149146-12-3

149146-12-3 structure

Name: Secretoneurin (mouse, rat) trifluoroacetate salt
Chemical Name: (5α,6β)-17-(Cyclopropylmethyl)-3-hydroxy-6-{[(2R)-4-methylene-5-oxotetrahydro-2-furanyl]methoxy}-4,5-epoxymorphinan-14-yl acetate
CAS Number: 149146-12-3
Molecular Formula: C₁₅₉H₂₅₂N₄₀O₅₈
Molecular Weight: 3651.95
Catalog: Research Areas Neurological Disease
Create Date: 2018-06-27 20:44:57
Modify Date: 2024-01-20 17:12:09
Secretoneurin, rat, a 33-amino acid polypeptide, is generated by proteolytic processing of secretogranin II (SgII). Secretoneurin, rat induces dopamine release in the rat striatum in vivo and in vitro, and it exerts a very strong chemotactic effect on monocytes and eosinophils but not on granulocytes[1].

Name	(5α,6β)-17-(Cyclopropylmethyl)-3-hydroxy-6-{[(2R)-4-methylene-5-oxotetrahydro-2-furanyl]methoxy}-4,5-epoxymorphinan-14-yl acetate
Synonyms	(5α,6β)-17-(Cyclopropylmethyl)-3-hydroxy-6-{[(2R)-4-methylene-5-oxotetrahydro-2-furanyl]methoxy}-4,5-epoxymorphinan-14-yl acetate (5α,6β)-17-(cyclopropylmethyl)-3-hydroxy-6-{[(2R)-4-methylidene-5-oxotetrahydrofuran-2-yl]methoxy}-4,5-epoxymorphinan-14-yl acetate 2(3H)-Furanone, 5-[[[(5α,6β)-14-(acetyloxy)-17-(cyclopropylmethyl)-4,5-epoxy-3-hydroxymorphinan-6-yl]oxy]methyl]dihydro-3-methylene-, (5R)-

Description	Secretoneurin, rat, a 33-amino acid polypeptide, is generated by proteolytic processing of secretogranin II (SgII). Secretoneurin, rat induces dopamine release in the rat striatum in vivo and in vitro, and it exerts a very strong chemotactic effect on monocytes and eosinophils but not on granulocytes[1].
Related Catalog	Signaling Pathways >> Others >> Others Research Areas >> Neurological Disease
References	[1]. Troger J, et al. Secretoneurin in the peripheral ocular innervation. Invest Ophthalmol Vis Sci. 2005 Feb;46(2):647-54.