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T11644Impurity C of Alfacalcidol；阿法骨化醇杂质 CImpurity C of Alfacalcidol
Impurity of Alfacalcidol is an impurity of Alfacalcidol. Alfacalcidol is a non-selective VDR activator medication.
价 格：￥电议型 号：T11644产 地：中国大陆
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T11643Impurity B of Calcitriol；化合物 T116431β,25-Dihydroxyvitamin-D3|||1-Epicalcitriol；1β,25-Dihydroxyvitami
Impurity B of Calcitriol is an impurity of Calcitriol. Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
价 格：￥电议型 号：T11643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
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T11630IFN alpha-IFNAR-IN-1 hydrochloride；化合物IFN alpha-IFNAR-IN-1 hydrochlorideIFN alpha-IFNAR-IN-1 hydroch
IFN alpha-IFNAR-IN-1 hydrochloride is an inhibitor of the interaction between IFN-α and IFNAR. IFN alpha-IFNAR-IN-1 hydrochloride inhibits MVA-induced IFN-α responses by BM-pDCs with IC50 of 2-8 μM.
价 格：￥电议型 号：T11630产 地：中国大陆
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T1163Betamethasone valerate；倍他米松戊酸酯Betnovate|||Betaderm|||Betamethasone 17-valerate|||Luxiq；Betnovate|||倍
Betamethasone valerate (Luxiq) is a synthetic glucocorticoid with metabolic, immunosuppressive and anti-inflammatory actions.
价 格：￥电议型 号：T1163产 地：中国大陆
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T11610Idelalisib D5；化合物 T11610CAL-101 D5|||GS-1101 D5；CAL-101 D5|||GS-1101 D5
Idelalisib D5, a version of Idelalisib marked with deuterium, is an orally bioavailable and highly selective inhibitor of p110δ.
价 格：￥电议型 号：T11610产 地：中国大陆
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T11599Ibiglustat (L-Malic acid)；化合物Ibiglustat (L马来酸)Ibiglustat L-Malic acid|||GZ402671 (L-Malic acid)|||Ve
Ibiglustat (L-Malic acid) (Ibiglustat L-Malic acid) is a selective, brain-penetrant, and allosteric inhibitor of glucosylceramide synthase. Ibiglustat (L-Malic acid) can be used in studies about PD Parkinson’s disease, SRT in Fabry’s and Gaucher’s.
价 格：￥电议型 号：T11599产 地：中国大陆
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T1156Palonosetron hydrochloride；盐酸帕洛诺司琼RS 25259 197|||Palonosetron HCl|||RS 25259；盐酸帕洛诺司琼|||RS 25259 197|
Palonosetron hydrochloride (RS 25259) is a 5-HT3 antagonist used in the prevention and treatment of chemotherapy-induced nausea and vomiting.
价 格：￥电议型 号：T1156产 地：中国大陆
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T11558Hexyl gallate没食子酸己酯没食子酸己酯|||Gallic acid hexyl ester|||Hexyl 3,4,5-trihydroxybenzoate
Hexyl gallate (Gallic acid hexyl ester), an alkyl ester derivative of gallic acid, exhibits potent antimalarial activity against Plasmodium falciparum (IC50: 0.11 mM).
价 格：￥电议型 号：T11558产 地：中国大陆
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T11549Helioxanthin 8-1；化合物 T11549Helioxanthin analogue 8-1；Helioxanthin analogue 8-1
Helioxanthin 8-1, an analogue of helioxanthin, exhibits significant in vitro anti-HBV/HCV/HSV-1/HIV activity with EC50 of >5/10/1.4/15 μM.
价 格：￥电议型 号：T11549产 地：中国大陆
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T11535Haloperidol D4氟哌啶醇D4氟哌啶醇D4
Haloperidol D4 is deuterium-labeled haloperidol.
价 格：￥电议型 号：T11535产 地：中国大陆
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T1152Albendazole；阿苯达唑SKF-62979；SKF-62979|||阿苯达唑
Albendazole (SKF-62979) is used as a drug indicated for the treatment of a variety of worm infestations.
价 格：￥电议型 号：T1152产 地：中国大陆
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T11508Camicinal；化合物 T11508GSK962040；GSK962040
Camicinal is a selective motilin receptor agonist (pEC50: 7.9).
价 格：￥电议型 号：T11508产 地：中国大陆
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T11487LFiboflapon sodium；化合物 T11487LGSK2190915 sodium salt|||AM-803 sodium；GSK2190915 sodium salt|||AM-803
Fiboflapon sodium (GSK2190915) is an orally bioavailable 5-lipoxygenase-activating protein (FLAP) inhibitor with a potency of 2.9 nM in FLAP binding, an IC50 of 76 nM for inhibition of LTB4 in human blood.
价 格：￥电议型 号：T11487L产 地：中国大陆
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T11475GSK-J1 lithium salt化合物 T11475GSKJ1 lithium salt|||GSK J1 lithium salt|||GSK-J-1 lithium salt
GSK-J1 lithium salt is an effective inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A, with an IC 50 of 60 nM for KDM6B.
价 格：￥电议型 号：T11475产 地：中国大陆
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T1146Nifedipine；硝苯地平BAY-a-1040|||Procardia XL|||Procardia|||Adalat；BAY-a-1040|||Procardia XL|||Procardia|
Nifedipine (Procardia) is a dihydropyridine calcium channel blocking agent. Nifedipine inhibits the transmembrane influx of extracellular calcium ions into myocardial and vascular smooth muscle cells, causing dilatation of the main coronary and systemic arteries and decreasing myocardial contractility. This agent also inhibits the drug efflux pump P-glycoprotein which is overexpressed in some multi-drug resistant tumors and may improve the efficacy of some antineoplastic agents.
价 格：￥电议型 号：T1146产 地：中国大陆
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T1144Lidocaine hydrochloride盐酸利多卡因Lidocaine HCL|||盐酸利多卡因|||Lignocaine hydrochloride|||Xyloneural|||Lidoth
Lidocaine hydrochloride (Lignocaine hydrochloride) is a local anesthetic and cardiac depressant used as an antiarrhythmic agent. Its actions are more intense and its effects more prolonged than those of PROCAINE but its duration of action is shorter than that of BUPIVACAINE or PRILOCAINE.
价 格：￥电议型 号：T1144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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T11427Antibacterial compound 2；抗菌化合物2Antibacterial compound 2
Antibacterial compound 2 is a potent antimicrobial agent effective against many human veterinary pathogens, inhibiting multi-drug resistant staphylococci, enterococci and streptococci, as well as anaerobic bacteria.
价 格：￥电议型 号：T11427产 地：中国大陆
