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  • T0247AcarboseAcarbose,BAY g 5421,

    Acarbose is an inhibitor of α-Glucosidases with antihyperglycemic activity.

    价 格:¥电议型 号:T0247产 地:美洲

  • T0250Ciprofloxacin hydrochlorideCiprofloxacin hydrochloride,Bay-09867 (hydrochloride),Ciprofloxacin HCl

    Ciprofloxacin hydrochloride is a broad-spectrum antimicrobial carboxyfluoroquinoline.

    价 格:¥电议型 号:T0250产 地:美洲

  • T0331Moxifloxacin hydrochlorideMoxifloxacin hydrochloride,BAY-128039,Moxifloxacin HCl

    Moxifloxacin is a fourth generation fluoroquinolone with expanded activity against gram-positive bacteria as well as atypical pathogens. Moxifloxacin has been linked to mild ALT elevations during therapy and to rare instances of idiosyncratic acute liver

    价 格:¥电议型 号:T0331产 地:美洲

  • T0343NimodipineNimodipine,BAY-e 9736,

    Nimodipine, a 1, 4-dihydropyridine calcium channel blocker, acts primarily on vascular smooth muscle cells.

    价 格:¥电议型 号:T0343产 地:美洲

  • T0506ClotrimazoleClotrimazole,BAY b 5097,FB 5097

    Clotrimazole, an imidazole derivative with a broad spectrum of antimycotic activity, inhibits biosynthesis of the sterol ergostol.

    价 格:¥电议型 号:T0506产 地:美洲

  • T0711NiclosamideNiclosamide,BAY2353,Niclocide

    Niclosamide(BAY2353) is used to treat most tapeworm infections by inhibiting DNA replication.

    价 格:¥电议型 号:T0711产 地:美洲

  • T0812Propranolol hydrochloridePropranolol hydrochloride,Propranolol HCl,AY-64043

    Propranolol hydrochloride is a widely used non-cardioselective beta-adrenergic antagonist. Propranolol has been used for MYOCARDIAL INFARCTION; ARRHYTHMIA; ANGINA PECTORIS; HYPERTENSION; HYPERTHYROIDISM; MIGRAINE; PHEOCHROMOCYTOMA; and ANXIETY but adverse

    价 格:¥电议型 号:T0812产 地:美洲

  • T1002EtodolacEtodolac,AY-24236,Etodolic acid

    Etodolac inhibits the activity of cyclooxygenase I and II, thereby preventing the formation of prostaglandin which is involved in the induction of pain, fever, and inflammation. Etodolac is a pyranocarboxylic acid and non-steroidal anti-inflammatory drug

    价 格:¥电议型 号:T1002产 地:美洲

  • T10270BAY 2416964BAY 2416964

    BAY 2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist extracted from patent WO2018146010A1 (example 192, IC50: 341 nM). It has the potential for cancer treatment.

    价 格:¥电议型 号:T10270产 地:美洲

  • T10464LAtuveciclib RacemateAtuveciclib Racemate,BAY-1143572 Racemate,

    Atuveciclib is a potent and highly selective, oral P-TEFb/CDK9 inhibitor which supresses CDK9/CycT1 with an IC50 of 13 nM. Atuveciclib Racemate (BAY-1143572 Racemate) is the racemate mixture of Atuveciclib.

    价 格:¥电议型 号:T10464L产 地:美洲

  • T10466BAY-1797BAY-1797

    BAY-1797 is an orally active and selective P2X4 antagonist (IC50: 211 nM against human P2X4) with anti-nociceptive and anti-inflammatory effects. BAY-1797 displays no or very weak activity on the other P2X ion channels.

    价 格:¥电议型 号:T10466产 地:美洲

  • T10467BAY-1816032BAY-1816032

    BAY-1816032 is a potent and orally available inhibitor of bidding uninhibited by benzimidazoles 1 ( BUB1) kinase (IC50: 7 nM).

    价 格:¥电议型 号:T10467产 地:美洲

  • T10470BAY-545BAY-545

    BAY-545 is a potent and selective A2B adenosine receptor antagonist (IC50: 59 nM). BAY-545 also exhibits IC50s of 66, 280, 400 nM for human, rat, mouse A2B adenosine receptor in cells, respectively.

    价 格:¥电议型 号:T10470产 地:美洲

  • T10472Bay 65-1942 R formBay 65-1942 R form

    Bay 65-1942 R form is the less active R-form of Bay 65-1942. Bay 65-1942 is a selective and ATP-competitive IKKβ inhibitor.

    价 格:¥电议型 号:T10472产 地:美洲

  • T10473BAY-678BAY-678

    BAY-678 is an orally bioavailable, selective and cell-permeable inhibitor of human neutrophil elastase (HNE; IC50: 20 nM).

    价 格:¥电议型 号:T10473产 地:美洲

  • T10473LBAY-677BAY-677

    BAY-677 is an inactive control for BAY-678. BAY-678 is an orally bioavailable, highly potent, selective and cell-permeable inhibitor of human neutrophil elastase (HNE), with an IC50 of 20 nM[1] and it is also nominated as a chemical probe to the public vi

    价 格:¥电议型 号:T10473L产 地:美洲

  • T10477BAY-985BAY-985

    BAY-985 is a potent, selective, and orally active ATP-competitive dual inhibitor of TBK1 and IKKε (IC50s: 2/30 and 2 nM for TBK1 (low/high ATP) and IKKε) with antitumor efficacy.

    价 格:¥电议型 号:T10477产 地:美洲

  • T10479BAY885BAY885

    BAY885 is a new ERK5 inhibitor.

    价 格:¥电议型 号:T10479产 地:美洲

  • T10480Bay 41-4109 (less active enantiomer)Bay 41-4109 (less active enantiomer)

    Bay 41-4109 less active enantiomer shows less activity than Bay 41-4109. BAY 41-4109 is a potent HBV inhibitor (IC50: 53 nM).

    价 格:¥电议型 号:T10480产 地:美洲

  • T10480LBay 41-4109Bay 41-4109

    BAY 41-4109 is a potent inhibitor of human hepatitis B virus (HBV)(IC50 : 53 nM).

    价 格:¥电议型 号:T10480L产 地:美洲

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