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(1S,3aS,5aR,8aS)-1,7,7-trimethyl-1,2,3,3a,5a,6,7,8-octahydrocyclopenta[c]pentalene-4-carboxylic acid
go.drugbank.com/drugs/DB06903ExperimentalSynonyms: (1S,3aS,5aR,8aS)-1,7,7-trimethyl-1,2,3,3a,5a,6,7,8-octahydrocyclopenta[c]pentalene-4-carboxylic acidNUC-7738
go.drugbank.com/drugs/DB19148InvestigationalNUC-7738 is under investigation in clinical trial NCT03829254 (A Safety, Pharmacokinetic and Clinical Activity Study of NUC-7738 in Patients With Advanced Solid Tumours and Lymphoma).
Categories: Heterocyclic Compounds, 2-RingSynonyms: L-Alanine, N-(3′-deoxy-P-phenyl-5′-adenylyl)-, phenylmethyl ester (ACI)Beta-(1,3)-D glucan
go.drugbank.com/drugs/DB16468InvestigationalSynonyms: Poly(1-3)-beta-D-glucan, PC-3 type glucanTirzepatide
go.drugbank.com/drugs/DB15171ApprovedInvestigational[A246265] Tirzepatide was approved by the FDA on May 13, 2022, under the brand name MOUNJARO by the FDA for the treatment of adults with type 2 diabetes, making it the first and only GIP and GLP-1 receptor … [A246260] Tirzepatide comprises a 39 amino acid linear synthetic peptide conjugated to a C20 fatty diacid moiety.
Categories: Receptors, G-Protein-Coupled, GLP-1 AgonistsProducts: Mounjaro 5 mg/0,5 ml Enjeksiyonluk Çözelti, 4 ADET, Mounjaro 2,5 mg/0,5 ml Enjeksiyonluk Çözelti, 4 ADETDihematoporphyrin ether
go.drugbank.com/drugs/DB15351InvestigationalDihematoporphyrin ether is under investigation in clinical trial NCT00118222 (High Light and Low Light Dose PDT in Glioma).
Synonyms: bis-1-(8-(1-hydroxyethyl)deuteroporphyrin-3-yl)ethyl etherCategories: Heterocyclic Compounds with 4 or More Rings, Heterocyclic Compounds, 1-RingInterferon beta-1a
go.drugbank.com/drugs/DB00060ApprovedInvestigationalHuman interferon beta (166 residues), glycosylated, MW=22.5kD. It is produced by mammalian cells (Chinese Hamster Ovary cells) into which the human interferon beta gene has been introduced.
Synonyms: Interferon beta 1-a, IFN β-1aCategories: Interferon Type I, Cytochrome P-450 CYP1A2 InhibitorsDexchlorpheniramine maleate
go.drugbank.com/drugs/DB09555ApprovedDexchlorpheniramine is the S-enantiomer of chlorpheniramine which is a 1st generation anti-histamine. … Dexchlorpheniramine has more pharmacological activity than the R and so is more potent than the racemic mixture.
Mixtures: HUFADEXTA-M, INTUNAL-FCategories: Cytochrome P-450 Substrates, Cytochrome P-450 CYP2D6 InhibitorsTiphenamil
go.drugbank.com/drugs/DB19367ExperimentalSynonyms: -phenyl-, s-(2-(diethylamino)ethyl) ester, Benzeneethanethioic acid, a-phenyl-, s-(2-(diethylamino)ethyl) ester2-[(2e,6e,10e,14e,18e,22e,26e)-3,7,11,15,19,23,27,31-Octamethyldotriaconta-2,6,10,14,18,22,26,30-Octaenyl]Phenol
go.drugbank.com/drugs/DB03232ExperimentalSynonyms: 2-[(2e,6e,10e,14e,18e,22e,26e)-3,7,11,15,19,23,27,31-Octamethyldotriaconta-2,6,10,14,18,22,26,30-Octaenyl]Phenol7-(2,5-dihydropyrrol-1-yl)-6-phenyl-pyrido[6,5-d]pyrimidin-2-amine
go.drugbank.com/drugs/DB08146ExperimentalSynonyms: 7-(2,5-dihydropyrrol-1-yl)-6-phenyl-pyrido[6,5-d]pyrimidin-2-amine