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产品数：86101
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T6738Z-FA-FMKSARS coronavirus,SARS-CoV,RRMs,DNA fragmentation,DEVDase,Caspase,Cathepsin,Inhibitor,externa
Z-FA-FMK can irreversibly inhibit cysteine protease and also inhibit effector caspases.
价 格：￥电议型 号：T6738产 地：中国大陆
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T9304(S)-SunvozertinibHER1,Her2,(S)Sunvozertinib,mutant forms of ErbB,Epidermal growth factor receptor,(S
DZD9008 is a rationally designed selective, irreversible EGFR/HER2 inhibitor.
价 格：￥电议型 号：T9304产 地：中国大陆
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TN1416Ayaninhypertension,airway hyperresponsiveness,Phosphodiesterase (PDE),Inhibitor,inhibit,respiratory
Ayanin has vasorelaxant activity, it also may have the potential for use in treating allergic asthma. The IC50 value of Ayanin is 2.2microM for inhibiting interleukin IL-4 production from purified basophils. Ayanin is a non-selective phosphodiesterase1-4 inhibitor and can be used for respiratory disease researches.
价 格：￥电议型 号：TN1416产 地：中国大陆
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T6711Tyrphostin AG1296Fms like tyrosine kinase 3,PDGF,Apoptosis,CD117,inhibit,platelet-derived,CD135,SCFR
Tyrphostin AG 1296 is an inhibitor of PDGFR with IC50 of 0.3-0.5 μM, no activity to EGFR.
价 格：￥电议型 号：T6711产 地：中国大陆
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T6714URB-597Mitochondrial Autophagy,Mitophagy,bioavailable,Autophagy,inhibit,Fatty acid amide hydrolase,K
URB597 is an effective, orally bioavailable FAAH inhibitor (IC50: 4.6 nM), and no effect on other cannabinoid-related targets.
价 格：￥电议型 号：T6714产 地：中国大陆
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T9698UC2288Attenuator,786-O,Inhibitor,UC-2288,MDM-2/p53,inhibit,UC2288,ovarian,RCC,HK2,UC 2288,p21,sorafe
UC2288 is a relatively selective p21 attenuator which is synthesized based Sorafenib. UC2288 attenuates p21 protein levels with minimal effect on p21 protein stability.
价 格：￥电议型 号：T9698产 地：中国大陆
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TP1809TATPeptide,Inhibitor,HIV-1,HIV,TAT,inhibit,Human immunodeficiency virus
TAT (YGRKKRRQRRR) is a cell-penetrating peptide derived from the transactivator of transcription (TAT) of human immunodeficiency virus-1 (HIV-1). TAT can increase the yields and the solubility of heterologous proteins[1].
价 格：￥电议型 号：TP1809产 地：中国大陆
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T9008NPD8733Inhibitor,inhibit,ATPase,p97,fibroblast,cancer,NPD 8733,NPD8733,VCP,migration,NPD-8733
NPD8733 is an inhibitor of cancer cell-enhanced fibroblast migration. It specifically binds to valosin-containing protein (VCP)/p97.
价 格：￥电议型 号：T9008产 地：中国大陆
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T8541Lenvatinib mesylatePDGFR,Inhibitor,Lenvatinib mesylate,inhibit,VEGFR,c-Kit,RET,Vascular endothelial
Lenvatinib mesylate is an oral and multi-targeted inhibitor of VEGFR1-3, FGFR1-4, PDGFR, KIT, and RET, with potent antitumor activities.
价 格：￥电议型 号：T8541产 地：中国大陆
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T8007VU 0238429VU 0238429,VU-0238429,Muscarinic acetylcholine receptor,Inhibitor,inhibit,mAChR
VU0238429 is positive allosteric modulator of muscarinic acetylcholine receptor subtype 5 (mAChR5 or M5)( EC50 : 1.16 μM).
