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Chemotaxis protein CheA
go.drugbank.com/bio_entities/BE0001431TargetThermotoga maritima (strain ATCC 43589 / MSB8 / DSM 3109 / JCM 10099)CheA is autophosphorylated; it can transfer its phosphate group to either CheB or CheY (By similarity).
Polypeptides: Chemotaxis protein CheAPadeliporfin
go.drugbank.com/drugs/DB15575ApprovedInvestigational[A244699] Padeliporfin was first approved by the European Commission on November 10, 2017, for the treatment of low-risk prostate cancer in adults meeting certain clinical criteria.[L39799] … It aims to destroy only cancerous lesions of the prostate, rather than ablating the entire prostate gland.
Taiwanofungus camphoratus fruiting body
go.drugbank.com/drugs/DB19272InvestigationalSynonyms: Botanical agent LEAC-102Pentaerythritol tetranitrate
go.drugbank.com/drugs/DB06154ApprovedWithdrawnIt is recognized by the FDA to be a coronary vasodilator in the treatment of heart conditions such as angina [L2395]. … It is a pentaerythritol nitrate in which all four hydroxy groups of pentaerythritol have been converted to the corresponding nitrate ester.
Synonyms: Tetranitrato de pentaeritritilo, Tetranitrate de pentaerithrityleProducts: เพอริเตรท(R) (10 มก.)Lorcaserin
go.drugbank.com/drugs/DB04871ApprovedInvestigationalWithdrawnIn February 2020, the FDA issued a Drug Safety Communication requesting the manufacturer of Belviq (lorcaserin hydrochloride tablets, 10 mg) and Belviq XR (lorcaserin hydrochloride extended-release tablets … , 20 mg) to voluntarily withdraw these products from the U.S. market, and the company has submitted a request to voluntarily withdraw the drug.
Carbon monoxide
go.drugbank.com/drugs/DB11588ApprovedInvestigationalThe technique was first described 100 years ago, and applied to clinical practice many years after. … Since 2002, FDA has favorably reviewed three GRAS notifications for carbon monoxide use in fresh meat packaging [L2537].
Mixtures: Co-NE-O2-N2 Mixture, Co-HE-O2-N2 MixtureNaxitamab
go.drugbank.com/drugs/DB15965ApprovedInvestigational[L24454] This approval requires naxitamab to be co-administered only with GM-CSF, a factor known to enhance the granulocyte-mediated antibody-dependent cytotoxicity of anti-GD2 therapies,[A224604] making … [L24929] Naxitamab-gqgk (Danyelza) was granted accelerated approval by the FDA in November 2020 for the treatment of high-risk relapsed/refractory neuroblastoma of the bone or bone marrow.
Ketobemidone
go.drugbank.com/drugs/DB06738InvestigationalThe most commonly cited equalisation ratio for analgesic doses is 25 mg of ketobemidone hydrobromide to 60 mg of morphine hydrochloride or sulfate and circa 8 mg of ketobemidone by injection. … It also has some NMDA-antagonist properties. This makes it useful for some types of pain that don't respond well to other opioids.
Policresulen
go.drugbank.com/drugs/DB13492InvestigationalProducts: ALBOTHYL VAGINAL SUPPOSITORY 90 mgInsulin-like growth factor II
go.drugbank.com/drugs/DB14472InvestigationalIt is believed to be a major fetal growth factor in contrast to insulin-like growth factor I, which is a major growth factor in adults. … The insulin-like growth factor II is a well-characterized neutral peptide believed to be secreted by the liver and to circulate in the blood.
Synonyms: CG-IGF2Products: HUCORD HSCM-100 Ampoule