Ogerin
CAS No. 1309198-71-7
Ogerin( —— )
Catalog No. M23467 CAS No. 1309198-71-7
Ogerin is a selective GPR68 positive allosteric modulator (pEC50: 6.83). Ogerin blocks recall in fear conditioning in mice.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 70 | In Stock |
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| 5MG | 62 | In Stock |
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| 10MG | 105 | In Stock |
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| 25MG | 216 | In Stock |
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| 50MG | 354 | In Stock |
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| 100MG | 527 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameOgerin
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NoteResearch use only, not for human use.
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Brief DescriptionOgerin is a selective GPR68 positive allosteric modulator (pEC50: 6.83). Ogerin blocks recall in fear conditioning in mice.
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DescriptionOgerin is a selective GPR68 positive allosteric modulator (pEC50: 6.83). Ogerin blocks recall in fear conditioning in mice. Ogerin displays inverse agonist and antagonist activity (Ki, 220 nM) at A2A receptor and weak antagonist activity (Ki, 736 nM) at 5-HT2B receptor.
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In VitroCell Proliferation Assay Cell Line:Primary human lung fibroblasts (PHLFs) (TGF-β induced)Concentration:50, 100 μMIncubation Time:72 hResult:Inhibited TGF-β stimulated proliferation.Cell Viability Assay Cell Line:HEK293 cells (stably expressing HA-GPR68) Concentration:50 μM Incubation Time:10 min Result:Activated PKA and p42/p44 MAP kinase.RT-PCR Cell Line:Primary human lung fibroblasts (PHLFs) (TGF-β induced)Concentration: 50-150 μM Incubation Time:48 h Result:Suppressed TGF-β induced Col1A1 and Col3A1 mRNA levels in a dose-dependent manner.Western Blot Analysis Cell Line:Primary human lung fibroblasts (PHLFs) (TGF-β induced)Concentration:150 μM Incubation Time:40 min (pre-treat)Result:Induced CREB phosphorylation in both non-fibrotic and fibrotic PHLFs.Western Blot Analysis Cell Line:Primary human lung fibroblasts (PHLFs) (TGF-β induced)Concentration:50-150 μM Incubation Time:72 hResult:Inhibited TGF-β induced αSMA expression in a dose-dependent manner.
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In VivoAnimal Model:GPR68 knockout and WT mice.Dosage:10 mg/kg Administration:Single (30 min before the training)Result:Suppressed recall in fear conditioning in wild-type, but not in GPR68 knockout mice.
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Synonyms——
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PathwayEndocrinology/Hormones
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Target5-HT Receptor
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Recptor5-HT2B|A2A|GPR68
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Research Area——
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Indication——
Chemical Information
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CAS Number1309198-71-7
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Formula Weight307.35
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Molecular FormulaC17H17N5O
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Purity>98% (HPLC)
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SolubilityDMSO:250 mg/mL (813.40 mM; Need ultrasonic)
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SMILESOCC1=C(C2=NC(N)=NC(NCC3=CC=CC=C3)=N2)C=CC=C1
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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
1.Huang XP, et al. Allosteric ligands for the pharmacologically dark receptors GPR68 and GPR65. Nature. 2015 Nov 26;527(7579):477-83.
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