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ChemicalBook--->CAS DataBase List--->39793-31-2

39793-31-2

39793-31-2 Structure

39793-31-2 Structure
IdentificationBack Directory
[Name]

4H-THIENO[3,2-B]PYRROLE-5-CARBOXYLIC ACID
[CAS]

39793-31-2
[Synonyms]

79793-31-2
AKOS BB-9991
CHEMBRDG-BB 4012315
D-Amino Acid Oxidase Inhibitor
Thieno[2,3-b]pyrrole-5-carboxylic acid
4-Thieno[3,2-b]pyrrole-5-carboxylic acid
4H-thieno[2,3-d]pyrrole-5-carboxylic acid
4H-THIENO[3,2-B]PYRROLE-5-CARBOXYLIC ACID
4H-thieno[3,2-b]pyrrole-5-carboxylic acid(SALTDATA: FREE)
D-Amino Acid Oxidase Inhibitor - CAS 39793-31-2 - Calbiochem
[Molecular Formula]

C7H5NO2S
[MDL Number]

MFCD07368542
[MOL File]

39793-31-2.mol
[Molecular Weight]

167.19
Chemical PropertiesBack Directory
[Melting point ]

180 °C
[Boiling point ]

437.4±25.0 °C(Predicted)
[density ]

1.609
[storage temp. ]

+2C to +8C
[solubility ]

DMF: 30 mg/ml; DMSO: 30 mg/ml; DMSO:PBS (pH 7.2) (1:2): 0.3 mg/ml; Ethanol: 2 mg/ml
[form ]

Beige solid
[pka]

4.36±0.30(Predicted)
[color ]

Light brown to gray
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xn,Xi
[Risk Statements ]

22-36/37/38
[Safety Statements ]

22-26-36/37/39
[WGK Germany ]

3
Hazard InformationBack Directory
[Synthesis Reference(s)]

Journal of the American Chemical Society, 79, p. 2556, 1957 DOI: 10.1021/ja01567a053
[General Description]

A cell-permeable thienopyrrole compound that potently inhibits the cellular activity of transfected D-amino acid oxidase (DAO/DAAO/DAMOX/OXDA) in CHO cells (IC50 against human and rat DAO = 145 and 114 nM, respectively), while exhibiting no activity towards D-aspartate oxidase (DDO; IC50 >5 μM), P450 enzymes CYP3A4/2D6/3C9 (IC50 >10 μM), and a panel of over 150 other enzymes, receptors, and ion channels. Although in vivo treatment of Compound 8 (200 mg/kg, i.p.) is shown to effectively inhibit DAO activity in rat brain and kidney (by 96% and 80%, respectively), the resulting D-serine concentration increase in the periphery and central nervous system appears to be far from sufficient to produce adequate antipsychotic and cognitive enhancing effects.
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