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441742-93-4

441742-93-4 Structure

441742-93-4 Structure
IdentificationBack Directory
[Name]

(E)-4-(2-((2-methyl-1H-indol-3-yl)methylene)hydrazinyl)-5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidine
[CAS]

441742-93-4
[Synonyms]

pyrimidine-indole hybrid
(E)-4-(2-((2-methyl-1H-indol-3-yl)methylene)hydrazinyl)-5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidine
4-{(2E)-2-[(2-methyl-1H-indol-3-yl)methylidene]hydrazinyl}-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidine
[Molecular Formula]

C20H19N5S
[MOL File]

441742-93-4.mol
[Molecular Weight]

361.46
Chemical PropertiesBack Directory
[Boiling point ]

627.8±55.0 °C(Predicted)
[density ]

1.45±0.1 g/cm3(Predicted)
[pka]

9.14±0.20(Predicted)
Hazard InformationBack Directory
[Description]

PIH is an inhibitor of ciliogenesis through microtubule destabilization. It acts by antagonizing Hh signaling by repressing cilia biogenesis and disassembly of alpha tubulin in its stabilized form.
[Uses]

Pyrimidine-indole hybrid is a compound that inhibits ciliogenesis and has the activity of antagonizing the Hedgehog signaling pathway by destabilizing microtubules. Pyrimidine-indole hybrid exerts its biological effects by inhibiting ciliogenesis and deconstructing the stable form of α-tubulin. Pyrimidine-indole hybrid has shown its unique mechanism of action in in vitro cell experiments and zebrafish embryo models, interfering with microtubule dynamics[1].
[References]

[1] Hedgehog Antagonist Pyrimidine-Indole Hybrid Molecule Inhibits Ciliogenesis through Microtubule Destabilisation DOI:10.1002/cbic.201700631
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