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T16708R-268712；化合物R-268712R-268712
R-268712 is a specific activin receptor-like kinase 5 (ALK5) inhibitor(IC50 of 2.5 nM). It is also an orally active transforming growth factor-β type I receptor inhibitor.
价 格：￥电议型 号：T16708产 地：中国大陆
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T16268Namitecan；化合物 T16268ST-1968；ST-1968
Namitecan is an effective inhibitor of topoisomerase I. It has antitumor property.
价 格：￥电议型 号：T16268产 地：中国大陆
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T15690L-902688；化合物 T15690L-902688
L-902688 is an orally active EP4 receptor agonist (Ki: 0.38 nM; EC50: 0.6 nM). L-902688 displays >4,000-fold selective for EP4 over other EP and prostanoid receptors.
价 格：￥电议型 号：T15690产 地：中国大陆
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T15268FAAH-IN-2；4-(3-氯-4-氟苯氨基)-7-甲氧基喹唑啉-6-醇O-Desmorpholinopropyl Gefitinib；O-Desmorpholinopropyl Gefitinib
FAAH-IN-2 (O-Desmorpholinopropyl Gefitinib) is a potent inhibitor of FAAH(fatty acid amide hydrolase).
价 格：￥电议型 号：T15268产 地：中国大陆
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T1434Clarithromycin；克拉霉素A-56268；A-56268|||克拉霉素
Clarithromycin (A-56268) is a Macrolide Antimicrobial. The mechanism of action of clarithromycin is as a Cytochrome P450 3A4 Inhibitor, and Cytochrome P450 3A Inhibitor, and P-Glycoprotein Inhibitor. The chemical classification of clarithromycin is Macrolides.
价 格：￥电议型 号：T1434产 地：中国大陆
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T14268Aminooxy-PEG3-methyl ester；化合物 T14268Aminooxy-PEG3-methyl ester
Aminooxy-PEG3-methyl ester, a PEG-based PROTAC linker, serves as a pivotal element in the synthesis of PROTACs[1].
价 格：￥电议型 号：T14268产 地：中国大陆
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T13268USP7-IN-1；化合物USP7-IN-1USP7-IN-1
USP7-IN-1 is a selective and reversible ubiquitin-specific protease 7 (USP7) inhibitor (IC50 = 77 μM).
价 格：￥电议型 号：T13268产 地：中国大陆
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T131268Compound N039-0037；化合物 N039-0037Compound N039-0037
Compound N039-0037 is a useful organic compound for research related to life sciences and the catalog number is T131268.
价 格：￥电议型 号：T131268产 地：中国大陆
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T12689Ramelteon metabolite M-II；化合物 T12689Ramelteon metabolite M-II
Ramelteon metabolite M-II is the major Ramelteon metabolite(human melatonin receptors (MT1 or MT2) with IC50s of 208 pM, 1470 pM). Ramelteon is an agonist of selective melatonin.
价 格：￥电议型 号：T12689产 地：中国大陆
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T12685RAF mutant-IN-1；化合物 T12685RAF mutant-IN-1
RAF mutant-IN-1 is an inhibitor of RAF kinase(IC50 values of 21 nM, 30 nM and 392 nM for C-RAF 340D/Y341D, B-RAFV600E and B-RAFWT, respectively).
价 格：￥电议型 号：T12685产 地：中国大陆
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T12684Radioprotectin-1；化合物Radioprotectin-15-chloro-2-[4-(1,3-dioxobenzo[de]isoquinolin-2-yl)butylsulfamoyl
Radioprotectin-1 is a selective agonist of LPA2 with EC50 of 25 nM for murine LPA2 GPCR and exerts radioprotective and radiomitigative action.
价 格：￥电议型 号：T12684产 地：中国大陆
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T12682Emzadirib；化合物EmzadiribCYT-0851|||RAD51-IN-2；CYT-0851|||RAD51-IN-2
Emzadirib (RAD51-IN-2) is a potent RAD51 inhibitor with potential anticancer activity for the study of DNA damage repair.
价 格：￥电议型 号：T12682产 地：中国大陆
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T12680(±)-Darifenacin；化合物 T12680(±)-UK-88525；(±)-UK-88525
(±)-Darifenacin is the racemate of Darifenacin. Darifenacin is a selective antagonist of M3 muscarinic receptor.
价 格：￥电议型 号：T12680产 地：中国大陆
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T1268Dixanthogen；二黄原酸Scabicidol|||Aulinogen|||Auligen；Scabicidol|||二黄原酸|||Aulinogen|||Auligen|||四硫双酯
Dixanthogen (Auligen) is an ectoparasiticide. Dixanthogen is a thiocarbonyl compound.
价 格：￥电议型 号：T1268产 地：中国大陆
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T126268Chalepin；化合物 ChalepinChalepin
Chalepin is a useful organic compound for research related to life sciences. The catalog number is T126268 and the CAS number is 118389-19-8.
价 格：￥电议型 号：T126268产 地：中国大陆
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T125268Poncitrin；化合物 PoncitrinPoncitrin
Poncitrin is a useful organic compound for research related to life sciences. The catalog number is T125268 and the CAS number is 22980-57-0.
价 格：￥电议型 号：T125268产 地：中国大陆
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T124268Chalcostrobamine；化合物 ChalcostrobamineChalcostrobamine
Chalcostrobamine is a useful organic compound for research related to life sciences and the catalog number is T124268.
价 格：￥电议型 号：T124268产 地：中国大陆
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T12268NTP42；化合物NTP42NTP42
NTP42 is an antagonist of thromboxane A2 (TXA2) receptor(IC50 of 3.278 nM)
价 格：￥电议型 号：T12268产 地：中国大陆
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T12195NCI172112；化合物 T12195NSC268497|||NSC172112；NSC268497|||NSC172112
NCI172112 is is used to develop antitumor agents effective against CNS tumors.
价 格：￥电议型 号：T12195产 地：中国大陆
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T11268FD 12-9；化合物 T11268Ac12Az9；Ac12Az9
FD 12-9, Anti-glioblastoma activity. is a flavonoid dimer, acts as a dual inhibitor of P-gp and BCRP, with EC50s of 285 nM and 0.9 nM, respectively.
价 格：￥电议型 号：T11268产 地：中国大陆
