成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Home Cart 0 Sign in  

[ CAS No. 482-36-0 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 482-36-0
Chemical Structure| 482-36-0
Structure of 482-36-0 * Storage: {[proInfo.prStorage]}

Please Login or Create an Account to: See VIP prices and availability

Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Search after Editing

* Storage: {[proInfo.prStorage]}

* Shipping: {[proInfo.prShipping]}

Quality Control of [ 482-36-0 ]

Related Doc. of [ 482-36-0 ]

Alternatived Products of [ 482-36-0 ]
Product Citations

Product Citations

Liezel Gouws ; Helena Dorathea Janse van Rensburg ; Gisella Terre' , et al. DOI:

Abstract: Rooibos (Aspalathus linearis) and Honeybush (Cyclopia intermedia) are popular tisanes in South Africa and are of growing interest due to the wide variety of flavonoids and other phytochemicals they contain. Despite their history as herbal teas and traditional medicines, the chemical constituents of these tisanes have yet to be studied for their effects on adenosine receptors. Flavonoids have previously shown promising affinity toward the adenosine receptors. A series of 30 commercially available constituents of Rooibos and Honeybush were investigated via radioligand binding studies to determine their adenosine A1 and A2A receptor affinity at both rat and human subtypes in order to establish structure-activity relationships and identify novel adenosine receptor ligands. In addition, in silico evaluations of the 30 test compounds were also performed to investigate their physiochemical and pharmacokinetic properties. The most promising constituent was kaempferol (28) which showed sub-micromolar affinity towards the rat A1 subtype (rA1Ki = 0.7287 μM; hA1Ki = 9.88 μM) and acted as an antagonist toward adenosine rA1 receptors. Additionally, quercetin (2), chrysoeriol (8), luteolin (9), eriodyctiol (12), and naringenin (27) also showed adenosine A1 and/or A2A receptor affinity. It was observed that a flavonol scaffold is preferred to flavone and flavanone scaffolds, and within the flavonols, C4’-OH substitution on ring B is preferred to C3’,4’-diOH substitution. These phytochemicals, specifically kaempferol (28), may be considered lead-like and valuable in designing novel ligands, based on in vitro and in silico evaluation.

Keywords: Rooibos ; Honeybush ; adenosine A1 receptor ; adenosine A2A receptor ; structure-activity relationships

Purchased from AmBeed: ; ;

Product Details of [ 482-36-0 ]

CAS No. :482-36-0 MDL No. :MFCD00016933
Formula : C21H20O12 Boiling Point : -
Linear Structure Formula :C15H10O6(C6H10O4)O2 InChI Key :OVSQVDMCBVZWGM-DTGCRPNFSA-N
M.W : 464.38 Pubchem ID :5281643
Synonyms :
Quercetin-3-O-galactoside;NSC 407304;Quercetin 3-D-galactoside;Quercetin 3-galactoside;Hyperin
Chemical Name :2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

Safety of [ 482-36-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:
Recommend Products
Same Skeleton Products

Technical Information

Historical Records
; ;