Misplaced Pages

Aplysamine-2

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.

Aplysamine-2
Names

Preferred IUPAC name (2Z)-3-(3-Bromo-4-methoxyphenyl)-N-(2-{3,5-dibromo-4-phenyl}ethyl)-2-(hydroxyimino)propanamide
Identifiers
CAS Number	172486-24-7
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL465038
ChemSpider	4919384
PubChem CID	6411696
CompTox Dashboard (EPA)	DTXSID401317884
InChI InChI=1S/C23H28Br3N3O4/c1-29(2)9-4-10-33-22-18(25)12-16(13-19(22)26)7-8-27-23(30)20(28-31)14-15-5-6-21(32-3)17(24)11-15/h5-6,11-13,31H,4,7-10,14H2,1-3H3,(H,27,30)/b28-20-Key: RCOAHKXJTMBQLI-RRAHZORUSA-N InChI=1/C23H28Br3N3O4/c1-29(2)9-4-10-33-22-18(25)12-16(13-19(22)26)7-8-27-23(30)20(28-31)14-15-5-6-21(32-3)17(24)11-15/h5-6,11-13,31H,4,7-10,14H2,1-3H3,(H,27,30)/b28-20-Key: RCOAHKXJTMBQLI-RRAHZORUBY
SMILES CN(C)CCCOC1=C(C=C(C=C1Br)CCNC(=O)/C(=N\O)/CC2=CC(=C(C=C2)OC)Br)Br
Properties
Chemical formula	C₂₃H₂₈Br₃N₃O₄
Molar mass	650.198
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references

Chemical compound

Aplysamine-2 is a bio-active isolate of marine sponge.

References

Kottakota, SK; Evangelopoulos, D; Alnimr, A; Bhakta, S; McHugh, TD; Gray, M; Groundwater, PW; Marrs, EC; Perry, JD; Spilling, CD; Harburn, JJ (2012). "Synthesis and biological evaluation of purpurealidin E-derived marine sponge metabolites: aplysamine-2, aplyzanzine A, and suberedamines A and B". J Nat Prod. 75 (6): 1090–101. doi:10.1021/np300102z. PMID 22620987.

This article about an alkaloid is a stub. You can help Misplaced Pages by expanding it.

v
t
e