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T6524GW0742GW0742,inhibit,GW 610742,Inhibitor,PPAR,Peroxisome proliferator-activated receptors,GW-0742,GW
GW0742 (GW610742) is an effective and specific PPARδ agonist (EC50: 1 nM/1.1 μM/2 μM, for human PPARδ/α/γ).
价 格：￥电议型 号：T6524产 地：中国大陆
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T6738Z-FA-FMKSARS coronavirus,SARS-CoV,RRMs,DNA fragmentation,DEVDase,Caspase,Cathepsin,Inhibitor,externa
Z-FA-FMK can irreversibly inhibit cysteine protease and also inhibit effector caspases.
价 格：￥电议型 号：T6738产 地：中国大陆
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T9640Diethylnorspermine HCl
Diethylnorspermine HCl potently induces SSAT (spermidine/spermine N1-acetyltransferase) mRNA and effectively stabilizes SSAT enzyme activity.
价 格：￥电议型 号：T9640产 地：中国大陆
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T9076SpinosadInhibitor,neuronal,insecticide,antioxidant,Nicotinic acetylcholine receptors,Spinosad,fermen
Spinosad is a naturally-occurring insecticide found in the the soil bacterium S. spinosa.?It is a mixture of the macrocyclic lactones spinosyn A and spinosyn D, which act as agonists of insect nicotinic acetylcholinesterase receptors (nAChRs).
价 格：￥电议型 号：T9076产 地：中国大陆
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T60919SARS-CoV-2-IN-13
SARS-CoV-2-IN-13 (compound 5) is an analogue of niclosamide. SARS-CoV-2-IN-13 is more stable than niclosamide in human plasma and liver S9 enzymes assay. SARS-CoV-2-IN-13 can improve bioavailability and half-life when administered orally. SARS-CoV-2-IN-13 is a potent SARS-CoV-2 inhibitor with an IC 50 of 0.057 μM [1].
价 格：￥电议型 号：T60919产 地：中国大陆
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T7700LersivirineHIV,non-nucleoside reverse transcription,Reverse Transcriptase,HIV virus,UK 453061,Inhibi
Lersivirine(UK 453061) is a second-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) under development for HIV infection therapy.
价 格：￥电议型 号：T7700产 地：中国大陆
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T19786HematinInhibitor,Hematin,inhibit,fibrin clot,clotting factors,rat,hemostatic proteins,acute porphyri
Hematin is an iron-containing porphyrin. It is used for testing in vitro activities of the Rx-01 oxazolidinones against hospital and community pathogens.
价 格：￥电议型 号：T19786产 地：中国大陆
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T9066MerafloxacinMerafloxacin,frameshifting,SARS-CoV,bacteria,antibacterial,fluoroquinolone,Inhibitor,CI9
Merafloxacin is a fluoroquinolone antibacterial, which was also identified as a 1 PRF inhibitor of SARS-CoV-2.
价 格：￥电议型 号：T9066产 地：中国大陆
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T8374LJ570inhibit,Peroxisome proliferator-activated receptors,LJ-570,LJ 570,LJ570,Inhibitor,PPAR
LJ570 is the first PPARα/γ dual agonist (PPARα,PPARγ with EC50s of 1.05 and 0.12 μM, respectively[)
价 格：￥电议型 号：T8374产 地：中国大陆
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T9626CycloleucineIonotropic glutamate receptors,inhibit,glycine,NMDA,cytostatic,nucleic,Inhibitor,Cyclole
Cycloleucine is an antagonist of NMDA receptor associated glycine receptor with a Ki of 600 μM. Cycloleucine is also a competitive inhibitor of S-adenosyl-methionine mediated methylation with anxiolytic and cytostatic effects.
价 格：￥电议型 号：T9626产 地：中国大陆
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T7318Elimusertibresponse,damage,ATM/ATR,stress,Inhibitor,BAY1895344,tumors,DNA,instability,lymphomas,inhi
BAY 1895344 is a potent, highly selective and orally available ATR inhibitor with an IC50 of 7 nM.BAY 1895344 shows potent anti-tumor efficacy in monotherapy and strong combination potential with the targeted alpha therapy Radium-223 dichloride.
