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T10786Charantin；化合物 T10786Charantin
Charantin is a steroidal saponin isolated from Momordica charantia. It increases the release of insulin and slowing down gluconeogenesis. Charantin can inhibit GSK-3.
价 格：￥电议型 号：T10786产 地：中国大陆
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T10785Chalcone 4 hydrate；查耳酮 4 水合物Chalcone 4 hydrate
Chalcone 4 hydrate, an anti-parasite compound, inhibits the growth of Theileria and Babesia.
价 格：￥电议型 号：T10785产 地：中国大陆
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T10784CH6953755；化合物CH6953755CH6953755
CH6953755 is an orally active, potent and selective YES1 kinase inhibitor (IC50:1.8 nM).CH6953755 has anticancer activity and inhibits cancer cell proliferation by inhibiting YES1 kinase.
价 格：￥电议型 号：T10784产 地：中国大陆
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T10783CGS 15435；化合物CGS 15435CGS 15435
CGS 15435 is a potent thromboxen (TxA2) synthetase inhibitor (IC50: 1 nM). CGS 15435 acts on PGI2 synthase, cyclooxygenase and liposynthase with much less selectivity than on thromboxin synthase.
价 格：￥电议型 号：T10783产 地：中国大陆
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T10782CGP52411；化合物CGP52411DAPH；DAPH
CGP52411 is an orally active, and ATP-competitive inhibitor of EGFR (IC50: 0.3 μM). CGP52411 blocks the toxic influx of Ca2+ ions into neuronal cells and dramatically inhibits and reverses the formation of β-amyloid Aβ42 fibril aggregates. CGP52411 can be used in studies about Alzheimer´s diseases.
价 格：￥电议型 号：T10782产 地：中国大陆
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T10780CGP-53153；化合物 T10780CGP-53153
CGP-53153 is a steroidal inhibitor of 5 alpha-reductase (IC50s: 36 and 262 nM in rat and human prostatic tissue).
价 格：￥电议型 号：T10780产 地：中国大陆
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T1078Sulfadimethoxine；磺胺二甲氧嗪Sulphadimethoxine；Sulphadimethoxine|||磺胺二甲氧嗪
Sulfadimethoxine (Sulphadimethoxine) is a sulfanilamide that is used as an anti-infective agent.
价 格：￥电议型 号：T1078产 地：中国大陆
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T10778CGP 20712 A；化合物 CGP 20712 ACGP 20712 mesylate；CGP 20712 mesylate
CGP 20712 A (CGP 20712 mesylate) is a selective and potent β1-adrenergic receptor antagonist (IC50: 0.7 nM) with antihypertensive activity that reverses RKT-induced gastric relaxation.
价 格：￥电议型 号：T10778产 地：中国大陆
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T10766Ceritinib D7；化合物 T10766LDK378 D7；LDK378 D7
Ceritinib D7 (LDK378 D7) is a deuterium-labeled Ceritinib. Ceritinib is an ATP-competitive inhibitor of ALK tyrosine kinase.
价 格：￥电议型 号：T10766产 地：中国大陆
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T10678Carboxypeptidase G2 (CPG2) Inhibitor；羧肽酶G2抑制剂CPG2 Inhibitor|||Carboxypeptidase G2 Inhibitor；CPG2 Inh
Carboxypeptidase G2 (CPG2) Inhibitor (CPG2 Inhibitor) is a new CPG2 Inhibitor with antitumor activity.
价 格：￥电议型 号：T10678产 地：中国大陆
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T10595LBQ-788 sodium salt；化合物 T10595LBQ-788 sodium salt
BQ-788 sodium salt is a potent and selective antagonist of ETB receptor(ETB receptors with an IC50 of 1.2 nM in human Girrardi heart cells).
价 格：￥电议型 号：T10595L产 地：中国大陆
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T10595BQ-788；化合物BQ-788BQ788；BQ788
BQ-788 is a selective and potent ETB receptor antagonist with potential hypertensive activity.BQ-788 inhibits ET-1 binding to ETB receptors and inhibits exogenous ET-1-induced elevation of coronary artery perfusion pressure.
价 格：￥电议型 号：T10595产 地：中国大陆
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T10552Bitopertin (R enantiomer)；化合物 T10552RO4917838 (R enantiomer)|||RG1678 (R enantiomer)|||Bitopertin R
Bitopertin R enantiomer (RG1678 R enantiomer) is the R-enantiomer of Bitopertin. Bitopertin is a noncompetitive glycine reuptake inhibitor and inhibits glycine uptake at human GlyT1 (IC50: 25 nM).
价 格：￥电议型 号：T10552产 地：中国大陆
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T10478BAY-Y 3118化合物 T10478BAY-Y3118|||BAY Y 3118|||BAY-Y 3118
BAY-Y 3118, a new chlorofluoroquinolone, has antimicrobial activity.
价 格：￥电议型 号：T10478产 地：中国大陆
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T10475BAY-784；化合物 T10475BAY-784
BAY-784 is a gonadotropin-releasing hormone receptor (GnRH-R) antagonist (IC50s: 21 and 24 nM for human and rat GnRH-R).
价 格：￥电议型 号：T10475产 地：中国大陆
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T10473BAY-678；化合物BAY-678BAY-678
BAY-678 is a human neutrophil elastase (HNE; IC50: 20 nM) inhibitor with oral bioactivity, potency and selectivity.BAY-678 is a chemical probe recommended by the Structural Genomics Consortium (SGC).
价 格：￥电议型 号：T10473产 地：中国大陆
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T10378Artelinic acid；化合物 Artelinic acidArtelinic acid
Artelinic acid is a water-soluble artemisinin analog with antimalarial activity and is used for the treatment of multi-drug resistant strains of Plasmodium falciparum.
价 格：￥电议型 号：T10378产 地：中国大陆
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T10354APX-115；化合物APX-115Ewha-18278；Ewha-18278
APX-115 (Ewha-18278) (Ewha-18278) is a potent, orally active pan NADPH oxidase (Nox) inhibitor (Kis: 1.08 μM, 0.57 μM, and 0.63 μM for Nox1, Nox2, and Nox4). APX-115 effectively prevents kidney injury.
价 格：￥电议型 号：T10354产 地：中国大陆
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T10353APX-115 free base；化合物APX-115 free baseEwha-18278 free base；Ewha-18278 free base
APX-115 free base (Ewha-18278 free base) (Ewha-18278 free base) is a potent, orally active pan NADPH oxidase (Nox) inhibitor (Kis: 1.08 μM, 0.57 μM, and 0.63 μM for Nox1, Nox2, and Nox4). APX-115 effectively prevents kidney injury.
价 格：￥电议型 号：T10353产 地：中国大陆
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T10278Alamethicin；丙甲菌素Alamethicin
Alamethicin is isolated from Trichoderma viride. It is a channel-forming peptide antibiotic and induces voltage-gated conductance in model and cell membranes.
价 格：￥电议型 号：T10278产 地：中国大陆
