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.
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- CAS No.: 43000-65-3
- Formule: C31H44Cl2N2O3
- Masse moléculaire:563.60
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Activité biologique
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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] |
Chemical Information
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CAS No. 43000-65-3
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Masse moléculaire 563.60
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Formule C31H44Cl2N2O3
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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
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)