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产品数：86101
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TP1166ZINC77292789inhibit,Inhibitor,ZINC77292789,ZINC-77292789
Fmoc-Thr[GalNAc(Ac)3-α-D]-OH is a reagent for the preparation of a synthetic MUC1 Glycopeptide Bearing βGalNAc-?Thr as a Tn antigen isomer which induces the antibody production against tumor cells. Fmoc-Thr[GalNAc(Ac)3-α-D]-OH is a starting material to make trimeric MUC1 immunodominant motif antigen-?based anti-?cancer vaccine candidates.
价 格：￥电议型 号：TP1166产 地：中国大陆
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T11163EGFR-IN-9EGFRIN9,EGFR IN 9
EGFR-IN-9 is a potent EGFR kinase inhibitor with IC50s of 7 nM, 28 nM for the wild type EGFR kinase and double mutant EGFR kinase (L858R/T790M). EGFR-IN-9 has antitumor activity.
价 格：￥电议型 号：T11163产 地：中国大陆
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TN11661,3,6-Tri-O-galloyl-beta-D-glucoseinhibit,Inhibitor,1,3,6TriOgalloylbetaDglucose,1,3,6 Tri O galloyl
1,3,6-Tri-O-galloyl-beta-D-glucose is a phenolic compound in Black Walnut Kernels. It shows anti-inflammatory activity.
价 格：￥电议型 号：TN1166产 地：中国大陆
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T8973HS-1793HIF-1α,Inhibitor,MCF-7,HS 1793,breast cancer,inhibit,ERK,HCT116,resveratrol,VEGF,Apoptosis,HS
HS-1793, a resveratrol analogue, downregulates the expression of hypoxia-induced HIF-1 and VEGF and inhibits tumor growth of human breast cancer cells in a nude mouse xenograft model
价 格：￥电议型 号：T8973产 地：中国大陆
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T8487EmpesertibBAY-1161909,Empesertib,Inhibitor,inhibit,Mps1,BAY1161909,Monopolar spindle 1
Empesertib is an orally bioavailable and selective inhibitor Mps1(IC50 < 1 nM), with potential antineoplastic activity.
价 格：￥电议型 号：T8487产 地：中国大陆
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TP1305LLEP(116-130)(mouse)TFA(258276-95-8 free base)LEP(116 130)(mouse)TFA(258276 95 8 free base),LEP(11613
LEP(116-130)(mouse) is a synthetic leptin peptide fragment.
价 格：￥电议型 号：TP1305L产 地：中国大陆
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TP1168N-Formyl-Met-Leu-Phe-LysInhibitor,N Formyl Met Leu Phe Lys,inhibit,NFormylMetLeuPheLys
N-Formyl-Met-Leu-Phe-Lys (fMLFK) is a peptide, acts as a potent and selective agonist of FPR1, with EC50s of 3.5 nM, 6.7 μM and 0.88 μM for FPR1, FPR2 and FPR2-D2817.32G, respectively.Chemotactic peptide (fMLFK) binds specifically to receptors on leukocyte membranes. Uptake of chemotactic peptides can contribute to quantitative assessment of neutrophils in localized inflammatory processes and is independent of associated edema formation or microcirculatory compromise.
价 格：￥电议型 号：TP1168产 地：中国大陆
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TP1116LKinetensin acetate(103131-69-7 free base)Kinetensin acetate(103131697 free base),Kinetensin acetate(
Kinetensin acetate is isolated from pepsin-treated human plasma.Kinetensin acetate is a neurotensin-like peptide.
价 格：￥电议型 号：TP1116L产 地：中国大陆
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T60022WAY-604116WAY604116,WAY 604116
WAY-604116 has anti-inflammatory, antitumor and antiasthmatic effects.
