Antiproliferative agent-81
Antiproliferative agent-81 is a Homocamptothecin-derived ADC payload (ADC Payload) featuring an expanded seven-membered β-hydroxylactone ring. Antiproliferative agent-81 exhibits antiproliferative activity against multiple cancer cell lines with varying HER2 expression levels. Antiproliferative agent-81 is applicable to ADC synthesis-related research.
For research use only. We do not sell to patients.
- Formula: C27H29FN2O6
- Molecular Weight:496.53
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| MDA-MB-231 | IC50 |
0.3901 nM
|
Antiproliferative activity against human MDA-MB-231 breast carcinoma cells assessed as reduction in cell viability by proliferation inhibition assay.
Antiproliferative activity against human MDA-MB-231 breast carcinoma cells assessed as reduction in cell viability by proliferation inhibition assay.
|
42720475 |
| JIMT-1 | IC50 |
4.374 nM
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Antiproliferative activity against human JIMT-1 breast carcinoma cells assessed as reduction in cell viability by proliferation inhibition assay.
Antiproliferative activity against human JIMT-1 breast carcinoma cells assessed as reduction in cell viability by proliferation inhibition assay.
|
42720475 |
| NCI-N87 | IC50 |
1.118 nM
|
Antiproliferative activity against human NCI-N87 gastric carcinoma cells assessed as reduction in cell viability by proliferation inhibition assay.
Antiproliferative activity against human NCI-N87 gastric carcinoma cells assessed as reduction in cell viability by proliferation inhibition assay.
|
42720475 |
In Vitro
Antiproliferative agent-81 (Serially diluted concentrations) exhibits superior intrinsic cytotoxicity against MDA-MB-231 (IC50 = 0.3901 nM), JIMT-1 (IC50 = 4.374 nM), and NCI-N87 (IC50 = 1.118 nM) cancer cell lines compared to conventional six-membered α-hydroxylactone analogs[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
Chemical Information
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Molecular Weight 496.53
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Formula C27H29FN2O6
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SMILES
OCCCCC1=C2C(C(N3C2)=CC([C@@](O)(CC)[C@H](OC)C(OC4)=O)=C4C3=O)=NC5=CC(F)=C(C)C=C51
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
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RNA extraction experimental
By lysing cells, releasing RNA, and removing impurities such as proteins and DNA, high-purity RNA products are finally obtained. The commonly used traditional method is the guanidine isothiocyanate/phenol/chloroform method (Trizol), which is suitable for a variety of animal materials including animal tissues, microorganisms, cultured cells, etc., and most plant materials.
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Cell Viability Determination by MTT Colorimetric Assay
The following protocol uses the MTT colorimetric assay as a classic literature-established method for assessing cell viability/metabolic activity in cultured mammalian cells. MTT[3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] is reduced by metabolically active cells to a colored formazan product; the amount of formazan is quantified spectrophotometrically and provides an indirect measure of metabolically active viable cells. Importantly, MTT reduction reflects cellular oxidoreductase/metabolic activity rather than an absolute direct count of living cells, so changes in cellular metabolism can alter the signal independently of cell number.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)