Physicochemical Properties
| Molecular Formula | C44H60FN3O4 |
| Molecular Weight | 713.96 |
| Exact Mass | 713.456 |
| CAS # | 2251753-58-7 |
| PubChem CID | 145982275 |
| Appearance | Typically exists as solid at room temperature |
| Density | 1.2±0.1 g/cm3 |
| Boiling Point | 868.9±65.0 °C at 760 mmHg |
| Flash Point | 479.3±34.3 °C |
| Vapour Pressure | 0.0±3.3 mmHg at 25°C |
| Index of Refraction | 1.586 |
| LogP | 8.21 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 7 |
| Heavy Atom Count | 52 |
| Complexity | 1570 |
| Defined Atom Stereocenter Count | 7 |
| SMILES | FC1C=CC(=CC=1)NC(C1(CC1)C(NCCNC([C@]12CCC(C)(C)C[C@H]1C1=CC[C@@H]3[C@@]4(C)CC(=C)C(C(C)(C)[C@@H]4CC[C@@]3(C)[C@]1(C)CC2)=O)=O)=O)=O |
| InChi Key | QGKCNAYWPGAXOU-LBWRYPOYSA-N |
| InChi Code | InChI=1S/C44H60FN3O4/c1-27-25-40(6)32(39(4,5)34(27)49)15-16-42(8)33(40)14-13-30-31-26-38(2,3)17-19-43(31,20-18-41(30,42)7)35(50)46-23-24-47-36(51)44(21-22-44)37(52)48-29-11-9-28(45)10-12-29/h9-13,31-33H,1,14-26H2,2-8H3,(H,46,50)(H,47,51)(H,48,52)/t31-,32-,33+,40-,41+,42+,43-/m0/s1 |
| Chemical Name | 1-N-[2-[[(4aS,6aR,6aS,6bR,8aR,12aR,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-11-methylidene-10-oxo-1,3,4,5,6,6a,7,8,8a,12,13,14b-dodecahydropicene-4a-carbonyl]amino]ethyl]-1-N'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide |
| HS Tariff Code | 2934.99.9001 |
| Storage |
Powder-20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| Shipping Condition | Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs) |
Biological Activity
| ln Vitro | Anti-CSCs agent-1 (compound 48) inhibits A375 and B16F10 cell migration and colony formation in a dose-dependent manner [1]. In a dose-dependent way, anti-CSCs agent-1 (0, 1, 2, 3, 4 µM; 48 h) increases the expression of cleaved PARP, cleaved caspase-3, P-53, and Bax while inducing apoptosis[1]. The expression of E-cadherin is considerably upregulated in a dose-dependent manner to reverse the epithelial-mesenchymal transition by anti-CSCs agent-1 (0, 0.25, 0.5, 1.0, and 2.0 µM; 24 hours) [1]. Anti-CSC agent -1 (0-10 µM; 15 days) decreases CSC viability; for spheroid A357 and B16F10 cells, the IC50 values are 3.04 and 1.24 µM, respectively[1]. ROS generation in CSCs is greatly increased in a dose-dependent manner by anti-CSCs agent-1 (0-2 µM; 24 h) [1]. |
| ln Vivo | In mice, anti-tumor activity of anti-CSCs agent-1 (5 mg/kg; ip; daily for 15 days) has been demonstrated [1]. |
| Cell Assay |
Cell Proliferation Assay[1] Cell Types: MDA-MB-231, 4T1, A375, B16F10, PANC-1, A549, LLC cells Tested Concentrations: 0-50 µM Incubation Duration: 48 h Experimental Results: demonstrated antiproliferative activity with IC50s of 3.152, 0.7401, 0.8929, 0.6744, 1.107, 11.56, 0.9066 µM for MDA-MB-231, 4T1, A375, B16F10, PANC-1, A549, LLC cells, respectively. Apoptosis Analysis[1] Cell Types: A375, B16F10 cells Tested Concentrations: 0, 1, 2, 3 µM Incubation Duration: 48 h Experimental Results: Induced cell apoptosis in a dose-dependent manner. Western Blot Analysis[1] Cell Types: A375, B16F10 cells Tested Concentrations: 0, 1, 2, 3, 4 µM Incubation Duration: 48 h Experimental Results: Increased the expression of cleaved PARP, cleaved casepase-3, P-53 and Bax in a dose-dependent manner. |
| Animal Protocol |
Animal/Disease Models: C57BL/6J mice (A375 cells)[1] Doses: 5 mg/kg Route of Administration: Ip; daily for 15 days Experimental Results: Dramatically inhibited tumor growth. |
| References |
