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T12920Sirt2-IN-1Sirt2IN1,Sirt2 IN 1,Sirt-2-IN-1
Sirt2-IN-1 is an inhibitor of sirtuin 2 (IC50 = 163 nM).
价 格：￥电议型 号：T12920产 地：中国大陆
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T21720GP-82996
GP-82996 (CINK4) is a pharmacological inhibitor of CDK4/6. GP-82996 has IC 50 s of 1.5, 5.6 and 25 μM for CDK4/cyclin D1, CDK6/cyclin D1 and Cdk5/p35, respectively. GP-82996 induces the apoptosis of cancer cells U2OS which can be used in the research of cancer [1] [2].
价 格：￥电议型 号：T21720产 地：中国大陆
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T38604C12-200C-12-200,C12200,C12 200
C12-200 is a benchmark ionizable cationic lipidoid along with helper lipids and can be used in the delivery of mRNA.
价 格：￥电议型 号：T38604产 地：中国大陆
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T9518Inarigivir ammoniuminhibit,HCV,HBV,RIG-I,Huh7,SB9000,ORI-9020,SB 9000,SB-9000,antiviral,Inarigivir a
Inarigivir ammonium is a dinucleotide antiviral compound that significantly reduces HBV DNA in transgenic mice expressing hepatitis B virus. Inarigivir is an agonist of retinoic acid-inducible gene-I (RIG-I) that activates intracellular innate immunity.
价 格：￥电议型 号：T9518产 地：中国大陆
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T978520-(tert-Butoxy)-20-oxoicosanoic acid20 (tert Butoxy) 20 oxoicosanoic acid,Inhibitor,inhibit,ADC Lin
20-(tert-Butoxy)-20-oxoicosanoic acid is a alkyl-chain-based PROTAC linker. 20-(tert-Butoxy)-20-oxoicosanoic acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T9785产 地：中国大陆
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T8312DerenofyllineInhibitor,P1 receptor,Derenofylline,Adenosine Receptor,SLV320,fibrosis,uraemic,SLV-320,
Derenofylline is a selective and potent adenosine A(1) antagonist in vitro (Ki=1 nM)
价 格：￥电议型 号：T8312产 地：中国大陆
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TQ0205Procyanidin B1Procyanidin B1,Toll-like Receptor (TLR),Inhibitor,Procyanidin B-1,inhibit,Procyanidin
Procyanidin B1, isolated from commonly eaten fruits, binds to the TLR4/MD-2 complex and has anti-inflammatory activity.
价 格：￥电议型 号：TQ0205产 地：中国大陆
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TP2204LCCK Octapeptide, non-sulfated acetateCCK Octapeptide, nonsulfated acetate,CCK Octapeptide, non sulfa
CCK Octapeptide, non-sulfated acetate is a synthetic desulfated peptide of cholecystokinin.
价 格：￥电议型 号：TP2204L产 地：中国大陆
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TP2051LCTCE 9908 acetateCTCE 9908 acetate
CTCE 9908 acetate is an antagonist of CXCR4 and inhibits migration in CXCR4-expressing ovarian cancer cells.
价 格：￥电议型 号：TP2051L产 地：中国大陆
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T17006TC-I 2014TCI 2014,TC I 2014
TC-I 2014 shows antiallodynic properties in pain models. TC-I 2014 is a potent and orally active Benzimidazole-containing transient receptor potential melastatin 8 antagonist (IC50: 0.8 nM, 3.0 nM, and 4.4 nM for canine, human and rat channels respectively).
价 格：￥电议型 号：T17006产 地：中国大陆
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T7007UNC2025Inhibitor,inhibit,FLT3,leukemia,CD135,Fms like tyrosine kinase 3,acute,Cluster of differentia
UNC-2025（ IC50 of 0.74 nM and 0.8 nM） is a potent and orally bioavailable dual MER/FLT3 inhibitor. UNC-2025 is about 20-fold selectivity higher than Axl and Tyro3.
价 格：￥电议型 号：T7007产 地：中国大陆
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T20692LSchistoflrfamide acetateSchistoflrfamide acetate
Schistoflrfamide acetate is isolated from the grasshopper, Schistocerca gregaria. Schistoflrfamide acetate elicited an immediate effect on the basal membrane potential of the opalescent tubule gland cells in insects.
价 格：￥电议型 号：T20692L产 地：中国大陆
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T7320TozadenantP1 receptor,SYN-115,Adenosine Receptor,SYN 115,Tozadenant,Inhibitor,inhibit
Tozadenant is an adenosine A2A receptor antagonist(Ki of 11.5 nM and 6 nM on human and rhesus,respectively)
价 格：￥电议型 号：T7320产 地：中国大陆
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T7206L2-Iminobiotin hydrobromideNitric oxide synthases,NOS,NO Synthase,2-Iminobiotin,2Iminobiotin hydrobro
2-Iminobiotin hydrobromide is a cyclic guanidino analog of biotin that acts as a reversible inhibitor of inducible nitric oxide synthase (iNOS) and neuronal NOS (nNOS; Ki of 21.8 and 37.5 μM for mouse iNOS and rat nNOS, respectively).
价 格：￥电议型 号：T7206L产 地：中国大陆
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TN4220Homobutein
Homobutein is a dual inhibitor of HDACs and NF-κB with IC50s of 190 and 38 μM. Homobutein is an iron chelator with anticancer, anti-inflammatory, antiparasite, and antioxidation activities.
价 格：￥电议型 号：TN4220产 地：中国大陆
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T9020GSK620Inhibitor,oral,GSK 620,phenotype,selectivity,GSK-620,whole,anti-inflammatory,GSK620,Epigenetic
GSK620 is a pan-BD2 inhibitor, which shows an anti-inflammatory phenotype in human whole blood with excellent broad selectivity, developability, and in vivo oral pharmacokinetics.GSK620 is highly selective for the BET-BD2 family of proteins, with >200-fold selectivity over all other bromodomains. GSK620 shows an anti-inflammatory phenotype in human whole blood.
价 格：￥电议型 号：T9020产 地：中国大陆
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T13553Arimoclomolaggregation,Heat shock proteins,HSP,co-inducer,system,BRX220,motor,Arimoclomol,inhibit,ub
Arimoclomol is a co-inducer of heat shock proteins (HSP) and can be used in studies about the treatment of amyotrophic lateral sclerosis (ALS).
价 格：￥电议型 号：T13553产 地：中国大陆
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TCS2070Homogentisic acidHomogentisic acid,inhibit,Endogenous Metabolite,Inhibitor
1. Homogentisic acid shows interesting antioxidant and antiradical activities, and protective effect against thermal-cholesterol degradation, comparable to those of well known antioxidants. 2. Homogentisic acid is the primary precursor of melanin synthesis in Vibrio cholerae, a Hyphomonas strain, and Shewanella colwelliana. 3. A derivative of homogentisic acid which inhibits Pfnek-1 with an IC(5) around 1.8 muM, this product is moderately active in vitro against a FcB1 P. falciparum strain (IC(5
价 格：￥电议型 号：TCS2070产 地：中国大陆
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T8727TH1020interaction,inhibit,Bacterial,flagellin,TH-1020,TH1020,Toll-like Receptor (TLR),TLR5,protein-p
TH1020 is a novel Inhibitor of Toll-Like Receptor 5 (TLR5)/Flagellin Complex with promising activity (IC50 =0.85±0.12 μm) and specificity.
价 格：￥电议型 号：T8727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
