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Merck
CN

SML3860

Sigma-Aldrich

Conolidine

≥98% (HPLC)

别名:

(+)-Conolidine, (+)-Ervaticine, (2R,4E,5S)-4-Ethylidene-1,4,5,7-tetrahydro-2,5-ethano-2H-azocino[4,3-b]indol-6(3H)-one, Ervaticine

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关于此项目

经验公式(希尔记法):
C17H18N2O
CAS Number:
分子量:
266.34
UNSPSC代码:
51111800
NACRES:
NA.77
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质量水平

方案

≥98% (HPLC)

表单

powder

颜色

white to beige

溶解性

DMSO: >2 mg/mL, clear

储存温度

-10 to -25°C

SMILES字符串

O=C(C1=C(C[N@](CC2)C/3)C4=C(C=CC=C4)N1)[C@@H]2C3=C(C)\[H]

InChI

1S/C17H18N2O/c1-2-11-9-19-8-7-12(11)17(20)16-14(10-19)13-5-3-4-6-15(13)18-16/h2-6,12,18H,7-10H2,1H3/b11-2-/t12-/m0/s1

InChI key

DBGBUYFOJXOYNY-RENATIMJSA-N

相关类别

生化/生理作用

Natural analgesic that induces pain relieve though activation of atypical scavenger receptor for chemokines and opioid peptides ACKR3 (CXCR7).



Conolidine is a natural analgesic isolated from tropical flowering shrub Tabernaemontana divaricate, which exhibits potent analgesia in in vivo models of tonic and persistent pain. Conolidine induces pain relieve though activation of atypical scavenger receptor for chemokines and opioid peptides ACKR3 (CXCR7). It appears that conolidine inhibits scavenging functions of ACKR3 therefore increasing levels of endogenous opioid peptides.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 3

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Saori Naoe et al.
The Journal of organic chemistry, 81(13), 5690-5698 (2016-06-09)
A total synthesis of (+)-conolidine has been achieved via the gold(I)-catalyzed cascade cyclization of a conjugated enyne. Remarkably, this strategy allowed for the simultaneous formation of the indole ring and the ethylidene-substituted piperidine moiety of (+)-conolidine under homogeneous gold catalysis
Conolidine: A Novel Plant Extract for Chronic Pain
Amber N Edinoff
Anesthesiology Keywords Review, 11(6) (2021)
The natural analgesic conolidine targets the newly identified opioid scavenger ACKR3/CXCR7.
Martyna Szpakowska et al.
Signal transduction and targeted therapy, 6(1), 209-209 (2021-06-03)

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