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T10842Clomipramine D3氯米帕明 D3氯米帕明 D3
Clomipramine D3 is the deuterium-labeled Clomipramine. Clomipramine is a serotonin transporter, norepinephrine transporter dopamine transporter blocker (Ki: 0.14, 54 and 3 nM).
价 格：￥电议型 号：T10842产 地：中国大陆
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T10841CM-675；化合物CM-675CM-675
CM-675 is a dual inhibitor of phosphodiesterase 5 (PDE5) and class I histone deacetylases (IC50s: 114 nM and 673 nM for PDE5 and HDAC1) with the potential to treat Alzheimer’s disease.
价 格：￥电议型 号：T10841产 地：中国大陆
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T10840LCM-579；化合物CM-579CM-579
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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T10840CM-579 trihydrochloride (1846570-40-8 free base)；化合物 T10840CM-579 trihydrochloride；CM-579 trihydroch
CM-579 trihydrochloride is a first-in-class reversible and dual inhibitor of G9a and DNMT (IC50s: 16 nM, 32 nM) with potent in vitro cellular activity in a wide range of cancer cells.
价 格：￥电议型 号：T10840产 地：中国大陆
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T1084Apramycin sulfate；硫酸安普霉素Nebramycin II|||Ai3-29795；Nebramycin II|||Ai3-29795|||硫酸安普霉素|||硫酸阿布拉霉素
Apramycin sulfate (Nebramycin II) is an aminoglycoside antibiotic.
价 格：￥电议型 号：T1084产 地：中国大陆
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T10835L1Cletoquine hydrochloride；盐酸氯托喹Cletoquine hydrochloride( 4298-15-1 Free base)；Cletoquine hydrochlorid
Cletoquine hydrochloride is a major active metabolite of Hydroxychloroquine. Cletoquine hydrochloride is a Chloroquine derivative and exhibits the ability to against the chikungunya virus (CHIKV). Cletoquine hydrochloride exhibits antimalarial effects.
价 格：￥电议型 号：T10835L1产 地：中国大陆
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T10834CL656；化合物 T10834c-[2’FdAMP(S)-2’FdIMP(S)]；c-[2’FdAMP(S)-2’FdIMP(S)]
CL656 is a stimulator of interferon genes (STING) activator.
价 格：￥电议型 号：T10834产 地：中国大陆
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T10833CL264；化合物CL264CL264
CL264, a selective agonist of TLR7, can be used in studies about innate immune signals.
价 格：￥电议型 号：T10833产 地：中国大陆
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T10830CL 316243；化合物CL 316243CL 316243
CL316243 is a highly potent selective agonist of β3-adrenoceptor, with a EC50 of 3 nM. CL316243 is an effective stimulant of adipocyte lipolysis and increases brown adipose tissue thermogenesis and metabolic rate. CL316243 has the potential for the treatment obesity, diabetes and urge urinary incontinence.
价 格：￥电议型 号：T10830产 地：中国大陆
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T1083Theophylline；茶碱Theo-24|||1,3-Dimethylxanthine；Theo-24|||1,3-Dimethylxanthine|||茶碱
Theophylline (1,3-Dimethylxanthine) is a methyl xanthine derivative from tea with diuretic, smooth muscle relaxant, bronchial dilation, cardiac and central nervous system stimulant activities. Theophylline inhibits the 3´, 5´-CYCLIC NUCLEOTIDE PHOSPHODIESTERASE that degrades CYCLIC AMP thus potentiates the actions of agents that act through ADENYLYL CYCLASES and cyclic AMP.
价 格：￥电议型 号：T1083产 地：中国大陆
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T10824cis-Urocanic acid；顺式-尿刊酸cis-UCA|||(Z)-Imidazole-4-acrylic acid|||(Z)-Urocanic acid|||(E)-Urocanic ac
cis-Urocanic acid ((E)-Urocanic acid) is a 5-HT2A receptor agonist (Kd: 4.6 nM). It is an immune modulator that induces immunosuppression by binding to the 5-HT2A receptor.
