UNC 3230

Modify Date: 2024-01-09 10:43:53

UNC 3230 Structure
UNC 3230 structure
Common Name UNC 3230
CAS Number 1031602-63-7 Molecular Weight 344.431
Density 1.4±0.1 g/cm3 Boiling Point N/A
Molecular Formula C17H20N4O2S Melting Point N/A
MSDS N/A Flash Point N/A

 Use of UNC 3230


UNC3230 is a potent, selective and ATP-competitive phosphatidylinositol 4-phosphate 5 kinase type 1C (PIP5K1C) inhibitor with an IC50 of ~41 nM. UNC3230 also inhibits PIP4K2C and does not inhibit any of the other lipid kinases. UNC3230 has antinociceptive and anticancer effects[1].

 Names

Name 2-Anilino-5-[(cyclohexylcarbonyl)amino]-1,3-thiazole-4-carboxamide
Synonym More Synonyms

 UNC 3230 Biological Activity

Description UNC3230 is a potent, selective and ATP-competitive phosphatidylinositol 4-phosphate 5 kinase type 1C (PIP5K1C) inhibitor with an IC50 of ~41 nM. UNC3230 also inhibits PIP4K2C and does not inhibit any of the other lipid kinases. UNC3230 has antinociceptive and anticancer effects[1].
Related Catalog
Target

IC50: ~41 nM (phosphatidylinositol 4-phosphate 5 kinase type 1C (PIP5K1C))[1]

In Vitro Membrane PIP2 levels are significantly reduced by ~45% in dorsal root ganglia (DRG) neurons treated with 100 nM UNC3230 (~2-fold above the IC50) relative to vehicle controls. UNC3230 significantly reduces lysophosphatidic acid (LPA)-evoked calcium signaling in cultured DRG neurons relative to vehicle[1].
In Vivo UNC3230 (2 nmol) significantly increases noxious heat-evoked paw withdrawal latency for two hours after intrathecal injection in wild-type mice, indicating an antinociceptive effect[1]. UNC3230 (2 nmol; intrathecal injection) is administered then one hour later co-injected 1 nmol LPA with UNC3230 (2 nmol, intrathecal injection). UNC3230 significantly blunts thermal hyperalgesia and mechanical allodynia compared to vehicle[1]. UNC3230 (2 nmol; intrathecal injection) significantly blunts thermal hyperalgesia and mechanical allodynia in the complete Freund’s adjuvant (CFA)-inflamed hindpaw (relative to vehicle control) but does not affect thermal or mechanical sensitivity in the control (non-inflamed) hindpaw over a multiday time course[1].
References

[1]. Wright BD, et al. The lipid kinase PIP5K1C regulates pain signaling and sensitization. Neuron. 2014 May 21;82(4):836-47.

[2]. Peng W, et al. Type Iγ phosphatidylinositol phosphate kinase promotes tumor growth by facilitating Warburg effect in colorectal cancer. EBioMedicine. 2019 Jun;44:375-386.

[3]. Wright BD, et al. Development of a High-Throughput Screening Assay to Identify Inhibitors of the Lipid Kinase PIP5K1C. J Biomol Screen. 2015 Jun;20(5):655-62.

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Molecular Formula C17H20N4O2S
Molecular Weight 344.431
Exact Mass 344.130707
LogP 2.49
Index of Refraction 1.687
Storage condition -20°C

 Synonyms

2-Anilino-5-[(cyclohexylcarbonyl)amino]-1,3-thiazole-4-carboxamide
4-Thiazolecarboxamide, 5-[(cyclohexylcarbonyl)amino]-2-(phenylamino)-
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