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T15768LM985；化合物 T15768LM985
LM985 is one of a series of compounds based on the flavone ring structure. It has anti-tumor activities.
价 格：￥电议型 号：T15768产 地：中国大陆
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T15767LLY-283；化合物LLY-283LLY-283
LLY-283 is a potent, selective and oral protein arginine methyltransferase 5 (PRMT5) inhibitor, with an IC50 of 22 nM and a Kd of 6 nM for PRMT5:MEP50 complex, and shows antitumor activity.
价 格：￥电议型 号：T15767产 地：中国大陆
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T15766Lirimilast；化合物 T15766BAY 19-8004；BAY 19-8004
Lirimilast is an effective, selective, and orally active phosphodiesterase-4 (PDE4) inhibitor (IC50: 49 nM). Lirimilast has potently anti-inflammatory properties. Lirimilast can be used for the treatment of asthma or chronic obstructive pulmonary disease.
价 格：￥电议型 号：T15766产 地：中国大陆
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T15765Lipoamido-PEG4-azide；化合物 T15765Lipoamido-PEG4-azide
Lipoamido-PEG4-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：T15765产 地：中国大陆
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T15764Lipoamido-PEG4-acid；化合物 T15764Lipoamido-PEG4-acid
Lipoamido-PEG4-acid 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：T15764产 地：中国大陆
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T15763Lipoamido-PEG3-OH；化合物 T15763Lipoamido-PEG3-OH
Lipoamido-PEG3-OH, also known as compound TA-TEG-G2CN, is a PEG-based PROTAC linker utilized in PROTAC synthesis. It is instrumental in the creation of a robust, dendronized gold nanoparticle (AuNP)-based drug delivery platform[1].
价 格：￥电议型 号：T15763产 地：中国大陆
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T15762Lipoamido-PEG2-OH；化合物 T15762Lipoamido-PEG2-OH
Lipoamido-PEG2-OH 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：T15762产 地：中国大陆
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T15761Lipoamide-PEG3-Mal；化合物 T15761Lipoamide-PEG3-Mal
Lipoamide-PEG3-Mal 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：T15761产 地：中国大陆
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T15760LLintopride HCl；Lintopride 盐酸盐Lintopride HCl（107429-63-0 Free base)；Lintopride HCl（107429-63-0 Free b
Lintopride HCl is a 5HT-4 antagonist.
价 格：￥电议型 号：T15760L产 地：中国大陆
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T15760Lintopride；林托必利Lintopride
Lintopride is an antagonist of 5HT4. It has moderate 5HT3 antagonist properties.
价 格：￥电议型 号：T15760产 地：中国大陆
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T1576Iopamidol；碘帕醇SQ-13396|||Niopam|||Iopamiron|||Iopamiro|||B-15000|||Isovue；SQ-13396|||Niopam|||Iopamir
Iopamidol (SQ-13396) is a benzenedicarboxamide compound. It has a role as a radioopaque medium, an environmental contaminant and a xenobiotic.
价 格：￥电议型 号：T1576产 地：中国大陆
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T15706Lanicemine；拉尼西明AZD6765；AZD6765|||拉尼西明
Lanicemine is a low-trapping NMDA channel blocker. It also has a binding (Ki: 0.56-2.1 μM).
价 格：￥电议型 号：T15706产 地：中国大陆
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T15676KY-556化合物 T15676N556
KY-556 is a promising and orally-active pro-drug of disodium cromoglycate (DSCG). It also against allergic diseases.
价 格：￥电议型 号：T15676产 地：中国大陆
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T15617JNJ-38877618；化合物JNJ-38877618OMO-1；OMO-1
JNJ-38877618 (OMO-1) is an effective and highly selective inhibitor of Met kinase (IC50s: 2 and 3 nM for wild type and mutant Met, respectively).
价 格：￥电议型 号：T15617产 地：中国大陆
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T15591Ipenoxazone；伊培沙宗NC-1200|||MLV-6976；NC-1200|||MLV-6976|||伊培沙宗
Ipenoxazone is an effective and centrally acting muscle relaxant.
价 格：￥电议型 号：T15591产 地：中国大陆
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T15568Imirestat；咪瑞司他Alcon 1576|||AL 1576|||HOE 843；Alcon 1576|||AL 1576|||咪瑞司他|||HOE 843
Imirestat (HOE 843) is an aldose reductase inhibitor that can be used in diabetes research.
价 格：￥电议型 号：T15568产 地：中国大陆
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T15476Hexaethylene glycol；化合物 T15476Hexaethylene glycol
Hexaethylene glycol 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：T15476产 地：中国大陆
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T15453GW7647化合物GW76472-[[4-[2-[[环己基氨基)羰基](4-环己基丁基)氨基]乙基]苯基]硫基]-2-甲基丙酸
GW7647 is a potent agonist of PPARα (EC50s: 6 nM, 1.1 μM, and 6.2 μM for human PPARα, PPARγ, and PPARδ, respectively).
价 格：￥电议型 号：T15453产 地：中国大陆
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T15452GW7604；化合物 T15452GW7604
GW7604 is an antiestrogen and it also is the metabolite of GW5638. GW5638 is an antagonist of high-affinity estrogen receptor (ER).
价 格：￥电议型 号：T15452产 地：中国大陆
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T15440GSK376501A；化合物GSK376501AGSK376501A
GSK376501A is a selective and effective modulator of peroxisome proliferator-activated receptor γ (PPARγ) for the study of type 2 diabetes.
价 格：￥电议型 号：T15440产 地：中国大陆
