction inhibitor extracted from patent WO2017222976A1, compound Example 1, has an IC50 of ≤100 nM[1].

PD-1/PD-L1-IN 6

HY-130625 Get quote Ask for price
Description: PD-1/PD-L1-IN 6 (compound A13) is a potent PD-1/PD-L1 interaction inhibitor, with an IC50 of 132.8 nM. PD-1/PD-L1-IN 6 exhibits outstanding immunoregulatory activity. PD-1/PD-L1-IN 6 significantly elevates interferon-γ secretion in a Hep3B/OS-8/hPD-L1 and CD3 T cell co-culture model, without significant toxic effect. PD-1/PD-L1-IN 6 restores the immune response in a T cell-tumor co-culture model[1].

PD-1/PD-L1-IN-NP19

HY-131347 10 mg
EUR 1948.08
Description: PD-1/PD-L1-IN-NP19 is a PD-1/PD-L1 inhibitor, with an IC50 of 12.5 nM for human PD-1/PD-L1 interaction. PD-1/PD-L1-IN-NP19 could activate the immune microenvironment in tumor, which may contribute to its antitumor effects[1].

PD-1/PD-L1-IN-9

HY-132192 10 mg
EUR 984.86
Description: PD-1/PD-L1-IN-9 is a potent and orally active inhibitor of PD-1/PD-L1 interaction, with an IC50 of 3.8 nM. PD-1/PD-L1-IN-9 can enhance the killing activity of tumor cells by immune cells. PD-1/PD-L1-IN-9 also exhibits significant in vivo antitumor activity in a CT26 mouse model[1].

PD-1/PD-L1-IN-10

HY-132202 10 mg
EUR 779.23
Description: PD-1/PD-L1-IN-10 (compound B2) is an orally active PD-1/PD-L1 inhibitor (IC50 of 2.7 nM) with potent anticancer efficacy[1].

PD-1/PD-L1-IN-13

HY-145239 1 mg
EUR 3517.37
Description: PD-1/PD-L1-IN-13 (Compound 43) is a potent immune checkpoint PD-1/PD-L1 inhibitor with an IC50 value of 10.2 nM. PD-1/PD-L1-IN-13 promots CD8+ T cell activation and delays the tumor growth in the Hepa1-6 syngeneic mouse model[1].

PD-1/PD-L1-IN-18

HY-145768 Get quote Ask for price
Description: PD-1/PD-L1-IN-18 (Compound L31) is a small-molecule inhibitor of the PD-1/PD-L1 protein-protein interaction. PD-1/PD-L1-IN-18 blocks PD-1/PD-L1 with the IC50 of 1.054 μM. Antitumor Activity[1].

PD-1/PD-L1-IN-19

HY-145770 Get quote Ask for price
Description: PD-1/PD-L1-IN-19 (Example 22) is a small-molecule inhibitor of the PD-1/PD-L1 protein-protein interaction. PD-1/PD-L1-IN-19 blocks PD-1/PD-L1 with the IC50 of 62.3 nM. PD-1/PD-L1-IN-19 can be used for the research of cancers, infectious diseases and autoimmune diseases[1].

PD-1/PD-L1-IN-20

HY-145771 Get quote Ask for price
Description: PD-1/PD-L1-IN-20 (Example 21) is a small-molecule inhibitor of the PD-1/PD-L1 protein-protein interaction. PD-1/PD-L1-IN-20 blocks PD-1/PD-L1 with the IC50 of 5.29 nM. PD-1/PD-L1-IN-20 can be used for the research of cancers, infectious diseases and autoimmune diseases[1].

PD-1/PD-L1-IN-21

HY-145772 Get quote Ask for price
Description: PD-1/PD-L1-IN-21 (Example 22) is a small-molecule inhibitor of the PD-1/PD-L1 protein-protein interaction. PD-1/PD-L1-IN-21 blocks PD-1/PD-L1 with the IC50 of 4.99 μM. PD-1/PD-L1-IN-21 can be used for the research of cancers, infectious diseases and autoimmune diseases[1].

PD-1/PD-L1-IN-22

HY-145773 Get quote Ask for price
Description: PD-1/PD-L1-IN-22 (Example 2) is a small-molecule inhibitor of the PD-1/PD-L1 protein-protein interaction. PD-1/PD-L1-IN-22 blocks PD-1/PD-L1 with the IC50 of 0.732 μM. PD-1/PD-L1-IN-22 can be used for the research of cancers, infectious diseases and autoimmune diseases[1].

