DLin-MC3-DMA
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ATX-126 is a thiocarbamate-containing ionizable lipid investigated in siRNA nanoparticles and identified as an LNP component in the PMDA assessment of Kostaive.
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The published lipid 10p study provides a defined siRNA screening composition and mouse Factor VII silencing data. Separate regulatory studies describe tissue persistence after intramuscular administration; these results belong to different formulations and routes.
ATX-126 is identified by chemical name in the PMDA report and matches lipid 10p in Rajappan et al. The mouse siRNA screen and the regulatory vaccine studies are presented as separate evidence records.
| Component | DC Chemicals product | Molecular weight | Molar ratio | Mass at 1 µmol total lipid (mg) |
|---|---|---|---|---|
| ATX-126 | DC57046 | 755.23 | 58 | 0.438033 |
| DSPC | DC57005 | 790.15 | 7 | 0.055311 |
| Cholesterol | DCD-041 | 386.65 | 33.5 | 0.129528 |
| DMG-PEG2000 | DC40169 | 2507 | 1.5 | 0.037605 |
Rajappan 2020 siRNA formulation: 58:7:33.5:1.5 mol%; total lipid:RNA approximately 30:1 by mass. The 30:1 ratio is not N/P. DMG-PEG2000 MW 2507 follows the catalog calculation convention. This is not asserted to be the Kostaive manufacturing composition.
Prefilled proportions follow the source specified above. Molecular weights and ratios are editable. Results are calculated, not measured study data. No N/P or RNA dose is inferred.
| Component | MW | Molar ratio | Mass (mg) | Mass % |
|---|---|---|---|---|
| ATX-126 | ||||
| DSPC | ||||
| Cholesterol | ||||
| DMG-PEG2000 |
| Parameter | Reported finding | Source |
|---|---|---|
| Apparent pKa | 6.38 in the formulated-lipid study | Rajappan 2020, Table 8 |
| siRNA encapsulation | The study reports >90% across its tested lipid formulations | Experimental Section: siRNA Formulation into Lipid Nanoparticles |
| Regulatory LNP components | ATX-126, DSPC, cholesterol, PEG2000-DMG; ratio not assigned here | PMDA PDF p9, section 2.2.1 |
| Study | Finding | Interpretation |
|---|---|---|
| FVII siRNA, female BALB/c mice, intravenous, 48-hour endpoint | 99% FVII knockdown at 0.03 mg/kg siRNA | Lipid 10p, Tables 7–8; target-specific knockdown, not general mRNA efficacy |
| Mouse plasma stability | 100% lipid remaining at 2 hours | Table 8; does not support a rapid-clearance claim |
| Short mouse tolerability study | No abnormal observations reported at 3 mg/kg siRNA | Nontargeting-siRNA LNP assessment with 72-hour observation; not chronic or human safety |
| Context | Finding | Boundary |
|---|---|---|
| ARCT-021 repeated intramuscular rabbit study | ATX-126 remained detectable in liver, spleen, muscle and ovary on Day 57; no histopathological findings of toxicological significance were reported in these tissues | PMDA PDF pp16–17, section 4.2.2; not the intravenous siRNA formulation |
| ATX-126 metabolism assessment | Slow turnover and prolonged tissue persistence are described | PMDA PDF pp17–19; ester groups alone do not establish rapid elimination |
| CAS No. | 2230647-37-5 |
| Chemical Name | ATX-126(ATX-0126, lipid 10p) |
| Synonyms | ATX126, ATX 126,ATX 0126, ATX0126,ATX100,ATX-100, ATX 100 |
| SMILES | CCCCCCCC(CCCCCCC)OC(=O)CCCN(CCCC(=O)OC(CCCCCCC)CCCCCCC)C(=O)SCCCN(C)C |
| Formula | C44H86N2O5S |
| M.Wt | 755.23 |
| Purity | >95% by ELSD-HPLC |
| Storage | Pure form: −20 °C, 1 year; In solvent: −80 °C, 6 months; −20 °C, 1 month. Sealed and protected from light. |
| Shipping condition | Ships from Shanghai. Pure lipid is stable during ice-pack transport. |
| Publication |
The product molecular weight is prefilled when available and remains editable. Confirm solvent compatibility and solubility before preparation.
Solvent volumes update from the molecular weight above.
| Mass | 1 mM | 5 mM | 10 mM |
|---|---|---|---|
| 10 mg | 13.2410 mL | 2.6482 mL | 1.3241 mL |
| 25 mg | 33.1025 mL | 6.6205 mL | 3.3102 mL |
| 50 mg | 66.2050 mL | 13.2410 mL | 6.6205 mL |
| 100 mg | 132.4100 mL | 26.4820 mL | 13.2410 mL |
| 250 mg | 331.0250 mL | 66.2050 mL | 33.1025 mL |
Contact our team with the catalog number and requested quantity.