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产品数：86101
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TN2139Regaloside Blongiflorum,COX,Inhibitor,phenylpropanoid,iNOS,Lilium,Cyclooxygenase,COX-2,anti-inflamma
Regaloside B can inhibit the expression of iNOS and COX-2. Regaloside B is a phenylpropanoid isolated from Lilium longiflorum.It has anti-inflammatory activity.
价 格：￥电议型 号：TN2139产 地：中国大陆
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TN7038Regaloside HRegaloside H,gluconeogenesis,glucose,Inhibitor,inhibit
Regaloside H, a glyceryl phenylpropionate glycoside, is a gluconeogenesis inhibitor.
价 格：￥电议型 号：TN7038产 地：中国大陆
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T6946Pimavanserin tartrateInhibitor,Pimavanserin hemitartrate,5-hydroxytryptamine Receptor,ACP-103 hemita
Pimavanserin is an effective and specific serotonin 5-HT2A inverse agonist (pIC50: 8.73), used in the therapy of psychosis associated with Parkinson´s disease.
价 格：￥电议型 号：T6946产 地：中国大陆
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TN1962Myricetin 3-O-galactosideMyricetin 3 O galactoside,Myricetin 3Ogalactoside
Myricetin 3-O-galactoside has cytotoxicity, antioxidant, anti-genotoxic, antinociceptive and anti-inflammatory effects, the effects are related to peripheral inhibition of nitric oxide synthesis, mainly inducible nitric oxide synthase (iNOS).
价 格：￥电议型 号：TN1962产 地：中国大陆
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T9430Venadaparibinhibit,PARP,Venadaparib,IDX1197,Inhibitor,solid,IDX 1197,tumors,anticancer,poly ADP ribo
Venadaparib (IDX-1197) is a potent, selective and orally active PARP inhibitor with IC50s of 1.4 nM and 1.0 nM for PARP1 and PARP2, respectively. Venadaparib is insensitive to PARP-5. Venadaparib prevents the repair of DNA single-strand breaks (SSBs) and can be used in solid tumor research.
价 格：￥电议型 号：T9430产 地：中国大陆
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TN7025CanololCanolol
Canolol is an antioxidant phenolic compound that has potential use as a COX-2 inhibitor.
价 格：￥电议型 号：TN7025产 地：中国大陆
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T8247(+)-Aromadendrene(+)Aromadendrene,(+) Aromadendrene
(+)-Aromadendrene is a natural product that has significant antibacterial activity against the Gram-positive and Gram-negative bacteria.
价 格：￥电议型 号：T8247产 地：中国大陆
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TJS03684-Phenyl-7,8-dihydroxycoumarin4Phenyl7,8dihydroxycoumarin,inhibit,Inhibitor,bronchiectasiss,4 Phenyl
7,8-Dihydroxy-4-phenylcoumarin inhibits the activity of Staphylococcus aureus DNA helicase
价 格：￥电议型 号：TJS0368产 地：中国大陆
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T21060LNPC 567 acetateNPC 567 acetate
NPC 567 acetate is a bradykinin B2 antagonist and can be used in studies about the treatment of allergic airway disease.
价 格：￥电议型 号：T21060L产 地：中国大陆
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T9346CVN424penetrant,CVN 424,GPR6,inhibit,orally,CVN424,brain,Inhibitor,Parkinson,CVN-424,disease
CVN424 is a selective and novel GPR6 Inverse agonist effective in models of Parkinson Disease.
价 格：￥电议型 号：T9346产 地：中国大陆
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T26861BMS-817399BMS 817399
BMS-817399 is an orally active antagonist of CCR1 with IC50s of binding affinity and chemotaxis inhibition potencies and can be used in studies about rheumatoid arthritis.
价 格：￥电议型 号：T26861产 地：中国大陆
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T33429MK-2295MK 2295,MK2295
MK-2295 is a potent TRPV1 antagonist. MK-2295 can be used in studies about the treatment of chronic pain.
价 格：￥电议型 号：T33429产 地：中国大陆
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T73792-D08Ubiquitin ligase,Axl,2-D08,Tyro3,E3 ligating enzyme,Ubiquitin activating enzyme,Inhibitor,E1 ac
2-D08 is a synthetic flavone that inhibits sumoylation, also inhibits Axl with an IC50 of 0.49 nM.2-D08 showed anti-aggregatory and neuroprotective effect.
价 格：￥电议型 号：T7379产 地：中国大陆
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T8512BAY-545Inhibitor,BAY 545,BAY545,Adenosine Receptor,BAY-545,P1 receptor,inhibit
BAY-545 is an antagonist of A2B adenosine receptor(IC50 : 59 nM).
价 格：￥电议型 号：T8512产 地：中国大陆
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TP2219LAlytesin acetateAlytesin acetate
Alytesin acetate is an amphibian bombesin-like peptide.
价 格：￥电议型 号：TP2219L产 地：中国大陆
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T8232PEG6-(CH2CO2H)2PEG6 (CH2CO2H)2,PROTAC Linkers,PEG-6-(CH2CO2H)2,PEG6-(CH2CO2H)2,PEG6(CH2CO2H)2,inhibi
PEG6-(CH2CO2H)2 is a symmetric PEG PROTAC linker.
价 格：￥电议型 号：T8232产 地：中国大陆
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TMA0835Deapi-platycodin D3inhibit,Deapi-platycodin D3,Deapiplatycodin D3,Deapi platycodin D3,Deapi-platycod
Deapi-platycodin D3 is a natural product isolate from the root of Platycodon grandiflorum.
价 格：￥电议型 号：TMA0835产 地：中国大陆
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T6828ZL0420inhibit,Epigenetic Reader Domain,(E/Z)-ZL0420,BRD4,airway inflammation,immune response genes,Z
ZL0420 is a potent and selective bromodomain-containing protein 4 ( BRD4 ) inhibitor with nanomolar binding affinities to bromodomains (BDs) of BRD4. ZL0420 has IC 50 values of 27 nM against BRD4 BD1 and 32 nM against BRD4 BD2.
价 格：￥电议型 号：T6828产 地：中国大陆
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T9019JHU37152JHU37152,inhibit,hM3Dq,Clozapine,Inhibitor,DREADD,Muscarinic acetylcholine receptor,mAChR,hM
JHU 37152 is a Designer Receptors Exclusively Activated by Designer Drug (DREADD) agonist with Ki of 1.8 nM and 8.7 nM for human muscarinic acetylcholine M3 receptors (hM3Dq) and hM4Di in vitro, respectively. And EC50 values are 5 nM and 0.5 nM for hM3Dq and hM4Di in fluorescent and BRET-based assays in HEK-293 cells, respectively.
价 格：￥电议型 号：T9019产 地：中国大陆
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T7813α-MSHMelanocortin Receptor,hormone,αMSH,inhibit,Inhibitor,α MSH,neuroimmunomodulatory,inflammation,e
α-MSH is amide stimulates melanocortin 1 receptor that results in the activation of adenylyl cyclase.
价 格：￥电议型 号：T7813产 地：中国大陆
