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T68108LMoxilubant HCl；化合物Moxilubant盐酸盐Moxilubant hcl(146978-48-5 Free base)；Moxilubant hcl(146978-48-5 Free
Moxilubant HCl is a small molecule leukotriene B4 receptor 1 (LTB4R) antagonist for the treatment of immune system disorders, skin and musculoskeletal disorders, and may be used in studies of psoriasis and rheumatoid arthritis.
价 格：￥电议型 号：T68108L产 地：中国大陆
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T68108Moxilubant；化合物MoxilubantMoxilubant
Moxilubant is a small molecule leukotriene B4 receptor 1 (LTB4R) antagonist for the treatment of immune system disorders, skin and musculoskeletal disorders, and may be used in studies of psoriasis and rheumatoid arthritis.
价 格：￥电议型 号：T68108产 地：中国大陆
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T67108Boc-Phenylalaninol；化合物 Boc-PhenylalaninolBoc-Phenylalaninol
Boc-Phenylalaninol is a useful organic compound for research related to life sciences. The catalog number is T67108 and the CAS number is 66605-57-0.
价 格：￥电议型 号：T67108产 地：中国大陆
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T66108N-Cbz-D-glutamic Acid；化合物 N-Cbz-D-glutamic AcidN-Cbz-D-glutamic Acid
N-Cbz-D-glutamic Acid is a useful organic compound for research related to life sciences. The catalog number is T66108 and the CAS number is 63648-73-7.
价 格：￥电议型 号：T66108产 地：中国大陆
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T6591Nodinitib-1；化合物ML130ML130|||CID-1088438；ML130|||CID-1088438
Nodinitib-1 (CID-1088438) is a potent and selective NOD1 inhibitor with an IC50 of 0.56 μM.
价 格：￥电议型 号：T6591产 地：中国大陆
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T65108Boc-Met-OH；化合物 Boc-Met-OHBoc-Met-OH
Boc-Met-OH is a useful organic compound for research related to life sciences. The catalog number is T65108 and the CAS number is 2488-15-5.
价 格：￥电议型 号：T65108产 地：中国大陆
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T6481Droxinostat；4-(4-氯-2-甲基苯氧基)-N-羟基丁酰胺NS 41080；NS 41080|||4-(4-氯-2-甲基苯氧基)-N-羟基丁酰胺
Droxinostat (NS 41080) is a selective inhibitor of HDAC, mostly for HDACs 6 and 8 with IC50 of 2.47 μM and 1.46 μM, greater than 8-fold selective against HDAC3 and no inhibition to HDAC1, 2, 4, 5, 7, 9, and 10.
价 格：￥电议型 号：T6481产 地：中国大陆
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T64108DX3-235；化合物 DX3-235DX3-235
DX3-235 is an inhibitor of oxidative phosphorylation (OXPHOS). In galactose-containing media, DX3-235 inhibits complex I function and ATP production by nanomolar amounts and is significantly cytotoxic.
价 格：￥电议型 号：T64108产 地：中国大陆
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T63108CDK7-IN-14；化合物 CDK7-IN-14CDK7-IN-14
CDK7-IN-14 is a pyrimidine-derived compound that is a potent inhibitor of CDK7. CDK7-IN-14 has the potential to be investigated in a variety of cancers, particularly those with transcriptional dysregulation.
价 格：￥电议型 号：T63108产 地：中国大陆
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T63041DS01080522；化合物 DS01080522DS01080522
DS01080522 is an inhibitor of PRKACA. DS01080522 inhibited PRKACA kinase activity (IC50.0.8 nM) and CREB phosphorylation (IC50.66 nM). DS0108052 can be used to study cancer.
价 格：￥电议型 号：T63041产 地：中国大陆
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T62851SLF1081851 TFA；化合物 SLF1081851 TFASLF1081851 TFA
SLF1081851 (TFA) is a Spns2 inhibitor with an IC50 value of 1.93 μM for inhibition of S1P release.SLF1081851 (TFA) plays a key role in development and the immune system.
价 格：￥电议型 号：T62851产 地：中国大陆
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T62108ErSO-DFP；化合物 ErSO-DFPErSO-DFP
ErSO-DFP is an expected activator of the unfolded protein response (a-UPR). erSO-DFP improves selectivity for oestrogen receptor alpha+ (ERα+) cancer cells with higher selectivity than ErSO. erSO-DFP has anti-tumour effects and significantly eliminates MCF-7 tumours in a mouse model.
价 格：￥电议型 号：T62108产 地：中国大陆
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T62076LPM4870108；化合物 LPM4870108LPM4870108
LPM4870108 is a potent, orally active pan-Trk (WT/MT) inhibitor that acts on TrkC (IC50: 0.2 nM), TrkA (IC50: 2.4 nM), TrkAG595R (IC50: 3.5 nM) and TrkAG667C (IC50: 2.3 nM), and is more selective for Trk than ALK (IC50: 2.3 nM). LPM4870108 showed anti-tumour effects.
价 格：￥电议型 号：T62076产 地：中国大陆
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T61112SLF1081851；化合物SLF1081851SLF1081851
SLF1081851 is a Spns2 inhibitor. SLF1081851 inhibits S1P release with IC50 of 1.93 μM.
价 格：￥电议型 号：T61112产 地：中国大陆
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T61108YXL-13；化合物 YXL-13YXL-13
YXL-13 is a highly effective inhibitor of Pseudomonas aeruginosa (PAO1), with an IC50 value of 3.686 μM. It effectively hinders the expression of virulence factors and inhibits biofilm formation in PAO1. Moreover, YXL-13 significantly diminishes both the pathogenicity and drug resistance of PAO1 by inhibiting the quorum sensing (QS) system. Thus, YXL-13 holds great potential for studying antibacterial properties [1].
价 格：￥电议型 号：T61108产 地：中国大陆
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T61088Propiomazine；化合物 PropiomazinePropiomazine
Propiomazine is an orally active antihistamine agent that possesses sedative properties. It finds utility in insomnia research [1] [2].
价 格：￥电议型 号：T61088产 地：中国大陆
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T61087THK-5105；化合物 THK-5105THK-5105
THK-5105, an arylquinoline derivative, demonstrates a high binding affinity for tau fibrils, protein aggregates, and tau-rich Alzheimer´s disease (AD) brain homogenates, indicative of its potential as a tau imaging PET (Positron Emission Tomography) probe with the radiolabeled version, 18F-THK-5105 [1].
价 格：￥电议型 号：T61087产 地：中国大陆
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T61086HN37；化合物 HN37HN37
HN37 as a potent and chemically stable antiepileptic drug candidate, with an EC 50 of 37 nM for KCNQ2 [1].
价 格：￥电议型 号：T61086产 地：中国大陆
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T61085TGP-377/421；化合物TGP-377/421Targapre-miR-377/421；Targapre-miR-377/421
TGP-377/421 (Targapre-miR-377/421) is a potent miR-377 and miR-421 dual inhibitor that inhibits miR-377 and miR-421 by binding to their functional sites.
价 格：￥电议型 号：T61085产 地：中国大陆
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T61084Tubulin polymerization-IN-37；化合物 Tubulin polymerization-IN-37Tubulin polymerization-IN-37
Tubulin polymerization-IN-37 is a potent inhibitor (IC50: 2.3 μΜ) of tubulin polymerization by binding specifically to the colchicine site of tubulin and preventing colchicine binding. It has potential applications in cancer research, notably for lymphomas [1].
价 格：￥电议型 号：T61084产 地：中国大陆
