1. GPCR/G Protein
  2. LPL Receptor
  3. 1-Oleoyl lysophosphatidic acid

1-Oleoyl lysophosphatidic acid  (Synonyms: 1-Oleoyl-sn-glycero-3-phosphate; 1-Oleoyl-LPA)

Cat. No.: HY-137862 Purity: 99.90%
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1-Oleoyl lysophosphatidic acid (1-Oleoyl-sn-glycero-3-phosphate) is an abundant lysophosphatidic acid (LPA) species with high biological activity due to its strong affinity for the LPA receptors. 1-Oleoyl lysophosphatidic acid is commonly used in most laboratories as a reagent for LPA receptor activation. 1-Oleoyl lysophosphatidic acid increases SRE-driven β-galactosidase activity.

For research use only. We do not sell to patients.

CAS No. : 65528-98-5

Size Price Stock Quantity
Solvent
1 mg (22.91 mM * 100 μL in Ethanol) In-stock
Solvent
5 mg (22.91 mM * 500 μL in Ethanol) In-stock
Solvent
10 mg (22.91 mM * 1 mL in Ethanol) In-stock
Solvent
25 mg (22.91 mM * 2.5 mL in Ethanol) In-stock

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Customer Review

Based on 3 publication(s) in Google Scholar

Other Forms of 1-Oleoyl lysophosphatidic acid:

Top Publications Citing Use of Products

    1-Oleoyl lysophosphatidic acid purchased from MedChemExpress. Usage Cited in: Neurobiol Stress. 2024 Apr 4:30:100632.  [Abstract]

    Western blot analysis showed that in the brains of mice, LPA (1-Oleoyl lysophosphatidic acid) injection into the lateral ventricles affected the expression of synaptic-related proteins in the hippocampus

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    Description

    1-Oleoyl lysophosphatidic acid (1-Oleoyl-sn-glycero-3-phosphate) is an abundant lysophosphatidic acid (LPA) species with high biological activity due to its strong affinity for the LPA receptors. 1-Oleoyl lysophosphatidic acid is commonly used in most laboratories as a reagent for LPA receptor activation[1]. 1-Oleoyl lysophosphatidic acid increases SRE-driven β-galactosidase activity[2].

