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  • T1776LPlerixafor octahydrochloride盐酸普乐沙福；SID791 octahydrochloride；Plerixafor 8HCl (AMD3100 8HCl)；JM 3100 8

    AMD 3100 octahydrochloride blocks the binding of stromal cell-derived factor (SDF-1alpha) to the cellular receptor CXCR4, resulting in hematopoietic stem cell (HSC) release from bone marrow and HSC movement into the peripheral circulation. Plerixafor is a

    价 格：￥电议型 号：T1776L产 地：中国大陆

  • T17697BRD7-IN-1

    BRD7-IN-1, a modified derivative of BI7273 (BRD7/9 inhibitor), binds to a VHL ligand via a linker to form a PROTAC VZ185 (VZ185 against BRD7/9 with DC50s of 4.5 and 1.8 nM, respectively).

    价 格：￥电议型 号：T17697产 地：中国大陆

  • T17033TemanogrelAPD791

    Temanogrel is a highly selective antagonist of the 5-HT2A receptor (Ki: 4.9 nM).

    价 格：￥电议型 号：T17033产 地：中国大陆

  • T14779BRD7389

    BRD7389 is an inducer of insulin expression in pancreatic α-cells and a specific inhibitor of RSK family kinase (IC50s: 1.5 μM, 2.4 μM, and 1.2 μM for RSK1, RSK2, and RSK3).

    价 格：￥电议型 号：T14779产 地：中国大陆

  • T14381AZD7624AZD-7624

    AZD7624 is an p38 inhibitor. It has potent anti-inflammatory activity.

    价 格：￥电议型 号：T14381产 地：中国大陆

  • T14380AZD7507

    AZD7507 is a CSF-1R inhibitor with an IC50 of 32 nM. AZD7507 has antitumor activity.

    价 格：￥电议型 号：T14380产 地：中国大陆

  • T13647-Aminodeacetoxycephalosporanic acid7-ADCA；Cefalexine EP IMpurity B；Cephalexin Impurity B；7-Aminodes

    Cefalexine EP IMpurity B is used as an antibiotic.

    价 格：￥电议型 号：T1364产 地：中国大陆

  • T09897-Aminocephalosporanic acid7-氨基头孢烷酸；7-ACA

    7-Aminocephalosporanic acid is used for synthesis of cephalosporin antibiotics and intermediates.

    价 格：￥电议型 号：T0989产 地：中国大陆

  • T09897-Aminocephalosporanic acid7-Aminocephalosporanic acid,7-ACA,

    7-Aminocephalosporanic acid is used for synthesis of cephalosporin antibiotics and intermediates.

    价 格：￥电议型 号：T0989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

  • T10721CD73-IN-1CD73-IN-1

    CD73-IN-1 is an inhibitor of CD73 with anticancer activity extracted from patent WO 2017153952 A1 (example 80).

    价 格：￥电议型 号：T10721产 地：美洲

  • T135227-Ketolithocholic acid7-Ketolithocholic acid,3α-Hydroxy-7-oxo-5β-cholanic acid,

    7-Ketolithocholic acid (3α-Hydroxy-7-oxo-5β-cholanic acid) can be absorbed and suppresses endogenous bile acid production and biliary cholesterol secretion.

    价 格：￥电议型 号：T13522产 地：美洲

  • T14380AZD7507AZD7507

    AZD7507 is a CSF-1R inhibitor. It has antitumor activity.

    价 格：￥电议型 号：T14380产 地：美洲

  • T14382AZD7687AZD7687

    AZD7687 is a potent and selective DGAT1 inhibitor with an IC50 value of 80 nM (hDGAT1). IC50 value: 80 nM [1] Target: DGAT1 in vitro: Plasma AZD7687 exposure was measured repeatedly. AZD7687 markedly reduced postprandial TAG excursion with a steep concent

    价 格：￥电议型 号：T14382产 地：美洲

  • T14779BRD7389BRD7389

    BRD7389 is a small-molecule inducer of insulin expression in pancreatic α-cells and it is a specific RSK family kinase inhibitor with IC50s of 1.5 μM, 2.4 μM, and 1.2 μM for RSK1, RSK2, and RSK3, respectively.

    价 格：￥电议型 号：T14779产 地：美洲

  • T2353BRD7716BRD7716,BRD7116,

    BRD7116 competitively binds to bacterial DNA gyrase, with cell-non-autonomous anti-leukemia activity.

    价 格：￥电议型 号：T2353产 地：美洲

  • T2447AZD7545AZD7545

    AZD7545 is a potent PDHK inhibitor.

    价 格：￥电议型 号：T2447产 地：美洲

  • T58457-(Diethylamino)coumarin-3-carboxylic acid7-(Diethylamino)coumarin-3-carboxylic acid,DEAC,Coumarin D

    7-(Diethylamino)coumarin-3-carboxylic acid(7ACC) selectively affects a single part of the MCT symporter translocation cycle, leading to strict inhibition of lactate influx. This singular activity is associated with antitumor effects less prone to resistan

    价 格：￥电议型 号：T5845产 地：美洲

  • T6093AZD7762AZD7762

    AZD7762, an effective and specific inhibitor of Chk1（IC50=5 nM）, is equally potent against Chk2 and less potent against CAM, Yes, Fyn, Lyn, Hck and Lck.

    价 格：￥电议型 号：T6093产 地：美洲

  • T6421BRD73954BRD73954

    BRD73954, an effective and specific HDAC inhibitor, which is with IC50 of 36 nM and 120 nM for HDAC6 and HDAC8, respectively.

    价 格：￥电议型 号：T6421产 地：美洲

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