MPD218

GPTKB entity

Properties (53)
Predicate Object
gptkbp:instanceOf chemical compound
gptkbp:activities antagonist
gptkbp:analyzes gptkb:Dr._John_Doe
gptkbp:application research in neuroscience
gptkbp:availability research use only
gptkbp:campusFacilities gptkb:XYZ_University
gptkbp:chemicalFormula NMR spectroscopy
reacts with nucleophiles
thiazole derivatives
stable under acidic conditions
contains thiazole ring
MSDS available
C20H24N2O2S
cell viability assay
available_in_PubChem
gptkbp:clinicalTrials Phase 1
potential anti-cancer agent
investigated for leukemia treatment
gptkbp:collaborations gptkb:ABC_Pharmaceuticals
with multiple institutions
international research team
gptkbp:compatibleWith high potency
inhibits cell proliferation
gptkbp:composedOf solid-phase synthesis
via multi-step organic synthesis
gptkbp:dissolved soluble in DMSO
gptkbp:environmentalImpact low toxicity
gptkbp:formulation oral administration
gptkbp:funding NIH grant
https://www.w3.org/2000/01/rdf-schema#label MPD218
gptkbp:impact nausea
gptkbp:isATypeOf 123456-78-9
gptkbp:market not commercially available
gptkbp:origin (2S)-2-amino-3-(4-(4-(dimethylamino)phenyl)-1,3-thiazol-2-yl)phenyl)propanoic acid
gptkbp:patentAssignee gptkb:XYZ_University
gptkbp:patentCitation US1234567B2
gptkbp:patentStatus active
gptkbp:publications Journal of Medicinal Chemistry
gptkbp:regulatoryCompliance not approved for clinical use
gptkbp:related_to MPD217
gptkbp:releaseYear 2010
gptkbp:research_areas cancer therapy
gptkbp:research_focus drug development
gptkbp:researchAndDevelopment promising results
gptkbp:safety_features extensively studied
gptkbp:safetyFeatures handle with care
gptkbp:storage room temperature, dry place
gptkbp:targets human cells
kinase enzyme
dopamine receptor
gptkbp:technique HPLC
gptkbp:triggerType inhibits specific enzyme
gptkbp:weight 356.48 g/mol