[CAS NO. 591-12-8] α-Angelica lactone
PRODUCTS SPECIFICATIONS [591-12-8]
DESCRIPTION [591-12-8]
Overview
| MDL | MFCD00005375 |
|---|---|
| Molecular Weight | 98.10 |
| Molecular Formula | C5H6O2 |
| SMILES | O=C1OC(C)=CC1 |
1 Publications Citing Use of MCE
Summary
α-Angelica lactone is a naturally occurring anticarcinogen and an vinylogous nucleophile. α-Angelica lactone can give the chiral δ-amino γ,γ-disubstituted butenolide carbonyl derivatives and exhibitselectrophilic trapping at the γ-carbon. α-Angelica lactone exerts strong chemoprotective effects by selective enhancement of glutathione-S-thansferase (GST) and UDP-glucononosyltransferase (UGT) detoxification enzymes [1] [2] [3] [4] .
IC50 & Target
Appearance
Oil
Shipping
Room temperature in continental US; may vary elsewhere.
Storage
4°C, sealed storage, away from moisture
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
Solvent & Solubility
DMSO : 100 mg/mL ( 1019.37 mM ; Need ultrasonic)
Stock Solutions
| Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
|---|
| 1 mM | 10.1937 mL | 50.9684 mL | 101.9368 mL |
| 5 mM | 2.0387 mL | 10.1937 mL | 20.3874 mL |
| 10 mM | 1.0194 mL | 5.0968 mL | 10.1937 mL |
References
- [1] W A Nijhoff, et al. Quantification of Induction of Rat Oesophageal, Gastric and Pancreatic Glutathione and Glutathione S-transferases by Dietary Anticarcinogens. Carcinogenesis. 1994 Sep;15(9):1769-72.
- [2] E M J van der Logt, et al. Induction of Rat Hepatic and Intestinal UDP-glucuronosyltransferases by Naturally Occurring Dietary Anticarcinogens. Carcinogenesis. 2003 Oct;24(10):1651-6.
- [3] Lin Zhou, et al. Catalytic Asymmetric Vinylogous Mannich-type (AVM) Reaction of Nonactivated α-Angelica Lactone. Org Lett. 2011 Jun 17;13(12):3056-9.
- [4] Jessica A Griswold, et al. Diastereoselective Organocatalytic Addition of α-Angelica Lactone to β-Halo-α-ketoesters. J Org Chem. 2017 Feb 17;82(4):2276-2280.
Synonyms