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Chemical Structure : LH1753
Catalog No.: PC-22695Not For Human Use, Lab Use Only.
LH1753 is an orally bioavailable inhibitor of L-cystine crystallization for cystinuria, prevents stone formation effectively in the Slc3a1-knockout mouse model.
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LH1753 is an orally bioavailable inhibitor of L-cystine crystallization for cystinuria, prevents stone formation effectively in the Slc3a1-knockout mouse model.
| M.Wt | 630.57 | |
| Formula | C22H40N6O2S2.4ClH | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Hu L, et al. ACS Med Chem Lett. 2024 Jun 6;15(7):1026-1031.
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