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Levofacetoperane
go.drugbank.com/drugs/DB19849ExperimentalLevofacetoperane is a small molecule drug. Levofacetoperane has a monoisotopic molecular weight of 233.14 Da.
Categories: Heterocyclic Compounds, 1-RingSynonyms: (r,r)-(-)-phacetoperaneCinoxopazide
go.drugbank.com/drugs/DB19851ExperimentalCinoxopazide is a small molecule drug. Cinoxopazide has a monoisotopic molecular weight of 371.18 Da.
Flesinoxan
go.drugbank.com/drugs/DB19853ExperimentalFlesinoxan is a small molecule drug. The usage of the INN stem '-oxan(e)' in the name indicates that Flesinoxan is a benzodioxane derivative. … Flesinoxan has a monoisotopic molecular weight of 415.19 Da.
Categories: Heterocyclic Compounds, 1-RingIprotiazem
go.drugbank.com/drugs/DB19857ExperimentalIprotiazem is a small molecule drug. Iprotiazem has a monoisotopic molecular weight of 647.34 Da.
Betamipron
go.drugbank.com/drugs/DB19858ExperimentalBetamipron is a small molecule drug. Betamipron has a monoisotopic molecular weight of 193.07 Da.
Synonyms: N-benzoyl-.beta.-alanineDichlorophenarsine
go.drugbank.com/drugs/DB19861ExperimentalDichlorophenarsine is a small molecule drug. Dichlorophenarsine has a monoisotopic molecular weight of 252.9 Da.
MIP-1095 I-131
go.drugbank.com/drugs/DB14978InvestigationalMIP-1095 I-131 is under investigation in clinical trial NCT03030885 (Use of an Experimental Radiopharmaceutical (131I-MIP-1095) in Men With Metastatic Castration-Resistant Prostate Cancer (mCRPC)).
Martinostat
go.drugbank.com/drugs/DB14979InvestigationalMartinostat is under investigation in clinical trial NCT03721211 (Imaging With [11C]Martinostat in Breast Cancer).
Nomacopan
go.drugbank.com/drugs/DB14991InvestigationalNomacopan is under investigation in clinical trial NCT03427060 (Coversin in PNH in Patients With Resistance to Eculizumab Due to Complement C5 Polymorphisms).
Categories: Recombinant Protein Inhibitor of Complement Factor 5Pegunigalsidase alfa
go.drugbank.com/drugs/DB14992ApprovedInvestigationalPegunigalsidase alfa (PRX-102) is a recombinant form of human α-galactosidase-A indicated for long-term enzyme replacement therapy in patients with Fabry disease, a rare genetic disorder characterized … to a different glycosylation pattern.