天堂网亚洲,天天操天天搞,91视频高清,菠萝蜜视频在线观看入口,美女视频性感美女视频,95丝袜美女视频国产,超高清美女视频图片

ChemicalBook--->CAS DataBase List--->808118-40-3

808118-40-3

808118-40-3 Structure

808118-40-3 Structure
IdentificationBack Directory
[Name]

FG-4592
[CAS]

808118-40-3
[Synonyms]

CS-185
ASP1517
FG-4592
FibroGen
ROXADUSTAT
CM4309 TsOH
FG-4592/FG4592
FG-4592(ASP1517)
FG-4592 USP/EP/BP
FG-4592 (Roxadustat)
Roxadustat (FG-4592)
Roxadustat intermediates
Roxadustat Impurity ABCDEFGHJKL
FG-4592 - Roxadustat | ASP 1517
ROXADUSTAT;ASP1517;ASP-1517;FG 4592;FG4592
(4-hydroxy-1-methyl-7-phenoxyisoquinoline-3-carbonyl)glycine
N-[(4-Hydroxy-1-Methyl-7-phenoxy-3-isoquinolinyl)carbonyl]glycine
Glycine, N-[(4-hydroxy-1-Methyl-7-phenoxy-3-isoquinolinyl)carbonyl]-
2-(4-hydroxy-1-Methyl-7-phenoxyisoquinoline-3-carboxaMido)acetic acid
2-[(4-hydroxy-1-Methyl-7-phenoxyisoquinoline-3-carbonyl)aMino]acetic acid
[[(4-Hydroxy-1-Methyl-7-phenoxyisoquinolin-3-yl)carbonyl]aMino]acetic Acid
[(4-Hydroxy-1-methyl-7-phenoxy-isoquinoline-3-carbonyl)-amino]-acetic acid
FG-4592; 2-(4-HYDROXY-1-METHYL-7-PHENOXYISOQUINOLINE-3-CARBOXAMIDO)ACETIC ACID
2-(4-HYDROXY-1-METHYL-7-PHENOXYISOQUINOLINE-3-CARBOXAMIDO)ACETIC ACID(Roxadustat)
[(4-Hydroxy-1-methyl-7-phenoxy-isoquinoline-3-carbonyl)-amino]-acetic acid(FG-4592)
Glycine, N-[(4-hydroxy-1-methyl-7-phenoxy-3-isoquinolinyl)carbonyl]- (Related Reference)
[[(4-Hydroxy-1-methyl-7-phenoxyisoquinolin-3-yl)carbonyl]amino]acetic acid Roxadustat (FG-4592)
N-[(4-Hydroxy-1-methyl-7-phenoxy-3-isoquinolinyl)carbonyl]glycine [[(4-Hydroxy-1-methyl-7-phenoxyisoquinolin-3-yl)carbonyl]amino]acetic acid
[EINECS(EC#)]

813-400-2
[Molecular Formula]

C19H16N2O5
[MDL Number]

MFCD20040519
[MOL File]

808118-40-3.mol
[Molecular Weight]

352.341
Chemical PropertiesBack Directory
[Melting point ]

199-215°C
[Boiling point ]

684.3±55.0 °C(Predicted)
[density ]

1.389
[storage temp. ]

-20°C
[solubility ]

Soluble in DMSO (up to at least 25 mg/ml).
[form ]

solid
[pka]

2.46±0.10(Predicted)
[color ]

Off-white or white
[Stability:]

Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 2 months.
[InChI]

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)
[InChIKey]

YOZBGTLTNGAVFU-UHFFFAOYSA-N
[SMILES]

C(O)(=O)CNC(C1=C(O)C2=C(C(C)=N1)C=C(OC1=CC=CC=C1)C=C2)=O
Raw materials And Preparation ProductsBack Directory
[Raw materials]

4-phenoxy-1,2-benzenedicarboxylic acid
Hazard InformationBack Directory
[Description]

