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T11870Losartan D4；氯沙坦 D4DuP-753 D4；氯沙坦 D4|||DuP-753 D4
Losartan D4, the deuterium-labeled version of Losartan, functions as an angiotensin II receptor antagonist. It inhibits the interaction between angiotensin II and AT1 receptors by competing for binding, achieving an IC50 value of 20 nM.
价 格：￥电议型 号：T11870产 地：中国大陆
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T11869Losartan (D4 Carboxylic Acid)；氯沙坦羧酸 D4E-3174 D4|||EXP-3174 D4；E-3174 D4|||氯沙坦羧酸 D4|||EXP-3174 D4
Losartan D4 Carboxylic Acid is the deuterium labeled Losartan, which is an angiotensin II receptor antagonist.
价 格：￥电议型 号：T11869产 地：中国大陆
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T1186Ifenprodil Tartrate；酒石酸艾芬地尔Ifenprodil Tartrate
Ifenprodil is a selective NMDA receptor (glutamate) antagonist.
价 格：￥电议型 号：T1186产 地：中国大陆
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T11855Lipopolysaccharides；化合物LipopolysaccharidesLPS；脂多糖|||LPS
Lipopolysaccharides (LPS) is a unique component of the cell wall of Gram-negative bacteria and consists of three regions: lipid A, oligosaccharide core, and O-specific polysaccharide (O-antigen). Lipopolysaccharides help maintain the integrity of the outer cell membrane and protect bacteria from damage by bile salts and lipid antibiotics. Lipopolysaccharides is a highly immunogenic antigen that can enhance immune responses and can be used for inflammation model construction.
价 格：￥电议型 号：T11855产 地：中国大陆
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T11847LLiarozole；利阿唑R75251 dihydrochloride；R75251 dihydrochloride|||利阿唑
Liarozole (R75251 dihydrochloride) is a cytochrome P450 (CYP450) dependent inhibitor, orally active, it also a potent inhibitor of estrogen (via inhibition of aromatase) and testicular androgen synthesis (inhibition of 17 ,20-lyase).Liarozole dihydrochloride is an imidazole derivative; it is being investigated as a non-hormonal agent in prostate cancer and in the treatment of various other cancers and skin disorders.
价 格：￥电议型 号：T11847L产 地：中国大陆
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T11847Liarozole dihydrochloride；化合物 T11847R75251 dihydrochloride；R75251 dihydrochloride
Liarozole dihydrochloride is a cytochrome P450 (CYP450) dependent inhibitor, orally active, it also a potent inhibitor of estrogen (via inhibition of aromatase) and testicular androgen synthesis (inhibition of 17 ,20-lyase).Liarozole dihydrochloride is an imidazole derivative; it is being investigated as a non-hormonal agent in prostate cancer and in the treatment of various other cancers and skin disorders.
价 格：￥电议型 号：T11847产 地：中国大陆
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T1184Rivaroxaban；利伐沙班BAY 59-7939；BAY 59-7939|||利伐沙班
Rivaroxaban (BAY 59-7939) is an orally bioavailable oxazolidinone derivative and direct inhibitor of the coagulation factor Xa with anticoagulant activity. Upon oral administration, rivaroxaban selectively binds to both free factor Xa and factor Xa bound in the prothrombinase complex. This interferes with the conversion of prothrombin (factor II) to thrombin and eventually prevents the formation of cross-linked fibrin clots. Rivaroxaban does not affect existing thrombin levels.
价 格：￥电议型 号：T1184产 地：中国大陆
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T11832Ledipasvir D-tartrate；雷迪帕韦 D-酒石酸GS-5885 D-tartrate；GS-5885 D-tartrate|||雷迪帕韦 D-酒石酸
Ledipasvir D-tartrate with EC50 values of 34 pM against GT1a and 4 pM against GT1b replicon. is an inhibitor of the hepatitis C virus NS5A.
价 格：￥电议型 号：T11832产 地：中国大陆
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T1182LLevocarnitine propionate；化合物 T1182LL-Propionylcarnitine|||ST261|||ST 261|||Propionyl-L-carnitine|||S
Propionylcarnitine is present in high abundance in the urine of patients with Methylmalonyl-CoA mutase (MUT) deficiency.
价 格：￥电议型 号：T1182L产 地：中国大陆
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T1182Levocarnitine propionate hydrochloride；丙酰左旋肉碱盐酸盐Propionyl-L-carnitine hydrochloride|||L-Propionylcar
Levocarnitine propionate hydrochloride (ST-261) is used for the treatment of the deterioration of renal function, congestive heart failure, intermittent claudication, and other diseases.
