Chemical Structure : JN-170
CAS No.: 3032920-98-9
Catalog No.: PC-25027Not For Human Use, Lab Use Only.
JN-170 is a highly selective, first-in-class, orally bioavailable inhibitor of SLC6A19 (B0AT1) with IC50 of 97 nM against mouse SLC6A19 in the isoleucine transport assay, > 10-fold less potent against human SLC6A19 (IC50=1.25 μM).
| Packing | Price | Stock | Quantity |
|---|---|---|---|
| 2 mg | $298 | In stock | |
| 5 mg | $498 | In stock | |
| 10 mg | $788 | In stock | |
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| 100 mg | Get quote |
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JN-170 is a highly selective, first-in-class, orally bioavailable inhibitor of SLC6A19 (B0AT1) with IC50 of 97 nM against mouse SLC6A19 in the isoleucine transport assay, > 10-fold less potent against human SLC6A19 (IC50=1.25 μM).
JN-170 (50 -250 mg/kg, oral) caused a dose-dependent increase in urinary amino acid excretion in WT C57Bl/6J mice.
JN-170 significantly drove reductions in plasma Phe in an exposure-related manner.
| M.Wt | 434.42 | |
| Formula | C20H21F3N6O2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
(S)-N-(2-(1-aminocyclopropyl)ethyl)-3-(3-(4-cyanophenyl)-1,2,4-oxadiazol-5-yl)-3-(trifluoromethyl)pyrrolidine-1-carboxamide |
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1. Wobst HJ, et al. JCI Insight. 2024 Nov 8;9(21):e182876.

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