Lactandrate
Lactandrate is a D-high nitrogen steroid alkylating agent. It can interact with the ligand-binding domain (LBD) of estrogen receptor-alpha (ERα). Lactandrate has a growth inhibitory effect on breast cancer cells, with a GI50 value ranging from 5 to 65 μM. It shows anti-tumor activity in mouse breast tumors (MXT and CD8F1) as well as in human xenograft MX-1.
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。
- CAS 番号: 43000-65-3
- 分子式: C31H44Cl2N2O3
- 分子量:563.60
-
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 |
|---|---|---|---|---|
| Hs 766 | IC50 |
>100 μM
Compound: 104
|
Cytotoxicity against human Hs766T cells assessed as reduction in cell viability after 48 h by MTT assay
Cytotoxicity against human Hs766T cells assessed as reduction in cell viability after 48 h by MTT assay
|
[PMID: 29649739] |
| Hs 766 | IC50 |
>100 μM
Compound: 104
|
Cytotoxicity against human Hs766T cells assessed as reduction in cell viability after 48 by MTT assay
Cytotoxicity against human Hs766T cells assessed as reduction in cell viability after 48 by MTT assay
|
[PMID: 29649739] |
| MCF7 | GI50 |
5 μM
Compound: 104
|
Growth inhibition of human MCF7 cells after 48 h by MTT assay
Growth inhibition of human MCF7 cells after 48 h by MTT assay
|
[PMID: 29649739] |
| MCF7 | GI50 |
5 μM
Compound: 104
|
Growth inhibition of human MCF7 cells after 48 by MTT assay
Growth inhibition of human MCF7 cells after 48 by MTT assay
|
[PMID: 29649739] |
| MIA PaCa-2 | IC50 |
>100 μM
Compound: 104
|
Cytotoxicity against human MIAPaCa2 cells assessed as reduction in cell viability after 48 h by MTT assay
Cytotoxicity against human MIAPaCa2 cells assessed as reduction in cell viability after 48 h by MTT assay
|
[PMID: 29649739] |
| MIA PaCa-2 | IC50 |
>100 μM
Compound: 104
|
Cytotoxicity against human MIAPaCa2 cells assessed as reduction in cell viability after 48 by MTT assay
Cytotoxicity against human MIAPaCa2 cells assessed as reduction in cell viability after 48 by MTT assay
|
[PMID: 29649739] |
| PANC-1 | IC50 |
>100 μM
Compound: 104
|
Cytotoxicity against human PANC1 cells assessed as reduction in cell viability after 48 h by MTT assay
Cytotoxicity against human PANC1 cells assessed as reduction in cell viability after 48 h by MTT assay
|
[PMID: 29649739] |
| PANC-1 | IC50 |
>100 μM
Compound: 104
|
Cytotoxicity against human PANC1 cells assessed as reduction in cell viability after 48 by MTT assay
Cytotoxicity against human PANC1 cells assessed as reduction in cell viability after 48 by MTT assay
|
[PMID: 29649739] |
| T47D | GI50 |
5 μM
Compound: 104
|
Growth inhibition of human T47D cells after 48 h by MTT assay
Growth inhibition of human T47D cells after 48 h by MTT assay
|
[PMID: 29649739] |
| T47D | GI50 |
5 μM
Compound: 104
|
Growth inhibition of human T47D cells after 48 by MTT assay
Growth inhibition of human T47D cells after 48 by MTT assay
|
[PMID: 29649739] |
化学情報
-
CAS 番号 43000-65-3
-
分子量 563.60
-
分子式 C31H44Cl2N2O3
-
SMILES
C[C@@]12[C@]3([H])[C@](CC[C@@]1([H])C[C@H](CC2)OC(CC4=CC=C(C=C4)N(CCCl)CCCl)=O)([H])[C@@]5([H])[C@](CC3)(NC(CC5)=O)C
-
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)