An inhibitor of HIF-PH enzymes
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Isomer(s)
11573IOX2
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Roxadustat

Item No. 15294

Technical Information
Formal Name
N-[(4-hydroxy-1-methyl-7-phenoxy-3-isoquinolinyl)carbonyl]-glycine
CAS Number
808118-40-3
Synonyms
  • ASP1517
  • FG-4592
Molecular Formula
C19H16N2O5
Formula Weight
Purity
≥98%
A crystalline solid
DMF: 50 mg/mlDMSO: 30 mg/mlEthanol: 0.1 mg/ml
λmax
223, 261, 314, 333 nm
SMILES
OC1=C(C(NCC(O)=O)=O)N=C(C)C2=C1C=CC(OC3=CC=CC=C3)=C2
InChi Code
InChI=1S/C19H16N2O5/c1-11-15-9-13(26-12-5-3-2-4-6-12)7-8-14(15)18(24)17(21-11)19(25)20-10-16(22)23/h2-9,24H,10H2,1H3,(H,20,25)(H,22,23)
InChi Key
YOZBGTLTNGAVFU-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Roxadustat is an analog of 2-OG that has been developed as an inhibitor of HIF-PHs. While little has been published regarding the actions of this compound, similar HIF-PH inhibitors suppress HIF degradation and in this way induce erythropoietin expression, promoting erythropoiesis or preventing anemia in vivo.1

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Hsieh, M.M., Linde, N.S., Wynter, A., et alHIF-prolyl hydroxylase inhibition results in endogenous erythropoietin induction, erythrocytosis, and modest fetal hemoglobin expression in rhesus macaque. Blood 110(6), 2140-2147 (2007).

    Product Citations

    Kremer, D.M., Nelson, B.S., Lin, L., et alGOT1 inhibition primes pancreatic cancer for ferroptosis through the autophagic release of labile iron. bioRxiv (2020).

    Wu, D., Su, X., Lu, J., et alBidirectional modulation of HIF-2 activity through chemical ligands. Nat. Chem. Biol. 15(4), 367-376 (2019).