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产品数：86101
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T8880PFM01Inhibitor,derivative,MRE11,PFM-01,NHEJ,Mirin,DSB,endonuclease,N-alkylated,PFM01,PFM 01,inhibit
PFM01 is an inhibitor of MRE11 endonuclease. PFM01 can regulate double-strand break repair (DSBR) by nonhomologous end-joining (NHEJ) versus homologous recombination (HR).
价 格：￥电议型 号：T8880产 地：中国大陆
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TN6925Pristanehydrocarbon oil,Inhibitor,plants,Pristane,mineral oil,Norphytane,non-antigenic adjuvant,mari
Pristane is a natural product from shark liver oil and a non-antigenic adjuvant.
价 格：￥电议型 号：TN6925产 地：中国大陆
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T11053DJ001DJ-001,DJ001
DJ001 is a highly specific, selective and non-competitive protein tyrosine phosphatase σ (PTPσ) inhibitor with IC50 of 1.43 μM. DJ001 promotes the regeneration of hematopoietic stem cells.
价 格：￥电议型 号：T11053产 地：中国大陆
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TN1140Onjisaponin BAutophagy,Onjisaponin B,Inhibitor,inhibit
Onjisaponin B induces autophagy via the AMPK-mTOR signaling pathway, increases the NGF level and accelerates both the removal of mutant huntingtin and A53T α±-synuclein, it may have potential therapeutic effects on Parkinson disease, Alzheimer disease and Huntington disease.
价 格：￥电议型 号：TN1140产 地：中国大陆
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TN2246SwertiajaponinInhibitor,inhibit,Tyrosinase,Swertiajaponin
Swertiajaponin possesses antimicrobial activity.
价 格：￥电议型 号：TN2246产 地：中国大陆
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TQ0155Miglustat hydrochlorideN-Butyldeoxynojirimycin,OGT-918,type I gaucher disease,Miglustat,Miglustat hy
Miglustat hydrochloride is an inhibitor of glucosylceramide synthase and can be used for studies about Type I Gaucher disease.
价 格：￥电议型 号：TQ0155产 地：中国大陆
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T9765TJ-M2010-5ischemia,MIRI,Anoxia,factor,MyD88,injury,reoxygenation,inhibit,reperfusion,differentiation
TJ-M2010-5 is a MyD88 inhibitor that binds to the TIR domain to interfere with its homodimerization and suppress MyD88 signaling. TJ-M2010-5 can be used in myocardial ischemia/reperfusion injury studies.
价 格：￥电议型 号：T9765产 地：中国大陆
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T27683JNJ-42253432JNJ42253432,JNJ 42253432
JNJ-42253432 is a potent and selective antagonist of central nervous system-penetrant P2X7.
价 格：￥电议型 号：T27683产 地：中国大陆
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T7265HSP27 inhibitor J2Heat shock proteins,inhibit,HSP-27 inhibitor J2,HSP27 inhibitor J2,Inhibitor,J 2,H
HSP27 inhibitor J2 (J2) is a HSP27 inhibitor, inhibits a production of HSP27 giant polymers, thereby having an effect of inhibiting a chaperone function of the HSP27 and reducing a cell protection function.
价 格：￥电议型 号：T7265产 地：中国大陆
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TQ0010Brepocitinibinhibit,Janus kinase,PF06700841,JAK,Brepocitinib,Inhibitor,PF 06700841
Brepocitinib is a potent dual JAK1/TYK2 inhibitor (IC50s: 17 nM/23 nM). Brepocitinib also inhibits JAK2/3 (IC50s: 77 nM/6.49 μM).
价 格：￥电议型 号：TQ0010产 地：中国大陆
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TQ0292GrapiprantRQ 00000007,Inhibitor,Grapiprant,CJ 023423,RQ00000007,Prostaglandin Receptor,AAT 007,inhib
Grapiprant is a selective EP4 receptor antagonist. Grapiprant displaces [3H]-PGE2 (1 nM) binding to dog recombinant EP4 receptor (IC50: 35 nM, Ki: 24 nM).
