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T11871Loteprednol Etabonate D5；化合物 T11871Loteprednol Etabonate D5
Loteprednol Etabonate D5, a deuterium-labeled variant of Loteprednol etabonate (LE), is an orally active, anti-inflammatory soft steroid within a distinctive class of glucocorticoids. It is deployed in optometry and ophthalmology for its anti-inflammatory properties.
价 格：￥电议型 号：T11871产 地：中国大陆
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T11837Leptomycin A；来普霉素ALeptomycin A
Leptomycin A, a metabolite derived from Streptomyces, acts as an inhibitor of CRM1 (exportin 1) and effectively suppresses HIV-1 replication. Compared to Leptomycin B, it exhibits lesser potency. Leptomycin A hampers the interaction between CRM1 and nuclear export signals, effectively hindering the nuclear export of a wide array of proteins.
价 格：￥电议型 号：T11837产 地：中国大陆
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T11815Lanopepden；拉诺普登GSK 1322322|||GSK-1322322B|||GSK-1322322J；GSK 1322322|||GSK-1322322B|||GSK-1322322J
Lanopepden (GSK 1322322) is a potent peptide deformylase inhibitor of Staphylococcus aureus, inhibiting ATCC 29213 and ATCC 25923 strains, and can be used in the study of pneumonia, dermatological and infectious diseases.
价 格：￥电议型 号：T11815产 地：中国大陆
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T1171LMethylprednisolone Aceponate；醋丙甲泼尼龙MPA|||SH 440|||SH-440|||SH440|||Advantan；MPA|||SH 440|||SH-440|||
Methylprednisolone Aceponate (SH 440), a non-halogenated corticosteroid, is a potent anti-inflammatory agent.
价 格：￥电议型 号：T1171L产 地：中国大陆
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T11643Impurity B of Calcitriol；化合物 T116431β,25-Dihydroxyvitamin-D3|||1-Epicalcitriol；1β,25-Dihydroxyvitami
Impurity B of Calcitriol is an impurity of Calcitriol. Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
价 格：￥电议型 号：T11643产 地：中国大陆
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T11608Epanolol；化合物 T11608Visacor|||ICI141292；Visacor|||ICI141292
Epanolol is a potent β-adrenoceptor partial agonist with a greater affinity for β1- than β2-adrenoceptors.
价 格：￥电议型 号：T11608产 地：中国大陆
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T11555Heptasaccharide Glc4Xyl3；化合物 T11555Heptasaccharide Glc4Xyl3
Heptasaccharide Glc4Xyl3 is a covalent inhibitor of endo-xyloglucanases. It used for the identification and analysis of diverse xyloglucan-active enzymes in nature.
价 格：￥电议型 号：T11555产 地：中国大陆
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T11554Cathepsin Inhibitor 2；化合物 T11554Cathepsin Inhibitor 2
Cathepsin Inhibitor 2 is a potent Cathepsin S inhibitor (Ki: <20 nM).
价 格：￥电议型 号：T11554产 地：中国大陆
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T11553LHeptamidine；化合物 T11553LSBi4211；SBi4211
Heptamidine is an effective Pentamidine-related inhibitor of the calcium-binding protein S100B (Kd: 6.9 μM). It selectively kills melanoma cells with S100B over those without S100B. It is a useful tool for the investigation of Myotonic dystrophy.
价 格：￥电议型 号：T11553L产 地：中国大陆
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T11553Heptamidine dimethanesulfonate；化合物Heptamidine dimethanesulfonateSBi4211 dimethanesulfonate；SBi4211 d
Heptamidine dimethanesulfonate (SBi4211 dimethanesulfonate) serves as a potent inhibitor related to Pentamidine, targeting the calcium-binding protein S100B with a dissociation constant (Kd) of 6.9 ?M. It demonstrates specificity by preferentially killing melanoma cells overexpressing S100B compared to cells lacking this protein. Additionally, Heptamidine is employed as a valuable research tool in the study of Myotonic dystrophy (DM).
价 格：￥电议型 号：T11553产 地：中国大陆
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T11502Epelsiban；化合物 T11502GSK 557296；GSK 557296
Epelsiban is a selective and orally bioavailable oxytocin receptor antagonist (pKi: 9.9 for human oxytocin receptor).
价 格：￥电议型 号：T11502产 地：中国大陆
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T11500LGSK3368715 dihydrochlorideGSK3368715盐酸盐EPZ019997 dihydrochloride|||GSK3368715 2HCl|||EPZ019997 2HCl
GSK3368715 dihydrochloride (EPZ019997 dihydrochloride) is an orally active and potent inhibitor of type I protein arginine methyltransferases (PRMTs) with anticancer and antitumor activity, inhibiting PRMT1, PRMT3, PRMT4, PRMT6, and PRMT8, and can be used to study advanced solid tumors.
价 格：￥电议型 号：T11500L产 地：中国大陆
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T11500GSK3368715；化合物 T11500EPZ019997；EPZ019997
GSK3368715 is an orally active, reversible, and S-adenosyl-L-methionine (SAM) uncompetitive type I protein arginine methyltransferases (PRMTs) inhibitor (IC50s: 3.1 nM (PRMT1), 48 nM (PRMT3), 1148 nM (PRMT4), 5.7 nM (PRMT6), 1.7 nM (PRMT8)). It has strong anti-cancer activity.
价 格：￥电议型 号：T11500产 地：中国大陆
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T11417Glucocorticoid receptor agonist；化合物 T11417Glucocorticoid receptor agonist
Glucocorticoid receptor agonist is an effective glucocorticoid receptor agonist.
价 格：￥电议型 号：T11417产 地：中国大陆
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T11416Glucagon receptor antagonists-5；化合物 T11416Glucagon receptor antagonists-5
Glucagon receptor antagonists-5 is an orally bioavailable indazole-based glucagon receptor antagonist (Ki: 32 nM). It has potential for the treatment of type 2 diabetes mellitus (T2DM).
价 格：￥电议型 号：T11416产 地：中国大陆
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T11415Glucagon receptor antagonists-3；化合物 T11415Glucagon receptor antagonists-3
Glucagon receptor antagonist -3 is a highly effective glucagon receptor antagonist.
价 格：￥电议型 号：T11415产 地：中国大陆
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T11414Glucagon receptor antagonists-2；化合物 T11414Glucagon receptor antagonists-2
Glucagon receptor antagonist -2 is a highly effective glucagon receptor antagonist.
价 格：￥电议型 号：T11414产 地：中国大陆
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T11413Glucagon receptor antagonists-1；化合物 T11413Glucagon receptor antagonists-1
Glucagon receptor antagonist -1 is a highly effective glucagon receptor antagonist.
价 格：￥电议型 号：T11413产 地：中国大陆
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T11408Orforglipron；奥格列隆LY3502970|||GLP-1 receptor agonist 1；LY3502970|||GLP-1 receptor agonist 1
Orforglipron (LY3502970; GLP-1 receptor agonist 1) is an orally available glucagon-like peptide (GLP-1) receptor agonist for the study of obesity and type 1 diabetes in adults.
价 格：￥电议型 号：T11408产 地：中国大陆
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T11405GLP-1 receptor agonist 4；化合物 T11405GLP-1 receptor agonist 4
GLP-1 receptor agonist 4 is a glucagon-like peptide-1 receptor (GLP-1R) agonist , has an EC50 of 64.5 nM. GLP-1 receptor agonist 4 can be used in the research for treatment of diabetes.
价 格：￥电议型 号：T11405产 地：中国大陆
