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抑制剂&激动剂
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TargetMol产品目录中 "oligosaccharide"的结果
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TargetMol产品目录中 "

oligosaccharide

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  • 抑制剂&激动剂
    83
    TargetMol | Inhibitors_Agonists
  • 重组蛋白
    18
    TargetMol | Recombinant_Protein
  • 天然产物
    51
    TargetMol | Natural_Products
  • 检测抗体
    1
    TargetMol | Antibody_Products
  • 疾病造模
    2
    TargetMol | Disease_Modeling_Products
  • 分子与细胞研究
    22
    TargetMol | Inhibitors_Agonists
  • Raffinose
    棉子糖, Melitriose, Melitose
    T8144512-69-6
    Raffinose (Melitriose) 是不能够消化的短链寡糖,是由半乳糖,葡萄糖和果糖组成的三糖,能够在许多植物中找到。它能够被 α-半乳糖苷酶 (α-GAL) 水解为 D-半乳糖和蔗糖。
    • ¥ 150
    In stock
    规格
    数量
  • 2'-FUCOSYLLACTOSE
    2'-岩藻糖基乳糖, 2'-Fucosyl-D-lactose
    TN679641263-94-9
    2'-FUCOSYLLACTOSE (2'-Fucosyl-D-lactose) 是一种含岩藻糖的寡糖。
    • ¥ 333
    In stock
    规格
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  • Fructo-oligosaccharide DP11/GF10
    T19328137405-36-8
    Fructo-oligosaccharide DP11 GF10 is a fructooligosaccharide (FOS) compound with a degree of polymerization (DP) equal to 11. FOS consists of 10 fructose units connected by (2→1)-β-glycosidic bonds, with a single D-glucosyl unit present at the non-reducing end.
    • 待询
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  • GM1a Ganglioside oligosaccharide
    T8227767063-78-9
    GM1a Ganglioside oligosaccharide为ganglioside GM1的半合成形式,后者作为霍乱毒素的天然受体,在生长调节及激素诱导反应的耦合中具有关键功能。
    • 待询
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  • Fructo-oligosaccharide DP14
    T82369137405-38-0
    Fructo-oligosaccharide DP14为从Atractylodes lancea中提取的寡糖。
    • 待询
    规格
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  • Fructo-oligosaccharide DP13
    T82370137405-37-9
    Fructo-oligosaccharide DP13,一种Inulin型低聚果糖,可从Morinda Officinalis中分离。
    • 待询
    规格
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  • Chitosan oligosaccharide
    壳聚糖低聚乳酸酯, COS
    T10789148411-57-8
    Chitosan oligosaccharide (COS) 是 β-(1→4)-连接的 D-氨基葡萄糖的寡聚体,Chitosan oligosaccharide可激活 AMPK ,抑制NF-κB 和 MAPK在内的炎症信号通路。
    • ¥ 333
    In stock
    规格
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  • Fructo-oligosaccharide DP12/GF11
    蔗果十二糖
    T19329137405-40-4
    Fructo-oligosaccharide DP12 GF11 is a member of fructooligosaccharides (FOS) characterized by a degree of polymerization (DP) of 12. FOS compounds consist of 11 fructose units connected by (2→1)-β-glycosidic bonds, with a lone D-glucosyl unit located at the non-reducing end.
