Allocryptopine

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Allocryptopine
Allocryptopine-1.svg
Names
Preferred IUPAC name
3,4-Dimethoxy-6-methyl-5,7,8,15-tetrahydro-11H-[1,3]benzodioxolo[5,6-e][2]benzazecin-14(6H)-one
Other names
Thalictrimine; allo-Cryptopine; α-Fagarine; Fagarine I; α-Allocryptopine; β-Homochelidonine
Identifiers
  • 24240-04-8
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.006.933 Edit this at Wikidata
EC Number
  • 207-626-5
KEGG
  • InChI=1S/C21H23NO5/c1-22-7-6-14-9-19-20(27-12-26-19)10-15(14)17(23)8-13-4-5-18(24-2)21(25-3)16(13)11-22/h4-5,9-10H,6-8,11-12H2,1-3H3
    Key: HYBRYAPKQCZIAE-UHFFFAOYSA-N
  • CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C(=C(C=C4)OC)OC)OCO3
Properties
C21H23NO5
Molar mass 369.417 g·mol−1
Hazards
Main hazards H302 (100%): Harmful if swallowed, acute toxicity[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Allocryptopine is a bioactive alkaloid found in plants of the Papaveraceae family, including [2] Argemone mexicana , Eschscholtzia , Corydalis , Fumaria , Chelidonium , Hunnemannia fumariifolia Eschscholzia lobbii [3] and more other Papaveraceae plants.

[4][5]

See also[]

References[]

  1. ^ "Allocryptopine". PubChem: Open Chemistry Database. PubChem. Retrieved 24 May 2018.
  2. ^ Abu-Ghalyun, Y.; Masalmeh, A.; al-Khalil, S. (October 1997). "Effects of allocryptopine, an alkaloid isolated from Glaucium arabicum on rat isolated ileum and urinary bladder". General Pharmacology. 29 (4): 621–623. doi:10.1016/s0306-3623(96)00562-9. ISSN 0306-3623. PMID 9352312.
  3. ^ http://www.giftpflanzen.com/formelname.html#Allocryptopin
  4. ^ http://www.giftpflanzen.com/eschscholzia_californica.html
  5. ^ Brahmachari, Goutam; Gorai, Dilip; Roy, Rajiv (2013-05-01). "Argemone mexicana: Chemical and pharmacological aspects". Revista Brasileira de Farmacognosia. 23 (3): 559–575. doi:10.1590/S0102-695X2013005000021. ISSN 0102-695X.


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