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T6812LCyclo(-RGDfK) TFAligand,αvβ3 integrin,Cyclo( RGDfK) TFA,inhibit,Integrin,Microvasculature,cancer,Cyc
Cyclo(-RGDfK) is a selective αvβ3 integrin inhibitor(IC50 : 0.94 nM).
价 格：￥电议型 号：T6812L产 地：中国大陆
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T9073SRS16-86IRI,SRS16-86,Inhibitor,ferrostatin,SRS-16-86,ischemia-reperfusion injury,SCI,spinal cord inj
SRS16-86 is a novel third-generation ferrostatin, is an inhibitor of?ferroptosis.
价 格：￥电议型 号：T9073产 地：中国大陆
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T9174IcerguastatIFB 088,Sephin1,Inhibitor,misfolding,Sephin-1,prion,Icerguastat,IFB088,stress,eIF2α,scler
Sephin1 is a selective inhibitor of holophosphatase. Sephin1 safely and selectively inhibited a regulatory subunit of protein phosphatase 1 in vivo.
价 格：￥电议型 号：T9174产 地：中国大陆
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T7651Rose Bengal sodiumfluorescein,Inhibitor,dye,crimson-coloured,ophthalmic,antiviral,inhibit,Rose Benga
Rose Bengal is a potent inhibitor of VGlut and vesicular monoamine transporter (VMAT) (Ki of 19 and 64 nM for VGlut andVMAT, respectively）
价 格：￥电议型 号：T7651产 地：中国大陆
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T8544Masitinib mesylateSCFR,PDGFR,c-Kit,Apoptosis,AB 1010,Src,CD117,Masitinib,Platelet-derived growth fac
Masitinib mesylate is a selective and orally bioavailable c-Kit inhibitor (IC50 of 200 nM,540/800 nM,510 nM for human recombinant c-Kit;PDGFRα/β;LynB,respectively).
价 格：￥电议型 号：T8544产 地：中国大陆
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T36683VedaprofenVedaprofen,Inhibitor,nonsteroidal,PM150,PM-150,Escherichia coli,inhibit,CERM-10202,CERM102
Vedaprofen inhibits COX-1 and reduces prostaglandin H2 synthesis with anti-inflammatory activities. Vedaprofen is an inhibitor of Escherichia coli sliding clamp with the IC50 of 222 μM and Ki of 131 μM.
价 格：￥电议型 号：T36683产 地：中国大陆
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T8421TED-347PPI,irreversible,protein-protein,YAP,allosteric,TEAD4?Yap1,transcriptional,glioblastoma,TED 3
TED-347 is an irreversible and covalent inhibitor of TEAD4-Yap1 protein-protein interaction(EC50 of 5.9 μM), and inhibits glioblastoma cell viability.
价 格：￥电议型 号：T8421产 地：中国大陆
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T8242Sabineneskeletal muscle atrophy,L6 cells,bicyclic monoterpene,Makino essential oil,Chrysanthemum bor
Sabinene is a natural product that has antifungal and anti-inflammatory properties
价 格：￥电议型 号：T8242产 地：中国大陆
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T37042SCH529074
SCH529074 is a selective activator of p53 (Ki = 1 μM) and can be used in studies about non-small-cell lung carcinoma. SCH529074 restores mutant p53 function and interrupts HDM2-mediated ubiquitination of wild Type p53.
价 格：￥电议型 号：T37042产 地：中国大陆
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T7002Trihexyphenidyl hydrochloridemAChR,inhibit,dystonia,Inhibitor,Trihexyphenidyl,Muscarinic acetylcholi
Trihexyphenidyl hydrochloride is an antiparkinsonian agent of the antimuscarinic class.
