Anticancer agent 45
Anticancer agent 46 (compound 2b) is a potent and selective anticancer agent. Anticancer agent 46 shows cytotoxicity activity in cancer cells. Anticancer agent 46 induces apoptosis. Anticancer agent 46 shows low toxicity towards activated lymphocytes of human blood.
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- CAS. Nr.: 2770943-87-6
- Formel: C22H14ClN3O6S2
- Molecular Weight:515.95
-
Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biologische Aktivität
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| 786-0 | GI50 |
1.23 μM
Compound: 2b
|
Anticancer activity against human 786-0 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human 786-0 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| A549 | GI50 |
3.11 μM
Compound: 2b
|
Anticancer activity against human A549 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human A549 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| A549 | GI50 |
7.25 μM
Compound: 2b
|
Anticancer activity against human A549 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
Anticancer activity against human A549 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
|
[PMID: 35533562] |
| ACHN | GI50 |
1.36 μM
Compound: 2b
|
Anticancer activity against human ACHN cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human ACHN cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| BALB/3T3 | IC50 |
>100 μM
Compound: Les-6287
|
Cytotoxicity against mouse BALB/3T3 cells assessed reduction in cellular metabolic activity incubated for 24 to 72 hrs by MTT assay
Cytotoxicity against mouse BALB/3T3 cells assessed reduction in cellular metabolic activity incubated for 24 to 72 hrs by MTT assay
|
[PMID: 37579525] |
| Breast carcinoma cell | IC50 |
1 μM
Compound: Les-6287
|
Cytotoxicity against human Breast carcinoma cell assessed as inhibition of cell growth measured at 72 hrs
Cytotoxicity against human Breast carcinoma cell assessed as inhibition of cell growth measured at 72 hrs
|
[PMID: 37579525] |
| BT-549 | GI50 |
2.03 μM
Compound: 2b
|
Anticancer activity against human BT-549 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human BT-549 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| CAKI-1 | GI50 |
1.15 μM
Compound: 2b
|
Anticancer activity against human CAKI-1 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human CAKI-1 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| CCRF-CEM | GI50 |
0.385 μM
Compound: 2b
|
Anticancer activity against human CCRF-CEM cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human CCRF-CEM cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| COLO 205 | GI50 |
1.83 μM
Compound: 2b
|
Anticancer activity against human COLO 205 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human COLO 205 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| Colon carcinoma cell | IC50 |
1 μM
Compound: Les-6287
|
Cytotoxicity against human Colon carcinoma cell assessed as inhibition of cell growth measured at 72 hrs
Cytotoxicity against human Colon carcinoma cell assessed as inhibition of cell growth measured at 72 hrs
|
[PMID: 37579525] |
| DU-145 | GI50 |
1.72 μM
Compound: 2b
|
Anticancer activity against human DU-145 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human DU-145 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| EKVX | GI50 |
3.25 μM
Compound: 2b
|
Anticancer activity against human EKVX cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human EKVX cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| Glioblastoma cell line | IC50 |
1 μM
Compound: Les-6287
|
Cytotoxicity against human Glioblastoma cell line assessed as inhibition of cell growth measured at 72 hrs
Cytotoxicity against human Glioblastoma cell line assessed as inhibition of cell growth measured at 72 hrs
|
[PMID: 37579525] |
| HaCaT | GI50 |
73.6 μM
Compound: 2b
|
Cytotoxicity against human HaCaT cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
Cytotoxicity against human HaCaT cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
|
[PMID: 35533562] |
| HaCaT | IC50 |
>100 μM
Compound: Les-6287
|
Cytotoxicity against human HaCaT cells assessed reduction in cellular metabolic activity incubated for 24 to 72 hrs by MTT assay
Cytotoxicity against human HaCaT cells assessed reduction in cellular metabolic activity incubated for 24 to 72 hrs by MTT assay
|
[PMID: 37579525] |
| HaCaT | IC50 |
73.6 μM
Compound: Les-6287
|
Cytotoxicity against human HaCaT cells assessed reduction in cellular metabolic activity incubated for 72 hrs by MTT assay
Cytotoxicity against human HaCaT cells assessed reduction in cellular metabolic activity incubated for 72 hrs by MTT assay
|
[PMID: 37579525] |
| HCC 2998 | GI50 |
1.48 μM
Compound: 2b
|
Anticancer activity against human HCC 2998 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human HCC 2998 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| HCT-116 | GI50 |
0.751 μM
Compound: 2b
|
Anticancer activity against human HCT-116 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human HCT-116 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| HCT-116 | GI50 |
