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T10481LBAY 73-6691；化合物 T10481L(R)-BAY 73-6691；(R)-BAY 73-6691
BAY 73-6691 is an inhibitor of brain penetrant PDE9A.
价 格：￥电议型 号：T10481L产 地：中国大陆
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T10481BAY 73-6691 racemate；化合物 T10481BAY 73-6691 racemate
BAY 73-6691 racemate is a phosphodiesterase 9 inhibitor.
价 格：￥电议型 号：T10481产 地：中国大陆
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T10480LBay 41-4109；化合物 T10480LBay 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：中国大陆
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T10480Bay 41-4109 (less active enantiomer)；化合物 T10480Bay 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：中国大陆
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T1048Estradiol；雌二醇E2|||17β-Estradiol|||17β-Oestradiol|||β-Estradiol；雌二醇|||E2|||17β-Estradiol|||17β-Oestra
Estradiol (E2) is a naturally occurring steroidal sex hormone that is essential for female fertility and maintenance of secondary sexual characteristics. Estradiol upregulates IL-6 expression through estrogen receptor beta (ERβ).
价 格：￥电议型 号：T1048产 地：中国大陆
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T10478BAY-Y 3118化合物 T10478BAY-Y3118|||BAY Y 3118|||BAY-Y 3118
BAY-Y 3118, a new chlorofluoroquinolone, has antimicrobial activity.
价 格：￥电议型 号：T10478产 地：中国大陆
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T10477BAY-985；化合物BAY-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：中国大陆
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T10476BAY-899；化合物 T10476BAY-899
BAY-899 is an orally active and selective antagonist of the luteinizing hormone receptor (LH-R), exhibiting IC50 values of 185 nM and 46 nM for human LH (hLH) and rat LH (rLH) respectively. In vivo studies have demonstrated that BAY-899 effectively reduces sex hormone levels[1].
价 格：￥电议型 号：T10476产 地：中国大陆
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T10475BAY-784；化合物 T10475BAY-784
BAY-784 is a gonadotropin-releasing hormone receptor (GnRH-R) antagonist (IC50s: 21 and 24 nM for human and rat GnRH-R).
价 格：￥电议型 号：T10475产 地：中国大陆
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T10474BAY-7598；化合物 T10474BAY-7598
BAY-7598 is a potent, selective, and orally bioavailable MMP12 inhibitor (IC50s: 0.085, 0.67, and 1.1 nM for human/murine/rat MMP12).
价 格：￥电议型 号：T10474产 地：中国大陆
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T10473LBAY-677；化合物 T10473LBAY-677
BAY-677, serving as an inactive control for BAY-678, is distinguished by BAY-678´s capabilities as an orally bioavailable, selective, and cell-permeable inhibitor of human neutrophil elastase (HNE), showcasing a high potency with an IC50 of 20 nM[1]. Furthermore, BAY-678 has been publicly nominated as a chemical probe by the Structural Genomics Consortium (SGC)[2].
价 格：￥电议型 号：T10473L产 地：中国大陆
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T10473BAY-678；化合物BAY-678BAY-678
BAY-678 is a human neutrophil elastase (HNE; IC50: 20 nM) inhibitor with oral bioactivity, potency and selectivity.BAY-678 is a chemical probe recommended by the Structural Genomics Consortium (SGC).
价 格：￥电议型 号：T10473产 地：中国大陆
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T10472LBay 65-1942 free base；化合物 T10472LBay 65-1942 free base
Bay 65-1942 free base is an inhibitor of ATP-competitive and selective IKKβ.
价 格：￥电议型 号：T10472L产 地：中国大陆
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T10472Bay 65-1942 (R form)；化合物 T10472Bay 65-1942 R form；Bay 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：中国大陆
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T10471BAY 60-2770；化合物 T10471BAY 60-2770
BAY 60-2770 is a selective and orally active soluble guanylyl cyclase (sGC) activator with antifibrotic effect. It increases the activity of sGC in a nitric oxide-independent manner.
价 格：￥电议型 号：T10471产 地：中国大陆
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T10469BAY-298；化合物 T10469BAY-298
BAY-298 is an orally active and selective luteinizing hormone receptor (LH-R) antagonist with IC 50 s of 96 nM, 23 nM and 78 nM for hLH (human LH) and rLH (rat LH) and cLH (cynomolgus monkey LH), respectively. BAY-298 is the first nanomolar hLH-R antagonist reducing sex hormone levels in vivo[1].
价 格：￥电议型 号：T10469产 地：中国大陆
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T10468Elimusertib hydrochloride(1876467-74-1 free base)；化合物 Elimusertib hydrochlorideBAY-1895344 hydrochlo
Elimusertib hydrochloride(1876467-74-1 free base) (BAY-1895344 hydrochloride) is a effective, orally available and selective ATR inhibitor with anti-tumor activity.
价 格：￥电议型 号：T10468产 地：中国大陆
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T10467BAY-1816032；化合物BAY-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：中国大陆
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T10466BAY-1797；化合物BAY-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：中国大陆
