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T4554AG 1406；化合物AG 1406AG 1406
AG 1406 is a selective inhibitor of the receptor tyrosine kinase VEGF receptor 2.
价 格：￥电议型 号：T4554产 地：中国大陆
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T4343A-196；化合物A196A 196；A 196
A-196 is a potent and selective inhibitor of SUV420 h1 and SUV420 h2 with IC50 values of 0.025 and 0.144 μM, respectively; more than 100-fold selective over other histone methyltransferases and non-epigenetic targets.
价 格：￥电议型 号：T4343产 地：中国大陆
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T4118SB 271046 hydrochloride；化合物SB 271046 hydrochlorideSB 271046A；SB 271046A
SB 271046 hydrochloride (SB 271046A) is selective, orally active 5-HT6 antagonist (pKi values are 9.02-8.92, 6.35, 6.55, 6.27 at 5-HT6, 5-HT1A, 5-HT1D and D3, and 6.05, 5.95, 5.76, 5.73, 5.62, 5.55, 5.41, 5.39, 5.27 and < 4.99 at 5-HT1B, 5-HT1F, α1B, 5-HT2C, 5-HT2A, D2, 5-HT2B, 5-HT7, 5-HT4 and 5-HT1E respectively) and is > 200-fold selective over 55 other receptors, enzymes and ion channels. It increases extracellular aspartate and glutamate in the frontal cortex and exhibits anticonvulsant act
价 格：￥电议型 号：T4118产 地：中国大陆
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T40575ADPM06；ADPM06ADPM06
ADPM06, an azadipyrromethene compound, is a new nonporphyrin photodynamic therapeutic (PDT) agent with potential as a lead candidate. It demonstrates significant IC50 values in the micro-molar range in human tumor cells, as well as inducing apoptosis.
价 格：￥电议型 号：T40575产 地：中国大陆
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T40553ACAT-IN-6；ACAT-IN-6ACAT-IN-6
ACAT-IN-6, an acyl-Coenzyme A: cholesterol acyltransferase (ACAT) inhibitor, displays potent inhibition of NF-κB mediated transcription.
价 格：￥电议型 号：T40553产 地：中国大陆
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T3989SMI-16a；化合物SMI-16aPIM1/2 Kinase Inhibitor VI；PIM1/2 Kinase Inhibitor VI
SMI-16a (PIM1/2 Kinase Inhibitor VI) , a cell-permeable thiazolidinedione compound, acts as an effective, ATP-competitive inhibitor against Pim-1/2 kinases (IC50: 150/20 nM) while exhibiting little or no activity against a panel of 57 other kinases (≤18% inhibition at 5 μM).
价 格：￥电议型 号：T3989产 地：中国大陆
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T39758ARX-1796ARX-1796ARX-1796|||AV-006
ARX-1796 (AV-006), an Avibactam prodrug, is an orally bioavailable β-lactamase inhibitor. Avibactam has a spectrum of inhibition of class A and C β-lactamases, including ESBLs, AmpC and Klebsiella pneumoniae carbapenemase (KPC) enzymes.
价 格：￥电议型 号：T39758产 地：中国大陆
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T3975AZD9496；化合物AZD9496AZD9496|||AZD 9496|||AZD 9496|||AZD-9496|||AZD-9496|||Estrogen Receptor/ERR|||inhi
AZD9496 is an orally available selective estrogen receptor(ERα) antagonist, with potential antineoplastic activity.
价 格：￥电议型 号：T3975产 地：中国大陆
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T38881Antibacterial agent 56；Antibacterial agent 56Antibacterial agent 56
Antibacterial agent 56 (example 22) is a antibacterial agent.
价 格：￥电议型 号：T38881产 地：中国大陆
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T38871Antibacterial agent 46；Antibacterial agent 46Antibacterial agent 46
Antibacterial agent 46, serves as a potent antibacterial compound. With its versatile properties, this agent demonstrates considerable potential for supporting research on bacterial infections.
