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T12389711-Dehydroxymogroside III；化合物 11-Dehydroxymogroside III11-Dehydroxymogroside III
11-Dehydroxymogroside III is a useful organic compound for research related to life sciences. The catalog number is T123897 and the CAS number is 942612-68-2.
价 格：￥电议型 号：T123897产 地：中国大陆
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T12361Parcetasal；化合物ParcetasalMR-897；MR-897
Parcetasal (MR-897) is a non-steroidal anti-inflammatory agent that can be used in pain relief studies.
价 格：￥电议型 号：T12361产 地：中国大陆
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T12297Oleuropeinic acid；橄榄苦苷酸Oleuropeinic acid
Oleuropeinic acid, initially present in olive tissues or produced through the thermal oxidation of oleuropein, is an antioxidant-soluble fiber.
价 格：￥电议型 号：T12297产 地：中国大陆
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T12273NVP-CGM097 sulfate；化合物 T12273CGM097 sulfate；CGM097 sulfate
NVP-CGM097 sulfate is a potent and selective inhibitor of MDM2 (hMDM2, IC50 of 1.7±0.1 nM).
价 格：￥电议型 号：T12273产 地：中国大陆
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T12269LNUCC-390 dihydrochloride (1060524-97-1 free base)；化合物 T12269LNUCC-390 dihydrochloride；NUCC-390 dihyd
NUCC-390 dihydrochloride is selective agonist of small-molecule CXCR4 receptor.
价 格：￥电议型 号：T12269L产 地：中国大陆
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T12230Nitazoxanide-d4；硝唑尼特 D4NTZ D4|||NSC-697855 D4|||Nitazoxanide D4；NTZ D4|||NSC-697855 D4|||硝唑尼特 D4|||N
Nitazoxanide D4 is the deuterium labeled Nitazoxanide.
价 格：￥电议型 号：T12230产 地：中国大陆
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T12200Firsocostat S enantiomer；化合物 T12200ND-630 S enantiomer|||NDI-010976 S enantiomer|||GS-0976 S enantio
Firsocostat S enantiomer is the less active S enantiomer of Firsocostat.
价 格：￥电议型 号：T12200产 地：中国大陆
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T12197NCT-506；化合物 T12197NCT-506
NCT-506 is an orally bioavailable inhibitors of aldehyde dehydrogenase 1A1 (ALDH1A1) (IC50 of 7 nM).
价 格：￥电议型 号：T12197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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T12101MPP dihydrochloride (289726-02-9 Free base)化合物MPP dihydrochloride (289726-02-9 Free base)MPP dihydro
MPP dihydrochloride is a highly selective antagonist of estrogen receptor alpha (ERα).
价 格：￥电议型 号：T12101产 地：中国大陆
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T12097Morphothiadin；莫非赛定GLS4；GLS4|||莫非赛定
Morphothiadin (GLS4) is a potent inhibitor on the replication of both wild-type and adefovir-resistant HBV (IC50 of 12 nM).
价 格：￥电议型 号：T12097产 地：中国大陆
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T12088Mofegiline hydrochloride；化合物 T12088MDL72974A；MDL72974A
Mofegiline hydrochloride is a potent and selective enzyme-activated irreversible MAO-B inhibitor.
价 格：￥电议型 号：T12088产 地：中国大陆
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T11997MELK-IN-1；尼达尼布杂质LNintedanib Impurity L|||MELK inhibitor 17；Nintedanib Impurity L|||MELK inhibitor 17
MELK-IN-1 (MELK inhibitor 17) is a potent inhibitor of maternal embryonic leucine zipper kinase (MELK),(IC50:3nm;Ki:0.39 nM).
价 格：￥电议型 号：T11997产 地：中国大陆
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T11979McN5691；化合物 McN5691MCN 5691|||RWJ26240；MCN 5691|||RWJ26240
McN5691 (RWJ26240) is a voltage-dependent calcium channel blocker with antihypertensive activity that can be used in the study of diseases caused by vascular smooth muscle abnormalities.
价 格：￥电议型 号：T11979产 地：中国大陆
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T11978McN3716；帕莫酸甲酯NSC359682|||Methyl palmoxirate；NSC359682|||Methyl palmoxirate
McN3716 is a carnitine palmitoyltransferase I (CPT-1) inhibitor for the study of metabolic diseases.
价 格：￥电议型 号：T11978产 地：中国大陆
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T11977Mcl1-IN-9；化合物 T11977Mcl1-IN-9
Mcl1-IN-9 is a potent myeloid cell leukemia-1 (Mcl-1) Inhibitor with an IC50 of 446 nM in reengineered BCR-ABL+ B-ALL cells and a Ki of 0.03 nM.
价 格：￥电议型 号：T11977产 地：中国大陆
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T11976Mcl1-IN-4；化合物 T11976Mcl1-IN-4
Mcl1-IN-4 is an inhibitor of Mcl1 ( IC50:0.2 μM).
价 格：￥电议型 号：T11976产 地：中国大陆
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T11975PROTAC Mcl1 degrader-1；化合物 T11975PROTAC Mcl1 degrader-1
PROTAC Mcl1 degrader-1 induces the ubiquitination and proteasomal degradation of Mcl-1 by introducing the E3 ligase cereblon (CRBN)-binding ligand pomalidomide to Mcl-1 inhibitor S1-6 with μM-range affinity. PROTAC Mcl1 degrader-1, a proteolysis targeting chimera (PROTAC), is a potently and selectively Mcl-1 inhibitor with an IC50 of 0.78 μM.
价 格：￥电议型 号：T11975产 地：中国大陆
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T11974Mcl1-IN-12；化合物 T11974Mcl1-IN-12
Mcl1-IN-12 has anti-tumor activity.It is a selective Mcl-1 inhibitor, less potent at Bcl-2, with Kis of 0.29 and 3.1 μM, respectively.
价 格：￥电议型 号：T11974产 地：中国大陆
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T11973Mcl1-IN-11；化合物 T11973Mcl1-IN-11
Mcl1-IN-11 (Compound G) is a selective Mcl-1 inhibitor, less potent at Bcl-2, with Kis of 0.06 and 4.2 μM, respectively.
价 格：￥电议型 号：T11973产 地：中国大陆