    • 待询
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    数量
  • Fructo-​oligosaccharide DP7/GF6
    蔗果七糖, Fructoheptasaccharide
    T579162512-20-3
    Fructo-​oligosaccharide DP7/GF6 (Fructoheptasaccharide) 属于一种聚果糖,聚合度 (DP=7)。其中 Fructo-oligosaccharides (FOS) 由 6 个果糖单元通过 (2→1)-β-糖苷键连接,并在非还原性末端具有 1 个 D-葡萄糖单元。
    • ¥ 497
    In stock
    规格
    数量
    TargetMol | Inhibitor Sale
  • Fructo-oligosaccharide DP9/GF8
    蔗果九糖, Fructo-oligosaccharide DP9 GF8
    T8154143625-74-5
    Fructo-oligosaccharide DP9/GF8 (Fructo-oligosaccharide DP9 / GF8) 是一种低聚果糖(FOS),其聚合度DP=9。低聚果糖(FOS)由 8 个果糖单元通过 (2→1)-β-糖苷键连接,并在非还原性末端具有 1 个 D-葡萄糖单元。
    • ¥ 418
    In stock
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  • Fructo-oligosaccharide DP10/GF9
    蔗果十糖
    TN2358118150-64-4
    Fructo-oligosaccharide DP10/GF9是一种聚合度(DP)为10的聚果糖,由非还原性末端的1个D-葡萄糖(Glucose)单元和通过(2→1)-β-糖苷键连接的9个果糖(Fructose)单元组成。
    • ¥ 628
    In stock
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  • Fructo-oligosaccharide DP8/GF7
    蔗果八糖, Fructo-oligosaccharide DP8 GF7
    TN237662512-21-4
    Fructo-oligosaccharide DP8 GF7 (Fructo-oligosaccharide DP8 GF7) 是一种聚果糖,聚合度(DP=8)。Fructo-oligosaccharides 由 7 个果糖单元通过 (2→1)-β-糖苷键连接,并在非还原性末端具有 1 个 D-葡萄糖单元。
    • ¥ 347
    In stock
    规格
    数量
    TargetMol | Inhibitor Sale
  • Fructooligosaccharides
    低聚果糖, Oligolevulose, FOS
    T0582308066-66-2
    Fructooligosaccharides (低聚果糖,FOS)是一种天然存在的功能性寡糖,由2~10个果糖分子与葡萄糖分子结合而成,广泛存在于香蕉、洋葱、大蒜、菊苣、蜂蜜等天然植物中。作为一种典型的益生元,低聚果糖不能被人体消化吸收,但能被肠道中的益生菌(如双歧杆菌)选择性利用,促进肠道健康、调节肠道菌群平衡、增强免疫力。
    • ¥ 123
    In stock
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  • Lipopolysaccharides
    脂多糖, LPS
    T11855
    Lipopolysaccharides(LPS)来源于大肠杆菌O55:B5,是革兰氏阴性菌外膜的重要成分,由脂质A、核心寡糖和O-特异性多糖组成,具有高免疫原性,能激活免疫细胞TLR4受体,诱导细胞迁移体分泌,并有助于维持细菌外膜完整性、抵御胆汁盐和脂类抗生素的破坏,常用于炎症模型的构建,如关节炎、慢性阻塞性肺病(COPD)、急性呼吸窘迫综合征(ARDS)、以及消化系统等疾病模型的构建。
    • ¥ 449
    In stock
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    TargetMol | Inhibitor Hot
  • D(+)-Raffinose pentahydrate
    五水棉子糖, Raffinose pentahydrate, D-Raffinose pentahydrate, D(+)-五水棉子糖
    T3S030917629-30-0
    D(+)-Raffinose pentahydrate (D-Raffinose pentahydrate) 是果糖,半乳糖和葡萄糖组成的三糖,天然存在于各种蔬菜和谷物中。D(+)-Raffinose pentahydrate 是一种功能性低聚糖。
    • ¥ 163
    In stock
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  • Podecdysone B
    罗汉松甾酮B
    T1382222612-27-7
    Podecdysone B 是一种从露水草中分离出来的植物蜕皮激素。
    • ¥ 633
    In stock
    规格
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    TargetMol | Inhibitor Sale
  • α-L-Fucopyranos
    α-L-Fucose, L-(-)-海藻糖, Deoxy-a-L-galactopyranose, Alpha-L-Fucose, Alpha-L-Fucopyranose
    T2038196696-41-9
    α-L-fucopyranose(L-(-)-海藻糖)是一种内源性代谢物和六碳脱氧己糖,存在于许多细胞表面寡糖配体的末端或前端位置,介导细胞识别和粘附信号通路,是在包括肿瘤在内的病理过程中一个潜在的关键分子。
    • ¥ 1300
    In stock
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  • Aplanin
    T3009765098-54-6
    Aplanin is an Oligosaccharide containing glucose as monomeric unit with an additional N-containing moiety.
    • 待询
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  • Lacto-N-fucopentaose I
    LNFI,LNF I,LNF-I
    T325307578-25-8
    Lacto-N-fucopentaose I is a milk oligosaccharide.
