4-(4-氟苯基)-2-(4-羥基-1-丁炔)-1-(3-苯基丙基)-5-(4-吡啶基)咪唑
| 中文名稱 | 4-(4-氟苯基)-2-(4-羥基-1-丁炔)-1-(3-苯基丙基)-5-(4-吡啶基)咪唑 |
|---|---|
| 中文同義詞 | 4-(4-氟苯基)-2-(4-羥基-1-丁炔)-1-(3-苯基丙基)-5-(4-吡啶基)咪唑;RWJ 67657,P38Α和P38Β抑制劑;4-[4-(4-氟苯基)-1-(3-苯基丙基)-5-(4-吡啶基)-1H-咪唑-2-基]-3-丁Γ-1-OL;化合物RWJ-67657,10 MM DMSO 溶液 |
| 英文名稱 | 4-[4-(4-Fluorophenyl)-1-(3-phenylpropyl)-5-(4-pyridinyl)-1H-imidazol-2-yl]-3-butyn-1-ol |
| 英文同義詞 | 4-[4-(4-Fluorophenyl)-1-(3-phenylpropyl)-5-(4-pyridinyl)-1H-imidazol-2-yl]-3-butyn-1-ol;RWJ 67657;4-(4-Fluorophenyl)-2-(4-hydroxy-1-butynyl)-1-(3-phenylpropyl)-5-(4-Pyridyl)iMidazole;JNJ 3026582;RWJ-67657;JNJ-3026582;CS-1470;RWJ-67657; RWJ-67657; RWJ-67657;3-Butyn-1-ol, 4-[4-(4-fluorophenyl)-1-(3-phenylpropyl)-5-(4-pyridinyl)-1H-imidazol-2-yl]- |
| CAS號 | 215303-72-3 |
| 分子式 | C27H24FN3O |
| 分子量 | 425.5 |
| EINECS號 | |
| 相關(guān)類別 | |
| Mol文件 | 215303-72-3.mol |
| 結(jié)構(gòu)式 |  |
4-(4-氟苯基)-2-(4-羥基-1-丁炔)-1-(3-苯基丙基)-5-(4-吡啶基)咪唑 性質(zhì)
| 熔點(diǎn) | 124℃ |
|---|---|
| 沸點(diǎn) | 611.8±65.0 °C(Predicted) |
| 密度 | 1.14±0.1 g/cm3(Predicted) |
| 儲存條件 | Store at RT |
| 溶解度 | 乙醇中≤10mg/ml；DMSO 中≤5mg/ml；二甲基甲酰胺中≤2mg/ml |
| 酸度系數(shù)(pKa) | 14.37±0.10(Predicted) |
| 形態(tài) | 黃色粉末 |
| 顏色 | 淺黃至黃色 |
| InChI | 1S/C27H24FN3O/c28-24-13-11-22(12-14-24)26-27(23-15-17-29-18-16-23)31(25(30-26)10-4-5-20-32)19-6-9-21-7-2-1-3-8-21/h1-3,7-8,11-18,32H,5-6,9,19-20H2 |
| InChIKey | QSUSKMBNZQHHPA-UHFFFAOYSA-N |
| SMILES | OCCC#CC1=NC(C2=CC=C(F)C=C2)=C(C3=CC=NC=C3)N1CCCC4=CC=CC=C4 |
|
p38α 1 μM (IC 50 ) |
p38β 11 μM (IC 50 ) |
RWJ-67657 inhibits the release of TNF-α by lipopolysaccharide (LPS)-treated human peripheral blood mononuclear cells with an IC
50
of 3 nM, as well as the release of TNF-α from peripheral blood mononuclear cells treated with the superantigen staphylococcal enterotoxin B, with an IC
50
value of 13 nM.
RWJ67657 (10 μM; 24 hours) decreases colony formation in MCF-7 cells.
Cell Proliferation Assay
| Cell Line: | MCF-7 breast carcinoma cells |
| Concentration: | 10 μM |
| Incubation Time: | 24 hours |
| Result: | Decreased colony formation. |
RWJ-67657 inhibits TNF-alpha production in lipopolysaccharide-injected mice (87% inhibition at 50 mg/kg) and in rats (91% inhibition at 25 mg/kg) after oral administration.
RWJ-67657 (50 mg/kg; administered orally; once per day for 7 consecutive days) displays a potent anti-inflammatory effect. By both improving the functioning of endothelial progenitor cells (EPCs) and reducing inflammation, EPC transplantation plus RWJ-67657 administration synergistically promotes angiogenesis and neurogenesis after diabetic stroke.
| Animal Model: | The db/db mice (male, 8 weeks old) with EPCs |
| Dosage: | 50 mg/kg |
| Administration: | Administered orally; once per day for 7 consecutive days |
| Result: | Increased angiogenesis and neurogenesis of diabetic mice after cotreatment with EPCs transplantation. |
安全信息
| WGK Germany | WGK 3 |
|---|---|
| 存儲類別 | 11 - 可燃固體 |
| 更新日期 | 產(chǎn)品編號 | 產(chǎn)品名稱 | CAS號 | 包裝 | 價(jià)格 |
|---|---|---|---|---|---|
| 2026/06/05 | HY-15505R | 4-(4-氟苯基)-2-(4-羥基-1-丁炔)-1-(3-苯基丙基)-5-(4-吡啶基)咪唑 RWJ-67657 (Standard) | 215303-72-3 | 5 mg | 1750元 |
| 2026/06/05 | HY-15505R | 4-(4-氟苯基)-2-(4-羥基-1-丁炔)-1-(3-苯基丙基)-5-(4-吡啶基)咪唑 RWJ-67657 (Standard) | 215303-72-3 | 10 mg | 2800元 |