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T10610Brexpiprazole-d8；化合物 T10610OPC-34712 D8；OPC-34712 D8
Brexpiprazole D8 (OPC-34712 D8) is a deuterium-labeled Brexpiprazole. Brexpiprazole is a partial agonist of human 5-HT1A and dopamine receptors (Ki: 0.12 nM and 0.3 nM).
价 格：￥电议型 号：T10610产 地：中国大陆
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T10590Zatolmilast；化合物BPN14770BPN14770；BPN14770
Zatolmilast (BPN14770) is an allosteric inhibitor of selective phosphodiesterase 4D (PDE4D; IC50s: 7.8 nM and 7.4 nM for PDE4D7 and PDE4D3).
价 格：￥电议型 号：T10590产 地：中国大陆
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T10581Boc-MLF TFA (67247-12-5 free base)；化合物 T10581Boc-Met-Leu-Phe-OH (TFA)|||Boc-MLF TFA；Boc-Met-Leu-Phe-
Boc-MLF (TFA) is a specific antagonist of formyl peptide receptor (FPR) and also inhibits signaling through FPRL1 at higher concentrations.
价 格：￥电议型 号：T10581产 地：中国大陆
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T10568BMS-470539 dihydrochloride；化合物 T10568BMS-470539 dihydrochloride
BMS-470539 dihydrochloride is a highly potent and selective agonist of the melanocortin-1 receptor (MC-1R; IC50: 120 nM; EC50: 28 nM) with anti-inflammatory properties. It does not activate MC-3R and is a very weak partial agonist at MC-4R and MC-5R.
价 格：￥电议型 号：T10568产 地：中国大陆
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T10547BioE-1115；化合物BioE-1115BioE-1115
BioE-1115 is a selective and potent inhibitor of serine-threonine protein kinase (PASK, IC50 = 4 nM). BioE-1115 is a potent inhibitor of CK2α (IC50 = 10 μM).
价 格：￥电议型 号：T10547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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T10447BAA473；化合物 T10447BAA473
BAA473 is a bile acid analog that is a potent activator of the pyrin inflammasome. BAA473 can induce secretion of interleukin-18 (IL-18) through activation of the inflammasome in both myeloid and intestinal epithelial cells [1].
价 格：￥电议型 号：T10447产 地：中国大陆
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T10347LApidaecin IB acetate；化合物Apidaecin IB acetateApidaecin IB acetate (123276-94-8 Free base)；Apidaecin I
Apidaecin IB acetate is an insect antibacterial peptide. The minimum concentration of apidaecin IB acetate against Escherichia coli (E. coli ML35, o18k1h7 and ATCC 25922) is 8 μM.
价 格：￥电议型 号：T10347L产 地：中国大陆
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T10347Apidaecin IB；化合物 T10347Apidaecin IB
Apidaecin IB is an insect antimicrobial peptide, with MIC values of 8 μM for E. coli (O18K1H7, ML35 and ATCC 25922).
价 格：￥电议型 号：T10347产 地：中国大陆
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T10204A-317491 sodium salt hydrate；化合物 T10204A-317491 sodium salt hydrate (475205-49-3 free base)；A-317491
A-317491 sodium salt hydrate is a non-nucleotide P2X3 and P2X2/3 receptor antagonist, which inhibits calcium flux mediated by the receptors.
价 格：￥电议型 号：T10204产 地：中国大陆
