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T14688BMS CCR2 22BMS CCR2 22,BMS CCR-2 22
BMS CCR2 22 is a potent and selective antagonist of CCR2 with calcium flux IC50 of 18 nM, chemotaxis IC50 of 1 nM, and binding IC50 of 5.1 nM.
价 格：￥电议型 号：T14688产 地：中国大陆
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T6893MK-886leukotriene,FLAP,5-LOX,5-LO activating protein,non-competitive,L-663536,L663536,keratin-1,Leuk
MK-886 is an inhibitor of leukotriene biosynthesis, inhibiting 5-lipoxygenase-activating protein (FLAP). It is also a moderately potent PPARα antagonist.
价 格：￥电议型 号：T6893产 地：中国大陆
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T9468FR054FR054,FR 054,TNBC,HBP,inhibit,Negative,Cancer,Inhibitor,Breast,Triple,PGM3,FR-054
FR054 is an inhibitor of the Hexosamine Biosynthetic Pathway (HBP) enzyme PGM3, with a remarkable anti-breast cancer effect. FR054 induces in different breast cancer cells a dramatic decrease in cell proliferation and survival.
价 格：￥电议型 号：T9468产 地：中国大陆
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T36683VedaprofenVedaprofen,Inhibitor,nonsteroidal,PM150,PM-150,Escherichia coli,inhibit,CERM-10202,CERM102
Vedaprofen inhibits COX-1 and reduces prostaglandin H2 synthesis with anti-inflammatory activities. Vedaprofen is an inhibitor of Escherichia coli sliding clamp with the IC50 of 222 μM and Ki of 131 μM.
价 格：￥电议型 号：T36683产 地：中国大陆
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TQ0068NVP-LCQ195NVP-LCQ195,AT-9311,NVPLCQ195,NVP-LCQ-195,inhibit,Cyclin dependent kinase,Inhibitor,AT 9311
NVP-LCQ195 (AT9311) is a potent inhibitor of CDK1, CDK2, CDK3 and CDK5 (IC50: 1-42 nM).
价 格：￥电议型 号：TQ0068产 地：中国大陆
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T6817DeguelinAutophagy,inhibit,Deguelin,Protein kinase B,Akt,PKB,Inhibitor,Apoptosis
Deguelin is a PI3K/AKT Inhibitor, which is a natural product isolated from plants in the Mundulea sericea family.
价 格：￥电议型 号：T6817产 地：中国大陆
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T6S1688(1E,6E)-Bis(demethoxy)curcumin(E,E)-Curcumin III,Bisdemethoxycurcumin,inhibit,(E,E)-Didemethoxycurcu
(1E,6E)-Bis(demethoxy)curcumin is a natural demethoxy derivative of curcumin,with anti-inflammatory and anti-cancer activities.
价 格：￥电议型 号：T6S1688产 地：中国大陆
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T36899INCB086550
INCB086550 (example 24) is a PD-1/PD-L1 inhibitor, with an IC50 <= 10 nM.
价 格：￥电议型 号：T36899产 地：中国大陆
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T8068o-Toluic acidEndogenous Metabolite,metabolite,o-Toluic acid,2-Methylbenzoic acid,oToluic acid,Inhibi
o-Toluic acid, also 2-methylbenzoic acid, is an aromatic carboxylic acid. It is a human xenobiotic metabolite.
价 格：￥电议型 号：T8068产 地：中国大陆
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T8688(Rac)-X77SARS-CoV,(Rac)-X77,protease,SARS coronavirus,inhibit,Inhibitor,(Rac) X77,(Rac)-X-77,coronav
CPD77 is a potent SARS- CoV- 2 main protease inhibitor.
价 格：￥电议型 号：T8688产 地：中国大陆
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T8686VUN65671Compound 35
Compounds 35 are superior inhibitors of Ebola (Mayinga) and Marburg (Angola) infectious viruses.
价 格：￥电议型 号：T8686产 地：中国大陆
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T6441CGS 21680 HydrochlorideCGS-21680,Inhibitor,CGS 21680,inhibit,CGS21680,CGS 21680 Hydrochloride,Adenos
CGS 21680 HCl（ IC50=22 nM）, an adenosine receptor agonist, exhibits 140-fold potency in A2 receptor over A1 receptor.
价 格：￥电议型 号：T6441产 地：中国大陆
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T7673ATH686ATH686,inhibit,CD135,Inhibitor,Apoptosis,ATH-686,ATP-competitive,FLT3,antileukemic,Fms like ty
ATH 686 is an potent and selective Inhibitor of FLT3.
价 格：￥电议型 号：T7673产 地：中国大陆
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T6898MotolimodMotolimod,inhibit,VTX378,VTX 378,Inhibitor,Toll-like Receptor (TLR),VTX 2337,VTX2337
Motolimod (VTX-2337) is an effective and specific Toll-like receptor (TLR) 8 agonist (EC50: 100 nM), > 50-fold selectivity over TLR7.
价 格：￥电议型 号：T6898产 地：中国大陆
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T6768AZ6102AZ 6102,PARP,AZ-6102,Inhibitor,poly ADP ribose polymerase,inhibit,AZ6102
AZ6102 is a potent TNKS1/2 inhibitor that has 100-fold selectivity against other PARP family enzymes and shows IC50 of 5 nM for Wnt pathway inhibition in DLD-1 cells.
价 格：￥电议型 号：T6768产 地：中国大陆
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T9168NSC 617145NSC 617145,breaks,NHEJ,helicase,DSB,abnormalities,WRN,DNA/RNA Synthesis,strand,Rad51,chrom
NSC617145 is an inhibitor of WRN helicase that inhibits the ATPase, but not exonuclease, activity of WRN helicase in a concentration-dependent manner.
价 格：￥电议型 号：T9168产 地：中国大陆
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T8468CIL62CIL-62,CIL62
CIL62 is a caspase-3/7-independent inducer of cell death. The mechanism of action of CIL62 is Necrostatin-1 dependent cell death [1].
价 格：￥电议型 号：T8468产 地：中国大陆
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T40685LOrphan GPCR SP9155 agonist P550 (mouse, rat) acetateOrphan GPCR SP9155 agonist P550 (mouse, rat) ace
Orphan GPCR SP9155 agonist P550 (mouse, rat) acetate is a member of the RFamide peptide family with orexigenic effects.
价 格：￥电议型 号：T40685L产 地：中国大陆
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T6968RiociguatInhibitor,inhibit,BAY-632521,Riociguat,Guanylate Cyclase,BAY632521
Riociguat is a stimulator of guanylate cyclase which causes relaxation of vascular smooth muscle and is used to treat severe pulmonary arterial hypertension.
价 格：￥电议型 号：T6968产 地：中国大陆
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T6858Hydroxyprogesterone caproateHydroxyprogesterone caproate,Inhibitor,inhibit
Hydroxyprogesterone Caproate is a synthetic progestational agent. It binds to and activates nuclear progesterone receptors in the reproductive system and inhibits ovulation and an alteration in the cervical mucus and endometrium.
价 格：￥电议型 号：T6858产 地：中国大陆
