KOENIMBINE
KOENIMBINE ??? ???
?? ??:
21087-98-9
???:
KOENIMBINE
???(??):
Koenimbin;Kenimbine;NSC 127152;KOENIMBINE;Koenimbine-RM;3,11-Dihydro-8-methoxy-3,3,5-trimethylpyrano[3,2-a]carbazole;8-Methoxy-3,3,5-trimethyl-3,11-dihydro-chromeno[5,6-b]indole;Pyrano[3,2-a]carbazole, 3,11-dihydro-8-methoxy-3,3,5-trimethyl-
CBNumber:
CB11424103
???:
C19H19NO2
??? ??:
293.36
MOL ??:
21087-98-9.mol
KOENIMBINE ??
???
194-195℃
?? ?
482.1±45.0 °C(Predicted)
??
1.193
?? ?? (pKa)
17.02±0.40(Predicted)
InChI
InChI=1S/C19H19NO2/c1-11-9-15-14-10-12(21-4)5-6-16(14)20-17(15)13-7-8-19(2,3)22-18(11)13/h5-10,20H,1-4H3
InChIKey
OSERHKINMDLESD-UHFFFAOYSA-N
SMILES
N1C2=C(C=C(OC)C=C2)C2=C1C1C=CC(C)(C)OC=1C(C)=C2
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?? ? ???? ?? (GHS)
????(GHS):
?? ?:
Warning
??·?? ??:
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P- ??
H319
?? ?? ??? ???
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?? 2A
??
P264, P280, P305+P351+P338,P337+P313P
H413
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?? 4
??????:
P305+P351+P338
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KOENIMBINE C??? ??, ??, ??
??
Isolated from the fruit of Murraya koenigii Spreng. this base is closely allied to
the two preceding bases as may be seen from the structure. The ultraviolet
spectrum, however, differs from that of koenimbidine, having absorption maxima
at 230, 240, 300, 340 and 360 mJI. The double bond in the pyrone ring may be
reduced with the formation of the dihydro derivative, m.p. 250°C.
?? ??
Narasimhan, Paradkar, Chitguppi., Tetrahedron Lett., 5501 (I968)
KOENIMBINE ?? ?? ? ???
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KOENIMBINE ?? ??
???( 21)?? ??
China 18
United States 3
Global 21