Roxadustat (808118-40-3) is an orally administered, small molecule hypoxia-inducible factor (HIF) prolyl hydroxylase inhibitor that is being developed by FibroGen, in collaboration with Astellas and AstraZeneca, for the treatment of anaemia in patients with dialysis-dependent chronic kidney disease (CKD), non-dialysis-dependent CKD and in patients with myelodysplastic syndromes.
Roxadustat (FG-4592), an oral medication, is one of the medications currently undergoing Phase 3 studies. In their phase 2a study studying anemic CKD patients, the medication showed increases in erythropoietin and hemoglobin levels as well as a reduction in hepcidin concentrations with 0.7 to 2.0 mg/kg given 2 or 3 times per week compared to controls within 4 weeks of treatment with no adverse events observed. Roxadustat was then studied in hemodialysis and peritoneal dialysis patients and raised hemoglobin by 20 g/L in 7 weeks of treatment with 4.3 mg/kg weekly for 12 weeks. The current phase 3 studies will continue to evaluate Roxadustat compared to epoetin alpha(NCT02174731 ) and epoetin alpha or darbepoetin alpha (NCT02278341) in CKD patients on dialysis.
[Uses]

FG-4592 is an HIF α prolyl hydroxylase inhibitor.
[Uses]

N-[(4-Hydroxy-1-methyl-7-phenoxy-3-isoquinolinyl)carbonyl]glycine is a hypoxia-inducible factor (HIF) prolyl hydroxylase inhibitor used to increase white blood cell levels in blood and hematopoietic progenitor cells in bone marrow.
[Definition]

ChEBI: An N-acylglycine resulting from the formal condensation of the amino group of glycine with the carboxy group of 4-hydroxy-1-methyl-7-phenoxyisoquinoline-3-carboxylic acid. It is an inhibitor of hypoxia inducible factor prolyl hydroxylase (HIF-PH).
[Side effects]

The most common side effects include hypertension, vascular access thrombosis (formation of blood clots in the blood vessels associated with dialysis), diarrhea, peripheral edema (swelling especially of the ankles and feet), hyperkalemia and nausea.
[Synthesis]

Preparation of roxadustat(808118-40-3) of formula 1 was described in a patent application WO2004108681, where the roxadustat is prepared in 11 steps from initial chemical compound 4-nitro-1,2-dicarbonitrile of formula 2. Reaction of dicarbonitrile of formula 2 with phenol and potash in the first step leads to preparation of corresponding phenoxy derivate of formula 3, 4-phenoxyphthalic acid of formula 4 is prepared by the following hydrolysis effect of potassium hydroxide in methanol, from which a solid-phase mixture with glycine is created for reaction in a melt with temperature of 210°C to 220°C, which provides corresponding phthalimide of formula 5. After that, phthalimide of formula 5 is esterified to corresponding methyl ester of formula 6. Then, expansion of the ring is performed by the effect of sodium butanolate to butyl-7-phenoxy-1,4-dihydroxy isoquinoline-3-carboxylate of formula 7. Hydroxyl group of derivative of formula 7 in a position 1 is then replaced by bromine using phosphorus oxybromide under the alkaline conditions resulting in creation of isoquinoline derivative of formula 8. Further the alkaline hydrolysis is carried out to provide an acid of formula 9. Then the lithiation is carried out, capture of lithium salt with methyl iodide, and in the second step, the hydroxyl group and carboxyl function are protected by benzyl group resulting in the derivative of formula 10. By the effect of potassium hydroxide the derivative of formula 10 is hydrolyzed to the carboxylic acid of formula 11, from which the derivative 12 is prepared under the conditions of glycine benzyl ester. The final step of synthesis of roxadustat of formula 1 is deprotection of benzyl groups by means of hydrogenation reaction (Diagram 1).
synthesis of roxadustat
A Scalable Synthesis of Roxadustat (FG-4592)
[target]

HIF α prolyl hydroxylase
[IC 50]

IC50 = 591.4 nM (HIF-PH).IC50 values for inhibition of peak and late components of delayed rectifier calcium currents are 5.71 and 1.32 μM in pituitary tumor cells.
[Metabolism]

