XANTHOXYLETIN

Details

Stereochemistry	ACHIRAL
Molecular Formula	C15H14O4
Molecular Weight	258.2693
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

COC1=C2C=CC(C)(C)OC2=CC3=C1C=CC(=O)O3

InChI

InChIKey=JSJIIHRNDMLJGK-UHFFFAOYSA-N

InChI=1S/C15H14O4/c1-15(2)7-6-10-12(19-15)8-11-9(14(10)17-3)4-5-13(16)18-11/h4-8H,1-3H3

HIDE SMILES / InChI

Molecular Formula	C15H14O4
Molecular Weight	258.2693
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/21875271 | https://www.ncbi.nlm.nih.gov/pubmed/20433072

Xanthoxyletin is a coumarin isolated from Erythrina variegata. It has been reported that Xanthoxyletin possesses antibacterial, fungicidal, and algicidal properties. Xanthoxyletin induces S phase arrest and apoptosis in human gastric adenocarcinoma SGC-7901 cells. Xanthoxyletin may be promising anticancer agent and has worth for further mechanistic and therapeutic studies against gastric cancer.

Approval Year

Targets

Primary Target	Pharmacology	Potency
Apoptosis 155 Target ID: map04210 Sources: https://www.ncbi.nlm.nih.gov/pubmed/21875271	Activator 1430
Cyclooxygenase-2 196 Target ID: CHEMBL4321 Sources: https://www.ncbi.nlm.nih.gov/pubmed/18636311	Inhibitor 8297
thromboxane A2 signaling pathway 5 Target ID: GO:0038193 Sources: https://www.ncbi.nlm.nih.gov/pubmed/1523611	Inhibitor 8297
Carbonic anhydrase IX 35 Target ID: CHEMBL3594 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22892213	Inhibitor 8297	0.74 µM [Ki]
Carbonic anhydrase XII 30 Target ID: CHEMBL3242 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22892213	Inhibitor 8297	0.96 µM [Ki]
Carbonic anhydrase XIII 10 Target ID: CHEMBL3912 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22892213	Inhibitor 8297	3.15 µM [Ki]

Conditions

Condition	Modality	Targets	Highest Phase	Product
Gastric cancer 53 Sources: https://www.ncbi.nlm.nih.gov/pubmed/21875271	Primary		Basic research	Unknown Approved Use Unknown

PubMed

Title	Date	PubMed
Cytotoxic coumarins and lignans from extracts of the northern prickly ash (Zanthoxylum americanum).	2001 Aug	11507740
[Studies on the coumarins in the root of Zanthoxylum dimorphophyllum].	2003 Apr	15139146
Anti-HBV and cytotoxic activities of pyranocoumarin derivatives.	2009 Aug 15	19635670
Inhibitory effect of oxycoumarins isolated from the Thai medicinal plant Clausena guillauminii on the inflammation mediators, iNOS, TNF-alpha, and COX-2 expression in mouse macrophage RAW 264.7.	2009 Jan	18636311
Isolation of xanthyletin, an inhibitor of ants' symbiotic fungus, by high-speed counter-current chromatography.	2009 May 8	19296958

Patents

Sample Use Guides

In Vivo Use Guide

Unknown

Route of Administration: Unknown

In Vitro Use Guide

After treating the SGC-7901 cells with 200 and 400 uM of Xanthoxyletin for 48 h, ROS production was detected and the ratios of DCF-positive cells were 18.66% and 32.86% respectively as compared to 8.27% in the control group. Xanthoxyletin induced apoptosis in SGC-7901 cells and percentage of apoptotic cells was 41.47% after the exposure of 400 uM of Xanthoxyletin for 48 h as compared to 2.6% in the control group.

Substance Class	Chemical Created by `admin` on `Fri Dec 15 19:44:30 GMT 2023` Edited by `admin` on `Fri Dec 15 19:44:30 GMT 2023`
Record UNII	69MPX4M5VD
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

XANTHOXYLETIN

Common Name

English

7-HYDROXY-5-METHOXY-2,2-DIMETHYL-2H-1-BENZOPYRAN-6-ACRYLIC ACID .DELTA.-LACTONE

Common Name

English

NSC-35542

Code

English

XANTHOXYLIN N

Common Name

English

XANTHOXYLETIN [MI]

Common Name

English

XANTHOXYLOIN

Common Name

English

Code System Code Type Description

CAS

84-99-1