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三叶新科每月上新,持续为科研人员提供新颖性研究工具,助力科研创新与突破。
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Osemitamab
目录号:SY-109521
Osemitamab(TST001)是一种针对claudin-18.2的人源化单克隆抗体,由人鼠嵌合体TST001的γ-1链与κ链的二聚体构成,具有对NK细胞介导的肿瘤杀伤活性,可用于胃/胃食管结合部腺癌,PDAC和肺癌。
¥667.00
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Tonabersat
目录号:SY-109522
Tonabersat (SB-220453,托那博沙) 是一种新型和可口服的的gap-junction 调节剂和CSD(Cortical spreading depression)抑制剂, 调节三叉神经节神经细胞和胶质细胞之间的细胞通讯并抑制神经源性炎症,用于治疗偏头痛和癫痫。
¥561.00
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Meclofenamic acid
目录号:SY-109523
Meclofenamic acid (Meclofenamate) 是一种非特异性 gap-junction 阻滞剂和特异性脂肪量和肥胖相关 (FTO) 酶抑制剂。 Meclofenamic acid 具有抗炎活性。
¥943.00
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Connexin mimetic peptide 40GAP27
目录号:SY-109524
Connexin mimetic peptide 40GAP27 是一种生物活性肽,对应于主要的血管连接蛋白Cx40第二个细胞外环的GAP27结构域(40Gap27)。该化合物在研究氧化应激所致的损伤以及间隙连接通讯机制中有应用。40Gap27能够在给药后减少内皮依赖性的内膜下平滑肌的超极化现象。
¥724.00
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Meclofenamate sodium hydrate
目录号:SY-109525
Meclofenamate sodium is a potent non-steroidal anti-inflammatory agent, which can specifically inhibit chemokine-induced human polymorphonuclear leukocyte function: chemotaxis, degranulation, and superoxide anion free radical production.
询价
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Rotigaptide
目录号:SY-109526
Rotigaptide is a novel and specific modulator of Cx43 and is a potent AAP. Rotigaptide prevents the uncoupling of Cx43-mediated gap junction communication and normalizes cell-to-cell communication during acute metabolic stress.
¥5796.00
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TAT-Gap19
目录号:SY-109527
Cx43 hemichannel blocker (IC50 ~7 μM). No significant affinity for gap junctions or Panx1 channels. N-terminal transactivator of transcription (TAT) motif promotes membrane permeability and increases inhibitory effect of Gap19. Active in vivo. Brain penet
¥1694.00
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AT-1001
目录号:SY-109528
AT-1001 (Larazotide) 是一种具有口服活性的紧密连接调节剂及连蛋白 (Zonulin) 拮抗剂。它通过阻断 Zonulin 受体信号通路维持肠道上皮细胞间紧密连接的完整性,能有效降低乳糜泻及炎症性肠病模型中的肠道通透性。
¥1586.00
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Peptide5
目录号:SY-109529
Connexin43 mimetic peptide. Reduces swelling, astrogliosis, neuroinflammation and neuronal cell death following spinal cord injury ex vivo and in vivo. Exhibits analgesic effects in models of neuropathic pain. O'Carroll et al (2008) Connexin 43 mimetic peptides reduce swelling, astrogliosis and neuronal cell death after spinal cord injury. Cell.Commun.Adhes. 15 27 PMID:18649176 |Mao et al (2017) Characterisation of Peptide5 systemic administration for treating traumatic spinal cord injured rats. Exp.Brain.Res. 235 3033 PMID:28725925 |Kim et al (2017) Characterising the mode of action of extracellular Connexin43 channel mimetic peptides in an in vitro ischemia injury model. Biochem.Biophys.Acta. 1861 68 PMID:27816754 |Tonkin et al (2017) Attenuation of mechanical pain hypersensitivity by treatment with Peptide5, a connexin-43 mimetic peptide, involves inhibition of NLRP3 inflammasome in nerve-injured mice. Exp.Neurol. 300 1 PMID:29055716
¥1184.00
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