PD-0325901
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PD 0325901 |
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MBS132263-100mg | 100mg | EUR 1065 |
PD 0325901 |
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MBS132263-500mg | 500mg | EUR 2775 |
PD 0325901 |
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GL5463-1 | 1 | EUR 68.9 |
PD 0325901 |
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GL5463-25 | 25 | EUR 228.1 |
PD 0325901 |
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GL5463-5 | 5 | EUR 98.4 |
PD 0325901 |
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MBS696352-10mg | 10mg | EUR 215 |
PD 0325901 |
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MBS696352-25mg | 25mg | EUR 325 |
PD 0325901 |
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MBS696352-5x25mg | 5x25mg | EUR 1410 |
EZSolution? PD-0325901, Sterile-Filtered |
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1990-1 | each | EUR 326.4 |
PD-325901, Free Base (PD 0325901, MEK1/2 Inhibitor III) |
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MBS6061791-10mg | 10(mg | EUR 255 |
PD-325901, Free Base (PD 0325901, MEK1/2 Inhibitor III) |
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MBS6061791-25mg | 25mg | EUR 450 |
PD-325901, Free Base (PD 0325901, MEK1/2 Inhibitor III) |
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MBS6061791-5x25mg | 5x25mg | EUR 1865 |
PD150606 (PD 150606; PD-150606) |
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MBS131512-100mg | 100mg | EUR 1495 |
PD 312236, PD 312237 Mixture |
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P217850 | 10mg | EUR 230 |
PD-1/PD-L1 Inhibitor 2 |
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B1050-25 | each | EUR 679.2 |
PD-1/PD-L1 Inhibitor 2 |
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B1050-5 | each | EUR 242.4 |
PD-1/PD-L1 Inhibitor 1 |
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B1213-25 | each | EUR 679.2 |
PD-1/PD-L1 inhibitor 2 |
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B6023-25 | 25 mg | EUR 268 |
Description: PD-1/PD-L1 interaction inhibitor |
PD-1/PD-L1 inhibitor 2 |
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B6023-5 | 5 mg | EUR 84 |
Description: PD-1/PD-L1 interaction inhibitor |
PD-1/PD-L1 inhibitor 1 |
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B6172-25 | 25 mg | EUR 278 |
Description: PD-1/PD-L1 interaction inhibitor |
PD-1/PD-L1 inhibitor 1 |
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B6172-5 | 5 mg | EUR 82 |
Description: PD-1/PD-L1 interaction inhibitor |
PD-1/PD-L1 Inhibitor 3 |
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B6191-1 | 1 mg | EUR 249 |
Description: PD-1/PD-L1 interaction inhibitor |
PD-1/PD-L1 Inhibitor 3 |
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B6191-5 | 5 mg | EUR 838 |
Description: PD-1/PD-L1 interaction inhibitor |
PD-1/PD-L1-IN-10 |
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T9616-10mg | 10mg | Ask for price |
Description: PD-1/PD-L1-IN-10 |
PD-1/PD-L1-IN-10 |
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T9616-1g | 1g | Ask for price |
Description: PD-1/PD-L1-IN-10 |
PD-1/PD-L1-IN-10 |
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T9616-1mg | 1mg | Ask for price |
Description: PD-1/PD-L1-IN-10 |
PD-1/PD-L1-IN-10 |
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T9616-50mg | 50mg | Ask for price |
Description: PD-1/PD-L1-IN-10 |
PD-1/PD-L1-IN-10 |
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T9616-5mg | 5mg | Ask for price |
Description: PD-1/PD-L1-IN-10 |
PD-1/PD-L1-IN-9 |
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T9651-10mg | 10mg | Ask for price |
Description: PD-1/PD-L1-IN-9 |
PD-1/PD-L1-IN-9 |
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T9651-1g | 1g | Ask for price |
Description: PD-1/PD-L1-IN-9 |
PD-1/PD-L1-IN-9 |
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T9651-1mg | 1mg | Ask for price |
Description: PD-1/PD-L1-IN-9 |
PD-1/PD-L1-IN-9 |
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T9651-50mg | 50mg | Ask for price |
Description: PD-1/PD-L1-IN-9 |
PD-1/PD-L1-IN-9 |
