CAS 86632-03-3
:Acido (1α,3R,4α,5R)-3,4,5-Tris[[(2E)-3-(3,4-diidrossifenil)-1-osso-2-propen-1-il]ossi]-1-idrossicicloesanocarboxilico
Descrizione:
La sostanza chimica nota come "Acido (1α,3R,4α,5R)-3,4,5-Tris[[(2E)-3-(3,4-diidrossifenil)-1-osso-2-propen-1-il]ossi]-1-idrossicicloesanocarboxilico," con il numero CAS 86632-03-3, è un composto organico complesso caratterizzato dalla sua struttura multifunzionale. Presenta un nucleo di acido cicloesano-carbossilico, che è sostituito da più gruppi fenolici, contribuendo alla sua potenziale attività biologica. La presenza di gruppi idrossilici suggerisce che potrebbe mostrare forti capacità di legame idrogeno, influenzando la sua solubilità e reattività. La stereochimica del composto, indicata dalle specifiche configurazioni alfa e beta, potrebbe svolgere un ruolo cruciale nella sua interazione con obiettivi biologici, influenzando potenzialmente le sue proprietà farmacologiche. Tali composti sono spesso studiati per le loro attività antiossidanti, antinfiammatorie o anticancro a causa della presenza di moieties fenolici. In generale, questa sostanza rappresenta una classe di composti che potrebbero avere implicazioni significative nella chimica medicinale e nelle applicazioni terapeutiche, sebbene specifiche attività biologiche richiederebbero ulteriori indagini.
Formula:C34H30O15
InChI:InChI=1S/C34H30O15/c35-21-7-1-18(13-24(21)38)4-10-29(41)47-27-16-34(46,33(44)45)17-28(48-30(42)11-5-19-2-8-22(36)25(39)14-19)32(27)49-31(43)12-6-20-3-9-23(37)26(40)15-20/h1-15,27-28,32,35-40,46H,16-17H2,(H,44,45)/b10-4+,11-5+,12-6+/t27-,28-,32-,34+/m1/s1
InChI key:InChIKey=OAFXTKGAKYAFSI-YOWOTECTSA-N
SMILES:O(C(/C=C/C1=CC(O)=C(O)C=C1)=O)[C@H]2[C@@H](OC(/C=C/C3=CC(O)=C(O)C=C3)=O)[C@H](OC(/C=C/C4=CC(O)=C(O)C=C4)=O)C[C@@](C(O)=O)(O)C2
Sinonimi:- (1α,3R,4α,5R)-3,4,5-Tris[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-1-hydroxycyclohexanecarboxylic acid
- Cyclohexanecarboxylic acid, 3,4,5-tris[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-1-hydroxy-, [1R-[1α,3α(E),4α(E),5β(E)]]-
- Cyclohexanecarboxylic acid, 3,4,5-tris[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-1-hydroxy-, (1α,3R,4α,5R)-
- Cyclohexanecarboxylic acid, 3,4,5-tris[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-1-hydroxy-, (1α,3R,4α,5R)-
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7 prodotti.
(1α,3R,4α,5R)-3,4,5-Tris[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-1-hydroxycyclohexanecarboxylic acid
CAS:Formula:C34H30O15Purezza:99%Colore e forma:SolidPeso molecolare:678.5930(1S,3R,4S,5R)-3,4,5-Tris(((E)-3-(3,4-dihydroxyphenyl)acryloyl)oxy)-1-hydroxycyclohexane-1-carboxylic acid
CAS:(1S,3R,4S,5R)-3,4,5-Tris(((E)-3-(3,4-dihydroxyphenyl)acryloyl)oxy)-1-hydroxycyclohexane-1-carboxylic acidPurezza:99%Peso molecolare:678.6g/mol3,4,5-Tricaffeoylquinic acid
CAS:<p>3,4,5-Tricaffeoylquinic acid may attenuate the TNF-α±- and LPS-stimulated production of inflammatory mediators in keratinocytes by suppressing the Toll-like</p>Formula:C34H30O15Purezza:98%Colore e forma:SolidPeso molecolare:678.593,4,5-Tricaffeoylquinic acid
CAS:<p>3,4,5-Tricaffeoylquinic acid is a caffeoylquinic acid derivative that exerts an inhibitory effect on the Toll-like receptor. It also has anti-inflammatory properties. 3,4,5-Tricaffeoylquinic acid has been shown to exhibit strong antiviral and antibacterial activity against infectious diseases such as influenza and tuberculosis. The compound has also been used as a natural dye for food products and cosmetics. 3,4,5-Tricaffeoylquinic acid is used in vitro assays for the identification of compounds with potential antioxidant activity. This compound is also used as a matrix effect to determine the bioavailability of other drugs in vitro and may be useful in analytical methods for determining benzalkonium chloride levels.</p>Formula:C34H30O15Purezza:Min. 95%Colore e forma:PowderPeso molecolare:678.59 g/mol3,4,5-Tricaffeoylquinic acid
CAS:<p>3,4,5-Tricaffeoylquinic acid is a polyphenolic compound, which is found in certain plants, notably within the family Asteraceae. This compound is a type of chlorogenic acid, recognized for its significant antioxidant activity. It is biosynthesized via the phenylpropanoid pathway, where caffeic acid residues are esterified with quinic acid.</p>Formula:C34H30O15Purezza:Min. 95%Colore e forma:PowderPeso molecolare:678.59 g/mol(1S,3R,4S,5R)-3,4,5-Tris(((E)-3-(3,4-dihydroxyphenyl)acryloyl)oxy)-1-hydroxycyclohexane-1-carboxylic Acid
CAS:Prodotto controllatoFormula:C34H30O15Colore e forma:NeatPeso molecolare:678.593