价 格：￥电议型 号：T7002产 地：中国大陆
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T6S1917Schisandrol BTJN 101,antioxidant,Hepato-protective,BCL-2,TJN101,inhibit,P-glycoprotein,Inhibitor,CYP
1. Gomisin A may exert neuroprotective effects by attenuating the microglia-mediated neuroinflammatory response via inhibiting the TLR4-mediated NF-κB and MAPKs signaling pathways. 2. Gomisin A has anti-inflammatory property, potentially result from the inhibition of COX-2, iNOS, IL-6, TNF-α and NO through the down-regulation of RIP2 and NF-κB activation. 3. Gomisin A induces marked protective effects against hepatic and renal injury induced by CCl(4) exposure through differential regulation of
价 格：￥电议型 号：T6S1917产 地：中国大陆
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T9018JHU37160Inhibitor,hM4Di,Clozapine,hM3Dq,DREADD,inhibit,Muscarinic acetylcholine receptor,JHU-37160,J
JHU 37160 is a Designer Receptors Exclusively Activated by Designer Drug (DREADD) agonist with Ki of 1.9 nM and 3.6 nM for human muscarinic acetylcholine M3 receptors (hM3Dq) and hM4Di in vitro, respectively. And EC50 values are 18.5 nM and 0.2 nM for hM3Dq and hM4Di in fluorescent and BRET-based assays in HEK-293 cells, respectively.
价 格：￥电议型 号：T9018产 地：中国大陆
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T6407β-LapachoneARQ 501,ARQ501,Topoisomerase,Inhibitor,NSC26326,β-Lapachone,Apoptosis,NSC 26326,Autophagy
Beta-Lapachone is a specific DNA topoisomerase I inhibitor, and no inhibitory activities against DNA topoisomerase II or ligase.
价 格：￥电议型 号：T6407产 地：中国大陆
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T8491VorolanibVEGFR,PDGFR,X82,Vascular endothelial growth factor receptor,CM 082,transporter,angiogenesis
Vorolanib is an orally active VEGFR/PDGFR dual inhibitor.
价 格：￥电议型 号：T8491产 地：中国大陆
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T12871Talmapimodcytotoxicity,multiple,inhibit,tumor,SCIO 469,SCIO469,cells,Hsp27,Inhibitor,phosphorylation
Talmapimod is an selective, orally active, and ATP-competitive p38α inhibitor with IC50 of 9 nM and 90 nM for p38α and p38β, respectively. Talmapimod exhibits at least 2000-fold selectivity over a panel of 20 kinases, including other MAPKs.
价 格：￥电议型 号：T12871产 地：中国大陆
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T9889M4 mAChR agonist-1?inhibit,M4 mAChR agonist1?,Inhibitor,Muscarinic acetylcholine receptor,mAChR,M4 m
M4 mAChR agonist-1 is an effective agonist of M4 mAChR (EC50 >10 μM).
价 格：￥电议型 号：T9889产 地：中国大陆
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TQ0266MSC2530818Cyclin dependent kinase,Inhibitor,CDK,MSC2530818,inhibit,MSC 2530818,MSC-2530818
MSC2530818 is an effective, selective and orally available CDK8 inhibitor (IC50: 2.6 nM).
价 格：￥电议型 号：TQ0266产 地：中国大陆
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T6711Tyrphostin AG1296Fms like tyrosine kinase 3,PDGF,Apoptosis,CD117,inhibit,platelet-derived,CD135,SCFR
Tyrphostin AG 1296 is an inhibitor of PDGFR with IC50 of 0.3-0.5 μM, no activity to EGFR.
价 格：￥电议型 号：T6711产 地：中国大陆
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T9024OUL35ARTD10,PARP,inhibit,DNA,OUL 35,NSC 39047,apoptosis,NSC-39047,PARP10,poly ADP ribose polymerase,
OUL35 is a selective PARP-10 inhibitor, and small-molecule ARTD10 inhibitor. OUL35 has been shown to rescue cells from ARTD10-induced cell death.
价 格：￥电议型 号：T9024产 地：中国大陆
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T8541Lenvatinib mesylatePDGFR,Inhibitor,Lenvatinib mesylate,inhibit,VEGFR,c-Kit,RET,Vascular endothelial
Lenvatinib mesylate is an oral and multi-targeted inhibitor of VEGFR1-3, FGFR1-4, PDGFR, KIT, and RET, with potent antitumor activities.
价 格：￥电议型 号：T8541产 地：中国大陆
