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T5361T-26c
T-26c is highly potent and selective matrix metalloproteinase-13 (MMP-13) inhibitor (IC50: 6.75 pM).
价 格：￥电议型 号：T5361产 地：中国大陆
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T23861CAY10526CAY-10526；CAY 10526；BTH
CAY10526 is a selective mPGES-1 inhibitor that acts as an inhibitor of the NF-κB signaling pathway.
价 格：￥电议型 号：T23861产 地：中国大陆
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T5361T-26cT-26c
T-26c is highly potent and selective matrix metalloproteinase-13 (MMP-13) inhibitor (IC50: 6.75 pM).
价 格：￥电议型 号：T5361产 地：美洲
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T8726Cyclo(RGDyK)化合物 T8726Cyclo(RGDyK)
Cyclo(RGDyK) is a potent and selective αVβ3 integrin inhibitor with IC50 of 20 nM.
价 格：￥电议型 号：T8726产 地：中国大陆
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T83959CELT-426；化合物 CELT-426CELT-426
CELT-426 is a potent, partially selective fluorescent antagonist of the human D2 dopamine receptor, exhibiting Ki values of 89.3 nM, 194.8 nM, and 263.6 nM for D2, D3, and D4 dopamine receptors, respectively, in radioligand binding assays. This compound serves as an effective fluorescent probe for dopamine receptors, facilitating its application in a range of techniques including fluorescence binding assays, live cell imaging, flow cytometry, and fluorescence polarization assays. It provides an
价 格：￥电议型 号：T83959产 地：中国大陆
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T82684Connexin mimetic peptide 40,37GAP26；化合物 Connexin mimetic peptide 40,37GAP26Connexin mimetic peptide
Connexin mimetic peptide 40,37GAP26, a biologically active peptide, matches the GAP26 domain of the extracellular loop of major vascular connexins Cx37 and Cx40, referred to as 37,40Gap26 based on Cx homology. It has been utilized to examine gap junctions´ involvement in propagating endothelial hyperpolarizations induced by cyclopiazonic acid (CPA) in the rodent iliac artery wall. Abundant gap junction plaques comprising Cx37 and Cx40 are present in the endothelium, and the peptide exerts
价 格：￥电议型 号：T82684产 地：中国大陆
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T82664CTX-2026；化合物 CTX-2026CTX-2026
CTX-2026, a fully human antibody, targets and binds to CD277, demonstrating an anti-tumor effect in ovarian tumor models, and is utilized in cancer research [1].
价 格：￥电议型 号：T82664产 地：中国大陆
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T80282cPcAMP1/26；化合物 cPcAMP1/26cPcAMP1/26
cPcAMP1/26, an antimicrobial peptide, exhibits potent bactericidal activity against A. hydrophila and S. aureus by inducing depolarization of the bacterial plasma membrane and elevating intracellular ROS (Reactive Oxygen Species) levels [1].
价 格：￥电议型 号：T80282产 地：中国大陆
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T79631CDK9-IN-26；化合物 CDK9-IN-26CDK9-IN-26
CDK9-IN-26, also known as compound 1, is a potent inhibitor of Cyclin-Dependent Kinase 9 (CDK9) with an IC50 value of 0.18 μM.[1]
价 格：￥电议型 号：T79631产 地：中国大陆
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T78947CST626；化合物 CST626CST626
CST626 (Compound 9), a pan-IAP degrader PROTAC, effectively degrades XIAP, cIAP1, and cIAP2 in MM.1S cells with DC50 values of 0.7, 2.4, and 6.2 nM, respectively [1].
价 格：￥电议型 号：T78947产 地：中国大陆
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T69252CPD26；化合物 CPD26CPD26
CPD26 is a novel non-RBD binding modulator to inhibit SARS-CoV-2 by prohibiting the conformational change of the spike (S) protein.
价 格：￥电议型 号：T69252产 地：中国大陆
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T69186CP26；化合物 CP26CP26
CP26 is a novel inhibitor of ER-to-cytosol protein dislocation, exhibiting anti-dengue and anti-Zika virus activity.
价 格：￥电议型 号：T69186产 地：中国大陆
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T68208CL 118326；化合物 CL 118326CL 118326
CL 118326 is a phospholipase A2 inhibitor.
价 格：￥电议型 号：T68208产 地：中国大陆
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T63480COX-2-IN-26；化合物 COX-2-IN-26COX-2-IN-26
COX-2-IN-26 is a potent, orally active, selective COX-2 inhibitor that acts on COX-1 (IC50: 10.61 μM), COX-2 (IC50: 0.067 μM), and 15-LOX (IC50: 1.96 μM).COX-2-IN-26 is anti-inflammatory and has a gastrointestinal safety profile.
价 格：￥电议型 号：T63480产 地：中国大陆
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T61757Cap-dependent endonuclease-IN-26；化合物 Cap-dependent endonuclease-IN-26Cap-dependent endonuclease-IN-2
Cap-dependent endonuclease-IN-26, a potent inhibitor of cap-dependent endonuclease (CEN) with an IC50 of 286 nM, exhibits significant antiviral activity against a broad spectrum of influenza A and B strains [1].
价 格：￥电议型 号：T61757产 地：中国大陆
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T5361T-26c；化合物T-26cT-26c
T-26c is highly potent and selective matrix metalloproteinase-13 (MMP-13) inhibitor (IC50: 6.75 pM).
价 格：￥电议型 号：T5361产 地：中国大陆
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T37860T 26c disodium salt；T 26c disodium saltT 26c disodium|||T 26c|||T 26c disodium salt；T 26c disodium||
Highly potent and selective MMP13 inhibitor (IC50 = 6.9 pM). Exhibits >2600-fold selectivity for MMP13 over related MMPs. Inhibits degradation of bovine nasal septum cartilage explants in vitro . Orally bioavailable.
价 格：￥电议型 号：T37860产 地：中国大陆
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T36194CAY10726；CAY10726CAY10726；CAY10726
CAY10726 is an arylurea fatty acid. It decreases ATP production by 28% in MDA-MB-231 breast cancer cells when used at a concentration of 10 μM. CAY10726 decreases proliferation and initiates apoptosis in MDA-MB-231 cells via depletion of the phospholipid cardiolipin and its precursor phosphatidylglycerol from the mitochondrial membrane.
价 格：￥电议型 号：T36194产 地：中国大陆
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T36087PI3K-IN-22；CAY10626CAY10626；CAY10626
PI3K-IN-22 is a dual kinase inhibitor of PI3Kα and mTOR, with IC50s of 0.9 and 0.6 nM respectively. PI3K-IN-22 could be used in cancer.
价 格：￥电议型 号：T36087产 地：中国大陆
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T31126CX-659S；化合物 T31126CX659S|||UNII-YG2F04AVMQ|||CX 659S；CX659S|||UNII-YG2F04AVMQ|||CX 659S
CX-659S is a novel diaminuracil derivative that indirectly inhibits Langerhans cell function by blocking the MEK1/2 -- ERK1/2 pathway in keratinocytes. CX-659S can inhibit the contact hypersensitivity induced by haptens in mice.
价 格：￥电议型 号：T31126产 地：中国大陆
