Anthelmintic used in grazing animals for fasciola and cestode infestations.

Oxyma Pure is used in the synthesis of difficult peptides and can act as an acidic modifier to prevent aspartimide formation.

Oxyresveratrol is a natural hydroxystilbene with similar bioactivity to resveratrol.

Oxyresveratrol is isolated from the herbs of Dracaena angustifolia. Because toxicity to glia could be beneficial by inhibiting reactive gliosis, Oxyresveratro is useful to trauma models. Oxyresveratrol can reduce neuronal oxidative damage and protect hepatocytes against oxidative stress and mitochondrial dysfunction, which may be associated with activation of Nrf2.

Sophocarpidine comes from the root of Styphnolobium japonicum (L.) Schott. Sophocarpine could decrease the level of serum transaminase, improve lipid metabolism, reduce synthesis of inflammatory cytokines TNF-α, TGF-β1 and IL-6, activate protective adipocytokine adiponectin, might be a drug for colonic inflammation and NASH.

A tetracycline analog isolated from the actinomycete streptomyces rimosus and used in a wide variety of clinical conditions.

Oxytetracycline Hydrochloride is the hydrochloride salt form of oxytetracycline, a tetracycline derivative produced by Streptomyces rimosus exhibiting antimicrobial activity. Oxytetracycline hydrochloride interferes with binding of aminoacyl-tRNA to the mRNA-ribosome complex, thereby preventing peptide elongation and inhibiting protein synthesis. It is often used to treat skin conditions.

Free acid form of oxytocin, which is a hormone involved in many aspects of mammalian reproduction as well as other physiological processes such as bond pairing and cardiovascular homeostasis.

Oxytocin is a hormone that is produced by the hypothalamus and secreted by the pituitary gland. It is used in pharmacology to treat various conditions, such as postpartum haemorrhage, uterine contractions, labour induction, and to stimulate milk production. Oxytocin has been shown to activate G-protein coupled receptors (GPCRs) and ion channels. The oxytocin receptor is […]

Oxytocin is an Oxytocic. The physiologic effect of oxytocin is by means of Increased Uterine Smooth Muscle Contraction or Tone.

Ozagrel is a thromboxane A2 synthase inhibitor used as an antiplatelet agent. It reduces the risk of neurological impairment and the volume of brain damage.

Ozanimod is a potent and selective S1P1 and S1P5 receptor agonist with EC50s of 410±160 pM and 11±4.3 nM in [35S]-GTPγS binding, respectively.

Ozenoxacin is a Quinolone Antimicrobial.

p-Nitrophenylacetonitrile is used as a radical inhibitor in the polymerization of vinyl acetate.

P(t-Bu)3 Pd G3 is an organic noble metal catalyst, which is mainly used as a catalyst in coupling reactions such as Suzuki, Kumada, and Negishi.

P(t-Bu)3 Pd G4 is a powerful ligand for classic cross-coupling reactions combined with the Buchwald Fourth Generation Palladacycle. Bench stable, soluble in most organic solvents.

5′-Dimethoxytrityl-N-phenoxyacetyl-Adenosine is an immensely potent phosphoramidite, boasting significant utility in the research and development of oligonucleotides intended for diverse biomedical purposes. Notably, its employment expedites the incorporation of Phenoxyacetyl-Adenosine moieties into DNA molecules, thereby facilitating comprehensive examination of DNA-protein interactions while concurrently streamlining gene sequencing endeavors.

Pachymic acid, a natural lanostrane-type triterpenoid derived from the root of Wolfiporia cocos (Schw.) Ryv., demonstrates anti-inflammatory, anti-emetic and anti-cancer activities.

Paclitaxel is a tetracyclic diterpenoid isolated originally from the bark of the Pacific yew tree, Taxus brevifolia. It is a mitotic inhibitor used in cancer chemotherapy. Note that the use of the former generic name ‘taxol’ is now limited, as Taxol is a registered trade mark. It has a role as a microtubule-stabilising agent, a […]

Paclitaxel is an antineoplastic that used to treat patients with lung, ovarian, breast cancer, head and neck cancer, and advanc ed forms of Kaposis sarcoma.

