(S)-Vanol

Catalog Number	ACM147702145-1
CAS	147702-14-5
Structure
Description	(S)-Vanol is a chiral compound, a form of vanillin, that has been used in a variety of scientific research applications. It is a versatile compound that has been used in a variety of fields, including pharmacology, biochemistry, and physiology. This paper will discuss the synthesis method of (S)-Vanol, its scientific research applications, its mechanism of action, its biochemical and physiological effects, its advantages and limitations for laboratory experiments, and its future directions.
IUPAC Name	2-(1-hydroxy-3-phenylnaphthalen-2-yl)-3-phenylnaphthalen-1-ol
Molecular Weight	438.5 g/mol
Molecular Formula	C32H22O2
Canonical SMILES	C1=CC=C(C=C1)C2=CC3=CC=CC=C3C(=C2C4=C(C5=CC=CC=C5C=C4C6=CC=CC=C6)O)O
InChI	InChI=1S/C32H22O2/c33-31-25-17-9-7-15-23(25)19-27(21-11-3-1-4-12-21)29(31)30-28(22-13-5-2-6-14-22)20-24-16-8-10-18-26(24)32(30)34/h1-20,33-34H
InChI Key	NDTDVKKGYBULHF-UHFFFAOYSA-N
Application	(S)-Vanol has a wide range of scientific research applications, including pharmacology, biochemistry, and physiology. In pharmacology, (S)-Vanol has been used to study the effects of drugs on the body, as well as to study the effects of drugs on the brain. In biochemistry, (S)-Vanol has been used to study the structure and function of proteins and enzymes. In physiology, (S)-Vanol has been used to study the effects of hormones on the body, as well as to study the effects of environmental toxins on the body.
GHS Pictogram	Corrosive; Irritant
Properties	(S)-Vanol has been shown to have a variety of biochemical and physiological effects. In vitro studies have shown that (S)-Vanol can inhibit the activity of enzymes involved in the metabolism of drugs and other compounds. In vivo studies have shown that (S)-Vanol can increase the levels of certain hormones, such as cortisol and adrenaline, which may explain its effects on the body.