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产品数：86101
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T8620piperacillinβ-lactamase,inhibit,Gram-positive,piperacillin,semisynthetic penicillin,Inhibitor,Bacter
Piperacillin is a semisynthetic penicillin with wide spectrum of antimicrobial activity(particularly pseudomonas strains)
价 格：￥电议型 号：T8620产 地：中国大陆
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T9020GSK620Inhibitor,oral,GSK 620,phenotype,selectivity,GSK-620,whole,anti-inflammatory,GSK620,Epigenetic
GSK620 is a pan-BD2 inhibitor, which shows an anti-inflammatory phenotype in human whole blood with excellent broad selectivity, developability, and in vivo oral pharmacokinetics.GSK620 is highly selective for the BET-BD2 family of proteins, with >200-fold selectivity over all other bromodomains. GSK620 shows an anti-inflammatory phenotype in human whole blood.
价 格：￥电议型 号：T9020产 地：中国大陆
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T9620Sodium Tetradecyl SulfateInhibitor,Sodium Tetradecyl Sulfate,Tetradecyl sulfate,varicose veins,inhib
Sodium Tetradecyl Sulfate is a detergent sclerosant with antithrombotic effects and commonly used for the treatment of varicose veins.
价 格：￥电议型 号：T9620产 地：中国大陆
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T62083Camonsertib
Camonsertib is an orally active, selective ATR kinase inhibitor (IC50= 1.00 nM). Camonsertib exhibits 30-fold selectivity for ATR over mTOR (IC50=120 nM) and >2,000-fold selectivity over ATM, PI3Kα kinases, and DNA-PK. Camonsertib exhibits potent antitumor activity.
价 格：￥电议型 号：T62083产 地：中国大陆
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TN1620Eriocalyxin BEriocalyxin B,inhibit,Apoptosis,Inhibitor
Eriocalyxin B induces apoptosis and cell cycle arrest in pancreatic adenocarcinoma cells through caspase- and p53-dependent pathways, should be considered a candidate for pancreatic cancer treatment; it is a specific inhibitor of STAT3, it directly targets STAT3 through a covalent linkage to inhibit the phosphorylation and activation of STAT3 and induces apoptosis of STAT3-dependent tumor cells.
价 格：￥电议型 号：TN1620产 地：中国大陆
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T6620Ospemifeneinhibit,Ospemifene,Inhibitor,Estrogen Receptor/ERR
Ospemifene is a new selective non-hormonal estrogen receptor modulator (SERM) that is used for the treatment of moderate to severe dyspareunia, a symptom of vulvar and vaginal atrophy, due to menopause. FDA approved on February 26, 2013.
价 格：￥电议型 号：T6620产 地：中国大陆
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T7609ARS-1620inhibit,Ras,Inhibitor,ARS-1620,ARS 1620,ARS1620
ARS-1620 is a covalent inhibitor of K-RASG12C.
价 格：￥电议型 号：T7609产 地：中国大陆
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T62042BDZ-g
BDZ-g is a potent and selective antagonist of AMPA receptor. BDZ-g can be used for the research of various neurological disorders involving excessive activity of AMPA receptors.
价 格：￥电议型 号：T62042产 地：中国大陆
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T36200AZD 3147AZD 3147
AZD 3147 is an inhibitor of mTORC with IC50s of 40.7 and 5.75 nM for mTORC1 and mTORC2. AZD 3147 shows IC50s of 912, 5495, 9333, and 6310 nM for PI3Kα, PI3Kβ, PI3Kδ, and PI3Kγ, respectively.
价 格：￥电议型 号：T36200产 地：中国大陆
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T6846VesatolimodHepatitis B virus,Vesatolimod,HCV,inhibit,Apoptosis,GS9620,Human immunodeficiency virus,G
GS-9620 is an effective and specific orally active agonist of Toll-like receptor 7.
价 格：￥电议型 号：T6846产 地：中国大陆
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TQ0225VelsecoratAZD 7594,Inhibitor,AZD-7594,Velsecorat,Glucocorticoid Receptor,AZ-13189620,AZ 13189620,inh
AZD7594 is an effective and selective nonsteroidal glucocorticoid receptor modulator (IC50: 0.9 nM).
价 格：￥电议型 号：TQ0225产 地：中国大陆
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T9595LP-261NCI-H522,tubulin polymerization,tumor,SW-620,BXPC-3,H522,anti-mitotic,inhibit,LP261,MCF-7,Inhi
LP-261 is a novel tubulin targeting anticancer agent that binds at the colchicine site on tubulin, inducing G2/M arrest.
价 格：￥电议型 号：T9595产 地：中国大陆
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T6104Cerdulatinib hydrochloridePRT 062070,PRT 2070,Inhibitor,malignancies,Tyk2,Cerdulatinib hydrochloride
Cerdulatinib (PRT-062070) is an oral active, multi-targeted tyrosine kinase inhibitor with IC50 of 12 nM/6 nM/8 nM/0.5 nM and 32 nM for JAK1/JAK2/JAK3/TYK2 and Syk, respectively. Also inhibits 19 other tested kinases with IC50 less than 200 nM.
价 格：￥电议型 号：T6104产 地：中国大陆
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T6575LY2119620Muscarinic acetylcholine receptor,Inhibitor,inhibit,mAChR,LY-2119620,LY 2119620,LY2119620
LY2119620 is a specific, and allosteric agonist of human M2 and M4 muscarinic acetylcholine receptors.
价 格：￥电议型 号：T6575产 地：中国大陆
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TQ0033ZegocractinInhibitor,inhibit,Calcium release-activated channels,Ca2+ release-activated Ca2+ channels
CM4620 is a calcium-release activated calcium-channel (CRAC channel) inhibitor.
价 格：￥电议型 号：TQ0033产 地：中国大陆
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T9994WAY-620521WAY620521,WAY 620521
WAY-620521 is a cell-based high-throughput assay to identify small molecules that inhibit phospholipid biosynthesis in animal cells.
价 格：￥电议型 号：T9994产 地：中国大陆
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T9991WAY-620645WAY 620645,WAY620645
WAY-620645 is a CCK antagonist with antitumor and analgesic activities.
价 格：￥电议型 号：T9991产 地：中国大陆
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T76202,4,6-Tribromophenyl caproateFungal,2,4,6Tribromophenyl caproate,Inhibitor,inhibit,2,4,6-Tribromophe
2,4,6-Tribromophenyl caproate is a potent antifungal agent.
价 格：￥电议型 号：T7620产 地：中国大陆
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T9033BTYNBInhibitor,inhibit,ES-2,BTYNB,c-Myc,IMP1,Myc,IGROV-1,cancer cell,SK-MEL2
MDK6620?is an inhibitor of the oncofetal mRNA-binding protein IMP1 (IC50 = 5 μM for IMP1 binding to c-Myc mRNA).?MDK6620?downregulates β-TrCP1 mRNA and reduces activation of nuclear transcriptional factors-kappa B (NF-κB).?It disrupts this enhancer function by impairing IGF2 mRNA-binding protein 1 (IGF2BP1)-RNA association
价 格：￥电议型 号：T9033产 地：中国大陆
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T8356FPL 62064Cyclooxygenase,FPL 62064,LOX,5-lipoxygenase,FPL62064,inhibit,FPL-62064,Prostaglandin,5-LOX,
FPL 62064 is a potent dual inhibitor of 5-lipoxygenase (5-LOX) and COX (IC50 of 3.5 μM and 3.1 μM for RBL-1 cytosolic 5-lipoxygenase and prostaglandin synthetase, respectively).
价 格：￥电议型 号：T8356产 地：中国大陆