Roxadustat(808118-40-3) is metabolized by cytochrome P450 (CYP)2C8 and uridine diphosphate-glucuronosyltransferase (UGT)1A9. Roxadustat is primarily metabolized through 2 main metabolic pathways: hydroxylation/oxidation followed by sulfation, producing metabolites 4'-hydroxy roxadustat and 4'-O-sulfate conjugates of 4'-hydroxy roxadustat, together accounting for 20% of the radioactive dose. The O-glucuronidation produces metabolite 4-O-β-glucuronide of roxadustat, representing 28% of the dose. Minor metabolic routes included glucosidation producing 4-O-β-glucoside of roxadustat (8.1% of the dose), acyl glucuronidation producing acyl-1-O-β-glucuronide of roxadustat (0.6% of the dose), and demethylation producing N-descarboxymethyl roxadustat oxide and Ndescarboxymethyl roxadustat (together ~3.6% of the dose).
[storage]

Store at -20°C
[Clinical claims and research]

Roxadustat (FG-4592,808118-40-3), an oral medication, is one of the medications currently undergoing Phase 3 studies. In their phase 2a study studying anemic CKD patients, the medication showed increases in erythropoietin and hemoglobin levels as well as a reduction in hepcidin concentrations with 0.7 to 2.0 mg/kg given 2 or 3 times per week compared to controls within 4 weeks of treatment with no adverse events observed. Roxadustat was then studied in hemodialysis and peritoneal dialysis patients and raised hemoglobin by 20 g/L in 7 weeks of treatment with 4.3 mg/kg weekly for 12 weeks. The current phase 3 studies will continue to evaluate Roxadustat compared to epoetin alpha(NCT02174731 ) and epoetin alpha or darbepoetin alpha (NCT02278341) in CKD patients on dialysis.
[Current market and forecast]

Roxadustat(808118-40-3) is approved in EU member states, including the EEA countries, as well as in Japan, China, Chile and South Korea for the treatment of anemia of CKD in adult patients on dialysis (DD) and not on dialysis (NDD). Several other licensing applications for roxadustat have been submitted by Astellas and AstraZeneca to regulatory authorities across the globe and are currently in review.
Astellas and FibroGen are collaborating on the development and commercialization of roxadustat for the potential treatment of anemia of CKD in territories including Japan, Europe, Turkey, Russia and the Commonwealth of Independent States, the Middle East, and South Africa. FibroGen and AstraZeneca are collaborating on the development and commercialization of roxadustat for the potential treatment of anemia of CKD in the U.S., China, other markets in the Americas, in Australia/New Zealand, and Southeast Asia.
[Mode of action]

Roxadustat(808118-40-3) is a novel, orally bioavailable, potent and reversible HIF-PH inhibitor (HIF-PHI) that transiently induces HIF stabilization and leads to a functional HIF transcriptional response that mimics the erythropoietic response associated with exposure of humans to intermittent hypoxia. roxadustat increases hemoglobin levels with a mechanism of action that is different from that of ESAs. Roxadustat activates the body’s natural protective response to reduced oxygen levels in the blood. This response involves the regulation of multiple, complementary processes that promote a coordinated erythropoietic response and increase the blood’s oxygen-carrying capacity.
[References]

