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产品数：86101
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T7613β-Casomorphin, humaninhibit,β Casomorphin, human,Inhibitor,β-Casomorphin, human,βCasomorphin, human,
β-Casomorphin, human(TFA) is an opioid receptor agonist.
价 格：￥电议型 号：T7613产 地：中国大陆
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T6571Lomerizine dihydrochlorideCa2+ channels,Ca channels,inhibit,Lomerizine,KB 2796,KB2796,Lomerizine dih
Lomerizine dihydrochloride is an antagonist of L- and T-type voltage-gated calcium channels used to treat migraine.
价 格：￥电议型 号：T6571产 地：中国大陆
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TN1922Meranzin hydrateMeranzin hydrate,Meranzin,inhibit,Inhibitor
Meranzin hydrate exhibits antidepressive and prokinetic-like effects through the regulation of the common mediator, the alpha 2-adrenoceptor , and α±-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors; it produces a rapid effect mediated by AMPA receptors and involving BDNF modulation through the ERK1/2 pathway.
价 格：￥电议型 号：TN1922产 地：中国大陆
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T7158OmbitasvirABT267,Hepatitis C virus,Inhibitor,inhibit,HCV,Ombitasvir,ABT 267
Ombitasvir is an orally bioavailable and potent inhibitor of the hepatitis C virus (HCV) non-structural protein 5A (NS5A).with EC50s of 0.82 to 19.3 pM against HCV genotypes 1 to 5, and 366 pM against genotype 6a
价 格：￥电议型 号：T7158产 地：中国大陆
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TP1724LPUMA BH3 acetatePUMA BH-3 acetate,PUMA BH3 acetate
PUMA BH3 acetate is a p53 positive regulator of apoptosis (PUMA) BH3 domain polypeptide that acts as a direct activator of Bak with a Kd of 26 nM.
价 格：￥电议型 号：TP1724L产 地：中国大陆
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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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TN30915,7-Diacetoxy-8-methoxyflavone
5,7-Diacetoxy-8-methoxyflavone is derived from the roots of Scutellaria baicalensis and inhibits cAMP phosphodiesterase.
价 格：￥电议型 号：TN3091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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T11915LY88074LY88074,LY-88074
Raloxifene is a selective estrogen receptor modulator, and reduces fracture risk at least in part by improving the mechanical properties of bone in a cell- and estrogen receptor-independent manner. LY88074 is a Raloxifene analog lacking the basic side chain.
价 格：￥电议型 号：T11915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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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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T1986Atopaxarplatelets,Atopaxar,receptor-1,signaling,PAR-1,inhibit,E-5555,Inhibitor,receptor,Protease Act
Atopaxar, a reversible PAR-1 thrombin receptor antagonist, interferes with platelet signaling. Atopaxar has been investigated for the treatment of Coronary Artery Disease and Acute Coronary Syndrome.
价 格：￥电议型 号：T1986产 地：中国大陆
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T36010p38 MAPK Inhibitorp-38 MAPK Inhibitor,p38 MAPK Inhibitor
p38 MAPK inhibitor is a potent inhibitor of p38 MAP kinase (IC50 = 35 nM). It inhibits senescence induced by the oncogene RAS.
价 格：￥电议型 号：T36010产 地：中国大陆
