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  • T101524-Methylamino antipyrine4-Methylamino antipyrine

    4-Methylamino antipyrine is an active metabolite of Metamizole. Metamizole is a pyrazolone non-steroidal anti-inflammatory drug (NSAID) and inhibits COX. 4-Methylamino antipyrine has analgesic, antipyretic, and relatively weak anti-inflammatory properties

    价 格:¥电议型 号:T10152产 地:美洲

  • T10157Regorafénib N-oxyde (M2)Regorafénib N-oxyde (M2)

    Regorafénib N-oxyde M2 is an active metabolite of Regorafenib. Regorafenib is a multi-target inhibitor for VEGFR1/2/3, PDGFRβ, RET, Kit, and Raf-1 (IC50s: 13/4.2/46, 1.5, 22, 7, and 2.5 nM).

    价 格:¥电议型 号:T10157产 地:美洲

  • T1015842-(2-Tetrazolyl)rapamycin42-(2-Tetrazolyl)rapamycin

    42-(2-Tetrazolyl)rapamycin is a prodrug compound of a rapamycin analog extracted from patent US 20080171763 A1, Example 1.

    价 格:¥电议型 号:T10158产 地:美洲

  • T1016Vitamin E AcetateVitamin E Acetate,Tocopherol acetate,

    A natural tocopherol and one of the most potent antioxidant tocopherols. It exhibits antioxidant activity by virtue of the phenolic hydrogen on the 2 h-1-benzopyran-6-ol nucleus. It has four methyl groups on the 6-chromanol nucleus. The natural d form of

    价 格:¥电议型 号:T1016产 地:美洲

  • T101836-Methoxytricin6-Methoxytricin

    6-Methoxytricin is a flavonoid isolated from Artemisia iwayomogi. It is an inhibitor on aldose reductase (AR) and advanced glycation endproduct (AGE) formation activities (IC50s: 30.29 μM and 134.88 μM). 6-Methoxytricin has potential as an anti-diabetic c

    价 格:¥电议型 号:T10183产 地:美洲

  • T101866-Quinoxalinecarboxylic acid, 2,3-bis(bromomethyl)-6-Quinoxalinecarboxylic acid, 2,3-bis(bromomethyl

    6-Quinoxalinecarboxylic acid, 2,3-bis(bromomethyl)-, derived from 2,3-Bis(bromomethyl)quinoxaline, shows antibacterial activity.

    价 格:¥电议型 号:T10186产 地:美洲

  • T101917-Chlorokynurenic acid sodium salt7-Chlorokynurenic acid sodium salt,7-CKA sodium salt,

    7-Chlorokynurenic acid sodium salt (7-CKA sodium salt) is a potent and selective antagonist of the glycine B coagonist site of the NMDA receptor (IC50: 0.56 μM). It is also a potent inhibitor of the reuptake of glutamate into synaptic vesicles (Ki: 0.59 μ

    价 格:¥电议型 号:T10191产 地:美洲

  • T10191L7-Chlorokynurenic acid7-Chlorokynurenic acid,7-CKA,

    7-Chlorokynurenic acid (7-CKA) is a potent and selective antagonist of the glycine B coagonist site of the N-methyl-D-aspartate (NMDA) receptor (IC50=0.56 μM). 7-Chlorokynurenic acid is also a potent inhibitor of the reuptake of glutamate into synaptic ve

    价 格:¥电议型 号:T10191L产 地:美洲

  • T101957-O-Geranylscopoletin7-O-Geranylscopoletin,7-Geranyloxy-6-methoxycoumarin,

    7-O-Geranylscopoletin is a natural coumarin from the root of Atalantia monophylla. Various parts of this plant have been used for folk medicine for several purposes such as the treatment of chronic rheumatism, antispasmodic, paralysis, hemiplegia, and sti

    价 格:¥电议型 号:T10195产 地:美洲

  • T101978,?9-?Epoxy-?3-?isobutyryloxy-?10-?(2-?methylbutanoyl)?thymol8,?9-?Epoxy-?3-?isobutyryloxy-?10-?(2-?

