CAS 86632-03-3
:(1α,3R,4α,5R)-3,4,5-Tris[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-1-hydroxycyclohexanecarboxylic acid
Description:
The chemical substance known as "(1α,3R,4α,5R)-3,4,5-Tris[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-1-hydroxycyclohexanecarboxylic acid," with the CAS number 86632-03-3, is a complex organic compound characterized by its multi-functional structure. It features a cyclohexanecarboxylic acid core, which is substituted with multiple phenolic groups, contributing to its potential biological activity. The presence of hydroxyl groups suggests that it may exhibit strong hydrogen bonding capabilities, influencing its solubility and reactivity. The compound's stereochemistry, indicated by the specific alpha and beta configurations, may play a crucial role in its interaction with biological targets, potentially affecting its pharmacological properties. Such compounds are often studied for their antioxidant, anti-inflammatory, or anticancer activities due to the presence of phenolic moieties. Overall, this substance represents a class of compounds that may have significant implications in medicinal chemistry and therapeutic applications, although specific biological activities would require further investigation.
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
Synonyms:- (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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Found 7 products.
(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:C34H30O15Purity:99%Color and Shape:SolidMolecular weight:678.5930(1S,3R,4S,5R)-3,4,5-Tris(((E)-3-(3,4-dihydroxyphenyl)acryloyl)oxy)-1-hydroxycyclohexane-1-carboxylic acid
CAS:<p>(1S,3R,4S,5R)-3,4,5-Tris(((E)-3-(3,4-dihydroxyphenyl)acryloyl)oxy)-1-hydroxycyclohexane-1-carboxylic acid</p>Purity:99%Molecular weight: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:C34H30O15Purity:98%Color and Shape:SolidMolecular weight: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:C34H30O15Purity:Min. 95%Color and Shape:PowderMolecular weight: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:C34H30O15Purity:Min. 95%Color and Shape:PowderMolecular weight: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:Controlled ProductFormula:C34H30O15Color and Shape:NeatMolecular weight:678.593






