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产品数：86101
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T6524GW0742GW0742,inhibit,GW 610742,Inhibitor,PPAR,Peroxisome proliferator-activated receptors,GW-0742,GW
GW0742 (GW610742) is an effective and specific PPARδ agonist (EC50: 1 nM/1.1 μM/2 μM, for human PPARδ/α/γ).
价 格：￥电议型 号：T6524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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T7700LersivirineHIV,non-nucleoside reverse transcription,Reverse Transcriptase,HIV virus,UK 453061,Inhibi
Lersivirine(UK 453061) is a second-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) under development for HIV infection therapy.
价 格：￥电议型 号：T7700产 地：中国大陆
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TN6961Heneicosaneinhibit,alkane,Heneicosane,aroma,Fungal,Inhibitor,pheromone
Heneicosane is a pheromone that inhibits the production of aflatoxins. Heneicosane is an aroma component isolated from Streptomyces philanthi RL-1-178 or Serapias cordigera.
价 格：￥电议型 号：TN6961产 地：中国大陆
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T7614Eniluracil5-fluorouracil,cancer,Inhibitor,inhibit,Eniluracil,5-FU,tumor,combination
Eniluracil is an orally activedihydropyrimidine dehydrogenase (DPD) inhibitor,increases the oral bioavailability of 5-FU to 100%, facilitating uniform absorption and predictable toxicity.
价 格：￥电议型 号：T7614产 地：中国大陆
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T61068AMPA receptor antagonist-2
AMPA receptor antagonist-2 is an AMPA receptor antagonist.
价 格：￥电议型 号：T61068产 地：中国大陆
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T6961PX-478Inhibitor,Autophagy,HIFs,inhibit,PX-478,PX 478,HIF-PH,HIF/HIF Prolyl-Hydroxylase,PX478,Hypoxia
PX-478 2HCl is an orally active, and selective inhibitor of hypoxia-inducible factor-1α (HIF-1α).
价 格：￥电议型 号：T6961产 地：中国大陆
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T61589c-Fms-IN-13
c-Fms-IN-13 (compound 14) is a potent FMS kinase inhibitor (IC50= 17 nM). c-Fms-IN-13 is an anti-inflammatory agent.
价 格：￥电议型 号：T61589产 地：中国大陆
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T8482Ripretinibc-Kit,Inhibitor,DCC2618,Vascular endothelial growth factor receptor,CD135,CD117,Platelet-d
Ripretinib is an orally bioavailable inhibitor of KIT and PDGFRA.
价 格：￥电议型 号：T8482产 地：中国大陆
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T86198-CHLOROQUINAZOLIN-4(1H)-ONE8 CHLOROQUINAZOLIN 4(1H) ONE,8CHLOROQUINAZOLIN4(1H)ONE
8-CHLOROQUINAZOLIN-4(1H)-ONE is inhibitor of Poly [ADP-ribose] polymerase 1 (human)
价 格：￥电议型 号：T8619产 地：中国大陆
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T8615ISOTHIAZOLINE 1,1-DIOXIDEISOTHIAZOLINE 1,1 DIOXIDE,ISOTHIAZOLINE 1,1DIOXIDE
ISOTHIAZOLINE 1,1-DIOXIDE is a reactant used in the synthesis of orally bioavailable hebatits B caspid inhibitors, and in the preparation of cryptochrome imhibitors as antidiabetic agents.
价 格：￥电议型 号：T8615产 地：中国大陆
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TP1617LChemerin-9 (149-157) acetateChemerin 9 (149 157) acetate,Chemerin9 (149157) acetate
Chemerin-9 (149-157) acetate, The nonapeptide 149,YFPGQFAFS157 (chemerin-9), corresponding to the C terminus of processed chemerin, retained most of the activity of the full-size protein, with regard to agonism toward the chemerinR.the natural ligand of ChemR23 (chemerinR).
价 格：￥电议型 号：TP1617L产 地：中国大陆
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T15614JJKK 048inhibit,JJKK-048,JJKK048,MAGL,Inhibitor,Monoacylglycerol lipase,JJKK 048
JJKK 048 is a potent and selective MAGL inhibitor.
价 格：￥电议型 号：T15614产 地：中国大陆
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T7261Grp94 Inhibitor-1HSP,Heat shock proteins,integrin αL,Inhibitor,inhibit,integrin α2,Grp-94 Inhibitor-
Grp94 Inhibitor-1 is a potent, selective Grp94 inhibitor (IC50 : 2 nM).
价 格：￥电议型 号：T7261产 地：中国大陆
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TQ0161MulberrinMulberrin,Inhibitor,inhibit
Mulberrin is an inhibitor of OATP2B1-mediated estrone-3-sulfate (E3S) uptake (IC50: 1.8 ±1.5 μM).
价 格：￥电议型 号：TQ0161产 地：中国大陆
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TN6120Nauclefine
Nauclefine is a plant indole alkaloid natural product and induces apoptosis of diverse cancer cells via a PDE3A-SLFN12 dependent death pathway. Nauclefine binds PDE3A but does not inhibit the PDE3A´s phosphodiesterase activity.
价 格：￥电议型 号：TN6120产 地：中国大陆
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T8991BMS986187leu-enkephalin,inhibit,PAM,BMS 986187,δ-opioid,Opioid Receptor,CHO-OPRD1 cell,BMS986187,BMS
BMS986187 is a novel Potent and Selective Positive Allosteric Modulators of the delta-Opioid Receptor.
价 格：￥电议型 号：T8991产 地：中国大陆
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T8061CitronellalCitronellal,Inhibitor,inhibit
Citronellal is a monoterpene predominantly formed by the secondary metabolism of plants, producing antithrombotic, antiplatelet, and antihypertensive activities.
价 格：￥电议型 号：T8061产 地：中国大陆
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T67741SU0561,3Dioxolo[4,5g]furo[3,4b]quinolin8(5H)one,9(3fluorophenyl)6,9dihydro5(2hydroxyethyl)
SU056 is a YB-1 inhibitor. SU056 interacts with YB-1 and inhibits and downstream proteins and pathways. SU056 can induce cell-cycle arrest, apoptosis, and inhibit cell migration in ovarian cancer cells.
价 格：￥电议型 号：T67741产 地：中国大陆
