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T10362LAR453588 hydrochloride；化合物 T10362LAR453588 hydrochloride
AR453588 hydrochloride is an orally bioavailable anti-diabetic glucokinase activator (EC50: 42 nM) with anti-hyperglycemic activity.
价 格：￥电议型 号：T10362L产 地：中国大陆
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T10362AR453588化合物 T10362AR-453588|||AR453588
AR453588 is an orally bioavailable anti-diabetic glucokinase activator (EC50: 42 nM) with anti-hyperglycemic activity.
价 格：￥电议型 号：T10362产 地：中国大陆
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T10358L2Netarsudil mesylate；化合物 T10358L2AR-13324 (mesylate)；AR-13324 (mesylate)
Netarsudil mesylate is an inhibitor of Rho-associated protein kinase (ROCK) and norepinephrine transporter (NET) with effective in intraocular pressure (IOP) reduction.
价 格：￥电议型 号：T10358L2产 地：中国大陆
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T10358LAR-13324 M1 metabolite；化合物 T10358LAR-13324 M1 metabolite
AR-13324 M1 metabolite is a hydrolysis metabolite of AR-13324 mesylate.
价 格：￥电议型 号：T10358L产 地：中国大陆
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T10358Netarsudil Dihydrochloride；化合物Netarsudil DihydrochlorideAR-13324 Dihydrochloride；AR-13324 Dihydrochl
Netarsudil Dihydrochloride (AR-13324 Dihydrochloride) is an inhibitor of Rho-associated protein kinase (ROCK) and norepinephrine transporter (NET) with effective in intraocular pressure (IOP) reduction.
价 格：￥电议型 号：T10358产 地：中国大陆
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T103187Compound 0833-0158；化合物 0833-0158Compound 0833-0158
Compound 0833-0158 is a useful organic compound for research related to life sciences and the catalog number is T103187.
价 格：￥电议型 号：T103187产 地：中国大陆
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T10302Amibegron hydrochloride；化合物 T10302SR 58611A；SR 58611A
Amibegron hydrochloride is a selective β3-adrenoceptor agonist (EC50: 3.5 nM for β-adrenoceptor in rat colon). It has anxiolytic and antidepressant activity.
价 格：￥电议型 号：T10302产 地：中国大陆
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T1028Moxonidine；莫索尼定BDF5895；莫索尼定|||BDF5895|||莫索尼啶
Moxonidine (BDF5895) is a selective agonist at the imidazoline receptor subtype 1, acting as an antihypertensive drug.
价 格：￥电议型 号：T1028产 地：中国大陆
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T10258AFP464 free base；化合物 T10258NSC710464 free base；NSC710464 free base
AFP464 (NSC710464) free base is an active HIF-1α inhibitor (IC50: 0.25 μM) and a potent aryl hydrocarbon receptor (AhR) activator.
价 格：￥电议型 号：T10258产 地：中国大陆
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T10240ACP-5862；化合物 T10240ACP-5862
ACP-5862 is a major active and pyrrolidine ring-opened metabolite of Acalabrutinib (IC50: 5.0 nM for BTK). Acalabrutinib is an irreversible and highly selective BTK inhibitor (IC50: 3 nM; EC50: 8 nM).
价 格：￥电议型 号：T10240产 地：中国大陆
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T10210A-9758；化合物 T10210A-9758
A-9758 is a RORγ ligand and a selective RORγt inverse agonist (IC50: 5 nM) and exhibits robust potency against IL-17A release. It is effective in suppressing both Th17 differentiation and Th17 effector function. A-9758 significantly attenuates IL-23 driven psoriasiform dermatitis.
价 格：￥电议型 号：T10210产 地：中国大陆
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T1015842-(2-Tetrazolyl)rapamycin；化合物 T1015842-(2-Tetrazolyl)rapamycin
42-(2-Tetrazolyl)rapamycin is a prodrug compound of a rapamycin analog.
