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Home > Lesinurad for Sale > Lesinuard(RDEA594) Pharma Grade
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Lesinuard(RDEA594) Pharma Grade

Unit Price: Get Latest Price
CAS No.:

878672-00-5

Grade:

Pharmaceutical Grade

Port:

SHANGHAI

Packaging:

1kg/0.12kg Bag

Price valid (until):

2017-06-29

Company Type:
Manufactory
Location:
China
Payment Terms:
L/C,D/A
Qualification:
Main Products:

CAL-101 Tedizolid Afatinib Nintedanib Lenvatinib,Neratinib Olaparib Rucaparib and intermediates

  • Product Description

  • Seller Information

  • Description

    Chemical Information

    Product name: Lesinurad(RDEA594)

    Synonyms: 2-[[5-Bromo-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-yl]thio]acetic acid; RDEA 594

    CAS No.: 878672-00-5

    Molecular Formula: C17H14BrN3O2S

    Molecular weight: 404.28

    Technicel Data

    Appearance: Tech pack

    purity: 99.0%min

    Solubility: DMSO

    Package: Packaging according to customer requirements

    Storage: −20°C 2 years

    Shipping condition: Conventional transport

    http://www.shinningpharm.com/products_detail_e/id/29.html

    ECHEMI Editorial Reference
    Lesinurad is a URAT1 and OAT inhibitor, is determined to be a substrate for the kidney transporters OAT1 and OAT3 with Km values of 0.85 and 2 µM, respectively.
    Lesinurad is a member of the class of triazoles that is [(3-bromo-1,2,4-triazol-5-yl)sulfanyl]acetic acid substituted at position 1 of the triazole ring by a 4-cyclopropylnaphthalen-1-yl group. Used for treatment of gout. It has a role as a uricosuric drug. It is a member of triazoles, a member of naphthalenes, a member of cyclopropanes, an organobromine compound, an aryl sulfide and a monocarboxylic acid.|Lesinurad is an oral uric acid transporter 1 (URAT1) inhibitor indicated for the treatment of hyperuricemia associated with gout. It reduces serum uric acid concentration through the inhibition of URAT1, an enzyme responsible for reuptake of uric acid from the renal tubule, and OAT4, another uric acid transporter associated with diuretic-induced hyperuricemia. Marketed as the product Zurampic, it is indicated for use in combination with a xanthine oxidase inhibitor for the treatment of hyperuricemia associated with gout in patients who have not achieved target serum uric acid levels with a xanthine oxidase inhibitor alone. In August 2017, a combination oral therapy consisting of lesinurad and [DB00437] was FDA-approved under the brand name Duzallo indicated for the treatment of gout-related hyperuricemia in patients with uncontrolled gout.|Lesinurad is an Urate Transporter 1 Inhibitor. The mechanism of action of lesinurad is as an Urate Transporter 1 Inhibitor, and Cytochrome P450 3A Inducer.|Lesinurad is a selective inhibitor of uric acid reabsorption which is used in combination with other agents in the therapy of gout. Lesinurad has had limited clinical use, but has not been associated with serum enzyme elevations during therapy or with instances of clinically apparent liver injury.

    Basic Info
    Product Name:

    Lesinurad

    Other Name:

    Acetic acid,2-[[5-bromo-4-(4-cyclopropyl-1-naphthalenyl)-4H-1,2,4-triazol-3-yl]thio]-;Acetic acid,[[5-bromo-4-(4-cyclopropyl-1-naphthalenyl)-4H-1,2,4-triazol-3-yl]thio]-;2-[[5-Bromo-4-(4-cyclopropyl-1-naphthalenyl)-4H-1,2,4-triazol-3-yl]thio]acetic acid;Lesinurad;RDEA 594;2-[[5-Bromo-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-yl]thio]acetic acid;Lesinida;Zurampic;READ 594;2-[[5-Bromo-4-(4-cyclopropylnaphthalen-1-yl)-1,2,4-triazol-3-yl]sulfanyl]acetic acid

    CAS No.:

    878672-00-5

    Molecular Formula:

