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产品数：86101
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TN7036N-(3-Methoxybenzyl)-(9Z,12Z,15Z)-octadecatrienamidebone formation,Beta catenin,inhibit,Inhibitor,N (
N-3-methoxylBenzyllinolenicamide induces osteogenic differentiation and subsequent bone formation of mesenchymal stem cells by activating the canonical Wnt/β-catenin signaling pathway that can be used for osteoporosis research.
价 格：￥电议型 号：TN7036产 地：中国大陆
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T9057norbergeninradical,norbergenin,antioxidant,Reactive Oxygen Species,bergenin,scavenging,inhibit,Inhib
Norbergenin is a chemical compound. It is the O-demethylated derivative of bergenin. It can be isolated from rhizomes of Bergenia stracheyi.
价 格：￥电议型 号：T9057产 地：中国大陆
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T19418LMethionine
Methionine (MRX-1024; D-Methionine) is an effective chemoprotective agent which can also inhibit the neuronal activity through GABAA receptor activation.
价 格：￥电议型 号：T19418L产 地：中国大陆
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TQ0069MI-503Inhibitor,MI503,inhibit,MI 503,MI-503,Epigenetic Reader Domain
MI-503 is a highly effective and orally bioavailable inhibitor of the menin-mLL interaction.
价 格：￥电议型 号：TQ0069产 地：中国大陆
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T9402Thalidomide-O-C4-NH2 hydrochlorideThalidomide O C4 NH2 hydrochloride,E3 Ligase Ligand-Linker Conjuga
Thalidomide-linker 9 is a synthesized?E3 ligase ligand-linker conjugate?that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
价 格：￥电议型 号：T9402产 地：中国大陆
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T21777VU0359595
VU0359595 is a potent and selective pharmacological phospholipase D1 (PLD1) inhibitor with an IC50 of 3.7 nM. VU0359595 is >1700-fold selective for PLD1 over PLD2 (IC50 of 6.4 μM). VU0359595 can be used for the research of cancer, diabetes, neurodegenerative and inflammatory diseases.
价 格：￥电议型 号：T21777产 地：中国大陆
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T2310LCHIR-99021 HCl
Laduviglusib (CHIR-99021) monohydrochloride is a potent and selective GSK-3α/β inhibitor with IC 50 s of 10 nM and 6.7 nM. Laduviglusib monohydrochloride shows over 500-fold selectivity for GSK-3 over CDC2, ERK2 and other protein kinases. Laduviglusib monohydrochloride is also a potent Wnt/β-catenin signaling pathway activator. Laduviglusib monohydrochloride enhances mouse and human embryonic stem cells self-renewal. Laduviglusib monohydrochloride induces autophagy [1] [2] [3].
价 格：￥电议型 号：T2310L产 地：中国大陆
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TP1730Lβ-catenin peptide acetate(265669-37-2 free base)βcatenin peptide acetate(265669372 free base),β cate
β-catenin peptide(βCATp) acetate is a naturally occurring self-peptide presented by Kb that very efficiently mediates positive selection of the OT-I thymocytes.
价 格：￥电议型 号：TP1730L产 地：中国大陆
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T9164BMS-986242glucuronidation,potent,Indoleamine 2,3-Dioxygenase (IDO),cancer,Inhibitor,BMS 986242,inhib
BMS-986242 is an orally active, potent and selective inhibitor of indoleamine-2,3-dioxygenase 1 (IDO1), and it can be used for the research of cancer.
价 格：￥电议型 号：T9164产 地：中国大陆
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T22963McN-A 343McN A 343,McNA 343
McN-A 343 is a selective M1 muscarinic agonist that stimulates muscarinic transmission in sympathetic ganglia. McN-A-343 reduces inflammation and oxidative stress in an experimental model of ulcerative colitis.
价 格：￥电议型 号：T22963产 地：中国大陆
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T8592CTK8A3536CTK-8A3536,CTK8A3536
CTK8A3536 is an inhibitor of Androgen receptor.
价 格：￥电议型 号：T8592产 地：中国大陆
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TP1166ZINC77292789inhibit,Inhibitor,ZINC77292789,ZINC-77292789
Fmoc-Thr[GalNAc(Ac)3-α-D]-OH is a reagent for the preparation of a synthetic MUC1 Glycopeptide Bearing βGalNAc-?Thr as a Tn antigen isomer which induces the antibody production against tumor cells. Fmoc-Thr[GalNAc(Ac)3-α-D]-OH is a starting material to make trimeric MUC1 immunodominant motif antigen-?based anti-?cancer vaccine candidates.
价 格：￥电议型 号：TP1166产 地：中国大陆
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T8815AzumoleneSOCE,inhibit,Azumolene,EU-4093,ryanodine,Inhibitor,Ca channels,EU 4093,Calcium Channel,rela
Azumolene
价 格：￥电议型 号：T8815产 地：中国大陆
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T8698Hydrazinium hydroxideHydrazinium hydroxide
Hydrazinium hydroxide is a bioactive compound
价 格：￥电议型 号：T8698产 地：中国大陆
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T73197-MethylguanosineEndogenous Metabolite,Nucleoside Antimetabolite/Analog,7-Methylguanosine,7Methylgua
7-Methylguanosine is a novel cNIIIB nucleotidase inhibitor (IC50 : 87.8 ± 7.5 μM).
价 格：￥电议型 号：T7319产 地：中国大陆
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TN3695Coniine hydrochlorideConiine hydrochloride
Coniine hydrochloride, a polyketide-derived alkaloid, is poisonous to humans and animals. It is a nicotinic acetylcholine receptor antagonist, which leads to inhibition of the nervous system.
价 格：￥电议型 号：TN3695产 地：中国大陆
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T9842WAY-388264-AWAY388264A,WAY 388264 A
5-HT2B antagonist-1 is an orally active 5-HT2B receptor antagonist with an IC 50 of 33.4 nM. It can be used in studies of diseases characterized by 5-HT2B receptor signaling, such as hepatocellular carcinoma, cardiovascular disease or gastrointestinal disease [1] [2].
价 格：￥电议型 号：T9842产 地：中国大陆
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T38776LP-922056cortical,Pectinacetylesterase,thickness,orally,femur,inhibit,Wnt,lipase,bone,LP-922056,Notu
LP-922056 is an inhibitor of Notum Pectinacetylesterase with EC50 values of 21 nM, 55 nM for human and mouse, respectively.
价 格：￥电议型 号：T38776产 地：中国大陆
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TP1994LM871 acetateM871 acetate,M-871 acetate(908844-75-7 Free base)
M871 acetate is a selective galanin GAL2 receptor antagonist (Ki values are 13.1 and 420 nM at GAL2 and GAL1 receptors, respectively).It blocks pronociceptive effects of GAL2 agonists including AR-M1896.
价 格：￥电议型 号：TP1994L产 地：中国大陆
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T6588Mitoxantroneleukaemia,NSC301739,PKC,MCF-7,NSC 301739,lymphocytes,Topoisomerase,Mitoxantrone,HL60 cel
Mitoxantrone is an anthracenedione antibiotic with antineoplastic activity. Mitoxantrone intercalates into and crosslinks DNA, thereby disrupting DNA and RNA replication. This agent also binds to topoisomerase II, resulting in DNA strand breaks and inhibition of DNA repair. Mitoxantrone is less cardiotoxic compared to doxorubicin.
价 格：￥电议型 号：T6588产 地：中国大陆