4.52 μM
Compound: 2b
|
Anticancer activity against human HCT-116 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
Anticancer activity against human HCT-116 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
|
[PMID: 35533562] |
| HCT-15 | GI50 |
0.472 μM
Compound: 2b
|
Anticancer activity against human HCT-15 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human HCT-15 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| HeLa | GI50 |
6.13 μM
Compound: 2b
|
Anticancer activity against human HeLa cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
Anticancer activity against human HeLa cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
|
[PMID: 35533562] |
| HL-60 | GI50 |
2.44 μM
Compound: 2b
|
Anticancer activity against human HL-60 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human HL-60 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| HOP-62 | GI50 |
2.26 μM
Compound: 2b
|
Anticancer activity against human HOP-62 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human HOP-62 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| HOP-92 | GI50 |
1.62 μM
Compound: 2b
|
Anticancer activity against human HOP-92 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human HOP-92 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| Hs-578T | GI50 |
2.8 μM
Compound: 2b
|
Anticancer activity against human Hs-578T cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human Hs-578T cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| HT-29 | GI50 |
0.847 μM
Compound: 2b
|
Anticancer activity against human HT-29 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human HT-29 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| IGROV-1 | GI50 |
1.2 μM
Compound: 2b
|
Anticancer activity against human IGROV-1 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human IGROV-1 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| Jurkat | GI50 |
1.3 μM
Compound: 2b
|
Anticancer activity against human Jurkat cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
Anticancer activity against human Jurkat cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
|
[PMID: 35533562] |
| K562 | GI50 |
0.603 μM
Compound: 2b
|
Anticancer activity against human K562 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human K562 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| KB 3-1 | GI50 |
8 μM
Compound: 2b
|
Anticancer activity against human KB 3-1 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
Anticancer activity against human KB 3-1 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
|
[PMID: 35533562] |
| KM12 | GI50 |
1.83 μM
Compound: 2b
|
Anticancer activity against human KM12 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human KM12 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| Leukemic tumor cell line | IC50 |
1 μM
Compound: Les-6287
|
Cytotoxicity against human Leukemic tumor cell line assessed as inhibition of cell growth measured at 72 hrs
Cytotoxicity against human Leukemic tumor cell line assessed as inhibition of cell growth measured at 72 hrs
|
[PMID: 37579525] |
| Lung cancer cell line | IC50 |
1 μM
Compound: Les-6287
|
Cytotoxicity against human Lung cancer cell line assessed as inhibition of cell growth measured at 72 hrs
Cytotoxicity against human Lung cancer cell line assessed as inhibition of cell growth measured at 72 hrs
|
[PMID: 37579525] |
| Lymphocyte | GI50 |
51.2 μM
Compound: 2b
|
Cytotoxicity against mitogen activated human peripheral blood lymphocytes assessed as cell growth inhibition incubated for 48 hrs by MTT assay
Cytotoxicity against mitogen activated human peripheral blood lymphocytes assessed as cell growth inhibition incubated for 48 hrs by MTT assay
|
[PMID: 35533562] |
| Lymphocyte | GI50 |
67.1 μM
Compound: 2b
|
Cytotoxicity against mitogen activated human peripheral blood lymphocytes assessed as cell growth inhibition incubated for 24 hrs by MTT assay
Cytotoxicity against mitogen activated human peripheral blood lymphocytes assessed as cell growth inhibition incubated for 24 hrs by MTT assay
|
[PMID: 35533562] |
| M14 | GI50 |
1.46 μM
Compound: 2b
|
Anticancer activity against human M14 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human M14 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| Malme-3M | GI50 |
2.31 μM
Compound: 2b
|
Anticancer activity against human Malme-3M cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human Malme-3M cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| MCF7 | GI50 |
1.21 μM
Compound: 2b
|
Anticancer activity against human MCF7 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human MCF7 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| MCF7 | GI50 |
4 μM
Compound: 2b
|
Anticancer activity against human MCF7 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
Anticancer activity against human MCF7 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
|
[PMID: 35533562] |
| MDA-MB-231 | GI50 |
2.14 μM
Compound: 2b
|
Anticancer activity against human MDA-MB-231 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human MDA-MB-231 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| MDA-MB-231 | GI50 |