Paclitaxel is a potent anticancer medication which can promote microtubule (MT) assembly, inhibit MT depolymerization, and change MT dynamics required for mitosis and cell proliferation.

Paclitaxel is a potent anticancer medication which can promote microtubule (MT) assembly, inhibit MT depolymerization, and change MT dynamics required for mitosis and cell proliferation.

Pacritinib is a small molecule Janus kinase inhibitor that is used in the treatment of intermediate or high risk, primary or secondary myelofibrosis. Pacritinib is associated with transient and usually mild elevations in serum aminotransferase during therapy but has not been linked instances of clinically apparent acute liver injury.

Paeoniflorin is a herbal constituent extracted from the root of Paeonia albiflora Pall. Paeoniflorin has antiandrogenic properties. Paeoniflorin inhibits the production of testosterone and promotes the activity of aromatase-the enzyme that converts testosterone into estrogen.

Paeonol acting as a β-Secretase inhibitor an anti-apoptotic agent is used in the treatment of memory loss after ischemic stroke.

Used in the preparation of lipophilic human glucagon-like peptide-1 derivatives with protracted action profiles.

Palbociclib is a selective CDK4 and CDK6 inhibitor with IC50s of 11 and 16 nM, respectively. Palbociclib is a drug for the treatment of ER-positive and HER2-negative breast cancer.

Palbociclib Impurity 53 is an impurity of Palbociclib, a medication for the treatment of HR-positive and HER2-negative breast cancer. It is a selective inhibitor of the cyclin-dependent kinases CDK4 and CDK6.

Palbociclib Impurity 63 is an impurity of Palbociclib, a medication for the treatment of HR-positive and HER2-negative breast cancer. It is a selective inhibitor of the cyclin-dependent kinases CDK4 and CDK6.

Palbociclib Impurity 42 is an impurity of Palbociclib, a medication for the treatment of HR-positive and HER2-negative breast cancer. It is a selective inhibitor of the cyclin-dependent kinases CDK4 and CDK6.

An impurity of Palbociclib which is a selective inhibitor of the cyclin-dependent kinases CDK4 and CDK6.

Paliperidone is an Atypical Antipsychotic.

A benzisoxazole derivative and active metabolite of RISPERIDONE that functions as a DOPAMINE D2 RECEPTOR ANTAGONIST and SEROTONIN 5-HT2 RECEPTOR ANTAGONIST. It is an ANTIPSYCHOTIC AGENT used in the treatment of SCHIZOPHRENIA.

A fourth generation (G4) Buchwald precatalyst that is similar to the third generation (G3) precatalysts except that the amino group on the biphenyl backbone is methylated. This modification helps to prevent the limitations found when using the third generation precatalysts. It is air, moisture, and thermally-stable and shows good solubility in common organic solvents.

Palmitoylethanolamide is a natural substance produced by the body and it is very effective and safe to use as a supplement for pain and reduce inflammation.

Palmitoylethanolamide can be used as organic synthesis intermediates and pharmaceutical intermediates, which are mainly used in laboratory research and development process and chemical production process.

Adjuvant to chemotherapy

2-pyridinylmethylsulfinylbenzimidazole proton pump inhibitor that is used in the treatment of GASTROESOPHAGEAL REFLUX and PEPTIC ULCER.

Pantoprazole sodium hydrate is a proton pump inhibitor drug used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease.

powerful analgesic

Paricalcitol is a synthetic vitamin D analog. Paricalcitol has been used to reduce parathyroid hormone levels. Paricalcitol is indicated for the prevention and treatment of secondary hyperparathyroidism associated with chronic renal failure.

Parthenolide is a sesquiterpene lactone and active principle of Feverfew (Tanacetum parthenium). It has a role as a non-steroidal anti-inflammatory drug, a non-narcotic analgesic, a peripheral nervous system drug, an inhibitor and a drug allergen.

Pasireotide is a stable cyclohexapeptide somatostatin mimic that exhibits unique high-affinity binding to human somatostatin receptors.