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Vadadustat

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Company Name: Chongqing jooe co., ltd
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Products Intro: Product Name:Vadadustat
CAS:1000025-07-9
Purity:0.99 Package:25KG;5KG;1KG
Company Name: Beijing Ruqueen Biotech., Co., Ltd.
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Products Intro: Product Name:Vadadustat
CAS:1000025-07-9
Purity:99.5% Package:1kg;|10kg;|25kg;
Company Name: Shochem(Shanghai) Co.,Ltd
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Products Intro: Product Name:Vadadustat
CAS:1000025-07-9
Purity:98% Package:10g;USD|100g;USD
Company Name: BOC Sciences
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Products Intro: Product Name:Vadadustat
CAS:1000025-07-9
Purity:>98% Package:50 mg Remarks:Reach out to us for more information about custom solutions.
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:Vadadustat
CAS:1000025-07-9
Remarks:NME250239P

Vadadustat manufacturers

  • Vadadustat
  • Vadadustat pictures
  • $0.00 / 1kg
  • 2025-08-05
  • CAS:1000025-07-9
  • Min. Order: 1kg
  • Purity: 99.5%
  • Supply Ability: EX:100kg
  • Vadadustat
  • Vadadustat pictures
  • $0.00 / 1g
  • 2024-11-01
  • CAS:1000025-07-9
  • Min. Order: 1g
  • Purity: 98%
  • Supply Ability: 1000kgs
  • Vadadustat
  • Vadadustat pictures
  • $9.80 / 1.79999995231628KG
  • 2020-01-09
  • CAS:1000025-07-9
  • Min. Order: 1g
  • Purity: ≥99%
  • Supply Ability: 100kg

Related articles

  • Synthesis of Vadadustat
  • Vadadustat is used as raw material of boronic acid and is prepared by coupling, substitution and hydrolysis reactions.
  • Dec 22,2023
Vadadustat Basic information
Product Name:Vadadustat
Synonyms:AKB-6548; AKB 6548; AKB6548; PG-1016548; PG 1016548; PG1016548; B-506; B506; VADADUSTAT;PG-1016548;AKB-6548;Vadadustat;Vadadustat(AKB-6548/PG-1016548);Vadadustat (AKB-6548);AKB-6548;PG 1016548;PG1016548
CAS:1000025-07-9
MF:C14H11ClN2O4
MW:306.7
EINECS:
Product Categories:API
Mol File:1000025-07-9.mol
Vadadustat Structure
Vadadustat 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)
form Solid
pka4.09±0.40(Predicted)
color Pale Beige to Light Beige
Stability:Hygroscopic
InChIInChI=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)
InChIKeyJGRXMPYUTJLTKT-UHFFFAOYSA-N
SMILESC(O)(=O)CNC(C1=NC=C(C2=CC=CC(Cl)=C2)C=C1O)=O
Safety Information
MSDS Information
Vadadustat Usage And Synthesis
DescriptionVadadustat 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.
UsesVadadustat 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 actionVadadustat inhibits PDH and reduces the degradation of HIF-α, thereby increasing the production of endogenous erythropoietin (EPO) and improving anemia symptoms.
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
Vadadustat Preparation Products And Raw materials
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