价 格：￥电议型 号：TQ0292产 地：中国大陆
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T38680RJW100RJW100,RJW-100
RJW100 is a potent liver receptor homolog 1 (LRH-1, NR5A2) and steroidogenic factor-1 (SF-1, NR5A1) agonist with pEC 50 s of 6.6 and 7.5, respectively. RJW100 also causes strong activation of the miR-200c (miRNA-200c, microRNA-200c) promoter.
价 格：￥电议型 号：T38680产 地：中国大陆
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T7946AER-271Inhibitor,AER-271,AQP4,AER-270,stroke,inhibit,aquaporin-4,injury,AER 271,acute,AER271,CNS,isc
AER-271 is an inhibitor of aquaporin-4.
价 格：￥电议型 号：T7946产 地：中国大陆
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TN4661NodosinI. Japonicus,Isodon trichocarpus,inhibit,Nodosin,Inhibitor,diterpenoid
Nodosin has an anti-inflammatory function via inhibition of IL-2. Nodosin perfusion provides a potential protective effect by inducing HO-1 expression to attenuate ischemia/reperfusion injury in liver transplantation.
价 格：￥电议型 号：TN4661产 地：中国大陆
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T8933JNJ-63576253 free baseJNJ 63576253 free base,resistant,TRC 253,JNJ63576253,TRC-253,CRPC,JNJ63576253
JNJ-63576253 is a potent and orally active full antagonist of androgen receptor (AR), with IC50s of 37 and 54 nM for F877L mutant AR and wild-type AR in LNCaP cells. JNJ-63576253 can be used for the research of castration-resistant prostate cancer (CRPC).
价 格：￥电议型 号：T8933产 地：中国大陆
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TN1403Arjunolic acidhepatocyte injury,hyperglycemia,Inhibitor,type 1 diabetes,antimicrobial,antioxidant,Re
Arjunolic acid has antioxidant, anti-inflammatory, antinociceptive and anticholinesterasic (AChE and BuChE) activities, it may as promising targets for the development of innovative multi-functional medicines for Alzheimer desease treatment.
价 格：￥电议型 号：TN1403产 地：中国大陆
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T8742G5-7antiangiogenic,inhibit,Apoptosis,JAK,Glioma,G-5-7,cycle,G5 7,phase,G57,STAT3,cell,Inhibitor,EGFR
JAK2 inhibitor G5-7 is an orally active JAK2 inhibitor, selectively inhibits JAK2–mediated phosphorylation and activation of EGFR (Tyr1068) and STAT3 by binding to JAK2. G5-7 has the potential for glioma study
价 格：￥电议型 号：T8742产 地：中国大陆
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TN2343Pseudojervine
Pseudojervine is derived from Veratrum nigrum L. Pseudojervine exhibits feeble inhibition activity against platelet aggregation.
价 格：￥电议型 号：TN2343产 地：中国大陆
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TJS03684-Phenyl-7,8-dihydroxycoumarin4Phenyl7,8dihydroxycoumarin,inhibit,Inhibitor,bronchiectasiss,4 Phenyl
7,8-Dihydroxy-4-phenylcoumarin inhibits the activity of Staphylococcus aureus DNA helicase
价 格：￥电议型 号：TJS0368产 地：中国大陆
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T9019JHU37152JHU37152,inhibit,hM3Dq,Clozapine,Inhibitor,DREADD,Muscarinic acetylcholine receptor,mAChR,hM
JHU 37152 is a Designer Receptors Exclusively Activated by Designer Drug (DREADD) agonist with Ki of 1.8 nM and 8.7 nM for human muscarinic acetylcholine M3 receptors (hM3Dq) and hM4Di in vitro, respectively. And EC50 values are 5 nM and 0.5 nM for hM3Dq and hM4Di in fluorescent and BRET-based assays in HEK-293 cells, respectively.
价 格：￥电议型 号：T9019产 地：中国大陆
