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T191394-Nitrophenyl α-D-galactopyranoside；4-硝基苯-α-D-吡喃半乳糖苷PNP-alpha-D-Gal|||PNP-α-D-Gal；PNP-alpha-D-Gal|||
4-Nitrophenyl α-D-galactopyranoside (PNP-alpha-D-Gal) (PNP-alpha-D-Gal) is an artificial substrate of 4-nitrophenyl (pNP) glycopyranoside for detecting α-galactosidase activity. The amount of released pNP is significantly increased when PNP-alpha-D-Gal is used as substrates.
价 格：￥电议型 号：T19139产 地：中国大陆
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T18139m-PEG12-Hydrazide；化合物 T18139m-PEG12-Hydrazide
m-PEG12-Hydrazide 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：T18139产 地：中国大陆
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T17245VU0467485化合物 T17245AZ13713945
VU0467485 is a potent and selective muscarinic acetylcholine receptor 4 positive allosteric modulator. VU0467485 potentiates the activity of ACh at M4 (EC50s: 26.6 nM and 78.8 nM at the rat and human M4 receptors, respectively). VU0467485 displays selectivity for M4 over human and rat M1/2/3/5.
价 格：￥电议型 号：T17245产 地：中国大陆
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T17139Tos-PEG7-OH；化合物 T17139Tos-PEG7-OH
Tos-PEG7-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：T17139产 地：中国大陆
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T16139MRS2698；化合物 T16139MRS2698
MRS2698 is an effective and highly selective agonist of the P2Y2 receptor (EC50: 8 nM). MRS2698 also is >300-fold P2Y2-selective versus the P2Y4 and P2Y6 receptors.
价 格：￥电议型 号：T16139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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T1549Raloxifene hydrochloride；盐酸雷洛昔芬LY156758 hydrochloride|||Raloxifene HCl|||LY139481 hydrochloride|||Ke
Raloxifene hydrochloride (LY156758 hydrochloride) is a second generation selective estrogen receptor modulator (SERM) used to prevent osteoporosis in postmenopausal women. It has estrogen agonist effects on bone and cholesterol metabolism but behaves as a complete estrogen antagonist on mammary gland and uterine tissue.
价 格：￥电议型 号：T1549产 地：中国大陆
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T15367Gadoxetate Disodium；钆塞酸二钠Gd-EOB-DTPA Disodium|||ZK 139834；Gd-EOB-DTPA Disodium|||钆塞酸二钠|||ZK 139834
Gadoxetate Disodium is used to evaluate focal liver lesions, such as hepatocellular carcinoma or liver metastasis on T1-weighted imaging. It is a contrast agent in magnetic resonance imaging (MRI) of the hepatobiliary system. It accumulates in normal, functioning hepatocytes.
价 格：￥电议型 号：T15367产 地：中国大陆
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T15139DLin-KC2-DMA；化合物DLin-KC2-DMADLin-KC2-DMA
DLin-KC2-DMA is a cationic/ionizable lipid. Which is used for siRNA delivery.
价 格：￥电议型 号：T15139产 地：中国大陆
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T14198ALX-1393；化合物ALX-1393ALX-1393
ALX-1393 is a selective GlyT2 inhibitor that effectively reduces neuronal action potential activity in a concentration-dependent manner and inhibits the activity of spontaneous networks by inducing glycinergic tetanic currents in the abdominal horn of the spinal cord. Antiinjurious effects on thermal, mechanical and chemical stimuli in rat models of acute pain.
价 格：￥电议型 号：T14198产 地：中国大陆
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T14139Aganepag；化合物 T14139AGN 210937；AGN 210937
Aganepag, a potent Prostanoid EP2 receptor agonist, exhibits remarkable selectivity with an EC50 of 0.19 nM, demonstrating no activity at the EP4 receptor. Its applications are primarily in the fields of wound healing, scar reduction, scar prevention, and the treatment and prevention of wrinkles.
价 格：￥电议型 号：T14139产 地：中国大陆
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T139981-(t-Boc-Aminooxy)-3-aminooxy-propane；化合物 T139981-(t-Boc-Aminooxy)-3-aminooxy-propane
1-(t-Boc-Aminooxy)-3-aminooxy-propane is an alkyl/ether-based PROTAC linker utilized in the synthesis of PROTACs[1].
价 格：￥电议型 号：T13998产 地：中国大陆
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T13997AU-224；化合物 AU-224AU-224
AU-224 is an orally available benzamide derivative that is a potent gastrointestinal prokinetic.
价 格：￥电议型 号：T13997产 地：中国大陆
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T139961-Naphthohydroxamic acid；1-萘羟肟酸1-Naphthohydroxamic acid
1-Naphthohydroxamic acid (Compound 2) is a potent and selective HDAC8 inhibitor with an IC50 of 14 μM, and it is more selectively for HDAC8 than class I HDAC1 and class II HDAC6 (IC50 >100 μM). 1-Naphthohydroxamic acid does not increase global histone H4 acetylation and also does not reduce total intracellular HDAC activity[1][2], But it can induce tubulin acetylation.
价 格：￥电议型 号：T13996产 地：中国大陆
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T139951-Methyl-7-nitroisatoic anhydride；化合物1-Methyl-7-nitroisatoic anhydride1M7；1M7
1-Methyl-7-nitroisatoic anhydride (1M7) is a reagent. It detects local nucleotide flexibility, for probing 2´-hydroxyl reactivity.
价 格：￥电议型 号：T13995产 地：中国大陆
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T139941-Isothiocyanato-PEG4-alcohol；化合物 T139941-Isothiocyanato-PEG4-alcohol
1-Isothiocyanato-PEG4-alcohol is a polyethylene glycol (PEG)-derived linker compound suitable for the incorporation into Proteolysis Targeting Chimeras (PROTACs)[1].
价 格：￥电议型 号：T13994产 地：中国大陆
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T139931-Isothiocyanato-PEG3-azide；化合物 T139931-Isothiocyanato-PEG3-azide
1-Isothiocyanato-PEG3-azide is a PEG-based PROTAC linker utilized for PROTAC synthesis[1].
价 格：￥电议型 号：T13993产 地：中国大陆
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T13992CHF5407；化合物CHF5407SVT-47060；SVT-47060
CHF5407（SVT-47060） is a potent and selective muscarinic M3 receptor antagonist with prolonged action at muscarinic receptors.CHF5407 has an effect on bronchospasm and may be used in the study of respiratory disorders.CHF5407 is a potent and selective muscarinic M3 receptor antagonist with prolonged action at muscarinic receptors.
价 格：￥电议型 号：T13992产 地：中国大陆
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T139911,7-Bis-Boc-1,4,7-triazaheptane；化合物 T139911,7-Bis-Boc-1,4,7-triazaheptane
1,7-Bis-Boc-1,4,7-triazaheptane is an alkyl/ether-based PROTAC linker utilized for the synthesis of PROTACs[1].
价 格：￥电议型 号：T13991产 地：中国大陆
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T139901,3-Bis-aminooxy propane；化合物 T139901,3-Bis-aminooxy propane
1,3-Bis-aminooxy propane is an alkyl chain-derived PROTAC linker utilized for synthesizing PROTACs[1].
价 格：￥电议型 号：T13990产 地：中国大陆