    8,9-Epoxy-3-isobutyryloxy-10-(2-methylbutanoyl)thymol is a chemical composition of essential oils from Telekia speciosa. It also shows marked antipro-liferative activity against human cancer cell lines in vitro.

    价 格:¥电议型 号:T10197产 地:美洲

  • T101988-M-PDOT8-M-PDOT,AH-002,

    8-M-PDOT (AH-002) is a selective melatonin MT2 receptor agonist. It is 5.2-fold selective for MT2 over MT1 receptors. 8-M-PDOT binds human recombinant MT2 and MT2 receptors (pKi: 8.23 and 8.95).

    价 格:¥电议型 号:T10198产 地:美洲

  • T10199GNF-PF-3777GNF-PF-3777,8-Nitrotryptanthrin,

    GNF-PF-3777 (8-Nitrotryptanthrin) is a potent inhibitor of human indoleamine 2,3-dioxygenase 2 (hIDO2; Ki: 0.97 μM).

    价 格:¥电议型 号:T10199产 地:美洲

  • T10585BozitinibBozitinib,PLB-1001,CBT-101

    Bozitinib (PLB-1001) is a highly selective inhibitor of the c-MET kinase with blood-brain barrier permeability. Bozitinib binds to the conventional ATP-binding pocket of the tyrosine kinase superfamily.

    价 格:¥电议型 号:T10585产 地:美洲

  • T10871CP-809101 hydrochlorideCP-809101 hydrochloride

    CP-809101 hydrochloride is a potent and selective 5-HT2C receptor agonist (pEC50: 9.96/7.19/6.81 for human 5-HT2C/5-HT2B/5-HT2A receptors).

    价 格:¥电议型 号:T10871产 地:美洲

  • T10926CYT-1010CYT-1010

    CYT-1010 is an mu-opioid receptor agonist extracted from patent WO2013173730A2. The EC50 for the inhibition of β-arrestin recruitment and cAMP production is 13.1 nM and 0.0053 nM, respectively.

    价 格:¥电议型 号:T10926产 地:美洲

  • T1101Minocycline hydrochlorideMinocycline hydrochloride,Minocycline HCl,

    Minocycline is a tetracycline antibiotic with excellent absorption and tissue penetration that is used for several bacterial infections as well as treatment of acne. Minocycline can cause both an acute hepatitis-like syndrome occurring within 1 to 3 month

    价 格:¥电议型 号:T1101产 地:美洲

  • T11011Dexpramipexole dihydrochlorideDexpramipexole dihydrochloride,(R)-Pramipexole dihydrochloride,R-(+)-P

    Dexpramipexole dihydrochloride ((R)-Pramipexole dihydrochloride) is a neuroprotective agent and is a weak non-ergoline dopamine agonist.

    价 格:¥电议型 号:T11011产 地:美洲

  • T11012DextranDextran,Dextran 40,

    Dextran (Dextran 40) has an inhibitory effect on platelet aggregation and coagulation factors, and is used as an agent for increasing plasma volume.

    价 格:¥电议型 号:T11012产 地:美洲

  • T11013Dextrorotation nimorazole phosphate esterDextrorotation nimorazole phosphate ester

    D-rotation nimorazole phosphate is an anti-anaerobic and anti-parasitic agent. D-morpholine ornidazole organic phosphate is a newly developed, highly efficient, well-tolerated fourth-generation nitroimidazole derivative. Objective: Antibacterial and antip

    价 格:¥电议型 号:T11013产 地:美洲

  • T11014DFP00173DFP00173

    DFP00173 is a potent and selective aquaporin 3 (AQP3) inhibitor. DFP00173 inhibits mouse and human AQP3 with IC50 of ~0.1-0.4 μM. Compared with the homologous AQP subtypes AQP7 and AQP9, DFP00173 is selective for AQP3.

    价 格:¥电议型 号:T11014产 地:美洲

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