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产品数：86101
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TP1606LNLS PKKKRKV acetate(95088-49-6 free base)NLS PKKKRKV acetate(95088 49 6 free base),NLS PKKKRKV ace
NLS PKKKRKV acetate is a peptide derived from the 40 tumor antigen of the great ape virus (SV40 big T antigen), which is a method to enhance the nuclear portal in the research field of gene transfer.
价 格：￥电议型 号：TP1606L产 地：中国大陆
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T1016011β-HSD1-IN-111β-HSD-1-IN-1,11βHSD1IN1,11β HSD1 IN 1
11β-HSD1-IN-1 is an inhibitor of 11β-hydroxydehydrogenase 1 (11β-HSD1, IC50: 52 nM), and used for the treatment of pain.
价 格：￥电议型 号：T10160产 地：中国大陆
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T7160Lofexidineinhibit,Inhibitor,Lofexidine,Beta Receptor,Adrenergic Receptor
Lofexidine is a selective α2-receptor agonist, Lofexidine reduces narcotic withdrawal symptoms.
价 格：￥电议型 号：T7160产 地：中国大陆
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TN1601EffusolInhibitor,Effusol,inhibit
Effusol is a natural product, exhibits potent scavenging activity for DPPH and ABTS radicals(IC50 values of 79 μM and 2.73 μM, respectively). Effusol rescues CA1 LTP attenuated by corticosterone, defending the hippocampal function against stress-induced cognitive decline. Effusol can induce caspase-3-mediated cytotoxicity in HT22 cells.
价 格：￥电议型 号：TN1601产 地：中国大陆
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T31602Ecopipam
Ecopipam is a potent, selective and orally active antagonist of dopamine D1/D5 receptor, with Kis of 1.2 nM and 2.0 nM, respectively. Ecopipam shows more than 40-flod selectivity over D2, D4, 5-HT, and α2a receptor (Ki=0.98, 5.52, 0.08, and 0.73 μM, respectively). Ecopipam can be used for the research of schizophrenia, cocaine addition, and obesity.
价 格：￥电议型 号：T31602产 地：中国大陆
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TMA1603Parishin CParishin C,Inhibitor,inhibit
Parishin C is a phenolic glycoside and a major component of G. elata, have antioxidant property
价 格：￥电议型 号：TMA1603产 地：中国大陆
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TP1604LThioredoxin reductase peptide acetateThioredoxin reductase peptide acetate
Thioredoxin reductase peptide acetate corresponds to residues 53–67 in thioredoxin reductase (TrxR), used in thioredoxin reductase research.Mammalian thioredoxin reductase (TR) catalyzes the reduction of the redox-active disulfide bond of thioredoxin (Trx) and is similar in structure and mechanism to glutathione reductase except for a C-terminal 16-amino acid extension containing a rare vicinal selenylsulfide bond.
价 格：￥电议型 号：TP1604L产 地：中国大陆
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T16040Mepazinediffuse,B cell,inhibit,large,mucosa associated lymphoid tissue lymphoma translocation gene 1
Mepazine is a potent and selective inhibitor of MALT1. Mepazine inhibits GSTMALT1 full length and GSTMALT1 325-760 with IC50s of 0.83 μM and 0.42 μM. Mepazine enhances apoptosis and affects the cell viability.
价 格：￥电议型 号：T16040产 地：中国大陆
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T60160STX-0119STX0119
STX-0119 is a selective, orally active STAT3 dimerization inhibitor. STX-0119 inhibits STAT3 transcription with an IC50 of 74 μM.
价 格：￥电议型 号：T60160产 地：中国大陆
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T8160EGCG OctaacetateInhibitor,EGCG Octaacetate,prodrug,gram-negative bacteria,Bacterial,inhibit,colitis-
EGCG Octaacetate, a prodrug of EGCG, is utilized to enhance the stability and bioavailability of EGCG in vivo. It has high efficacy, bioavailability, anti-oxidation, and anti-angiogenesis capacities.
价 格：￥电议型 号：T8160产 地：中国大陆
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T91604-Chloroquinolin-8-ol4 Chloroquinolin 8 ol,4Chloroquinolin8ol
4-Chloroquinolin-8-ol is a building block
价 格：￥电议型 号：T9160产 地：中国大陆
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TQ0160HydrastineHydrastine,Inhibitor,inhibit
Hydrastine is a natural alkaloid that is present in Hydrastis Canadensis.
价 格：￥电议型 号：TQ0160产 地：中国大陆
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T61025GSK-1482160
GSK-1482160 is a CNS-penetrant negative allosteric modulator of P2X7 receptor with oral activity. The P2X7 receptor is involved in the production of pro-inflammatory cytokines by central and peripheral immune cells, so GSK-1482160 has the potential to study inflammatory diseases. GSK-1482160 shows excellent in vitro potency (in functional and electrophysiological assays at recombinant and naive P2X7 receptors across multiple species including humans) and cross-target selectivity.
价 格：￥电议型 号：T61025产 地：中国大陆
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T24160IM-54
IM-54 is a cell-permeable, effective, and selective necrosis inhibitor.
价 格：￥电议型 号：T24160产 地：中国大陆
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T67845ARUK2001607
ARUK2001607 is a selective inhibitor of phosphatidylinositol 5-phosphate 4-kinase γ (PI5P4Kγ, Kd= 7.1 nM). ARUK2001607 exhibits high selectivity over other >150 kinases.
价 格：￥电议型 号：T67845产 地：中国大陆
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TN1600Eclalbasaponin IEclalbasaponin I,inhibit,Inhibitor
Eclalbasaponin I has anti-oxidative, and antitumor activities, it reduces oxidative stress-induced neural cell death by autophagy activation, it can dose-dependently inhibit the proliferation of hepatoma cell smmc-7721 with the IC(50) value of 111.1703 ug/ml.
价 格：￥电议型 号：TN1600产 地：中国大陆
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T8808LLYN-1604 dihydrochlorideanti-tumor,Unc-51 like kinase,negative,LYN-1604,LYN 1604,cancer,Autophagy,br
LYN-1604 is a novel ULK1 activator.It inducing cell death involved in ATF3, RAD21, and caspase3, accompanied by autophagy and apoptosis.
价 格：￥电议型 号：T8808L产 地：中国大陆
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TP1605L1Allatostatin IV TFA(123338-13-6 free base)Allatostatin IV TFA(123338136 free base),Allatostatin IV T
Allatostatin IV TFA, an octapeptide amine, is a member of the allatoregulatory peptide family found in insects which either inhibit (allatostatins) or stimulate (allatotropins) juvenile hormone (JH) synthesis.
价 格：￥电议型 号：TP1605L1产 地：中国大陆
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T7680GSNKGAIIGLM(131602-53-4(free base))GSNKGAIIGLM(131602 53 4(free base)),GSNKGAIIGLM(131602534(free ba
GSNKGAIIGLM is the fragment Aβ(25-35) of the Alzheimer´s amyloid β-peptide.
价 格：￥电议型 号：T7680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
