2313525-20-9

2313525-20-9 structure

Name: SET2
Chemical Name: SET 2
CAS Number: 2313525-20-9
Molecular Formula: C₁₇H₂₁F₃N₄O₂S
Molecular Weight: 402.44
Catalog: Signaling Pathways Membrane Transporter/Ion Channel TRP Channel
Create Date: 2022-03-27 20:47:24
Modify Date: 2024-07-12 12:51:20
SET2 is a selective TRPV2 antagonist (IC50=0.46 μM). SET2 blocks the TRP channel and suppresses prostate cancer cells migration. SET2 reduces the lysophosphatidic acid (LPA, a TRPV2 activator)-induced cytoplasmic calcium increases[1].

Name	SET 2
Synonyms	N-(2-Furanylmethyl)-3-[[4-(methylpropylamino)-6-(trifluoromethyl)-2-pyrimidinyl]thio]propanamide

Description	SET2 is a selective TRPV2 antagonist (IC50=0.46 μM). SET2 blocks the TRP channel and suppresses prostate cancer cells migration. SET2 reduces the lysophosphatidic acid (LPA, a TRPV2 activator)-induced cytoplasmic calcium increases[1].
Related Catalog	Signaling Pathways >> Membrane Transporter/Ion Channel >> TRP Channel Research Areas >> Cancer
Target	TRPV2:0.46 μM (IC50)
In Vitro	SET2 (20 μM；24 小时) 消除表达 TRPV2 的 PC-3M 细胞的迁移[1]。 SET2 (20 μM；24 小时) 抑制瞬时共转染 TRPV2 和 LPAR1 的 HEK293T 细胞中的 2-APB 诱发电流[1]。 SET2 (20 μM；24 小时) 抑制 LPA (0.1 μM；3 分钟) 诱导的细胞质钙增加和 LPA 诱导的 PC-3M 细胞迁移[1]。 Cell Migration Assay [1] Cell Line: PC-3M prostate cancer cells Concentration: 0, 5 μM, 10 μM, and 20 μM Incubation Time: 24 hr and 48 hr Result: Inhibited cell migration of PC-3M cells, without inhibiting cell viability at 48 hours.
References	[1]. Chai H, et al. Structure-Based Discovery of a Subtype-Selective Inhibitor Targeting a Transient Receptor Potential Vanilloid Channel. J Med Chem. 2019 Feb 14;62(3):1373-1384.

Molecular Formula	C₁₇H₂₁F₃N₄O₂S
Molecular Weight	402.44