(S)-Monastrol
(S)-Monastrol ((+)-Monastrol) is an allosteric inhibitor of the mitotic kinesin Eg5 that exhibits an antiproliferative effect against several cancer cell lines. (S)-Monastrol arrests mammalian cells in mitosis with monopolar spindles.
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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。
- CAS 番号: 254753-54-3
- 分子式: C14H16N2O3S
- 分子量:292.35
-
保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
Kinesin アイソフォーム固有の製品をすべて表示
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生物活性
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| 786-0 | GI50 |
4 μg/mL
Compound: BA2, monastrol
|
Growth inhibition of human 786-0 cells after 48 hrs by sulforhodamine B assay
Growth inhibition of human 786-0 cells after 48 hrs by sulforhodamine B assay
|
[PMID: 22410248] |
| A-431 | IC50 |
53 μg/mL
Compound: Monastrol
|
Cytotoxicity against human A431 cells after 48 hrs by MTT assay
Cytotoxicity against human A431 cells after 48 hrs by MTT assay
|
[PMID: 21620531] |
| A549 | IC50 |
>10 μM
Compound: Monastrol
|
Cytotoxicity against human A549 cells after 48 hrs by SRB assay
Cytotoxicity against human A549 cells after 48 hrs by SRB assay
|
[PMID: 21856161] |
| A549 | IC50 |
>100 μM
Compound: 1
|
Antiproliferative activity against human A549 cells incubated for 72 hrs by MTT assay
Antiproliferative activity against human A549 cells incubated for 72 hrs by MTT assay
|
[PMID: 31673316] |
| A549 | IC50 |
118 μg/mL
Compound: Monastrol
|
Cytotoxicity against human A549 cells after 48 hrs by MTT assay
Cytotoxicity against human A549 cells after 48 hrs by MTT assay
|
[PMID: 21620531] |
| AGS | IC50 |
>10 μM
Compound: Monastrol
|
Cytotoxicity against human AGS cells after 48 hrs by SRB assay
Cytotoxicity against human AGS cells after 48 hrs by SRB assay
|
[PMID: 21856161] |
| BXPC-3 | EC50 |
>100 nM
Compound: rac-monastrol
|
Antiproliferative activity against human BxPC3 cells after 72 hrs by Alamar blue assay
Antiproliferative activity against human BxPC3 cells after 72 hrs by Alamar blue assay
|
[PMID: 20597485] |
| C6 | IC50 |
>200 μM
Compound: 1
|
Antiproliferative activity against rat C6 cells after 24 hrs by MTS assay
Antiproliferative activity against rat C6 cells after 24 hrs by MTS assay
|
[PMID: 30108989] |
| C6 | IC50 |
87.83 μM
Compound: Manastrol
|
Cytotoxicity against rat C6 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Cytotoxicity against rat C6 cells assessed as reduction in cell viability after 48 hrs by MTT assay
|
[PMID: 30151081] |
| COLO 205 | IC50 |
164 μg/mL
Compound: Monastrol
|
Cytotoxicity against human COLO205 cells after 48 hrs by MTT assay
Cytotoxicity against human COLO205 cells after 48 hrs by MTT assay
|
[PMID: 21620531] |
| HCT-116 | EC50 |
1.2 μM
Compound: monastrol
|
Effect on cell cycle progression in human HCT116 cells assessed as mitotic arrest measured by doubling DNA content by fluorescence microscopy
Effect on cell cycle progression in human HCT116 cells assessed as mitotic arrest measured by doubling DNA content by fluorescence microscopy
|
[PMID: 18793847] |
| HCT-116 | EC50 |
1.5 μM
Compound: monastrol
|
Effect on cell cycle progression in human HCT116 cells assessed as increase in phospho-histone H3 by fluorescence microscopy
Effect on cell cycle progression in human HCT116 cells assessed as increase in phospho-histone H3 by fluorescence microscopy
