SML3190
Dehydroevodiamine hydrochloride
≥98% (HPLC)
Synonym(s):
8,14-Dihydro-14-methyl-indolo[2′,3′:3,4]pyrido[2,1-b]quinazolin-5(7H)-one hydrochloride, Dehydroevodiamine chloride, Indolo[2,3:3,4]pyrido[2,1-b]quinazolin-5(7H)-one, 8,14-dihydro-14-methyl-, hydrochloride (1:1)
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About This Item
Empirical Formula (Hill Notation):
C19H15N3O · HCl
CAS Number:
Molecular Weight:
337.80
UNSPSC Code:
12352107
NACRES:
NA.77
MDL number:
Assay:
≥98% (HPLC)
Form:
powder
Storage condition:
desiccated
Quality Segment
assay
≥98% (HPLC)
form
powder
storage condition
desiccated
color
white to beige
solubility
DMSO: 2 mg/mL, clear (warmed)
storage temp.
2-8°C
SMILES string
O=C1C2=C(C=CC=C2)N(C)C3=C4C(CCN31)=C(C=CC=C5)C5=N4.Cl
InChI
1S/C19H15N3O.ClH/c1-21-16-9-5-3-7-14(16)19(23)22-11-10-13-12-6-2-4-8-15(12)20-17(13)18(21)22;/h2-9H,10-11H2,1H3;1H
InChI key
SVOMSEHNGXLQRU-UHFFFAOYSA-N
Biochem/physiol Actions
Dehydroevodiamine is the major alkaloid of Evodia rutaecarpa that exhibit cardiovascular effects such as bradycardia, hypotension, and vasorelaxation. Dehydroevodiamine potently inhibits hERG channels. Apparently it is a blocker of IKr (rapid delayed rectifier current) with proarrhythmic effects in vitro and in vivo. Dehydroevodiamine ameliorates the spatial memory impairment in the scopolamine-induced amnestic rats. It reduced neurotoxicity and the production of A?-induced ROS in primary cortical neurons.
potently inhibits hERG channels; reduced neurotoxicity and the production of A?-induced ROS in primary cortical neurons
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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