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产品数：86101
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T21980PD 198306MAPK,inhibit,neuropathic,Inhibitor,MAP2K,rabies,mitogen-activated protein,drug,MAPKK,PD-198
PD 198306 is a selective inhibitor of MAPK/ERK-kinase (MEK) with antihyperalgesic effects. PD 198306 reduces the Streptozocin-induced increase in the level of active ERK1.
价 格：￥电议型 号：T21980产 地：中国大陆
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T11986Mebeverine acidDrug Metabolite,inhibit,Mebeverine acid,Inhibitor
Mebeverine acid is a secondary metabolite of Mebeverine and can be used as a marker of oral exposure to Mebeverine.
价 格：￥电议型 号：T11986产 地：中国大陆
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T8722iKIX1antifungal,Inhibitor,drug-resistant,Fungal,CgGal11A,CgPdr1,infection,C. glabrata,iKIX1,inhibit,
iKIX1 is an Pdr1-dependent gene activation. It re-sensitizes drug-resistant C. glabrata to azole antifungals in vitro and in animal models for disseminated and urinary tract C. glabrata infection.
价 格：￥电议型 号：T8722产 地：中国大陆
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T9100BP 897inhibit,BP-897,BP897,cocaine drug-seeking,BP 897,Dopamine Receptor,Inhibitor,addiction,behavio
2-Naphthalenecarboxamide, N-[4-[4-(2-methoxyphenyl)-1-piperazinyl]butyl]- is a potent and selective dopamine D3 receptor agonist, and a weak dopamine D2 receptor antagonist, with Kis of 0.92 nM and 61 nM for D3 and D2 receptors, and shows low affinities at D1 and D4 receptors (Kis, 3 and 0.3 μM, respectively).
价 格：￥电议型 号：T9100产 地：中国大陆
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T9014SKI-178resistant,SphK,cytotoxic,myeloid,Inhibitor,Apoptosis,leukemia,multi-drug,inhibit,SKI-178,canc
SKI-178 is a sphingosine kinase 1 (SphK1) inhibitor with IC50 of 0.1-1.8 μM. It induces prolonged mitosis followed by apoptotic cell death through the intrinsic apoptotic cascade. The sustained activation of CDK1 during prolonged mitosis, mediated by SKI-178 leads to the simultaneous phosphorylation of the prosurvival Bcl-2 family members, Bcl-2 and Bcl-xl, as well as the phosphorylation and subsequent degradation of Mcl-1.
价 格：￥电议型 号：T9014产 地：中国大陆
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T9784Docosanedioic acid?Antibody-drug conjugates linkers,Docosanedioic acid,inhibit,Docosanedioic acid?,I
BEHENIC ACID is a alkyl-chain-based PROTAC linker. BEHENIC ACID is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T9784产 地：中国大陆
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T6741SPDPSPDP,ADC Linkers,Antibody-drug conjugates linkers,inhibit,Inhibitor
SPDP is a short-chain crosslinker, which is used for amine-to-sulfhydryl conjugation via NHS-ester and pyridyldithiol reactive groups that form cleavable (reducible) disulfide bonds with cysteine sulfhydryls. SPDP could activate equal amounts of anti-CD11c and anti-CTLA-4 Abs (in borate buffered saline; pH 8.5).
价 格：￥电议型 号：T6741产 地：中国大陆
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T8115MenthofuranInhibitor,peppermint oil biosynthesis,inhibit,monoterpene reductase,Menthofuran,Drug Meta
Menthofuran is a natural product.
价 格：￥电议型 号：T8115产 地：中国大陆
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T8175DL-LaudanosineDrug Metabolite,DLLaudanosine,DL Laudanosine,DL-Laudanosine,Inhibitor,inhibit
Laudanosine is a recognized metabolite of atracurium and cisatracurium.
价 格：￥电议型 号：T8175产 地：中国大陆
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T9982PU23MRP4,PU23,resistance,PU-23,Inhibitor,inhibit,protein,PU 23,6-Mercaptopurine,multidrug
PU 23 is an inhibitor of multidrug-resistant protein 4 (MRP4).
