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T16999Tavapadon；化合物TavapadonPF-6649751|||CVL-751；PF-6649751|||CVL-751
Tavapadon (CVL-751) is an orally active and highly selective dopamine D1/D5 receptor partial agonist.
价 格：￥电议型 号：T16999产 地：中国大陆
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T16751Rilapladib；瑞拉帕地SB 659032；SB 659032
Rilapladib (SB 659032) is a selective inhibitor of Lipoprotein-Associated Phospholipase A2(Lp-PLA2, IC50 = 230 pM) and an antagonist of the platelet activating factor receptor.
价 格：￥电议型 号：T16751产 地：中国大陆
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T16154MS417；化合物MS417GTPL7512；GTPL7512
MS417 (GTPL7512) is an inhibitor of BET-specific BRD4(BRD4-BD1 and BRD4-BD2 with IC50s of 30, 46 nM and Kds of 36.1, 25.4 nM, respectively), with weak selectivity at CBP BRD with IC50 of 32.7 μM.
价 格：￥电议型 号：T16154产 地：中国大陆
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T14751Boc-NH-PEG6-azide；化合物 T14751Boc-NH-PEG6-azide
Boc-NH-PEG6-azide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T14751产 地：中国大陆
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T13751L-Threonine derivative-1；L-苏氨酸衍生物-1L-Threonine derivative-1
L-Threonine derivative-1 is acetylsalicylic acid-L-threonine ester with potential analgesic activity.
价 格：￥电议型 号：T13751产 地：中国大陆
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T13398ZINC13466751；化合物ZINC13466751ZINC13466751
ZINC13466751 is a potent HIF-1α/von Hippel-Lindau interaction inhibitor(IC50 = 2.0 ?M).
价 格：￥电议型 号：T13398产 地：中国大陆
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T12848SB-657510；化合物SB-657510SB-657510
SB-657510 is a urotensin II (UII) receptor (UT) antagonist. The Ki values of UT for human, monkey, cat, rat and mouse were 61, 17, 30, 65 and 56 nM, respectively. SB-657510 plays an anti-inflammatory role by inhibiting UII-induced inflammatory mediators, such as adhesion molecules, in human vascular endothelial cells and upregulation of cytokines and tissue factors. SB 657510 has a therapeutic effect on diabetes-related atherosclerotic disease in diabetic mouse models.
价 格：￥电议型 号：T12848产 地：中国大陆
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T12751RORγt agonist 1；化合物 T12751RORgammat agonist 1|||RORγt agonist 1|||RORγt agonist 1|||RORrt agonist 1；
RORγt agonist 1 is a potent, orally bioavailable agonist of RORγt(EC50 of 20.8 nM).
价 格：￥电议型 号：T12751产 地：中国大陆
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T125751Eriodictyol-8-glucoside；化合物 Eriodictyol-8-glucosideEriodictyol-8-glucoside
Eriodictyol-8-glucoside is a useful organic compound for research related to life sciences and the catalog number is T125751.
价 格：￥电议型 号：T125751产 地：中国大陆
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T124751Junceic acid；化合物 Junceic acidJunceic acid
Junceic acid is a useful organic compound for research related to life sciences. The catalog number is T124751 and the CAS number is 50816-25-6.
价 格：￥电议型 号：T124751产 地：中国大陆
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T12429PF-06751979；化合物 T12429PF-06751979
PF-06751979 is an inhibitor of β-site amyloid precursor protein cleaving enzyme 1 (BACE1) (IC50 of 7.3 nM in BACE1 binding assay).
价 格：￥电议型 号：T12429产 地：中国大陆
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T1203476751-0002；化合物 6751-00026751-0002
Glucagon-like peptide 1 receptor, Potency: 2238.7 nM
价 格：￥电议型 号：T120347产 地：中国大陆
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T11798L-692429；化合物L-692429MK-0751；MK-0751
L-692429 (MK-0751) is a potent nonpeptidyl growth hormone secretagogue (GHS) agonist, a benzolactam derivative, which reverses the inhibition of GH secretion by glucocorticoids.L-692429 has a high affinity for the G protein-coupled receptor and can be used in the study of acromegaly and obesity. L-692429 has a high affinity for G protein-coupled receptor and can be used to study acromegaly and obesity.
价 格：￥电议型 号：T11798产 地：中国大陆
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T11751KDOAM-25；化合物 T11751KDOAM-25
KDOAM-25, a potent and highly selective inhibitor of histone lysine demethylases 5 (KDM5) with IC50 values of 71 nM for KDM5A, 19 nM for KDM5B, 69 nM for KDM5C, and 69 nM for KDM5D, enhances global H3K4 methylation at transcriptional start sites and reduces proliferation in multiple myeloma MM1S cells.
价 格：￥电议型 号：T11751产 地：中国大陆
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T10751Cefetrizole；头孢三唑Cefetrizole
Ceftezole is an α-Glucosidase inhibitor (IC50: 2.1 μM; Ki: 0.578 μM).
价 格：￥电议型 号：T10751产 地：中国大陆
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T0751Furazolidone呋喃唑酮呋喃唑酮|||Furoxone
Furazolidone (Furoxone), a nitrofuran derivative, inhibits AML1-ETO transformed cells with IC50 value of 12.7 μM. It is antibacterial and antiprotozoal activity,
价 格：￥电议型 号：T0751产 地：中国大陆
