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T6652Salbutamol hemisulfateAdrenergic Receptor,Beta Receptor,Inhibitor,Salbutamol hemisulfate,AH-3365 hem
Salbutamol Sulfate is a short-acting β2-adrenergic receptor agonist with an IC50 of 8.93 μM.
价 格：￥电议型 号：T6652产 地：中国大陆
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T6997SU6656PTK2 protein tyrosine kinase 2,Focal adhesion kinase,FAK,Akt,SU-6656,PTK2,Inhibitor,Protein ki
SU 6656 is a selective inhibitor of Src family kinases, with IC50 of 280 nM, 20 nM, 130 nM, and 170 nM for Src, Yes, Lyn, and Fyn, respectively.
价 格：￥电议型 号：T6997产 地：中国大陆
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T6653Salmeterol Xinafoatecorticosteroid,Salmeterol,Beta Receptor,therapy,inhibit,Adrenergic Receptor,GR 3
Salmeterol Xinafoate is a long-acting β2-adrenergic receptor agonist with anti-inflammatory effects, used in the treatment of asthma symptoms and chronic obstructive pulmonary disease (COPD) symptoms.
价 格：￥电议型 号：T6653产 地：中国大陆
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T6654SaponinsSaponins,Inhibitor,Fungal,inhibit,Bacterial
Sapogenins glycosides are a mixture of triterpene and steroid saponins isolated from medicinal plants such as Aesculus hippocastanum L., Hedera helix L. and Ruscus aculeatus L., which are claimed to be effective for the treatment/prevention of venous insufficiency.
价 格：￥电议型 号：T6654产 地：中国大陆
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T7665[Leu5]-Enkephalin TFA(58822-25-6(free bas))[Leu5] Enkephalin TFA(58822 25 6(free bas)),[Leu-5]-Enkep
[Leu5]-Enkephalin is the most potent δ-receptor ago
价 格：￥电议型 号：T7665产 地：中国大陆
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TP1895L1KYL acetate(676657-00-4 free base)KYL acetate(676657 00 4 free base),KYL acetate(676657004 free base
EphA4 receptor tyrosine kinase inhibitor (Kd = 0.8 μM); inhibits EphA4-EphrinA5 interactions (IC50 = 6.34 μM). Prevents AβO induced synaptic damage, dendritic spine loss and prevents the blocking of LTP in hippocampal CA3-CA1 transmissions. Exhibits a long half life in cell culture media (8 and 12 hours in PC3 and C2C12 media respectively). Neuroprotective.
价 格：￥电议型 号：TP1895L1产 地：中国大陆
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TQ0167ZimlovisertibInterleukin-1 receptor associated kinase,inhibit,Zimlovisertib,Inhibitor,IL-1R associat
PF06650833 is an effective, selective and orally active inhibitor of interleukin-1 receptor-associated kinase 4 (IRAK4) (IC50s: 0.2 and 2.4 nM in the cell and PBMC assay).
价 格：￥电议型 号：TQ0167产 地：中国大陆
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T12629LMIK665
MIK665 (S-64315) has an inhibitory effect on myeloid leukemia.
价 格：￥电议型 号：T12629L产 地：中国大陆
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T6S1665IrisflorentinNOS,Irisflorentin,inhibit,Inhibitor,iNOS,Nitric oxide synthases,macrophages,inflammator
1. Irisflorentin blocks apoptosis pathways, by exerting its effects by promoting rpn-3 expression to enhance the activity of proteasomes and down-regulating egl-1 expression. 2. Irisflorentin has anti-inflammatory mechanism in LPS-activated RAW 264.7 macrophages, by reducing the transcriptional and translational levels of inducible nitric oxide synthase (iNOS) as well as the production of NO.
价 格：￥电议型 号：T6S1665产 地：中国大陆
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T28374PF-06651481-00
PF-06651481-00 is a Bosutinib analog and a Bcr-Abl inhibitor.
