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TargetMol | Tags 通过 靶点 筛选
  • Antibiotic
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抑制剂&激动剂
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TargetMol产品目录中 "precursors"的结果
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TargetMol产品目录中 "

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  • 抑制剂&激动剂
    47
    TargetMol | Inhibitors_Agonists
  • 重组蛋白
    45
    TargetMol | Recombinant_Protein
  • 多肽产品
    5
    TargetMol | Peptide_Products
  • 抗体抑制剂
    1
    TargetMol | Inhibitory_Antibodies
  • PROTAC
    1
    TargetMol | PROTAC
  • 天然产物
    14
    TargetMol | Natural_Products
  • 同位素
    1
    TargetMol | Isotope_Products
  • 分子与细胞研究
    3
    TargetMol | Inhibitors_Agonists
  • 1-Phenylpropane-1,2-dione
    Acetyl benzoyl, 1-苯基-1,2-丙二酮, 1-Phenyl-1,2-propanedione
    T7450579-07-7
    1-Phenylpropane-1,2-dione (Acetyl benzoyl) 是麻黄素生物碱的生物合成前体,分离自从嫩麻黄中。
    • ¥ 108
    In stock
    规格
    数量
  • MRT-81
    T95321263132-08-6
    MRT-81 是一种人和啮齿动物 smoothened 受体的有效拮抗剂,能够抑制 hedgehog 的活性,在 Shh-light2 细胞中的IC50值为 41 nM。它可用于研究癌症。
    • ¥ 463
    In stock
    规格
    数量
  • heparin cofactor II precursor (SERPIND1) fragment [Homo sapiens]
    TP2256
    Heparin cofactor II precursor (SERPIND1) fragment [Homo sapiens] is a peptide with the sequence H2N-Phe-Thr-Val-Asp-Arg- Pro-Phe-Leu-Phe-Leu-Ile-Tyr-Glu-His-Arg-OH, MW=1953.25.
    • ¥ 483
    待询
    规格
    数量
  • Ketoprofen
    酮洛芬, 酮基布洛芬, RP-19583
    T083922071-15-4
    Ketoprofen (RP-19583) 是一种非甾体抗炎剂,能够有效地抑制COX 的活性,在人血单核细胞中,对 COX-1 和 COX-2 的IC50值分别为 2 nM 和 26 nM。
    • ¥ 333
    In stock
    规格
    数量
  • Ibuprofen
    布洛芬, Motrin, Brufen, Advil, (±)-Ibuprofe
    T139415687-27-1
    Ibuprofen (Advil) 是一种丙酸衍生物和非甾体抗炎药 (NSAID),具有抗炎、镇痛和解热作用。它是COX-1和COX-2的抑制剂,IC50值分别为 13 和 370 μM,导致前列腺素和血栓素前体的形成减少。
    • ¥ 333
    In stock
    规格
    数量
    TargetMol | Citations 客户已引用
  • Aniline
    苯胺
    T20705362-53-3
    Aniline是最简单的芳香胺,其特征是一个氨基连接在苯环上。Aniline是一种具有重要工业意义的大宗化学品,也是精细化学合成的多功能起始材料,其主要用途是制造聚氨酯前体、染料和其他工业化学品。与大多数挥发性胺类一样,它具有类似烂鱼的独特难闻气味,易于点燃,燃烧时产生芳香族化合物特有的烟雾,并且对人类具有接触毒性。
    询价
  • Bromfenac sodium hydrate
    Bromfenac sodium sesquihydrate, Bromfenac monosodium salt sesquihydrate
    T2403120638-55-3
    Bromfenac sodium hydrate (Bromfenac monosodium salt sesquihydrate) 是一种可口服的 COX 抑制剂,抑制 COX-1和COX-2的IC50值分别为 5.56 和 7.45 nM。它是一种溴化非甾体类抗炎药,有用于白内障的术后炎症和疼痛以及假晶状体囊状黄斑水肿的研究。
    • ¥ 178
    In stock
    规格
    数量
  • 4-​Hydroxyphenylpyruvic acid
