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抑制剂&激动剂
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TargetMol产品目录中 "s 312"的结果
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s 312

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  • 抑制剂&激动剂
    7
    TargetMol | Inhibitors_Agonists
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    TargetMol | Recombinant_Protein
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    TargetMol | Peptide_Products
  • S 312
    T71260120004-07-1
    S 312 is a calcium antagonist.
    • ¥ 10600
    6-8周
    规格
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  • Dehydrodeoxy donepezil
    T71258120013-45-8
    Dehydrodeoxy donepezil is an inhibitor of acetylcholinesterase (AChE)
    • ¥ 10600
    6-8周
    规格
    数量
  • S-312-d
    S312-d, S-312d, S 312-d, S 312d
    T28646120056-57-7
    S-312d is a calcium channel antagonist. S-312-d can offer marked neuronal protective effects against ischemic injury.
    • ¥ 10600
    6-8周
    规格
    数量
  • CRS-3123
    REP-3123, REP 3123, CRS 3123
    T270881013915-71-3
    CRS-3123, a methionyl-tRNA synthetase inhibitor, is used potentially for the treatment of enteric infections.
    • 待询
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  • CRS3123 dihydrochloride
    T641491013915-99-5
    CRS3123 (REP-3123) dihydrochloride 是一种口服具有活力的全合成抗菌剂,能够有效抑制 Clostridioides difficile 甲硫氨酰-tRNA 合成酶 (MetRS)。CRS3123 dihydrochloride 能够用于 Clostridioides difficile 感染 (CDI) 的研究。
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  • Anti-inflammatory agent 84
    T209635
    Anti-inflammatory agent 84 (Compound 4D) 是一种 Coumarin 衍生物,具有抗菌和抗炎作用。它能够抑制 E. coli、Candida albicans、Staphylococcus aureus 和 耐甲氧西林 S. aureus (MRSA),其 MIC 分别为 312、156、19 和 316 μg/mL。此外,Anti-inflammatory agent 84 抑制 S. aureus、E. coli 和 MRSA 的生物膜形成,IC50 分别为 185、321 和 99 μM。它还可抑制 Lipopolysaccharide 刺激的 RAW264.7 巨噬细胞中一氧化氮的生成。
    • 待询
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  • PAR2 (1-6) amide (human) (trifluoroacetate salt)
    PAR2 (1-6) amide (human) (trifluoroacetate salt)
    T359552379569-17-0
    PAR2 (1-6) amide is a synthetic peptide agonist of proteinase-activated receptor 2 (PAR2) that corresponds to residues 1-6 of the amino terminal tethered ligand sequence of human PAR2 and residues 37-42 of the full-length sequence.1It binds to NCTC 2544 cells expressing human PAR2 (Ki= 9.64 μM in a radioligand binding assay) and induces calcium mobilization in the same cells (EC50= 0.075 μM).2PAR2 (1-6) amide (100 μM) reduces colony formation of A549 lung cancer cells.1It induces superoxide production and degranulation in isolated human eosinophils when used at a concentration of 500 μM.3PAR2 (1-6) amide (5 μmol/kg) induces tear secretion in rats when used in combination with amastatin .4 1.Bohm, S.K., Kong, W., Bromme, D., et al.Molecular cloning, expression and potential functions of the human proteinase-activated receptor-2Biochem. J.314(Pt 3)1009-1016(1996) 2.Kanke, T., Ishiwata, H., Kabeya, M., et al.Binding of a highly potent protease-activated receptor-2 (PAR2) activating peptide, [3H]2-furoyl-LIGRL-NH2, to human PAR2Br. J. Pharmacol.145(2)255-263(2005) 3.Miike, S., McWilliam, A.S., and Kita, H.Trypsin induces activation and inflammatory mediator release from human eosinophils through protease-activated receptor-2J. Immunol.167(11)6615-6622(2001) 4.Nishikawa, H., Kawai, K., Tanaka, M., et al.Protease-activated receptor-2 (PAR-2)-related peptides induce tear secretion in rats: Involvement of PAR-2 and non-PAR-2 mechanismsJ. Pharmacol. Exp. Ther.312(2)324-331(2005)
    • ¥ 1560
    35日内发货
    规格
    数量