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T6582LMezlocillin；化合物 T6582LBay-f 1353|||Meslocillin|||Melocin|||Baypen|||Mezlin；Bay-f 1353|||Meslocillin|
Meloxicillin is a broad-spectrum penicillin antibiotic that is active against both Gram-negative bacteria and some Gram-positive bacteria. Unlike most other broad-spectrum penicillin, it is excreted by the liver and can therefore be used to treat biliary tract infections, such as ascending cholangitis.
价 格：￥电议型 号：T6582L产 地：中国大陆
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T6582Mezlocillin Sodium；美洛西林钠Baycipen；美洛西林钠|||Baycipen
Mezlocillin Sodium (Baycipen) is a penicillin beta-lactam antibiotic used in the treatment of bacterial infections caused by susceptible, usually gram-positive, organisms.
价 格：￥电议型 号：T6582产 地：中国大陆
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T6383Amikacin hydrate；阿米卡星水合物BAY416651 hydrate；阿米卡星水合物|||BAY416651 hydrate
Amikacin hydrate (BAY416651 hydrate) is an aminoglycoside antibiotic used to treat different types of bacterial infections.
价 格：￥电议型 号：T6383产 地：中国大陆
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T6382Amikacin disulfate；阿米卡星硫酸盐Pierami|||BAY-416651 sulfate|||BB-K8|||Amikacin sulfate；硫酸阿米卡星|||Pierami||
Amikacin disulfate (BAY-416651 sulfate) is a semi-synthetic aminoglycoside antibiotic derived from kanamycin A.
价 格：￥电议型 号：T6382产 地：中国大陆
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T63756BAY-204；化合物 BAY-204BAY-204
BAY-204 is a CSNK1α/δ inhibitor that can be used in the treatment of proliferative diseases.
价 格：￥电议型 号：T63756产 地：中国大陆
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T6322Copanlisib；库潘尼西BAY 80-6946；BAY 80-6946|||可泮利塞|||库潘尼西
Copanlisib (BAY 80-6946) is a phosphoinositide 3-kinase (PI3K) inhibitor with potential antineoplastic activity. Copanlisib inhibits the activation of the PI3K signaling pathway, which may result in inhibition of tumor cell growth and survival in susceptible tumor cell populations. Activation of the PI3K signaling pathway is frequently associated with tumorigenesis and dysregulated PI3K signaling may contribute to tumor resistance to a variety of antineoplastic agents.
价 格：￥电议型 号：T6322产 地：中国大陆
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T63204BAY-888；化合物 BAY-888BAY-888
BAY-888 is capable of acting on CSNK1A1 (IC50: 1.5 nM) and CSNK1D (IC50: 5.5 nM).
价 格：￥电议型 号：T63204产 地：中国大陆
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T62881(R)-BAY-899；化合物 (R)-BAY-899(R)-BAY-899
(R)-BAY-899 is an R-isomer of BAY-899. BAY-899 is a selective, orally active luteinizing hormone receptor (LH-R) antagonist that acts on hLH (human LH) (IC50: 185 nM) and rLH (rat LH) (IC50: 46 nM).
价 格：￥电议型 号：T62881产 地：中国大陆
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T62795BAY 2476568；化合物 BAY 2476568BAY 2476568
BAY 2476568 is a selective and potent EGFR inhibitor that acts on both wild-type EGFR (IC50 <0.2 nM) and mutant EGFR (IC50 <0.2 nM).
价 格：￥电议型 号：T62795产 地：中国大陆
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T62014(R,R)-BAY-Y 3118；化合物 (R,R)-BAY-Y 3118(R,R)-BAY-Y 3118
(R,R)-BAY-Y 3118, the R-enantiomer of BAY-Y 3118, exhibits weak bactericidal activity.
价 格：￥电议型 号：T62014产 地：中国大陆
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T61934Repinotan；瑞匹诺坦BAY x 3702 free base；BAY x 3702 free base
Repinotan (BAY x 3702 free base) is an orally active and selective 5-HT1A receptor agonist that crosses the blood-brain barrier (BBB), has neuroprotective activity, antagonizes morphine-induced depression of ventilation in anesthetized rats, and can be used in studies of acute ischemic stroke and traumatic brain injury.
价 格：￥电议型 号：T61934产 地：中国大陆
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T6166Telatinib；替拉替尼Bay 57-9352；Bay 57-9352|||替拉替尼
Telatinib (Bay 57-9352) is an effective inhibitor of VEGFR2/3, c-Kit, and PDGFRα. The IC50s of Telatinib forVEGFR2/3, c-Kit and PDGFRα are 6 nM/4 nM, 1 nM, and 15 nM, respectively.
价 格：￥电议型 号：T6166产 地：中国大陆
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T60147BAY-091；化合物BAY-091BAY-091
BAY-091 is a novel potent and highly selective PIP4K2A kinase inhibitor.
价 格：￥电议型 号：T60147产 地：中国大陆
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T5622BAY-218；化合物AHR antagonist 1AHR antagonist 1；AHR antagonist 1
BAY-218 (AHR antagonist 1) is an aryl hydrocarbon receptor (AHR) antagonist , has an IC50 of 39.9 nM in human cell line.
价 格：￥电议型 号：T5622产 地：中国大陆
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T5418BAY-293；化合物BAY-293BAY-293
BAY-293 is a potent, cell-active SOS1 inhibitor that disrupts the KRAS-SOS1 interaction (IC50: 21 nM).
价 格：￥电议型 号：T5418产 地：中国大陆
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T5325Nifurtimox；硝呋替莫BAY-2502|||BAY-A-2502；硝呋替莫|||BAY-2502|||BAY-A-2502
Nifurtimox (BAY-A-2502) is an antiprotozoal agent (IC50s = 9.91, 12.28, and 10.44 μM against Taluahuén, LQ, and Brener strains of T. cruzi- epimastigotes, respectively).
价 格：￥电议型 号：T5325产 地：中国大陆
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T5208BAY-8002；化合物BAY-8002BAY8002|||BAY 8002；BAY8002|||BAY 8002
BAY-8002 is a potent dual MCT1/2 inhibitor (IC50 values are 3, 8, and 12 nM at rat (C6), human (DLD-1) and mouse (4T1) MCT1 respectively).
价 格：￥电议型 号：T5208产 地：中国大陆
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T4263BAY 61-3606；化合物BAY 61-3606Syk inhibitor IV；2-[[7-(3,4-二甲氧基苯基)咪唑并[1,2-C]嘧啶-5-基]氨基]-3-吡啶甲酰胺|||Syk inhi
BAY 61-3606 (Syk inhibitor IV) is a potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase activity (Ki= 7.5 nM), exhibiting no inhibitory effect against Btk, Fyn, Itk, Lyn, and Src.
价 格：￥电议型 号：T4263产 地：中国大陆
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T41214(S)-BAY-293；异构体BAY-293BAY 294|||BAY 293 Negative Control；BAY 294|||BAY 293 Negative Control
(S)-BAY-293 is a potent pan-KRAS inhibitor for the study of primary non-small lung and pancreatic cancers.
价 格：￥电议型 号：T41214产 地：中国大陆
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T4097Vardenafil hydrochloride trihydrate盐酸瓦地那非三水合物Vardenafil HCl Trihydrate|||BAY38-9456|||盐酸瓦地那非三水合物
Vardenafil hydrochloride trihydrate (BAY38-9456) is a new type PDE inhibitor with IC50 of 0.7 and 180 nM for PDE5 and PDE1, respectively.
价 格：￥电议型 号：T4097产 地：中国大陆
