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T64280ODN 2216；化合物 ODN 2216ODN 2216
ODN 2216 is a TLR9 (toll-like receptor 9) ligand or agonist that induces the production of large amounts of IFN-α and IFN-β. ODN 2216 can induce IFN-α using pDC (plasma cell-like DC) and IL-12 (p40) using DC (dendritic cells). ODN 2216 is capable of indirectly stimulating IFN-γ production by peripheral blood mononuclear cells (PBMC), mediated by IFN-α/β. ODN 2216 activates NK cells and induces IFN-γ production by TCR-triggered CD4+ T cells.
价 格：￥电议型 号：T64280产 地：中国大陆
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T62216Influenza virus-IN-5；化合物 Influenza virus-IN-5Influenza virus-IN-5
Influenza virus-IN-5 (Compound 5f) is an influenza virus hemagglutinin (HA) inhibitor that acts on the A/H3N2 virus (EC50: 1 nM).
价 格：￥电议型 号：T62216产 地：中国大陆
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T60608FPFT-2216；化合物FPFT-2216FPFT-2216
FPFT-2216 is a "molecular glue" compound that degrades IKZF6, IKZF1, DE1D, and CK3α. FPFT-2216 has potential antitumor activity and can be used to study immune system diseases.
价 格：￥电议型 号：T60608产 地：中国大陆
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T5148Atosiban acetate醋酸阿托西班RW22164|||Atosiban acetate (90779-69-4 free base)|||RWJ22164|||醋酸阿托西班
Atosiban acetate (RW22164) is an inhibitor of the hormones oxytocin and vasopressin. It is used as an intravenous medication as a labour repressant (tocolytic) to halt premature labor. Atosiban acetate (RW22164) inhibits the oxytocin-mediated release of inositol trisphosphate from the myometrial cell membrane. As a result, there is reduced release of intracellular, stored calcium from the sarcoplasmic reticulum of myometrial cells, and reduced influx of Ca2+ from the extracellular space through
价 格：￥电议型 号：T5148产 地：中国大陆
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T4996Atosiban；阿托西班RWJ22164|||RW22164；阿托西班|||RWJ22164|||RW22164
Atosiban (RW22164) is an inhibitor of the hormones oxytocin and vasopressin. It is used as an intravenous medication as a labour repressant (tocolytic) to halt premature labor. Atosiban inhibits the oxytocin-mediated release of inositol trisphosphate from the myometrial cell membrane. As a result, there is reduced release of intracellular, stored calcium from the sarcoplasmic reticulum of myometrial cells, and reduced influx of Ca2+ from the extracellular space through voltage gated channels. In
价 格：￥电议型 号：T4996产 地：中国大陆
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T32552Lamtidine；化合物 T32552AH-22216|||AH22216|||AH 22216；AH-22216|||AH22216|||AH 22216
Lamtidine is a biochemical.
价 格：￥电议型 号：T32552产 地：中国大陆
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T32216Isolinearol；化合物 T32216Isolinearol
Isolinearol is a secodolastane diterpene.
价 格：￥电议型 号：T32216产 地：中国大陆
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T31604Edivoxetine；化合物 T31604LY-2216684|||LY 2216684|||LY2216684；LY-2216684|||LY 2216684|||LY2216684
Edivoxetine( LY2216684) is a selective norepinephrine reuptake inhibitor being developed as a treatment for attention deficit hyperactivity disorder (ADHD) and antidepressants.
价 格：￥电议型 号：T31604产 地：中国大陆
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T30618Butachlor丁草胺丁草胺|||NSC 221683|||CP 53619|||SHA 112301|||BRN 2873811
Butachlor is a chloroacetanalide herbicide. Butachlor is commonly used for weed control in rice as well as cotton, maize, wheat and other crops.