价 格：￥电议型 号：T60022产 地：中国大陆
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T6583MG-101RKO,MG-101,colon cancer,Bax,HepG2,Proteasome,MG 101,Inhibitor,mitochondria,HCT116,inhibit,Apop
MG-101 (ALLN) is a cell-permeable and potent inhibitor of cysteine proteases including calpains and lysosomal cathepsins.
价 格：￥电议型 号：T6583产 地：中国大陆
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T9973WAY-311677MCF-7,B16-F10,cancer,PTK2,FAK,WAY311677,Inhibitor,inhibit,WAY 311677,PTK2 protein tyrosine
WAY-311677 has potential antiproliferative activity and is a FAK inhibitor.
价 格：￥电议型 号：T9973产 地：中国大陆
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T7116Sodium gualenateSodium gualenate,Inhibitor,inhibit,Guaiazulenesulfonate
Sodium gualenate (Guaiazulenesulfonate sodium), a hydrophilic derivative of guaiazulene (GA), is an unstable compound. It has anti-inflammatory and wound-healing effects.
价 格：￥电议型 号：T7116产 地：中国大陆
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T8800NSAHDNA/RNA Synthesis,HCT116,MDA-231,Panc1,Inhibitor,NSAH,inhibit,S-phase
NSAH is a nonnucleoside inhibitor of human ribonucleotide reductase (hRR).with cell-free IC50 of 32 μM and cell-based IC50 of ~250 nM, respectively.
价 格：￥电议型 号：T8800产 地：中国大陆
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TN11601,2,3,6-TetragalloylglucoseInhibitor,1,2,3,6-Tetragalloylglucose,1,2,3,6Tetragalloylglucose,inhibit,
1,2,3,6-Tetragalloylglucose has antioxidative activity, it also shows the most potent anticomplement activity (IC50 = 34 microM). 1,2,3,6-Tetragalloylglucose is also a potent inhibitor of UDP glucuronosyltransferase 1 A1 (UGT1A1, Ki = 1.68 μM).
价 格：￥电议型 号：TN1160产 地：中国大陆
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T8500VLX600iron,HCT116,Autophagy,glycolytic,VLX 600,colon,chelator,cancer,OXPHOS,VLX600,Mitochondrial Met
VLX600 is an iron-chelating oxidative phosphorylation (OXPHOS) inhibitor, is a cell-permeable anticancer agent. It acts by reducing mitochondrial oxidative phosphorylation in tumor cells.
价 格：￥电议型 号：T8500产 地：中国大陆
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T9117BSJ-4-116CDK,degrader,antiproliferative,inhibit,Kelly,C1039F,BSJ 4 116,Cyclin dependent kinase,PROTA
BSJ-4-116 is a highly potent and selective CDK12 degrader (PROTAC) with an IC50 of 6 nM. It downregulates DDR genes through a premature termination of transcription, primarily through increasing poly(adenylation).
价 格：￥电议型 号：T9117产 地：中国大陆
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TQ0116LY 3000328Cathepsin,LY3000328,LY 3000328,Inhibitor,LY-3000328,inhibit
LY 3000328 is a potent, highly selective Cathepsin S (Cat S) inhibitor (IC50s: 7.7 and 1.67 nM for hCat S and mCat S).
价 格：￥电议型 号：TQ0116产 地：中国大陆
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T7394Toceranib PhosphateSU11654,inhibit,SU-11654,Toceranib,Toceranib Phosphate,VEGFR,PHA 291639E,Platelet
Toceranib phosphate, is a selective inhibitor of the tyrosine kinase activity of several members of the split kinase RTK family, including Flk-1/KDR, PDGFR
价 格：￥电议型 号：T7394产 地：中国大陆
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T6116LBleomycin hydrochlorideBleomycinhydrochloride
Bleomycin hydrochloride is a DNA synthesis inhibitor. Bleomycin hydrochloride is a DNA damaging agent. Bleomycin hydrochloride is an antitumor antibiotic.
价 格：￥电议型 号：T6116L产 地：中国大陆
