1914-58-5 | Trans-styrylacetic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$21.00	$15.00
5g	98%	in stock	$69.00	$49.00

Description

• Catalog Number: AB12831
• Chemical Name: Trans-styrylacetic acid
• CAS Number: 1914-58-5
• Molecular Formula: C10H10O2
• Molecular Weight: 162.1852
• MDL Number: MFCD00002783
• SMILES: OC(=O)C/C=C/c1ccccc1

Computed Properties

• Complexity: 167
• Covalently-Bonded Unit Count: 1
• Defined Bond Stereocenter Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 2.3

Literature

• Fragrance material review on 4-phenyl-3-buten-2-ol.

  Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20120901

• Synthesis and antimalarial and antituberculosis activities of a series of natural and unnatural 4-methoxy-6-styryl-pyran-2-ones, dihydro analogues and photo-dimers.

  Bioorganic & medicinal chemistry 20120215

• p38 MAPK activation, JNK inhibition, neoplastic growth inhibition, and increased gap junction communication in human lung carcinoma and Ras-transformed cells by 4-phenyl-3-butenoic acid.

  Journal of cellular biochemistry 20120101

• Enhanced neuropeptide Y synthesis during intermittent hypoxia in the rat adrenal medulla: role of reactive oxygen species-dependent alterations in precursor peptide processing.

  Antioxidants & redox signaling 20110401

• Probing the peptidylglycine alpha-hydroxylating monooxygenase active site with novel 4-phenyl-3-butenoic acid based inhibitors.

  ChemMedChem 20100903

• Anti-inflammatory effects of 4-phenyl-3-butenoic acid and 5-(acetylamino)-4-oxo-6-phenyl-2-hexenoic acid methyl ester, potential inhibitors of neuropeptide bioactivation.

  The Journal of pharmacology and experimental therapeutics 20070301

• Study of polarized IR spectra of the hydrogen bond system in crystals of styrylacetic acid.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20061001

• Isolation and antifungal activity of 4-phenyl-3-butenoic acid from Streptomyces koyangensis strain VK-A60.

  Journal of agricultural and food chemistry 20051005

• Streptomyces koyangensis sp. nov., a novel actinomycete that produces 4-phenyl-3-butenoic acid.

  International journal of systematic and evolutionary microbiology 20050101

• Peptidyl-glycine alpha-amidating monooxygenase targeting and shaping of atrial secretory vesicles: inhibition by mutated N-terminal ProANP and PBA.

  Circulation research 20041210

• Reversal of the transformed phenotype and inhibition of peptidylglycine alpha-monooxygenase in Ras-transformed cells by 4-phenyl-3-butenoic acid.

  Molecular carcinogenesis 20041201

• Oleic acid derived metabolites in mouse neuroblastoma N18TG2 cells.

  Biochemistry 20041005

• Glycine-extended adrenomedullin exerts vasodilator effect through amidation in the rat aorta.

  Regulatory peptides 20030515

• Intracellular angiotensin II increases the long isoform of PDGF mRNA in rat hepatoma cells.

  Journal of molecular and cellular cardiology 20021101

• The phenylacetyl-CoA catabolon: a complex catabolic unit with broad biotechnological applications.

  Molecular microbiology 20010301