价 格：￥电议型 号：T38871产 地：中国大陆
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T378116-Chloro-3-indolyl-β-D-Glucuronide CHA；6-Chloro-3-indolyl-β-D-Glucuronide 环已胺盐16beta-Methyl-16alpha,
6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) is a chromogenic substrate for β-glucuronidase. 6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) can be used in the histochemical analysis of β-glucuronidase activity.
价 格：￥电议型 号：T37811产 地：中国大陆
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T37180Avanafil metabolite M16；Avanafil metabolite M16Avanafil metabolite M16
Avanafil metabolite M16 is a major inactive metabolite of the phosphodiesterase 5 (PDE5) inhibitor avanafil . Avanafil is metabolized by the cytochrome P450 (CYP450) isoforms CYP3A4 and CYP2C to the major metabolites avanafil metabolite M16 and avanafil metabolite M4 , as well as minor metabolites.
价 格：￥电议型 号：T37180产 地：中国大陆
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T368966α-hydroxy Paclitaxel；6-羟基泰素6alpha-hydroxypaclitaxel；6alpha-hydroxypaclitaxel
6α-hydroxy Paclitaxel (6α-OH-PTX) is a major metabolite of the anticancer compound paclitaxel and is partially cytotoxic.
价 格：￥电议型 号：T36896产 地：中国大陆
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T3624A-366；化合物A366A 366|||A366；A 366|||A366
A-366 is a highly selective peptide-competitive histone methyltransferase G9a inhibitor with IC50s of 3.3 and 38 nM for G9a and GLP, respectively.It is more than 1,000-fold selective for G9a and GLP over the other 21 methyltransferases. It is an inhibitor of the Spindlin1-H3K4me3 interaction with an IC50 of 182.6 nM.It exhibits high affinity for human H3R with a Ki value of 17 nM, and shows subtype selectivity between subgroups of the histaminergic and dopaminergic receptor families.
价 格：￥电议型 号：T3624产 地：中国大陆
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T3513GSK180736A；化合物GSK180736AGSK180736；GSK180736
GSK180736A is an effective and selective GRK2 inhibitor (IC50: 0.77 μM) and >100-fold selectivity over other GRKs. It is a weak inhibitor of PKA (IC50: 30 μM), but highly effective against ROCK1 (IC50: 100 nM).
价 格：￥电议型 号：T3513产 地：中国大陆
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T34766T-808；化合物 T34766AVI-680；AVI-680
T-808 is a tau tracer which may be used in radiographic labeling of Tau aggregates during Alzheimer´s disease.
价 格：￥电议型 号：T34766产 地：中国大陆
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T34765T6A；化合物t6AN-(6-Nebularinylcarbamoyl)threonine|||t 6 A|||t-6-A|||t(6)A|||N6-Threonylcarbamoyladenosin
T6A (N6-Threonylcarbamoyladenosine) is a ubiquitously conserved nucleoside, which is essential for modification. T6A is found in the tRNA responsible for transporting the ANN codon.
价 格：￥电议型 号：T34765产 地：中国大陆
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T33686Nitrocaphane；化合物 T33686AT 1258|||AT-1258|||AT1258；AT 1258|||AT-1258|||AT1258
Nitrocaphane, in combination with 5-FU (fluorouracil), chemotherapy is considered as a protocol of choice in the treatment of malignant trophoblastic tumor.
价 格：￥电议型 号：T33686产 地：中国大陆
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T33563N6-Allyladenosine；化合物 T33563N Allyladenosine|||a6A|||N-Allyladenosine；N Allyladenosine|||a6A|||N-All
N6-allyladenosine is an RNA labeling probe that acts through metabolic and enzyme - assisted approaches.
价 格：￥电议型 号：T33563产 地：中国大陆
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T33511ms2i6A；化合物 T33511ms2i6-2-6|||ms2i6 2 6；ms2i6-2-6|||ms2i6 2 6
ms2i6A is a mitochondrial tRNA-specific modification, which regulates efficient mitochondrial translation and energy metabolism in mammals.
价 格：￥电议型 号：T33511产 地：中国大陆
