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Phosphoaminophosphonic acid guanylate ester
go.drugbank.com/drugs/DB02082ExperimentalThe nucleotide is a potent stimulator of adenylate cyclase. … A non-hydrolyzable analog of GTP, in which the oxygen atom bridging the beta to the gamma phosphate is replaced by a nitrogen atom. It binds tightly to G-protein in the presence of Mg2+.
Synonyms: Gpp(NH)p, 5'-guanylylimidodiphosphateCategories: Heterocyclic Compounds, 2-RingN,N-dimethylglycine
go.drugbank.com/drugs/DB02083ExperimentalSynonyms: N,N-dimethylglycine, N,N-Dimethylaminoacetic acidCategories: N-substituted GlycinesCytidine
go.drugbank.com/drugs/DB02097InvestigationalSynonyms: 4-amino-1-β-D-ribofuranosylpyrimidin-2(1H)-one, 4-amino-1β-D-ribofuranosyl-2(1H)-pyrimidinoneCategories: Heterocyclic Compounds, 1-Ring6-Hydroxymethyl-7,8-Dihydropterin
go.drugbank.com/drugs/DB02119ExperimentalSynonyms: 6-Hydroxymethyl-7,8-DihydropterinCategories: Heterocyclic Compounds, 2-RingChlorophyll A
go.drugbank.com/drugs/DB02133ExperimentalSynonyms: Chlorophyll ACategories: Heterocyclic Compounds, 1-Ring, Heterocyclic Compounds with 4 or More RingsNandrolone decanoate
go.drugbank.com/drugs/DB08804ApprovedIllicitInvestigationalNandrolone decanoate, also known as nandrolone caprinate, is an alkylated anabolic steroid indicated in the management of anemia of renal insufficiency and as an adjunct therapy in the treatment of senile … [A233789,A233849,L32564,L9464] The process for creating esters of [nandrolone] was patented in Spain in 1959[L33244] and in 1960, it was described as having a long duration of action and strong anabolic
Categories: Monoamine Oxidase A Inhibitors for interaction with Monoamine Oxidase A substratesProducts: PARABOLIN RETARD 5 MG AMPUL, 2 ADET, DECA - DURABOLIN® 50 MGLurasidone
go.drugbank.com/drugs/DB08815ApprovedInvestigationalLurasidone is an atypical antipsychotic developed by Dainippon Sumitomo Pharma. It was approved by the U.S. … Food and Drug Administration (FDA) for treatment of schizophrenia on October 29, 2010 and is currently pending approval for the treatment of bipolar disorder in the United States.
Categories: Cytochrome P-450 Substrates, Heterocyclic Compounds, 1-RingProducts: LURAP® 40, LURAP ® 80Lomitapide
go.drugbank.com/drugs/DB08827ApprovedLomitapide, marketed under the brand names Juxtapid (USA) and Lojuxta (EU), is a first-in-class, small-molecule inhibitor of microsomal triglyceride transfer protein (MTP). … [A7367] Lomitapide was first approved by the FDA in December 2012 and the EMA in July 2013 as an adjunct to a low-fat diet and other lipid-lowering treatments.[A275444, A275446]
Synonyms: 9H-FLUORENE-9-CARBOXAMIDE, N-(2,2,2-TRIFLUOROETHYL)-9-(4-(4-(((4'-(TRIFLUOROMETHYL)(1,1'-BIPHENYL)-2-YL)CARBONYL)AMINO)-1-PIPERIDINYL)BUTYL)-, N-(2,2,2-TRIFLUOROETHYL)-9-(4-(4-(((4'-(TRIFLUOROMETHYL)BIPHENYL-2-YL)CARBONYL)AMINO)PIPERIDIN-1-YL)BUTYL)-9H-FLUORENE-9-CARBOXAMIDECategories: Cytochrome P-450 CYP3A4 Substrates with a Narrow Therapeutic Index, Cytochrome P-450 CYP3A Inhibitors