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产品数：86101
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T6382Amikacin disulfateBacterial,bacillary,aminoglycosides,Gram-negative,ototoxic,Inhibitor,BAY 41-6551 d
Amikacin sulfate(BAY416651 sulfate) is a semi-synthetic aminoglycoside antibiotic derived from kanamycin A.
价 格：￥电议型 号：T6382产 地：中国大陆
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T8205Norwogonincytotoxicity,Enterovirus,Norwogonin,inhibit,Inhibitor,antiviral,EV71,HRV,HEVs,baicalensis,
Norwogonin, isolated from Scutellaria baicalensis Georgi, possesses antiviral activity against Enterovirus 71 (IC50: 31.83 μg/ml).
价 格：￥电议型 号：T8205产 地：中国大陆
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TP2333cyclo(L-Pro-L-Tyr)inhibit,Cyclo(Tyr-Pro),Alternaria alternata,anti-cancer,liver cancer,non-toxicity,
Maculosin is a secondary metabolite of fungi and bacteria.
价 格：￥电议型 号：TP2333产 地：中国大陆
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T7860SM-324405Inhibitor,Toll-like Receptor (TLR),low toxicity,TLR7,SM-324405,cytokine,diseases,immunother
SM 324405 is an agonist of TLR7.
价 格：￥电议型 号：T7860产 地：中国大陆
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TN1078SeneciphyllineP-450,hydrase,Inhibitor,Gutathione S-transferase,Cytochrome P450,Toxic,alkaloid,cytoch
Seneciphylline, one of the hepatotoxic pyrolizidine alkaloids, has mutagenic activity in Drosophila and their transfer into rat milk.Seneciphylline can significantly increased the activities of epoxide hydrase and glutathione-S-transferase but cause reduction of cytochrome P-450 and related monooxygenase activities.
价 格：￥电议型 号：TN1078产 地：中国大陆
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TN2182SarraceninInhibitor,Sarracenin,Patrinia,cytotoxic,tumor,inhibit,heterophylla,Iridoid
Sarracenin is a natural product. Sarracenin shows cytotoxic activities against tumor cells.
价 格：￥电议型 号：TN2182产 地：中国大陆
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T6612NU6027inhibit,Ataxia telangiectasia mutated,Cyclin dependent kinase,ATM/ATR,NU 6027,cytotoxicity,NU6
NU6027 is a potent ATR/CDK inhibitor, inhibits CDK1/2, ATR and DNA-PK with Ki of 2.5 μM/1.3 μM, 0.4 μM and 2.2 μM, enter cells more readily than the 6-aminopurine-based inhibitors.
价 格：￥电议型 号：T6612产 地：中国大陆
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T12871Talmapimodcytotoxicity,multiple,inhibit,tumor,SCIO 469,SCIO469,cells,Hsp27,Inhibitor,phosphorylation
Talmapimod is an selective, orally active, and ATP-competitive p38α inhibitor with IC50 of 9 nM and 90 nM for p38α and p38β, respectively. Talmapimod exhibits at least 2000-fold selectivity over a panel of 20 kinases, including other MAPKs.
价 格：￥电议型 号：T12871产 地：中国大陆
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T8646URB937FAAH,URB 937,Inhibitor,URB937,low,toxicity,inhibit,Fatty acid amide hydrolase,OEA,URB-937
URB937 is an inhibitor of FAAH and increases anandamide levels(IC50 : 26.8 nM).
价 格：￥电议型 号：T8646产 地：中国大陆
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TP1444Magainin 2protozoa,cytotoxicity,Bacterial,AMP,phospholipid,Inhibitor,bacteria,antimicrobial peptide,
Magainin II is a member of the antimicrobial peptides family
价 格：￥电议型 号：TP1444产 地：中国大陆
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T7495Hexa-D-arginineinhibit,furin,Furin Inhibitor II,TNF-α,PACE4,noncytotoxic,PC1,anthrax,PEA,HexaDargini
Hexa-D-arginine is an inhibitor of furin,blocks the activation of Pseudomonas aeruginosa exotoxin A in vivo.
价 格：￥电议型 号：T7495产 地：中国大陆
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TN1807IsoverticineIsoverticine,cytotoxicity,alkaloid,isosteroidal,Inhibitor,antitumor,inhibit
Isoverticine exhibits significant antitussive, expectorant and anti-inflammatory activities, it also displays significant cytotoxicity.
价 格：￥电议型 号：TN1807产 地：中国大陆
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T9267Aureobasidin AAureobasidin A,ceramide,inositolphosphorylceramides,Fungal,Inhibitor,intoxication,inhi
Aureobasidin A is a cyclic peptide and an antifungal antibiotic. Aureobasidin A is an inhibitor of the inositolphosphorylceramide synthase AUR1.
价 格：￥电议型 号：T9267产 地：中国大陆
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T8756KRAS inhibitor-9non-small,proliferation,inhibit,KRAS inhibitor 9,KRAS inhibitor9,cytotoxicity,Apopto
KRAS inhibitor-9 is a potent KRAS inhibitor with Kd of 92 μM that blocks the formation of GTP-KRAS and downstream activation of KRAS. KRAS inhibitor-9 causes G2/M cell cycle arrest and induces apoptosis. KRAS inhibitor-9 selectively inhibits the proliferation of NSCLC cells with KRAS mutation but not normal lung cells
价 格：￥电议型 号：T8756产 地：中国大陆
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T9918DaratumumabAnti-Human CD38, Human Antibody,myeloma,inhibit,tumor,antibody,cell,adhesion,cytotoxicity
Daratumumab is a human monoclonal antibody that targets CD38 a cell surface protein that is overexpressed on multiple myeloma MM) cells.
价 格：￥电议型 号：T9918产 地：中国大陆
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T6500Ferrostatin-1ROS,inhibit,Fer1,cell,neurotoxicity,cytosolic,Ferrostatin1,Fungal,antifungal,antioxidan
Ferrostatin-1 is a potent ferroptosis inhibitor (EC50: 60 nM).
价 格：￥电议型 号：T6500产 地：中国大陆
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T7413JNJ-5207852sleep,low,JNJ5207852,Histamine Receptor,JNJ-5207852,JNJ 5207852,Inhibitor,REM,toxicity,in
JNJ-5207852 is a novel, non-imidazole histamine H3 receptor antagonist, with high affinity at the rat (pKi=8.9) and human (pKi=9.24) H3 receptor.
价 格：￥电议型 号：T7413产 地：中国大陆
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T8492BO-264inhibit,cytotoxicity,antitumor,Fibroblast growth factor receptor,BO-264,Apoptosis,Inhibitor,TA
BO-264 is a highly potent and orally active inhibitor of transforming acidic coiled-coil 3 (TACC3, IC50 of 188 nM and a Kd of 1.5 nM).
价 格：￥电议型 号：T8492产 地：中国大陆
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T36964BML-259BML-259,protein,p53,CDK,death,disease,neurotoxicity,cell,Inhibitor,inhibit,Cyclin dependent k
BML-259 is an inhibitor of CDK5 and CDK2 with IC50s of 64 and 98 nM, respectively. BML-259 can be used in studies about the treatment of cancer and neurodegenerative diseases.
价 格：￥电议型 号：T36964产 地：中国大陆
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T9575MRTX9768SDMA,toxicity,glioblastoma,orally,MRTX9768,low,Inhibitor,hematological,MRTX-9768,MTAP,CDKN2A
MRTX-9768 is a synthetic lethal-based inhibitor designed to bind the PRMT5-MTA complex and selectively target MTAP/CDKN2A-deleted tumors.
价 格：￥电议型 号：T9575产 地：中国大陆