    Cellular Effect
    Cell Line Type Value Description References
    CHO EC50
    0.26 μM
    Compound: 1, LPA 18:1
    Agonist activity at mouse LPA4 expressed in CHO cells by Fura-2AM dye based Ca2+ mobilization assay
    Agonist activity at mouse LPA4 expressed in CHO cells by Fura-2AM dye based Ca2+ mobilization assay
    [PMID: 25100502]
    HEK293 EC50
    18 nM
    Compound: LPA (18:1)
    Agonist activity at human LPA1 receptor transfected in HEK293 cells after 1 hr by TGFalpha shedding assay
    Agonist activity at human LPA1 receptor transfected in HEK293 cells after 1 hr by TGFalpha shedding assay
    [PMID: 23395664]
    HEK293 EC50
    29 nM
    Compound: LPA (18:1)
    Agonist activity at human LPA2 receptor transfected in HEK293 cells after 1 hr by TGFalpha shedding assay
    Agonist activity at human LPA2 receptor transfected in HEK293 cells after 1 hr by TGFalpha shedding assay
    [PMID: 23395664]
    HEK293 EC50
    55 nM
    Compound: LPA (18:1)
    Agonist activity at human LPA5 receptor transfected in HEK293 cells after 1 hr by TGFalpha shedding assay in presence of Ki16425
    Agonist activity at human LPA5 receptor transfected in HEK293 cells after 1 hr by TGFalpha shedding assay in presence of Ki16425
    [PMID: 23395664]
    HEK293 EC50
    77 nM
    Compound: LPA (18:1)
    Agonist activity at human LPA3 receptor transfected in HEK293 cells after 1 hr by TGFalpha shedding assay
    Agonist activity at human LPA3 receptor transfected in HEK293 cells after 1 hr by TGFalpha shedding assay
    [PMID: 23395664]
    HEK293 EC50
    8.1 nM
    Compound: LPA (18:1)
    Agonist activity at human LPA4 receptor transfected in HEK293 cells after 1 hr by TGFalpha shedding assay in presence of Ki16425
    Agonist activity at human LPA4 receptor transfected in HEK293 cells after 1 hr by TGFalpha shedding assay in presence of Ki16425
    [PMID: 23395664]
    HEK293 EC50
    970 nM
    Compound: LPA (18:1)
    Agonist activity at human LPA6 receptor transfected in HEK293 cells after 1 hr by TGFalpha shedding assay in presence of Ki16425
    Agonist activity at human LPA6 receptor transfected in HEK293 cells after 1 hr by TGFalpha shedding assay in presence of Ki16425
    [PMID: 23395664]
    HEK293 IC50
    442 nM
    Compound: LPA
    Inhibition of 6x-histidine-tagged human recombinant ATX expressed in HEK293 cells using bisP-nitrophenyl phosphate as a substrate
    Inhibition of 6x-histidine-tagged human recombinant ATX expressed in HEK293 cells using bisP-nitrophenyl phosphate as a substrate
    [PMID: 20536182]
    MEF EC50
    0.002 μM
    Compound: 1, LPA 18:1
    Agonist activity at human LPA2 expressed in LPA1xLPA2 double knockout mouse MEF cells by Fura-2AM dye based Ca2+ mobilization assay
    Agonist activity at human LPA2 expressed in LPA1xLPA2 double knockout mouse MEF cells by Fura-2AM dye based Ca2+ mobilization assay
    [PMID: 25100502]
    MEF EC50
    0.35 μM
    Compound: 1, LPA 18:1
    Agonist activity at human LPA1 expressed in LPA1xLPA2 double knockout mouse MEF cells up to 10 uM by Fura-2AM dye based Ca2+ mobilization assay
    Agonist activity at human LPA1 expressed in LPA1xLPA2 double knockout mouse MEF cells up to 10 uM by Fura-2AM dye based Ca2+ mobilization assay
    [PMID: 25100502]
    MEF EC50
    0.83 μM
    Compound: 1, LPA 18:1
    Agonist activity at human LPA3 expressed in LPA1xLPA2 double knockout mouse MEF cells by Fura-2AM dye based Ca2+ mobilization assay
    Agonist activity at human LPA3 expressed in LPA1xLPA2 double knockout mouse MEF cells by Fura-2AM dye based Ca2+ mobilization assay
    [PMID: 25100502]
    N1E-115 IC50
    10 nM
    Compound: oleoyl-LPA
    Displacement of [32P]diazirine-LPA from LPA receptor in mouse N1E-115 cells preincubated for 1 hr in dark followed by UV irradiation for 5 mins by scintillation counting analysis
    Displacement of [32P]diazirine-LPA from LPA receptor in mouse N1E-115 cells preincubated for 1 hr in dark followed by UV irradiation for 5 mins by scintillation counting analysis
    10.1039/C4MD00333K
    RH7777 EC50
    0.83 μM
    Compound: LPA
    Agonist activity at LPA1 receptor (unknown origin) stably expressed in rat RH7777 cells assessed as increase in intracellular calcium level by Fluo-4 NW dye based fluorescence assay
    Agonist activity at LPA1 receptor (unknown origin) stably expressed in rat RH7777 cells assessed as increase in intracellular calcium level by Fluo-4 NW dye based fluorescence assay
    [PMID: 31790581]
    Sf9 IC50
    499.8 nM
    Compound: 1-O-Oleoyl-LPA
    Inhibition of human recombinant autotaxin expressed in insect Sf9 cells using FS-3 as substrate preincubated for 10 mins prior substrate addition measured up to 60 mins by FRET-based analysis
    Inhibition of human recombinant autotaxin expressed in insect Sf9 cells using FS-3 as substrate preincubated for 10 mins prior substrate addition measured up to 60 mins by FRET-based analysis
    [PMID: 22460025]
    In Vivo

    1-Oleoyl lysophosphatidic acid (1-Oleoyl-sn-glycero-3-phosphate) (0.4-2 μg; i.c.v.; 9-week-old male Wistar rats) induces anxiety-like responses in the elevated plus maze (EPM) under novelty conditions[1].

    MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

    Animal Model: 9-week-old male Wistar rats[1]
    Dosage: 0.4-2 μg
    Administration: I.c.v.
    Result: Reduced open arm exploration under novelty conditions and had no effect under habituated conditions in the EPM.
    Molecular Weight

    436.52

    Formula

    C21H41O7P

    CAS No.
    Appearance

    Liquid

    Color

    Colorless to light yellow

    SMILES

    CCCCCCCC/C=C\CCCCCCCC(OC[C@@H](O)COP(O)(O)=O)=O

    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage

    Solution, -20°C, 2 years

    Purity & Documentation

    Purity: 99.96%

    References
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      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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    Product Name:
    1-Oleoyl lysophosphatidic acid
    Cat. No.:
    HY-137862
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