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T16202N-Boc-diethanolamine；化合物 T16202N-Boc-diethanolamine
N-Boc-diethanolamine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T16202产 地：中国大陆
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T16201N-(Biotin)-N-bis(PEG1-alcohol)；化合物 T16201N-(Biotin)-N-bis(PEG1-alcohol)
N-(Biotin)-N-bis(PEG1-alcohol) is a PEG-based PROTAC linker employed for the synthesis of PROTACs[1].
价 格：￥电议型 号：T16201产 地：中国大陆
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T16200N-Benzyl-N-bis-PEG4；化合物 T16200N-Benzyl-N-bis-PEG4
N-Benzyl-N-bis-PEG4 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：T16200产 地：中国大陆
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T1620Pazufloxacin Mesylate；帕珠沙星甲磺酸盐Pazucross|||Pazufloxacin mesilate|||T-3762|||Pazufloxacin methanesulfo
Pazufloxacin Mesylate (T-3762) is a fluoroquinolone antibiotic.
价 格：￥电议型 号：T1620产 地：中国大陆
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T16132MRE3008F20；化合物 MRE3008F20MRE3008F20
MRE3008F20 is a species-selective and potent adenosine A3 receptor (AA3R) antagonist that inhibits Cl-IB-MECA-induced cAMP production and can be used in glaucoma and asthma studies.CAS ??13483-88-88-9
价 格：￥电议型 号：T16132产 地：中国大陆
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T16120MLT-748；化合物 T16120MLT-748
MLT-748 is an effective, selective, and allosteric MALT1 inhibitor. It binds MALT1 in the allosteric Trp580 pocket (IC50: 5 nM).
价 格：￥电议型 号：T16120产 地：中国大陆
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T1603Glipizide格列吡嗪CP 28720|||K 4024|||格列吡嗪
Glipizide (CP 28720) is a short-acting, second-generation sulfonylurea with hypoglycemic activity.
价 格：￥电议型 号：T1603产 地：中国大陆
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T15946MA-2029；化合物 T15946MA-2029
MA-2029 is selective for the motilin receptor over various other receptors and ion channels. MA-2029 is a selective and competitive motilin receptor antagonist (IC50=4.9 nM). MA-2029 may be useful for gastrointestinal disorders associated with disturbed gastrointestinal motility.
价 格：￥电议型 号：T15946产 地：中国大陆
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T15945MA-0204；化合物MA-0204MA-0204
MA-0204 is a highly selective and orally available peroxisome proliferator-activated receptor δ (PPARδ) modulator (EC50s: 0.4 nM, 7.9 nM and 10 nM for human, mouse and rat PPARδ, respectively). It is a potential treatment for Duchene Muscular Dystrophy (DMD).
价 格：￥电议型 号：T15945产 地：中国大陆
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T15920m-PEG7-Amine；化合物 T15920m-PEG7-Amine
m-PEG7-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15920产 地：中国大陆
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T15820Mibampator；化合物MibampatorLY451395；LY451395
Mibampator (LY451395) is an effective and selective AMPA receptor potentiator.
价 格：￥电议型 号：T15820产 地：中国大陆
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T15757Limaprost；利马前列素17α,20-dimethyl-δ2-PGE1|||OP1206|||ONO1206；17α,20-dimethyl-δ2-PGE1|||利马前列素|||OP1206||
Limaprost (17α,20-dimethyl-δ2-PGE1) is an analog of PGE1 with structural modifications intended to give it a prolonged half-life and greater potency.It is a potent and orally active vasodilator. Limaprost increases blood flow and inhibits platelet aggregation. Limaprost (17α,20-dimethyl-δ2-PGE1) can be used for pain relief, has antianginal effects, and has potential for ischaemic symptoms treatment.
价 格：￥电议型 号：T15757产 地：中国大陆
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T15728LDN-212320；化合物LDN-212320LDN-0212320|||LDN/OSU-0212320|||OSU-0212320；LDN-0212320|||LDN/OSU-0212320|||
LDN-212320 (OSU-0212320) is a glutamate transporter EAAT2 activator. It also enhances EAAT2 levels by > 6 fold at concentrations < 5 μM after 24 h.
价 格：￥电议型 号：T15728产 地：中国大陆
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T15720Lathosterol；化合物LathosterolLathosterol
Lathosterol, a molecule akin to cholesterol, serves as a biomarker for the body´s total cholesterol synthesis, as indicated by its serum concentration.
价 格：￥电议型 号：T15720产 地：中国大陆
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T15677KY1220；化合物KY1220KY1220
KY1220 destabilizes both β-catenin and Ras by targeting the Wnt/β-catenin pathway. It has an IC50 of 2.1 μM in HEK293 reporter cells.
价 格：￥电议型 号：T15677产 地：中国大陆
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T15669KT5720；化合物 T15669KT5720
KT5720 is a cell-permeable, reversible, and ATP-competitive inhibitor of protein kinase A (PKA) (Ki: 60 nM).
价 格：￥电议型 号：T15669产 地：中国大陆
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T1565Deferiprone；去铁酮Deferidone|||CP20；去铁酮|||Deferidone|||CP20
Deferiprone (Deferidone) is an Iron Chelator. The mechanism of action of deferiprone is as an Iron Chelating Activity.
价 格：￥电议型 号：T1565产 地：中国大陆
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T15646KBU2046；化合物KBU2046KBU2046
KBU2046 is an orally administered compound that inhibits cell motility and invasion, effectively suppressing cancer metastasis and extending lifespan. This compound uniquely targets and binds to chaperone heterocomplexes, selectively modifying the interaction of client proteins involved in motility regulation, while avoiding the characteristics typical of classical HSP90 inhibitors.
价 格：￥电议型 号：T15646产 地：中国大陆
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T15623JNJ-61432059；化合物JNJ-61432059JNJ-61432059
JNJ-61432059 is an oral active and selective negative modulator of TARP γ?8 Selective AMPAR(pIC50: 9.7).
价 格：￥电议型 号：T15623产 地：中国大陆
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T15597ISA-2011B；化合物ISA-2011BISA-2011B
ISA-2011B is an inhibitor of PIP5K1α and can be used in anticancer studies.
价 格：￥电议型 号：T15597产 地：中国大陆