价 格：￥电议型 号：T7318产 地：中国大陆
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T9399Menin-MLL inhibitor 20Epigenetic Reader Domain,mixed-lineage,MeninMLL inhibitor 20,irreversible,leuk
Menin-MLL inhibitor 20 is an irreversible inhibitor of menin-MLL interaction with antitumor activities (WO2020142557A1, compound 6).
价 格：￥电议型 号：T9399产 地：中国大陆
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T23016MRS1220
MRS1220, a highly potent and selective human A3 adenosine receptor (hA3AR) antagonist with a Ki of 0.59 nM, has therapeutic potential for the research of diseases of the central nervous system. MRS1220 reduces glioblastoma tumor size and blood vessel formation in vivo.
价 格：￥电议型 号：T23016产 地：中国大陆
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T8169DecursinolDecursinol,inhibit,Inhibitor
Decursinol is isolated from the roots of Angelica Gigas with an antinociceptive effect. It also has anti-tumor and anti-metastasis activity.
价 格：￥电议型 号：T8169产 地：中国大陆
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T7108OmberacetamInhibitor,Omberacetam,iGluR,Ionotropic glutamate receptors,SGS 111,GVS 111,SGS111,inhibit
Omberacetam is a synthetic dipeptide that has been shown to produce positive nootropic and cognitive effects in animal models by a mechanism similar to other related racetam compounds.
价 格：￥电议型 号：T7108产 地：中国大陆
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TQ0002A-317491flux,calcium,P2X Receptor,A 317491,Inhibitor,neuropathic,inhibit,P2X2/3,A317491,P2X3,P2XRs,p
A-317491 is a non-nucleotide P2X3 ( Ki: 22 nM) and P2X2/3 receptor (Ki: 9 nM) antagonist, which inhibits calcium flux mediated by the receptors.
价 格：￥电议型 号：TQ0002产 地：中国大陆
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T8333Aurintricarboxylic acidTopoisomerase,Apoptosis,receptor,P2XRs,Influenza Virus,glioblastoma,anti-infl
Aurintricarboxylic acid is a strong inhibitor of topoisomerases and other nucleases. It is a potent inhibitor of ribonuclease and topoisomerase II by preventing the binding of the nucleic acid to the enzyme.
价 格：￥电议型 号：T8333产 地：中国大陆
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T9116SMCCSMCC,ADC Linkers,inhibit,Antibody-drug conjugates linkers,Inhibitor
N-Succinimidyl 4-(N-maleimidomethyl)cycl(SMCC), also known as succinimidyl-4-[N-maleimidomethyl]cyclohexane-1-carboxylate, is a heterobifunctional protein crosslinker.
价 格：￥电议型 号：T9116产 地：中国大陆
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T8689ChloroquineInhibitor,SARS coronavirus,Chloroquine,SARS-CoV,malaria,Autophagy,rheumatoid,COVID-19,Tol
Chloroquine is an autophagy and toll-like receptors (TLRs) inhibitor. Chloroquine is an antimalarial and anti-inflammatory agent widely used to treat malaria and rheumatoid arthritis. Chloroquine is highly effective in the control of SARS-CoV-2 (COVID-19) infection in vitro with EC50 of 1.13 μM.
价 格：￥电议型 号：T8689产 地：中国大陆
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TN6735Bigelovininhibit,Autophagy,Inhibitor,Retinoic acid receptors,Bigelovin,Retinoid X receptors,Apoptosi
Bigelovin is a selective retinoid X receptor α agonist. Bigelovin suppresses tumor growth through inducing apoptosis and autophagy via the inhibition of mTOR pathway regulated by ROS generation.It is also known as a potent cytotoxic sesquiterpene lactone from Inula sp.
价 格：￥电议型 号：TN6735产 地：中国大陆