PD-1/PD-L1-IN-23

HY-145774 10 mg
EUR 4058.51
Description: PD-1/PD-L1-IN-23 is a potent and orally active inhibitor of PD-1/PD-L1. PD-1/PD-L1-IN-23 is an ester proagent of L7. L7 is a benzo[c][1,2,5]oxadiazole derivative and biologically evaluated as inhibitors of PD-L1. PD-1/PD-L1-IN-23 displays significant antitumor effects in tumor models of syngeneic and PD-L1 humanized mice[1].

PD-1/PD-L1-IN-27

HY-146740 Get quote Ask for price
Description: PD-1/PD-L1-IN-27 is a potent PD-1/PD-L1 inhibitor with an IC50 value of 134 nM. PD-1/PD-L1-IN-27 shows antitumor effects with low T cell cytotoxicity. PD-1/PD-L1-IN-27 has the ability to activate CD8+ T cells and reduces T cell exhaustion[1].

PD-1/PD-L1-IN-28

HY-148305 Get quote Ask for price
Description: PD-1/PD-L1-IN-28 (compound 3) is an immune checkpoint inhibitor of PD-1/PD-L1 signaling pathway (IC50=0.744 µM). PD-1/PD-L1-IN-28 shows good research potential in tumor immunity[1].

PD-1/PD-L1-IN-25

HY-143305 Get quote Ask for price
Description: PD-1/PD-L1-IN-25 (compound D2) is an inhibitor of PD-1/PD-L1 interaction with an IC50 value of 16.17 nM. PD-1/PD-L1-IN-25 activates the antitumor immunity of T cells efficiently in PBMCs. PD-1/PD-L1-IN-25 can be used for the research of cancer[1].

PD-1/PD-L1-IN-14

HY-144258 10 mg
EUR 2543.33
Description: PD-1/PD-L1-IN-14 (compound 17) is a bifunctional inhibitor of PD-1/PD-L1 interactions, with an IC50 of 27.8 nM. PD-1/PD-L1-IN-14 (compound 17) inhibits PD-1/PD-L1 interactions and promotes dimerization, internalization, and degradation of PD-L1[1].

PD-1/PD-L1-IN-15

HY-144442 Get quote Ask for price
Description: PD-1/PD-L1-IN-15 (Compound M17) is a potent inhibitor of PD-1/PD-L1 with an IC50 value of 60.1 nM. PD-1/PD-L1-IN-15 has the potential for the research of tumor immunoresearch[1].

PD-1/PD-L1-IN-16

HY-144443 Get quote Ask for price
Description: PD-1/PD-L1-IN-16 (Compound M23) is a potent inhibitor of PD-1/PD-L1 with an IC50 value of 53.2 nM. PD-1/PD-L1-IN-16 has the potential for the research of tumor immunoresearch[1].

PD-1/PD-L1-IN-17

HY-144447 Get quote Ask for price
Description: PD-1/PD-L1-IN-17 (Compound P20) is a potent inhibitor of PD-1/PD-L1 with an IC50 value of 26.8 nM. PD-1/PD-L1-IN-17 is a promising lead compound for the development of inhibitors of the PD-1/PD-L1 interaction. PD-1/PD-L1-IN-17 has the potential for the research of cancer diseases[1].

PD-1/PD-L1-IN-24

HY-144649 Get quote Ask for price
Description: PD-1/PD-L1-IN-24 is a highly potent PD-1/PD-L1 inhibitor with IC50 value of 1.57 nM. PD-1/PD-L1-IN-24 can restore T-cell function at the cellular level by significantly elevating the IFN-γ level. PD-1/PD-L1-IN-24 has low toxicity on the PBMCs[1].

PD-1/PD-L1-IN-26

HY-144746 Get quote Ask for price
Description: PD-1/PD-L1-IN-26 (Compound II-14) is a potent inhibitor of PD-1/PD-L1 with an IC50 of 0.0380 μM. PD-1/PD-L1-IN-26 activates the immune microenvironment by promoting the infiltration of CD4+ T cells into tumor tissues. PD-1/PD-L1-IN-26 has the potential for the research of cancer diseases[1].

