ChemicalBook--->CAS DataBase List--->915082-52-9

915082-52-9

915082-52-9 Structure

915082-52-9 Structure
IdentificationBack Directory
[Name]

A 33
[CAS]

915082-52-9
[Synonyms]

A-33
PDE4B-IN-2
Benzeneacetic acid, 4-[[2-(5-chloro-2-thienyl)-5-ethyl-6-methyl-4-pyrimidinyl]amino]-
[Molecular Formula]

C19H18ClN3O2S
[MDL Number]

MFCD31699853
[MOL File]

915082-52-9.mol
[Molecular Weight]

387.88
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

38.7mg/ml in DMSO
[form ]

Solid
[color ]

White to off-white
[InChI]

InChI=1S/C19H18ClN3O2S/c1-3-14-11(2)21-19(15-8-9-16(20)26-15)23-18(14)22-13-6-4-12(5-7-13)10-17(24)25/h4-9H,3,10H2,1-2H3,(H,24,25)(H,21,22,23)
[InChIKey]

FDVSPBLZPJMXFV-UHFFFAOYSA-N
[SMILES]

C1(CC(O)=O)=CC=C(NC2C(CC)=C(C)N=C(C3SC(Cl)=CC=3)N=2)C=C1
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

PDE4B-IN-2 is an orally active and selective PDE4B inhibitor with an IC50 of 15 nM. PDE4B-IN-2 inhibits PDE4D (IC50=1.7 μM). PDE4B-IN-2 exhibits potent anti-inflammatory effects[1].
[Biochem/physiol Actions]

A-33 (A33) is a potent and selective catalytic site-targeting PDE4B inhibitor (IC50 = 15 nM/PDE4B vs. 1.7 μM/PDE4D) that effectively prevents PDE4B-medicated cellular cAMP hydrolysis (150%/320% increased cAMP level with 100 nM/1 μM A-33 pre-treament in murine hippocampal HT-22 cells following 10 nM isoproterenol stimulation) in vitro and inhibits LPS-induced TNF-α production in mice in vivo (ID50 = 14 mg/kg p.o.). When administered via intraperitoneal injection, A-33 improves cognitive function in a rat model of traumatic brain injury (0.3 mg/kg i.p.) and exhibits antidepressant property in mice (0.3-1 mg/kg i.p.) in vivo.
[in vivo]

PDE4B-IN-2 (compound 33; 2 mg/kg; po) has a Cmax of 8.7 μg/mL and an AUC of 52.3 μg h/mL in mice[1].

[IC 50]

PDE4B: 15 nM (IC50); PDE4D: 1.7 μM (IC50)
[storage]

Store at -20°C
[References]

[1] Kenji Naganuma, et al. Discovery of selective PDE4B inhibitors. Bioorg Med Chem Lett. 2009 Jun 15;19(12):3174-6. DOI:10.1016/j.bmcl.2009.04.121
Spectrum DetailBack Directory
[Spectrum Detail]

A 33(915082-52-9)1HNMR
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