DC12096 |
Pinacidil monohydrate (Pinacidil hydrate)
Featured
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Pinacidil monohydrate, an antihypertensive drug, is a potassium channel activator. |
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DCAPI1413 |
pioglitazone hydrochloride
Featured
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Pioglitazone Hydrochloride is the hydrochloride salt preparation of Pioglitazone, a specific ligand of PPAR-γ (peroxisome proliferator-activated receptor-γ). Pioglitazone is a thiazolidinedione compound described to produce antiinflammatory and antiarteri |
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DC10113 |
Pipequaline
Featured
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Pipequaline (PK 8165) is a partial benzodiazepine receptor agonist with anxiolytic activity. |
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DCAPI1533 |
Piperaquine Phosphate |
Piperaquine Phosphate |
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DC24186 |
Piperazine Erastin
Featured
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Piperazine Erastin is an analog of Erastin, which can induces ferroptosis in cancer cells, an iron-dependent form of nonapoptotic cell death.. |
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DC9691 |
Piperlongumine
Featured
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Piperlongumine induces cell death and increases the level of reactive oxygen species (ROS) in cancer cells with both wild-type and normal p53. |
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DC10115 |
Piperoxan hydrochloride
Featured
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Piperoxan hydrochloride is an α2 adrenoceptor antagonist. |
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DC9629 |
Azaphen (dihydrochloride monohydrate) |
Pipofezine(Azafen or Azaphen) is a potent inhibitor of the reuptake of serotonin. |
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DCAPI1330 |
Piracetam |
Piracetam is a cyclic derivative of the neurotransmitter ã-aminobutyric acid (GABA), used in treatment of a wide range of cognitive disorders. |
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DC23685 |
Piragliatin |
Piragliatin (RO 4389620. |
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DC8112 |
Pirarubicin(THP)
Featured
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Pirarubicin is an analogue of the anthracycline anti-neoplastic doxorubicin, which is an inhibitor of Topo II. |
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DC8792 |
Pirfenidone(AMR69)
Featured
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Pirfenidone(AMR69) is an inhibitor for TGF-β production and TGF-β stimulated collagen production, reduces production of TNF-α and IL-1β, and also has anti-fibrotic and anti-inflammatory properties. Phase 3. |
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DCAPI1575 |
Pirlimycin |
Pirlimycin |
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DC12558 |
Pirlindole Mesylate |
Pirlindole is a novel potent inhibitor of Enteroviruse that targets Viral Protein 2C, inhibits EV-B and EV-D through the inhibition of genome replication (CV-B3 EC50=9.91 uM). . |
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DC10012 |
Pirmenol hydrochloride
Featured
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Pirmenol hydrochloride inhibits IK.ACh by blocking muscarinic receptors. The IC50 of Pirmenol for inhibition of Carbachol-induced IK.ACh is 0.1 μM. |
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DC10364 |
(±)-Pirmenol
Featured
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Pirmenol inhibits IK.ACh by blocking muscarinic receptors. The IC50 of Pirmenol for inhibition of Carbachol-induced IK.ACh is 0.1 μM. |
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DC7155 |
Pirodavir (R 77975)
Featured
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Pirodavir (R 77975) is the prototype of a novel class of broad-spectrum antipicornavirus compounds; potent human rhinovirus (HRV) capsid-binding inhibitor. |
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DC9071 |
Piroxicam |
Piroxicam (Feldene) is a non-selective COX inhibitor with an IC50 of 6 mM. |
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DC20506 |
PIT-1 |
PIT-1 is a specific PIP3 antagonist that disrupts PIP3/Akt PH domain binding with IC50 of 30 uM, Kd of 43.2 uM. |
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DCAPI1385 |
Ropinirole HCl |
Pitavastatin Calcium is a competitive inhibitor of the enzyme HMGCR (HMG-CoA reductase) results in a reduction in LDL cholesterol synthesis. |
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DCAPI1470 |
Pitavastatin Calcium
Featured
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Pitavastatin Calcium is a competitive inhibitor of the enzyme HMGCR (HMG-CoA reductase) results in a reduction in LDL cholesterol synthesis. Alternate studies show that pitavastatin can suppress oxygen production in endothelial cells by inhibiting NADPH o |
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DC9465 |
Pitolisant (hydrochloride)
Featured
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Pitolisant Hcl(BF2.649;Ciproxidine ) is a novel, potent, and selective nonimidazole inverse agonist at the recombinant human H3 receptor (Ki=0.16 nM).
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DC9357 |
Pivmecillinam (hydrochloride) |
Pivmecillinam(Amdinocillin pivoxil) is an orally active prodrug of mecillinam, an extended-spectrum penicillin antibiotic. |
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DCAPI1216 |
Pizotifen malate |
Pizotifen malate |
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DC21940 |
Pizuglanstat
Featured
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Pizuglanstat is a potent, selective prostaglandin D synthase inhibitor.. |
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DC7237 |
PJ34 HCl
Featured
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PJ34 HCl is the hydrochloride salt of PJ34, which is a PARP inhibitor with EC50 of 20 nM and is equally potent to PARP1/2. |
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DC21512 |
PJ-68 |
PJ-68 is a potent, selective inhibitor of arginine methyltransferase PRMT5 with IC50 of 517 nM, shows no inhibitory activity against type I PRMT family members ( (PRMT1, 3, 4, 6, and 8). |
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DC22109 |
PK4C9 |
PK4C9 (Homocarbonyltopsentin) is a small-molecule stem-loop RNA structure TSL2-binding compound (EC50=16.1 uM) that increases SMN2 exon 7 (E7) splicing and rescues downstream molecular alterations in SMA cells. |
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DC23280 |
PK-7088 |
PK-7088 is a small molecule mutant p53 Y220C reactivator, promotes correct folding of Y220 mutant p53 and induces expression of p53 targets p21 and the Noxa, triggers nuclear export of the pro-apoptotic Bax protein to mitochondria.. |
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DC7634 |
PKC-412 (Midostaurin)
Featured
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PKC-412 is a broad spectrum protein kinase inhibitor. Inhibits conventional PKC isoforms (α, β, γ), PDFRβ, VEGFR2, Syk, PKCη, Flk-1, Flt3, Cdk1/B, PKA, c-Kit, c-Fgr, c-Src, VEGFR1 and EGFR. Displays potent antitumor activity. |
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