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Progesterone
go.drugbank.com/drugs/DB00396ApprovedInvestigationalVet approvedPharmaceutical progesterone is made from a plant source as a starting material and is chemically identical to progesterone of human ovarian origin [FDA label]. … A low progesterone concentration or an insufficient response to progesterone can cause infertility and pregnancy loss [A175609].
Synonyms: (S)-4-Pregnene-3,20-dione, (S)-Pregn-4-en-3,20-dioneMixtures: SYNERGAL® DOBLE, Minoxidil 7% / Progesterone 0.1%Colloidal oatmeal
go.drugbank.com/drugs/DB11286ApprovedNutraceuticalColloidal oatmeal is a FDA-approved skin protectant that temporarily protects and helps relieve minor skin irritation and itching due to rashes, eczema, poison ivy, oak, sumac, or insect bites. … It is available in topical products as a skin soothing agent.
Mixtures: Pediadermics Eczema 3, 5% Oat Facial CleanserProducts: A Bit Hippy, TMC-A Hair TonicFrovatriptan
go.drugbank.com/drugs/DB00998ApprovedFrovatriptan is a triptan drug developed by Vernalis for the treatment of migraine headaches, in particular those associated with menstruation.
Categories: Serotonin 5-HT1 Receptor Agonists, Selective Serotonin 5-HT1 Receptor AgonistsProducts: EUMITAN 2.5MG FTA, NEWART 2.5 MG TABLET, 3 ADETAtrial natriuretic peptide receptor 1
go.drugbank.com/bio_entities/BE0000556TargetHumansReceptor for the atrial natriuretic peptide NPPA/ANP and the brain natriuretic peptide NPPB/BNP which are potent vasoactive hormones playing a key role in cardiovascular homeostasis (PubMed:39543315).
Polypeptides: Atrial natriuretic peptide receptor 1Synonyms: Atrial natriuretic peptide receptor type A, ANP-ATagraxofusp
go.drugbank.com/drugs/DB14731ApprovedInvestigationalTagraxofusp is a CD123-directed cytotoxin. … [A253762, A253887, L43702] Tagraxofusp received its first global approval by the FDA on December 21, 2018 as the first FDA-approved treatment for blastic plasmacytoid dendritic cell neoplasm, which is
Synonyms: Diphtheria toxin-il-3 fusion protein targeting IL-3 receptorNucleoside diphosphokinase
go.drugbank.com/bio_entities/BE0009626EnzymeHumansPhosphorylates the GNB1 subunit of heterotrimeric G proteins at 'His-266', generating a high-energy phosphate group that promotes GTP formation and enables receptor-independent activation of heterotrimeric … Catalyzes the transfer of a gamma-phosphoryl group from a nucleoside triphosphate, mainly ATP, to a nucleoside diphosphate via a ping-pong mechanism involving a phosphohistidine intermediate, therefore
Polypeptides: Nucleoside diphosphate kinase ASynonyms: NDPK A, NDP kinase APiracetam
go.drugbank.com/drugs/DB09210ApprovedWithdrawnPiracetam is a nootropic drug in the racetams group, with chemical name 2-oxo-1-pyrrolidine acetamide. … It shares the same 2-oxo-pyrrolidone base structure with pyroglutamic acid and is a cyclic derivative of the neurotransmitter γ-aminobutyric acid (GABA).
Categories: Compounds used in a research, industrial, or household setting, Heterocyclic Compounds, 1-RingProducts: PIRACETAM RATIO 800MG FTA, PIRACETAM - CT 1200MG FTAEscitalopram
go.drugbank.com/drugs/DB01175ApprovedInvestigationalEscitalopram is a selective serotonin re-uptake inhibitor (SSRI) and the S-enantiomer of racemic [citalopram]. … that the R-enantiomer of racemic citalopram actively dampens the activity of escitalopram rather than existing simply as an inactive enantiomer.
Synonyms: (S)-Citalopram, S(+)-CitalopramCategories: Monoamine Oxidase A Substrates, Cytochrome P-450 SubstratesMethylprednisolone
go.drugbank.com/drugs/DB00959ApprovedInvestigationalVet approvedMethylprednisolone is a [prednisolone] derivative glucocorticoid with higher potency than [prednisone].[A188811] It was first described in the literature in the late 1950s. … [A188811,A188814] Methylprednisolone was granted FDA approval on 24 October 1957.
Mixtures: P-Care D80, P-Care D40Categories: Compounds used in a research, industrial, or household setting, Corticosteroid Hormone Receptor AgonistsExemestane
go.drugbank.com/drugs/DB00990ApprovedInvestigationalExemestane is an oral steroidal aromatase inhibitor used in the adjuvant treatment of hormonally-responsive (also called hormone-receptor-positive, estrogen-responsive) breast cancer in postmenopausal
Synonyms: 6-methyleneandrosta-1,4-diene-3,17-dioneCategories: Cytochrome P-450 Substrates, Cytochrome P-450 CYP3A Substrates