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T9308AzoMethine-H Monosodium salt hydrateAzoMethineH Monosodium salt hydrate,AzoMethine H Monosodium salt
AzoMethine-H Monosodium salt hydrate is a reagent used for the colorimetric determination of boron in soil, plants, composts, manure, water and nutrient solutions.
价 格：￥电议型 号：T9308产 地：中国大陆
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TQ0219MK-8033bladder cancer,breast cancer,MK8033,EBC-1,H1993,MK 8033,MK-8033,anti-tumor,Inhibitor,GTL-16,r
MK-8033 is a new and selective dual ATP competitive c-Met/Ron inhibitor (IC50: 1 nM Wt c-Met).
价 格：￥电议型 号：TQ0219产 地：中国大陆
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T6938PF-4989216Apoptosis,inhibit,Phosphoinositide 3-kinase,PF4989216,PF-4989216,PI3K,Inhibitor
PF-4989216 is a potent and selective PI3K inhibitor with IC50 of 2 nM, 142 nM, 65 nM, 1 nM, and 110 nM for p110α, p110β, p110γ, p110δ, and VPS34, respectively.
价 格：￥电议型 号：T6938产 地：中国大陆
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T9356(E/Z)-GO289Inhibitor,cancer,(E/Z)GO289,circadian,(E/Z)-GO-289,cell,clock,rhythms,growth,(E/Z) GO289,
(E/Z)-GO289, which strongly lengthened circadian period, is a potent and selective inhibitor of CK2. (E/Z)-GO289 exhibited cell type-dependent inhibition of cancer cell growth that correlated with cellular clock function. The discovery of (E/Z)-GO289 provides a direct link between the circadian clock and cancer regulation and reveals unique design principles underlying kinase selectivity.
价 格：￥电议型 号：T9356产 地：中国大陆
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T6931PD0166285PD-0166285,Wee1,Inhibitor,inhibit,PD 0166285,Apoptosis,PD0166285
PD0166285 is a potent Wee1 and Chk1 inhibitor with activity at nanomolar concentrations.PD0166285 is a novel G2 checkpoint abrogator.
价 格：￥电议型 号：T6931产 地：中国大陆
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T6930Pazopanib Hydrochlorideinhibit,CD117,CSF1R,GW-786034,Vascular endothelial growth factor receptor,col
Pazopanib HCl (GW786034 HCl) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFR, FGFR, c-Kit and c-Fms with IC50 of 10 nM, 30 nM, 47 nM, 84 nM, 74 nM, 140 nM and 146 nM in cell-free assays, respectively.
价 格：￥电议型 号：T6930产 地：中国大陆
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T93351,1’-Methylenedi-2-naphthol1,1’Methylenedi2naphthol,1,1’ Methylenedi 2 naphthol
1,1´-Methylenedi-2-naphthol target CYP2C19 - cytochrome P450 family 2 subfamily C member 19 (human).
价 格：￥电议型 号：T9335产 地：中国大陆
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T93234-Amino-6-(trifluoromethyl)benzene-1,3-disulfonamide4Amino6(trifluoromethyl)benzene1,3disulfonamide,
4-Amino-6-(trifluoromethyl)benzene-1,3-disulfonamide is a carbonic anhydrase inhibitor, used as a potential anti-tumor and antiglaucoma drug.
价 格：￥电议型 号：T9323产 地：中国大陆
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TP1385Neurokinin A(4-10) TFA(97559-35-8 free base)Neurokinin A(410) TFA(97559358 free base),Neurokinin A(4
Neurokinin A (4-10) TFA is a tachykinin NK2 receptor agonist[1].
价 格：￥电议型 号：TP1385产 地：中国大陆
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TN7093N-CaffeoyltryptophanN Caffeoyltryptophan,NCaffeoyltryptophan
N-Caffeoyltryptophan, a potential Sirt inhibitor, is screened using coffee extract. N-Caffeoyltryptophan inhibited Sirt2 (IC50; 8.7 μM) better than Sirt1(IC50; 34μM).
价 格：￥电议型 号：TN7093产 地：中国大陆
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T9331Bemnifosbuvir hemisulfateInhibitor,antiviral,phosphoramidate,HCV,nucleotide,SARS-CoV,pangenotypic,Be
Bemnifosbuvir hemisulfate is a potent inhibitor of HCV virus replication.
价 格：￥电议型 号：T9331产 地：中国大陆
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T9358N,N,O-TridesmethylvenlafaxineInhibitor,N,N,O-Tridesmethylvenlafaxine,inhibit,Endogenous Metabolite,N
N,N,O-Tridesmethylvenlafaxine is a huamn endogenous metabolite.
价 格：￥电议型 号：T9358产 地：中国大陆
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T39370tri-GalNAc-COOHtri GalNAc COOH,triGalNAcCOOH
tri-GalNAc-COOH is an asialoglycoprotein receptor (ASGPR) ligand that can be used for LYsosome TArgeting Chimera (LYTAC) research.
价 格：￥电议型 号：T39370产 地：中国大陆
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T10936D-I03
D-I03 is a selective RAD52 inhibitor with a Kd of 25.8 ?M. D-I03 specifically inhibits RAD52-dependent single-chain annealing (SSA) and D-loop formation, with IC50 of 5 ?M and 8 ?M, respectively. D-I03 inhibited the growth of BRCA1 and BRCA2 deficient cells and inhibited the formation of damage-induced RAD52 foci, but does not effect on RAD51 foci induced by Cisplatin.
价 格：￥电议型 号：T10936产 地：中国大陆
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T9375IU1-248Deubiquitinase,IU1-248,IU1 248,DUBs,IU-1-248,Inhibitor,inhibit,IU1248
IU1-248 is a derivative of IU1. IU1-248 is a potent and selective USP14 inhibitor with an IC50 of 0.83?μM[1].
价 格：￥电议型 号：T9375产 地：中国大陆
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TP1938LRS09 2TFA (1449566-36-2 free base)RS09 2TFA (1449566362 free base),RS09 2TFA (1449566 36 2 free base
RS09 2TFA is a TLR4 agonist. Promotes NF-κB nuclear translocation and induces inflammatory cytokine secretion in RAW264.7 macrophages in vitro. It acts as an adjuvant in vivo and enhances X-15 specific antibody serum concentrations.
价 格：￥电议型 号：TP1938L产 地：中国大陆
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T12935SMN-C3
SMN-C3 is an orally active modulator of SMN2 splicing, and has the potential to treat spinal muscular atrophy (SMA).
价 格：￥电议型 号：T12935产 地：中国大陆
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T6932PD168393Autophagy,EGFR,ErbB-1,HER1,PD 168393,PD168393,Apoptosis,PDGFR,Epidermal growth factor recept
PD168393 is an irreversible EGFR inhibitor (IC50: 0.70 nM), irreversibly alkylate Cys-773; inactive against PKC, FGFR, PDGFR, and insulin.
价 格：￥电议型 号：T6932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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T16936SS-208
SS-208 is a selective inhibitor of HDAC6 (IC50 = 12 nM) with anti-tumor activity. SS-208 shows selectivity over other HDAC subtypes.
价 格：￥电议型 号：T16936产 地：中国大陆
