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T40700IKK-IN-3；IKK-IN-3IKK-IN-3
IKK-IN-3 is a highly potent and selective inhibitor of IkappaB kinase 2 (IKK2 or IKKβ). It exhibits impressive inhibitory activity against IKK2 (IC50 = 19 nM), while also demonstrating significant efficacy against IKK1 (or IKKα) with an IC50 value of 400 nM.
价 格：￥电议型 号：T40700产 地：中国大陆
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T40577TAK1-IN-3；TAK1 抑制剂3TAK1-IN-3；TAK1-IN-3
TAK1-IN-3 is a novel ATP-competitive TAK1 inhibitor for the study of cancer.
价 格：￥电议型 号：T40577产 地：中国大陆
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T405672,6,6-Trimethylbicyclo[3.1.1]heptan-3-ol；2,6,6-Trimethylbicyclo[3.1.1]heptan-3-ol2,6,6-Trimethylbicy
2,6,6-Trimethylbicyclo[3.1.1]heptan-3-ol is isolated from Chrysanthemum indicum L..
价 格：￥电议型 号：T40567产 地：中国大陆
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T40551ACAT-IN-3；ACAT-IN-3ACAT-IN-3
ACAT-IN-3, a potent inhibitor of acyl-Coenzyme A: cholesterol acyltransferase (ACAT), effectively suppresses NF-κB dependent transcription.
价 格：￥电议型 号：T40551产 地：中国大陆
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T40356PDE4-IN-3PDE4-IN-3PDE4-IN-3
PDE4-IN-3 is a newly developed oral compound that acts as a potent inhibitor of the enzyme phosphodiesterase 4 (PDE4), displaying a high affinity for inhibition with an IC50 value of 4.2 nM.
价 格：￥电议型 号：T40356产 地：中国大陆
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T40335AChE-IN-3；AChE抑制剂VIAChE-IN-3
AChE-IN-3 had inhibitory effect on AChE and stronger inhibitory effect on NO, with EC50 of 0.57 μM.
价 格：￥电议型 号：T40335产 地：中国大陆
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T40267RdRP-IN-3；RdRP-IN-3RdRP-IN-3
RdRP-IN-3, a potential anti-influenza drug candidate, functions by inhibiting the activity of RNA-dependent RNA polymerase (RdRp).
价 格：￥电议型 号：T40267产 地：中国大陆
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T40222FTO-IN-3；化合物FTO-IN-3FTO-IN-3
FTO-IN-3 is a FTO inhibitor. FTO-IN-3 impairs self-renewal in glioblastoma stem cells.
价 格：￥电议型 号：T40222产 地：中国大陆
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T40210eIF4E-IN-3eIF4E-IN-3eIF4E-IN-3
eIF4E-IN-3 is a highly effective inhibitor of eukaryotic initiation factor 4e (eIF4e), exhibiting noteworthy potential for investigating eIF4e dependent diseases, particularly cancer research (WO2021003157A1, compound 485).
价 格：￥电议型 号：T40210产 地：中国大陆
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T40066SENP1-IN-3SENP1-IN-3SENP1-IN-3
SENP1-IN-3 is a distinct inhibitor of the deSUMOylation protease 1 (SENP1), designed to enhance tumor radiosensitivity.
价 格：￥电议型 号：T40066产 地：中国大陆
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T40031Thalidomide-O-C6-NH2 hydrochloride；萨力多胺-O-C6-氨基盐酸盐4-((6-aminohexyl)oxy)-2-(2,6-dioxopiperidin-3-yl)i
Thalidomide-O-C6-NH2 hydrochloride (4-((6-aminohexyl)oxy)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione hydrochloride) is a synthesized E3 ligase ligand-linker conjugate.
价 格：￥电议型 号：T40031产 地：中国大陆
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T40026Pomalidomide 4’-alkylC3-acid；化合物 Pomalidomide 4’-alkylC3-acid4-[[2-(2,6-dioxopiperidin-3-yl)-1,3-dio
Butanoic acid, 4-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]amino]- (4-[[2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindol-4-yl]amino]butanoic acid) is a Cereblon ligand with alkyl linker and terminal acid for onward chemistry.
价 格：￥电议型 号：T40026产 地：中国大陆
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T40018SY2-062；化合物 SY2-0624-Bromo-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione；4-Bromo-2-(2,6-dioxopipe
4-Bromo-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione has potential as an anticancer, prodrug for the treatment of Parkinson´s disease, and as an anti-inflammatory agent.
价 格：￥电议型 号：T40018产 地：中国大陆
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T3S1250Ophiogenin 3-O-α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside；化合物T3S1250Ophiogenin-3-O-alpha-L-rhaMno
Ophiogenin 3-O-α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside (Ophiogenin-3-O-alpha-L-rhaMnopyranosyl-(1->2)-beta-D-glucopyranoside) is a natural product, and has good pharmacological effects on the cardiovascular system.
价 格：￥电议型 号：T3S1250产 地：中国大陆
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T3S0895Spirostan-3-ol；剑麻皂苷元Sarsaponin；剑麻皂苷元|||Sarsaponin
Spirostan-3-ol (Sarsaponin) is a stereoisomer of Sarsasapogenin (S142505), a steroid glycoside isolated from plant materials. A saponin with with potential anti-tumor activity via apoptosis.
价 格：￥电议型 号：T3S0895产 地：中国大陆
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T39986LOX-IN-3 dihydrochloride；化合物LOX-IN-3 dihydrochlorideLOX-IN-3 dihydrochloride
LOX-IN-3 dihydrochloride is an inhibitor of lysyl oxidase (LOX). LOX-IN-3 dihydrochloride inhibited bovine LOX (IC50<10 μM) and human LOXL2 (IC50<1 μM)activities.
价 格：￥电议型 号：T39986产 地：中国大陆
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T39984PKM2-IN-3PKM2-IN-3PKM2-IN-3
PKM2-IN-3 is a potent PKM2 kinase inhibitor, displaying an IC 50 value of 4.1 μM. The compound effectively suppresses PKM2-mediated glycolysis and NLRP3 activation, thereby exerting an anti-neuroinflammatory effect.
价 格：￥电议型 号：T39984产 地：中国大陆
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T39805LDHA-IN-3；LDHA抑制剂3PSTMB|||1-(phenylseleno)-4-(trifluoromethyl) benzene；PSTMB|||1-(phenylseleno)-4-(t
LDHA-IN-3 (1-(phenylseleno)-4-(trifluoromethyl) benzene) is a potent non-competitive lactate dehydrogenase (LDHA) inhibitor with an IC50 value of 145.2 nM.LDHA-IN-3 is a selenobenzene compound that can be used in cancer research.
价 格：￥电议型 号：T39805产 地：中国大陆
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T39732BCR-ABL-IN-3；BCR-ABL-IN-3BCR-ABL-IN-3
BCR-ABL-IN-3 is a highly effective and irreversibly binding inhibitor of Bcr-Abl, displaying a remarkable potency with an IC50 value of ≤100 nM for Ba/F3 Bcr-Abl T3151. This compound exhibits significant anti-cancer activity.
价 格：￥电议型 号：T39732产 地：中国大陆
