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TN6770Malabaricone AMalabaricone A
Malabaricone A is a bioactive chemical.
价 格：￥电议型 号：TN6770产 地：中国大陆
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T7703PK11007PK11007,inhibit,MDM-2/p53,Reactive Oxygen Species,Inhibitor,PK 11007,PK-11007
PK11007 is an anti-p53 drug.
价 格：￥电议型 号：T7703产 地：中国大陆
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T12770RR-11a analog
RR-11a analog is an inhibitor of asparaginyl endopeptidase with IC50s of 4.5 nM, 4.5 nM and 31 nM for AE1 in Trichomonas Vaginalis, AE in Ixodes ricinus and AE in Schistosoma mansoni, respectively.
价 格：￥电议型 号：T12770产 地：中国大陆
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T9770Samelisant
Samelisant is a selective and inverse agonist of H3 receptor with Kis of 8.7 nM and 9.8 nM for human and rat. Samelisant has anticataplectic effects and can be used in studies about narcolepsy.
价 格：￥电议型 号：T9770产 地：中国大陆
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T7558CID-1067700ML282,competitively,CID1067700,brain,Rab7,ML 282,GTPase,Ras,machinery,Ras-related,CID-106
CID-1067700 is one of the first identified competitive inhibitors of nucleotide binding by Ras-related GTPases（Rab7 with a Ki of 13 nM).
价 格：￥电议型 号：T7558产 地：中国大陆
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T7709(E/Z)-GSK5182(E/Z)GSK5182,(E/Z) GSK5182,(E/Z)-GSK-5182
(E/Z)-GSK5182 is a racemate of (E)-GSK5182 and (Z)-GSK5182 isomers. GSK5182 is a highly selective and orally active inverse agonist of estrogen-related receptor γ (ERRγ) with an IC 50 of 79 nM [1]. GSK5182 also induces reactive oxyen species (ROS) generation in hepatocellular carcinoma [1] [2] [3].
价 格：￥电议型 号：T7709产 地：中国大陆
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T12861SB-277011
SB-277011 is a specific antagonist of the dopamine D3 receptor with pKi values of 8.0, 6.0, 5.0, and <5.2 for D3 receptor, D2 receptor, 5-HT1D, and 5-HT1B respectively.
价 格：￥电议型 号：T12861产 地：中国大陆
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TP2485difelikefalin acetate(1024828-77-0 Free base)difelikefalin acetate(1024828770 Free base),difelikefal
is a ketone and a building block.
价 格：￥电议型 号：TP2485产 地：中国大陆
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T27703JZP-361
JZP-361 is a specific MAGL inhibitor with IC50s of 46 nM, 7.24 μM, and 1.79 μM for human recombinant MAGL, human recombinant FAAH, and human hABHD6. JZP-361 displays anti-histaminergic activities. JZP-361 can be used in studies about asthma.
价 格：￥电议型 号：T27703产 地：中国大陆
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T7701Boc-NH-PEG3PROTAC Linker10,PROTAC Linker-10,Boc-NH-PEG-3,Inhibitor,BocNHPEG3,PROTAC Linkers,inhibit,
Boc-NH-PEG3 is a PEG derivative containing a hydroxyl group and Boc-protected amino group, and is a PROTAC linker.
价 格：￥电议型 号：T7701产 地：中国大陆
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T7708DL-Buthionine-(S,R)-sulfoximineBSO,DL Buthionine (S,R) sulfoximine,Buthionine sulfoximine,DLButhioni
D,L-Buthionine-(S,R)-sulfoximine is an inhibitor of γ-glutamylcysteine synthetase for the treatment of solid tumors.
价 格：￥电议型 号：T7708产 地：中国大陆
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T27704K00135
K00135 is a selective inhibitor of Pim kinases and can be used in studies about gastric cancer and antileukemic therapeutics.
价 格：￥电议型 号：T27704产 地：中国大陆
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T7700LersivirineHIV,non-nucleoside reverse transcription,Reverse Transcriptase,HIV virus,UK 453061,Inhibi
Lersivirine(UK 453061) is a second-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) under development for HIV infection therapy.
价 格：￥电议型 号：T7700产 地：中国大陆
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TN1770Isomogroside VInhibitor,inhibit,Isomogroside V
Isomogroside V is a sweetener extracted from Siraitia grosvenorii that is approximately 500 times sweeter than 0.5% (w/v) sucrose.
价 格：￥电议型 号：TN1770产 地：中国大陆
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T7770Ethylhexyl Triazoneinhibit,Inhibitor,Ethylhexyl Triazone
Ethylhexyl triazone is an ultraviolet-B (UV-B) chemical filter for commercial sunscreens.
价 格：￥电议型 号：T7770产 地：中国大陆
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T7704KY-226inhibit,anti-diabetic,leptin,ZO-1,LPS,insulin,phosphorylated,KY-226,Akt,KY226,anti-obesity,PTP
KY-226 is a potent inhibitor of protein tyrosine phosphatase 1B (PTP1B)(IC50: 0.25 μM,)
价 格：￥电议型 号：T7704产 地：中国大陆
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T67708Thiolutin
Thiolutin is an inhibitor of endothelial cell adhesion and produced by Streptomyces. Thiolutin shows antibiotic and anti-angiogenic properties. Thiolutin induces the phosphorylation of Hsp27 rapidly.
价 格：￥电议型 号：T67708产 地：中国大陆
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T6770AZD0156AZD-0156,inhibit,Inhibitor,AZD0156,Ataxia telangiectasia mutated,ATM and RAD3 related,Apoptos
AZD0156 , an effective and specific inhibitors of ATM kinase, is potential antineoplastic activities and chemo-/radio-sensitizing.
价 格：￥电议型 号：T6770产 地：中国大陆
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T17157TRAF-STOP inhibitor 6877002
TRAF-STOP inhibitor 6877002, is a selective inhibitor of CD40-TRAF6 interaction. TRAF-STOP 6877002 reduces leukocyte recruitment, and reduces macrophage activation; reduces macrophage proliferation in atherosclerotic plaques.
价 格：￥电议型 号：T17157产 地：中国大陆
