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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
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T60093CHEMBL1380345
CHEMBL1380345 exhibits antibacterial activity against Staphylococcus aureus, Bacillus cereus, and Escherichia coli with pMIC values of 3.64, 3.56, and 3.70, respectively.
价 格：￥电议型 号：T60093产 地：中国大陆
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T7118DimethocaineInhibitor,inhibit,Dimethocaine,Dopamine Receptor
Dimethocaine is a local anesthetic with reported stimulant properties most similar to cocaine.
价 格：￥电议型 号：T7118产 地：中国大陆
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T60108PDGFR Tyrosine Kinase Inhibitor III
PDGFR Tyrosine Kinase Inhibitor III (PDGF Receptor Tyrosine Kinase Inhibitor III) is a multikinase inhibitor that inhibits PDGFR, EGFR, FGFR, PKA, and PKC, respectively. PDGFR Tyrosine Kinase Inhibitor III can be used for the research of amyotrophic lateral sclerosis [1].
价 格：￥电议型 号：T60108产 地：中国大陆
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T26815BILB-1941
BILB-1941 is an inhibitor of HCV NS5B polymerase and can be used in studies about HCV infection.
价 格：￥电议型 号：T26815产 地：中国大陆
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T80802-?Methylhexanoic acidInhibitor,2-?Methylhexanoic acid,2 ?Methylhexanoic acid,2?Methylhexanoic acid,
2-Methylhexanoic acid is a flavouring ingredient.
价 格：￥电议型 号：T8080产 地：中国大陆
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T8275(+)-IsopulegolInhibitor,Parasite,(+)-Isopulegol,inhibit,(+)Isopulegol,Terpenoid,phagostimulatory,fee
(+)-Isopulegol is a monoterpenoid from Mentha canadensis L.
价 格：￥电议型 号：T8275产 地：中国大陆
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T6670Silymarinthistle,angiogenesis,Inhibitor,hepatocellular,resistance,SARS coronavirus,chemopreventive,i
Silymarin (Silybin B) is a polyphenolic flavonoid that extracts from the milk thistle or seeds of Silybum marianum. It is used in the prevention and treatment of liver diseases.
价 格：￥电议型 号：T6670产 地：中国大陆
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T15387GLP-1R Antagonist 1GLP 1R Antagonist 1,GLP1R Antagonist 1
GLP-1R Antagonist 1 is an orally active, CNS penetrant and non-competitive glucagon-like peptide 1 receptor (GLP-1R) antagonist (IC50: 650 nM).
价 格：￥电议型 号：T15387产 地：中国大陆
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TN2376Fructo-oligosaccharide DP8/GF7inhibit,Fructo oligosaccharide DP8/GF7,Fructooligosaccharide DP8/GF7,F
Fructo-oligosaccharide DP8 / GF7 belongs to fructooligosaccharides (FOS) with degree of polymerization (DP=8). Fructo-oligosaccharides (FOS) are composed of 7 fructose units linked by (2→1)-β-glycosidic bonds and having a single D-glucosyl unit at the non-reducing end.
价 格：￥电议型 号：TN2376产 地：中国大陆
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T13378Z-Asp-CH2-DCBZAspCH2DCB,Z Asp CH2 DCB,Z-Asp-CH-2-DCB
Z-Asp-CH2-DCB is an irreversible inhibitor of broad spectrum caspase.
价 格：￥电议型 号：T13378产 地：中国大陆
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TL0016SulforapheneInhibitor,Sulforaphene,ERK,NF-κB,Nuclear factor-κB,Nuclear factor-kappaB,Extracellular s
Sulforaphene is a natural product isolated from radish seeds, exhibits an ED50 against velvetleaf seedlings approximately 2 x 10 -4 M. Sulforaphene promotes cancer cells apoptosis and inhibits migration via inhibiting EGFR, p-ERK1/2, NF‐κB and other signals.
价 格：￥电议型 号：TL0016产 地：中国大陆