价 格：￥电议型 号：T8007产 地：中国大陆
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T8065TiamulinAntibiotic,Inhibitor,inhibit,pneumonia,Bacterial,veterinary,Tiamulin,dysentery,enzootic,swin
Tiamulin is a semisynthetic pleuromutilin antibiotic
价 格：￥电议型 号：T8065产 地：中国大陆
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TN119216-Epivoacarpine16-Epivoacarpine,Inhibitor,16 Epivoacarpine,16Epivoacarpine,inhibit
16-Epivoacarpine is a natural product from Gelsemium elegans.
价 格：￥电议型 号：TN1192产 地：中国大陆
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T6S2384PoliumosidePoliumoside,RLAR,AGE,Aldose Reductase,Inhibitor,aldose,advanced,glycation,product,Brandis
Poliumoside is a natural compound which exhibits significant inhibition of advanced glycation end product formation with IC50 value of 4.6-25.7 μM, it also exhibits great inhibitory effects on rat lens aldose reductase with IC50 values of 0.85 μM.Poliumoside has oxidant scavenging, antibacterial and hemostasis capacities, it can inhibit Biofilm-forming Staphylococcus aureus in mice.
价 格：￥电议型 号：T6S2384产 地：中国大陆
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T10835CletoquineNdesethylation,inhibit,CHIKV,P23pro-zbd,Parasite,antimalarial,CYP2D6,Influenza Virus,CYP3A
Cletoquine is a major active metabolite of Hydroxychloroquine. Cletoquine has the ability to against the chikungunya virus (CHIKV). Cletoquine has antimalarial effects and has the potential for autoimmune disease treatment.
价 格：￥电议型 号：T10835产 地：中国大陆
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T9578ELOVL1-IN-1chain,inhibit,adrenoleukodystrophy,Inhibitor,ELOVL1IN1,ALD,fatty,ELOVL-1-IN-1,acid,ELOVL1
ELOVL1-IN-1 is an ELOVL1 inhibitor. ELOVL1-IN-1 can reduce the levels of very long chain fatty acids. ELOVL1-IN-1 can be used in the study of adrenoleukodystrophy (ALD).
价 格：￥电议型 号：T9578产 地：中国大陆
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T60019VPC-70063VPC70063,Anticancer,LNCaP,VPC 70063,inhibit,Myc-Max,UBE2C,Apoptosis,VPC-70063,c-Myc,PARP,AR
VPC-70063 is an inhibitor of c-Myc-MAX. VPC-70063 exhibits Myc-Max transcriptional activity inhibition of 106% with an IC50 of 8.9 μM and Myc-Max/UBE2C downstream pathway inhibition of 94%. VPC-70063 can be used for studies about anticancer.
价 格：￥电议型 号：T60019产 地：中国大陆
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T6780Benzamideneuroprotective,dopamine,Benzenecarboxamide,Inhibitor,PARP,poly ADP ribose polymerase,Pheny
Benzamide, an inhibitor of poly(ADP-ribose) polymerase, is a derivative of benzoic acid.
价 格：￥电议型 号：T6780产 地：中国大陆
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T60919SARS-CoV-2-IN-13
SARS-CoV-2-IN-13 (compound 5) is an analogue of niclosamide. SARS-CoV-2-IN-13 is more stable than niclosamide in human plasma and liver S9 enzymes assay. SARS-CoV-2-IN-13 can improve bioavailability and half-life when administered orally. SARS-CoV-2-IN-13 is a potent SARS-CoV-2 inhibitor with an IC 50 of 0.057 μM [1].
价 格：￥电议型 号：T60919产 地：中国大陆
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T17115TolycaineTolycaine,anesthetic,inhibit,analog,convulsion,Inhibitor
Tolycaine is a compound of local anesthetic.
价 格：￥电议型 号：T17115产 地：中国大陆
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T6377AloperineInhibitor,Filovirus,Aloperine,Apoptosis,Autophagy,Human immunodeficiency virus,inhibit,HIV
Aloperine exhibits anti-inflammatory, antibacterial, antiviral, and anti-tumor properties.
价 格：￥电议型 号：T6377产 地：中国大陆
