Hasubanan

Hasubanan
Names
	IUPAC name (3aS-cis)-2,3,4,5-Tetrahydro-3a,9b-butano-1H-benz[e]indole
Identifiers
CAS Number	14510-67-9 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:35647 ;
ChemSpider	20152973 ;
PubChem CID	6857499;
CompTox Dashboard (EPA)	DTXSID60425891 ;
	InChI InChI=1S/C16H21N/c1-2-6-14-13(5-1)7-10-16-9-4-3-8-15(14,16)11-12-17-16/h1-2,5-6,17H,3-4,7-12H2/t15-,16+/m1/s1 Key: RKWPQIQYRNOTMT-CVEARBPZSA-N ; InChI=1/C16H21N/c1-2-6-14-13(5-1)7-10-16-9-4-3-8-15(14,16)11-12-17-16/h1-2,5-6,17H,3-4,7-12H2/t15-,16+/m1/s1 Key: RKWPQIQYRNOTMT-CVEARBPZBP;
	SMILES C2C[C@]14CCCC[C@@]4(CCN1)c3ccccc23;
Properties
Chemical formula	C16H21N
Molar mass	227.351 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

Hasubanan is an alkaloid with the chemical formula of C₁₆H₂₁N. It forms the central core of a class of alkaloids known collectively as hasubanans.[1] The compound is derived from reticuline, as is morphinan, but is comparatively more oxidized and rearranged. It is similar to acutumine.

References

Zhang H, Yue J (2005). "Hasubanan type alkaloids from Stephania longa". J Nat Prod. 68 (8): 1201–7. doi:10.1021/np0500833. PMID 16124761.

External links

Synthesis at chem.wisc.edu

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[1] Zhang H, Yue J (2005). "Hasubanan type alkaloids from Stephania longa". J Nat Prod. 68 (8): 1201–7. doi:10.1021/np0500833. PMID 16124761.

Hasubanan

See also

References

External links