PYRIB-SO 2
PYRIB-SO 2 is a potent antimitotic agent. PYRIB-SO 2 shows antiproliferative activity and induces cell cycle arrest at G2/M phase. PYRIB-SO 2 reduces and disruptes microtubule structures. PYRIB-SO 2 binds to the colchicine-binding site (C-BS) of α, β-tubulin.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 分子式: C14H12ClN3O4S
- 分子量:353.78
-
保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| HaCaT | IC50 |
17 nM
Compound: 2
|
Antiproliferative activity against human HaCaT cells assessed as inhibition of cell growth incubated for 48 hrs by SRB assay
Antiproliferative activity against human HaCaT cells assessed as inhibition of cell growth incubated for 48 hrs by SRB assay
|
[PMID: 38614151] |
| MCF7 | IC50 |
50 nM
Compound: 2
|
Antiproliferative activity against human MCF7 cells assessed as inhibition of cell growth incubated for 48 hrs by SRB assay
Antiproliferative activity against human MCF7 cells assessed as inhibition of cell growth incubated for 48 hrs by SRB assay
|
[PMID: 38614151] |
| MDA-MB-231 | IC50 |
220 nM
Compound: 2
|
Antiproliferative activity against human MDA-MB-231 cells assessed as inhibition of cell growth incubated for 48 hrs by SRB assay
Antiproliferative activity against human MDA-MB-231 cells assessed as inhibition of cell growth incubated for 48 hrs by SRB assay
|
[PMID: 38614151] |
| MDA-MB-468 | IC50 |
9 nM
Compound: 2
|
Antiproliferative activity against human MDA-MB-468 cells assessed as inhibition of cell growth incubated for 48 hrs by SRB assay
Antiproliferative activity against human MDA-MB-468 cells assessed as inhibition of cell growth incubated for 48 hrs by SRB assay
|
[PMID: 38614151] |
PYRIB-SO 2 (150 nM; 24 h) induces cell cycle arrest at G2/M phase [1].
PYRIB-SO 2 (138 nM; 24 h) reduces and disruptes microtubule structures in MCF7 cells [1].
PYRIB-SO 2 (5, 50 µM) reduces the formation of the EBI:β-tubulin adduct [1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:MCF7, MDA-MB-468, MDA-MB-231 cells
-
Concentration:0-500 nM
-
Incubation Time:48 h
-
Result:Showed antiproliferative activity with IC50s of 50, 9, 220 nM for MCF7, MDA-MB-468 and MDA-MB-231 cells, respectively.
-
Cell Line:MCF7 cells
-
Concentration:150 nM
-
Incubation Time:24 h
-
Result:Iduced cell cycle arrest at G2/M phase with the percentage of 77%.
化学情報
-
分子量 353.78
-
分子式 C14H12ClN3O4S
-
SMILES
ClC1=CC(OS(=O)(C2=CC=C(C=C2)N3CCNC3=O)=O)=CN=C1
-
輸送条件
Room temperature in continental US; may vary elsewhere.
-
保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)