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产品数：86101
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T9221UNC926 hydrochlorideUNC926,methyl-lysine,L3MBTL3,Epigenetic Reader Domain,UNC-926 hydrochloride,UNC9
UNC926 hydrochloride is a methyl-lysine (Kme) reader domain inhibitor.
价 格：￥电议型 号：T9221产 地：中国大陆
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T6762AS1842856AS 1842856,AS-1842856,inhibit,AS1842856,Autophagy,Inhibitor
AS1842856, a cell-permeable inhibitor, can block the transcription activity of Foxo1 (IC50: 33 nM). It can directly bind to the active Foxo1, but not the Ser256-phosphorylated form.
价 格：￥电议型 号：T6762产 地：中国大陆
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TN2081Maohuoside Aorally,MAPK,osteogenesis,Maohuoside A,inhibit,Transforming growth factor beta receptors,
Maohuoside A promotes osteogenesis of rat mesenchymal stem cells via BMP and MAPK signaling pathways.
价 格：￥电议型 号：TN2081产 地：中国大陆
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T7847Apelin-13 triTFA(217082-58-1(free base))Apelin 13 triTFA(217082 58 1(free base)),Apelin13 triTFA(217
Apelin-13 triTFA is the endogenous ligand of the APJ receptor, activating this G protein-coupled receptor with an EC50 value of 0.37 nM.
价 格：￥电议型 号：T7847产 地：中国大陆
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T9013Autogramin-2Autogramin-2,Inhibitor,inhibit,Autogramin2,Autophagy,Autogramin 2
Autogramin-2 potently inhibits?autophagy?induced by either starvation with IC50 of 0.27 μM, and inhibits mTORC1 (Rapamycin; IC50:0.14 μM)
价 格：￥电议型 号：T9013产 地：中国大陆
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T7959(+)-ISOPINOCAMPHEOL(+) ISOPINOCAMPHEOL,(+)ISOPINOCAMPHEOL
(+)-ISOPINOCAMPHEOL is a natural product.
价 格：￥电议型 号：T7959产 地：中国大陆
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T67758Pumecitinib3Azetidineacetonitrile,3[3amino4(7Hpyrrolo[2,3d]pyrimidin4yl)1Hpyrazol1yl]1[(1methylethyl
Pumecitinib is a Janus kinase (JAK) inhibitor. Pumecitinib exhibits anti-inflammatory activity.
价 格：￥电议型 号：T67758产 地：中国大陆
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T7292FITMFITM,mGluR,Metabotropic glutamate receptors,inhibit,Inhibitor
FITM is a potent negative allosteric modulator of mGlu1 receptor(Ki : 2.5 nM).
价 格：￥电议型 号：T7292产 地：中国大陆
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T9816ArofyllineLAS-31025,inhibit,Arofylline,LAS31025,Phosphodiesterase (PDE),Inhibitor
Arofylline is a PDE4 inhibitor and can be used for asthma studies.
价 格：￥电议型 号：T9816产 地：中国大陆
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T60128N,N-Didesethyl Sunitinib HydrochlorideN,NDidesethylSunitinibHydrochloride
N,N-Didesethyl Sunitinib Hydrochloride is a potent AMPK inhibitor with IC50 of 393 nM and 141 nM for AMPKα1 and AMPK2,respectively.
价 格：￥电议型 号：T60128产 地：中国大陆
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TN3231PratolPratol
Pratol significantly increased melanin content and tyrosinase activity in the cells without being cytotoxic.
价 格：￥电议型 号：TN3231产 地：中国大陆
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T60125(2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid(2S,3S)3Hydroxy2methyl3phenylpropanoicacid
(2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid is a chemical synthesis intermediate.
价 格：￥电议型 号：T60125产 地：中国大陆
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T6915DarolutamideBAY1841788,BAY 1841788,ODM201,ODM 201,Inhibitor,Androgen Receptor,Darolutamide,inhibit
ODM-201 is an androgen receptor (AR) antagonist that blocks AR nuclear translocation (Ki: 11 nM).
价 格：￥电议型 号：T6915产 地：中国大陆
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T21782A 77636 hydrochloride
A-77636 hydrochloride is a potent, orally active, selective and long acting dopamine D1 receptor agonist (pKi=7.40; Ki=39.8 nM). A-77636 hydrochloride shows antiparkinsonian activity. A-77636 hydrochloride is functionally inactive at dopamine D2 receptor.
价 格：￥电议型 号：T21782产 地：中国大陆
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T94432-Chloro-4-nitrophenol2Chloro4nitrophenol,2 Chloro 4 nitrophenol
2-Chloro-4-nitrophenol is a chemical compound.
价 格：￥电议型 号：T9443产 地：中国大陆
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T60075Thieno[2,3-b]pyridine-2-carboxamide, 3-amino-N-[5-[4-(2,3-dichlorophenyl)-1-piperazinyl]pentyl]-4,6-
Thieno[2,3-b]pyridine-2-carboxamide, 3-amino-N-[5-[4-(2,3-dichlorophenyl)-1-piperazinyl]pentyl]-4,6-dimethyl- is a ligand targeting the dopamine D2 receptor.
价 格：￥电议型 号：T60075产 地：中国大陆
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T20535Carnidazole
Carnidazole shows antiprotozoal activity and can be used in studies about the treatment of Trichomonas infection.
价 格：￥电议型 号：T20535产 地：中国大陆
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T8329AR 231453inhibit,GPR119,AR-231453,G Protein-Coupled Receptor 119,diabetes,AR231453,AR 231453,insulin
AR 231453 is a selective and orally available GPR119 agonist,can stimulate β-cell replication and improve islet graft function.
价 格：￥电议型 号：T8329产 地：中国大陆
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T25192Butyrolactone I
Butyrolactone I is an ATP-competitive inhibitor of CDK and cdc2 kinase family. Butyrolactone I shows antitumor effects in non-small cell lung, small cell lung, and prostate cancer cell lines.
价 格：￥电议型 号：T25192产 地：中国大陆
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T9121AG-636inhibit,oral,AG 636,AG-636,reversible,DHODH,anticancer,AG636,Inhibitor,Dihydroorotate Dehydrog
AG-636 is a potent, reversible, selective and orally active DHODH inhibitor(IC50 of 17 nM). It has strong anticancer effects.
价 格：￥电议型 号：T9121产 地：中国大陆
