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Rotenolone is an antiproliferative agent. Rotenolone shows antiproliferative activity against the ovarian cancer A2780, breast cancer BT-549, prostate cancer DU 145, NSCLC NCI-H460, and colon cancer HCC-2998 cell lines, with IC50s of 0.95, 1.6, 2.7, 2.0, and 2.9 μM, respectively.

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Rotenolone Chemical Structure

Rotenolone Chemical Structure

CAS No. : 509-96-6

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Based on 1 publication(s) in Google Scholar

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  • Biological Activity

  • Purity & Documentation

  • References

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Description

Rotenolone is an antiproliferative agent. Rotenolone shows antiproliferative activity against the ovarian cancer A2780, breast cancer BT-549, prostate cancer DU 145, NSCLC NCI-H460, and colon cancer HCC-2998 cell lines, with IC50s of 0.95, 1.6, 2.7, 2.0, and 2.9 μM, respectively[1].

Cellular Effect
Cell Line Type Value Description References
697 IC50
0.5 μM
Compound: 7
Cytotoxicity against human 697 cells after 72 hrs by MTS assay
Cytotoxicity against human 697 cells after 72 hrs by MTS assay
[PMID: 23895019]
697 IC50
0.7 μM
Compound: 7
Cytotoxicity against human 697 cells after 48 hrs by MTS assay
Cytotoxicity against human 697 cells after 48 hrs by MTS assay
[PMID: 23895019]
A2780 IC50
0.95 μM
Compound: 5
Antiproliferative activity against human A2780 cells after 96 hrs by CellTiter-Glo luminescent cell viability assay
Antiproliferative activity against human A2780 cells after 96 hrs by CellTiter-Glo luminescent cell viability assay
[PMID: 20804165]
BT-549 IC50
1.6 μM
Compound: 5
Antiproliferative activity against human BT549 cells after 96 hrs by CellTiter-Glo luminescent cell viability assay
Antiproliferative activity against human BT549 cells after 96 hrs by CellTiter-Glo luminescent cell viability assay
[PMID: 20804165]
DU-145 IC50
2.7 μM
Compound: 5
Antiproliferative activity against human DU145 cells after 96 hrs by CellTiter-Glo luminescent cell viability assay
Antiproliferative activity against human DU145 cells after 96 hrs by CellTiter-Glo luminescent cell viability assay
[PMID: 20804165]
HCC 2998 IC50
2.9 μM
Compound: 5
Antiproliferative activity against human HCC2998 cells after 96 hrs by CellTiter-Glo luminescent cell viability assay
Antiproliferative activity against human HCC2998 cells after 96 hrs by CellTiter-Glo luminescent cell viability assay
[PMID: 20804165]
HCT-116 IC50
0.055 ug
Compound: 6
Cytotoxicity against human HCT116 cells measured per disk after 5 days by hemocytometer counting
Cytotoxicity against human HCT116 cells measured per disk after 5 days by hemocytometer counting
[PMID: 21452840]
HT-29 IC50
0.1 μM
Compound: 7
Cytotoxicity against human HT-29 cells after 72 hrs by SRB assay
Cytotoxicity against human HT-29 cells after 72 hrs by SRB assay
[PMID: 23895019]
NCI-H460 IC50
2 μM
Compound: 5
Antiproliferative activity against human NCI-H460 cells after 96 hrs by CellTiter-Glo luminescent cell viability assay
Antiproliferative activity against human NCI-H460 cells after 96 hrs by CellTiter-Glo luminescent cell viability assay
[PMID: 20804165]
Raji IC50
2.4 μM
Compound: 7
Cytotoxicity against human Raji cells after 72 hrs by MTS assay
Cytotoxicity against human Raji cells after 72 hrs by MTS assay
[PMID: 23895019]
Raji IC50
5.6 μM
Compound: 7
Cytotoxicity against human Raji cells after 48 hrs by MTS assay
Cytotoxicity against human Raji cells after 48 hrs by MTS assay
[PMID: 23895019]
U-937 IC50
0.07 μM
Compound: 4, 12a-hydroxyrotenone
Antiproliferative activity against human U937 cells after 48 hrs by WST-8 assay
Antiproliferative activity against human U937 cells after 48 hrs by WST-8 assay
[PMID: 17158054]
U-937 IC50
0.09 μM
Compound: 4, 12a-hydroxyrotenone
Antiproliferative activity against human U937 cells after 72 hrs by WST-8 assay
Antiproliferative activity against human U937 cells after 72 hrs by WST-8 assay
[PMID: 17158054]
U-937 IC50
3.6 μM
Compound: 4, 12a-hydroxyrotenone
Antiproliferative activity against human U937 cells after 24 hrs by WST-8 assay
Antiproliferative activity against human U937 cells after 24 hrs by WST-8 assay
[PMID: 17158054]
Molecular Weight

410.42

Formula

C23H22O7

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

O=C1[C@@]2([C@]([H])(OC3=C1C=CC4=C3C[C@@H](O4)C(C)=C)COC5=C2C=C(C(OC)=C5)OC)O

Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Powder -20°C 3 years
In solvent -80°C 6 months
-20°C 1 month
Solvent & Solubility
In Vitro: 

DMSO : 100 mg/mL (243.65 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.4365 mL 12.1826 mL 24.3653 mL
5 mM 0.4873 mL 2.4365 mL 4.8731 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

  • Molarity Calculator

  • Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass
=
Concentration
×
Volume
×
Molecular Weight *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

×
Volume (start)

V1

=
Concentration (final)

C2

×
Volume (final)

V2

In Vivo:

Select the appropriate dissolution method based on your experimental animal and administration route.

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

  • Protocol 1

    Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

    Solubility: ≥ 2.5 mg/mL (6.09 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

    Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
  • Protocol 2

    Add each solvent one by one:  10% DMSO    90% Corn Oil

    Solubility: ≥ 2.5 mg/mL (6.09 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL Corn oil, and mix evenly.

In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
%
DMSO +
+
%
Tween-80 +
%
Saline
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Calculation results:
Working solution concentration: mg/mL
Method for preparing stock solution: mg drug dissolved in μL  DMSO (Stock solution concentration: mg/mL).
The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only. If necessary, please contact MedChemExpress (MCE).
Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline.
 If the continuous dosing period exceeds half a month, please choose this protocol carefully.
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Purity & Documentation
References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.4365 mL 12.1826 mL 24.3653 mL 60.9132 mL
5 mM 0.4873 mL 2.4365 mL 4.8731 mL 12.1826 mL
10 mM 0.2437 mL 1.2183 mL 2.4365 mL 6.0913 mL
15 mM 0.1624 mL 0.8122 mL 1.6244 mL 4.0609 mL
20 mM 0.1218 mL 0.6091 mL 1.2183 mL 3.0457 mL
25 mM 0.0975 mL 0.4873 mL 0.9746 mL 2.4365 mL
30 mM 0.0812 mL 0.4061 mL 0.8122 mL 2.0304 mL
40 mM 0.0609 mL 0.3046 mL 0.6091 mL 1.5228 mL
50 mM 0.0487 mL 0.2437 mL 0.4873 mL 1.2183 mL
60 mM 0.0406 mL 0.2030 mL 0.4061 mL 1.0152 mL
80 mM 0.0305 mL 0.1523 mL 0.3046 mL 0.7614 mL
100 mM 0.0244 mL 0.1218 mL 0.2437 mL 0.6091 mL
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Rotenolone Related Classifications

Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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