Lamellarin D

Lamellarin D
Names
	Preferred IUPAC name 3,11-Dihydroxy-14-(4-hydroxy-3-methoxyphenyl)-2,12-dimethoxy-6H-[1]benzopyrano[4′,3′:4,5]pyrrolo[2,1-a]isoquinolin-6-one
Identifiers
CAS Number	97614-65-8 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL373114 ;
ChemSpider	8067814 ;
PubChem CID	9892144;
UNII	YEF6XD93VE ;
CompTox Dashboard (EPA)	DTXSID501031665 ;
	InChI InChI=1S/C28H21NO8/c1-34-21-9-14(4-5-17(21)30)24-25-16-11-23(36-3)19(32)12-20(16)37-28(33)27(25)29-7-6-13-8-18(31)22(35-2)10-15(13)26(24)29/h4-12,30-32H,1-3H3 Key: ATHLLZUXVPNPAW-UHFFFAOYSA-N ; InChI=1S/C28H21NO8/c1-34-21-9-14(4-5-17(21)30)24-25-16-11-23(36-3)19(32)12-20(16)37-28(33)27(25)29-7-6-13-8-18(31)22(35-2)10-15(13)26(24)29/h4-12,30-32H,1-3H3 Key: ATHLLZUXVPNPAW-UHFFFAOYSA-N;
	SMILES COC1=C(C=CC(=C1)C2=C3C4=CC(=C(C=C4C=CN3C5=C2C6=CC(=C(C=C6OC5=O)O)OC)O)OC)O;
Properties
Chemical formula	C28H21NO8
Molar mass	499.475 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Lamellarins are a group of pyrrole alkaloids first isolated in 1985 from the marine mollusk Lamellaria in the waters of Palau. Over 70 lamellarins and similar compounds were subsequently isolated. Other similar compounds include ningalins, lukianols, polycitones, and storniamides.^[1]

^ Bailly, Christian; Newman, David J. (2015). Written at Pierre Fabre Research Institute. "Download Limit Exceeded" (PDF). Marine Drugs. 13 (3). 2015-02-19: 1105–1123. doi:10.3390/md13031105. ISSN 1660-3397. PMC 4377975. PMID 25706633.{{cite journal}}: CS1 maint: location (link)

[1] Bailly, Christian; Newman, David J. (2015). Written at Pierre Fabre Research Institute. "Download Limit Exceeded" (PDF). Marine Drugs. 13 (3). 2015-02-19: 1105–1123. doi:10.3390/md13031105. ISSN 1660-3397. PMC 4377975. PMID 25706633.{{cite journal}}: CS1 maint: location (link)

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