价 格：￥电议型 号：T10824产 地：中国大陆
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T10820L1Ciraparantag acetate；化合物Ciraparantag acetateCiraparantag acetate(1438492-26-2 Free base)；Ciraparanta
Ciraparantag acetate, an anticoagulant reversal agent, is a small molecule specifically designed to bind noncovalently by charge-charge interaction to unfractionated heparin and low-molecular-weight heparin.?It shows binding characteristics that are similar to those of direct oral anticoagulants (DOACs).
价 格：￥电议型 号：T10820L1产 地：中国大陆
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T10814Cinacalcet metabolite M4；3-三氟甲基苯丙胺Rarechem AL BW 1078；3-三氟甲基苯丙胺|||Rarechem AL BW 1078
Cinacalcet metabolite M4 (Rarechem AL BW 1078) is a metabolite of Cinacalcet. Cinacalcet is an allosteric agonist of Ca receptor.
价 格：￥电议型 号：T10814产 地：中国大陆
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T10809LCHPG hydrochloride；化合物CHPG盐酸盐CHPG hydrochloride(170846-74-9 Free base)；CHPG hydrochloride(170846-74-
CHPG hydrochloride is a selective agonist of mGluR5.
价 格：￥电议型 号：T10809L产 地：中国大陆
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T10804CHMFL-PI3KD-317；化合物CHMFL-PI3KD-317CHMFL-PI3KD-317
CHMFL-PI3KD-317 is a highly potent, selective and orally active PI3Kδ inhibitor, with an IC50 of 6 nM, and exhibits over 10-1500 fold selectivity over other class I, II and III PIKK family isoforms, such as PI3Kα (IC50, 62.6 nM), PI3Kβ (IC50, 284 nM), PI3Kγ (IC50, 202.7 nM), PIK3C2A (IC50, >10000 nM), PIK3C2B (IC50, 882.3 nM), VPS34 (IC50, 1801.7 nM), PI4KIIIA (IC50, 574.1 nM) and PI4KIIIB (IC50, 300.2 nM). CHMFL-PI3KD-317 inhibits PI3Kδ-mediated Akt T308 phosphorylation in Raji cells, with an E
价 格：￥电议型 号：T10804产 地：中国大陆
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T10792LCHK1-IN-4 hydrochloride；化合物CHK1-IN-4盐酸盐CHK1-IN-4 hydrochloride（2120398-41-4 Free base）；CHK1-IN-4 hyd
CHK1-IN-4 hydrochloride is a potent inhibitor of checkpoint kinase 1 (chk1). CHK1-IN-4 hydrochloride potently inhibits chk1 phosphorylation in the tumor cells. CHK1-IN-4 hydrochloride has anti-tumor activity.
价 格：￥电议型 号：T10792L产 地：中国大陆
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T10792CHK1-IN-4；化合物 T10792CHK1-IN-4
CHK1-IN-4 is a potent inhibitor of checkpoint kinase 1 (chk1) and potently inhibits chk1 phosphorylation in the tumor cells with anti-tumor activity.
价 格：￥电议型 号：T10792产 地：中国大陆
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T10785Chalcone 4 hydrate；查耳酮 4 水合物Chalcone 4 hydrate
Chalcone 4 hydrate, an anti-parasite compound, inhibits the growth of Theileria and Babesia.
价 格：￥电议型 号：T10785产 地：中国大陆
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T10784CH6953755；化合物CH6953755CH6953755
CH6953755 is an orally active, potent and selective YES1 kinase inhibitor (IC50:1.8 nM).CH6953755 has anticancer activity and inhibits cancer cell proliferation by inhibiting YES1 kinase.
价 格：￥电议型 号：T10784产 地：中国大陆
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T10783CGS 15435；化合物CGS 15435CGS 15435
CGS 15435 is a potent thromboxen (TxA2) synthetase inhibitor (IC50: 1 nM). CGS 15435 acts on PGI2 synthase, cyclooxygenase and liposynthase with much less selectivity than on thromboxin synthase.
价 格：￥电议型 号：T10783产 地：中国大陆
