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T11893Lurasidone metabolite 14326；化合物 T11893Lurasidone metabolite 14326
Lurasidone metabolite 14326, an active metabolite of the atypical antipsychotic Lurasidone, functions effectively in the body.
价 格：￥电议型 号：T11893产 地：中国大陆
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T11490LGSK2945 hydrochloride (1438071-12-5 free base)；化合物 T11490LGSK2945 hydrochloride；GSK2945 hydrochlorid
GSK2945 hydrochloride is a highly specific Rev-erbα/REV-ERBα (mouse/human reverse erythroblastosis virus α) antagonist (EC50s: 21.5 μM and 20.8 μM). It enhances cholesterol 7α-hydroxylase (CYP7A1) level and cholesterol metabolism.
价 格：￥电议型 号：T11490L产 地：中国大陆
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T11439GNE-616；化合物 T11439GNE-616
GNE-616 is a highly potent, metabolically stable, orally bioavailable, and subtype-selective Nav1.7 inhibitor (Ki: 0.79 nM, Kd: 0.38 nM for hNav1.7) for the treatment of chronic pain.
价 格：￥电议型 号：T11439产 地：中国大陆
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T11438GNE-1858；化合物GNE-1858GNE-1858
GNE-1858 is an ATP-competitive hematopoietic progenitor kinase-1 (HPK1) inhibitor (IC50s of 1.9 nM, 1.9 nM, and 4.5 nM for wild-type and the active mimetic mutants HPK1-TSEE and HPK1-SA).
价 格：￥电议型 号：T11438产 地：中国大陆
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T11437GNE-0439；化合物 T11437GNE-0439
GNE-0439 is a novel Nav1.7-selective inhibitor (IC50: 0.34 uM) and inhibits Nav1.5 (IC50: 38.3 μM). GNE-0439 inhibits mutant N1742K channels (IC50: 0.37 uM) in membrane potential assays.
价 格：￥电议型 号：T11437产 地：中国大陆
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T11436GNA002；化合物 T11436GNA002
GNA002 is a highly potent, specific, and covalent EZH2 (Enhancer of zeste homolog 2) inhibitor (IC50: 1.1 μM).
价 格：￥电议型 号：T11436产 地：中国大陆
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T11435GlyT1 Inhibitor 1；化合物 T11435GlyT1 Inhibitor 1
GlyT1 Inhibitor 1 is a potent and selective GlyT1 inhibitor (IC50: 38 nM for rGlyT1) with antipsychotic activity.
价 格：￥电议型 号：T11435产 地：中国大陆
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T11434GlyRS-IN-1；化合物 T11434GlyRS-IN-1
GlyRS-IN-1 is an inhibitor of glycyl-tRNA synthase (GlyRS). It can inhibit the growth of bacteria.
价 格：￥电议型 号：T11434产 地：中国大陆
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T11433Glyoxalase I inhibitor；化合物 T11433Glyoxalase I inhibitor
Glyoxalase I inhibitor, a candidate for anticancer agents, is a potent Glyoxalase I (GLO1) inhibitor.
价 格：￥电议型 号：T11433产 地：中国大陆
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T11432Glyoxalase I inhibitor free base；化合物 T11432Glyoxalase I inhibitor free base
Glyoxalase I inhibitor (free base), a candidate for anticancer agents, is a potent Glyoxalase I (GLO1) inhibitor.
价 格：￥电议型 号：T11432产 地：中国大陆
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T11431Glycosidase-IN-2；化合物 T11431Glycosidase-IN-2
Glycosidase-IN-2 is a glycosidase inhibitor with hypoglycemic activity.
价 格：￥电议型 号：T11431产 地：中国大陆
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T11430Glycosidase-IN-1；化合物 T11430Glycosidase-IN-1
Glycosidase-IN-1 is a glycosidase inhibitor synthesized from D-mannose with hypoglycemic activity. It can be used to synthesize some immunosuppressive agents and β-glucosidase inhibitors.
价 格：￥电议型 号：T11430产 地：中国大陆
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T1143Carbenicillin disodium；羧苄青霉素钠BRL-2064|||Sodium carbenicillin；BRL-2064|||羧苄青霉素钠|||Sodium carbenicilli
Carbenicillin disodium (BRL-2064) is a broad-spectrum, semi-synthetic penicillin antibiotic with bactericidal and beta-lactamase resistant activity.
价 格：￥电议型 号：T1143产 地：中国大陆
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T11209EOAI3402143；化合物EOAI3402143EOAI3402143
EOAI3402143 inhibits Usp9x and Usp24 activity, increases tumor cell apoptosis. EOAI3402143 phenocopies the FAS induction and apoptotic sensitization of Usp5 knockdown and fully blocks melanoma tumor growth.
价 格：￥电议型 号：T11209产 地：中国大陆
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T11143EB-47；化合物EB-47EB-47
EB-47 mimics the substrate NAD+ and extends from the nicotinamide to the adenosine subsite.EB-47, a potent and selective PARP-1/ARTD-1 inhibitor with an IC50 value of 45 nM, shows modest potency against ARTD5 with an IC50 value of 410 nM.
价 格：￥电议型 号：T11143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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T10465Atuveciclib S-Enantiomer；化合物 T10465BAY-1143572 S-Enantiomer；BAY-1143572 S-Enantiomer
Atuveciclib S-Enantiomer (BAY-1143572 S-Enantiomer) is the (S)-enantiomer of BAY-1143572. Atuveciclib S-Enantiomer is a potent and selective CDK9 inhibitor, which inhibits CDK9 / CycT1 with an IC 50 of 16 nM.
价 格：￥电议型 号：T10465产 地：中国大陆
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T10464LAtuveciclib Racemate；阿维西利BAY-1143572 Racemate；BAY-1143572 Racemate|||阿维西利
Atuveciclib Racemate (BAY-1143572 Racemate) is the racemate mixture of Atuveciclib, which is a potent and highly selective, oral P-TEFb/CDK9 inhibitor which supresses CDK9/CycT1 with an IC50 of 13 nM.
价 格：￥电议型 号：T10464L产 地：中国大陆
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T10464Atuveciclib；化合物 T10464BAY-1143572；BAY-1143572
Atuveciclib (BAY-1143572) is a potent and highly selective, oral PTEFb / CDK9 inhibitor that inhibits CDK9 / CycT1 with an IC 50 of 13 nM [1].
价 格：￥电议型 号：T10464产 地：中国大陆
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T0199Cephradine；头孢拉定Anspor|||Cephradin|||Velosef|||SQ-11436|||Sefril；Anspor|||Cephradin|||Velosef|||SQ-11
Cephradine (Anspor) is a beta-lactam, first-generation cephalosporin antibiotic with bactericidal activity.
价 格：￥电议型 号：T0199产 地：中国大陆
