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产品数：86101
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TN1926Methyl caffeateinhibit,stress,antimicrobial,Bacterial,antimycobacterial,Methyl caffeate,α-glucosidas
Methyl caffeate acid
价 格：￥电议型 号：TN1926产 地：中国大陆
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T8118BekanamycinBekanamycin,Gram-negative,inhibit,influx,action,Antibiotic,calcium,Inhibitor,presynaptic,
Bekanamycin is an aminoglycoside antibiotic.
价 格：￥电议型 号：T8118产 地：中国大陆
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TN1121EvocarpineEvocarpine,Ca2+,HL-60,inhibit,antimycobacterial,Inhibitor,leukaemia,Bacterial,Apoptosis,In
Evocarpine shows antimycobacterial, and vasorelaxant effects, it can inhibit Ca2+ influx through voltage-dependent calcium channels.
价 格：￥电议型 号：TN1121产 地：中国大陆
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T6845GNE-317inhibit,GNE-317,Inhibitor,Phosphoinositide 3-kinase,Mammalian target of Rapamycin,mTOR,GNE 31
GNE-317, a PI3K/mTOR inhibitor, can pass through the blood-brain barrier (BBB).
价 格：￥电议型 号：T6845产 地：中国大陆
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TQ0155Miglustat hydrochlorideN-Butyldeoxynojirimycin,OGT-918,type I gaucher disease,Miglustat,Miglustat hy
Miglustat hydrochloride is an inhibitor of glucosylceramide synthase and can be used for studies about Type I Gaucher disease.
价 格：￥电议型 号：TQ0155产 地：中国大陆
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T22297Clindamycin hydrochloride monohydrate
Clindamycin hydrochloride monohydrate is an oral protein synthesis inhibitory agent that has the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin hydrochloride monohydrate resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin hydrochloride monohydrate decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-staphylo
价 格：￥电议型 号：T22297产 地：中国大陆
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T6740Bafilomycin A1Autophagy,Proton Pump,Bafilomycin A 1,Bafilomycin A1,Bafilomycin A-1,Antibiotic,BafA1,
Bafilomycin A1 induces caspase-independent cell death in hepatocellular carcinoma cells via targeting of autophagy and MAPK pathways. Bafilomycin A1 is a vacuolar H+-ATPase inhibitor (IC50: 0.44 nM). It is also found to inhibit autophagy while induces apoptosis.Bafilomycin A1 triggers proliferative potential of senescent cancer cells in vitro and in NOD/SCID mice.
价 格：￥电议型 号：T6740产 地：中国大陆
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TP2311C-MYC PEPTIDE EPITOPE TFACMYC PEPTIDE EPITOPE TFA,C MYC PEPTIDE EPITOPE TFA
C-MYC PEPTIDE EPITOPE TFA, the product of the c-myc proto-oncogene, is a helix-loop-helix leucine zipper phosphoprotein that regulates gene transcription in cell proliferation, cell differentiation and apoptosis. This peptide is a human c-myc epitope.
价 格：￥电议型 号：TP2311产 地：中国大陆
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T6557KU-0060648mTOR,inhibit,KU-0060648,Phosphoinositide 3-kinase,Inhibitor,Mammalian target of Rapamycin,
KU-0060648 is a dual inhibitor of DNA-PK and PI3Kα, PI3Kβ, PI3Kδ with IC50 of 8.6 nM and 4 nM, 0.5 nM, 0.1 nM respectively, less inhibition of PI3Kγ with IC50 of 0.59 μM.
价 格：￥电议型 号：T6557产 地：中国大陆
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T8838CCI-007CCI 007,MLL-r,CALM-AF10,HOXA9,MEIS1,Apoptosis,CMYC,CCI-007,SET-NUP214,inhibit,Inhibitor,CCI00
CCI 007 is a selective inhibitor of MLL-r, CALM-AF10 and SET-NUP214 leukemia with IC50 of 3.5 uM against MLL-r leukemia cell line PER-485
价 格：￥电议型 号：T8838产 地：中国大陆
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T13303Virginiamycin M1
Virginiamycin M1 is a macrocyclic lactone peptide antibiotic and is a member of the streptogramin A group of antibiotics.