6.2 μM
Compound: 2b
|
Anticancer activity against human MDA-MB-231 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
Anticancer activity against human MDA-MB-231 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
|
[PMID: 35533562] |
| MDA-MB-435 | GI50 |
2.01 μM
Compound: 2b
|
Anticancer activity against human MDA-MB-435 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human MDA-MB-435 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| MDA-MB-468 | GI50 |
1.87 μM
Compound: 2b
|
Anticancer activity against human MDA-MB-468 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human MDA-MB-468 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| MOLT-4 | GI50 |
0.534 μM
Compound: 2b
|
Anticancer activity against human MOLT-4 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human MOLT-4 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| NCI/ADR-RES | GI50 |
2.13 μM
Compound: 2b
|
Anticancer activity against human NCI/ADR-RES cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human NCI/ADR-RES cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| NCI-H226 | GI50 |
2.41 μM
Compound: 2b
|
Anticancer activity against human NCI-H226 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human NCI-H226 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| NCI-H23 | GI50 |
1.56 μM
Compound: 2b
|
Anticancer activity against human NCI-H23 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human NCI-H23 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| NCI-H322M | GI50 |
2.34 μM
Compound: 2b
|
Anticancer activity against human NCI-H322M cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human NCI-H322M cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| NCI-H460 | GI50 |
2.55 μM
Compound: 2b
|
Anticancer activity against human NCI-H460 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human NCI-H460 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| NCI-H522 | GI50 |
1.86 μM
Compound: 2b
|
Anticancer activity against human NCI-H522 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human NCI-H522 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| OVCAR-3 | GI50 |
0.604 μM
Compound: 2b
|
Anticancer activity against human OVCAR-3 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human OVCAR-3 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| OVCAR-4 | GI50 |
5.13 μM
Compound: 2b
|
Anticancer activity against human OVCAR-4 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human OVCAR-4 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| OVCAR-5 | GI50 |
1.91 μM
Compound: 2b
|
Anticancer activity against human OVCAR-5 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human OVCAR-5 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| OVCAR-8 | GI50 |
2.16 μM
Compound: 2b
|
Anticancer activity against human OVCAR-8 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human OVCAR-8 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| PC-3 | GI50 |
0.906 μM
Compound: 2b
|
Anticancer activity against human PC-3 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human PC-3 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| RPMI-8226 | GI50 |
0.295 μM
Compound: 2b
|
Anticancer activity against human RPMI-8226 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human RPMI-8226 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| RXF 393 | GI50 |
1.53 μM
Compound: 2b
|
Anticancer activity against human RXF 393 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human RXF 393 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| SCC-15 | EC50 |
24.85 μM
Compound: Les-6287
|
Cytotoxicity against human SCC-15 cells assessed as LDH release incubated for 24 hrs
Cytotoxicity against human SCC-15 cells assessed as LDH release incubated for 24 hrs
|
[PMID: 37579525] |
| SCC-15 | EC50 |
32.75 μM
Compound: Les-6287
|
Cytotoxicity against human SCC-15 cells assessed as LDH release incubated for 48 hrs
Cytotoxicity against human SCC-15 cells assessed as LDH release incubated for 48 hrs
|
[PMID: 37579525] |
| SCC-15 | IC50 |
17.69 μM
Compound: Les-6287
|
Cytotoxicity against human SCC-15 cells assessed as decrease in cellular metabolic activity incubated for 24 hrs by resazurin reduction assay
Cytotoxicity against human SCC-15 cells assessed as decrease in cellular metabolic activity incubated for 24 hrs by resazurin reduction assay
|
[PMID: 37579525] |
| SCC-15 | IC50 |
6.72 μM
Compound: Les-6287
|
Cytotoxicity against human SCC-15 cells assessed as decrease in cellular metabolic activity incubated for 48 hrs by resazurin reduction assay
Cytotoxicity against human SCC-15 cells assessed as decrease in cellular metabolic activity incubated for 48 hrs by resazurin reduction assay
|
[PMID: 37579525] |
| SF-268 | GI50 |
2.43 μM
Compound: 2b
|
Anticancer activity against human SF-268 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human SF-268 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| SF-295 | GI50 |
1.31 μM
Compound: 2b
|
