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产品数：86101
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T6785BI-847325BI 847325,inhibit,Apoptosis,MEK,MAPKK,MAP2K,Inhibitor,Aurora Kinase,Mitogen-activated prote
BI-847325 is a selective dual inhibitor of MEK and aurora kinases (AK) with IC50 values of 4 and 15 nM for human MEK2 and AK-C, respectively.
价 格：￥电议型 号：T6785产 地：中国大陆
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TN7108Urolithin Cinsulin,Ca channels,Apoptosis,Polyphenols,ROS,mitochondria,anti-diabetic,gut-microbial,Re
Urolithin C is a gut metabolite of ellagic acid. Urolithin C induces apoptosis in PC12 cells through a mitochondria-mediated pathway.
价 格：￥电议型 号：TN7108产 地：中国大陆
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T6433CAY10505PI3K,CAY10505,Apoptosis,Phosphoinositide 3-kinase,CAY-10505,CAY 10505,inhibit,Inhibitor
CAY10505, a form of dehydroxyl of AS-252424, is a PI3Kγ inhibitor (IC50: 33 nM).
价 格：￥电议型 号：T6433产 地：中国大陆
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T7177CapsazepineApoptosis,Transient receptor potential channels,TRP Channel,Inhibitor,inhibit,Capsazepine
Capsazepine is an antagonist of TRPV1 receptor ( IC50 : 562 nM). Capsazepine blocks the painful sensation of heat caused by capsaicin (the active ingredient of chilli pepper) which activates the TRPV1 ion channel. It is therefore considered to be a capsaicin antagonist.
价 格：￥电议型 号：T7177产 地：中国大陆
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T8333Aurintricarboxylic acidTopoisomerase,Apoptosis,receptor,P2XRs,Influenza Virus,glioblastoma,anti-infl
Aurintricarboxylic acid is a strong inhibitor of topoisomerases and other nucleases. It is a potent inhibitor of ribonuclease and topoisomerase II by preventing the binding of the nucleic acid to the enzyme.
价 格：￥电议型 号：T8333产 地：中国大陆
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T7040Angiotensin II humanAngiotensin II human,Apoptosis,Angiotensin Receptor,Inhibitor,inhibit
Angiotensin II is mediated by AT1 and AT2 receptors. AT1 and AT2 receptors have seven transmembrane glycoproteins with 30% sequence similarity.Angiotensin I convert Angiotensin II human through removing of two C-terminal residues by the enzyme angiotensin-converting enzyme (ACE).
价 格：￥电议型 号：T7040产 地：中国大陆
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T7791IberdomideCELMoD,H929,CRBN,Ligands for E3 Ligase,KMS12PE,KMS11,orally,sub-G1,Apoptosis,Iberdomide,ce
Iberdomide is a modulator of cereblon( IC50 value of 60 nM in a competitive TR-FRET assay).
价 格：￥电议型 号：T7791产 地：中国大陆
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T16766Ro 08-2750growth,MSI,Ro 082750,p75NTR,TRKA,RNA-binding,Nerve,NGF,Inhibitor,leukemia,Apoptosis,AML,Ro
Ro 08-2750 is a non-peptide and reversible nerve growth factor (NGF) inhibitor which binds to NGF, and with an IC50 of ~ 1 ?M. Ro 08-2750 is a selective MSI RNA-binding activity inhibitor, with an IC50 of 2.7 μM. Ro 08-2750 inhibits NGF binding to p75NTR selectively over TRKA.
价 格：￥电议型 号：T16766产 地：中国大陆
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T3055Liensinine PerchlorateInhibitor,Apoptosis,inhibit,Liensinine Perchlorate,Liensinine,cancer,tumorigen
Liensinine is the active constituent of plumula nelambinis with anti-hypertension.
价 格：￥电议型 号：T3055产 地：中国大陆
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T6871L-Glutamic acid monosodium saltEndogenous Metabolite,Inhibitor,L-Glutamic acid monosodium,Apoptosis,
L-Glutamic acid monosodium salt (Monosodium glutamate) is an activator of mGlu1 receptor.
