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产品数：86101
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TN27302,5-Dihydroxybenzaldehyde2,5Dihydroxybenzaldehyde,inhibit,mastitis,2,5 Dihydroxybenzaldehyde,antisep
2,5-Dihydroxybenzaldehyde has antioxidant activity against Mycobacterium avium subsp. Paratuberculosis. 2,5-Dihydroxybenzaldehyde also inhibits S. aureus strains(MIC50: 500 mg/L).
价 格：￥电议型 号：TN2730产 地：中国大陆
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T8730BMS986260nuclear translocation,TGFβR1,BMS-986260,FOXP3 expression,MINK,Transforming growth factor be
BMS-986260 is a selective, and orally bioavailable TGFβR1 inhibitor(IC50 = 1.6 nM).
价 格：￥电议型 号：T8730产 地：中国大陆
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T61111UCB-5307
UCB-5307 is a TNF signaling inhibitor with a K D of 9 nM. UCB-5307 can penetrate the preformed hTNF/hTNFR1 complex [1].
价 格：￥电议型 号：T61111产 地：中国大陆
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T30828CGP 35949
CGP 35949 is an LTD4 antagonist with phospholipase inhibitory activity.
价 格：￥电议型 号：T30828产 地：中国大陆
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T9303MRTX1133KRAS,Ras,MRTX 1133,G12D,cells,active,wild-type,phosphorylation,mutant,MRTX1133,inactive,ERK,
MRTX1133 is a potent, selective, and noncovalent inhibitor of KRAS G12D. MRTX1133 exhibits an estimated KD against KRAS G12D of 0.2 pM. MRTX1133 inhibits mutant KRAS-dependent signal transduction by preventing SOS1-catalyzed nucleotide exchange and/or formation of the KRAS G12D/GTP/RAF1 complex. MRTX1133 selectively inhibits KRAS G12D mutant tumor cells with no effect on KRAS wild-type. MRTX1133 exhibits single digit nanomolar activity in cellular assays and marked in vivo efficacy in tumor mode
价 格：￥电议型 号：T9303产 地：中国大陆
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T9373DCH36_06HATs,hypoacetylation,Apoptosis,DCH-36_06,inhibit,antiproliferative,p300,HAT,DCH36_06,Inhibit
DCH36_06? as a bona fide is a potent p300/CBP inhibitor
价 格：￥电议型 号：T9373产 地：中国大陆
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T6S0630HypaconitineInhibitor,TNFR,TNF Receptor,inhibit,Tumor Necrosis Factor Receptor,Hypaconitine
Hypaconitine, an active and highly toxic constituent derived from Aconitum species, has anti-inflammatory activity, is widely used to treat rheumatism.
价 格：￥电议型 号：T6S0630产 地：中国大陆
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TQ0126Mirodenafil dihydrochlorideSK3530,Inhibitor,Wnt,Beta catenin,Mirodenafil,SK-3530,MRC-5 cells,Miroden
Mirodenafil dihydrochloride is a PDE-5 inhibitor developed for the treatment of erectile dysfunction.
价 格：￥电议型 号：TQ0126产 地：中国大陆
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T9212IMB-301Inhibitor,APOBEC3G,HIV-1,inhibit,Human immunodeficiency virus,IMB 301,HIV,IMB-301,replication
IMB-301 is a small molecular inhibitor via virtual screening according to the hA3G model.
价 格：￥电议型 号：T9212产 地：中国大陆
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TP1271LCalmodulin-Dependent Protein Kinase II 290-309 acetateCalmodulin Dependent Protein Kinase II 290 309
Calmodulin-Dependent Protein Kinase II 290-309 acetate is an effective antagonist of Ca2+/calmodulin-dependent protein kinase II (IC50 = 52 nM).
价 格：￥电议型 号：TP1271L产 地：中国大陆
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TP1330Cyclo(RADfK)Cyclo(RADfK),Inhibitor,inhibit,Integrin
Cyclo(RADfK) is a selective α(v)β(3) integrin ligand that has been extensively used for research, therapy, and diagnosis of neoangiogenesis.Cyclo(RADfK) is a negative control for the cyclo (-RGDfK-), the RGD peptide. RGD peptides are modulators of cell adhesion and are recognized by several members of the integrin family.
价 格：￥电议型 号：TP1330产 地：中国大陆
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TQ0302ThapsigarginCa2+ channels,stress,inhibit,unfolded,Thapsigargin,Inhibitor,Apoptosis,Ca channels,Calci
Thapsigargin is a microsomal Ca2+-ATPase inhibitor and Endoplasmic Reticulum stress-inducing agent.
价 格：￥电议型 号：TQ0302产 地：中国大陆
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T12307OMDM-6OMDM 6,OMDM6
OMDM-6 is a dual agonist of TRPV1(EC50 = 75 nM) and CB1 (Ki = 3.2 μM). OMDM-6 inhibits anandamide cellular uptake with a Ki of 7.0 μM.
价 格：￥电议型 号：T12307产 地：中国大陆
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T6633RanolazineNa+ channels,CVT-303,Ca2+ channels,inhibit,Sodium Channel,Ranolazine,Inhibitor,Calcium Cha
Ranolazine is a calcium uptake inhibitor via the sodium/calcium channel, used to treat chronic angina. It affects the sodium-dependent calcium channels during myocardial ischemia in rabbits by altering the intracellular sodium level.
价 格：￥电议型 号：T6633产 地：中国大陆
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T8426EncequidarMDR1,P-gp,Cluster of differentiation 243,inhibit,HM 30181,Encequidar,P-glycoprotein,Multid
Encequidar is a potent and selective P-glycoprotein inhibitor.
价 格：￥电议型 号：T8426产 地：中国大陆
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T6521GSK 2830371GSK-2830371,Inhibitor,GSK 2830371,Phosphatase,inhibit
GSK2830371 is an orally active, allosteric Wip1 phosphatase inhibitor with IC50 of 6 nM.
价 格：￥电议型 号：T6521产 地：中国大陆
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T7530PD146176inhibit,tau,brain,triple,NSC-168807,PD146176,Autophagy,pathology,amyloidosis,transgenic,reti
PD146176 is an inhibitor of 15-Lipoxygenase (15-LO) , it inhibits rabbit reticulocyte 15-LO with Ki of 197 nM and IC50 of 0.54 μM. PD146176 reverses cognitive impairment, brain amyloidosis, and tau pathology by stimulating autophagy in aged triple transgenic mice.
价 格：￥电议型 号：T7530产 地：中国大陆
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T22992ML 10302 hydrochlorideML 10302 hydrochloride
ML 10302 hydrochloride is a specific agonist 5-HT4 and binds 5-HT receptors with Kis of 1.07 nM and 782 nM for 5-HT4 and 5-HT3.
价 格：￥电议型 号：T22992产 地：中国大陆
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T24816SP-100030
SP-100030 is a potent NF-κB and activator protein-1 (AP-1) double inhibitor (IC50s=50 and 50 nM, respectively). SP-100030 inhibits IL-2, IL-8, and TNF-alpha production in Jurkat and other T cell lines. SP-100030 decreases murine collagen-induced arthritis (CIA).
价 格：￥电议型 号：T24816产 地：中国大陆