1) Lei?et al.?(2015)?Affinity-Based Fluorescence Polarization Assay for High-Throughput Screening of Prolyl Hydroxylase 2 Inhibitors, ACS Med. Chem. Lett.?6?12367 2) Liu?et al.?(2020) Roxadustat (FG-4592)?Treatment for Anemia in Dialysis-Dependent (DD) and Not Dialysis-Dependent (NDD) Chronic Kidney Disease Patients: A?, Hemodial. Int.?21(Suppl. 1)?S110 3) Tang?et al.?(2018)?FG-4592 Accelerates Cutaneous Wound Healing by Epidermal Stem Cell Activation via HIF-1α Stabilization, Cell Physiol. Biochem.?46?2460 4) Zhu?et al.?(2019)?Roxadustat Promotes Angiogenesis Through HIF-1α/VEGF/VEGFR2 Signaling and Accelerates Cutaneous Wound Healing in Diabetic Rats, Wound Repair Regen.?27?324 5) Zhang?et al.?(2019)?Radioprotective effects of roxadustat (FG-4592) in haematopoietic system, J. Cell Mol. Med. 23 349 6) Zhang?et al.?(2019)?Adipocyte Hypoxia-Inducible Factor 2α Suppresses Atherosclerosis by Promoting Adipose Ceramide Catabolism, Cell Metab.30?937
Spectrum DetailBack Directory
[Spectrum Detail]

Roxadustat(808118-40-3)1HNMR
808118-40-3 suppliers list
Company Name: Shanghai Famo Biotech Co Ltd
Tel: +86-36680037 +86-18550473860 , +86-18550473860
Website: www.famobiotech.com
Company Name: Beijing Hope Pharmaceutical Co., Ltd.
Tel: +86-010-67886402 +8613611125266 , +8613611125266
Website: en.hopelife.cn/
Company Name: BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
Tel: +86-18600796368 +86-18600796368 , +86-18600796368
Website: http://www.sjar-tech.com/
Company Name: Zison Pharmaceutical (Shandong) Co., Ltd.
Tel: +86-0086-531-88259693 +86-18660188356 , +86-18660188356
Website: https://www.zisonpharm.com/
Company Name: Hebei Mojin Biotechnology Co., Ltd
Tel: +86 13288715578 +8613288715578 , +8613288715578
Website: http://www.mojinchemical.com
Company Name: XuZhou Magic Biotechnology Co., Ltd.
Tel: +undefined13921770081 , +undefined13921770081
Website: http://www.approvedhomemanagement.com/ShowSupplierProductsList385090/0.htm
Company Name: shandong perfect biotechnology co.ltd
Tel: +86-53169958659 +86-13153181156 , +86-13153181156
Website: www.sdperfect.com/about_e/id/1.html
Company Name: Capot Chemical Co.,Ltd.
Tel: +86-(0)57185586718 +86-13336195806 , +86-13336195806
Website: www.capot.com
Company Name: Beijing Cooperate Pharmaceutical Co.,Ltd
Tel: 010-60279497
Website: http://www.cooperate-pharm.com
Company Name: Hangzhou FandaChem Co.,Ltd.
Tel: +8615858145714 , +8615858145714
Website: www.fandachem.com/
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Website: www.atkchemical.com
Company Name: Biochempartner
Tel: 0086-13720134139
Website: www.biochempartner.com
Company Name: Changzhou Ansciep Chemical Co., Ltd.
Tel: +86 519 86305871
Website: www.approvedhomemanagement.com/ShowSupplierProductsList31173/0.htm
Company Name: Hubei xin bonus chemical co. LTD
Tel: 86-13657291602
Website: www.approvedhomemanagement.com/ShowSupplierProductsList1549548/0.htm
Company Name: Shochem(Shanghai) Co.,Ltd
Tel: 86-21-50800795
Website: www.shochem.com
Company Name: Chongqing Chemdad Co., Ltd
Tel: +86-023-6139-8061 +86-86-13650506873 , +86-86-13650506873
Website: http://www.chemdad.com/
Company Name: Shanghai Jinghao Pharmaceutical Co.,Ltd
Tel: +86-21-68900963
Website: www.jinghaopharma.com/en
Company Name: China fortune way company
Tel: +8610 84669320 17865159269 , 17865159269
Website: www.sinopharm-science.com
Tags:808118-40-3 Related Product Information
1509958-11-5 3676-85-5 65399-05-5 57830-14-5 2301113-15-3 1421312-36-8 1708971-55-4 152459-95-5 60-56-0 150683-30-0 1421312-34-6 1455091-10-7 1403254-99-8 1009298-09-2 362-07-2 931398-72-0 1227158-85-1 53123-88-9