CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
Pantoprazole is a proton pump inhibitor drug used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease.
More Information
Supplier Page
CSNpharm
Pantoprazole is a proton pump inhibitor drug used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease.
More Information
Supplier Page
CSNpharm
Pantoprazole sodium is an inhibitor of proton pump that can suppress function of H+/K+ ATPase. It is used for the treatment of hyperacidity.
More Information
Supplier Page
CSNpharm
Pantoprazole sodium is an inhibitor of proton pump that can suppress function of H+/K+ ATPase. It is used for the treatment of hyperacidity.
More Information
Supplier Page
CSNpharm
Pantoprazole sodium is an inhibitor of proton pump that can suppress function of H+/K+ ATPase. It is used for the treatment of hyperacidity.
More Information
Supplier Page
CSNpharm
Paprotrain is reversible, non-ATP competitive inhibitor of mitotic kinesin-like protein 2 (MKLP-2) with Ki of 3.4 μM.
More Information
Supplier Page
CSNpharm
Paprotrain is reversible, non-ATP competitive inhibitor of mitotic kinesin-like protein 2 (MKLP-2) with Ki of 3.4 μM.
More Information
Supplier Page
CSNpharm
Paprotrain is reversible, non-ATP competitive inhibitor of mitotic kinesin-like protein 2 (MKLP-2) with Ki of 3.4 μM.
More Information
Supplier Page
CSNpharm
Paprotrain is reversible, non-ATP competitive inhibitor of mitotic kinesin-like protein 2 (MKLP-2) with Ki of 3.4 μM.
More Information
Supplier Page
CSNpharm
Paprotrain is reversible, non-ATP competitive inhibitor of mitotic kinesin-like protein 2 (MKLP-2) with Ki of 3.4 μM.
More Information
Supplier Page
CSNpharm
Paquinimod is an inhibitor of S100A9 which can prevent S100A9 from binding to TLR-4. Paquinimod is also known as ABR‑215757.
More Information
Supplier Page
CSNpharm
Paquinimod is an inhibitor of S100A9 which can prevent S100A9 from binding to TLR-4. Paquinimod is also known as ABR‑215757.
More Information
Supplier Page
CSNpharm
Paquinimod is an inhibitor of S100A9 which can prevent S100A9 from binding to TLR-4. Paquinimod is also known as ABR‑215757.
More Information
Supplier Page
CSNpharm
Paquinimod is an inhibitor of S100A9 which can prevent S100A9 from binding to TLR-4. Paquinimod is also known as ABR‑215757.
More Information
Supplier Page
CSNpharm
Paradol is an effective inhibitor of tumor promotion in mouse skin carcinogenesis, binds to cyclooxygenase (COX)-2 active site, it’s a pungent phenolic substance isolated and purified from ginger and other Zingiberaceae plants.
More Information
Supplier Page
CSNpharm
Paradol is an effective inhibitor of tumor promotion in mouse skin carcinogenesis, binds to cyclooxygenase (COX)-2 active site, it’s a pungent phenolic substance isolated and purified from ginger and other Zingiberaceae plants.
More Information
Supplier Page
CSNpharm
Paradol is an effective inhibitor of tumor promotion in mouse skin carcinogenesis, binds to cyclooxygenase (COX)-2 active site, it’s a pungent phenolic substance isolated and purified from ginger and other Zingiberaceae plants.
More Information
Supplier Page
CSNpharm
Paradol is an effective inhibitor of tumor promotion in mouse skin carcinogenesis, binds to cyclooxygenase (COX)-2 active site, it’s a pungent phenolic substance isolated and purified from ginger and other Zingiberaceae plants.
More Information
Supplier Page
CSNpharm
Paradol is an effective inhibitor of tumor promotion in mouse skin carcinogenesis, binds to cyclooxygenase (COX)-2 active site, it’s a pungent phenolic substance isolated and purified from ginger and other Zingiberaceae plants.
More Information
Supplier Page
CSNpharm
Parbendazole is a potent inhibitor of microtubule assembly, destabilizes tubulin, with an EC50 of 8.79 nM, and exhibits a broad-spectrum anthelmintic activity.
More Information
Supplier Page
CSNpharm
Parbendazole is a potent inhibitor of microtubule assembly, destabilizes tubulin, with an EC50 of 8.79 nM, and exhibits a broad-spectrum anthelmintic activity.