价 格：￥电议型 号：T30618产 地：中国大陆
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T30089AP-22161；化合物 T30089AP22161|||G7VE62573J|||UNII-G7VE62573J|||SCHEMBL7243003|||AP 22161；AP22161|||G7VE
AP-22161 selectively binds the Src SH2 domain by targeting highly conserved phosphotyrosine binding to cysteine residues in the pocket. AP-22161 selectively inhibits Src SH2 binding and can be used to inhibit osteoclast absorption.
价 格：￥电议型 号：T30089产 地：中国大陆
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T28367L(R)-PF-04822163；化合物(R)-PF-04822163(R)-PF-04822163
(R)-PF-04822163 is a biochemical reagent that can be used to synthesize other compounds.
价 格：￥电议型 号：T28367L产 地：中国大陆
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T28367PF-04822163；化合物PF-04822163PF-4822163|||PF 04822163|||PF4822163|||PF04822163|||PF 4822163；PF-4822163|
PF-04822163 is a potent inhibitor of PDE1 with IC50 value of 0.0024 μM.
价 格：￥电议型 号：T28367产 地：中国大陆
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T27383FR-221647；化合物 T27383FR-221647
FR-221647 is a non-nucleoside adenosine deaminase inhibitor, it has moderate activity and good pharmacokinetics compared with the known inhibitors EHNA and pentostatin.
价 格：￥电议型 号：T27383产 地：中国大陆
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T26701AZ12216052；化合物 AZ12216052AZ 12216052|||AZ-12216052；AZ 12216052|||AZ-12216052
AZ12216052 is a GRP8 antagonist with anxiolytic and anti-inflammatory activity and can be used to study obesity and metabolic disorders.
价 格：￥电议型 号：T26701产 地：中国大陆
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T2445FG-2216；化合物FG-2216YM-311|||FG2216|||FG 2216；YM-311|||FG2216|||FG 2216
FG-2216 (YM-311) is a potent HIF-prolyl hydroxylase inhibitor for the PDH2 enzyme (IC50: 3.9 uM); orally bioavailable and induced reversible and significant Epo induction in vivo.
价 格：￥电议型 号：T2445产 地：中国大陆
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T2221610-Undecen-1-ol；10-十一烯-1-醇10-Undecen-1-ol
10-Undecen-1-ol is converted from ricinoleic acid. 10-Undecen-1-ol can be used as a comonomer for the introduction of functional groups[1][2].
价 格：￥电议型 号：T22216产 地：中国大陆
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T2216Entacapone；恩他卡朋OR-611；OR-611|||恩他卡朋
Entacapone (OR-611) is a selective and reversible inhibitor of catechol-O-methyltransferase (COMT).
价 格：￥电议型 号：T2216产 地：中国大陆
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T13665DT2216；化合物DT2216DT2216
DT2216 inhibits various Bcl-XL-dependent leukemias and cancer cells, but is significantly less toxic to platelets.DT2216 is a selective B-cell lymphoma, extremely large (BCL-XL), proteolytic targeting chimera (PROTAC).DT2216 targets bcl-XL to the Von Hippel-Lindau (VHL) E3 ligase for degradation.
价 格：￥电议型 号：T13665产 地：中国大陆
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T12216LNF-56-EJ40 hydrochloride；化合物NF-56-EJ40盐酸盐NF-56-EJ40 hydrochloride
NF-56-EJ40 hydrochloride is a potent, high-affinity, and highly selective human SUCNR1 (GPR91) antagonist with an IC50 of 25 nM and a Ki of 33 nM, and shows almost no activity towards rat SUCNR1. NF-56-EJ40 hydrochloride has high affinity for humanized rat SUCNR1 with a Ki value of 17.4 nM.
价 格：￥电议型 号：T12216L产 地：中国大陆
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T12216NF-56-EJ40；化合物NF-56-EJ40NF-56-EJ40
NF-56-EJ40 is an effective and highly selective antagonist of human SUCNR1 with an IC50 of 25 nM and a Ki of 33 nM.
价 格：￥电议型 号：T12216产 地：中国大陆