价 格：￥电议型 号：T10158产 地：中国大陆
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T10058A2B receptor antagonist 1；化合物A2B receptor antagonist 1A2B receptor antagonist 1
A2B receptor antagonist 1 (EXAMPLE 9B) is a potent A2B adenosine receptor antagonist.
价 格：￥电议型 号：T10058产 地：中国大陆
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T100231-Naphthol；1-萘酚NSC 9586|||Nako TRB|||Furro ER；NSC 9586|||Nako TRB|||1-萘酚|||Furro ER
1-Naphthol (Furro ER) is an excited state proton transfer (ESPT) fluorescent molecular probe for sensing thermotropic microenvironmental changes of pluronic F127 in aqueous media.
价 格：￥电议型 号：T10023产 地：中国大陆
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T0958Penicillin G sodium salt；青霉素钠Penicillin G Sodium|||Benzylpenicillin sodium salt|||Benzylpenicillin S
Penicillin G sodium(Benzylpenicillin sodium) salt is a penicillin derivative commonly used in the form of its sodium or potassium salts in the treatment of a variety of infections. It is effective against most gram-positive bacteria and against gram-negative cocci. It has also been used as an experimental convulsant because of its actions on GAMMA-AMINOBUTYRIC ACID mediated synaptic transmission.
价 格：￥电议型 号：T0958产 地：中国大陆
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T0901Chlorobutanol；三氯叔丁醇Chlortran|||Chloretone|||YM-57158|||Chlorbutol|||Chloreton；Chlortran|||Chloretone
Chlorobutanol (Chlortran) is a chemical preservative, sedative hypnotic and weak local anaesthetic. It has Antibacterial and Antifungal properties. Chlorobutanol is typically used at a concentration of 0.5% where it lends long-term stability to multi-ingredient formulations.
价 格：￥电议型 号：T0901产 地：中国大陆
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T0858Flufenamic acid；氟芬那酸Arlef|||Nichisedan|||Achless；Arlef|||Nichisedan|||氟灭酸|||氟芬那酸|||Achless
Flufenamic acid (Arlef) is an anthranilic acid derivative with analgesic, anti-inflammatory, and antipyretic properties. It is used in musculoskeletal and joint disorders and administered by mouth and topically.
价 格：￥电议型 号：T0858产 地：中国大陆
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T0839LS-(+)-Ketoprofen；(S)-(+)-酮洛芬RP-19583|||Dexketoprofen|||(S)-(+)-Ketoprofen|||(S)-Ketoprofen；RP-19583|
S-(+)-Ketoprofen ((S)-(+)-Ketoprofen) works by blocking the action of a substance in the body called cyclo-oxygenase. It belongs to a class of medicines called non-steroidal anti-inflammatory drugs (NSAIDs). Cyclo-oxygenase is involved in the production of chemicals in the body called prostaglandins. Prostaglandins are produced in response to injury or certain diseases and would otherwise go on to cause swelling, inflammation and pain. By blocking cyclo-oxygenase, S-(+)-Ketoprofen prevents the p
价 格：￥电议型 号：T0839L产 地：中国大陆
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T0839Ketoprofen酮洛芬酮基布洛芬|||RP-19583|||酮洛芬
Ketoprofen (RP-19583) is a propionic acid derivate and nonsteroidal anti-inflammatory drug (NSAID) with anti-inflammatory, analgesic and antipyretic effects. Ketoprofen inhibits the activity of the enzymes cyclo-oxygenase I and II, resulting in a decreased formation of precursors of prostaglandins and thromboxanes. The resulting decrease in prostaglandin synthesis, by prostaglandin synthase, is responsible for the therapeutic effects of ibuprofen. Ketoprofen also causes a decrease in the formati
价 格：￥电议型 号：T0839产 地：中国大陆
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T0758Piroxicam；吡罗昔康CP-16171；吡罗昔康|||CP-16171
Piroxicam (CP-16171) is a non-specific COX inhibitor.
价 格：￥电议型 号：T0758产 地：中国大陆
