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T10882CPUY074020CPUY074020,CPUY-074020
CPUY074020 is a potent and orally bioavailable inhibitor of histone methyltransferase G9a (IC50: 2.18 μM) with anti-proliferative activity.
价 格：￥电议型 号：T10882产 地：中国大陆
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T11108DSR-6434DSR6434,DSR 6434
DSR-6434 is a selective agonist of TLR7 with antitumor effect. DSR-6434 exhibits EC50s of 7.2 nM and 4.6 nM for human and mouse.
价 格：￥电议型 号：T11108产 地：中国大陆
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T10827CK2/ERK8-IN-1
CK2/ERK8-IN-1 is a dual inhibitor of casein kinase 2 (CK2) (Ki: 0.25 ?M) and ERK8 (IC50s: 0.50 μM) with pro-apoptotic efficacy. CK2/ERK8-IN-1 also binds to PIM1, DYRK1A, and HIPK2 (Kis: 8.65 ?M, 11.9 ?M, and 15.25 ?M).
价 格：￥电议型 号：T10827产 地：中国大陆
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T6958Prucalopride Succinateinhibit,5-HT Receptor,Inhibitor,Prucalopride Succinate,Serotonin Receptor,R108
Prucalopride is a selective, high affinity 5-HT4 receptor agonist, inhibiting human 5-HT(4a) and 5-HT(4b) receptor with Ki value of 2.5 nM and 8 nM, respectively.
价 格：￥电议型 号：T6958产 地：中国大陆
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T7352PridopidineFR-310826,Dopamine Receptor,inhibit,Pridopidine,Inhibitor,ACR-16,ACR 16,ASP-2314,FR 31082
Pridopidine, a dopamine (DA) stabilizer, acts as a low affinity dopamine D2 receptor (D2R) antagonist, improves motor performance and shows neuroprotective effects in Huntington disease R6/2 mouse model.
价 格：￥电议型 号：T7352产 地：中国大陆
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T10840LCM-579CM 579,CM579
CM-579 is a dual inhibitor of G9a and DNMT( IC50:16 nM, 32 nM for G9a and DNMT). It has potent in vitro cellular activity in a wide range of cancer cells.
价 格：￥电议型 号：T10840L产 地：中国大陆
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T10876CPA inhibitor
CPA inhibitor is a potent carboxypeptidase A (CPA) inhibitor with a Ki of 0.32 μM.
价 格：￥电议型 号：T10876产 地：中国大陆
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T10800CHMFL-ABL-121CHMFLABL121,CHMFL ABL 121
CHMFL-ABL-121 is a highly potent inhibitor of type II ABL kinase (IC50s: 2 nM and 0.2 nM against purified inactive ABL wt and T315I kinase protein).
价 格：￥电议型 号：T10800产 地：中国大陆
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T40108Inaxaplin
Inaxaplin is an apolipoprotein L1 ( APOL1 ) function inhibitor (WO2020131807, compound 2). Inaxaplin can be used for the research of kidney disease.
价 格：￥电议型 号：T40108产 地：中国大陆
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T10839Clozic
Clozic exhibits reversible anti-proliferative effects and can be used in studies about serving as a potential anti-arthritic agent.
价 格：￥电议型 号：T10839产 地：中国大陆
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TN1081HirsuteineHirsuteine,Inhibitor,inhibit
Hirsuteine is a natural product. It non-competitively antagonizes nicotine-mediated dopamine release by blocking ion permeation through nicotinic receptor channel complexes.
价 格：￥电议型 号：TN1081产 地：中国大陆
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T6591Nodinitib-1Nodinitib1,CID1088438,Inhibitor,NOD-like Receptor (NLR),Nodinitib 1,ML-130,ML 130,Nodinit
Nodinitib-1 is a potent and selective NOD1 inhibitor with an IC50 of 0.56 μM.
价 格：￥电议型 号：T6591产 地：中国大陆
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T10835CletoquineNdesethylation,inhibit,CHIKV,P23pro-zbd,Parasite,antimalarial,CYP2D6,Influenza Virus,CYP3A
Cletoquine is a major active metabolite of Hydroxychloroquine. Cletoquine has the ability to against the chikungunya virus (CHIKV). Cletoquine has antimalarial effects and has the potential for autoimmune disease treatment.
价 格：￥电议型 号：T10835产 地：中国大陆
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T10813Cilobradine hydrochloride
Cilobradine hydrochloride is an HCN Channel blocker and an open channel blocker of neuronal Ih and related cardiac If channels.
价 格：￥电议型 号：T10813产 地：中国大陆
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T10888CRT0066854 hydrochlorideCRT-0066854 hydrochloride,CRT0066854 hydrochloride
CRT0066854 hydrochloride is an effective selective atypical PKCs inhibitor. CRT0066854 is against full-length (FL) PKCι, PKCζ, and ROCK-II kinases with IC50 values of 132 nM, 639 nM, and 620 nM, respectively.
价 格：￥电议型 号：T10888产 地：中国大陆
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T10893CS-722 Free baseCS722 Free base,CS 722 Free base
CS-722 Free base is a synthetic central muscle relaxant with muscle relaxant activity and inhibitory effect on spinal reflex. CS-722 Free base may inhibit spontaneous inhibitory post-synaptic current and excitatory post-synaptic current in hippocampal culture by inhibiting sodium current and calcium current.
价 格：￥电议型 号：T10893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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TN7108Urolithin Cinsulin,Ca channels,Apoptosis,Polyphenols,ROS,mitochondria,anti-diabetic,gut-microbial,Re
Urolithin C is a gut metabolite of ellagic acid. Urolithin C induces apoptosis in PC12 cells through a mitochondria-mediated pathway.
价 格：￥电议型 号：TN7108产 地：中国大陆
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TP1088N-Acetylcarnosinehistidine-containing,NAcetylcarnosine,Inhibitor,L-carnosine,pharmacological,catarac
N-acetylcarnosine (NAC) is thought to be able to combat some of the effects of oxidative stress as it has anti-oxidant properties.
价 格：￥电议型 号：TP1088产 地：中国大陆
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TP1085LNeuromedin N acetate(92169-45-4 free base)Neuromedin N acetate(92169 45 4 free base),Neuromedin N ac
Neuromedin N acetate is a neuropeptide derived from the same precursor polypeptide as neurotensin, and with similar but subtly distinct expression and effects.Neuromedin N is a potent modulator of dopamine D2 receptor agonist binding in rat neostriatal membranes.
价 格：￥电议型 号：TP1085L产 地：中国大陆
