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T6947PiperlongumineExtracellular signal regulated kinases,Ferroptosis,Bacterial,Inhibitor,inhibit,Apoptos
Piperlongumine is a natural alkaloid from Piper longum L. It selectively kills cancer cells and strengthens the level of reactive oxygen species (ROS).
价 格：￥电议型 号：T6947产 地：中国大陆
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TN2356TetradehydropodophyllotoxinInhibitor,Fungal,Tetradehydropodophyllotoxin,inhibit
Tetradehydropodophyllotoxin has anti-tumor activity.
价 格：￥电议型 号：TN2356产 地：中国大陆
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T7507γ-L-Glutamyl-L-alanineγLGlutamylLalanine,inhibit,Endogenous Metabolite,Inhibitor,γ L Glutamyl L alan
γ-L-Glutamyl-L-alanine, composed of gamma-glutamate and alanine, is the substrate of CRF21 (gamma-Glutamylcyclotransferase, GGCT).
价 格：￥电议型 号：T7507产 地：中国大陆
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T6386Ampicillin sodiumAmpicillin sodium,Antibiotic,inhibit,Inhibitor,Bacterial,Ampicillin
Ampicillin Sodium is the sodium salt form of ampicillin, a broad-spectrum semisynthetic derivative of aminopenicillin. Ampicillin sodium inhibits bacterial cell wall synthesis by binding to penicillin binding proteins, thereby inhibiting peptidoglycan synthesis, a critical component of the bacterial cell wall.
价 格：￥电议型 号：T6386产 地：中国大陆
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TN2080Pinoresinolapoptotic,sensitizer,Pinoresinol,caterpillar,inhibit,cancer,Apoptosis,Inhibitor,lignol,gl
Pinoresinol has antiinflammatory, hepatoprotective, and fungicidal activities, it can protect pial microcirculation from I-reperfusion injury, to increase nitric oxide release and to reduce oxidative stress preserving pial blood flow distribution; it may exert pharmacologically interesting effects via modulation of the insulin-like signalling pathway in C.elegans. Pinoresinol causes an upregulation of the CDK inhibitor p21(WAF1/Cip1) both at mRNA and protein levels, inhibits NF-kappaB and activa
价 格：￥电议型 号：TN2080产 地：中国大陆
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T6S0657Isorhynchophyllineinhibit,Inhibitor,Isorhynchophylline
1. Isorhyncophylline and rhyncophylline can directly inhibit the contractile responses induced by several agonists in small blood vessels of rat, they also can inhibit the hypertensive effect of angiotensin Ⅱ.
价 格：￥电议型 号：T6S0657产 地：中国大陆
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T9230KM 91104V-ATPase human HSC,a3-b2 subunits,KM-91104,KM 91104,Inhibitor,KM91104,Proton Pump,cell-perme
KM 91104 is a cell permeable inhibitor of V-ATPase. KM91104 specifically targets the interaction between V-ATPase subunit A3 and subunit B2.
价 格：￥电议型 号：T9230产 地：中国大陆
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T8101Nepsilon-Acetyl-L-lysineinhibit,Nepsilon Acetyl L lysine,NepsilonAcetylLlysine,Inhibitor,Endogenous
Nepsilon-Acetyl-L-lysine is a derivative of the lysine.
价 格：￥电议型 号：T8101产 地：中国大陆
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T13456(S)-Willardiine
(S)-Willardiine is present in the seeds of Acacia and Mimosa. (S)-Willardiine is an AMPA/kainate receptor agonist (EC50 = 44.8 μM).
价 格：￥电议型 号：T13456产 地：中国大陆
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T7426ALSTERPAULLONECDK5,GSK-3,p35,NSC-705701,9-Nitropaullone,NSC705701,ALSTERPAULLONE,Glycogen synthase k
Alsterpaullone is a Cyclin-Dependent Kinase Inhibitor, Mediated Toxicity in HeLa Cells Through Apoptosis-Inducing Effec
价 格：￥电议型 号：T7426产 地：中国大陆
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T6879LLY-507protein,inhibit,methyltransferase,methylation,breast,cancer,SMYD2,LLY-507,p53,Inhibitor,Histo
LLY-507 is an effective, cell-active, and specific inhibitor of protein-lysine Methyltransferase SMYD2.
价 格：￥电议型 号：T6879产 地：中国大陆
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TN2054Periplocymarinproliferation,inhibit,Inhibitor,cardiac,Periplocymarin,U937,anti-cancer,HCT-8,cells,gl
Periplocymarin, a cardiac glycoside, has potential anti-cancer activity.
价 格：￥电议型 号：TN2054产 地：中国大陆
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T9541CTBHATs,Inhibitor,neurons,CTB,Apoptosis,MCF-7 cell,cancer,potent,HAT,autophagic flux,inhibit,Histone
CTB (Cholera Toxin B subunit) is an activator of p300 histone acetyltransferase and induces apoptosis in MCF-7 cells.
价 格：￥电议型 号：T9541产 地：中国大陆
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T13867RH01386RH 01386,βTC6 cells,RH01386,RH-01386,inhibit,Apoptosis,Inhibitor,type 2 diabetes,β cell
RH01386 is a small molecule that can prevent ER stress-induced β cell dysfunction and death, and inhibits proapoptotic gene expression,has the potential for type 2 diabetes treatment. RH01386 restores ER stress-impaired glucose-stimulated insulin secretion responses.
价 格：￥电议型 号：T13867产 地：中国大陆
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TP1658LType A Allatostatin I acetateType A Allatostatin I acetate
Type A Allatostatin I acetate is a tridecapeptide. Allatostatins are pleiotropic neuropeptides for inhibition of juvenile hormone synthesis in insects.
价 格：￥电议型 号：TP1658L产 地：中国大陆
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T8233BRD3308β-cells,glucolipotoxicity,inflammatory,BRD-3308,Human immunodeficiency virus,BRD3308,Histone
BRD3308 is a highly selective inhibitor of HDAC3(IC50 of 54 nM), attenuating PE-mediated phosphorylation of ERK but not JNK.
价 格：￥电议型 号：T8233产 地：中国大陆
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T83161V209cell,polysaccharides,IP-10,intravenous,MCP-1,Tumor,1V-209,IL-6,1V209,Toll-like Receptor (TLR),c
1V209 is a Toll-like receptor 7 (TLR7) agonist and has anti-tumor effects.
价 格：￥电议型 号：T8316产 地：中国大陆
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T17117Tonapofylline
Tonapofylline is an orally active and selective antagonist of the A1 adenosine receptor (Ki: 7.4 nM for human A1). Tonapofylline can be used in studies about heart failure.
价 格：￥电议型 号：T17117产 地：中国大陆
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TP1497LMast Cell Degranulating Peptide HR-2 acetateMast Cell Degranulating Peptide HR 2 acetate,Mast Cell D
Mast Cell Degranulating Peptide HR-2 acetate from giant hornet Vespa orientalis that has biological effects similar to mast cell degranulating peptide from bee venom.
价 格：￥电议型 号：TP1497L产 地：中国大陆
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T6481DroxinostatHDAC3,hepatocellular carcinoma (HCC),Droxinostat,NS-41080,Apoptosis,Histone deacetylases,
Droxinostat is a selective inhibitor of HDAC, mostly for HDACs 6 and 8 with IC50 of 2.47 μM and 1.46 μM, greater than 8-fold selective against HDAC3 and no inhibition to HDAC1, 2, 4, 5, 7, 9, and 10.
价 格：￥电议型 号：T6481产 地：中国大陆
