1217471-69-6

(2S)-OMPT triethylamine, in ethanol:chloroform (1:1), 98% Chemical Structure
1217471-69-6

Chemical Structure

(2S)-OMPT triethylamine, in ethanol:chloroform (1:1), 98%

  • CAS. Nr.: 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].

Art. -Nr. Produktname Reinheit Beschreibung Pricing
HY-120967
(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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Amount:

USD 0.00

This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References