价 格：￥电议型 号：T13303产 地：中国大陆
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T6732WYE-687mTOR,Mammalian target of Rapamycin,WYE-687,Phosphoinositide 3-kinase,WYE687,PI3K,WYE 687,inhi
WYE-687 is an ATP-competitive and selective inhibitor of mTOR with IC50 of 7 nM; blocks mTORC1/pS6K(T389) and mTORC2/P-AKT(S473) but no effect observed on P-AKT(T308). Selectivity for mTOR is greater than PI3Kα (>100-fold) and PI3Kγ (>500-fold).
价 格：￥电议型 号：T6732产 地：中国大陆
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TN1040Skullcapflavone IIinhibit,inflammatory,Skullcapflavone II,Bacterial,antimicrobial,mycobacterial,diff
Skullcapflavone II is a flavonoid derived from Scutellaria baicalensis, a widely used herbal medicine in anti-inflammatory and anticancer therapy. Skullcapflavone II may have therapeutic potential for the treatment of allergic asthma.Skullcapflavone II regulates osteoclast differentiation, survival, and function. Skullcapflavone II exerts potent antimicrobial activity against M. aurum and M. bovis BCG
价 格：￥电议型 号：TN1040产 地：中国大陆
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T0906Salinomycin
Salinomycin, a polyether potassium ionophore antibiotic, selectively inhibits the growth of gram-positive bacteria. Salinomycin is a potent inhibitor of Wnt/β-catenin signaling, blocks Wnt-induced LRP6 phosphorylation. Salinomycin (Procoxacin) shows selective activity against human cancer stem cells.
价 格：￥电议型 号：T0906产 地：中国大陆
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TN1405Arnicolide DMammalian target of Rapamycin,Phosphoinositide 3-kinase,inhibit,Inhibitor,Caspase,mTOR,A
Arnicolide D is a sesquiterpene lactone. Arnicolide D isolates from Centipeda minima. Arnicolide D modulates the cell cycle, activates the caspase signaling pathway and inhibits the PI3K/AKT/mTOR and STAT3 signaling pathways. Arnicolide D inhibits Nasopharyngeal carcinoma (NPC) cell viability in a concentration- and time-dependent manner. Arnicolide D exerts strong cytotoxic activity on the human colon carcinoma HT-29 cell line.
价 格：￥电议型 号：TN1405产 地：中国大陆
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T8658NEO2734PER-403,SPOP,NEO-2734,CBP,NEO 2734,MYC,HAT,NEO2734,Epigenetic Reader Domain,TC-797,Histone Ac
NEO2734 is an orally active and selective inhibitor of p300/CBP and BET bromodomain(IC50 of <30 nM for both p300/CBP and BET bromodomains).
价 格：￥电议型 号：T8658产 地：中国大陆
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T9032MGH-CP1MGH CP1,Lats1/2 deletion,Myc,MGHCP1,TEAD auto-palmitoylation,Apoptosis,Epithelial,MGH-CP1,inh
MGH-CP1 is a potent and selective inhibitor TEAD palmitoylation. It exhibits dose-dependent and potent inhibition of TEAD2/4 auto-palmitoylation in vitro with IC50 of 710 nM and 672 nM, respectively.
价 格：￥电议型 号：T9032产 地：中国大陆
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T9370dCBP-1Inhibitor,p300,multiple,CRBN,myeloma,cell,degrader,PROTACs,MYC,CBP,inhibit,dCBP 1,dCBP1,hetero
dCBP-1 is a chemical degrader of p300/CBP. dCBP-1 hijacks the E3 ubiquitin ligase CRBN for selective degradation of p300/CBP. Degradation of p300/CBP by dCBP-1 leads to effective multiple myeloma cell killing.
价 格：￥电议型 号：T9370产 地：中国大陆
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T8262Fosfomycin sodiumXDR,multidrug-resistant,Bacterial,inhibit,Fosfomycin sodium,Antibiotic,MK-0955,drug
Fosfomycin is a bactericidal, low-molecular weight, broad-spectrum antibiotic, with putative activity against several bacteria, including multidrug-resistant Gram-negative bacteria, by irreversibly inhibiting an early stage in cell wall synthesis.
价 格：￥电议型 号：T8262产 地：中国大陆
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T9093NY2267c-Myc,inhibit,NY2267,Inhibitor,interaction,NY 2267,Myc,Max,NY-2267
NY2267 is a disruptor of Myc-Max interaction, with an IC50 of 36.5 μM.
价 格：￥电议型 号：T9093产 地：中国大陆