[1]. Synthesis and Discovery Novel Anti-Cancer Stem Cells Compounds Derived from the Natural Triterpenoic Acids. J Med Chem. 2018 Dec 13;61(23):10814-10833. |
Solubility Data
| Solubility (In Vitro) | May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples |
| Solubility (In Vivo) |
Note: Listed below are some common formulations that may be used to formulate products with low water solubility (e.g. < 1 mg/mL), you may test these formulations using a minute amount of products to avoid loss of samples. Injection Formulations (e.g. IP/IV/IM/SC) Injection Formulation 1: DMSO : Tween 80： Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution → 50 μL Tween 80 → 850 μL Saline) *Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH ₂ O to obtain a clear solution. Injection Formulation 2: DMSO : PEG300 ：Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL DMSO → 400 μLPEG300 → 50 μL Tween 80 → 450 μL Saline) Injection Formulation 3: DMSO : Corn oil = 10 : 90 (i.e. 100 μL DMSO → 900 μL Corn oil) Example: Take the Injection Formulation 3 (DMSO : Corn oil = 10 : 90) as an example, if 1 mL of 2.5 mg/mL working solution is to be prepared, you can take 100 μL 25 mg/mL DMSO stock solution and add to 900 μL corn oil, mix well to obtain a clear or suspension solution (2.5 mg/mL, ready for use in animals). Injection Formulation 4: DMSO : 20% SBE-β-CD in saline = 10 : 90 [i.e. 100 μL DMSO → 900 μL (20% SBE-β-CD in saline)] *Preparation of 20% SBE-β-CD in Saline (4°C，1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution. Injection Formulation 5: 2-Hydroxypropyl-β-cyclodextrin : Saline = 50 : 50 (i.e. 500 μL 2-Hydroxypropyl-β-cyclodextrin → 500 μL Saline) Injection Formulation 6: DMSO : PEG300 : castor oil : Saline = 5 : 10 : 20 : 65 (i.e. 50 μL DMSO → 100 μLPEG300 → 200 μL castor oil → 650 μL Saline) Injection Formulation 7: Ethanol : Cremophor : Saline = 10： 10 : 80 (i.e. 100 μL Ethanol → 100 μL Cremophor → 800 μL Saline) Injection Formulation 8: Dissolve in Cremophor/Ethanol (50 : 50), then diluted by Saline Injection Formulation 9: EtOH : Corn oil = 10 : 90 (i.e. 100 μL EtOH → 900 μL Corn oil) Injection Formulation 10: EtOH : PEG300：Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL EtOH → 400 μLPEG300 → 50 μL Tween 80 → 450 μL Saline) Oral Formulations Oral Formulation 1: Suspend in 0.5% CMC Na (carboxymethylcellulose sodium) Oral Formulation 2: Suspend in 0.5% Carboxymethyl cellulose Example: Take the Oral Formulation 1 (Suspend in 0.5% CMC Na) as an example, if 100 mL of 2.5 mg/mL working solution is to be prepared, you can first prepare 0.5% CMC Na solution by measuring 0.5 g CMC Na and dissolve it in 100 mL ddH2O to obtain a clear solution; then add 250 mg of the product to 100 mL 0.5% CMC Na solution, to make the suspension solution (2.5 mg/mL, ready for use in animals). Oral Formulation 3: Dissolved in PEG400 Oral Formulation 4: Suspend in 0.2% Carboxymethyl cellulose Oral Formulation 5: Dissolve in 0.25% Tween 80 and 0.5% Carboxymethyl cellulose Oral Formulation 6: Mixing with food powders Note: Please be aware that the above formulations are for reference only. InvivoChem strongly recommends customers to read literature methods/protocols carefully before determining which formulation you should use for in vivo studies, as different compounds have different solubility properties and have to be formulated differently. (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 1.4006 mL | 7.0032 mL | 14.0064 mL | |
| 5 mM | 0.2801 mL | 1.4006 mL | 2.8013 mL | |
| 10 mM | 0.1401 mL | 0.7003 mL | 1.4006 mL |