价 格：￥电议型 号：T28374产 地：中国大陆
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T8665Adinazolamγ-Aminobutyric acid Receptor,sickness,antihistamine,GABA Receptor,inhibit,Adinazolam,U-411
Adinazolam is a triazolobenzodiazepine (TBZD). It possesses anxiolytic, anticonvulsant, sedative, and antidepressant properties.
价 格：￥电议型 号：T8665产 地：中国大陆
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T6659SB 415286inhibit,GSK-3,Inhibitor,Glycogen synthase kinase 3,Glycogen synthase kinase-3,Apoptosis,SB-
SB415286 is a potent GSK3α inhibitor with IC50/Ki of 78 nM/31 nM with equally effective inhibition of GSK-3β.
价 格：￥电议型 号：T6659产 地：中国大陆
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T11665Ionomycin calciumCa2+ channels,PKC,ionophore,Calcium Channel,Ionomycin,SQ 23377,Ionomycin calcium,An
lonomycin calcium is a potent, selective calcium ionophore and an antibiotic produced by Streptomyces conglobatus. also induces the activation of protein kinase C (PKC). Ionomycin calcium is highly specific for divalent cations (Ca>Mg>Sr=Ba). Ionomycin promotes apoptosis.
价 格：￥电议型 号：T11665产 地：中国大陆
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T6665Sertaconazole nitrateCOX-2,Inhibitor,inhibit,Sertaconazole nitrate,MCF-7,HaCaT,Candida,HeLa,p38 MAPK
Sertaconazole nitrate, a topical broad-spectrum antifungal, is developed to supply an additional agent for the treatment of superficial cutaneous and mucosal infections.
价 格：￥电议型 号：T6665产 地：中国大陆
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T6651LSafinamide
Safinamide is a reversible and selective monoamine oxidase B (IC50 0.098μM) inhibitor, reducing the degradation of dopamine, and a glutamate release inhibitor (IC50 8μM). It also inhibits dopamine reuptake. Safinamide also blocks sodium and calcium channels. Potential additional uses of Safinamide might be Parkinson´s disease, restless leg syndrome and epilepsy.
价 格：￥电议型 号：T6651L产 地：中国大陆
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T6658SB-408124SB408124,SB 408124,inhibit,water,membrane,selectivity,Inhibitor,Orexin Receptor (OX Recepto
SB408124 is a non-peptide antagonist for OX1 receptor with Ki of 57 nM and 27 nM in both whole cell and membrane, respectively, exhibits 50-fold selectivity over OX2 receptor.
价 格：￥电议型 号：T6658产 地：中国大陆
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T6728VUF 101665-HT3A,VUF 10166,VUF10166,VUF-10166,neurotransmission,5-HT3AB,inhibit,5-HT3 receptor ligand
VUF10166 is a novel, potent and competitive antagonist for 5-HT3A receptor with Ki of 0.04 nM, its affinity at 5-HT3AB receptor is significantly lower.
价 格：￥电议型 号：T6728产 地：中国大陆
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T14911CD2665CD2665,CD-2665
CD2665 is an orally active antagonist of retinoic acid receptor (RAR). For RARγ and RARβ, the Kis are 110 nM and 306 nM.
价 格：￥电议型 号：T14911产 地：中国大陆
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T6651Safinamide mesylateEMD 1195686,Monoamine Oxidase,EMD-1195686,neuroprotective,inhibit,OGD/R,Glucose,n
Safinamide Mesylate, a mesylate salt of Safinamide, can reversibly and specifically inhibit MAO-B (IC50: 98 nM), has 5918-fold selectivity against MAO-A.
价 格：￥电议型 号：T6651产 地：中国大陆
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T22671CJ 0334665-HT Receptor,Inhibitor,inhibit,gastroprokinetic,CJ-033466,CJ033466,Serotonin Receptor,gast
CJ 033466 is a selective partial agonist of 5-HT4 receptor (EC50 = 9 nM) with gastroprokinetic effect.
价 格：￥电议型 号：T22671产 地：中国大陆
