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T61392NLRP3-IN-10
NLRP3-IN-10 is a potent NLRP3 inhibitor. NLRP3-IN-10 inhibits IL-1β release with an IC50 value of 251.1 nM. NLRP3-IN-10 attenuates ASC speck formation, leading to suppress activation of NLRP3 inflammasome.
价 格：￥电议型 号：T61392产 地：中国大陆
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T9192BIIB068ADME,inhibit,FcγR,Autoimmune,Bruton tyrosine kinase,TNFα,BIIB 068,ROS,Inhibitor,reversible,Bt
BIIB068 is an selective, reversible and orally active BTK inhibitor (IC50 = 1 nM, Kd = 0.3 nM). BIIB068 is 400 times more selective for BTK than other kinases.
价 格：￥电议型 号：T9192产 地：中国大陆
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T9268UlinastatinUlinastatin
Ulinastatin is a multivalent Kunitz-type serine protease inhibitor with anti-inflammatory properties.
价 格：￥电议型 号：T9268产 地：中国大陆
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T6924Riviciclib hydrochlorideinhibit,Inhibitor,Riviciclib,CDK,Riviciclib hydrochloride,Cyclin dependent k
P276-00 is a novel CDK1, CDK4 and CDK9 inhibitor with IC50 of 79 nM, 63 nM and 20 nM, respectively. Phase 2/3.
价 格：￥电议型 号：T6924产 地：中国大陆
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T8222SelpercatinibFVB/NRj mice,RET (WT),inhibit,Inhibitor,RET (G810R),LOXO 292,LOXO292,RET (V804M),Selper
Selpercatinib is a tyrosine kinase inhibitor with antineoplastic properties(IC50 of 14.0 nM, 24.1 nM, and 530.7 nM for RET (WT), RET (V804M) , and RET (G810R), respectively)
价 格：￥电议型 号：T8222产 地：中国大陆
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T9240sulfopinneuroblastoma,antiproliferative,PIN1-3,tumors,cancer,pancreatic,Inhibitor,sulfopin,inhibit,c
Sulfopin is a highly selective covalent inhibitor of Pin1 with an apparent Ki of 17nM. Sulfopin blocks Myc-driven tumors in vivo.
价 格：￥电议型 号：T9240产 地：中国大陆
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TN6920Methyl heptadecanoateinhibit,Methyl heptadecanoate,Inhibitor
Methyl heptadecanoate is a natural product.
价 格：￥电议型 号：TN6920产 地：中国大陆
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T12922Sirtuin modulator 1Inhibitor,Sirtuin,Sirtuin modulator1,inhibit,Sirtuin modulator-1,Sirtuin modulato
Sirtuin modulator 1 is a modulator of SIRT1 with EC1.5 of < 1 μM.
价 格：￥电议型 号：T12922产 地：中国大陆
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TN1926Methyl caffeateinhibit,stress,antimicrobial,Bacterial,antimycobacterial,Methyl caffeate,α-glucosidas
Methyl caffeate acid
价 格：￥电议型 号：TN1926产 地：中国大陆
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TQ0011PF-06869206inhibit,PF-06869206,Na+ channels,Sodium Channel,Na channels,PF 06869206,Inhibitor,PF06869
PF-06869206 is an oral selective inhibitor of the sodium-phosphate cotransporter NaPi2a (SLC34A1, IC50: 380 nM).
价 格：￥电议型 号：TQ0011产 地：中国大陆
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T9226CCG-143140CCG143140,CCG 143140
CCG-143140 is a GLP-1 receptor inverse agonists.
价 格：￥电议型 号：T9226产 地：中国大陆
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T19206β-Lactamase-IN-1
β-Lactamase-IN-1 is a β-Lactamase inhibitor and targets the infection of Neisseria gonorrhoeae.
价 格：￥电议型 号：T19206产 地：中国大陆
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TN6928L-Azetidine-2-carboxylic acidLAzetidine2carboxylic acid,Endogenous Metabolite,inhibit,L Azetidine 2
L-2-Azetidinecarboxylic acid is a toxic proline analogue produced by members of the Liliaceae and Agavaciae families.
价 格：￥电议型 号：TN6928产 地：中国大陆
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T64351GI-560192
GI-560192 is a potent smo cilial modulator with an EC50 value of 0.02 ?M. GI-560192 modulates the translocation and/or accumulation of smoothened to the primary cilia by hedgehog signaling pathway.
价 格：￥电议型 号：T64351产 地：中国大陆
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T9255Zolpidem tartrateZolpidem tartrate
Zolpidem is a prescription medication used for the treatment of insomnia, as well as some brain disorders. It is a short-acting nonbenzodiazepine hypnotic of the imidazopyridine class that potentiates gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter, by binding to GABAA receptors at the same location as benzodiazepines.
价 格：￥电议型 号：T9255产 地：中国大陆
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T9228Propionylpromazine hydrochloridePropiopromazine,Propionylpromazine,DRD2,Dopamine Receptor,Parkinson,
Propionylpromazine hydrochloride is a dopamine receptor D2 (DRD2) antagonist.
价 格：￥电议型 号：T9228产 地：中国大陆
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T9140NAcM-OPT HCl(2089293-61-6 free base)NAcMOPT HCl(2089293616 free base),NAcM OPT HCl(2089293 61 6 free
NAcM-OPT HCL is an orally bioavailable cullin neddylation 1 (DCN1) inhibitor that targets N-Acetyl-UBE2M (E2 conjugating enzyme, UBC12) interaction with DCN1 with IC50 of 79 nM.
价 格：￥电议型 号：T9140产 地：中国大陆
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T8592CTK8A3536CTK-8A3536,CTK8A3536
CTK8A3536 is an inhibitor of Androgen receptor.
价 格：￥电议型 号：T8592产 地：中国大陆
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TP1166ZINC77292789inhibit,Inhibitor,ZINC77292789,ZINC-77292789
Fmoc-Thr[GalNAc(Ac)3-α-D]-OH is a reagent for the preparation of a synthetic MUC1 Glycopeptide Bearing βGalNAc-?Thr as a Tn antigen isomer which induces the antibody production against tumor cells. Fmoc-Thr[GalNAc(Ac)3-α-D]-OH is a starting material to make trimeric MUC1 immunodominant motif antigen-?based anti-?cancer vaccine candidates.
价 格：￥电议型 号：TP1166产 地：中国大陆
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T38776LP-922056cortical,Pectinacetylesterase,thickness,orally,femur,inhibit,Wnt,lipase,bone,LP-922056,Notu
LP-922056 is an inhibitor of Notum Pectinacetylesterase with EC50 values of 21 nM, 55 nM for human and mouse, respectively.
价 格：￥电议型 号：T38776产 地：中国大陆
