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T18677SC-Val-Cit-PAB；化合物 T18677SC-Val-Cit-PAB
SC-Val-Cit-PAB is a cleavable ADC linker for antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T18677产 地：中国大陆
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T18657S-acetyl-PEG20-alcohol；化合物 T18657S-acetyl-PEG20-alcohol
S-acetyl-PEG20-alcohol 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：T18657产 地：中国大陆
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T16957Sulfo DBCO-PEG4-amine；化合物 T16957Sulfo DBCO-PEG4-amine
Sulfo DBCO-PEG4-amine 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：T16957产 地：中国大陆
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T16938ST034307；化合物ST034307ST034307
ST034307 is an effective and selective inhibitor of adenylyl cyclase 1 (IC50: 2.3 μM).
价 格：￥电议型 号：T16938产 地：中国大陆
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T16937ST 2825；化合物 T16937ST 2825
ST 2825 is a specific MyD88 dimerization inhibitor. ST2825 inhibition of IL-1β-mediated activation of NF-κB transcriptional activity.
价 格：￥电议型 号：T16937产 地：中国大陆
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T16917SPDP-PEG4-NHS ester；化合物 T16917SPDP-PEG4-NHS ester
SPDP-PEG4-NHS ester 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：T16917产 地：中国大陆
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T16907Soluflazine；化合物 T16907Soluflazine
Soluflazine is a nucleoside transport inhibitor. It also has anticonvulsant action.
价 格：￥电议型 号：T16907产 地：中国大陆
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T16877SHP394；化合物 T16877SHP394
SHP394 is an orally efficacious inhibitor of protein tyrosine phosphatase SHP2 (IC50: 23 nM).
价 格：￥电议型 号：T16877产 地：中国大陆
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T16857SB269652；化合物 T16857SB269652
SB269652 is the first drug-like allosteric modulator of the dopamine D2 receptor.
价 格：￥电议型 号：T16857产 地：中国大陆
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T16856SB228357；化合物SB228357SB228357
SB228357 is a potent and selective antagonist of the 5-HT receptor with pKis of 6.9, 8.0, and 9.0 for 5-HT2A, 5-HT2B, and 5-HT2C, respectively.
价 格：￥电议型 号：T16856产 地：中国大陆
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T16847SA 47；化合物 T16847SA 47
SA 47 is a selective and effective inhibitor of fatty acid amide hydrolase and carbamate.
价 格：￥电议型 号：T16847产 地：中国大陆
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T16837SAICAR；化合物 T16837SAICAR
SAICAR is an intermediate of de novo purine nucleotide biosynthesis, activates pyruvate kinase isoform M2 (PKM2) in an isozyme-selective manner (EC50: 0.3 mM).
价 格：￥电议型 号：T16837产 地：中国大陆
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T16827S-acetyl-PEG6-Tos；化合物 T16827S-acetyl-PEG6-Tos
S-acetyl-PEG6-Tos 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：T16827产 地：中国大陆
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T16377Odiparcil；化合物 T16377SB-424323；SB-424323
Odiparcil is an orally active beta-d-thioxyloside analog. Odiparcil is an indirect thrombin inhibitor that exerts its anticoagulant effect through activation of antithrombin II (heparin cofactor II). It also has an antithrombotic activity associated with a reduced risk of adverse bleeding events.
价 格：￥电议型 号：T16377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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T13887SJF620；化合物 T13887SJF620
SJF620 is a potent degrader of PROTAC BTK(DC50 : 7.9 nM).
价 格：￥电议型 号：T13887产 地：中国大陆
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T13667Dusquetide TFA (931395-42-5 free base)；化合物 T13667SGX942 TFA|||Dusquetide TFA；SGX942 TFA|||Dusquetide
Dusquetide TFA is a kind of innate defense regulator (IDR).Dusquetide TFA has been shown to be active in reducing inflammation and increasing clearance of bacterial infections.Dusquetide TFA regulates innate immune responses to PAMPs and DAMPs in combination with P62.
价 格：￥电议型 号：T13667产 地：中国大陆
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T131624(3S,5S,6R,10R,13S,17S) androstane-3,6,17-triol；化合物 (3S,5S,6R,10R,13S,17S) androstane-3,6,17-triol(3S
androstane-3,6,17-triol is a useful organic compound for research related to life sciences and the catalog number is T131624.
价 格：￥电议型 号：T131624产 地：中国大陆
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T13111Tegadifur；双喃氟啶40497S|||FD 1；40497S|||FD 1
Tegadifur (40497S) is an orally available antitumor compound with antimetabolic effects, often used with uracil and in the treatment of rectal adenocarcinoma.
价 格：￥电议型 号：T13111产 地：中国大陆
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T12998SR10067；化合物SR10067SR10067
SR10067 is a potent, selective and brain penetrant agonist of Rev-Erbβ(IC50 = 160 nM) and Rev-Erbα(IC50 = 170 nM) with anxiolytic activity.
价 格：￥电议型 号：T12998产 地：中国大陆