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T9651-5mg | 5mg | Ask for price |
Description: PD-1/PD-L1-IN-9 |
PD-1/PD-L1-IN 5 |
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T62193-10mg | 10mg | Ask for price |
Description: PD-1/PD-L1-IN 5 |
PD-1/PD-L1-IN 5 |
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T62193-1g | 1g | Ask for price |
Description: PD-1/PD-L1-IN 5 |
PD-1/PD-L1-IN 5 |
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T62193-1mg | 1mg | Ask for price |
Description: PD-1/PD-L1-IN 5 |
PD-1/PD-L1-IN 5 |
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T62193-50mg | 50mg | Ask for price |
Description: PD-1/PD-L1-IN 5 |
PD-1/PD-L1-IN 5 |
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T62193-5mg | 5mg | Ask for price |
Description: PD-1/PD-L1-IN 5 |
PD-1/PD-L1-IN-25 |
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T63329-10mg | 10mg | Ask for price |
Description: PD-1/PD-L1-IN-25 |
PD-1/PD-L1-IN-25 |
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T63329-1g | 1g | Ask for price |
Description: PD-1/PD-L1-IN-25 |
PD-1/PD-L1-IN-25 |
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T63329-1mg | 1mg | Ask for price |
Description: PD-1/PD-L1-IN-25 |
PD-1/PD-L1-IN-25 |
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T63329-50mg | 50mg | Ask for price |
Description: PD-1/PD-L1-IN-25 |
PD-1/PD-L1-IN-25 |
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T63329-5mg | 5mg | Ask for price |
Description: PD-1/PD-L1-IN-25 |
PD-1/PD-L1-IN-17 |
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T62501-10mg | 10mg | Ask for price |
Description: PD-1/PD-L1-IN-17 |
PD-1/PD-L1-IN-17 |
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T62501-1g | 1g | Ask for price |
Description: PD-1/PD-L1-IN-17 |
PD-1/PD-L1-IN-17 |
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T62501-1mg | 1mg | Ask for price |
Description: PD-1/PD-L1-IN-17 |
PD-1/PD-L1-IN-17 |
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T62501-50mg | 50mg | Ask for price |
Description: PD-1/PD-L1-IN-17 |
PD-1/PD-L1-IN-17 |
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T62501-5mg | 5mg | Ask for price |
Description: PD-1/PD-L1-IN-17 |
PD-1/PD-L1-IN-14 |
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T61929-10mg | 10mg | Ask for price |
Description: PD-1/PD-L1-IN-14 |
PD-1/PD-L1-IN-14 |
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T61929-1g | 1g | Ask for price |
Description: PD-1/PD-L1-IN-14 |
PD-1/PD-L1-IN-14 |
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T61929-1mg | 1mg | Ask for price |
Description: PD-1/PD-L1-IN-14 |
PD-1/PD-L1-IN-14 |
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T61929-50mg | 50mg | Ask for price |
Description: PD-1/PD-L1-IN-14 |
PD-1/PD-L1-IN-14 |
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T61929-5mg | 5mg | Ask for price |
Description: PD-1/PD-L1-IN-14 |
PD-1/PD-L1-IN 6 |
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T61968-10mg | 10mg | Ask for price |
Description: PD-1/PD-L1-IN 6 |
PD-1/PD-L1-IN 6 |
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T61968-1g | 1g | Ask for price |
Description: PD-1/PD-L1-IN 6 |
PD-1/PD-L1-IN 6 |
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T61968-1mg | 1mg | Ask for price |
Description: PD-1/PD-L1-IN 6 |
PD-1/PD-L1-IN 6 |
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T61968-50mg | 50mg | Ask for price |
Description: PD-1/PD-L1-IN 6 |
PD-1/PD-L1-IN 6 |
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T61968-5mg | 5mg | Ask for price |
Description: PD-1/PD-L1-IN 6 |
PD-1/PD-L1-IN-22 |
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T63607-10mg | 10mg | Ask for price |
Description: PD-1/PD-L1-IN-22 |
PD-1/PD-L1-IN-22 |
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T63607-1g | 1g | Ask for price |
Description: PD-1/PD-L1-IN-22 |
PD-1/PD-L1-IN-22 |
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T63607-1mg | 1mg | Ask for price |
Description: PD-1/PD-L1-IN-22 |
PD-1/PD-L1-IN-22 |
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T63607-50mg | 50mg | Ask for price |
Description: PD-1/PD-L1-IN-22 |
PD-1/PD-L1-IN-22 |
