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7H-Furo[3,2-g][1]benzopyran-7-one, 4-[(3,7-dimethyl-2,6-octadienyl)oxy]-9-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15905-39-2

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15905-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15905-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,0 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15905-39:
(7*1)+(6*5)+(5*9)+(4*0)+(3*5)+(2*3)+(1*9)=112
112 % 10 = 2
So 15905-39-2 is a valid CAS Registry Number.

15905-39-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-geranyloxy-8-methoxypsoralen

1.2 Other means of identification

Product number -
Other names 5-geranyloxy-8-methoxy-psoralen

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15905-39-2 SDS

15905-39-2Downstream Products

15905-39-2Relevant academic research and scientific papers

Structure-activity relationships for naturally occurring coumarins as β-secretase inhibitor

Marumoto, Shinsuke,Miyazawa, Mitsuo

, p. 784 - 788 (2012)

The present study was demonstrated to evaluate the effects of naturally occurring coumarins (NOCs) including simple coumarins, furanocoumarins, and pyranocoumarins on the inhibition of β-secretase (BACE1) activity. Of 41 NOCs examined, some furanocoumarins inhibited BACE1 activity, but simple coumarins and pyranocoumarins did not affect. The most potent inhibitor was 5-geranyloxy-8-methoxypsoralen (31), which has an IC50 value of 9.9 μM. Other furanocoumarin derivatives, for example, 8-geranyloxy-5- methoxypsoralen (35), 8-geranyloxypsoralen (24), and bergamottin (18) inhibited BACE1 activity, with the IC50 values 25.0 μM. Analyses of the inhibition mechanism by Dixon plots and Cornish-Bowden plots showed that compounds 18, 31 and 35 were mixed-type inhibitor. The kinetics of inhibition of BACE1 by coumarins 24 was non-competitive inhibitors.

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