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Riferminogene pecaplasmid
go.drugbank.com/drugs/DB06394InvestigationalRiferminogene pecaplasmid (non-viral fibroblast growth factor 1; NV1FGF) is a recombinant DNA plasmid in a pCOR backbone allowing expression of human FGF1.
DP-VPA
go.drugbank.com/drugs/DB05821InvestigationalDP-VPA is D-Pharm's proprietary lipid modified version of valproic acid (VPA) that demonstrate that DP-VPA is well-tolerated in patients with resistant epilepsy and has a marked effect on reducing seizure frequency.
NM-702
go.drugbank.com/drugs/DB05505InvestigationalM-702 is an orally active inhibitor of phosphodiesterase and thromboxane synthetase. … Nissan Chemical and Taisho have been jointly developing NM-702, a drug for the treatment of arteriosclerosis obliterans.
Lanthanum carbonate
go.drugbank.com/drugs/DB06792ApprovedLanthanum carbonate is a phosphate binder marketed under the trade name Fosrenol by Shire Pharmaceuticals. It is a large pill that requires thorough chewing to avoid choking and other gastrointestinal adverse effects. It is used to treat...
Categories: Drugs for Treatment of Hyperkalemia and HyperphosphatemiaSodium-dependent phosphate transporter 1
go.drugbank.com/bio_entities/BE0005055TransporterHumansMay play a role in extracellular matrix and cartilage calcification as well as in vascular calcification (PubMed:11009570).
Synonyms: Leukemia virus receptor 1 homolog, Gibbon ape leukemia virus receptor 1Platelet glycoprotein 4
go.drugbank.com/bio_entities/BE0010538TargetTransporterHumansMultifunctional glycoprotein that acts as a receptor for a broad range of ligands. … Receptor for thrombospondins, THBS1 and THBS2, mediating their antiangiogenic effects (By similarity).
Synonyms: Thrombospondin receptor, Platelet collagen receptorStarch, corn
go.drugbank.com/drugs/DB11599ApprovedInvestigationalNutraceuticalCorn starch may be added in some food products as a thickening agent or anti-caking agent, and is sometimes found in topical drugs as a skin protectant.
CX157
go.drugbank.com/drugs/DB05205InvestigationalMAO-A inhibitors of this class. … CX157,3-fluoro-7-(2,2,2,-trifluoroethoxy)phenoxathiin-10,10-dioxide, is a reversible, selective inhibitor of MAO-A designed to have improved oral bioavailability and reduced clearance compared to previous
PPI-2458
go.drugbank.com/drugs/DB05864InvestigationalIn preclinical studies to date, PPI-2458 has demonstrated the potent pharmacologic activity of this class of compounds while displaying an improved pharmacokinetic and toxicity profile.
Etilamfetamine
go.drugbank.com/drugs/DB13285ExperimentalHowever, being on the controlled drug and substance act does not necessitate that the drug is approved for sale on the market. … Like other amphetamines, this amphetamine analog was used as an appetite suppressant in the 1950s.