价 格：￥电议型 号：T6871产 地：中国大陆
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T8216T-1101 tosylateTAI95,T1101 tosylate,TAI-95,T1101,Apoptosis,Inhibitor,inhibit,T 1101,T-1101,PPI,TAI 9
T-1101 tosylate is an inhibitor of Hec1/Nek2, with antitumor activity.
价 格：￥电议型 号：T8216产 地：中国大陆
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T6911NSC-87877 disodiumApoptosis,Neuroblastoma,inhibit,Inhibitor,NSC 87877 disodium,PPAR,p53,Phosphatase,
NSC-87877 is a cell-permeable inhibitor of both SHP-1 and SHP-2 with IC50 values of 355 and 318 nM respectively. It also inhibits EGF-induced Erk1/2 activation in HEK293 cells and significantly reduces MDA-MB-468 cell viability/proliferation.
价 格：￥电议型 号：T6911产 地：中国大陆
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TN2190Scoulerineproliferation,Inhibitor,cancer,Beta-secretase,Scoulerine,Apoptosis,inhibit,microtubule,cyc
Scoulerine is an inhibitor of ?-site amyloid precursor protein cleaving enzyme 1(BACE1). Scoulerine a potent antimitotic compound that inhibits proliferation, arrests cell cycle, and induces apoptosis in cancer cells.
价 格：￥电议型 号：TN2190产 地：中国大陆
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T6129GSK-1070916Inhibitor,Aurora Kinase,GSK-1070916,GSK 1070916,Apoptosis,inhibit
GSK1070916 is a reversible and ATP-competitive inhibitor of Aurora B/C with IC50 of 3.5 nM/6.5 nM. It displays >100-fold selectivity against the closely related Aurora A-TPX2 complex. Phase 1.
价 格：￥电议型 号：T6129产 地：中国大陆
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T7020Z-VAD-FMKinhibit,Inhibitor,ZVADFMK,Hela,Z VAD FMK,Caspase,Antiapoptosis,cells,pan-caspase
Z-VAD-FMK (Caspase Inhibitor VI) is an irreversible pan-caspase inhibitor.
价 格：￥电议型 号：T7020产 地：中国大陆
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T8057Citronellyl acetateInhibitor,Apoptosis,inhibit,Citronellyl,Citronellyl acetate
Citronellyl acetate is a natural product
价 格：￥电议型 号：T8057产 地：中国大陆
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T8734Cholineapoptosis,orally active,inhibit,hydrogen oxidized,organic base,sphingomyelin,Choline,standard
Choline is a ubiquitous water soluble nutrient, often associated with the B vitamins
价 格：￥电议型 号：T8734产 地：中国大陆
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T6731WYE-354inhibit,Apoptosis,WYE354,WYE-354,WYE 354,Inhibitor,Autophagy,Mammalian target of Rapamycin,mT
WYE-354(IC50=5 nM) is an effective, selective and ATP-competitive mTOR inhibitor. It blocks mTORC2/P-AKT(S473) and mTORC1/P-S6K(T389), not P-AKT(T308). The selectivity for mTOR is higher than PI3Kα (>100-fold) and PI3Kγ (>500-fold).
价 格：￥电议型 号：T6731产 地：中国大陆
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TN31105-Geranoxy-7-methoxycoumarinApoptosis,5 Geranoxy 7 methoxycoumarin,Bacterial,Fungal,antifungal,inhib
5-Geranoxy-7-methoxycoumarin shows antifungal activity.
价 格：￥电议型 号：TN3110产 地：中国大陆
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TJS0387DesoxyrhaponticinInhibitor,Fatty Acid Synthase (FASN),inhibit,Desoxyrhaponticin,Apoptosis
1. Desoxyrhaponticin is an agent that is potentially effective in controlling postprandial hyperglycemia in diabetes, the in vivo antidiabetic action of this compound can be explained, in part at least, by inhibition of glucose transport in the small intestine and inhibition of glucose reabsorption in the kidney. 2. Desoxyrhaponticin and rhaponticin could be considered as promising fatty acid synthase(FAS) inhibitors, they could inhibit intracellular FAS activity and downregulate FAS expression
价 格：￥电议型 号：TJS0387产 地：中国大陆