价 格：￥电议型 号：T9982产 地：中国大陆
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T8924MFCD28987368MFCD28987368,ADC Linkers,inhibit,MFCD-28987368,Antibody-drug conjugates linkers,Inhibito
MFCD28987368 is a chemical compound
价 格：￥电议型 号：T8924产 地：中国大陆
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TN4660NiranthinNiranthin,inhibit,anti-leishmanial agent,leishmaniasis,Topoisomerase,Parasite,drug-resistan
Niranthin is a potent anti-leishmanial agent, inhibits the relaxation activity of heterodimeric type IB topoisomerase of L. donovani and acts as a non-competitive inhibitor interacting with both subunits of the enzyme. Niranthin also exhibits anti-hepatitis B virus, antiinflammatory and antiallodynic actions.
价 格：￥电议型 号：TN4660产 地：中国大陆
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TN6512TectolHL60,Ftase,Inhibitor,cell,anti-malarial,Parasite,cytotoxic,inhibit,leukemia,drug-resistant,Tec
Tectol has anti-plasmodial activity, it as a moderately active growth inhibitor with an IC50 of 3.44±0.20μM. It exhibited significant activity against human leukemia cell lines HL60 and CEM. Tectol may cause itchy dermatitis, the dermatitis appeared on the neck, upper legs, underarms, and trunk area.
价 格：￥电议型 号：TN6512产 地：中国大陆
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T8160EGCG OctaacetateInhibitor,EGCG Octaacetate,prodrug,gram-negative bacteria,Bacterial,inhibit,colitis-
EGCG Octaacetate, a prodrug of EGCG, is utilized to enhance the stability and bioavailability of EGCG in vivo. It has high efficacy, bioavailability, anti-oxidation, and anti-angiogenesis capacities.
价 格：￥电议型 号：T8160产 地：中国大陆
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T8262Fosfomycin sodiumXDR,multidrug-resistant,Bacterial,inhibit,Fosfomycin sodium,Antibiotic,MK-0955,drug
Fosfomycin is a bactericidal, low-molecular weight, broad-spectrum antibiotic, with putative activity against several bacteria, including multidrug-resistant Gram-negative bacteria, by irreversibly inhibiting an early stage in cell wall synthesis.
价 格：￥电议型 号：T8262产 地：中国大陆
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T7894Tazarotenic acidretinoid action,inhibit,retinoic acid receptor,AGN190299,Drug Metabolite,warty dyske
AGN-190299 is a retinoid prodrug which is converted to its active form
价 格：￥电议型 号：T7894产 地：中国大陆
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T9781Boc-C14-COOHADC Linkers,Antibody-drug conjugates linkers,Inhibitor,PROTAC Linkers,inhibit,Boc-C-14-C
Boc-C14-COOH is a alkyl-chain-based PROTAC linker. Boc-C14-COOH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T9781产 地：中国大陆
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T8667MC-Gly-Gly-Phe-GlyADC Linkers,MC Gly Gly Phe Gly,Antibody-drug conjugates linkers,inhibit,MCGlyGlyPh
DSN28369 is a heterobifunctional linker, and useful to make antibody drug conjuate (ADC).
价 格：￥电议型 号：T8667产 地：中国大陆
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TN1742Homovanillyl alcoholinhibit,Homovanillyl alcohol,Drug Metabolite,Inhibitor
Homovanillyl alcohol is a biological metabolite of Hydroxytyrosol. Hydroxytyrosol is a phenolic compound that is present in virgin olive oil (VOO) and wine. Homovanillyl alcohol displays high scavenging activities, it protects red blood cells from hemolysis in a dose-dependent manner. Homovanillyl alcohol has protective effect on cardiovascular disease and total mortality.
价 格：￥电议型 号：TN1742产 地：中国大陆
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T7060Amantadineinhibit,SARS coronavirus,Influenza Virus,antiviral drugs,anticancer,CDK,Bcl-2 Family,hepat
1-Adamantylamine is an antiviral, is a weak antagonist of the NMDA-type glutamate receptor, increases dopamine release, and blocks dopamine reuptake.
价 格：￥电议型 号：T7060产 地：中国大陆
