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T63028KRAS G12D inhibitor 12；化合物 KRAS G12D inhibitor 12KRAS G12D inhibitor 12
KRAS G12D inhibitor 12 is an effective inhibitor of KRAS G12D. The Ras protein family is an important intracellular signaling molecule, which plays an important role in growth and development. KRAS G12D inhibitor 12 has the potential to perform KRAS G12D-mediated cancer studies.
价 格：￥电议型 号：T63028产 地：中国大陆
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T62785KRAS G12C inhibitor 29；化合物 KRAS G12C inhibitor 29KRAS G12C inhibitor 29
KRAS G12C inhibitor 29 is an inhibitor of KRAS G12C and can be used to study cancer.
价 格：￥电议型 号：T62785产 地：中国大陆
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T62566KRAS G12C inhibitor 53；化合物 KRAS G12C inhibitor 53KRAS G12C inhibitor 53
KRAS G12C inhibitor 53 (Compound 1) is a KRAS G12C inhibitor.
价 格：￥电议型 号：T62566产 地：中国大陆
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T62485FabG1-IN-1；化合物 FabG1-IN-1FabG1-IN-1
FabG1-IN-1 (Compound 29) is a potent inhibitor of MabA (FabG1) (IC50: 38 μM).
价 格：￥电议型 号：T62485产 地：中国大陆
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T62228KRAS G12D inhibitor 14；KRAS G12D抑制剂14KRAS G12D inhibitor 14
KRAS G12D inhibitor 14 is a potent inhibitor of KRAS G12D that binds KRAS G12D protein (Kd: 33 nM). KRAS G12D inhibitor 14 inhibits the active form of KRAS G12D (KRAS G12D-GTP), but not KRAS G13D.
价 格：￥电议型 号：T62228产 地：中国大陆
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T61109HG122；化合物 HG122HG122
HG122 is a chemical compound that effectively facilitates the degradation of androgen receptor (AR) via the proteasome pathway, leading to the inhibition of castration-resistant prostate cancer.
价 格：￥电议型 号：T61109产 地：中国大陆
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T60870BRG1-IN-1；化合物 BRG1-IN-1BRG1-IN-1
BRG1-IN-1 (Compound 11d) is a potent BRG1 inhibitor with better efficacy than PFI-3 in sensitizing GBM cells to the antiproliferative and cell death inducing effects of Temozolomide in vitro. BRG1-IN-1 enhances the inhibitor effect of Temozolomide on the subcutaneous GBM tumors growth[1].
价 格：￥电议型 号：T60870产 地：中国大陆
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T60032BRM/BRG1 ATP Inhibitor-2；化合物 BRM/BRG1 ATP Inhibitor-2BRM/BRG1 ATP Inhibitor-2
BRM/BRG1 ATP Inhibitor-2 is an inhibitor of BRG1/BRM ATPase and can be used in studies about the treatment of BAF-related disorders.
价 格：￥电议型 号：T60032产 地：中国大陆
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T6001Nelfinavir Mesylate；甲磺酸奈非那韦Viracept|||Nelfin|||AG1343|||AG 1343 Mesylate；Viracept|||Nelfin|||AG1343|
Nelfinavir Mesylate (Viracept) is an effective HIV protease inhibitor (Ki: 2 nM).
价 格：￥电议型 号：T6001产 地：中国大陆
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T4661PKG drug G1；化合物PKG drug G1PKG drug G1
PKG drug G1 targets PKG Iα C42. PKG drug G1 can couple to vasodilation and blood pressure lowering by a C42 PKG Iα-independent mechanism.
价 格：￥电议型 号：T4661产 地：中国大陆
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T41096Propynyl-PEG1-Ac；Propynyl-PEG1-AcPropynyl-PEG1-Ac；Propynyl-PEG1-Ac
Propynyl-PEG1-Ac 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：T41096产 地：中国大陆
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T41047Benzyl-PEG10-alcohol；Benzyl-PEG10-alcoholBenzyl-PEG10-alcohol；Benzyl-PEG10-alcohol
Benzyl-PEG10-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：T41047产 地：中国大陆
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T4092AG126；化合物AG 126Tyrphostin AG126|||AG 126；Tyrphostin AG126|||AG 126
AG126 (Tyrphostin AG126) selectively inhibits the phosphorylation of ERK1 (p44) and ERK2 (p42) at 25-50 μM. It blocks the production of TNF-α in vitro2 and in vivo, attenuating signaling through NF-κB, the induced expression of COX-2 and iNOS, and the inflammatory response in diverse animal models. AG-126 weakly inhibits epidermal GFRK (IC50: 450 μM) and platelet-derived GFRK (IC50 > 100 μM).
价 格：￥电议型 号：T4092产 地：中国大陆
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T40914Biotin-PEG1-NH2Biotin-PEG1-NH2Biotin-PEG1-NH2
Biotin-PEG1-NH2 is a cleavable, 1-unit PEG linker employed in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T40914产 地：中国大陆
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T40702Decaethylene glycol dodecyl ether；Decaethylene glycol dodecyl etherPEG10-dodecyl；PEG10-dodecyl
Decaethylene glycol dodecyl ether, a PEG-based PROTAC linker, finds utility in PROTAC synthesis.
价 格：￥电议型 号：T40702产 地：中国大陆
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T40673Benzyl-PEG1-Ms；Benzyl-PEG1-MsBenzyl-PEG1-Ms；Benzyl-PEG1-Ms
Benzyl-PEG1-Ms 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：T40673产 地：中国大陆
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T40664Methyl acetate-PEG1；Methyl acetate-PEG1Methyl acetate-PEG1；Methyl acetate-PEG1
Methyl acetate-PEG1 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：T40664产 地：中国大陆
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T40632MS-PEG12-THP；MS-PEG12-THPMS-PEG12-THP；MS-PEG12-THP
MS-PEG12-THP 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：T40632产 地：中国大陆
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T40624Methyl acetate-PEG1-methyl acetate；Methyl acetate-PEG1-methyl acetateMethyl acetate-PEG1-methyl acet
Methyl acetate-PEG1-methyl acetate is a PEG-based linker compound utilized in PROTAC synthesis.
价 格：￥电议型 号：T40624产 地：中国大陆
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T40533THP-PEG10-THP；THP-PEG10-THPTHP-PEG10-THP；THP-PEG10-THP
THP-PEG10-THP 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：T40533产 地：中国大陆
