ChemicalBook Product Catalog Biochemical Engineering Inhibitors Angiogenesis HIF inhibitor Vadadustat

Vadadustat

Product NameVadadustat
CAS1000025-07-9
MFC14H11ClN2O4
MW306.7
EINECS
MOL File1000025-07-9.mol

Chemical Properties

Melting point	172-174°C
Boiling point	674.6±55.0 °C(Predicted)
Density	1.461±0.06 g/cm3(Predicted)
storage temp.	Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility	DMSO (Slightly), Methanol (Slightly)
pka	4.09±0.40(Predicted)
form	Solid
color	Pale Beige to Light Beige
Stability	Hygroscopic
InChI	InChI=1S/C14H11ClN2O4/c15-10-3-1-2-8(4-10)9-5-11(18)13(16-6-9)14(21)17-7-12(19)20/h1-6,18H,7H2,(H,17,21)(H,19,20)
InChIKey	JGRXMPYUTJLTKT-UHFFFAOYSA-N
SMILES	C(O)(=O)CNC(C1=NC=C(C2=CC=CC(Cl)=C2)C=C1O)=O

Usage And Synthesis

Description

Vadadustat is an inhibitor of hypoxia-inducible factor prolyl hydroxylase 2 (HIF-PH2) and HIF-PH3 (IC₅₀s = 1.1 and 0.39 micromolar, respectively). It stabilizes HIF-1α in mouse hepatocyte nuclear extracts. Vadadustat (50 and 100 mg/kg) increases erythropoietin levels in mouse serum.

Uses

Vadadustat is a novel HIF (Hypoxia-inducible factor) stabilizer. It provides an effective anemia treatment in nondialysis-dependent chronic kidney disease.

Indications

Vadadustat is used to treat anemia in dialysis-dependent and non-dialysis-dependent chronic kidney disease patients.

Mechanism of action

Vadadustat inhibits PDH and reduces the degradation of HIF-α, thereby increasing the production of endogenous erythropoietin (EPO) and improving anemia symptoms.

Safety

Phase 3 clinical trials in Japan have confirmed the efficacy and safety of vadadustat for the treatment of renal anemia in patients with both non-dialysis-dependent (NDD)-chronic kidney disease (CKD) and dialysis-dependent CKD. The incidence of adverse events (AEs) and serious AEs in the vadadustat treatment group was comparable to that observed in the erythropoiesis-stimulating agents (ESA) treatment group^[2].

Synthesis

Boronic acid 69 and pyridine nitrile 70 were coupled via Suzuki coupling to give biphenyl 71. Crystallization of 71 was required to remove small amounts of undesired regioisomer coupling products. One-pot reaction: aromatic substitution with methoxy anion. Hydrolysis of the nitrile was performed simultaneously. These two independent operations were performed in one pot to give compound 72 in 92% overall yield for the two steps. Carboxylic acid 72 and amine 73 were amidated using CDI (carbodiimide) as coupling agent to give compound 74. Aluminum-mediated demethylation of 74 removed the ester and ether functionalities to give vadadustat (XI) in 84% yield.
Vadadustat synthesis route

Advantages

Vadadustat offers the convenience of traditional injectable EPO stimulators, helping to improve patient compliance with treatment. In clinical trials, Vadadustat has been shown to improve hemoglobin levels in CKD patients and has good safety and tolerability.

References

[1] ROBERT LABES Kameliya R. Prolyl hydroxylase inhibitors, polydrug use, and the phosphoproteome[J]. Acta Physiologica, 2022, 237 1. DOI: 10.1111/apha.13898
[2] Nangaku, M., Sasaki, K., Bi, J., Ueta, K., Nishimura, K., Hashimoto, T., Hata, M. (2025). Real-World Safety and Effectiveness of Vadadustat in Patients with Chronic Kidney Disease-Related Anemia: Interim Analysis of Postmarketing Surveillance in Japan. Advances in Therapy, 42 9, 4486–4509. https://doi.org/10.1007/s12325-025-03272-x

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