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T26673AT-076；化合物 T26673AT 076；AT 076
AT-076 is a noncompetitive antagonist of the κ-opioid receptor (Ki = 1.14 nM) and nociceptin receptor (Ki = 1.75 nM) and a competitive antagonist of the μ-opioid receptor (Ki = 1.67 nM) and δ-opioid receptor (Ki = 19.6 nM).
价 格：￥电议型 号：T26673产 地：中国大陆
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T26668ASN06917370；化合物 T26668ASN 06917370|||ASN-06917370；ASN 06917370|||ASN-06917370
ASN06917370 is a GPR17 receptor modulator and can be used for neuroprotective and/or reparatory purposes.
价 格：￥电议型 号：T26668产 地：中国大陆
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T26642Aplaviroc hydrochloride；化合物 T26642AK602|||AK 602|||GW873140A|||GW-873140|||GW873140|||AK-602|||Aplav
Aplaviroc is a human cellular CC chemokine receptor 5 (CCR5) entry inhibitor. Aplaviroc binds specifically to CCR5 and demonstrates potent anti-human immunodeficiency virus activity in vitro in the subnanomolar range. In vitro studies show that aplaviroc selectively inhibits the binding of a particular monoclonal antibody, 45531, to CCR5.
价 格：￥电议型 号：T26642产 地：中国大陆
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T26627LAnatibant 2HCl；Anatibant二盐酸盐Anatibant 2HCl(209733-45-9 Free base)；Anatibant 2HCl(209733-45-9 Free ba
Anatibant 2HCl is a small molecule bradykinin B2 receptor antagonist for the treatment of neurological disorders and may be used in the study of brain injury.
价 格：￥电议型 号：T26627L产 地：中国大陆
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T26586AL-37350A；化合物 T26586AL-37350A
AL-37350A is a 5-HT2 receptor-selective agonist with ocular hypotensive activity.
价 格：￥电议型 号：T26586产 地：中国大陆
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T26573AG311；化合物 T26573AG 311|||AG-311；AG 311|||AG-311
AG311 is an inhibitor of complex I and hypoxia-induced HIF-1α stabilization. In vitro, AG311 induces rapid necrosis in numerous cancer cell lines. Within minutes, exposure to AG311 also results in mitochondrial depolarization, superoxide production, and increased intracellular calcium levels.
价 格：￥电议型 号：T26573产 地：中国大陆
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T26447A 78773；化合物 T26447A78773|||A-78773；A78773|||A-78773
A 78773 is a potent, selective, direct, and reversible 5-lipoxygenase inhibitor. It has activity in a variety of purified cells and in more complex biological systems such as whole blood, lung fragments, and tracheal tissues. A 78773 acts against inflammation and allergy, edema, inflammatory cell influx, and bronchospasm. It may treat asthma and inflammatory bowel disease.
价 格：￥电议型 号：T26447产 地：中国大陆
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T26439A 74273；化合物 T26439A-74273|||A74273；A-74273|||A74273
A 74273, a nonpeptidic and renin inhibitor, may be used to treat cardiovascular diseases due to renin inhibition.
价 格：￥电议型 号：T26439产 地：中国大陆
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T26438A 73209；化合物 T26438A73209|||A-73209；A73209|||A-73209
A 73209 is a nucleoside analog of the oxetanocin family. A-73209 appears to be a potent and selective agent against herpes simplex virus and varicella-zoster virus infections.
价 格：￥电议型 号：T26438产 地：中国大陆
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T2642PD173074；化合物PD173074PD173074
PD173074 is an effective FGFR1 inhibitor (IC50: 25 nM) and also inhibits VEGFR2 (IC50: 100-200 nM) in cell-free assays. The selectivity is higher ~1000-fold for FGFR1 than PDGFR and c-Src.
价 格：￥电议型 号：T2642产 地：中国大陆
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T26373(R)-Mequitazine；化合物 T26373V-0162|||V0162|||V 0162；V-0162|||V0162|||V 0162
(R)-Mequitazine, a muscarinic acetylcholine receptor (M-AChRs) antagonist, is used potentially for the treatment of asthma.
价 格：￥电议型 号：T26373产 地：中国大陆
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T26322L(-)-Vorozole；化合物(-)-Vorozole(-)-Vorozole(Isomer-129731-10-8)；(-)-Vorozole(Isomer-129731-10-8)
(-)-Vorozole is an orally active non-steroidal aromatase inhibitor with potency and selectivity. (-)-Vorozole has demonstrated antitumor activity in in vivo experiments. (-)-Vorozole is used in the study of breast cancer.
价 格：￥电议型 号：T26322L产 地：中国大陆
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T26304U 27391；化合物 T26304U-27391|||U27391；U-27391|||U27391
U 27391 is a metalloproteinase inhibitor. It acts by inhibits the action of human recombinant interleukin-1beta and glycosaminoglycan synthesis.
价 格：￥电议型 号：T26304产 地：中国大陆
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T26273Thioquinapiperifil；化合物 T26273KF-31327|||KF 31327|||KF-31327 free base|||KF31327；KF-31327|||KF 31327|
Thioquinapiperifil is a type of phosphodiesterase-5 (PDE-5) inhibitor found in dietary supplements.
价 格：￥电议型 号：T26273产 地：中国大陆
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T26173Safrazine Hydrochloride；化合物 T26173Safrazine Hydrochloride
Safrazine Hydrochloride is a monoamine oxidase inhibitor (MOI) that is irreversible.
价 格：￥电议型 号：T26173产 地：中国大陆
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T26142RS 87337；化合物 T26142RS87337|||RS-87337；RS87337|||RS-87337
RS 87337 is an antiarrhythmic that is chemically novel with an electrophysiologic profile characteristic of both class III and class Ia compounds.
价 格：￥电议型 号：T26142产 地：中国大陆
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T26140RS 5773；化合物 T26140RS-5773|||RS5773；RS-5773|||RS5773
RS 5773 is a benzothiazepine derivative with antianginal effects.
价 格：￥电议型 号：T26140产 地：中国大陆
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T2613Almorexant；阿莫伦特ACT 078573；阿莫伦特|||ACT 078573
Almorexant (ACT 078573) is a potent and competitive dual orexin 1 receptor (OX1)/orexin 2 receptor (OX2) antagonist with Ki values of 1.3 and 0.17 nM for OX1 and OX2, respectively.
价 格：￥电议型 号：T2613产 地：中国大陆
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T26105Ro 32-7315；化合物 T26105Ro-327315|||Ro327315|||Ro 32 7315；Ro-327315|||Ro327315|||Ro 32 7315
Ro 32-7315 is a selective inhibitor of ADAM17.
价 格：￥电议型 号：T26105产 地：中国大陆
