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T40775SSR411298；SSR411298SSR411298；SSR411298
SSR411298 is a reversible, orally active compound that selectively inhibits fatty acid amide hydrolase (FAAH). Its potential lies in the field of post-traumatic stress disorder (PTSD) research.
价 格：￥电议型 号：T40775产 地：中国大陆
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T407727-TFA-ap-7-Deaza-dG；7-TFA-ap-7-Deaza-dG7-TFA-ap-7-Deaza-dG
5´-O-TBDMS-dG, a modified nucleoside, is utilized in the synthesis of deoxyribonucleic acid or nucleic acid.
价 格：￥电议型 号：T40772产 地：中国大陆
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T4077PE859；化合物PE859PE859
PE859 is a potent inhibitor of both tau and Aβ aggregation.
价 格：￥电议型 号：T4077产 地：中国大陆
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T40769Maltooctaose；MaltooctaoseMaltooctaose
Maltooctaose, a defined maltooligosaccharide with a specific length, can be enzymatically synthesized using Pyrococcus furiosus thermostable amylase (PFTA).
价 格：￥电议型 号：T40769产 地：中国大陆
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T40768{Boc}-Phe-Leu-Phe-Leu-Phe；{Boc}-Phe-Leu-Phe-Leu-Phe{Boc}PheLeuPheLeuPhe|||{Boc}-Phe-Leu-Phe-Leu-Phe|
{Boc}-Phe-Leu-Phe-Leu-Phe ({Boc}-FLFLF) is a selective antagonist of the formyl peptide receptor (FPR) family, effectively inhibiting receptor activity in response to formyl peptides.
价 格：￥电议型 号：T40768产 地：中国大陆
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T40767Bananin；BananinBananin
Bananin, a potent inhibitor of the ATPase activity exhibited by the SARS Coronavirus helicase, demonstrates remarkable efficacy with an IC50 value of 2.3 μM.
价 格：￥电议型 号：T40767产 地：中国大陆
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T407661,2,3,4-Tetrahydro-β-carboline-1-carboxylic acid；1,2,3,4-四氢-β-咔啉-1-羧酸1,2,3,4-Tetrahydro-β-carboline-
1,2,3,4-Tetrahydro-β-carboline-1-carboxylic acid is a neuroactive compound utilized in neurodegenerative disease research.
价 格：￥电议型 号：T40766产 地：中国大陆
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T40765DMAC-SPDB-sulfo；DMAC-SPDB-sulfoDMAC-SPDB-sulfo
DMAC-SPDB-sulfo is a cleavable linker vital in ADC synthesis. DMAC-SPDB-sulfo joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness.
价 格：￥电议型 号：T40765产 地：中国大陆
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T40764DMAC-SPDB；DMAC-SPDBDMAC-SPDB
DMAC-SPDB is a cleavable linker vital in ADC synthesis. DMAC-SPDB joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness.
价 格：￥电议型 号：T40764产 地：中国大陆
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T40763NO2-SPDMV-sulfo；NO2-SPDMV-sulfoNO2-SPDMV-sulfo；NO2-SPDMV-sulfo
NO2-SPDMV-sulfo is a cleavable linker vital in ADC synthesis. NO2-SPDMV-sulfo joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness.
价 格：￥电议型 号：T40763产 地：中国大陆
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T40762NO2-SPDB-sulfo；NO2-SPDB-sulfoNO2-SPDB-sulfo；NO2-SPDB-sulfo
NO2-SPDB-sulfo is a cleavable linker vital in ADC synthesis. NO2-SPDB-sulfo joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness.
价 格：￥电议型 号：T40762产 地：中国大陆
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T40761NO2-SPP-sulfo；NO2-SPP-sulfoNO2-SPP-sulfo；NO2-SPP-sulfo
NO2-SPP-sulfo is a cleavable linker vital in ADC synthesis. NO2-SPP-sulfo joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness.
价 格：￥电议型 号：T40761产 地：中国大陆
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T40760Mal-PEG2-NH2 TFA；Mal-PEG2-NH2 TFAMal-PEG2-NH2 TFA；Mal-PEG2-NH2 TFA
Mal-PEG2-NH2 TFA 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：T40760产 地：中国大陆
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T4076Fondaparinux sodium；磺达肝癸钠Natural heparin pentasaccharide Sodium|||Fondaparin sodium|||SR-90107A|||Ar
Fondaparinux sodium (SR-90107A) is an antithrombin-dependent factor Xa inhibitor with antithrombotic activity.
价 格：￥电议型 号：T4076产 地：中国大陆
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T40759ddCTP；ddCTPddCTP
ddCTP is one of 2´,3´-dideoxyribonucleoside 5´-triphosphates (ddNTPs) that acts as chain-elongating inhibitor of DNA polymerase for DNA sequencing.
价 格：￥电议型 号：T40759产 地：中国大陆
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T40758Hydrastinine；HydrastinineHydrastinine
Hydrastinine, a key alkaloid component found in Hydrastis canadensis (goldenseal), serves as an effective hemostatic agent.
价 格：￥电议型 号：T40758产 地：中国大陆
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T407571-Stearoyl-2-arachidonoyl-sn-glycerol；1-Stearoyl-2-arachidonoyl-sn-glycerol1-Stearoyl-2-arachidonoyl
1-Stearoyl-2-arachidonoyl-sn-glycerol, a diacylglycerol (DAG) encompassing polyunsaturated fatty acids, possesses the ability to activate PKC. Moreover, this compound has the potential to enhance nonselective cation channel (NSCC) activity.
价 格：￥电议型 号：T40757产 地：中国大陆
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T40756[Asp5]-Oxytocin；[Asp5]-Oxytocin[Asp5]-Oxytocin；[Asp5]-Oxytocin
[Asp5]-Oxytocin is the first 5-position neurohypophyseal hormone analogue possessing significant biological activity.
价 格：￥电议型 号：T40756产 地：中国大陆
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T40755Glabrescione B；Glabrescione BGlabrescione B
Glabrescione B is a novel compound that specifically binds to Gli1, an important modulator of the Hedgehog (Hh) signaling pathway. By disrupting the Gli1-DNA interaction, Glabrescione B effectively impairs the activity of Gli1. Moreover, Glabrescione B demonstrates potent inhibitory effects on the growth of tumor cells that rely on Hedgehog signaling, as well as on the self-renewal capacity and clonogenicity of tumor-derived stem cells.
价 格：￥电议型 号：T40755产 地：中国大陆
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T40754m-PEG2-O-Ph-NH2；m-PEG2-O-Ph-NH2m-PEG2-O-Ph-NH2；m-PEG2-O-Ph-NH2
m-PEG2-O-Ph-NH2 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：T40754产 地：中国大陆
