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  • T1519LRimonabantSR141716;利莫那班

    Rimonabant is an inverse agonist for the cannabinoid receptor CB1. It is an anorectic anti-obesity drug produced and marketed by Sanofi-Aventis. Its main avenue of effect is a reduction in appetite. Rimonabant is the first selective CB1 receptor blocker t

    价 格:¥电议型 号:T1519L产 地:中国大陆

  • T15141DM4美登素 DM4;Ravtansine

    DM4 can be used in the preparation of antibody drug conjugate and it is an antitubulin agent. It can inhibit cell division.

    价 格:¥电议型 号:T15141产 地:中国大陆

  • T15019LCUR61414 hydrochloride

    CUR61414 is a novel, potent and cell permeable Hedgehog signaling pathway inhibitor (IC50 =100-200 nM). CUR61414 is a small-molecule aminoproline class compound and selectively binds to smoothened (Smo) with a Ki value of 44 nM. CUR-61414 can induce apop

    价 格:¥电议型 号:T15019L产 地:中国大陆

  • T14199ALZ-801

    ALZ-801 is an advanced and markedly improved candidate for the treatment of alzheimer’s disease. ALZ-801 is a potent and orally available small-molecule β-amyloid (Aβ) anti-oligomer and aggregation inhibitor, valine-conjugated prodrug of Tramiprosate with

    价 格:¥电议型 号:T14199产 地:中国大陆

  • T14194β-NETAα-NETA

    α-NETA is a stable, noncompetitive, slowly reversible choline acetyltransferase (ChAT) inhibitor with an IC50 of 9 μM and is a potent chemokine-like receptor-1 (CMKLR1) antagonist. α-NETA has anti-cancer activity[1][2]. α-NETA weakly inhibits cholinestera

    价 格:¥电议型 号:T14194产 地:中国大陆

  • T1419Azithromycin hydrate阿奇霉素二水物;阿奇霉素二水合物;Azithromycin dihydrate;CP-62993 dihydrate

    Azithromycin dihydrate is a semi-synthetic macrolide antibiotic structurally related to ERYTHROMYCIN. It has been used in the treatment of Mycobacterium avium intracellulare infections, toxoplasmosis, and cryptosporidiosis.

    价 格:¥电议型 号:T1419产 地:中国大陆

  • T14188ALLO-2

    ALLO-2 is a Inhibitor of Drug-Resistant Smo Mutant.It inhibits Smo agonist Hh-Ag1.5-induced luciferase expression in TM3-Gli-Luc cells with IC50 of 6 nM.

    价 格:¥电议型 号:T14188产 地:中国大陆

  • T1418617-ODYA17-十八炔酸;Alkynyl Stearic Acid

    Alkynyl Stearic Acid is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs.

    价 格:¥电议型 号:T14186产 地:中国大陆

  • T14185Alkynyl Palmitic Acid

    Alkynyl Palmitic Acid is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs.

    价 格:¥电议型 号:T14185产 地:中国大陆

  • T14181Alizarin Red S sodiumARS sodium;茜素红钠盐

    Alizarin Red S sodium (ARS sodium) is an anthraquinone dye. Which has been widely used to evaluate calcium deposits in cell culture[1].

    价 格:¥电议型 号:T14181产 地:中国大陆

  • T1418Bucladesine sodiumDibutyryl-cAMP sodium salt;Bucladesine;Sodium dibutyryl cAMP;DC2797;Dibutyryl-cAMP

    Bucladesine, PKA activator, is a cyclic nucleotide derivative that mimics the action of endogenous cAMP and is capable of permeating the cell membrane. It has vasodilator properties and is used as a cardiac stimulant.

    价 格:¥电议型 号:T1418产 地:中国大陆

  • T14177Alexidine dihydrochloride

    Alexidine dihydrochloride has antifungal and antibiofilm activity against a diverse range of fungal pathogens. Alexidine dihydrochloride is an anticancer agent that targets a mitochondrial tyrosine phosphatase, PTPMT1, in mammalian cells and causes mitoch

    价 格:¥电议型 号:T14177产 地:中国大陆

  • T14175Aldose reductase-IN-1

    Aldose reductase-IN-1 is a aldose reductase inhibitor (IC50: 28.9 pM).

    价 格:¥电议型 号:T14175产 地:中国大陆

  • T1417Mechlorethamine hydrochlorideMechlorethamine HCl;Chlormethine hydrochloride;恩比兴

    Mechlorethamine is the prototype of alkylating agents, it works by binding to DNA, crosslinking two strands and preventing cell duplication.

    价 格:¥电议型 号:T1417产 地:中国大陆

  • T1416Zidovudine齐多夫定;叠氮胸苷;AZT;Azidothymidine;ZDV;NSC 602670

    Zidovudine is a synthetic dideoxynucleoside. After intracellular phosphorylation to its active metabolite, zidovudine inhibits DNA polymerase, resulting in the inhibition of DNA replication and cell death. This agent also decreases levels of available pyr

    价 格:¥电议型 号:T1416产 地:中国大陆

  • T14151AKR1C1-IN-1

    AKR1C1-IN-1 is a human 20α-hydroxysteroid dehydrogenase (AKR1C1) inhibitor (Ki: 4 nM for AKR1C1).

    价 格:¥电议型 号:T14151产 地:中国大陆

  • T1415Gemfibrozil吉非罗齐;Jezil;CI-719;Lopid;Decrelip

    Gemfibrozil interacts with peroxisome proliferator-activated receptors (PPARalpha) resulting in PPARalpha-mediated stimulation of fatty acid oxidation and an increase in lipoprotein lipase (LPL) synthesis. Gemfibrozil is a fibric acid derivative with hypo

    价 格:¥电议型 号:T1415产 地:中国大陆

  • T14148AH 6809

    AH 6809 is an antagonist of EP and DP receptor(with Kis of 1217, 1150, 1597, and 1415 nM for the cloned human EP1, EP2, EP3-III, and DP receptor respectively). AH 6809 has a Ki of 350 nM for mouse EP2 receptor.

    价 格:¥电议型 号:T14148产 地:中国大陆

  • T14140Agaric acid落叶松蕈酸;Agaricinic Acid

    Agaricic acid is an adenine nucleotide translocase antagonist.It is obtained from various plants of the fungous tribe, i.e. Polyporus officinalis and Polyporus igniarius. Agaric acid induces mitochondrial permeability transition through its interaction wi

    价 格:¥电议型 号:T14140产 地:中国大陆

  • T1414Sodium 2-mercaptoethanesulfonate美司那;美司钠;Uromitexan;Mitexan;Mesna;Mesnum;Mesnex

    Mesna is a sulfhydryl compound used to prevent urothelial toxicity by inactivating metabolites from antineoplastic agents, such as ifosfamide or cyclophosphamide.

    价 格:¥电议型 号:T1414产 地:中国大陆

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