|
[PMID: 18793847] |
| HCT-116 | EC50 |
24155 nM
Compound: rac-monastrol
|
Antiproliferative activity against human HCT116 cells after 72 hrs by Alamar blue assay
Antiproliferative activity against human HCT116 cells after 72 hrs by Alamar blue assay
|
[PMID: 20597485] |
| HCT-116 | IC50 |
>50 μM
Compound: Monastrol
|
Cytotoxicity against human HCT116 cells after 72 hrs by MTT assay
Cytotoxicity against human HCT116 cells after 72 hrs by MTT assay
|
[PMID: 20934346] |
| HCT-116 | IC50 |
9 μM
Compound: 1
|
Antiproliferative activity against human HCT116 cells incubated for 72 hrs by MTT assay
Antiproliferative activity against human HCT116 cells incubated for 72 hrs by MTT assay
|
[PMID: 31673316] |
| HeLa | IC50 |
176.9 μM
Compound: Monastrol
|
Cytotoxicity against human HeLa cells assessed as decrease in cell viability after 72 hrs by MTT assay
Cytotoxicity against human HeLa cells assessed as decrease in cell viability after 72 hrs by MTT assay
|
[PMID: 29908443] |
| HeLa | IC50 |
51.3 μM
Compound: 1, monastrol
|
Induction of monoastral spindles in HeLa cells after 7 hrs
Induction of monoastral spindles in HeLa cells after 7 hrs
|
[PMID: 17587586] |
| HeLa | IC50 |
6.1 μM
Compound: 1, monastrol
|
Inhibition of Eg5 ATPase activity expressed in HeLa cells after 12 hrs
Inhibition of Eg5 ATPase activity expressed in HeLa cells after 12 hrs
|
[PMID: 17587586] |
| HL-60(TB) | IC50 |
0.147 μM
Compound: Monastrol
|
Growth inhibition of human HL-60(TB) cells incubated for 24 hrs by MTT assay
Growth inhibition of human HL-60(TB) cells incubated for 24 hrs by MTT assay
|
[PMID: 28667871] |
| HT-29 | GI50 |
29.6 μg/mL
Compound: BA2, monastrol
|
Growth inhibition of human HT-29 cells after 48 hrs by sulforhodamine B assay
Growth inhibition of human HT-29 cells after 48 hrs by sulforhodamine B assay
|
[PMID: 22410248] |
| K562 | EC50 |
>100 nM
Compound: rac-monastrol
|
Antiproliferative activity against human K562 cells after 72 hrs by Alamar blue assay
Antiproliferative activity against human K562 cells after 72 hrs by Alamar blue assay
|
[PMID: 20597485] |
| KB 3-1 | EC50 |
56494 nM
Compound: rac-monastrol
|
Antiproliferative activity against human KB3-1 cells after 72 hrs by Alamar blue assay in presence of zosuquidar
Antiproliferative activity against human KB3-1 cells after 72 hrs by Alamar blue assay in presence of zosuquidar
|
[PMID: 20597485] |
| KB 3-1 | EC50 |
85114 nM
Compound: rac-monastrol
|
Antiproliferative activity against human KB3-1 cells after 72 hrs by Alamar blue assay
Antiproliferative activity against human KB3-1 cells after 72 hrs by Alamar blue assay
|
[PMID: 20597485] |
| KB-V1 | EC50 |
45394 nM
Compound: rac-monastrol
|
Antiproliferative activity against human KBV1 cells overexpressing MDR1 after 72 hrs by Alamar blue assay in presence of zosuquidar
Antiproliferative activity against human KBV1 cells overexpressing MDR1 after 72 hrs by Alamar blue assay in presence of zosuquidar
|
[PMID: 20597485] |
| KB-V1 | EC50 |
99083 nM
Compound: rac-monastrol
|
Antiproliferative activity against human KBV1 cells overexpressing MDR1 after 72 hrs by Alamar blue assay
Antiproliferative activity against human KBV1 cells overexpressing MDR1 after 72 hrs by Alamar blue assay
|
[PMID: 20597485] |
| MCF7 | IC50 |
45 μg/mL