PD-1/PD-L1-IN-NP19

MBS5785098-10mg 10mg
EUR 555

PD-1/PD-L1-IN-NP19

MBS5785098-25mg 25mg
EUR 1350

PD-1/PD-L1-IN-NP19

MBS5785098-50mg 50(mg
EUR 1520

PD-1/PD-L1-IN-NP19

MBS5785098-5mg 5(mg
EUR 375

PD-1/PD-L1 inhibitor 1

MBS578522-10mg 10mg
EUR 250

PD-1/PD-L1 inhibitor 1

MBS578522-25mg 25mg
EUR 375

PD-1/PD-L1 inhibitor 1

MBS578522-2mg 2mg
EUR 160

PD-1/PD-L1 inhibitor 1

MBS578522-50mg 50mg
EUR 510

PD-1/PD-L1 inhibitor 1

MBS578522-5mg 5mg
EUR 190

PD-1/PD-L1-IN-10

MBS5786462-10mg 10(mg
EUR 250

PD-1/PD-L1-IN-10

MBS5786462-2mg 2(mg
EUR 180

PD-1/PD-L1-IN-10

MBS5786462-5mg 5(mg
EUR 195

PD-1/PD-L1-IN-9

MBS5801395-1mg 1(mg
EUR 225

PD-1/PD-L1-IN-9

MBS5801395-2mg 2mg
EUR 285

PD-1/PD-L1-IN-9

MBS5801395-5mg 5(mg
EUR 345

PD-1/PD-L1-IN-16

T63948-10mg 10mg Ask for price
Description: PD-1/PD-L1-IN-16

PD-1/PD-L1-IN-16

T63948-1g 1g Ask for price
Description: PD-1/PD-L1-IN-16

PD-1/PD-L1-IN-16

T63948-1mg 1mg Ask for price
Description: PD-1/PD-L1-IN-16

PD-1/PD-L1-IN-16

T63948-50mg 50mg Ask for price
Description: PD-1/PD-L1-IN-16

PD-1/PD-L1-IN-16

T63948-5mg 5mg Ask for price
Description: PD-1/PD-L1-IN-16

PD-1/PD-L1-IN-20

T64086-10mg 10mg Ask for price
Description: PD-1/PD-L1-IN-20

PD-1/PD-L1-IN-20

T64086-1g 1g Ask for price
Description: PD-1/PD-L1-IN-20

PD-1/PD-L1-IN-20

T64086-1mg 1mg Ask for price
Description: PD-1/PD-L1-IN-20

PD-1/PD-L1-IN-20

T64086-50mg 50mg Ask for price
Description: PD-1/PD-L1-IN-20

PD-1/PD-L1-IN-20

T64086-5mg 5mg Ask for price
Description: PD-1/PD-L1-IN-20

PD-1/PD-L1-IN-10

T9616-10mg 10mg Ask for price
Description: PD-1/PD-L1-IN-10

PD-1/PD-L1-IN-10

T9616-1g 1g Ask for price
Description: PD-1/PD-L1-IN-10

PD-1/PD-L1-IN-10

T9616-1mg 1mg Ask for price
Description: PD-1/PD-L1-IN-10

PD-1/PD-L1-IN-10

T9616-50mg 50mg Ask for price
Description: PD-1/PD-L1-IN-10

PD-1/PD-L1-IN-10

T9616-5mg 5mg Ask for price
Description: PD-1/PD-L1-IN-10

PD-1/PD-L1-IN-9

T9651-10mg 10mg Ask for price
Description: PD-1/PD-L1-IN-9

PD-1/PD-L1-IN-9

T9651-1g 1g Ask for price
Description: PD-1/PD-L1-IN-9

PD-1/PD-L1-IN-9

T9651-1mg 1mg Ask for price
Description: PD-1/PD-L1-IN-9

PD-1/PD-L1-IN-9

T9651-50mg 50mg Ask for price
Description: PD-1/PD-L1-IN-9

PD-1/PD-L1-IN-9

T9651-5mg 5mg Ask for price
Description: PD-1/PD-L1-IN-9

PD-1/PD-L1-IN-NP19

T36900-10mg 10mg Ask for price
Description: PD-1/PD-L1-IN-NP19

PD-1/PD-L1-IN-NP19

T36900-1g 1g Ask for price
Description: PD-1/PD-L1-IN-NP19

PD-1/PD-L1-IN-NP19

T36900-1mg 1mg Ask for price
Description: PD-1/PD-L1-IN-NP19

PD-1/PD-L1-IN-NP19

T36900-50mg 50mg Ask for price
Description: PD-1/PD-L1-IN-NP19

PD-1/PD-L1-IN-NP19