Anticancer activity against human SF-295 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human SF-295 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| SF-539 | GI50 |
1.72 μM
Compound: 2b
|
Anticancer activity against human SF-539 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human SF-539 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| SK-MEL-2 | GI50 |
2.74 μM
Compound: 2b
|
Anticancer activity against human SK-MEL-2 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human SK-MEL-2 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| SK-MEL-28 | GI50 |
1.95 μM
Compound: 2b
|
Anticancer activity against human SK-MEL-28 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human SK-MEL-28 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| SK-MEL-5 | GI50 |
1.92 μM
Compound: 2b
|
Anticancer activity against human SK-MEL-5 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human SK-MEL-5 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| SK-OV-3 | GI50 |
>100 μM
Compound: 2b
|
Anticancer activity against human SK-OV-3 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
Anticancer activity against human SK-OV-3 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
|
[PMID: 35533562] |
| SK-OV-3 | GI50 |
2.99 μM
Compound: 2b
|
Anticancer activity against human SK-OV-3 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human SK-OV-3 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| SN12C | GI50 |
1.6 μM
Compound: 2b
|
Anticancer activity against human SN12C cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human SN12C cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| SNB-19 | GI50 |
1.34 μM
Compound: 2b
|
Anticancer activity against human SNB-19 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human SNB-19 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| SR | GI50 |
0.394 μM
Compound: 2b
|
Anticancer activity against human SR cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human SR cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| SW-620 | GI50 |
0.684 μM
Compound: 2b
|
Anticancer activity against human SW-620 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human SW-620 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| T47D | GI50 |
2.45 μM
Compound: 2b
|
Anticancer activity against human T47D cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human T47D cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| TK-10 | GI50 |
1.92 μM
Compound: 2b
|
Anticancer activity against human TK-10 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human TK-10 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| U-251 | GI50 |
0.597 μM
Compound: 2b
|
Anticancer activity against human U-251 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human U-251 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| U-251 | GI50 |
1.1 μM
Compound: 2b
|
Anticancer activity against human U-251 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
Anticancer activity against human U-251 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
|
[PMID: 35533562] |
| UACC-257 | GI50 |
2.48 μM
Compound: 2b
|
Anticancer activity against human UACC-257 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human UACC-257 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| UACC-62 | GI50 |
1.67 μM
Compound: 2b
|
Anticancer activity against human UACC-62 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human UACC-62 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
| UO-31 | GI50 |
1.35 μM
Compound: 2b
|
Anticancer activity against human UO-31 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
Anticancer activity against human UO-31 cells assessed as growth inhibition incubated for 48 hrs by SRB assay
|
[PMID: 35533562] |
Anticancer agent 46 (compound 2b) (0-100 µM; 72 h) shows antitumor activity with GI50S of 1.30, 7.25, 4.00, 6.20, 8.00, 6.13, 4.52, 5.65, 1.10, >100, 73.62 µM for Jurkat, A549, MCF-7, MDA-MB-231, KB3-1, HeLa, HCT-116, HCT-116 p53-/-, U251, SK-OV-3, HaCaT cells, respectively[1].
Anticancer agent 46 (1.5 µM; 24 h) induces apoptosis by increases the expression of caspase 3, Bax and decreases the amount of anti-apoptotic Bcl-2 protein[1].
Anticancer agent 46 (compound 2b) (0-2 µM; 24, 48 h) shows low toxicity towards normal human keratinocytes of HaCaT line and mitogen-activated lymphocytes of peripheral blood of healthy human donor[1].
Anticancer agent 46 dose not induce significant DNA damage and changes in morphology of mitogen-activated lymphocytes of peripheral blood of healthy donor[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:Jurkat cells
-
Concentration:1.5 µM
-
Incubation Time:24 h
-
Result:Increased in the amount of pro-apoptotic proteins: caspase 3, Bax, and decreased the amount of anti-apoptotic Bcl-2 protein.
Chemical Information
-
CAS. Nr. 2770943-87-6
-
Molecular Weight 515.95
-
Formel C22H14ClN3O6S2
-
SMILES
O=C(C(N(C/1=O)C(SC1=C/C(Cl)=C/C2=CC=C([N+]([O-])=O)C=C2)=S)C3)N(C4=CC=C(O)C=C4)C3=O
-
Versand
Room temperature in continental US; may vary elsewhere.
-
Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Reinheit & Dokumentation
Verweise
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)