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Synonyms: Doxorubicin-LNAA-Boc
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | Legubicin (Doxorubicin-LNAA-Boc) is a conjugate of Doxorubicin linked with a peptide connector hydrolyzable by Legumain. Upon activation by Legumain, Legubicin releases leucine-Doxorubicin, potentially minimizing damage to normal tissues. It inhibits tumor cell growth and reduces DNA binding ability in cells lacking legumain expression. In mice with CT26 tumors, Legubicin completely suppresses tumor growth, making it useful for colon cancer (CRC) research. |
| In vivo | Legubicin (9.05 μmol/kg, intravenous injection, single dose) enhances the exposure of Doxorubicin in HT1080 tumor-bearing mice while reducing its presence in the heart and kidneys. In female SD rats and beagle dogs, Legubicin (intravenous injection, single dose, 56-day observation period) demonstrates a higher maximum tolerated dose (MTD) compared to conventional Doxorubicin and exhibits milder toxicity. When administered to SD rats, Legubicin (5-25 mg/kg, intravenous injection, once weekly, 4 weeks) induces dose-dependent toxicity. In beagle dogs, a dosage of Legubicin (3/1.5-20/10 mg/kg, intravenous injection, once weekly, 4 weeks) at 20/10 mg/kg results in an 80% mortality rate. Administered intraperitoneally, Legubicin (5-50 mg/kg, every other day, 3 doses total) completely inhibits tumor growth in Balb/C mice carrying CT26 tumors or WEHI nude mice with legumain 293, with no significant toxicity observed. |
| Synonyms | Doxorubicin-LNAA-Boc |
| Molecular Weight | 1013.06 |
| Formula | C48H64N6O18 |
| Cas No. | 606967-53-7 |
| Smiles | O([C@@H]1C2=C(C(O)=C3C(=C2O)C(=O)C=4C(C3=O)=CC=CC4OC)C[C@](C(CO)=O)(O)C1)[C@H]5C[C@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC(OC(C)(C)C)=O)C)=O)C)=O)CC(N)=O)=O)CC(C)C)=O)[C@H](O)[C@H](C)O5 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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