H2L5186303
CAS No. 139262-76-3
H2L5186303( ZINC33388081 )
Catalog No. M27634 CAS No. 139262-76-3
H2L5186303 is an LPA2 antagonist and can be used in studies about asthma treatment.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 88 | Get Quote |
|
| 10MG | 160 | Get Quote |
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| 25MG | 357 | Get Quote |
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| 50MG | 530 | Get Quote |
|
| 100MG | 759 | Get Quote |
|
| 500MG | 1557 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameH2L5186303
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NoteResearch use only, not for human use.
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Brief DescriptionH2L5186303 is an LPA2 antagonist and can be used in studies about asthma treatment.
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DescriptionH2L5186303 is an LPA2 antagonist and can be used in studies about asthma treatment.(In Vitro):The high cell invasion activity of HT1080-M6 cells is significantly suppressed by H2L5186303.(In Vivo):H2L5186303 shows strong suppressive efficacy when administered before OVA sensitization and challenge, such as suppression of airway hyper responsiveness, inflammatory cytokine levels, mucin production, and eosinophil numbers.
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In Vitro——
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In Vivo——
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SynonymsZINC33388081
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PathwayGPCR/G Protein
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TargetLPA Receptor
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number139262-76-3
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Formula Weight488.45
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Molecular FormulaC26H20N2O8
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (511.82 mM)
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SMILESO(C1=CC(OC2=CC=C(NC(/C=C\C(O)=O)=O)C=C2)=CC=C1)C3=CC=C(NC(/C=C\C(O)=O)=O)C=C3
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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AM095
AM095 is a potent LPA1 receptor antagonist with IC50 values of 0.98 and 0.73μM for recombinant human or mouse LPA1 respectively.
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AM095 free acid
AM095 (free acid) is a potent LPA1 receptor antagonist (IC50s: 0.98 and 0.73 μM for recombinant human or mouse LPA1).In vitro, AM095 was a potent LPA receptor antagonist because it inhibited GTPγS binding to Chinese hamster ovary (CHO) cell membranes overexpressing recombinant human or mouse LPA with IC values of 0.98 and 0.73 μM, respectively, and exhibited no LPA agonism.
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GRI977143
GRI977143 is a selective and non-lipid agonist of LPA2 (EC50 = 3.3 μM). GRI977143 inhibits the activation of caspases 3, 7, 8, and 9 and and reduces DNA fragmentation.
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