价 格：￥电议型 号：T1182产 地：中国大陆
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T11804β3-AR agonist 2；化合物 T11804β3-AR agonist 2
β3-AR agonist 2 is a potent and selective agonist of β3-adrenergic receptor (β3-AR with an EC50 of 8 nM).
价 格：￥电议型 号：T11804产 地：中国大陆
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T11761Tarlox-TKI；化合物 Tarlox-TKIKinase inhibitor-1；Kinase inhibitor-1
Tarlox-TKI (Kinase inhibitor-1) is a pan-ErbB inhibitor, the active ingredient of Tarloxotinib, with antitumor activity.Tarlox-TKI inhibits NRG1 and suppresses HER2 mutants.
价 格：￥电议型 号：T11761产 地：中国大陆
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T1175217-BFC；7-苄氧基-4-三氟甲基香豆素7-Benzyloxy-4-(trifluoromethyl)coumarin|||Y040-0031；7-Benzyloxy-4-(trifluoromet
7-BFC (7-Benzyloxy-4-(trifluoromethyl)coumarin) is a coumarin-like fluorescent substrate that serves as a biomarker for cytochrome P 450 and can be used to study CYP isoforms and cytochrome P 450 metabolism.
价 格：￥电议型 号：T117521产 地：中国大陆
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T1175Bromopride；溴灭吐灵Bromoprida|||Valopride|||Artomey；Bromoprida|||溴灭吐灵|||Valopride|||Artomey
Bromopride (Valopride) is a dopamine antagonist with prokinetic properties closely related to metoclopramide, and is widely used as an antiemetic. It is not available in the United States or the United Kingdom.
价 格：￥电议型 号：T1175产 地：中国大陆
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T11732JTV-519 hemifumarate；化合物 T11732K201 hemifumarate；K201 hemifumarate
JTV-519 hemifumarate,Antiarrhythmic and cardioprotective properties. is a Ca2+-dependent blocker of sarcoplasmic reticulum Ca2+-stimulated ATPase (SERCA) and a partial agonist of ryanodine receptors in striated muscle.
价 格：￥电议型 号：T11732产 地：中国大陆
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T11684Isoguvacine hydrochloride；异四氢烟酸1,2,3,6-tetrahydro-4-pyridinecarboxylic acid hydrochloride；1,2,3,6-te
Isoguvacine hydrochloride (1,2,3,6-tetrahydro-4-pyridinecarboxylic acid hydrochloride) is a GABA receptor agonist. Isoguvacine hydrochloride binds to rat synaptic cortical membranes and activates α1β2γ2S, α2β2γ2S, α3β2γ2S, α5β2γ2S, and ρ1 subunit GABAA receptors.
价 格：￥电议型 号：T11684产 地：中国大陆
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T11683Isoglycycoumarin；化合物 T11683Isoglycycoumarin
Isoglycycoumarin, a flavonoid derived from the roots of Glycyrrhiza uralensis, serves as a highly selective probe for human cytochrome P450 2A6.
价 格：￥电议型 号：T11683产 地：中国大陆
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T11682Isofistularin-3；化合物 T11682Isofistularin-3
Isofistularin-3, a direct DNA-competitive DNMT1 inhibitor with an IC50 of 13.5 μM, functions as a DNA demethylating agent, leading to cell cycle arrest and increased sensitivity to TRAIL in cancer cells. Additionally, it can be employed as an ADC cytotoxin.
价 格：￥电议型 号：T11682产 地：中国大陆
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T11675Irbesartan-d4；厄贝沙坦 D4SR-47436 D4|||BMS-186295 D4；厄贝沙坦 D4|||SR-47436 D4|||BMS-186295 D4
Irbesartan D4, a deuterium-labeled variant of Irbesartan, is a highly potent and specific antagonist of the angiotensin II type 1 (AT1) receptor.
价 格：￥电议型 号：T11675产 地：中国大陆
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T11630LIFN alpha-IFNAR-IN-1；化合物 T11630LIFN alpha-IFNAR-IN-1
IFN alpha-IFNAR-IN-1 is a nonpeptidic, low-molecular-weight inhibitor of the interaction between IFN-α and IFNAR. It inhibits MVA-induced IFN-α responses by BM-pDCs (IC50: 2-8 μM).
价 格：￥电议型 号：T11630L产 地：中国大陆
