144060-53-7 CAS NO.144060-53-7

Min.Order Quantity:: 100 Kilogram

Purity:: 99%

Port:: China Main Port

Payment Terms:: L/C,D/A,D/P,T/T,MoneyGram,Other

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Product Details

Keywords

RARECHEM AH PB 0251
144060-53-7
C16H16N2O3S

Quick Details

ProName: 144060-53-7
CasNo: 144060-53-7
Molecular Formula: C16H16N2O3S
Appearance: powder
Application: 144060-53-7
DeliveryTime: Within 3-7 days
PackAge: Depended
Port: China Main Port
ProductionCapacity: 300 Kilogram/Month
Purity: 99%
Storage: Refrigerator
Transportation: by air or by sea
LimitNum: 100 Kilogram
Valid Period: 6 month
Application: Multipurpose intermediate
Application: ISO/9001 Certificate

Superiority

febuxostat basic information

product description anti-gout drug drugs increasing the risk of gout intermediate application

product name:	febuxostat
synonyms:	febuxostat;tei-6720;2-[3-cyano-4-(2-methylpropoxy)phenyl]-4-methyl-1,3-thiazole-5-carboxylic acid;2-[3-cyano-4-isobutoxyphenyl]-4-methylthiazole-5-carboxylic acid;2-(3-cyano-4-isobutyloxyphenyl)-4-methyl-5-thiazolecarboxylic acid;2-[3-cyano-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid;tmx 67;febuxosta
cas:	144060-53-7
mf:	c16h16n2o3s
mw:	316.37
einecs:
product categories:	heterocycles;inhibitors;intermediates & fine chemicals;pharmaceuticals;zjh;api;febuxostat;trilipix;other apis;eterocycles
mol file:	144060-53-7.mol

febuxostat chemical properties

mp	238-239°(dec.)
storage temp.	refrigerator
cas database reference	144060-53-7(cas database reference)

safety information

msds information

febuxostat usage and synthesis

product description	febuxostat developed by teijin is a new generation of xanthine oxidase inhibitor, for the treatment of high uric acid disease (gout) on clinical , the structure is completely different from xanthine oxidase inhibitor drug developed 40 years ago, it is a new and efficient non-purine selective inhibitor of xanthine oxidase. xanthine oxidase is a key enzyme in the promotion of uric acid. febuxostat reduces blood uric acid level in gout patients with hyperuricemia , clinical studies show that the product is safe and effective, this product is metabolized by the liver, it does not depend on renal excretion, so for moderate - severe liver and kidney dysfunction patients it is not necessary to reduce the dose. dose is once 1 day, 40 mg or 80 mg once ,it is not recommended for the treatment of gout patients without hyperuricemia. in february 2009, the us food and drug administration (fda) approved febuxostat for long-term treatment of gout patients with hyperuricemia.
anti-gout drug	gout is a heterogeneous group of diseases, hereditary or acquired due to uric acid excretion decreasing and purine metabolism. because the body produces too much uric acid and renal clearance capacity decreases, uric acid accumulates in the body, leading to urate crystals deposited in the joints and organs. therefore, it means the treatment of gout usually taken to be: promote uric acid excretion, and suppression of uric acid, and adopt appropriate measures to improve related symptoms. uric acid formation is associated with purine metabolism, in the final step of purine metabolism, hypoxanthine becomes xanthine through the role of xanthine oxidoreductase (xor) ,then further generate uric acid ,inhibiting activity of the enzyme can effectively reduce uric acid production. febuxostat is currently the world's latest generation of non-purine selective inhibitor of xanthine oxidase, which acts highly selectively on the oxidase, then reduces uric acid synthesis, reduces uric acid levels, thus effectively treats ventilation diseases. 30 years, allopurinol is the only clinically used drugs to inhibit production of uric acid and is used as gold drugs widely in clinical treatment of gout, and achieves good results in the anti-gout treatment. compared with allopurinol, febuxostat has obvious advantages: (1) allopurinol only inhibit reduced xor while febuxostat shows a significant inhibitory effect on oxidized and reduced xor , so its role of reducing the uric acid is more powerful, long-lasting; (2) because allopurinol is a purine analog,it is inevitable affecting other purine and pyridine metabolic activity . therefore, allopurinol treatment should be repeated large doses of the drugs to maintain a high level. this also leads to serious or even fatal adverse reactions due to the accumulation of the drug-induced. however, febuxostat as non-purine xor inhibitors, has better security. the above information is edited by the chemicalbook of tian ye.
drugs increasing the risk of gout	diuretics: furosemide , hydrochlorothiazide ), metolazone salicylic acid: such as aspirin (aspirin) niacin cyclosporine (cyclosporineneoral) l-dopa (levodopa)
intermediate	4-hydroxy thiobenzamide cas no.:25984-63-8 appearance: light green to white powder. 2- (4-hydroxyphenyl) -4-methyl-thiazole-5-carboxylic acid ethyl ester cas: 161797-99-5 appearance: yellow powder. 2- (3-aldehyde-4-hydroxyphenyl) -4-methyl-thiazole-5-carboxylic acid ethyl ester cas no.:161798-01-2 appearance: light yellow to yellow powder. 2- [3-aldehyde-4-isobutyloxyphenyl] -4-methyl-thiazole-5-carboxylic acid ethyl ester cas no.:161798-03-4 appearance: light yellow to white powder. 2- [3-cyano-4-isobutoxy-phenyl] -4-methyl-thiazole-5-carboxylic acid ethyl ester cas no.:160844-75-7 appearance: white to white powder.
application	treatment of high uric acid disease (gout)
chemical properties	crystalline solid
usage	antihyperlipidemic
usage	xanthine oxidase/xanthine dehydrogenase inhibitor. used for treatment of hyperuricemia and chronic gout. 40-120 mg/day febuxostat was proven effective in lowering serum urate levels when administered to manage hyperuricemia in patients with gout.
usage	febuxostat is primarily indicated in conditions like gout, hyperuricemia

service we provide:

1. mixed container, we can mix different items in one container.

2. quality control, before shipment, free sample for test. after shipment, keep sample for 3 years

3. prompt shipment with professional documents

4. packing as your request, with photo before shipment

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