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  • T6S1587Notoginsenoside R2；三七皂苷R220(S)-Notoginsenoside R2|||Ginsenoside Ng-R2；三七皂苷R2|||20(S)-Notoginsenoside

    Notoginsenoside R2 (20(S)-Notoginsenoside R2) has neuroprotection against 6-OHDA-induced neurotoxicity, is associated with Notoginsenoside R2-mediated P90RSK and Nrf2 activation through MEK1/2-ERK1/2 pathways.

    价 格：￥电议型 号：T6S1587产 地：中国大陆

  • T69336NNC-11-1585；化合物 NNC-11-1585NNC-11-1585

    NNC-11-1585 is an M(1) and M(2) muscarinic acetylcholine receptor (mAChR) agonist.

    价 格：￥电议型 号：T69336产 地：中国大陆

  • T69158Ambenonium chloride tetrahydrate；化合物 Ambenonium chloride tetrahydrateAmbenonium chloride tetrahydrat

    Ambenonium chloride tetrahydrate is a salt of ambenonium --- a quaternary ammonium compound with parasympathomimetic activity. It is a cholinesterase inhibitor used in the management of myasthenia gravis. Myasthenia gravis occurs when the body produces antibodies against acetylcholine receptors, and thus inhibits signal transmission across the myoneural junction. Ambenonium chloride is a rapid indirect-acting cholinergic agonist that reversibly blocks the activity of acetylcholinesterase, thereb

    价 格：￥电议型 号：T69158产 地：中国大陆

  • T68805PSB-1584；化合物 PSB-1584PSB-1584

    PSB-1584 is a Potent Agonist of the Orphan G Protein-Coupled Receptor 84 (GPR84). GPR84, a Gi protein-coupled receptor that is activated by medium-chain (hydroxy)fatty acids, appears to play an important role in inflammation, immunity, and cancer.

    价 格：￥电议型 号：T68805产 地：中国大陆

  • T68741OKY 1581；化合物 OKY 1581OKY 1581

    OKY 1581 is a new thromboxane synthetase inhibitor

    价 格：￥电议型 号：T68741产 地：中国大陆

  • T6853GSK591；化合物GSK591GSK3203591|||EPZ015866；GSK3203591|||EPZ015866

    GSK591 (GSK3203591), Alternative Names are EPZ015866, GSK3203591, is a potent selective inhibitor of the arginine methyltransferase PRMT5 (IC50=11 nM).

    价 格：￥电议型 号：T6853产 地：中国大陆

  • T68499F15845 HBr；化合物 F15845 HBrF15845 HBr

    F 15845 is a blocker of the persistent sodium current prevents consequences of hypoxia in rat femoral artery. F15845 has been shown to selectively inhibit the persistent sodium current of Nav1.5[1] exerting cardioprotective effects following ischemia. In vitro testing showed minimal effects of F15845 on other important ion channels of the heart, including major Ca2+ and K+ channels.[1] This characteristic is thought to account for the limited effect of F15845 to change other heart parameters suc

    价 格：￥电议型 号：T68499产 地：中国大陆

  • T6798Tretazicar；化合物Tretazicar5-Aziridino-2,4-dinitrobenzamide|||CB1954|||NSC 115829；5-Aziridino-2,4-dinit

    CB1954(Tretazicar (NSC-115829)), an anticancer prodrug, is activated by NAD(P)H quinone oxidoreductase 2. It is converted in the presence of the enzyme NQO2 and co-substrate caricotamide ( EP-0152R) (EP) into a potent cytotoxic bifunctional alkylating agent.

    价 格：￥电议型 号：T6798产 地：中国大陆

  • T671584-Hydroxyphthalic acid；化合物 4-Hydroxyphthalic acid4-Hydroxyphthalic acid

    4-Hydroxyphthalic acid is a useful organic compound for research related to life sciences. The catalog number is T67158 and the CAS number is 610-35-5.

    价 格：￥电议型 号：T67158产 地：中国大陆

  • T661586-Chloro-3-hydroxypyrazine-2-carboxamide；化合物 6-Chloro-3-hydroxypyrazine-2-carboxamide6-Chloro-3-hydr

    6-Chloro-3-hydroxypyrazine-2-carboxamide is a useful organic compound for research related to life sciences. The catalog number is T66158 and the CAS number is 259793-90-3.

