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 |
5MG | 42 | In Stock |
|
10MG | 69 | In Stock |
|
25MG | 147 | In Stock |
|
50MG | 237 | In Stock |
|
100MG | 381 | In Stock |
|
200MG | Get Quote | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product NameD 159687
-
NoteResearch use only not for human use.
-
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.
-
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.
-
Synonyms——
-
PathwayAngiogenesis
-
TargetPDE
-
RecptorPDE4D
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1155877-97-6
-
Formula Weight366.85
-
Molecular FormulaC21H19ClN2O2
-
Purity>98% (HPLC)
-
SolubilityDMSO:150 mg/mL?(408.90 mM)
-
SMILESCOc1ccc(Cc2ccc(NC(N)=O)cc2)cc1-c1cccc(Cl)c1
-
Chemical Name[4-[[3-(3-Chlorophenyl)-4-methoxyphenyl]methyl]phenyl]urea
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
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.
molnova catalog
related products
-
Icariin
Icariin(Ieariline) is a major constituent of flavonoids from the Chinese medicinal herb Epimedium brevicornum.
-
Bullatine A
Bullatine A, a diterpenoid alkaloid of the genus Aconitum, possesses anti-rheumatic, anti-inflammatory and anti-nociceptive effects.
-
THPP-1
THPP-1 is a potent and orally bioavailable inhibitor of PDE10A(Ki of 1 nM and 1.3 nM for human and rat PDE10A, respectively).