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产品数：86101
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T8219VU0238441mAChR,Inhibitor,VU-0238441,VU0238441,Muscarinic acetylcholine receptor,VU 0238441,inhibit
VU0238441 is agonist of Muscarinic acetylcholine receptor M5 (human) with EC50 of 2.1μM.
价 格：￥电议型 号：T8219产 地：中国大陆
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T10874CP-060CP060,CP 060
CP-?060 is a potent Ca2+ antagonist and inhibits Ca2+ overload with antioxidant and cardioprotective activities.
价 格：￥电议型 号：T10874产 地：中国大陆
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T8505SC-236SC-236,gastric,PPAR,cancer,ischemia,Liver,inhibit,allodynia,Inhibitor,fibrogenesis,neuroprotec
Sc 236 is an orally active and selective inhibitor of COX-2 (IC50 of 0.005 μM and 17.8 μM for COX-2 and COX-1, respectively).
价 格：￥电议型 号：T8505产 地：中国大陆
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T15767LLY-283LLY283,LLY 283
LLY-283 is a potent, selective and oral protein arginine methyltransferase 5 (PRMT5) inhibitor, with an IC50 of 22 nM and a Kd of 6 nM for PRMT5:MEP50 complex, and shows antitumor activity.
价 格：￥电议型 号：T15767产 地：中国大陆
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TP1760LAMARA peptide acetate(163560-19-8 free base)AMARA peptide acetate(163560 19 8 free base),AMARA pep
AMARA peptide acetate is a substrate for SIK and AMPK.AMARA peptide is a minimal substrate of several members of the protein kinases family. It consists of the phosphorylation site for AMP-activated Protein Kinase (AMPK).
价 格：￥电议型 号：TP1760L产 地：中国大陆
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T8784IGS-1.76NCS-1,Ric8a,IGS 1.76,PPI,inhibit,IGS1.76,IGS-1.76,Inhibitor
IGS-1.76 shows a significantly increased affinity for hNCS-1 and is able to modulate the hNCS-1/Ric8a interaction efficiently.IGS-1.76 efficiently inhibits the human NCS-1/Ric8a complex.
价 格：￥电议型 号：T8784产 地：中国大陆
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TWP2911ThymidineThymidine,precursor,synchronizing,inhibit,NSC21548,DNA,NSC-21548,Inhibitor,replication,arre
1. Thymidine overload due to Thymidine phosphorylase deficiency, and mitochondrial toxicity caused by antiviral Thymidine analogues.
价 格：￥电议型 号：TWP2911产 地：中国大陆
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T8873BractoppinDNA break,Bractoppin,phosphopeptide,inhibit,DNA/RNA Synthesis,DNA damage,RAD51,G2 arrest,I
Bractoppin is a drug-like inhibitor of phosphopeptide recognition by the human BRCA1 tandem (t)BRCT domain (IC50 = 0.074 μM), which selectively inhibits substrate binding with nanomolar potency in vitro. Structure-activity exploration suggests that Bractoppin engages BRCA1 tBRCT residues recognizing pSer in the consensus motif, pSer-Pro-Thr-Phe, plus an abutting hydrophobic pocket that is distinct in structurally related BRCT domains, conferring selectivity.
价 格：￥电议型 号：T8873产 地：中国大陆
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T8132Iron sucroseIron sucrose,H2O2,pregnancy,ascorbate,Reactive Oxygen Species,IDA,Intravenous,ICAM-1,inh
Iron sucrose is treatment of iron deficiency anemia.
价 格：￥电议型 号：T8132产 地：中国大陆
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T7682Asymmetric dimethylarginineInhibitor,Endogenous Metabolite,NOS,NO Synthase,Asymmetric dimethylargini
Asymmetric dimethylarginine is an endogenous inhibitor of nitric oxide synthase (NOS)
价 格：￥电议型 号：T7682产 地：中国大陆
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TP1035LCyclic somatostatin Acetate(38916-34-6(free base))Cyclic somatostatin Acetate(38916346(free base)),C
Cyclic somatostatin Acetate is a cyclic tetradecapeptide regulating many endocrine and nervous system functions.
价 格：￥电议型 号：TP1035L产 地：中国大陆
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TN1968N-?Feruloyloctopaminecarcinoma,N-?Feruloyloctopamine,inhibit,Protein kinase B,MAPK,PKB,Inhibitor,Hep
N-Feruloyloctopamine is a natural product.
价 格：￥电议型 号：TN1968产 地：中国大陆
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T9683VX-150Na+ channels,VX-150,indications,Inhibitor,Na channels,orally,inhibit,pain,VX 150,VX150,Sodium
VX-150 is a highly selective NaV1.8 inhibitor relative to the other sodium channel subtypes (>400-fold).
价 格：￥电议型 号：T9683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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T80324-Pentenoic acidEndogenous Metabolite,inhibit,4 Pentenoic acid,4Pentenoic acid,4-Pentenoic acid,Inhi
4-Pentenoic acid, also known as allyl acetic acid or 4-pentenate, belongs to the class of organic compounds known as straight chain fatty acids. These are fatty acids with a straight aliphatic chain. 4-Pentenoic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.
价 格：￥电议型 号：T8032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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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
