ChemicalBook--->CAS DataBase List--->177355-84-9

177355-84-9

177355-84-9 Structure

177355-84-9 Structure
IdentificationBack Directory
[Name]

DBeQ
[CAS]

177355-84-9
[Synonyms]

JRF
DBeQ
JRF 12
CS-982
DBeQ (JRF 12)
DBeQ USP/EP/BP
JRF 12; JRF12; JRF-12
N,N'-Dibenzylquinazoline-2,4-diamine
N2,N4-Dibenzylquinazoline-2,4-diamine
N,N'-Dibenzyl-2,4-quinazolinediamine, 99%
N,N'-Dibenzylquinazoline-2,4-diamine DBeQ
N2,N4-Bis(phenylmethyl)-2,4-quinazolinediamine
2,4-QuinazolinediaMine, N,N'-bis(phenylMethyl)-
2,4-QuinazolinediaMine, N2,N4-bis(phenylMethyl)-
N2,N4-Dibenzylquinazoline-2,4-diamine DBeQ
[Molecular Formula]

C22H20N4
[MDL Number]

MFCD03691820
[MOL File]

177355-84-9.mol
[Molecular Weight]

340.421
Chemical PropertiesBack Directory
[Melting point ]

149 °C
[Boiling point ]

573.1±52.0 °C(Predicted)
[density ]

1.259±0.06 g/cm3(Predicted)
[storage temp. ]

room temp
[solubility ]

DMSO: ≥20mg/mL
[form ]

powder
[pka]

7.78±0.30(Predicted)
[color ]

white to beige
[Stability:]

Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 2 months.
[InChIKey]

QAIMUUJJAJBPCL-UHFFFAOYSA-N
[CAS DataBase Reference]

177355-84-9
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H319
[Precautionary statements ]

P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22-36
[Safety Statements ]

26
[WGK Germany ]

3
[HS Code ]

2933.59.8000
Hazard InformationBack Directory
[Description]

DBeQ (177355-84-9) is a potent, selective and reversible inhibitor of the AAA-ATPase p97 (ATPase associated with diverse cellular activities). Ki=3.2 μM. DBeQ blocks ubiquitin-dependent protein clearance pathways. Cell permeable.
[Uses]

The ATPase p97 is an ubiquitin-selective chaperone known to play a critical role in the degradation of misfolded membrane and secretory proteins and has been linked to various cellular processes that require unfolding and disassembly of protein complexes. DBeQ is a selective, reversible, and ATP-competitive inhibitor of the ATPase p97 (Ki = 3.2 μM; IC50 = 1.5 μM). It does not exhibit activity when tested against a panel 170 protein kinases at concentrations as high as 15 μM. At 10 μM it blocks endoplasmic reticulum-associated degradation, impairing the autophagy pathway and promoting the activation of caspase-3 and -7 in cancer cells.[Cayman Chemical]
[Biochem/physiol Actions]

DBeQ is a potent and specific inhibitor of ATPase p97, an integral component of the ubiquitin-fusion degradation (UFD) pathway. DBeQ inhibits the degradation of ubiquitinated proteins, the endoplasmic reticulum-associated degradation pathway, and autophagosome maturation. The compound also potently inhibits cellular proliferation and induces caspase 3/7 activity and apoptosis.
[storage]

Store at -20°C
[References]

1) Chou et al. (2011), Reversible inhibitor of p97, DBeQ, impairs both ubiquitin-dependent and autophagic protein clearance pathways; Proc. Natl. Acad. Sci. USA, 108 4834
Spectrum DetailBack Directory
[Spectrum Detail]

DBeQ(177355-84-9)1HNMR
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