(S)-BEL
(S)-BEL Basic information
- Product Name:
- (S)-BEL
- Synonyms:
-
- (S)-BEL
- (3S,6E)-6-(bromomethylidene)-3-naphthalen-1-yloxan-2-one
- (S)-BROMOENOL LACTONE
- 6E-(BROMOMETHYLENE)TETRAHYDRO-3-(1-NAPHTHALENYL)-2H-PYRAN-2-ONE
- 2H-Pyran-2-one, 6-(bromomethylene)tetrahydro-3-(1-naphthalenyl)-, (3S,6E)-
- (S)-Bromoenol lactone(solution in acetate)
- CAS:
- 478288-94-7
- MF:
- C16H13BrO2
- MW:
- 317.18
- Mol File:
- Mol File
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(S)-BEL Chemical Properties
- Boiling point:
- 467.0±45.0 °C(Predicted)
- Density
- 1.538±0.06 g/cm3(Predicted)
- storage temp.
- Store at -20°C, protect from light
- solubility
- DMF: 50 mg/ml; DMSO: 25 mg/ml; Ethanol: 5 mg/ml; PBS (pH 7.2): .05 mg/ml
- form
- Liquid
- color
- Colorless to light yellow
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(S)-BEL Usage And Synthesis
Uses
(S)-Bromoenol lactone ((S)-BEL) is an irreversible, chiral, mechanism-based inhibitor of calcium-independent phospholipase A2β (iPLA2β) that inhibits the vasopressin-induced release of arachidonate from cultured rat aortic smooth muscle (A10) cells with an IC50 of 2 μM[1].
Definition
ChEBI: (S)-Bromoenol lactone is a member of naphthalenes.
IC 50
PLA2
References
[1] Jenkins CM, et al. Identification of calcium-independent phospholipase A2 (iPLA2) beta, and not iPLA2gamma, as the mediator of arginine vasopressin-induced arachidonic acid release in A-10 smooth muscle cells. Enantioselective mechanism-based discriminati DOI:10.1074/jbc.M202568200
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