GANT61

製品コードS8075 バッチS807501

印刷

化学情報

Chemical Structure Synonyms NSC 136476 Storage
(From the date of receipt)		 3 years -20°C powder
1 years -80°C in solvent
化学式

C27H35N5
分子量 429.6 CAS No. 500579-04-4
Solubility (25°C)* 体外 Ethanol 12 mg/mL (27.93 mM)
DMSO Insoluble
Water Insoluble
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液（一定の濃度）を調合する

生物活性

製品説明 GANT61 (NSC 136476) is an inhibitor for GLI1 as well as GLI2-induced transcription, inhibits hedgehog with IC50 of 5 μM in GLI1 expressing HEK293T cell, displays selectivity over other pathways, such as TNF and glucocorticoid receptor gene transactivation. GANT61 induces apoptosis and activates protective autophagy in LX-2 cells.
in vitro GANT61 is an inhibitor for GLI1 as well as GLI2-induced transcription. This compound inhibits the DNA binding ability of GLI1. It inhibits hedgehog signaling with IC50 of 5 μM, displays selectivity over other pathways, such as TNF signaling/NFκB activation, glucocorticoid receptor gene transactivation, and the Ras–Raf–Mek–Mapk cascade. This chemical efficiently inhibited in vitro tumor cell proliferation in a GLI-dependent manner. [1] It induces apoptosis in chronic lymphocytic leukemia cells (CLL), but not in normal B lymphocytes. [2] This compound induces robust cytotoxicity and abolishs the clonogenicity in human colon carcinoma cell lines. [3] It induces inhibition of DNA replication in early S-phase in human colon carcinoma cell lines, leading to DNA damage signaling involving an ATM–Chk2 axis and induction of cell death. [4] This chemical (30 μM) causes growth arrest and apoptosis in acute myeloid leukemia (AML) cells. [5]
in vivo In nude mice injected with GLI1-positive 22Rv1 prostate cancer cells, GANT61 induces growth regression until no tumor is palpable. [1] In nude mice carrying SK-N-AS neuroblastoma xenografts, this compound treatment (oral gavage, 50 mg/kg) significantly inhibits tumor growth at Day 12 , as the tumor volume is reduced to 63% compared with controls. [6]

プロトコル(参考用のみ)

キナーゼアッセイ Dual Luciferase Assay
HEK293 cells are transfected with GLI1 expression plasmid, together with the reporter plasmids 12×GliBSLuc and R-Luc on 10-cm plates (day 0). Twenty-four hours later, cells are seeded in white 96-well plates with clear bottom at a density of 15,000 cells per well. Cells are allowed to attach, and this compound is added at a final concentration of 10 μM in DMSO (0.5% final DMSO concentration) (day 1.5). Cells are grown for another 24 h, subsequently lysed, and then analyzed by using the Dual Luciferase kit.
細胞アッセイ 細胞株 PANC1 or 22Rv1
濃度 ~5 μM
反応時間 48 h
実験の流れ BrdU Incorporation Assay. Subconfluent cells are grown in reduced FBS (2.5%) for 48 h in the presence of 5 μM test compound (or DMSO) on white 96-well plates with clear bottom. Subsequently, cells are labeled for 2 h with BrdU, fixed, and analyzed.
動物実験 動物モデル BALB/c nude mice with 22Rv1 cell xenograft
投薬量 50 mg/kg
投与方法 s.c.

参考

  • https://pubmed.ncbi.nlm.nih.gov/17494766/
  • https://pubmed.ncbi.nlm.nih.gov/20603613/
  • https://pubmed.ncbi.nlm.nih.gov/21135115/
  • https://pubmed.ncbi.nlm.nih.gov/21747117/
  • https://pubmed.ncbi.nlm.nih.gov/22398221/
  • https://pubmed.ncbi.nlm.nih.gov/22949014/

カスタマーフィードバック

, , Oncogene, 2017, 36(13): 1849-1861

, , Oncotarget. 2017, 8(30):48701-48710

Data from [Data independently produced by , , Cell Physiol Biochem, 2016, 38(4):1288-302.]

Selleckの高級品が、幾つかの出版された研究調査結果（以下を含む）で使われた：

The O-glycosyltransferase C1GALT1 promotes EWSR1::FLI1 expression and is a therapeutic target for Ewing sarcoma [ Nat Commun, 2025, 16(1):1267] PubMed: 39894896
Endothelial cell-derived SDF-1α elicits stemness traits of glioblastoma via dual-regulation of GLI1 [ Theranostics, 2025, 15(18):9819-9837] PubMed: 41041071
GPR137-RAB8A activation promotes ovarian cancer development via the Hedgehog pathway [ J Exp Clin Cancer Res, 2025, 44(1):22] PubMed: 39856733
PlexinD1 is a driver and a therapeutic target in advanced prostate cancer [ EMBO Mol Med, 2025, 17(2):336-364] PubMed: 39748059
Sonic Hedgehog potentiates BMP9-induced osteogenic differentiation of mesenchymal stem cells [ Genes Dis, 2025, 12(3):101308] PubMed: 40070367
Impact of Hedgehog modulators on signaling pathways in primary murine and human hepatocytes in vitro: insights into liver metabolism [ Arch Toxicol, 2025, 99(3):1105-1116] PubMed: 39714734
Identification of a distal enhancer regulating hedgehog interacting protein gene in human lung epithelial cells [ EBioMedicine, 2024, 101:105026] PubMed: 38417378
Inhibition of primary cilia-hedgehog signaling axis triggers autophagic cell death and suppresses malignant progression of VHL wild-type ccRCC [ Cell Death Dis, 2024, 15(10):739] PubMed: 39389955
Hedgehog pathway orchestrates the interplay of histone modifications and tailors combination epigenetic therapies in breast cancer [ Acta Pharm Sin B, 2023, 13(6):2601-2612] PubMed: 37425067
Hedgehog pathway orchestrates the interplay of histone modifications and tailors combination epigenetic therapies in breast cancer [ Acta Pharm Sin B, 2023, 13(6):2601-2612] PubMed: 37425067

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

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