ChemicalBook--->CAS DataBase List--->877618-79-6

877618-79-6

877618-79-6 Structure

877618-79-6 Structure
IdentificationBack Directory
[Name]

IWP-2-V2
[CAS]

877618-79-6
[Synonyms]

CS-1444
IWP-2-V2
INHIBITOR OF WNT PRODUCTION-2-V2
N-(6-methyl-2-benzothiazolyl)-2-[[3,4,6,7-tetrahydro-4-oxo-3-(phenylmethyl)thieno[3,2-d]pyrimidin-2-yl]thio]-acetamide
Acetamide, N-(6-methyl-2-benzothiazolyl)-2-[[3,4,6,7-tetrahydro-4-oxo-3-(phenylmethyl)thieno[3,2-d]pyrimidin-2-yl]thio]-
[Molecular Formula]

C23H20N4O2S3
[MDL Number]

MFCD05963653
[MOL File]

877618-79-6.mol
[Molecular Weight]

480.63
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

≤2mg/ml in DMSO;5mg/ml in dimethyl formamide
[form ]

crystalline solid
Hazard InformationBack Directory
[Uses]

IWP-2-V2 is a IWP-2 (HY-13912) analogue that retains activity against the Wnt/β-catenin pathway[1].
[Biological Activity]

iwp-2-v2 is a wnt production inhibitor.wnt signaling proteins are small secreted proteins that are active in tissue homeostasis, embryonic development, and tumorigenesis. wnt proteins bind to receptors, initiating a signaling cascade that results in β-catenin activation of gene transcription.
[in vitro]

iwp-2 was identified as an inhibitor of wnt production inactivating porcupine, a membrane-bound o-acyltransferase whose palmitoylation activity was essential for the signaling ability and secretion of wnt proteins. iwp-2-v2 is a less potent iwp-2 derivative whose chemical structure retains the benzothiazole group of its parent compound. iwp-2-v2 was used to evaluate which structural features of iwp-2 were critical for impairing wnt/β-catenin pathway activity [1].
[in vivo]

in cci rats, repetitive i.t. administration of iwp-2 (20 μm) in the early phase could significantly delay production of mechanical allodynia. the same drug administrated in the late phase produced long-lasting inhibitory effects on the established mechanical allodynia. such analgesia lasted 4–6 days for iwp-2 after termination of the third treatment. these results showed similar inhibitory effects of iwp-2 on thermal hyperalgesia after cci treatment [2].
[IC 50]

27 nm
[References]

[1] b. chen, m. e. dodge, w. tang, et al. small molecule-mediated disruption of wnt-dependent signaling in tissue regeneration and cancer. nature chemical biology 5(2), 100-107 (2009).
[2] y. zhang et al. wnt signaling underlies the pathogenesis of neuropathic pain in rodents. j clin invest. 2013 may 1; 123(5): 2268–2286.
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