Anticancer agent 222
Anticancer agent 222 (Compound 19) is an orally active anticancer agent that exhibits significant anticancer activity against Huh7, FOCUS, SNU475, SNU182, HepG2, and Hep3B cells (IC50 = 2.9–9.3 μM).
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- 화학식: C28H26F6N6
- 분자량:560.54
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| HCT-116 | IC50 |
10.8 μM
Compound: 19
|
Cytotoxicity against human HCT-116 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
Cytotoxicity against human HCT-116 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
|
[PMID: 38688437] |
| Hep 3B2 | IC50 |
10.3 μM
Compound: 19
|
Cytotoxicity against human Hep3B cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
Cytotoxicity against human Hep3B cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
|
[PMID: 38688437] |
| HepG2 | IC50 |
6.6 μM
Compound: 19
|
Cytotoxicity against human HepG2 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
Cytotoxicity against human HepG2 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
|
[PMID: 38688437] |
| Huh-7 | IC50 |
9.3 μM
Compound: 19
|
Cytotoxicity against human Huh-7 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
Cytotoxicity against human Huh-7 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
|
[PMID: 38688437] |
| Mahlavu | IC50 |
19.8 μM
Compound: 19
|
Cytotoxicity against human Mahlavu cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
Cytotoxicity against human Mahlavu cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
|
[PMID: 38688437] |
| MCF7 | IC50 |
6.1 μM
Compound: 19
|
Cytotoxicity against human MCF7 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
Cytotoxicity against human MCF7 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
|
[PMID: 38688437] |
| PLC | IC50 |
99.1 μM
Compound: 19
|
Cytotoxicity against human PLC cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
Cytotoxicity against human PLC cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
|
[PMID: 38688437] |
| SNU-182 | IC50 |
16.4 μM
Compound: 19
|
Cytotoxicity against human SNU-182 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
Cytotoxicity against human SNU-182 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
|
[PMID: 38688437] |
| SNU-387 | IC50 |
98.7 μM
Compound: 19
|
Cytotoxicity against human SNU-387 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
Cytotoxicity against human SNU-387 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
|
[PMID: 38688437] |
| SNU-398 | IC50 |
19 μM
Compound: 19
|
Cytotoxicity against human SNU-398 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
Cytotoxicity against human SNU-398 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
|
[PMID: 38688437] |
| SNU-423 | IC50 |
24.9 μM
Compound: 19
|
Cytotoxicity against human SNU-423 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
Cytotoxicity against human SNU-423 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
|
[PMID: 38688437] |
| SNU-449 | IC50 |
60.6 μM
Compound: 19
|
Cytotoxicity against human SNU-449 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
Cytotoxicity against human SNU-449 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
|
[PMID: 38688437] |
| SNU-475 | IC50 |
17 μM
Compound: 19
|
Cytotoxicity against human SNU-475 cells assessed as cell growth inhibition by SRB assay
Cytotoxicity against human SNU-475 cells assessed as cell growth inhibition by SRB assay
|
[PMID: 38688437] |
Chemical Information
-
분자량 560.54
-
화학식 C28H26F6N6
-
SMILES
FC(F)(F)C(C=C1)=CC=C1C2=NC3=C(N=CN=C3N2C4CCCC4)N(CC5)CCN5C6=CC=C(C(F)(F)F)C=C6
-
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)