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14755-02-3 | 2-Propenoic acid, 3-(3-hydroxyphenyl)-, (2E)-
CAS No: 14755-02-3 Catalog No: AG001EZB MDL No:MFCD00004390
Product Description
Catalog Number:
AG001EZB
Chemical Name:
2-Propenoic acid, 3-(3-hydroxyphenyl)-, (2E)-
CAS Number:
14755-02-3
Molecular Formula:
C9H8O3
Molecular Weight:
164.1580
MDL Number:
MFCD00004390
IUPAC Name:
(E)-3-(3-hydroxyphenyl)prop-2-enoic acid
InChI:
InChI=1S/C9H8O3/c10-8-3-1-2-7(6-8)4-5-9(11)12/h1-6,10H,(H,11,12)/b5-4+
InChI Key:
KKSDGJDHHZEWEP-SNAWJCMRSA-N
SMILES:
OC(=O)/C=C/c1cccc(c1)O
UNII:
KWJ2DDJ34H
Properties
Complexity:
186
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Exact Mass:
164.047g/mol
Formal Charge:
0
Heavy Atom Count:
12
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
164.16g/mol
Monoisotopic Mass:
164.047g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
57.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.8
Literature
| Title | Journal |
|---|---|
| Antimicrobial activity and phenolic content of natural site and micropropagated Limonium avei (De Not.) Brullo & Erben plant extracts. | Natural product research 20120101 |
| Structure-activity relationships of trans-substituted-propenoic acid derivatives on the nicotinic acid receptor HCA2 (GPR109A). | Bioorganic & medicinal chemistry letters 20110501 |
| Enhanced activity of antifungal drugs using natural phenolics against yeast strains of Candida and Cryptococcus. | Letters in applied microbiology 20110501 |
| Contribution of cinnamic acid analogues in rosmarinic acid to inhibition of snake venom induced hemorrhage. | Bioorganic & medicinal chemistry 20110401 |
| A chemical screening approach reveals that indole fluorescence is quenched by pre-fibrillar but not fibrillar amyloid-beta. | Bioorganic & medicinal chemistry letters 20090901 |
| Molecular modifications on carboxylic acid derivatives as potent histone deacetylase inhibitors: Activity and docking studies. | Bioorganic & medicinal chemistry 20090715 |
| Synthesis and structure--activity relationships of substituted cinnamic acids and amide analogues: a new class of herbicides. | Journal of agricultural and food chemistry 20090422 |
| Measurement of xanthine oxidase inhibition activity of phenolics and flavonoids with a modified cupric reducing antioxidant capacity (CUPRAC) method. | Analytica chimica acta 20090316 |
| Structure-activity relationships of 1'S-1'-acetoxychavicol acetate for inhibitory effect on NO production in lipopolysaccharide-activated mouse peritoneal macrophages. | Bioorganic & medicinal chemistry letters 20050401 |
| Microbial metabolites of ingested caffeic acid are absorbed by the monocarboxylic acid transporter (MCT) in intestinal Caco-2 cell monolayers. | Journal of agricultural and food chemistry 20041020 |
| Structure-activity relationships of trans-cinnamic acid derivatives on alpha-glucosidase inhibition. | Bioorganic & medicinal chemistry letters 20040607 |
| Orally administered rosmarinic acid is present as the conjugated and/or methylated forms in plasma, and is degraded and metabolized to conjugated forms of caffeic acid, ferulic acid and m-coumaric acid. | Life sciences 20040528 |
| Antiallergic principles from Alpinia galanga: structural requirements of phenylpropanoids for inhibition of degranulation and release of TNF-alpha and IL-4 in RBL-2H3 cells. | Bioorganic & medicinal chemistry letters 20031006 |
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