D 159687
CAS No. 1155877-97-6
D 159687( —— )
Catalog No. M20211 CAS No. 1155877-97-6
D159687 is a selective PDE4D inhibitorhad a procognitive profile as it improved memory in the novel object recognition test but had no antidepressant or anxiolytic benefit.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 29 | In Stock |
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| 5MG | 29 | In Stock |
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| 10MG | 44 | In Stock |
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| 25MG | 93 | In Stock |
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| 50MG | 147 | In Stock |
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| 100MG | 235 | In Stock |
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| 200MG | 350 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameD 159687
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NoteResearch use only, not for human use.
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Brief DescriptionD159687 is a selective PDE4D inhibitorhad a procognitive profile as it improved memory in the novel object recognition test but had no antidepressant or anxiolytic benefit.
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DescriptionD159687 is a selective PDE4D inhibitorhad a procognitive profile as it improved memory in the novel object recognition test but had no antidepressant or anxiolytic benefit.
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In VitroD159687 (1 μM, 0-24?hours) induces a transient increase in CREB phosphorylation which peaked at 6?hours after treatment.D159687 (0.01-1 μM, 6 hours) causes optimal CREB phosphorylation at 1?μM.Western Blot Analysis Cell Line:HT-22 (mouse hippocampal cell line)Concentration:1 μM Incubation Time: 0, 1, 3, 6, 12, 24?hours Result:Induced a transient increase in CREB phosphorylation which peaked at 6?hours after treatment. Western Blot Analysis Cell Line:HT-22 (mouse hippocampal cell line)Concentration:0.01 μM, 0.1 μM, 1 μM Incubation Time:6 hours Result:CREB phosphorylation was optimal at 1?μM.
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In VivoD159687 (0.05-5 mg/kg; oral daily for a week) shows a potential recruitment or enhancement of synaptic function with increased task difficulty in female Cynomolgus macaques. Animal Model:Female Cynomolgus macaques (4–6 year old) Dosage:0.05, 0.5, 5 mg/kg Administration:Oral daily for a week Result:A potential recruitment or enhancement of synaptic function with increased task difficulty.
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Synonyms——
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PathwayAngiogenesis
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TargetPDE
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RecptorPDE4D
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Research Area——
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Indication——
Chemical Information
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CAS Number1155877-97-6
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Formula Weight366.85
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Molecular FormulaC21H19ClN2O2
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Purity>98% (HPLC)
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SolubilityDMSO:150 mg/mL?(408.90 mM)
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SMILESCOc1ccc(Cc2ccc(NC(N)=O)cc2)cc1-c1cccc(Cl)c1
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Chemical Name[4-[[3-(3-Chlorophenyl)-4-methoxyphenyl]methyl]phenyl]urea
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.Zhang C et al. Comparison of the Pharmacological Profiles of Selective PDE4B and PDE4D Inhibitors in the Central Nervous System. Sci Rep. 2017 Jan 5;7:40115.
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