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ChemicalBook--->CAS DataBase List--->790663-33-1

790663-33-1

790663-33-1 Structure

790663-33-1 Structure
IdentificationBack Directory
[Name]

PBD-150
[CAS]

790663-33-1
[Synonyms]

PBD-150
[Molecular Formula]

C15H20N4O2S
[MDL Number]

MFCD32666996
[MOL File]

790663-33-1.mol
[Molecular Weight]

320.41
Chemical PropertiesBack Directory
[Melting point ]

160.0-161.0 °C(Solv: ethanol (64-17-5))
[Boiling point ]

502.7±60.0 °C(Predicted)
[density ]

1.22±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C
[solubility ]

Soluble in DMSO (25 mg/ml) or ethanol (25 mg/ml)
[form ]

solid
[pka]

12.29±0.70(Predicted)
[color ]

White
[Stability:]

Stable for 1 year as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 1 month.
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Description]

PBD-150 (790663-33-1) is an inhibitor of human glutaminyl cyclase (IC50 = 60 nM).1 PBD-150 diminished Ab plaque formation and gliosis while improving memory in a mouse model with small amounts of Ab3(pE)-40/42.2
[Uses]

PBD-150 is a human glutaminyl cyclase (hQC) Y115E-Y117E variant inhibitor, with a Ki value of 490 nM[1][2].
[in vivo]

PBD-150 is able to reduce the deposition of pyroglutamate-modified amyloid-β peptides in brain of transgenic mouse models of Alzheimer disease, leading to a significant improvement of learning and memory in those transgenic animals[3].

[References]

Buchholz et al. (2006), The first potent inhibitors for human glutaminyl cyclase: synthesis and structure-activity relationship; J. Med. Chem., 49 664 Schilling et al. (2008), Glutaminyl cyclase inhibition attenuates pyroglutamate Ab and Alzheimer’s disease-like pathology; Nat. Med., 14 1106
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