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T11071Dofequidar fumarate；化合物Dofequidar fumarateMS-209；MS-209
Dofequidar fumarate (MS-209)(MS-209 fumarate), a quinoline-based compound administered orally, is known for counteracting multidrug resistance (MDR) through the inhibition of ABCB1/P-glycoprotein (P-gp) and ABCC1/MDR-associated protein 1.
价 格：￥电议型 号：T11071产 地：中国大陆
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T10998Deriglidole；德格列哚SL 86-0715；SL 86-0715
Deriglidole (SL 86-0715) is a peripheral adrenergic receptor antagonist that is a selective inhibitor of alpha2 receptors. Deriglidole inhibits colistin and Idazoxan but does not show activity against prazosin and rat cortical and human platelet α2-adrenergic receptors.
价 格：￥电议型 号：T10998产 地：中国大陆
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T10778CGP 20712 A；化合物 CGP 20712 ACGP 20712 mesylate；CGP 20712 mesylate
CGP 20712 A (CGP 20712 mesylate) is a selective and potent β1-adrenergic receptor antagonist (IC50: 0.7 nM) with antihypertensive activity that reverses RKT-induced gastric relaxation.
价 格：￥电议型 号：T10778产 地：中国大陆
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T1071LDL-Adrenaline Hydrochloride；肾上腺素盐酸盐DL-Adrenaline Hydrochloride
DL-Adrenaline Hydrochloride is the hydrochloride salt of the naturally occurring sympathomimetic amine with vasoconstricting, intraocular pressure-reducing activities.
价 格：￥电议型 号：T1071L产 地：中国大陆
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T10719CCT365623 hydrochloride；化合物 T10719CCT365623 hydrochloride
CCT365623 hydrochloride is an orally active inhibitor of lysyl oxidase (LOX) (IC50: 0.89 μM). It suppresses EGFR (pY1068) and AKT phosphorylation driven by EGF.
价 格：￥电议型 号：T10719产 地：中国大陆
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T10718LCCT241533 hydrochloride；化合物 T10718LCCT241533 hydrochloride
CCT241533 hydrochloride is an effective and selective ATP competitive inhibitor of CHK2 (Ki: 1.16 nM; IC50: 3 nM).
价 格：￥电议型 号：T10718L产 地：中国大陆
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T10718CCT241533；化合物 T10718CCT241533
CCT241533 is an effective and selective ATP competitive inhibitor of CHK2 (Ki: 1.16 nM; IC50: 3 nM).
价 格：￥电议型 号：T10718产 地：中国大陆
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T10717Inobrodib；化合物CBP-IN-1CBP-IN-1；CBP-IN-1
Inobrodib (CBP-IN-1) is a potent inhibitor of p300/CBP bromodomain.
价 格：￥电议型 号：T10717产 地：中国大陆
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T10716CCR7 Ligand 1；化合物 T10716CCR7-Cmp2105；CCR7-Cmp2105
CCR7 Ligand 1 (CCR7-Cmp2105) is an allosteric Ligand and antagonist for human CC chemokine receptor 7 (CCR7) with a Kd of 3 nM. CCR7 Ligand 1, thiadiazole-dioxide ligan, suppresses arrestin binding in response to activation by CCL19 with an IC50 of 7.3 μM.
价 格：￥电议型 号：T10716产 地：中国大陆
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T10715CCR6 inhibitor 1；化合物CCR6 inhibitor 1CCR6 inhibitor 1
CCR6 inhibitor 1 is an effective and selective inhibitor of CCR6 (IC50 of monkey and human CCR6 was 0.45 nM and 6 nM, respectively). CCR6 is associated with both autoimmune and non-autoimmune diseases, so CCR6 inhibitor 1 is useful for in vitro and in vivo pathophysiology studies as a small molecule inhibitor of CCR6.
价 格：￥电议型 号：T10715产 地：中国大陆
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T10714CCR5 antagonist 1；化合物 T10714CCR5 antagonist 1
CCR5 antagonist 1 is a CCR5 antagonist extracted from WO 2004054974 A2. It can inhibit HIV replication.
价 格：￥电议型 号：T10714产 地：中国大陆
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T10713CCR4 antagonist 2；化合物 T10713CCR4 antagonist 2
CCR4 antagonist 2 (Compound 31) is a novel potent, orally bioavailable small molecule antagonists of CC chemokine receptor 4 (CCR4) that inhibits Treg trafficking into the Tumor Microenvironment without suppressing the number of Treg in healthy tissues. CCR4 antagonist 2 (Compound 31) exhibits IC50 values of Ca2+flux and (chemotaxis) CTX are 40 nM and 70 nM, respectively.
价 格：￥电议型 号：T10713产 地：中国大陆
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T10712CCR2 antagonist 3；化合物CCR2 antagonist 3AZD-2927|||AZD2927；AZD-2927|||AZD2927
CCR2 antagonist 3 (AZD-2927) is an antagonist of CCR2.
价 格：￥电议型 号：T10712产 地：中国大陆
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T10711CCR2 antagonist 1；化合物 T10711CCR2 antagonist 1
CCR2 antagonist 1 is a high-affinity and long-residence-time antagonist of CCR2 (Ki: 2.4 nM).
价 格：￥电议型 号：T10711产 地：中国大陆
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T10710CCR1 antagonist 9；化合物 T10710CCR1 antagonist 9
CCR1 antagonist 9 is an effective and selective CCR1 antagonist (IC50: 6.8 nM in calcium flux assay).
价 格：￥电议型 号：T10710产 地：中国大陆
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T10071Itch-Targeting Compound 1；化合物 T10071Itch-Targeting Compound 1
Itch-Targeting Compound 1 is an anti-itch compound. It is effective in preventing or treating reactions on insect´s bites, reactions on environmental allergens, skin infections, external vermination, or itches occurring in renal dialysis patients.
价 格：￥电议型 号：T10071产 地：中国大陆
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T0719Tetrabenazine；丁苯那嗪Xenazine|||Ro 1-9569；Xenazine|||丁苯那嗪|||Ro 1-9569
Tetrabenazine (Ro 1-9569) is a drug formerly used as an antipsychotic and treatment of various movement disorders. Tetrabenazine blocks neurotransmitter uptake into adrenergic storage vesicles and has been used as a high affinity label for the vesicle transport system.
价 格：￥电议型 号：T0719产 地：中国大陆
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T0718Brivudine；溴夫定Bromovinyldeoxyuridine|||BVDU；Bromovinyldeoxyuridine|||BVDU|||溴夫定
Brivudine (BVDU), an antiviral medicine, is used in the therapy of herpes zoster.
价 格：￥电议型 号：T0718产 地：中国大陆
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T0717LEnoxacin；依诺沙星NSC 629661|||AT 2266|||Pd107779|||CI 919；依诺沙星|||NSC 629661|||AT 2266|||Pd107779|||CI 91
Enoxacin (NSC-629661) is a broad-spectrum 6-fluoronaphthyridinone antibacterial agent (fluoroquinolones) structurally related to nalidixic acid.
价 格：￥电议型 号：T0717L产 地：中国大陆
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T0717Enoxacin hydrate；依诺沙星倍半水合物CI-919 hydrate|||Enoxacin Sesquihydrate|||AT-2266 hydrate；CI-919 hydrate||
Enoxacin hydrate (AT-2266 hydrate) is a broad-spectrum 6-fluoronaphthyridinone antibacterial agent.
价 格：￥电议型 号：T0717产 地：中国大陆
