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.
연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.
- CAS No.: 43000-65-3
- 화학식: C31H44Cl2N2O3
- 분자량:563.60
-
보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
|
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
-
CAS No. 43000-65-3
-
분자량 563.60
-
화학식 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
-
선적
Room temperature in continental US; may vary elsewhere.
-
보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)