BROMOENOL LACTONE manufacturers
- Bromoenol lactone
-
- $94.00
-
2026-07-25
- CAS:88070-98-8
- Purity: 99.98%
- Supply Ability: 10g
- Bromoenol lactone
-
- $94.00
-
2026-07-25
- CAS:88070-98-8
- Purity: 99.98%
- Supply Ability: 10g
|
| | BROMOENOL LACTONE Basic information |
| Product Name: | BROMOENOL LACTONE | | Synonyms: | E-6-(BROMOETHYLENE)TETRAHYDRO-3-(1-NAPHTHYL)-2H-PYRAN-2-ONE;(E)-6-(BROMOMETHYLENE)TETRAHYDRO-3-(1-NAPHTHALENYL)-2H-PYRAN-2-ONE;(E)-6-(BROMOMETHYLENE)TETRAHYDRO-3-(1-NAPTHALENYL)-2H-PYRAN-2-ONE;HELSS;HALOENOL LACTONE;HALOENOL LACTONE SUICIDE SUBSTRATE;BEL;BROMOENOL LACTONE | | CAS: | 88070-98-8 | | MF: | C16H13BrO2 | | MW: | 317.18 | | EINECS: | | | Product Categories: | | | Mol File: | 88070-98-8.mol |  |
| | BROMOENOL LACTONE Chemical Properties |
| Melting point | 103-106℃ | | Boiling point | 467.0±45.0 °C(Predicted) | | density | 1.538±0.06 g/cm3(Predicted) | | storage temp. | -20°C | | solubility | DMSO: Dilute in aqueous medium immediately prior to use and store on ice for no more than 12 hours.soluble | | form | White solid. | | color | White to yellow | | biological source | synthetic (organic) | | λmax | 224 nm | | InChI | 1S/C16H13BrO2/c17-10-12-8-9-15(16(18)19-12)14-7-3-5-11-4-1-2-6-13(11)14/h1-7,10,15H,8-9H2/b12-10+ | | InChIKey | BYUCSFWXCMTYOI-ZRDIBKRKSA-N | | SMILES | [H]\C(Br)=C1\CCC(C(=O)O1)c2cccc3ccccc23 |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26 | | WGK Germany | 3 | | Storage Class | 11 - Combustible Solids |
| | BROMOENOL LACTONE Usage And Synthesis |
| Uses | HELSS (Haloenol lactone suicide substrate, BEL, Bromoenol lactone) is an inhibitor of Ca-independent PLA2 and Mg-dependent PAP. | | Definition | ChEBI: Bromoenol lactone is a member of naphthalenes. | | Biological Activity | bromoenol lactone is a potent and irreversible inhibitor of myocardial cytosolic calcium-independent phospholipase a2 (ipla2) [1].the ipla2 has been involved in stimulus-induced arachidonic acid release and lysophospholipid generation. the catalytic action of ipla2 is responsible for phospholipid remodeling as a housekeeping function. arachidonic acid and lysophospholipid generated by ipla2 act as a signaling molecule in cellular functions, including eicosanoid production, glucose-induced insulin secretion, fas-induced apoptosis, cellular proliferation, membrane traffic in fusion, contribution to myocardial ischemia, and others [2].bel promoted apoptosis in a variety of cell lines, including u937, thp-1, and monomac (human phagocyte), raw264.7 (murine macrophage), jurkat (human t lymphocyte), and gh3 (human pituitary). long term treatment with bel (up to 24 h) increased annexin-v binding to the cell surface and nuclear dna damage. bel induced the proteolysis of procaspase-9 and procaspase-3 and increased cleavage of poly (adp-ribose) polymerase [1]. bel inhibited cellular phosphatidic acid phosphohydrolase (pap) activity in intact p388d1 macrophages with an ic50 of ～8 μm. bel blocked triacylglycerol biosynthesis in p388d1 cells by decreasing diacylglycerol availability [3]. | | Biochem/physiol Actions | Potent, irreversible inhibitor of calcium-independent phospholipase A2 and of magnesium-dependent phosphatidate phosphohydrolase from P388D macrophages (IC50 = 8μM); enzyme activated irreversible chymotrypsin inhibitor (Ki = 636 nM). | | IC 50 | PLA2: 7 μM (IC50) | | references | [1] fuentes l, pérez r, nieto m l, et al. bromoenol lactone promotes cell death by a mechanism involving phosphatidate phosphohydrolase-1 rather than calcium-independent phospholipase a2[j]. journal of biological chemistry, 2003, 278(45): 44683-44690.
[2] akiba s, sato t. cellular function of calcium-independent phospholipase a2[j]. biological and pharmaceutical bulletin, 2004, 27(8): 1174-1178.
[3] balsinde j, dennis e a. bromoenol lactone inhibits magnesium-dependent phosphatidate phosphohydrolase and blocks triacylglycerol biosynthesis in mouse p388d1 macrophages[j]. journal of biological chemistry, 1996, 271(50): 31937-31941. |
| | BROMOENOL LACTONE Preparation Products And Raw materials |
|