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Cat. No. Product Name Field of Application Chemical Structure
DC12096 Pinacidil monohydrate (Pinacidil hydrate) Featured Pinacidil monohydrate, an antihypertensive drug, is a potassium channel activator.
DCAPI1413 pioglitazone hydrochloride Featured 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
DC10113 Pipequaline Featured Pipequaline (PK 8165) is a partial benzodiazepine receptor agonist with anxiolytic activity.
DCAPI1533 Piperaquine Phosphate Piperaquine Phosphate
DC24186 Piperazine Erastin Featured Piperazine Erastin is an analog of Erastin, which can induces ferroptosis in cancer cells, an iron-dependent form of nonapoptotic cell death..
DC9691 Piperlongumine Featured Piperlongumine induces cell death and increases the level of reactive oxygen species (ROS) in cancer cells with both wild-type and normal p53.
DC10115 Piperoxan hydrochloride Featured Piperoxan hydrochloride is an α2 adrenoceptor antagonist.
DC9629 Azaphen (dihydrochloride monohydrate) Pipofezine(Azafen or Azaphen) is a potent inhibitor of the reuptake of serotonin.
DCAPI1330 Piracetam Piracetam is a cyclic derivative of the neurotransmitter ã-aminobutyric acid (GABA), used in treatment of a wide range of cognitive disorders.
DC23685 Piragliatin Piragliatin (RO 4389620.
DC8112 Pirarubicin(THP) Featured Pirarubicin is an analogue of the anthracycline anti-neoplastic doxorubicin, which is an inhibitor of Topo II.
DC8792 Pirfenidone(AMR69) Featured 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.
DCAPI1575 Pirlimycin Pirlimycin
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). .
DC10012 Pirmenol hydrochloride Featured Pirmenol hydrochloride inhibits IK.ACh by blocking muscarinic receptors. The IC50 of Pirmenol for inhibition of Carbachol-induced IK.ACh is 0.1 μM.
DC10364 (±)-Pirmenol Featured Pirmenol inhibits IK.ACh by blocking muscarinic receptors. The IC50 of Pirmenol for inhibition of Carbachol-induced IK.ACh is 0.1 μM.
DC7155 Pirodavir (R 77975) Featured Pirodavir (R 77975) is the prototype of a novel class of broad-spectrum antipicornavirus compounds; potent human rhinovirus (HRV) capsid-binding inhibitor.
DC9071 Piroxicam Piroxicam (Feldene) is a non-selective COX inhibitor with an IC50 of 6 mM.
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.
DCAPI1385 Ropinirole HCl Pitavastatin Calcium is a competitive inhibitor of the enzyme HMGCR (HMG-CoA reductase) results in a reduction in LDL cholesterol synthesis.
DCAPI1470 Pitavastatin Calcium Featured 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
DC9465 Pitolisant (hydrochloride) Featured Pitolisant Hcl(BF2.649;Ciproxidine ) is a novel, potent, and selective nonimidazole inverse agonist at the recombinant human H3 receptor (Ki=0.16 nM).
DC9357 Pivmecillinam (hydrochloride) Pivmecillinam(Amdinocillin pivoxil) is an orally active prodrug of mecillinam, an extended-spectrum penicillin antibiotic.
DCAPI1216 Pizotifen malate Pizotifen malate
DC21940 Pizuglanstat Featured Pizuglanstat is a potent, selective prostaglandin D synthase inhibitor..
DC7237 PJ34 HCl Featured 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.
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).
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.
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..
DC7634 PKC-412 (Midostaurin) Featured 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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