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Displaying results 171 - 180 of 4117 in total
  1. Drug

    S-Ethyl-N-Phenyl-Isothiourea

    go.drugbank.com/drugs/DB03707
    Experimental

    Synonyms: S-Ethyl-N-Phenyl-Isothiourea
  2. Drug

    (C8-S)-Hydantocidin 5'-phosphate

    go.drugbank.com/drugs/DB04460
    Experimental

    Synonyms: (C8-S)-Hydantocidin 5'-phosphate
  3. Drug

    S-METHYL-4,5,6,7-TETRABROMO-BENZIMIDAZOLE

    go.drugbank.com/drugs/DB04720
    Experimental

    Synonyms: S-METHYL-4,5,6,7-TETRABROMO-BENZIMIDAZOLE
  4. Drug

    Duloxetine

    go.drugbank.com/drugs/DB00476
    ApprovedInvestigational

    Duloxetine is a dual serotonin and norepinephrine reuptake inhibitor.[label] It was originally discovered in 1993 and developed by Eli Lilly and Company as LY248686. … [A178741] Duloxetine first received approval from the FDA in August, 2004 as Cymbalta for the treatment of Major Depressive Disorder.

    Categories: P-glycoprotein inhibitors, Cytochrome P-450 SubstratesSynonyms: (S)-duloxetine, (3S)-N-methyl-3-(1-naphthyloxy)-3-(2-thienyl)propan-1-amine
  5. Drug

    Levobunolol

    go.drugbank.com/drugs/DB01210
    Approved

    A nonselective beta-adrenoceptor antagonist used in the treatment of glaucoma.

    Categories: Cytochrome P-450 Substrates, Cytochrome P-450 CYP2D6 SubstratesSynonyms: (S)-5-(3-((1,1-dimethylethyl)amino)-2-hydroxypropoxy)-3,4-dihydro-1(2H)-naphthalenone
  6. Drug

    Linezolid

    go.drugbank.com/drugs/DB00601
    ApprovedInvestigational

    Linezolid is a synthetic antibiotic which is used for the treatment of infections caused by aerobic Gram-positive bacteria. … [A233425] A second member of this class, [tedizolid], was approved by the FDA in 2014 and is considered generally more effective and tolerable than its predecessor.

    Synonyms: N-(((S)-3-(3-Fluoro-4-morpholinophenyl)-2-oxo-5-oxazolidinyl)methyl)acetamideCategories: Monoamine Oxidase A Inhibitors for interaction with Monoamine Oxidase A substrates, Heterocyclic Compounds, 1-Ring
  7. Drug

    Levofloxacin

    go.drugbank.com/drugs/DB01137
    ApprovedInvestigational

    Levofloxacin is a fluoroquinolone antibiotic and the optical S-(-) isomer of racemic [ofloxacin]. … [L11638] Levofloxacin, along with other quinolones such as [gatifloxacin] and [moxifloxacin], is a member of the third generation of fluoroquinolones, colloquially referred to as the "respiratory quinolones

    Categories: 4-Quinolones, MATE 1 InhibitorsSynonyms: (S)-Ofloxacin, Ofloxacin S-(-)-form
  8. Drug

    Arginine

    go.drugbank.com/drugs/DB00125
    ApprovedInvestigationalNutraceutical

    An essential amino acid that is physiologically active in the L-form.

    Mixtures: AMINOACIDI S BIOINDUSTRIA L.I.M., AMINOPLASMAL® 10% ESynonyms: (S)-2-Amino-5-guanidinovaleric acid, (S)-2-amino-5-guanidinopentanoic acid
  9. Drug

    Rifabutin

    go.drugbank.com/drugs/DB00615
    ApprovedInvestigational

    A broad-spectrum antibiotic that is being used as prophylaxis against disseminated Mycobacterium avium complex infection in HIV-positive patients.

    Synonyms: 4-N-isobutylspiropiperidylrifamycin S, 4-Deoxo-3,4-(2-spiro(N-isobutyl-4-piperidyl)-2,5-dihydro-1H-imidazo)-rifamycin SCategories: P-glycoprotein inducers, Cytochrome P-450 Substrates
  10. Drug

    Darifenacin

    go.drugbank.com/drugs/DB00496
    ApprovedInvestigational

    It is unknown if M3 receptor selectivity is clinically advantageous in overactive bladder syndrome treatments. … Darifenacin (Enablex®, Novartis) is a medication used to treat urinary incontinence. Darifenacin blocks M3 muscarinic acetylcholine receptors, which mediate bladder muscle contractions.

    Synonyms: (S)-1-(2-(2,3-dihydro-5-benzofuranyl)ethyl)-α,α-diphenyl-3-pyrrolidineacetamideCategories: Cytochrome P-450 Substrates, Cytochrome P-450 CYP2D6 Inhibitors