SM-102
Recommended because it shares a closely related research category or delivery context. Formulation and performance are product- and study-specific.
View product →
Iso-A11B5C1 is an ionizable lipid investigated for muscle-selective mRNA delivery after intramuscular administration. In the cited mouse study, its LNP formulation retained local expression while limiting detectable liver and spleen reporter expression relative to the SM-102 comparator.
Open full Formulation & Performance →
The optimized muscle-delivery formulation uses a C14 PEG phospholipid. Its results should not be transferred to a formulation in which that component is replaced by DMG-PEG2000.
The results below describe the cited research formulations. Product specifications and commercial pack options are shown in the Specifications and ordering sections.
| Component | DC Chemicals product | Molecular weight | Molar ratio | Mass at 1 µmol total lipid (mg) |
|---|---|---|---|---|
| Iso-A11B5C1 | DC60510 | 662.1 | 60 | 0.397260 |
| DOPE | DC33634 | 744.03 | 10 | 0.074403 |
| Cholesterol | DCD-041 | 386.65 | 29 | 0.112128 |
| C14-PEG2000 (14:0 PEG2000 PE) | Not uniquely mapped | Not established | 1 | Not calculable from disclosed data |
Optimized molar composition = 60:10:29:1; ionizable lipid:mRNA = 10:1 by weight. The SI identifies 14:0 PEG2000 PE as the PEG lipid. Its exact commercial product mapping and molecular weight are not assigned here. This is not DMG-PEG2000; total mass fractions remain uncalculated until its molecular weight is specified. N/P was not reported.
Not all inputs are assigned to a single verified study formulation; unassigned fields are blank. Enter your own values to calculate a research scenario. 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 % |
|---|---|---|---|---|
| Iso-A11B5C1 | ||||
| DOPE | ||||
| Cholesterol | ||||
| C14-PEG2000 (14:0 PEG2000 PE) |
| Parameter | Evidence | Source / boundary |
|---|---|---|
| Apparent pKa | Approximately 7.2 | Main Fig. 3B; formulation ionization measurement. |
| Size / PDI | Particle-size and dispersity measurements are plotted | SI Fig. S4, p. 9. No exact mean is transcribed from the graph. |
| Encapsulation | >80% was an optimization selection criterion | The criterion is not a final-batch numerical encapsulation result. SI Table S2 compares screening formulations. |
| Helper-lipid identity | DOPE; C14-PEG2000 phospholipid | Methods and SI. Unverified substitutions are not used in the component calculator. |
| Cell model | Comparison with SM-102 LNPs | Interpretation |
|---|---|---|
| HeLa | 42-fold higher reporter expression | Main Fig. 3A; cell-line-specific comparison. |
| HepG2 | 28-fold lower reporter expression | Main Fig. 3A; supports reduced expression in this hepatic cell model. |
| Splenocytes | 24-fold lower reporter expression | Main Fig. 3A; does not imply absence of particle exposure. |
| Study | Conditions | Reported outcome |
|---|---|---|
| Luciferase mRNA | C57BL/6J mice; 0.3 mg/kg IM; 6 h; n = 3 | Local expression comparable to SM-102; no significant difference reported. Liver/spleen off-target expression was not detected under the assay conditions (Fig. 2). |
| Cre mRNA reporter | mTmG mice; 0.5 mg/kg IM; 36 h; n = 3 | Muscle reporter activation comparable to SM-102; Iso-A11B5C1 activation not detected in liver/spleen (Fig. 4). |
| SM-102 Cre comparator | Same reporter study | 83.83% liver and 72.67% spleen reporter activation reported for the comparator. These are reporter readouts, not injected-dose recovery. |
Five tissue sections were averaged per mouse in the Cre analysis. Cre-dependent recombination is distinct from CRISPR editing. Undetected expression does not demonstrate zero tissue exposure.
| Endpoint | Reported evidence | Limit |
|---|---|---|
| Trp2 mRNA / B16F10 model | Doses administered on days 7 and 12; tumour control exceeded MC3 but was less effective than SM-102 | Main Fig. 5; do not describe Iso-A11B5C1 as superior across all efficacy endpoints. |
| Acute cytokines | BALB/c mice, 0.5 mg/kg IM; six cytokines at 4 h showed no discernible difference from PBS | SI Fig. S8; one acute time point does not establish systemic or repeat-dose safety. |
Original Figures 2–5 and Supporting Information — Original source figures.
| CAS No. | Not available |
| Chemical Name | Iso-A11B5C1 |
| Synonyms | IsoA11B5C1, Iso A11B5C1, iso-A11B5C1, H3 |
| SMILES | CCCCCCCC/C=C\CCCCCCCCNC(=O)C(CCCCCOC(=O)CCC(C)CCCCC)NCCN1CCCC1 |
| Formula | C41H79N3O3 |
| M.Wt | 662.10 |
| 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 | 15.1035 mL | 3.0207 mL | 1.5103 mL |
| 25 mg | 37.7586 mL | 7.5517 mL | 3.7759 mL |
| 50 mg | 75.5173 mL | 15.1035 mL | 7.5517 mL |
| 100 mg | 151.0346 mL | 30.2069 mL | 15.1035 mL |
| 250 mg | 377.5865 mL | 75.5173 mL | 37.7586 mL |
Contact our team with the catalog number and requested quantity.