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  • T9518Inarigivir ammoniuminhibit,HCV,HBV,RIG-I,Huh7,SB9000,ORI-9020,SB 9000,SB-9000,antiviral,Inarigivir a

    Inarigivir ammonium is a dinucleotide antiviral compound that significantly reduces HBV DNA in transgenic mice expressing hepatitis B virus. Inarigivir is an agonist of retinoic acid-inducible gene-I (RIG-I) that activates intracellular innate immunity.

    价 格：￥电议型 号：T9518产 地：中国大陆

  • T7501Iso-H7 dihydrochlorideIso H7 dihydrochloride,Iso-H-7 dihydrochloride,IsoH7 dihydrochloride

    Iso-H7 dihydrochloride is a less potent inhibitor of phosphokinase C than H-7.

    价 格：￥电议型 号：T7501产 地：中国大陆

  • T6066SCH772984

    SCH 772984 is a potent inhibitor of ERK1/ERK2 (IC50: 4/1 nM) and has only weak inhibitory for other 300 tested kinases.

    价 格：￥电议型 号：T6066产 地：中国大陆

  • T5635CH7057288

    CH7057288 is an effective and selective TRK inhibitor with an IC50 value of 1.1 nM, 7.8 nM and 5.1 nM for TRKA, TRKB and TRKC, respectively.

    价 格：￥电议型 号：T5635产 地：中国大陆

  • T3599BFH772BFH-722

    BFH772, a structure analogue of BAW2881, is a potent and selective VEGF inhibitor. BFH772 is highly effective at targeting VEGFR2 kinase with an IC50 value of 3 nM. BFH772 inhibits the ligand induced autophosphorylation of RET, PDGFR, and KIT kinases, wit

    价 格：￥电议型 号：T3599产 地：中国大陆

  • T1974PH-797804PH797804

    PH-797804 is a pyridinone inhibitor of p38α (IC50: 26 nM, in a cell-free assay); 4-fold more selective versus p38β and does not inhibit JNK2.

    价 格：￥电议型 号：T1974产 地：中国大陆

  • T12870SCH79797 dihydrochloride

    SCH79797 dihydrochloride is an effective and selective antagonist of protease activated receptor 1 (PAR1) with an IC50 of 70 nM and a Ki of 35 nM. SCH79797 dihydrochloride has antiproliferative and pro-apoptotic effects.

    价 格：￥电议型 号：T12870产 地：中国大陆

  • T12870SCH79797 dihydrochlorideSCH79797 dihydrochloride

    SCH79797 dihydrochloride is a selective antagonist of nonpeptide protease activated receptor 1 (PAR1).

    价 格：￥电议型 号：T12870产 地：美洲

  • T1974PH797804PH797804

    PH-797804 is a pyridinone inhibitor of p38α (IC50: 26 nM, in a cell-free assay); 4-fold more selective versus p38β and does not inhibit JNK2.

    价 格：￥电议型 号：T1974产 地：美洲

  • T5635CH7057288CH7057288

    CH7057288 is an effective and selective TRK inhibitor with an IC50 value of 1.1 nM, 7.8 nM and 5.1 nM for TRKA, TRKB and TRKC, respectively.

    价 格：￥电议型 号：T5635产 地：美洲

  • T6066SCH772984SCH772984

    SCH 772984 is a potent inhibitor of ERK1/ERK2 (IC50: 4/1 nM) and has only weak inhibitory for other 300 tested kinases.

    价 格：￥电议型 号：T6066产 地：美洲

  • T82246H7；化合物 H7H7

    H7 is a second near-infrared (NIR-II) fluorophore [1].

    价 格：￥电议型 号：T82246产 地：中国大陆

  • T81845Maximin H7；化合物 Maximin H7Maximin H7

    Maximin H7, an antimicrobial peptide, originates from the toad Bombina maxima [1].

    价 格：￥电议型 号：T81845产 地：中国大陆

  • T80742Zelavespib hydrochloride；化合物 Zelavespib hydrochloridePU-H71 hydrochloride；PU-H71 hydrochloride

    Zelavespib (PU-H71) hydrochloride is a potent inhibitor of Hsp90, exhibiting an IC50 value of 51 nM in MDA-MB-468 cells.

    价 格：￥电议型 号：T80742产 地：中国大陆

  • T80357Bombinin H7；化合物 Bombinin H7Bombinin H7

    Bombinin H7, an antimicrobial peptide originating from the skin secretions of Bombina, exhibits bactericidal activity against Bacillus megaterium Bm11 at a lethal concentration of 25.2 μM [1].

    价 格：￥电议型 号：T80357产 地：中国大陆

  • T7501Iso-H7 dihydrochloride1-(5-硫代异喹啉)-3-甲基哌嗪二盐酸盐1-(5-硫代异喹啉)-3-甲基哌嗪二盐酸盐

    Iso-H7 dihydrochloride is a less potent inhibitor of phosphokinase C than H-7.

    价 格：￥电议型 号：T7501产 地：中国大陆

  • T71247PU-H71 hydrate；化合物 PU-H71 hydratePU-H71 hydrate

    PU-H71 hydrate is a potent inhibitor of heat shock protein 90 (Hsp90).

    价 格：￥电议型 号：T71247产 地：中国大陆

  • T6960LPU-H71 HCl；PU-H71盐酸盐PU-H71 HCl(873436-91-0 Free base)|||Zelavespib HCl；PU-H71 HCl(873436-91-0 Free b

    PU-H71 HCl (Zelavespib HCl) is a novel Hsp90 inhibitor, a novel purine-based analog, and a radiosensitizer that may be a promising agent for CIRT. PU-H71 HCL shows antitumor activity in many preclinical models of malignancy. PU-H71 HCL has an inhibitory effect on the protein expression levels of Rad51 and Ku70, which may be associated with the double chain break repair in the homologous recombination pathway and non-homologous end-joining pathway.

    价 格：￥电议型 号：T6960L产 地：中国大陆

  • T6960PU-H71；化合物PU-H71PU-H71

    PU-H71 is an effective selective HSP90 inhibitor with an IC50 of 51 nM.

    价 格：￥电议型 号：T6960产 地：中国大陆

  • T69513(–)-IHCH7041；化合物 (–)-IHCH7041(–)-IHCH7041

    (–)-IHCH7041 is a optical rotation negative isomer of IHCH7041. (–)-IHCH7041 is a DRD2 partial agonist. (–)-IHCH7041 showed EC50 = 1.38 nM in Gαi1–γ9 dissociation and 2.75 nM in β-arrestin2 recruitment. (–)-IHCH7041 exhibited a inhibition constant (Ki) of 22.44 nM binding affinity at DRD2. (–)-IHCH7041 has antidepressant properties and reverses cognitive impairment.

    价 格：￥电议型 号：T69513产 地：中国大陆

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