    • 待询
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  • Trigalacturonic Acid
    T369556037-45-2
    Trigalacturonic acid is an oligosaccharide that inhibits proteinase activity in tomato plants (ED50 = 2.6 μg plant).
    • ¥ 10936
    待询
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  • Chitoheptaose heptahydrochloride
    壳七糖七盐酸盐
    T37252127171-89-5
    Chitoheptaose heptahydrochloride is a chitosan oligosaccharide with antioxidant, anti-inflammatory, antiapoptotic, and cardioprotective properties. It effectively promotes the growth and photosynthesis parameters of wheat seedlings[1][2].
    • ¥ 7376
    待询
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    数量
  • Chitohexaose hexahydrochloride
    壳六糖六盐酸盐
    T37253127171-88-4
    Chitohexaose hexahydrochloride is a chitosan oligosaccharide compound that possesses anti-inflammatory properties. It exerts its anti-inflammatory effect by binding to the active sites of TLR4, thereby inhibiting inflammation induced by LPS. This compound has been supported by references [1] and [2].
    • ¥ 7000
    待询
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    数量
  • 6'-Sialyllactose Sodium Salt
    6'-N-Acetylneuraminyl-D-lactose sodium salt
    T37347157574-76-0
    6'-Sialyllactose Sodium Salt (6'-N-Acetylneuraminyl-D-lactose sodium salt)是一种存在于母乳中的低聚糖,对 LPS 诱导的 ALI 具有保护作用,通过抑制 STAT1 和 NF-κB 信号通路来减轻 LPS 诱导的肺损伤。
    • ¥ 198
    In stock
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  • Ganglioside GM1 Mixture (ovine) (ammonium salt)
    T375821007119-81-4
    Ganglioside GM1is a monosialylated ganglioside and the prototypic ganglioside for those containing one sialic acid residue.1,2It is found in a large variety of cells, including immune cells and neurons, and is enriched in lipid rafts in the cell membrane.3It associates with growth factor receptors, including TrkA, TrkB, and the GDNF receptor complex containing Ret and GFRα, and is required for TrkA expression on the cell surface. Ganglioside GM1interacts with other proteins to increase calcium influx, affecting various calcium-dependent processes, including inducing neuronal outgrowth during differentiation. Ganglioside GM1acts as a receptor for cholera toxin, which binds to its oligosaccharide group, facilitating toxin cell entry into epithelial cells of the jejunum.4,5Similarly, it is bound by the heat-labile enterotoxin fromE. coliin the pathogenesis of traveler's diarrhea.6Ganglioside GM1gangliosidosis, characterized by a deficiency in GM1-β-galactosidase, the enzyme that degrades ganglioside GM1, leads to accumulation of the gangliosides GM1and GA1in neurons and can be fatal in infants.1Levels of ganglioside GM1are decreased in the substantia nigra pars compacta in postmortem brain from patients with Parkinson's disease.3Ganglioside GM1mixture contains a mixture of ovine ganglioside GM1molecular species with primarily C18:0 fatty acyl chain lengths, among various others. [Matreya, LLC. Catalog No. 1544] 1.Kolter, T.Ganglioside biochemistryISRN Biochem.506160(2012) 2.Mocchetti, I.Exogenous gangliosides, neuronal plasticity and repair, and the neurotrophinsCell Mol. Life Sci.62(19-20)2283-2294(2005) 3.Ledeen, R.W., and Wu, G.The multi-tasked life of GM1 ganglioside, a true factotum of natureTrends Biochem. Sci.40(7)407-418(2015) 4.Turnbull, W.B., Precious, B.L., and Homans, S.W.Dissecting the cholera toxin-ganglioside GM1 interaction by isothermal titration calorimetryJ. Am. Chem. Soc.126(4)1047-1054(2004) 5.Blank, N., Schiller, M., Krienke, S., et al.Cholera toxin binds to lipid rafts but has a limited specificity for ganglioside GM1Immunol. Cell Biol.85(5)378-382(2007) 6.Minke, W.E., Roach, C., Hol, W.G., et al.Structure-based exploration of the ganglioside GM1 binding sites of Escherichia coli heat-labile enterotoxin and cholera toxin for the discovery of receptor antagonistsBiochemistry38(18)5684-5692(1999)
    • ¥ 2870
    35日内发货
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