T36900-5mg 5mg Ask for price
Description: PD-1/PD-L1-IN-NP19

PD-1/PD-L1-IN-14

T61929-10mg 10mg Ask for price
Description: PD-1/PD-L1-IN-14

PD-1/PD-L1-IN-14

T61929-1g 1g Ask for price
Description: PD-1/PD-L1-IN-14

PD-1/PD-L1-IN-14

T61929-1mg 1mg Ask for price
Description: PD-1/PD-L1-IN-14

PD-1/PD-L1-IN-14

T61929-50mg 50mg Ask for price
Description: PD-1/PD-L1-IN-14

PD-1/PD-L1-IN-14

T61929-5mg 5mg Ask for price
Description: PD-1/PD-L1-IN-14

PD-1/PD-L1-IN 6

T61968-10mg 10mg Ask for price
Description: PD-1/PD-L1-IN 6

PD-1/PD-L1-IN 6

T61968-1g 1g Ask for price
Description: PD-1/PD-L1-IN 6

PD-1/PD-L1-IN 6

T61968-1mg 1mg Ask for price
Description: PD-1/PD-L1-IN 6

PD-1/PD-L1-IN 6

T61968-50mg 50mg Ask for price
Description: PD-1/PD-L1-IN 6

PD-1/PD-L1-IN 6

T61968-5mg 5mg Ask for price
Description: PD-1/PD-L1-IN 6

PD-1/PD-L1-IN 5

T62193-10mg 10mg Ask for price
Description: PD-1/PD-L1-IN 5

PD-1/PD-L1-IN 5

T62193-1g 1g Ask for price
Description: PD-1/PD-L1-IN 5

PD-1/PD-L1-IN 5

T62193-1mg 1mg Ask for price
Description: PD-1/PD-L1-IN 5

PD-1/PD-L1-IN 5

T62193-50mg 50mg Ask for price
Description: PD-1/PD-L1-IN 5

PD-1/PD-L1-IN 5

T62193-5mg 5mg Ask for price
Description: PD-1/PD-L1-IN 5

PD-1/PD-L1-IN-17

T62501-10mg 10mg Ask for price
Description: PD-1/PD-L1-IN-17

PD-1/PD-L1-IN-17

T62501-1g 1g Ask for price
Description: PD-1/PD-L1-IN-17

PD-1/PD-L1-IN-17

T62501-1mg 1mg Ask for price
Description: PD-1/PD-L1-IN-17

PD-1/PD-L1-IN-17

T62501-50mg 50mg Ask for price
Description: PD-1/PD-L1-IN-17

PD-1/PD-L1-IN-17

T62501-5mg 5mg Ask for price
Description: PD-1/PD-L1-IN-17

PD-1/PD-L1-IN-25

T63329-10mg 10mg Ask for price
Description: PD-1/PD-L1-IN-25

PD-1/PD-L1-IN-25

T63329-1g 1g Ask for price
Description: PD-1/PD-L1-IN-25

PD-1/PD-L1-IN-25

T63329-1mg 1mg Ask for price
Description: PD-1/PD-L1-IN-25

PD-1/PD-L1-IN-25

T63329-50mg 50mg Ask for price
Description: PD-1/PD-L1-IN-25

PD-1/PD-L1-IN-25

T63329-5mg 5mg Ask for price
Description: PD-1/PD-L1-IN-25

PD-1/PD-L1-IN-22

T63607-10mg 10mg Ask for price
Description: PD-1/PD-L1-IN-22

PD-1/PD-L1-IN-22

T63607-1g 1g Ask for price
Description: PD-1/PD-L1-IN-22

PD-1/PD-L1-IN-22

T63607-1mg 1mg Ask for price
Description: PD-1/PD-L1-IN-22

PD-1/PD-L1-IN-22

T63607-50mg 50mg Ask for price
Description: PD-1/PD-L1-IN-22

PD-1/PD-L1-IN-22

T63607-5mg 5mg Ask for price
Description: PD-1/PD-L1-IN-22

PD-1/PD-L1-IN-15

T63614-10mg 10mg Ask for price
Description: PD-1/PD-L1-IN-15

PD-1/PD-L1-IN-15

T63614-1g 1g Ask for price
Description: PD-1/PD-L1-IN-15

PD-1/PD-L1-IN-15

T63614-1mg 1mg Ask for price
Description: PD-1/PD-L1-IN-15