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T63607-5mg | 5mg | Ask for price |
Description: PD-1/PD-L1-IN-22 |
PD-1/PD-L1-IN-15 |
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T63614-10mg | 10mg | Ask for price |
Description: PD-1/PD-L1-IN-15 |
PD-1/PD-L1-IN-15 |
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T63614-1g | 1g | Ask for price |
Description: PD-1/PD-L1-IN-15 |
PD-1/PD-L1-IN-15 |
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T63614-1mg | 1mg | Ask for price |
Description: PD-1/PD-L1-IN-15 |
PD-1/PD-L1-IN-15 |
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T63614-50mg | 50mg | Ask for price |
Description: PD-1/PD-L1-IN-15 |
PD-1/PD-L1-IN-15 |
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T63614-5mg | 5mg | Ask for price |
Description: PD-1/PD-L1-IN-15 |
PD-1/PD-L1-IN-16 |
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T63948-10mg | 10mg | Ask for price |
Description: PD-1/PD-L1-IN-16 |
PD-1/PD-L1-IN-16 |
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T63948-1g | 1g | Ask for price |
Description: PD-1/PD-L1-IN-16 |
PD-1/PD-L1-IN-16 |
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T63948-1mg | 1mg | Ask for price |
Description: PD-1/PD-L1-IN-16 |
PD-1/PD-L1-IN-16 |
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T63948-50mg | 50mg | Ask for price |
Description: PD-1/PD-L1-IN-16 |
PD-1/PD-L1-IN-16 |
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T63948-5mg | 5mg | Ask for price |
Description: PD-1/PD-L1-IN-16 |
PD-1/PD-L1-IN-20 |
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T64086-10mg | 10mg | Ask for price |
Description: PD-1/PD-L1-IN-20 |
PD-1/PD-L1-IN-20 |
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T64086-1g | 1g | Ask for price |
Description: PD-1/PD-L1-IN-20 |
PD-1/PD-L1-IN-20 |
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T64086-1mg | 1mg | Ask for price |
Description: PD-1/PD-L1-IN-20 |
PD-1/PD-L1-IN-20 |
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T64086-50mg | 50mg | Ask for price |
Description: PD-1/PD-L1-IN-20 |
PD-1/PD-L1-IN-20 |
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T64086-5mg | 5mg | Ask for price |
Description: PD-1/PD-L1-IN-20 |
PD-1/PD-L1-IN-NP19 |
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T36900-10mg | 10mg | Ask for price |
Description: PD-1/PD-L1-IN-NP19 |
PD-1/PD-L1-IN-NP19 |
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T36900-1g | 1g | Ask for price |
Description: PD-1/PD-L1-IN-NP19 |
PD-1/PD-L1-IN-NP19 |
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T36900-1mg | 1mg | Ask for price |
Description: PD-1/PD-L1-IN-NP19 |
PD-1/PD-L1-IN-NP19 |
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T36900-50mg | 50mg | Ask for price |
Description: PD-1/PD-L1-IN-NP19 |
PD-1/PD-L1-IN-NP19 |
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T36900-5mg | 5mg | Ask for price |
Description: PD-1/PD-L1-IN-NP19 |
PD-1/PD-L1-IN-9 |
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MBS5801395-1mg | 1(mg | EUR 225 |
PD-1/PD-L1-IN-9 |
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MBS5801395-2mg | 2mg | EUR 285 |
PD-1/PD-L1-IN-9 |
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MBS5801395-5mg | 5(mg | EUR 345 |
PD-1/PD-L1-IN-10 |
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MBS5786462-10mg | 10(mg | EUR 250 |
PD-1/PD-L1-IN-10 |
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MBS5786462-2mg | 2(mg | EUR 180 |
PD-1/PD-L1-IN-10 |
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MBS5786462-5mg | 5(mg | EUR 195 |
PD-1/PD-L1-IN-NP19 |
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MBS5785098-10mg | 10mg | EUR 555 |
PD-1/PD-L1-IN-NP19 |
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MBS5785098-25mg | 25mg | EUR 1350 |
PD-1/PD-L1-IN-NP19 |
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MBS5785098-50mg | 50(mg | EUR 1520 |
PD-1/PD-L1-IN-NP19 |
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MBS5785098-5mg | 5(mg | EUR 375 |
PD-1/PD-L1 inhibitor 1 |
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MBS578522-10mg | 10mg | EUR 250 |
PD-1/PD-L1 inhibitor 1 |
