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Atherosperminine

CAT: 1410-M29285-02Size: 5 mgDry Ice: NoHazardous: No
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CAT#:1410-M29285-02Size:5 mg
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Description
Atherosperminine shows cholinesterase inhibitory activity against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) . Atherosperminine exerts a non-specific relaxant effect on the trachealis, its major mechanism of action appears to be inhibition of cAMP phosphodiesterase.
CAS Number
5531-98-6
Stability
≥ 2 years
Purity
>98% (HPLC)
Weight
309.4
Molecular Formula
C20H23NO2
Notes
Research use only, not for human use.
Receptor
CAMP

Chemical Information

3,4-Dimethoxy-N,N-dimethyl-1-phenanthreneethanamine

Atherosperminine is an alkaloid.

CAS Number5531-98-6
PubChem CID96918
IUPAC Name2-(3,4-dimethoxyphenanthren-1-yl)-N,N-dimethylethanamine
Molecular FormulaC20H23NO2
Molecular Weight309.4
XLogP4.7
Topological Polar Surface Area21.7
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count5
Heavy Atom Count23
Formal Charge0
Complexity373
SMILES
CN(C)CCC1=CC(=C(C2=C1C=CC3=CC=CC=C32)OC)OC
InChI
InChI=1S/C20H23NO2/c1-21(2)12-11-15-13-18(22-3)20(23-4)19-16-8-6-5-7-14(16)9-10-17(15)19/h5-10,13H,11-12H2,1-4H3
InChIKey
UZZFAUDNCIFFPM-UHFFFAOYSA-N
Chemical Structure
2D Structure
2D structure of 3,4-Dimethoxy-N,N-dimethyl-1-phenanthreneethanamine
CAS: 5531-98-6
CID: 96918
Formula: C20H23NO2
MW: 309.4
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight309.4
XLogP34.7
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count5
Exact Mass309.172878976
Monoisotopic Mass309.172878976
Topological Polar Surface Area21.7 Ų
Heavy Atom Count23
Formal Charge0
Complexity373
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

Alternative Products

CatalogName
379640Atherosperminine

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