[CAS NO. 5786-54-9]  Hispidol

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PRODUCTS SPECIFICATIONS [5786-54-9]

Catalog
HY-102040
Brand
MCE
CAS
5786-54-9

DESCRIPTION [5786-54-9]

Overview

MDLMFCD00135406
Molecular Weight254.24
Molecular FormulaC15H10O4
SMILESO=C1C2=CC=C(O)C=C2O/C1=C\C3=CC=C(O)C=C3

For research use only. We do not sell to patients.

Summary

Hispidol ((Z)-Hispidol) is a potential therapeutic for inflammatory bowel disease; inhibits TNF-α induced adhesion of monocytes to colon epithelial cells with an IC 50 of 0.50 µM.


In Vitro

Hispidol shows potent inhibitory effect (>70%) on the TNF-α-induced adhesion of monocytes to colon epithelial cells, which is one of the hallmark events leading to inflammatory bowel disease (IBD). Hispidol shows strong inhibitory activities against TNF-α-induced monocytic-colonic epithelial cell adhesion as well as LPS-induced TNF-α expression, is as an excellent candidate for IBD drug development. This inhibition of TNF-α expression by hispidol corresponds to the additional inhibitory activity against AP-1 transcriptional activity, which is another transcription factor required for high level TNF-α expression [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


In Vivo

The oral administration of hispidol suppresses significantly and dose-dependently TNBS-induced rat colitis. Oral administration of hispidol suppresses TNBS-induced colitis in a dose-dependent manner. There is a significant recovery in body weight decrease and colon tissue edematous inflammation. A higher dose (30 mg/kg) of hispidol shows a similar recovery effect to that of 300 mg/kg sulfasalazine. In the colon tissues, TNBS induces a dramatic increase in the level of MPO, a biochemical marker of inflammation, which is suppressed significantly by hispidol in a dose-dependent manner [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month

Solvent & Solubility

In Vitro:

DMSO : ≥ 100 mg/mL ( 393.33 mM )

* "≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.9333 mL 19.6665 mL 39.3329 mL
5 mM 0.7867 mL 3.9333 mL 7.8666 mL
10 mM 0.3933 mL 1.9666 mL 3.9333 mL
* Please refer to the solubility information to select the appropriate solvent.


Synonyms

3(2H)-Benzofuranone, 6-hydroxy-2-[(4-hydroxyphenyl)methylene]-, (2Z)-
3(2H)-Benzofuranone, 6-hydroxy-2-(p-hydroxybenzylidene)-, (Z)-
3(2H)-Benzofuranone, 6-hydroxy-2-[(4-hydroxyphenyl)methylene]-, (Z)-
(2Z)-6-Hydroxy-2-[(4-hydroxyphenyl)methylene]-3(2H)-benzofuranone
Hispidol
4′,6-Dihydroxyaurone
(Z)-Hispidol
(Z)-6-Hydroxy-2-(4-hydroxybenzylidene)benzofuran-3(2H)-one