86456-17-9 Usage
Chemical structure
A xanthene dye with a diethylaminoethylamino group at position 1 and a hydroxy group at position 7.
Application
Widely used in biological and medical imaging applications.
Family
Belongs to the xanthene dyes family.
Function
Often used as a tracer to label proteins and cell membranes.
Techniques
Utilized in cell imaging and flow cytometry.
Fluorescence properties
Makes it a popular choice for visualizing and studying biological processes at the cellular and molecular level.
Research fields
Used in neuroscience, cardiology, and cancer research.
Selectivity
Ability to selectively label specific cell populations.
Photo-stability
High photo-stability, making it suitable for long-term imaging studies.
Check Digit Verification of cas no
The CAS Registry Mumber 86456-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,5 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86456-17:
(7*8)+(6*6)+(5*4)+(4*5)+(3*6)+(2*1)+(1*7)=159
159 % 10 = 9
So 86456-17-9 is a valid CAS Registry Number.
86456-17-9Relevant academic research and scientific papers
7-Hydroxylucanthone, 7-hydroxhycanthone and their analogs
-
, (2008/06/13)
7-Hydroxylucanthone and 7-hydroxyhycanthone derivatives have been found to have significant antitumor effect. The derivatives are of the general formula: STR1 wherein the radicals R1 and R2 are lower alkyl groups or other simple groups and R3 is OH where X=O, and H or OH where X=S.
Analogues of hycanthone and lucanthone as antitumor agents
Archer,Zayed,Rej,Rugino
, p. 1240 - 1246 (2007/10/02)
Hycanthone analogues (5 and 6) containing 7-substituted hydroxyl groups were prepared and evaluated as antitumor agents. These compounds were significantly more active than the corresponding unsubtituted derivatives. The 7-hydroxylated-4-(hydroxymethyl)-9H-xanthen-9-ones, 11 and 12, were also active antitumor agents. However, the 7-hydroxy-9H-xanthen-9-one counterparts of the 7-hydroxylucanthones were totally devoid of antitumor activity. Results obtained thus far are consistent with the hypothesis that 4-hydroxymethyl substituents in the 9H-xanthen-9-one and 9H-thioxanthen-9-one series are required for antitumor activity.