Compound: Monastrol
|
Cytotoxicity against human MCF7 cells after 48 hrs by MTT assay
Cytotoxicity against human MCF7 cells after 48 hrs by MTT assay
|
[PMID: 21620531] |
| MCF7 | IC50 |
59.1 μM
Compound: Monastrol
|
Cytotoxicity against human MCF7 cells assessed as decrease in cell viability after 72 hrs by MTT assay
Cytotoxicity against human MCF7 cells assessed as decrease in cell viability after 72 hrs by MTT assay
|
[PMID: 29908443] |
| MCF7 | IC50 |
73 μM
Compound: 1
|
Antiproliferative activity against human MCF7 cells incubated for 72 hrs by MTT assay
Antiproliferative activity against human MCF7 cells incubated for 72 hrs by MTT assay
|
[PMID: 31673316] |
| MM1.S | IC50 |
8.7 μM
Compound: 1
|
Antiproliferative activity against human MM1S cells incubated for 72 hrs by MTT assay
Antiproliferative activity against human MM1S cells incubated for 72 hrs by MTT assay
|
[PMID: 31673316] |
| MOLT-4 | IC50 |
0.215 μM
Compound: Monastrol
|
Growth inhibition of human MOLT4 cells incubated for 24 hrs by MTT assay
Growth inhibition of human MOLT4 cells incubated for 24 hrs by MTT assay
|
[PMID: 28667871] |
| NCI/ADR-RES | GI50 |
22.2 μg/mL
Compound: BA2, monastrol
|
Growth inhibition of human NCI-ADR-RES cells after 48 hrs by sulforhodamine B assay
Growth inhibition of human NCI-ADR-RES cells after 48 hrs by sulforhodamine B assay
|
[PMID: 22410248] |
| NCI-H1299 | EC50 |
>100 nM
Compound: rac-monastrol
|
Antiproliferative activity against human NCI-H1299 cells after 72 hrs by Alamar blue assay
Antiproliferative activity against human NCI-H1299 cells after 72 hrs by Alamar blue assay
|
[PMID: 20597485] |
| NCI-H460 | GI50 |
10.6 μg/mL
Compound: BA2, monastrol
|
Growth inhibition of human NCI-H460 cells after 48 hrs by sulforhodamine B assay
Growth inhibition of human NCI-H460 cells after 48 hrs by sulforhodamine B assay
|
[PMID: 22410248] |
| OVCAR-3 | GI50 |
14.4 μg/mL
Compound: BA2, monastrol
|
Growth inhibition of human OVCAR3 cells after 48 hrs by sulforhodamine B assay
Growth inhibition of human OVCAR3 cells after 48 hrs by sulforhodamine B assay
|
[PMID: 22410248] |
| PC-3 | GI50 |
5.6 μg/mL
Compound: BA2, monastrol
|
Growth inhibition of human PC3 cells after 48 hrs by sulforhodamine B assay
Growth inhibition of human PC3 cells after 48 hrs by sulforhodamine B assay
|
[PMID: 22410248] |
| U138-MG | IC50 |
>200 μM
Compound: 1
|
Antiproliferative activity against human U138MG cells after 24 hrs by MTS assay
Antiproliferative activity against human U138MG cells after 24 hrs by MTS assay
|
[PMID: 30108989] |
| U-251 | GI50 |
24 μg/mL
Compound: BA2, monastrol
|
Growth inhibition of human U251 cells after 48 hrs by sulforhodamine B assay
Growth inhibition of human U251 cells after 48 hrs by sulforhodamine B assay
|
[PMID: 22410248] |
化学情報
-
CAS 番号 254753-54-3
-
分子量 292.35
-
分子式 C14H16N2O3S
-
SMILES
O=C(C1=C(C)NC(N[C@H]1C2=CC=CC(O)=C2)=S)OCC
-
別名
(+)-Monastrol
-
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
[1]. Marques LA, et al. Antiproliferative activity of monastrol in human adenocarcinoma (MCF-7) and non-tumor (HB4a) breast cells. Naunyn Schmiedebergs Arch Pharmacol. 2016 Dec;389(12):1279-1288. [Content Brief]
[2]. Mayer TU, et al. Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen. Science. 1999 Oct 29;286(5441):971-4. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)