| Size | Price | |
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| 1mg | ||
| Other Sizes |
| ln Vitro |
Squamous NSCLC H157 cells' capacity to proliferate is inhibited by ABTL-0812 (ABTL0812; 10-100 μM; 48 hours) [1]. Treatment with ABTL0812 does not affect the human lung fibroblast cell line MRC-5 as it does not affect squamous non-small cell lung carcinoma H157 cells [1].
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| ln Vivo |
In human lung and pancreas xenografts, ABTL-0812 (ABTL0812; 120 mg/kg; oral gavage; 5 times per week; for 33 days) causes ER stress [1]. In vivo ER stress signals are induced by ABTL-0812. ATF4 and HSPA5 expression is upregulated in mice bearing A549 and MiaPaca2 xenografts, respectively, by ABTL-0812 [1].
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| Cell Assay |
Cell Viability Assay [1]
Cell Types: Human lung fibroblasts MRC5 and squamous non-small cell lung (NSCLC) H157 cells Tested Concentrations: 10, 30, 100 μM Incubation Duration: 48 hrs (hours) Experimental Results: Inhibition of squamous NSCLC H157 cells viability, but not the lung fibroblast cell line MRC-5. |
| Animal Protocol |
Animal/Disease Models: MiaPaca2 and A549 xenograft models in athymic female nude mice [1]
Doses: 120 mg/kg Route of Administration: po (oral gavage); 5 times per week for 33 days Experimental Results: In human lung and pancreas xenografts Inducing ER stress. |
| References | |
| Additional Infomation |
2-Hydroxylinoleic acid (2-hydroxylinoleic acid) is a 2-hydroxy fatty acid derived from linoleic acid. It functions as a metabolite of Arabidopsis thaliana, an antitumor agent, a PPARα agonist, and a PPARγ agonist. It is a 2-hydroxy fatty acid, a long-chain fatty acid, and a HODE. It is functionally related to linoleic acid. α-Hydroxylinoleic acid is being investigated in the clinical trial NCT04431258 (ABTL0812 combined with FOLFIRINOX as first-line treatment for metastatic pancreatic cancer). Ibuliraza is an orally bioavailable lipid analogue that is an inhibitor of target of rapamycin (mTOR) (mTOR complex 1; mTORC1), target of rapamycin (mTOR complex 2; mTORC2), and dihydrofolate reductase (DHFR), possessing potential antitumor activity. After oral administration, ibuliraza binds to and inhibits mTORC1 and mTORC2, which may lead to reduced apoptosis and proliferation of tumor cells expressing mTORC1/2. mTOR is a serine/threonine kinase that is upregulated in certain tumors; it plays a crucial role in the PI3K/Akt/mTOR signaling pathway, which is frequently dysregulated in cancer cells. Furthermore, ibrillazal inhibits dihydrofolate reductase (DHFR), an enzyme that reduces dihydrofolate to tetrahydrofolate, thereby blocking tetrahydrofolate synthesis, leading to nucleotide precursor depletion, and inhibiting the synthesis of DNA, RNA, and proteins. This induces autophagy-mediated cell death and further inhibits cell proliferation.
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| Molecular Formula |
C18H31NAO3
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|---|---|
| Molecular Weight |
318.4328
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| Exact Mass |
296.234
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| CAS # |
57818-44-7
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| PubChem CID |
21158511
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| Appearance |
Colorless to light yellow liquid
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| Density |
1.0±0.0 g/cm3
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| Boiling Point |
409.6±0.0 °C at 760 mmHg
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| Flash Point |
215.7±0.0 °C
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| Vapour Pressure |
0.0±0.0 mmHg at 25°C
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| Index of Refraction |
1.492
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| LogP |
6.24
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| Hydrogen Bond Donor Count |
2
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| Hydrogen Bond Acceptor Count |
3
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| Rotatable Bond Count |
14
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| Heavy Atom Count |
21
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| Complexity |
295
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| Defined Atom Stereocenter Count |
0
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| SMILES |
CCCCC/C=C\C/C=C\CCCCCCC(O)C(O)=O
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| InChi Key |
VFXKYDDSDQXKLC-NBTZWHCOSA-M
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| InChi Code |
InChI=1S/C18H32O3.Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(19)18(20)21/h6-7,9-10,17,19H,2-5,8,11-16H2,1H3,(H,20,21)/q+1/p-1/b7-6-,10-9-
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| Chemical Name |
sodium (9Z,12Z)-2-hydroxyoctadeca-9,12-dienoate
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| Synonyms |
ABTL0812 ABTL 0812ABTL-0812 sodium 2-hydroxylinoleate.
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| HS Tariff Code |
2934.99.9001
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| 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)
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| Solubility (In Vitro) |
DMSO : ~250 mg/mL (~843.34 mM)
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|---|---|
| Solubility (In Vivo) |
Solubility in Formulation 1: ≥ 2.08 mg/mL (7.02 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 20.8 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL. Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution. Solubility in Formulation 2: ≥ 2.08 mg/mL (7.02 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 20.8 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly. 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. View More
Solubility in Formulation 3: ≥ 2.08 mg/mL (7.02 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution. |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 3.1404 mL | 15.7020 mL | 31.4041 mL | |
| 5 mM | 0.6281 mL | 3.1404 mL | 6.2808 mL | |
| 10 mM | 0.3140 mL | 1.5702 mL | 3.1404 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration： mg/mL；
Method for preparing DMSO stock solution： mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:：Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O，mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.
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