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MBS578522-25mg | 25mg | EUR 375 |
PD-1/PD-L1 inhibitor 1 |
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MBS578522-2mg | 2mg | EUR 160 |
PD-1/PD-L1 inhibitor 1 |
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MBS578522-50mg | 50mg | EUR 510 |
PD-1/PD-L1 inhibitor 1 |
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MBS578522-5mg | 5mg | EUR 190 |
PD-1/PD-L1-IN 3 |
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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-18 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 6 |
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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 |
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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 |
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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 |
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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-14 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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-13 |
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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 5 |
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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-36 |
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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-25 |
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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-28 |
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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-31 |
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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-29 |
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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-34 |
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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 |
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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 |
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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 117519 |
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585228 | 5.0mg | EUR 230 |
PD-166285 |
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525796 | 5.0mg | EUR 275 |
PD 109488 |
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525816 | 50.0mg | EUR 1340 |
PD 135158 |
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525842 | 10.0mg | EUR 390 |
PD-176252 |
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525902 | 10.0mg | EUR 400 |
PD-198306 |
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525904 | 5.0mg | EUR 410 |
PD 146176 |
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530393 | 10.0mg | EUR 250 |
PD 150606 |
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531245 | 200.0mg | EUR 950 |
PD-85639 |
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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 180970 |
||
A8606-10 | 10 mg | EUR 302 |
Description: P210bcr/abl tyrosine kinase inhibitor |
PD 169316 |
||
A8689-10 | 10 mg | EUR 72 |
Description: P38 MAPK inhibitor |
PD 169316 |
||
A8689-5.1 | 10 mM (in 1mL DMSO) | EUR 106 |
Description: P38 MAPK inhibitor |
PD 169316 |
||
A8689-50 | 50 mg | EUR 271 |
Description: P38 MAPK inhibitor |
PD 173074 |
||
A8253-10 | 10 mg | EUR 40 |
Description: FGFR inhibitor |
PD 173074 |
||
A8253-5.1 | 10 mM (in 1mL DMSO) | EUR 48 |
Description: FGFR inhibitor |
PD 173074 |
||
A8253-50 | 50 mg | EUR 112 |
Description: FGFR inhibitor |
PD 173074 |
||
A8253-S | Evaluation Sample | EUR 22 |
Description: FGFR inhibitor |
PD-173212 |
||
598025 | 5.0mg | EUR 375 |
PD-166793 |
||
598116 | 10.0mg | EUR 360 |
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 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 082106 |
||
461981 | 5.0mg | EUR 300 |
PD 124966 |
||
414279 | 500.0µg | EUR 355 |
PD 81723 |
||
414815 | 10.0mg | EUR 335 |
PD-168393 |
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406105 | 25.0mg | EUR 300 |