    4-羟苯基丙酮酸, 4-Hydroxyphenylpyruvic acid
    T4858156-39-8
    4-Hydroxyphenylpyruvic acid 是一种苯丙氨酸代谢的中间产物,是一种酶抑制剂。
    • ¥ 259
    In stock
    规格
    数量
  • (E)-2-Butenoic acid
    巴豆酸, Crotonic acid, alpha-butenoic acid
    T5301107-93-7
    (E)-2-Butenoic acid (Crotonic acid) 是内源性代谢产物的一种。
    • ¥ 99
    待询
    规格
    数量
    TargetMol | Inhibitor Sale
  • L-Aspartic acid potasium salt
    Potassium L-aspartate, L-天冬氨酸钾盐, Aspartic acid potasium salt
    T652691115-63-5
    L-aspartic acid potasium salt(VX-548) 是一种广泛存在于动植物体内的氨基酸。L-aspartic acid potasium salt驱动氮氧化物的产生,从而促进吞噬作用,有助于提高鱼类的成活率。L-aspartic acid potasium salt 可对抗生素产生刺激,刺激作用可能与参与天冬氨酸-4-半醛生物合成的前体有关。
    • ¥ 137
    In stock
    规格
    数量
  • Oleylamine
    油胺, cis-1-Amino-9-octadecene
    T89046112-90-3
    Oleylamine(油胺)是一种长链伯胺,具有表面活性剂的特性,在工业中用途广泛,溶于多种有机溶剂且不溶于水。cis-1-Amino-9-octadecene用于控制纳米粒子的形态并防止聚集和将金属前体还原为金属纳米粒子。
    • ¥ 99
    In stock
    规格
    数量
  • Endo-β-N-acetylglucosaminidase
    T7617637278-88-9
    Endo-β-N-acetylglucosaminidase (Endo S) 是一种来自北拟杆菌的酶,可水解多支链复合物 N-聚糖,可在体内抑制抗体介导的炎症,广泛用于糖蛋白的聚糖分析和糖基化化合物前体的制备。
    • ¥ 662
    待询
    规格
    数量
    TargetMol | Inhibitor Sale
  • 3-Feruloyl-4-caffeoylquinic acid
    3-阿魏酰-4-咖啡酰奎尼酸
    TN707396990-65-7
    3-Feruloyl-4-caffeoylquinic acid 是一种绿原酸异构体。绿原酸是相关的咖啡品质标志、味道和香气前体以及重要的生物活性化合物。
    • ¥ 1300
    In stock
    规格
    数量
    TargetMol | Inhibitor Sale
  • Dynarrestin
    T151832222768-84-3
    Dynarrestin 是一种细胞质动力蛋白 1 和 2的氨基噻唑抑制剂。它能够快速的、可逆的抑制动力蛋白 1 驱动的微管在体外滑动和细胞内动力蛋白 1 和 2 依赖性过程,且不影响 ATP 水解和干扰纤毛发生。它可抑制神经元前体和肿瘤细胞的刺猬因子依赖性增殖。
    • ¥ 367
    In stock
    规格
    数量
  • Maleimido-tri(ethylene glycol)-propionic acid
    Mal-PEG3-acid
    T16008518044-40-1
    Maleimido-tri(ethylene glycol)-propionic acid is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Maleimido-tri(ethylene glycol)-propionic acid is used for the preparation of neolymphostin-based ADC precursors for site-spec
    • ¥ 693
    5日内发货
    规格
    数量
  • 5-Chloro-2'-deoxyuridine
    CldU, 5-氯-2-脱氧尿嘧啶核苷, 5-Chlorodeoxyuridine
    T1915150-90-8
    5-Chloro-2'-deoxyuridine (5-Chlorodeoxyuridine) 是胸腺嘧啶的类似物,可用于次氯酸对 DNA 和 DNA 前体的破坏作用的研究。
    • ¥ 158
    In stock
    规格
    数量
  • Cycloate
    R-2063, R2063, R 2063, HSDB-1712, HSDB 1712, Etsan
    T205301134-23-2
    Cycloate is a herbicide. It inhibits the biosynthesis of very-long-chain fatty acids, which is the essential constituents of plant suberin and waxes. Fatty acids also serve as precursors of aliphatic carbon chains in resorcinolic lipids.
