asimilobine
asimilobine Basic information
- Product Name:
- asimilobine
- Synonyms:
-
- 1-Methoxy-6abeta-noraporphin-2-ol
- R-(-)-asimilobine
- asimilobine
- (R)-5,6,6a,7-Tetrahydro-1-methoxy-4H-dibenzo[de,g]quinolin-2-ol
- 4H-Dibenzo[de,g]quinolin-2-ol, 5,6,6a,7-tetrahydro-1-methoxy-, (6aR)-
- CAS:
- 6871-21-2
- MF:
- C17H17NO2
- MW:
- 267.32
- Mol File:
- 6871-21-2.mol
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asimilobine Chemical Properties
- Melting point:
- 177-179℃ (acetone )
- InChI
- InChI=1S/C17H17NO2/c1-20-17-14(19)9-11-6-7-18-13-8-10-4-2-3-5-12(10)16(17)15(11)13/h2-5,9,13,18-19H,6-8H2,1H3/t13-/m1/s1
- InChIKey
- NBDNEUOVIJYCGZ-CYBMUJFWSA-N
- SMILES
- N1[C@@]2([H])C3=C(C(OC)=C(O)C=C3CC1)C1=CC=CC=C1C2
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asimilobine Usage And Synthesis
Uses
Asimilobine is an aporphine isoquinoline alkaloid isolated from plant species of Magnolia obobata Thun. Asimilobine is a dopamine biosynthesis inhibitor and a serotonergic receptor antagonist. Asimilobine shows an antimalarial and anti-cancer activity[1][2].
Definition
ChEBI: A natural product found in Annona glabra.
IC 50
Plasmodium; Dopamine Receptor; serotonergic receptor
References
[1] N Shoji, et al. Asimilobine and Lirinidine, Serotonergic Receptor Antagonists, From Nelumbo Nucifera. J Nat Prod. Jul-Aug 1987;50(4):773-4. DOI:10.1021/np50052a044
[2] Chun-Mei Jin, et al. Effects of Asimilobine on Dopamine Biosynthesis and l-DOPA-induced Cytotoxicity in PC12 Cells. J Asian Nat Prod Res. Jul-Aug 2008;10(7-8):747-55. DOI:10.1080/10286020802030892
asimilobineSupplier
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