PD-1/PD-L1-IN-15

T63614-50mg 50mg Ask for price
Description: PD-1/PD-L1-IN-15

PD-1/PD-L1-IN-15

T63614-5mg 5mg Ask for price
Description: PD-1/PD-L1-IN-15

PD 150606

A4413-10 10mg
EUR 145.6
Description: Proteases|Calpains

PD 150606

A4413-25 25 mg
EUR 304
Description: Proteases|Calpains

PD 150606

A4413-5 5 mg
EUR 87.2
Description: Proteases|Calpains

PD 150606

A4413-50 50mg
EUR 542.4
Description: Proteases|Calpains

PD 166793

A4438-10 10 mg
EUR 188
Description: Proteases|MMP

PD 166793

A4438-25 25 mg
EUR 432
Description: Proteases|MMP

PD 166793

A4438-5 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 166793

A4438-50 50mg
EUR 730
Description: MMP inhibitor

PD 180970

A8606-10 10 mg
EUR 344
Description: TGF-β / Smad Signaling|Bcr-Abl#Tyrosine Kinase|Bcr-Abl

PD 169316

A8689-10 10 mg
EUR 72
Description: MAPK Signaling|p38

PD 169316

A8689-5.1 10 mM (in 1mL DMSO)
EUR 105.6
Description: MAPK Signaling|p38

PD 169316

A8689-50 50 mg
EUR 271.2
Description: MAPK Signaling|p38

PD 173074

A8253-10 10 mg
EUR 40
Description: Tyrosine Kinase|FGFR#Tyrosine Kinase|VEGFR

PD 173074

A8253-5.1 10 mM (in 1mL DMSO)
EUR 48
Description: Tyrosine Kinase|FGFR#Tyrosine Kinase|VEGFR

PD 173074

A8253-50 50 mg
EUR 112
Description: Tyrosine Kinase|FGFR#Tyrosine Kinase|VEGFR

PD 173074

A8253-S Evaluation Sample
EUR 24
Description: Tyrosine Kinase|FGFR#Tyrosine Kinase|VEGFR

PD-166285

525796 5.0mg
EUR 275

PD 109488

525816 50.0mg
EUR 1340

PD 135158

525842 10.0mg
EUR 390

PD-176252

525902 10.0mg
EUR 400

PD-198306

525904 5.0mg
EUR 410

PD 146176

530393 10.0mg
EUR 250

PD 150606

531245 200.0mg
EUR 950

PD-85639

531389 5.0mg
EUR 250

PD-156707

532448 5.0mg
EUR 265

PD 158780

532449 10.0mg
EUR 470

PD 168368

532455 5.0mg
EUR 350

PD 117519

585228 5.0mg
EUR 230

PD-173212

598025 5.0mg
EUR 375

PD-166793

598116 10.0mg
EUR 360

PD-118057

561213 5.0mg
EUR 330

PD 124966

414279 500.0µg
EUR 355

PD-168393

406105 25.0mg
EUR 300

PD-173955

406164 25.0mg
EUR 250

PD-161570

407384 5.0mg
EUR 285

PD 81723

414815 10.0mg
EUR 335

PD-169316

510236 50.0mg
EUR 250

PD-151746

563384 5.0mg
EUR 280

PD 173074

27056 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 98059

1666-5 each
EUR 189.6

PD 173074

1675-1 each
EUR 164.4

PD 173074

1675-100 each Ask for price

PD 150,606

1906-25 each
EUR 444

PD 150,606

1906-5 each
EUR 164.4

PD-98059

abx076731-100l 100 µl
EUR 106.25

PD-98059

abx076731-1ml 1 ml Ask for price

PD-98059

abx076731-200l 200 µl
EUR 250

PD-325901

abx076765-100l 100 µl
EUR 118.75

PD-325901

abx076765-1ml 1 ml Ask for price

PD-325901

abx076765-200l 200 µl
EUR 300

PD-0325901