    • ¥ 10600
    6-8周
    规格
    数量
  • Pyruvate Carboxylase-IN-5
    T210370
    Pyruvate Carboxylase-IN-5 (compound 6m) 是一种具备高度选择性和渗透性的丙酮酸羧化酶 (pyruvate carboxylase) 抑制剂。丙酮酸羧化酶是一种线粒体酶,催化丙酮酸转化为草酰乙酸,这个过程在维持三羧酸循环中间体的稳态水平中扮演关键角色,而这些中间体是氨基酸、脂肪酸和葡萄糖等生物大分子合成的前体。
    询价
  • Artemisitene
    青蒿烯
    T21065101020-89-7
    Artemisitene 是青蒿素的氧化形式,是一种抗疟药。青蒿素前体是青蒿素生物合成的重要基础物质,包括青蒿素 B、青蒿素、青蒿酸等。
    • ¥ 763
    In stock
    规格
    数量
  • SC 19220
    SC19220
    T2333019395-87-0
    SC 19220 是一种前列腺素 E2 受体 EP1 拮抗剂。SC 19220通过抑制破骨细胞前体中的 RANK/RANKL 信号通路来抑制 RANKL 诱导的破骨细胞生成。
    • ¥ 350
    In stock
    规格
    数量
  • HPI-1 (hydrate)
    HPI-1 hydrate
    T355381262770-72-8
    HPI-1 (hydrate) is a Hedgehog (Hh) pathway inhibitor that suppresses signaling through Sonic Hh (IC50= 1.5 μM) without significantly affecting Wnt signaling (IC50≥ 30 μM).1HPI-1 suppresses Hh activation induced by loss of Suppressor of Fused or by Gli overexpression, suggesting action at posttranslational modification of Gli protein or at the interaction of Gli with a co-factor.1HPI-1 (hydrate) also inhibits signaling through the oncogenic Smoothened (Smo) mutant SmoM2 in neuron precursors, preventing cell proliferation.1 1.Hyman, J.M., Firestone, A.J., Heine, V.M., et al.Small-molecule inhibitors reveal multiple strategies for Hedgehog pathway blockadeProceedings of the National Academy of Sciences of the United States of America106(33)14132-14137(2009)
    • ¥ 10600
    待询
    规格
    数量
  • Concanamycin B
    T3611681552-33-2
    Concanamycin B is a macrolide antibiotic that selectively inhibits vacuolar type H+-ATPases, also known as V-ATPases (IC50 = 5 nM). In this way, it blocks the acidification of vacuolar organelles as well as early to late endosomal transport. Concanamycin B interferes with bone resorption and maturation of CD8 T lymphocytes. It also prevents processing of major histocompatibility complex (MHC) class II precursors in human B cells, inhibiting the expression of MHC class II molecules on the cell surface.
    • ¥ 14680
    待询
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  • Steryl Glucosides
    T37322
    Steryl glucosides are neutral glycolipids commonly found in plant cell membranes and vegetable oils that contain a glucose moiety conjugated to a sterol lipid. They function as glucose donors in the biosynthesis of glucocerebrosides in plant microsomes and are metabolic precursors to acylated/esterified steryl glucosides. Steryl glucosides are the major component of filter- and engine-damaging precipitates formed during biodiesel production from transesterification of vegetable oils. This product contains a mixture of steryl glucosides.
    • ¥ 993
    35日内发货
    规格
    数量
  • Glycerophospho-N-Arachidonoyl Ethanolamine
    T37530201738-25-2
    N-Acylated ethanolamines (NAE) are naturally-occurring lipids that have diverse bioactivities. The different types of NAE can be derived from glycerophospho-linked precursors by the activity of glycerophosphodiesterase 1 (GDE1). Glycerophospho-N-arachidonoyl ethanolamine is the precursor of arachidonoyl ethanolamide (AEA), also known as anandamide. AEA is an endogenous cannabinoid neurotransmitter that binds to both central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors. It inhibits the specific binding of [3H]-HU-243 to synaptosomal membranes with a Ki value of 52 nM, compared to 46 nM for δ9-THC.
    • ¥ 2130
    35日内发货
    规格
    数量