ILK抑制剂(ILK-IN-2)
ILK-IN-2
CAS: 2070015-22-2
Molecular Formula: C30H30F3N5O
ILK抑制剂(ILK-IN-2) - Names and Identifiers
| Name | ILK-IN-2 |
| Synonyms | OSU-T315 ILK-IN-2 OSU-T315 (ILK-IN-1) OSU-T315 (1,3-regioisomer) OSU-T315 (1,5-regioisomer) 1H-Pyrazole-5-propanamide, N-methyl-1-[4-(1-piperazinyl)phenyl]-3-[4'-(trifluoromethyl)[1,1'-biphenyl]-4-yl]- N-Methyl-3-(1-(4-(piperazin-1-yl)phenyl)-3-(4'-(trifluoromethyl)-[1,1'-biphenyl]-4-yl)-1H-pyrazol-5-yl)propanamide |
| CAS | 2070015-22-2 |
ILK抑制剂(ILK-IN-2) - Physico-chemical Properties
| Molecular Formula | C30H30F3N5O |
| Molar Mass | 533.59 |
| Solubility | DMSO : 50 mg/mL (93.70 mM);H2O : < 0.1 mg/mL (insoluble) |
| Storage Condition | 2-8°C(protect from light) |
ILK抑制剂(ILK-IN-2) - Preparation solution concentration reference
| 1mg | 5mg | 10mg | |
|---|---|---|---|
| 1 mM | 1.874 ml | 9.37 ml | 18.741 ml |
| 5 mM | 0.375 ml | 1.874 ml | 3.748 ml |
| 10 mM | 0.187 ml | 0.937 ml | 1.874 ml |
| 5 mM | 0.037 ml | 0.187 ml | 0.375 ml |
Last Update：2024-01-02 23:10:35
ILK抑制剂(ILK-IN-2) - Reference Information
| biological activity | OSU-T315 (ILK-IN-2) is a potent inhibitor of Integrin-Linked Kinase (ILK), the IC50 value was 0.6 μm. OSU-T315 induces autophagy and apoptosis, both of which are essential for its antiproliferative activity. OSU-T315 has anti-tumor activity. |
| Target | Value |
| ILK (Cell-free assay) | 0.6 μM |
| Cell Line: | PC-3 cells; MDA-MB-231 cells Prostate cancer cells: LNCaP, PC-3; breast cancer cells: MDA-MB-231, MDA-MB-468, SKBR3, MCF-7; PrEC and MEC cells PC-3 cells |
| Concentration: | 1 μM, 2 μM, 3 μM, 4 μM; 0.5 μM, 1 μM, 1.5 μM, 2 μM, 2.5 μM 0-5 μM 1 μM, 2 μM, 3 μM, 4 μM |
| Incubation Time: | 24 hours 24 hours 24 hours |
| Result: | Exhibited a dose-dependent decreasing effect on the phosphorylation of pS6, ERKs, and p38 in PC-3 cells and MDA-MB-231 cells. Suppressed cancer cells viability in breast and prostate cancer cells (IC (50), 1-2.5μM). Induced accumulation of LC3-II and PARP cleavage. Resulted in suppression of tumor growth relative to the vehicle control after 35 days of treatment (48% and 62% suppression for 25 and 50 mg/kg, respectively). |
| Animal Model: | Male NCr athymic nude mice with PC-3 tumor xenografts |
| Dosage: | 25 mg/kg; 50 mg/kg |
| Administration: | Oral gavage; single daily; 35 days |
Last Update：2024-04-09 20:52:54
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Product Name: OSU-T315 Visit Supplier Webpage Request for quotationCAS: 2070015-22-2
Tel: 609-228-6898
Email: sales@medchemexpress.com
tech@medchemexpress.com
Mobile: 609-228-6898
Spot supply
Product Name: OSU-T315 Visit Supplier Webpage Request for quotationCAS: 2070015-22-2
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922
Wechat: 18621343501
WhatsApp: +86-18621343501
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Product Name: ILK-IN-2 Visit Supplier Webpage Request for quotationCAS: 2070015-22-2
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328
WhatsApp: +86-18821248368
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Product Name: ILK-IN-2 Visit Supplier Webpage Request for quotationCAS: 2070015-22-2
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View History
ILK抑制剂(ILK-IN-2)
RINK AMIDE AM RESIN
Β-羟基丁酸,DL-3-羟基丁酸
PHENYLDIMETHYLCHLOROGERMANE
D-HYDROOROTIC ACIDStructure
2-[(Z)-(2-CHLORO-6-FLUOROPHENYL)METHYLIDENE]-1-AZABICYCLO[2.2.2]OCT-3-YL N-PHENYLCARBAMATE
3,4-DIAMINO ANISOLE
(2-甲基苄基)三苯基氯化膦
邻氯苯基丙酮(2-氯苯丙酮)
RINK AMIDE AM RESIN
Β-羟基丁酸,DL-3-羟基丁酸
PHENYLDIMETHYLCHLOROGERMANE
D-HYDROOROTIC ACIDStructure
2-[(Z)-(2-CHLORO-6-FLUOROPHENYL)METHYLIDENE]-1-AZABICYCLO[2.2.2]OCT-3-YL N-PHENYLCARBAMATE
3,4-DIAMINO ANISOLE
(2-甲基苄基)三苯基氯化膦
邻氯苯基丙酮(2-氯苯丙酮)