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产品数：86101
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T7837SR8278Duchenne muscular dystrophy,inhibit,metabolism,biological rhythm,Alzheimer’s disease,SR-8278,S
SR8278 is an REV-ERBα antagonist(EC50 = 0.47 μM), blocking activation of the receptor by the synthetic agonist GSK 4112
价 格：￥电议型 号：T7837产 地：中国大陆
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TN6832SulcatoneInhibitor,inhibit,Endogenous Metabolite,Sulcatone
6-Methyl-5-hepten-2-one is an alarm/panic pheromone produce by ant species.
价 格：￥电议型 号：TN6832产 地：中国大陆
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TQ0050NCGC00244536NCGC 00244536,inhibit,Histone Demethylase,NCGC00244536,Inhibitor,NCGC-00244536
NCGC00244536 is a potent KDM4B inhibitor (IC50: 10 nM).
价 格：￥电议型 号：TQ0050产 地：中国大陆
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T6725VU 0357121inhibit,VU-0357121,VU 0357121,VU0357121,Inhibitor,Metabotropic glutamate receptors,mGluR
VU0357121, a positive allosteric modulator of mGlu5 (EC50: 33 nM), is inactive or very weakly antagonizing at other mGlu receptor subtypes.
价 格：￥电议型 号：T6725产 地：中国大陆
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T87246-Methoxydihydrosanguinarinecancer,6-Methoxydihydrosanguinarine,SF-268,6 Methoxydihydrosanguinarine,
6-Methoxydihydrosanguinarine is a natural product. 6-Methoxydihydrosanguinarine shows strong cytotoxicity against MCF-7 and SF-268 cell lines with IC50 values of 0.61 μM and 0.54 μM, respectively.It has antibacterial activity against Methicillin-resistant Staphylococcus aureus (MRSA) strains with minimum inhibitory concentrations (MICs) ranging from1.9 to 3.9 microg/ml
价 格：￥电议型 号：T8724产 地：中国大陆
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T8192Pentacosanoic acidesters,fatty,Endogenous Metabolite,adrenoleukodystrophy,Inhibitor,cholesterol,acid
Pentacosanoic acid, belongs to the class of organic compounds known as very long-chain fatty acids.
价 格：￥电议型 号：T8192产 地：中国大陆
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T39668Methyl propyl disulfideMethyl propyl disulfide,anticaner,GST-P,inhibit,Inhibitor,volatile,Sulfur-con
Methyl propyl disulfide is a natural compound containing volatile sulfur produced in garlic and onions. Methyl propyl disulfide displays an anticaner effect.
价 格：￥电议型 号：T39668产 地：中国大陆
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T9230KM 91104V-ATPase human HSC,a3-b2 subunits,KM-91104,KM 91104,Inhibitor,KM91104,Proton Pump,cell-perme
KM 91104 is a cell permeable inhibitor of V-ATPase. KM91104 specifically targets the interaction between V-ATPase subunit A3 and subunit B2.
价 格：￥电议型 号：T9230产 地：中国大陆
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TQ0088Exatecan MesylateExatecan,Exatecan Mesylate,Topoisomerase,Inhibitor,inhibit
Exatecan Mesylate is a DNA topoisomerase I inhibitor (IC50: 2.2 μM, 0.975 μg/mL).
价 格：￥电议型 号：TQ0088产 地：中国大陆
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T60122AldometanibCompoundIA47
Aldometanib (LXY-05-029) is an orally active aldolase inhibitor. Aldometanib prevents FBP from binding to v-ATPase-associated aldolase and activates lysosomal AMPK. Aldometanib can be used for the research of metabolic homeostasis [1].
价 格：￥电议型 号：T60122产 地：中国大陆
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TN27032,3-Dihydroxy-4-methoxyacetophenoneinhibit,2,3Dihydroxy4methoxyacetophenone,Inhibitor,2,3 Dihydroxy
2,3-Dihydroxy-4-methoxyacetophenone is a natural product,it improves cognitive function and may be helpful for the treatment of Alzheimer´s disease.
价 格：￥电议型 号：TN2703产 地：中国大陆
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T6879LLY-507protein,inhibit,methyltransferase,methylation,breast,cancer,SMYD2,LLY-507,p53,Inhibitor,Histo
LLY-507 is an effective, cell-active, and specific inhibitor of protein-lysine Methyltransferase SMYD2.
价 格：￥电议型 号：T6879产 地：中国大陆
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T7309TAS-103 dihydrochlorideBMS247615,Topoisomerase,TAS-103,TAS103,inhibit,TAS 103 dihydrochloride,BMS-24
TAS-103 (dihydrochloride) is a novel anticancer agent targeting both topoisomerase (Topo) I and Topo II.
价 格：￥电议型 号：T7309产 地：中国大陆
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T9989WAY-298592neurological diseases,alzheimer’s disease,WAY 298592,Inhibitor,dementia,myasthenia gravis,
WAY-298592 is a small molecule used for high-throughput assays.
价 格：￥电议型 号：T9989产 地：中国大陆
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T7154trans-trans-Muconic acidtranstransMuconic acid,Endogenous Metabolite,inhibit,Inhibitor,trans trans M
trans-trans-Muconic acid is a urinary metabolite of benzene.
价 格：￥电议型 号：T7154产 地：中国大陆
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T80154-METHOXYCHALCONE4 METHOXYCHALCONE,4METHOXYCHALCONE
4-METHOXYCHALCONE is a natural compound that enhanced adipocyte differentiation,
价 格：￥电议型 号：T8015产 地：中国大陆
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T6446ClevudineOrthopoxvirus,half-life,nucleoside,DNA/RNA Synthesis,analog,Inhibitor,polymerase,Hepatitis
Clevudine is a synthetic pyrimidine analogue with activity against hepatitis B virus (HBV). Intracellularly, clevudine is phosphorylated to its active metabolites, clevudine monophosphate and triphosphate. The triphosphate metabolite competes with thymidine for incorporation into viral DNA, thereby causing DNA chain termination and inhibiting the function of HBV DNA polymerase (reverse transcriptase). Clevudine has a long half-life and shows significant reduction of covalently closed circular DN
价 格：￥电议型 号：T6446产 地：中国大陆
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TQ00011,4-CineoleTransient receptor potential channels,Inhibitor,1,4-Cineole,Endogenous Metabolite,inhibit
1,4-Cineole is a natural, oxygenated monoterpene. 1,4-Cineole can activate both human TRPM8 and human TRPA1.
价 格：￥电议型 号：TQ0001产 地：中国大陆
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T21967MEG hemisulfate
MEG hemisulfate is a potent and selective inhibitor of the inducible NO synthase (iNOS), with EC50s of 11.5, 110, and 60 μM for iNOS, ecNOS, and bNOS respectively in tissue homogenates. MEG hemisulfate is also a potent scavenger of peroxynitrite and inhibits peroxynitrite-induced oxidative processes. MEG hemisulfate has a protective effect in many experimental models of inflammation, including ischemia/reperfusion injury, periodontitis, hemorrhagic shock, inflammatory bowel disease, and endotoxi
价 格：￥电议型 号：T21967产 地：中国大陆
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T20094AdrenochromeAdrenochrome
Adrenochrome is a chemical compound produced by the oxidation of adrenaline.
价 格：￥电议型 号：T20094产 地：中国大陆