    C17H14BrN3O2S

    InChIKeys:

    InChIKey=FGQFOYHRJSUHMR-UHFFFAOYSA-N

    Molecular Weight:

    404.28096

    Exact Mass:

    404.28

    UNII:

    09ERP08I3W|Q59CAT99RS|73WY698HZ7

    ATC Code:

    M04AA51|M04AB05|M - Musculo-skeletal system

    Characteristics
    PSA:

    93.3

    XLogP3:

    4.7

    Density:

    1.72±0.1 g/cm3

    Boiling Point:

    643.7°C at 760 mmHg

    Flash Point:

    343.1±34.3 °C

    Refractive Index:

    1.776

    Hazard Identification

    Classification of the substance or mixture

    Acute toxicity - Category 4, Oral

    GHS label elements, including precautionary statements

    Pictogram(s)
    Signal word

    Warning

    Hazard statement(s)

    H302 Harmful if swallowed

    Precautionary statement(s)
    Prevention

    P264 Wash ... thoroughly after handling.

    P270 Do not eat, drink or smoke when using this product.

    Response

    P301+P317 IF SWALLOWED: Get medical help.

    P330 Rinse mouth.

    Storage

    none

    Disposal

    P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.

    Other hazards which do not result in classification

    no data available

    Handling and Storage

    Precautions for safe handling

    Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.

    Conditions for safe storage, including any incompatibilities

    Store the container tightly closed in a dry, cool and well-ventilated place. Store apart from foodstuff containers or incompatible materials.

  • Seller Information
    Business Type:

    Manufactory

    Main Products:

    CAL-101 Tedizolid Afatinib Nintedanib Lenvatinib,Neratinib Olaparib Rucaparib and intermediates

    Location:

    Ningyang Fine Chemicial Industry Park , Tai'an, Shandong.

    Payment Terms:

    L/C,D/A

    Total Annual Revenue:

    $5 million-$10 million

    Total Employees:

    51-100

    Shandong Shining Pharm Co., Ltd. is Investment and holding by a natural person, sets up three R&D Centers under Shining Pharm: Jinan Synovel Laboratory Co., Ltd., Tianjin Chemlike Scientific Co., Ltd. and Nanjing Leizheng Pharm Co., Ltd. Export agent: Taizhou Crene Biotechnology Co., Ltd.  Our manufactory Located in Ningyang  Fine Chemical  Industry Park, Tai’an ,Shangdong province.

     

    Shandong Shining Pharm is a high-tech manufactory, which is committed to producing high quality pharmaceutical intermediates, promoting innovation in API technology and provide customized services for global pharmaceutical companies, dedicates itself on research, develop and industrialize of high-end intermediates & API.   We have three R&D centers from Ji’nan, Tianjin and Nanjing, more than 40 R&D staff including 5 doctors, 20 masters and 18 synthesis assistants, along with their unique advantages in the product development, pilot and process optimization, of total hundred employees. Our products are highly praised by global customers as we are Closed cooperation with domestic pharmaceutical companies, with International market ofIndiaby intermediates, South American by APIs and actively develop the European and American market, cooperated with customers to DMF registration.

     

    Shandong Shining Pharm Covers an area of 40 mu (around 30000 square meter), located at Ningyang Fine Chemical Industry Park, Tai’an., which is a provincial chemical industry park, It is a high standard manufactory and about to set up cGMP quality system. Our plant including 500 analysis laboratories equipped with HPLC, LC-MS, GC and other analytical facilities, one pilot and four mass production workshop, the total reaction capacity can reach 35000L which can meet commercial production demands from kilos to hundreds of tons, is perfect for analysis and production.

     

    Shandong Shining Pharm provides the high-level products and the most reasonable price for our Partners. Our main products of intermediates:  Idelalisib ints, Tedizolid ints, Afatinib ints, Nintedanib ints, Lenvatinib ints  Trifluridine TAS-102ints, etc.

     

    “Social commitment, Professional services, Benefits society, Create better life” is Shandong Shining Pharm philosophy, Shandong Shining Pharm sincerely welcome global partners to get win-win cooperation, create a bright future!


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