More Information
Supplier Page
CSNpharm
Parbendazole is a potent inhibitor of microtubule assembly, destabilizes tubulin, with an EC50 of 8.79 nM, and exhibits a broad-spectrum anthelmintic activity.
More Information
Supplier Page
CSNpharm
Parbendazole is a potent inhibitor of microtubule assembly, destabilizes tubulin, with an EC50 of 8.79 nM, and exhibits a broad-spectrum anthelmintic activity.
More Information
Supplier Page
CSNpharm
Pardoprunox HCl is a partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist, D2 (pKi = 8.1) and D3 receptor (pKi = 8.6) partial agonist and 5-HT1A receptor (pKi = 8.5) full agonist.
More Information
Supplier Page
CSNpharm
Pardoprunox HCl is a partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist, D2 (pKi = 8.1) and D3 receptor (pKi = 8.6) partial agonist and 5-HT1A receptor (pKi = 8.5) full agonist.
More Information
Supplier Page
CSNpharm
Pardoprunox HCl is a partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist, D2 (pKi = 8.1) and D3 receptor (pKi = 8.6) partial agonist and 5-HT1A receptor (pKi = 8.5) full agonist.
More Information
Supplier Page
CSNpharm
Pardoprunox HCl is a partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist, D2 (pKi = 8.1) and D3 receptor (pKi = 8.6) partial agonist and 5-HT1A receptor (pKi = 8.5) full agonist.
More Information
Supplier Page
CSNpharm
Pardoprunox HCl is a partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist, D2 (pKi = 8.1) and D3 receptor (pKi = 8.6) partial agonist and 5-HT1A receptor (pKi = 8.5) full agonist.
More Information
Supplier Page
CSNpharm
Pardoprunox HCl is a partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist, D2 (pKi = 8.1) and D3 receptor (pKi = 8.6) partial agonist and 5-HT1A receptor (pKi = 8.5) full agonist.
More Information
Supplier Page
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
Parecoxib Sodium, a water-soluble and injectable prodrug of valdecoxib, is a COX2 inhibitor used for the short-term treatment of postoperative pain in adults.
More Information
Supplier Page
CSNpharm
Parecoxib Sodium, a water-soluble and injectable prodrug of valdecoxib, is a COX2 inhibitor used for the short-term treatment of postoperative pain in adults.
More Information
Supplier Page
CSNpharm
Parecoxib Sodium, a water-soluble and injectable prodrug of valdecoxib, is a COX2 inhibitor used for the short-term treatment of postoperative pain in adults.
More Information
Supplier Page
CSNpharm
Parecoxib Sodium, a water-soluble and injectable prodrug of valdecoxib, is a COX2 inhibitor used for the short-term treatment of postoperative pain in adults.
More Information
Supplier Page
CSNpharm
Pargyline is an irreversible non-selective monoamine oxidase (MAO) inhibitor drug (IC50 for MAO-A is 11.52 nM and for MAO-B is 8.2 nM) .
More Information
Supplier Page
CSNpharm
Pargyline is an irreversible non-selective monoamine oxidase (MAO) inhibitor drug (IC50 for MAO-A is 11.52 nM and for MAO-B is 8.2 nM) .
More Information
Supplier Page
CSNpharm
Pargyline HCl is an irreversible and selective MAO-B inhibitor with Ki values of 15 and 1.8 μM for MAO-A and MAO-B, respectively.
More Information
Supplier Page
CSNpharm
Pargyline HCl is an irreversible and selective MAO-B inhibitor with Ki values of 15 and 1.8 μM for MAO-A and MAO-B, respectively.
More Information
Supplier Page
CSNpharm
Pargyline HCl is an irreversible and selective MAO-B inhibitor with Ki values of 15 and 1.8 μM for MAO-A and MAO-B, respectively.
More Information
Supplier Page
CSNpharm
Paromomycin Sulfate is an aminoglycoside antibiotics inhibiting protein synthesis in non-resistant cells by binding to 16S ribosomal RNA.
More Information
Supplier Page
CSNpharm
Paromomycin Sulfate is an aminoglycoside antibiotics inhibiting protein synthesis in non-resistant cells by binding to 16S ribosomal RNA.
More Information
Supplier Page