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产品数：86101
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TP2063Lα-Conotoxin MII acetateαConotoxin MII acetate,α Conotoxin MII acetate
α-Conotoxin MII acetate is a 16-amino acid peptide from the venom of the marine snail Conus magus. α-Conotoxin MII acetate potently blocks nicotinic acetylcholine receptors composed of α3β2 subunits, with an IC50 of 0.5 nM. α-Conotoxin MII acetate potently blocks β3-containing neuronal nicotinic acetylcholine receptors.
价 格：￥电议型 号：TP2063L产 地：中国大陆
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T10063LDL-IN-3LDLIN3,LDL IN 3
LDL-IN-3 shows anti-atherosclerotic and antioxidant activities.
价 格：￥电议型 号：T10063产 地：中国大陆
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T6923Ozanimodneurosurgery,sphingosine 1-phosphate (S1P),LPL Receptor,inhibit,RPC1063,Lysophospholipid Rec
Ozanimod (RPC1063) is a specific oral S1P Receptor 1 modulator. Ozanimod has been used in trials studying the treatment of Crohn´s Disease, Ulcerative Colitis, Multiple Sclerosis, and Relapsing Multiple Sclerosis.
价 格：￥电议型 号：T6923产 地：中国大陆
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T6976SB 239063inhibit,SB 239063,SB-239063,Inhibitor,Autophagy,p38 MAPK
SB239063 is a potent and selective p38 MAPKα/β inhibitor with IC50 of 44 nM, showing no activity against the γ- and δ-kinase isoforms.
价 格：￥电议型 号：T6976产 地：中国大陆
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T12424PF-06305591
PF-06305591 is an effective and selective blocker of voltage-gated sodium channel NaV1.8 (IC50 = 15 nM).
价 格：￥电议型 号：T12424产 地：中国大陆
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TN7063N-AcetaminophenNAcetaminophen,N Acetaminophen
N-Acetaminophen is a methylated form of Colchicine.
价 格：￥电议型 号：TN7063产 地：中国大陆
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T60063WAY-323975
WAY-323975 is a nonfluorescent inhibitors of Fluorogen–Fluorogen Activating Protein Binding Pairn.
价 格：￥电议型 号：T60063产 地：中国大陆
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T8063Cephapirin BenzathineAntibiotic,Cephapirin Benzathine,Inhibitor,Bacterial,inhibit
Cephapirin Benzathine is a semisynthetic, broad-spectrum, first-generation cephalosporin with antibacterial activity.
价 格：￥电议型 号：T8063产 地：中国大陆
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T6S0630HypaconitineInhibitor,TNFR,TNF Receptor,inhibit,Tumor Necrosis Factor Receptor,Hypaconitine
Hypaconitine, an active and highly toxic constituent derived from Aconitum species, has anti-inflammatory activity, is widely used to treat rheumatism.
价 格：￥电议型 号：T6S0630产 地：中国大陆
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TP1785LPeptide T acetate(106362-32-7 free base)Peptide T acetate(106362 32 7 free base),Peptide T acetate(1
Peptide T acetate is an octapeptide from the V2 region of HIV-1 gp120. Peptide T is a synthetic octapeptide whose possible mechanism of action is the competitive inhibition of gp120 to the CD4 receptor as well as binding to vasointestinal peptide receptors and inhibiting cytokine action
价 格：￥电议型 号：TP1785L产 地：中国大陆
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T10630BuChE-IN-TM-10
BuChE-IN-TM-10 is a potent butyrylcholinesterase (BuChE) inhibitor, with an IC50 of 8.9 nM. BuChE inhibitor 1 inhibits and disaggregates self-induced Aβ aggregation, exhibiting potent antioxidant activity and good blood-brain barrier (BBB) penetration. Has potential to treat Alzheimer’s disease.
价 格：￥电议型 号：T10630产 地：中国大陆
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T7488BD1063 dhydrochlorideSigma Receptor,Inhibitor,inhibit,BD1063 dhydrochloride,BD-1063 dhydrochloride
BD1063 is a potent and selective sigma 1(σ1) receptor antagonist(Ki = 9 nM).
价 格：￥电议型 号：T7488产 地：中国大陆
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T9329BRD0639BRD0639,BRD-0639
BRD0639 is a first-in-class inhibitor of the PRMT5-substrate adaptor interaction. BRD0639 is a PRMT5 binding motif (PBM)-competitive inhibitor that can support studies of PBM dependent PRMT5 activities [1].
价 格：￥电议型 号：T9329产 地：中国大陆
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T60019VPC-70063VPC70063,Anticancer,LNCaP,VPC 70063,inhibit,Myc-Max,UBE2C,Apoptosis,VPC-70063,c-Myc,PARP,AR
VPC-70063 is an inhibitor of c-Myc-MAX. VPC-70063 exhibits Myc-Max transcriptional activity inhibition of 106% with an IC50 of 8.9 μM and Myc-Max/UBE2C downstream pathway inhibition of 94%. VPC-70063 can be used for studies about anticancer.
价 格：￥电议型 号：T60019产 地：中国大陆
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T11063DMT1 blocker 1DMT-1 blocker 1,DMT1 blocker 1
DMT1 blocker 1 is a blocker of divalent metal transporter 1 (DMT1) with IC50 of 0.64 μM, which is expected to block the absorption of iron by intestinal cells in vivo.
价 格：￥电议型 号：T11063产 地：中国大陆
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T9063N-[5-[(4-Bromophenyl)methylene]-4,5-dihydro-4-oxo-2-thiazolyl]-1-naphthalenesulfonamideInhibitor,ves
Pitstop 2 is a inhibitor of clathrin, and inhibits clathrin-mediated endocytosis (CME) by associating with the terminal domain of clathrin. It has the potential for anti-cancer research.
价 格：￥电议型 号：T9063产 地：中国大陆
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T10639C-021 dihydrochlorideInhibitor,C 021 dihydrochloride,CCL22,CCR4,C021,C021 dihydrochloride,CCR,C 021,
C-021 dihydrochloride is a potent CCR4 antagonist. It potently inhibits functional chemotaxis in human and mouse with IC50s of 140 nM and 39 nM.
价 格：￥电议型 号：T10639产 地：中国大陆
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T6338PHA-680632PHA 680632；PHA680632
PHA-680632 is potent inhibitor of Aurora A, Aurora B and Aurora C with IC50 of 27 nM, 135 nM and 120 nM, respectively. It has 10- to 200-fold higher IC50 for FGFR1, FLT3, LCK, PLK1, STLK2, and VEGFR2/3.
价 格：￥电议型 号：T6338产 地：中国大陆
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T6121TepotinibMSC2156119；EMD-1214063；特泊替尼
Tepotinib is an inhibitor of MET tyrosine kinase with potential antineoplastic activity.
价 格：￥电议型 号：T6121产 地：中国大陆
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T6063LY-411575LY411575
LY411575, a potent γ-secretase inhibitor, is with IC50 of 0.078 nM in the membrane and 0.082 nM in cell-based. It also suppresses Notch clevage with IC50 of 0.39 nM.
价 格：￥电议型 号：T6063产 地：中国大陆
