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Lodiperone
go.drugbank.com/drugs/DB21210ExperimentalLodiperone has a monoisotopic molecular weight of 435.09 Da. … Lodiperone is a small molecule drug. The usage of the INN stem '-perone' in the name indicates that Lodiperone is a tranquillizer, neuroleptic, 4'-fluoro-4-piperidinobutyrophenone derivative.
Murocainide
go.drugbank.com/drugs/DB21243ExperimentalMurocainide has a monoisotopic molecular weight of 377.2 Da. … Murocainide is a small molecule drug. The usage of the INN stem '-cain-' in the name indicates that Murocainide is a class I antiarrhythmic, procainamide and lidocaine derivative.
Zocainone
go.drugbank.com/drugs/DB21326ExperimentalZocainone has a monoisotopic molecular weight of 353.2 Da. … Zocainone is a small molecule drug. The usage of the INN stem '-cain-' in the name indicates that Zocainone is a class I antiarrhythmic, procainamide and lidocaine derivative.
Atrimustine
go.drugbank.com/drugs/DB21376ExperimentalAtrimustine has a monoisotopic molecular weight of 719.28 Da. … Atrimustine is a small molecule drug. The usage of the INN stem '-mustine' in the name indicates that Atrimustine is a antineoplastic, alkylating agent, (β-chloroethyl) amine derivative.
Pirenperone
go.drugbank.com/drugs/DB21405ExperimentalPirenperone has a monoisotopic molecular weight of 393.19 Da. … Pirenperone is a small molecule drug. The usage of the INN stem '-perone' in the name indicates that Pirenperone is a tranquillizer, neuroleptic, 4'-fluoro-4-piperidinobutyrophenone derivative.
Cinsebrutinib
go.drugbank.com/drugs/DB21640ExperimentalCinsebrutinib has a monoisotopic molecular weight of 383.2 Da. … Cinsebrutinib is a small molecule drug. The usage of the INN stem '-brutinib' in the name indicates that Cinsebrutinib is a agammaglobulinaemia tyrosine kinase (Bruton tyrosine kinase) inhibitor.
Surzetoclax
go.drugbank.com/drugs/DB21698InvestigationalSurzetoclax has a monoisotopic molecular weight of 1038.41 Da. … Surzetoclax is a small molecule drug. The usage of the INN stem '-toclax' in the name indicates that Surzetoclax is a B-cell lymphoma 2 (Bcl-2) inhibitor.
Metiamide
go.drugbank.com/drugs/DB08805ExperimentalMetiamide is an H-2 receptor antagonist derived from burimamide. It was an intermediate product on the path to developing cimetidine.
DG051
go.drugbank.com/drugs/DB05177ExperimentalDG051 is designed to decrease risk of heart attack by decreasing the production of leukotriene B4 (LTB4), an end product of the leukotriene pathway and a potent promoter of inflammation. … DG051 is a novel small-molecule inhibitor of leukotriene A4 hydrolase (LTA4H), the protein made by one of the genes in the leukotriene pathway that has been shown to link to risk of heart attack.
Imidafenacin
go.drugbank.com/drugs/DB09262InvestigationalImidafenacin is an antispasmodic agent with anticholinergic effects. It antagonizes muscarinic receptors in the bladder to reduce the frequency of urination in the treatment of overactive bladder.