ACETYLCORYNOLINE

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C23H23NO6
Molecular Weight	409.4318
Optical Activity	( + )
Defined Stereocenters	3 / 3
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

[H][C@]12N(C)CC3=C4OCOC4=CC=C3[C@@]1(C)[C@H](CC5=CC6=C(OCO6)C=C25)OC(C)=O

InChI

InChIKey=PUHCFWFODBLSAP-WWNPGLIZSA-N

InChI=1S/C23H23NO6/c1-12(25)30-20-7-13-6-18-19(28-10-27-18)8-14(13)22-23(20,2)16-4-5-17-21(29-11-26-17)15(16)9-24(22)3/h4-6,8,20,22H,7,9-11H2,1-3H3/t20-,22+,23-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C23H23NO6
Molecular Weight	409.4318
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	3 / 3
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
nitric oxide production involved in inflammatory response 17 Target ID: GO:0002537 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27472313	Inhibitor 8297

PubMed

Title	Date	PubMed
Corynoline Isolated from Corydalis bungeana Turcz. Exhibits Anti-Inflammatory Effects via Modulation of Nfr2 and MAPKs.	2016 Jul 27	27472313

Substance Class	Chemical Created by `admin` on `Sat Dec 16 17:30:46 GMT 2023` Edited by `admin` on `Sat Dec 16 17:30:46 GMT 2023`
Record UNII	6ZFQ6Y9RZD
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

ACETYLCORYNOLINE

Common Name

English

CHELIDONINE, 13-METHYL-, ACETATE (ESTER)

Systematic Name

English

O-ACETYLCORYNOLINE

Systematic Name

English

(+)-CORYNOLINE ACETATE

Systematic Name

English

(1,3)BENZODIOXOLO(5,6-C)-1,3-DIOXOLO(4,5-I)PHENANTHRIDIN-6-OL, 5B,6,7,12B,13,14-HEXAHYDRO-5B,13-DIMETHYL-, ACETATE (ESTER), (5BR,6S,12BR)-

Systematic Name

English

Code System Code Type Description

CAS

18797-80-3