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  • T13398ZINC13466751

    ZINC13466751 is a potent HIF-1α/von Hippel-Lindau interaction inhibitor(IC50 = 2.0 ?M).

    价 格：￥电议型 号：T13398产 地：中国大陆

  • T0751FurazolidoneFuroxone；呋喃唑酮

    Furazolidone, a nitrofuran derivative, inhibits AML1-ETO transformed cells with IC50 value of 12.7 μM. It is antibacterial and antiprotozoal activity,

    价 格：￥电议型 号：T0751产 地：中国大陆

  • T0751FurazolidoneFurazolidone,Furoxone,

    Furazolidone, a nitrofuran derivative, inhibits AML1-ETO transformed cells with IC50 value of 12.7 μM. It is antibacterial and antiprotozoal activity,

    价 格：￥电议型 号：T0751产 地：美洲

  • T12429PF-06751979PF-06751979

    PF-06751979 is an inhibitor of β-site amyloid precursor protein cleaving enzyme 1 (BACE1) (IC50 of 7.3 nM in BACE1 binding assay).

    价 格：￥电议型 号：T12429产 地：美洲

  • T12848SB-657510SB-657510

    SB-657510 is a selective antagonist of urotensin II (UII) receptor (UT).

    价 格：￥电议型 号：T12848产 地：美洲

  • T16154MS417MS417,GTPL7512,

    MS417 is an inhibitor of BET-specific BRD4(BRD4-BD1 and BRD4-BD2 with IC50s of 30, 46 nM and Kds of 36.1, 25.4 nM, respectively), with weak selectivity at CBP BRD with IC50 of 32.7 μM.

    价 格：￥电议型 号：T16154产 地：美洲

  • T16751RilapladibRilapladib,SB 659032,

    Rilapladib is a selective Lipoprotein-Associated Phospholipase A2 inhibitor (IC50: 230 pM). Rilapladib is also a Platelet Activating Factor Receptor antagonist.

    价 格：￥电议型 号：T16751产 地：美洲

  • T1751EliprodilEliprodil,SL-820715,

    Eliprodil(SL-820715), a non-competitive NR2B-NMDA receptor antagonist(IC50: 1 uM), less effective for NR2A- and NR2C-containing receptors(IC50> 100 uM). It has been used in trials studying the treatment of Parkinson Disease and Movement Disorders.

    价 格：￥电议型 号：T1751产 地：美洲

  • T1758ABT-751ABT-751,ABT751,ABT 751

    ABT-751 has been investigated for the treatment of Lung Cancer, Non-Small Cell Lung Cancer, and Non-Small-Cell Lung Cancer.

    价 格：￥电议型 号：T1758产 地：美洲

  • T1778AT 7519 hydrochloride saltAT 7519 hydrochloride salt,AT7519 Hydrochloride,AT7519 HCl

    AT7519 hydrochloride is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9.

    价 格：￥电议型 号：T1778产 地：美洲

  • T19022LDS-751LDS-751

    LDS-751 is a stain of nucleic acid.

    价 格：￥电议型 号：T19022产 地：美洲

  • T2410NedaplatinNedaplatin,NSC 375101D,

    Nedaplatin is a derivative of cisplatin and DNA damage agent for tumor colony forming units (IC50: 94 μM). Containing a novel ring structure in which glycolate is bound to the platinum by a bidentate ligand, nedaplatin forms reactive platinum complexes th

    价 格：￥电议型 号：T2410产 地：美洲

  • T2446KI8751KI8751

    KI8751 is a potent and selective inhibitor of VEGFR2 with IC50 of 0.9 nM.

    价 格：￥电议型 号：T2446产 地：美洲

  • T4751(2R,3R)-(-)-2,3-Butanediol(2R,3R)-(-)-2,3-Butanediol,levo-2,3-Butanediol,

    (2R,3R)-2,3-Butanediol is found in cocoa and cocoa products. (2R,3R)-2,3-Butanediol is isolated from cocoa butter and roots of Ruta graveolens (rue).2,3-Butanediol is one of the constitutional isomers of butanediol. The 2R,3R stereoisomer of 2,3-butanedio

    价 格：￥电议型 号：T4751产 地：美洲

  • T5751TigogeninTigogenin

    Tigogenin is one of steroidal sapogenins which is widely used for synthesizing steroid drugs. It might have protective effect on bone and be helpful in preventing the development of osteoporosis.

    价 格：￥电议型 号：T5751产 地：美洲

  • T6205AT7519AT7519

    AT7519 is a CDK1/2/4/6/9 inhibitor (IC50: 10-210 nM). It is less effective to CDK3 and little active to CDK7.

    价 格：￥电议型 号：T6205产 地：美洲

  • T8751AZD8931 diFuMaric acid化合物AZD8931 diFuMaric acid4-[[4-[(3-氯-2-氟苯基)氨基]-7-甲氧基-6-喹唑啉基]氧基]-N-甲基-1-哌啶乙酰胺二富

    AZD8931 is a reversible and ATP competitive inhibitor of EGFR, ErbB2 and ErbB3 (IC50 of 4 nM, 3 nM and 4 nM, respectively).

    价 格：￥电议型 号：T8751产 地：中国大陆

  • T8559Galnon TFA(475115-35-6(free base))；化合物Galnon TFAGalnon TFA(475115-35-6(free base))

    Galnon is a novel non-peptide galanin receptor agonist (GAL1 and GAL2 with Ki of 11.7 and 34.1 μM respectively).

    价 格：￥电议型 号：T8559产 地：中国大陆

  • T83751PUMA BH3 (human) TFA；化合物 PUMA BH3 (human) TFAPUMA BH3 (human) TFA

    PUMA BH3, a peptide that includes the BH3 domain from the p53-upregulated modulator of apoptosis (PUMA) and activates the pro-apoptotic protein Bak, demonstrates binding affinity to Bak with dissociation constants (Kds) of 290 nM in HEPES buffer and 26 nM in CHAPS buffer. This interaction with Bak induces its homo-oligomerization and facilitates Bak-mediated membrane permeabilization.

    价 格：￥电议型 号：T83751产 地：中国大陆

  • T82751Celloheptaose；化合物 CelloheptaoseCelloheptaose

    Celloheptaose, an oligosaccharide composed of seven glucose units, serves as a substrate for polysaccharide monooxygenases (PMOs), facilitating the production of oxidized cellulo-oligosaccharides [1] [2].

    价 格：￥电议型 号：T82751产 地：中国大陆

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