1217471-69-6
Chemical Structure
(2S)-OMPT triethylamine, in ethanol:chloroform (1:1), 98%
- CAS No.: 1217471-69-6
- Formula:C34H73N2O6PS
- Molecular Weight:668.99
IUPAC Name: triethylamine hemi((S)-O-(2-methoxy-3-(oleoyloxy)propyl) phosphorothioate)
InChIKey: SHELRVLEXVWOAY-JNYXYQEXSA-N
SMILES: O=C(CCCCCCC/C=C\CCCCCCCC)OC[C@@H](COP(O)(S)=O)OC.CCN(CC)CC.CCN(CC)CC
Biological Activity: (2S)-OMPT (triethylamine), in ethanol:chloroform (1:1), 98%, Lysophosphatidic acid analogue, is a LPA3 G-protein-coupled receptor agonist. (2S)-OMPT (triethylamine), in ethanol:chloroform (1:1), 98% selectively activates LPA3 G-protein-coupled receptor to trigger downstream cellular signaling events. (2S)-OMPT (triethylamine), in ethanol:chloroform (1:1), 98% induces calcium, IL-6 release in cancer cells and activates MAPK and Akt signaling pathways. (2S)-OMPT (triethylamine), in ethanol:chloroform (1:1), 98% can be used for the research of ovarian cancer[1].
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(2S)-OMPT triethylamine, in ethanol:chloroform (1:1), 98% | 99% | (2S)-OMPT (triethylamine), in ethanol:chloroform (1:1), 98%, Lysophosphatidic acid analogue, is a LPA3 G-protein-coupled receptor agonist. (2S)-OMPT (triethylamine), in ethanol:chloroform (1:1), 98% selectively activates LPA3 G-protein-coupled receptor to trigger downstream cellular signaling events. (2S)-OMPT (triethylamine), in ethanol:chloroform (1:1), 98% induces calcium, IL-6 release in cancer cells and activates MAPK and Akt signaling pathways. (2S)-OMPT (triethylamine), in ethanol:chloroform (1:1), 98% can be used for the research of ovarian cancer. | ||||||||||||||||||||
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