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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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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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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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T88684BP-TQS4BP TQS,allosteric agonist,transmembrane site,Inhibitor,α7 nAChR,inhibit,Nicotinic acetylchol
4BP-TQS is an allosteric agonist of α7 nAChRs.
价 格：￥电议型 号：T8868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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T7019Z-IETD-FMKinhibit,Inhibitor,Caspase,Z IETD FMK,ZIETDFMK
Z-IETD-FMK is a selective caspase 8 inhibitor, which has cell permeable.
价 格：￥电议型 号：T7019产 地：中国大陆
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T8409SYN1143c-Met/HGFR,SYN-1143,tumor,RON,dual,inhibit,SYN1143,SYN 1143,cancer,Inhibitor,c-Met
AMG-1 is a potent inhibitor of human RON and c-Met.In vitro kinase assays showed that compound I is a potent inhibitor of human RON and c-Met with IC50s of 9 and 4 nmol/L, respectively.
价 格：￥电议型 号：T8409产 地：中国大陆
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T67769MPT0B014MPT0B014
MPT0B014 is a potent tubulin polymerization inhibitor. MPT0B014 can induce cancer cell apoptosis.
价 格：￥电议型 号：T67769产 地：中国大陆
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TQ0067GSK484 hydrochlorideGSK484 hydrochloride,GSK 484,Protein Arginine Deiminase,GSK-484,GSK-484 hydrochl
GSK484 hydrochloride (GTPL8577) is a specifc and reversible peptidyl arginine deiminase 4 (PAD4) inhibitor. It demonstrates high-affinity binding to PAD4 with IC50s of 50 nM in the absence of Calcium.
价 格：￥电议型 号：TQ0067产 地：中国大陆
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T7486Imeglimin hydrochlorideEMD387008,inhibit,mitochondrial,lowering,insulin,Mitochondrial Metabolism,ora
Imeglimin hydrochloride prevents human endothelial cell death by inhibiting mitochondrial permeability transition without inhibiting mitochondrial respiration.
价 格：￥电议型 号：T7486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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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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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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T7489MART-1 (26-35) (human)inhibit,MART1 (2635) (human),Inhibitor,MART 1 (26 35) (human)
MART-1 (26-35) human is a peptide fragment of MART-1 protein.
价 格：￥电议型 号：T7489产 地：中国大陆
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T357022-Heptanol
2-Heptanol is one of chemical constituents identified in the essential oil of rhizome of Curcuma angustifolia and Curcuma zedoaria. Rhizome essential oil exhibited good antimicrobial and antioxidant activity.
价 格：￥电议型 号：T35702产 地：中国大陆
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T7949NCC007inhibit,NCC-007,Inhibitor,NCC007,NCC 007,Casein Kinase
NCC007 is a novel CKIα and CKIδ dual inhibitors by structural modification of N9 and C2 position of longdaysin.
价 格：￥电议型 号：T7949产 地：中国大陆
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T7679UBCS039Autophagy,UBCS039,UBCS 039,inhibit,Sirtuin,Inhibitor,UBCS-039
UBCS039 is the first synthetic Sirt6 activator(EC50 : 38 μM)
价 格：￥电议型 号：T7679产 地：中国大陆
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TN4569Minimolide FMinimolide F
Minimolide F, isolated from Centipeda minima, shows antiproliferative activity against human nasopharyngeal cancer cells with an IC50 of 17.4 μM.
价 格：￥电议型 号：TN4569产 地：中国大陆
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TP1049LOrnipressin Acetate（3397-23-7，free）Ornipressin Acetate（3397 23 7，free）,Ornipressin Acetate（3397237，f
Ornipressin Acetate is a potent vasoconstrictor, hemostatic and renal agent.
价 格：￥电议型 号：TP1049L产 地：中国大陆
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PDK0269Compound PDK0269Compound PDK0269
PBG (1-Phenylbiguanide HCl), as 5-HT3 receptor agonists(3–100 μM, pEC50 5.05±0.06), acutely increased XII (hypoglossal) burst frequency and regularity, and decreased bursts/episode . Phenylbiguanide produced a dose-related (10-500 microM) increase in the release of dopamine (280-2000%). When nomifensine (5 microM) was included in the Ringer solution, the effect of PBG on the release of dopamine was ameliorated or inhibited. Phenylbiguanide, infused intravenously for 15 min, elicited a sustained
价 格：￥电议型 号：PDK0269产 地：中国大陆
