Narceine

Narceine
Names
	Preferred IUPAC name 6-({6-[2-(Dimethylamino)ethyl]-4-methoxy-2H-1,3-benzodioxol-5-yl}acetyl)-2,3-dimethoxybenzoic acid
Identifiers
CAS Number	131-28-2;
3D model (JSmol)	Interactive image;
ChemSpider	8246;
ECHA InfoCard	100.004.566
EC Number	235-480-2;
KEGG	C09591;
PubChem CID	8564;
UNII	CTT09X2F1M;
CompTox Dashboard (EPA)	DTXSID40156833 ;
	InChI InChI=1S/C23H27NO8/c1-24(2)9-8-13-10-18-22(32-12-31-18)20(29-4)15(13)11-16(25)14-6-7-17(28-3)21(30-5)19(14)23(26)27/h6-7,10H,8-9,11-12H2,1-5H3,(H,26,27) Key: DEXMFYZAHXMZNM-UHFFFAOYSA-N; InChI=1/C23H27NO8/c1-24(2)9-8-13-10-18-22(32-12-31-18)20(29-4)15(13)11-16(25)14-6-7-17(28-3)21(30-5)19(14)23(26)27/h6-7,10H,8-9,11-12H2,1-5H3,(H,26,27) Key: DEXMFYZAHXMZNM-UHFFFAOYAJ;
	SMILES CN(C)CCC1=CC2=C(C(=C1CC(=O)C3=C(C(=C(C=C3)OC)OC)C(=O)O)OC)OCO2;
Properties
Chemical formula	C23H27NO8
Molar mass	445.468 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

Narceine is an opium alkaloid produced by the Papaver somniferum (opium poppy) plant.^[1] It is a bitter, crystalline compound with narcotic effects.^{[citation needed]} It was formerly used as a substitute for morphine.^{[medical citation needed]} Its name is derived from the Greek νάρκη (nárkē), meaning numbness, and the postfix -ine referring to an alkaloid.

References

^ van Itallie, L. (1946). "Investigations on poppies". Annales Pharmaceutiques Françaises. 4: 156–160.

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

[1] van Itallie, L. (1946). "Investigations on poppies". Annales Pharmaceutiques Françaises. 4: 156–160.

[1]

v t e Opium components
Alkaloids	16-Hydroxythebaine Berberine Canadine Codamine Coptisine Coreximine Cycloartenone Cyclolaudenol Dehydroreticuline Dihydrosanguinarine Glaucine Isoboldine Isocorypalmine Laudanidine Magnoflorine Narceine Narceinone Norlaudanosoline Norsanguinarine Oripavine Oxysanguinarine Palaudine Papaverrubine B (O-methyl-porphyroxine) Papaverrubine C (epiporphyroxine) Reticuline Salutaridine (sinoacutine) Sanguinarine Scoulerine Somniferine Stepholidine
Morphine group (Phenanthrenes. Includes opioids)	Codeine Morphine Narcotoline Neopine Perparin Papaverrubine D (porphyroxine) Pseudocodeine Pseudomorphine Thebaine
Isoquinolines	Cotarnine Eupaverine Hydrocotarnine Laudanosine Laudanine Noscapine (narcotine) Papaverine Papaveraldine Xanthaline
Protopine group	α-Allocryptopine Corycavamine Corycavine Cryptopine Protopine
Tetrahydroprotoberberine group	Corydaline Corybulbine Isocorybulbine Capaurine
Aporphine group	Dicentrine Glaucine Corytuberine Cularine Corydine Isocorydine Bulbocapnine
Phtalide-isoquinolines	Adulmine Bicuculline Bicucine Corlumine
α-Naphthaphenanthridines	Chelidonine β-Homochelidonoine Chelerythrine Sanguinarine
Other components	Meconic acid Cycloartenol

Names

Preferred IUPAC name 6-({6-[2-(Dimethylamino)ethyl]-4-methoxy-2H-1,3-benzodioxol-5-yl}acetyl)-2,3-dimethoxybenzoic acid
Identifiers
CAS Number	131-28-2
3D model (JSmol)	Interactive image
ChemSpider	8246
ECHA InfoCard	100.004.566
EC Number	235-480-2
KEGG	C09591
PubChem CID	8564
UNII	CTT09X2F1M
CompTox Dashboard (EPA)	DTXSID40156833
InChI InChI=1S/C23H27NO8/c1-24(2)9-8-13-10-18-22(32-12-31-18)20(29-4)15(13)11-16(25)14-6-7-17(28-3)21(30-5)19(14)23(26)27/h6-7,10H,8-9,11-12H2,1-5H3,(H,26,27) Key: DEXMFYZAHXMZNM-UHFFFAOYSA-N InChI=1/C23H27NO8/c1-24(2)9-8-13-10-18-22(32-12-31-18)20(29-4)15(13)11-16(25)14-6-7-17(28-3)21(30-5)19(14)23(26)27/h6-7,10H,8-9,11-12H2,1-5H3,(H,26,27) Key: DEXMFYZAHXMZNM-UHFFFAOYAJ
SMILES CN(C)CCC1=CC2=C(C(=C1CC(=O)C3=C(C(=C(C=C3)OC)OC)C(=O)O)OC)OCO2
Properties
Chemical formula	C₂₃H₂₇NO₈
Molar mass	445.468 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

Narceine

See also

References

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