    价 格：￥电议型 号：T66158产 地：中国大陆

  • T65158Ethyl sorbate；化合物 Ethyl sorbateEthyl sorbate

    Ethyl sorbate is a useful organic compound for research related to life sciences. The catalog number is T65158 and the CAS number is 2396-84-1.

    价 格：￥电议型 号：T65158产 地：中国大陆

  • T64279ODN 21158；化合物 ODN 21158ODN 21158

    ODN 21158 is a potent, non-cytotoxic inhibitor of G-modified TLR3 and TLR9. ODN 21158 dose-dependently inhibits IFN-α secretion.

    价 格：￥电议型 号：T64279产 地：中国大陆

  • T64277ODN 1585；化合物 ODN 1585ODN 1585

    ODN 1585 is a potent inducer of IFN and TNFα production, a potent stimulator of NK (natural killer) and can be used as a vaccine adjuvant.ODN 1585 enhances the function of CD8+ T cells, including CD8+ T cell-mediated IFN-γ production.ODN 1585 induces regression of established melanomas in mice and has been shown to inhibit malaria in mice. ODN 1585 can be used to study acute myelogenous leukaemia (AML) and malaria.

    价 格：￥电议型 号：T64277产 地：中国大陆

  • T64158Nenocorilant；化合物 NenocorilantNenocorilant

    Nenocorilant (Relacorilant) is an orally active glucocorticoid receptor (GR) antagonist (Ki: 0.15 nM). Nenocorilant can be used to study tumours.

    价 格：￥电议型 号：T64158产 地：中国大陆

  • T63196DS17701585；化合物 DS17701585DS17701585

    DS17701585 is an orally active, selective inhibitor of EP300 and CBP, capable of acting on CBP (IC50: 0.040 μM), EP300 (IC50: 0.15 μM), H3K27 (IC50: 0.45 μM) and SOX2 (IC50: 0.7 μM), and can be used to study cancer.

    价 格：￥电议型 号：T63196产 地：中国大陆

  • T63158hCAIX-IN-10；化合物 hCAIX-IN-10hCAIX-IN-10

    hCAIX-IN-10 (Compound 6i) is a selective inhibitor of carbonic anhydrase IX and XII, acting on hCA IX (Ki: 61.5 nM) and hCA XII (Ki: 586.8 nM). hCA IX and hCA XII are transmembrane isoforms of carbonic anhydrase that act as biomarkers for some types of tumours. hCA XII contributes to the maintenance of acid-base homeostasis in normal and tumour cells.

    价 格：￥电议型 号：T63158产 地：中国大陆

  • T62158AMG9678；化合物 AMG9678AMG9678

    AMG9678 is a selective, potent, orally active TRPM8 antagonist (IC50: 31.2 nM).

    价 格：￥电议型 号：T62158产 地：中国大陆

  • T61589c-Fms-IN-13；化合物c-Fms-IN-13c-Fms-IN-13

    c-Fms-IN-13 (compound 14) is a potent FMS kinase inhibitor (IC50= 17 nM). c-Fms-IN-13 is an anti-inflammatory agent.

    价 格：￥电议型 号：T61589产 地：中国大陆

  • T61588AGN 192870；化合物AGN 192870AGN 192870

    AGN 192870 is a potent retinoic acid receptor (RAR) antagonist.AGN 192870 can be used to study cell growth arrest, differentiation and apoptosis.

    价 格：￥电议型 号：T61588产 地：中国大陆

  • T61587ATR-IN-15；化合物 ATR-IN-15ATR-IN-15

    ATR-IN-15 (compound 1) is a highly potent and orally active inhibitor of ATR kinase with an IC50 of 8 nM. Additionally, ATR-IN-15 demonstrates inhibitory activity against several targets, including human colon tumor cells LoVo, DNA-PK, and PI3K, with IC50 values of 47, 663, and 5131 nM, respectively [1].

    价 格：￥电议型 号：T61587产 地：中国大陆

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