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产品数：86101
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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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T7013VorapaxarProtease Activated Receptor (PAR),Inhibitor,SCH-530348,Vorapaxar,SCH530348,Thrombin recepto
Vorapaxar (SCH 530348) is an effective and orally active thrombin receptor (PAR-1) antagonist (Ki: 8.1 nM).
价 格：￥电议型 号：T7013产 地：中国大陆
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TN1153Polyporenic acid Ccell,Apoptosis,inhibit,Inhibitor,lung,cancer,NSCLC,Polyporenic acid C
Polyporenic acid C shows inhibitory activity against human collagenase.
价 格：￥电议型 号：TN1153产 地：中国大陆
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T6653Salmeterol Xinafoatecorticosteroid,Salmeterol,Beta Receptor,therapy,inhibit,Adrenergic Receptor,GR 3
Salmeterol Xinafoate is a long-acting β2-adrenergic receptor agonist with anti-inflammatory effects, used in the treatment of asthma symptoms and chronic obstructive pulmonary disease (COPD) symptoms.
价 格：￥电议型 号：T6653产 地：中国大陆
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T12530PPTNPPTN
PPTN is a high-affinity, competitive and highly selective antagonist of P2Y14 receptor(KB value of 434 pM), with anti-inflammatory and immune activity.
价 格：￥电议型 号：T12530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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T9953BT173BT173
BT173 is a novel inhibitor of homeodomain interacting protein kinase 2 (HIPK2 ), attenuating renal fibrosis through suppression of the TGF-?1/Smad3 pathway.
价 格：￥电议型 号：T9953产 地：中国大陆
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T67836AT-533Benzamide,2[(trans4hydroxycyclohexyl)amino]4(4,5,6,7tetrahydro3,6,6trimethyl4oxo1Hindazol1yl)
AT-533 is a potent inhibitor of Hsp90 and HSV. AT-533 blocks the HIF-1α/VEGF/VEGFR-2 signaling pathway, leading to suppress tumor growth and angiogenesis. AT-533 also inhibits the activation of the downstream pathways, including Erk1/2, FAK, Akt/mTOR/p70S6K,. AT-533 inhibits the cell migration, invasion, and the tube formation of human umbilical vein endothelial cells (HUVECs).
价 格：￥电议型 号：T67836产 地：中国大陆
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T7727Se-Methylselenocysteinecaspase-3,A253,neck,SKOV-33,FaDu,Apoptosis,chemopreventive,cancer,cells,Se-Me
Se-Methylselenocysteine is a potent chemopreventive agent in many test systems and has been shown to inhibit tumor promotion and induce apoptosis.
价 格：￥电议型 号：T7727产 地：中国大陆
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T25253Cinnamtannin B-1
Cinnamtannin B1 is an A-type proanthocyanidin contained in several plant species such as Vaccinium vitis-idaea, Laurus nobilis L., Cinnamomum zeylanicum, and Lindera umbellata. It is a potent antioxidant and protective agent against oxidative stress and apoptosis in human platelets. It is a Cox-2 inhibitor.
价 格：￥电议型 号：T25253产 地：中国大陆
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T7553(+)-PD 128907 hydrochloride(+)-PD 128907,Dopamine Receptor,inhibit,(+) PD 128907 hydrochloride,Inhib
(+)-PD 128907 hydrochloride is an agonist of D3 dopamine receptor .
价 格：￥电议型 号：T7553产 地：中国大陆
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T41275PF-04753299PF04753299,PF 04753299
PF-04753299 is a potent and selective inhibitor of UDP-3-O-(R-3-hydroxymyristol)-N-acetylglucosamine deacetylase (LpxC). PF-04753299 is bactericidal for the gonococcal isolates. PF-04753299 inhibits E. coli, P. aeruginosa and K. pneumoniae strains with MIC 90 values of 2 μg/ml, 4 μg/ml and 16 μg/ml, respectively. PF-04753299 is used for the study of gram-negative bacteria infection [1].
价 格：￥电议型 号：T41275产 地：中国大陆
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T13553Arimoclomolaggregation,Heat shock proteins,HSP,co-inducer,system,BRX220,motor,Arimoclomol,inhibit,ub
Arimoclomol is a co-inducer of heat shock proteins (HSP) and can be used in studies about the treatment of amyotrophic lateral sclerosis (ALS).
价 格：￥电议型 号：T13553产 地：中国大陆
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TQ0133Amifostine thiol dihydrochlorideWR1065,Amifostine thiol dihydrochloride,Inhibitor,MDM-2/p53,WR-1065,
WR-1065 dihydrochloride can activate p53 through a JNK-dependent signaling pathway. It also protects normal tissues from the toxic effects of certain cancer drugs.
价 格：￥电议型 号：TQ0133产 地：中国大陆
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T15387GLP-1R Antagonist 1GLP 1R Antagonist 1,GLP1R Antagonist 1
GLP-1R Antagonist 1 is an orally active, CNS penetrant and non-competitive glucagon-like peptide 1 receptor (GLP-1R) antagonist (IC50: 650 nM).
价 格：￥电议型 号：T15387产 地：中国大陆
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T8953LAcetyl hexapeptide 38 AcetateAcetyl hexapeptide 38 Acetate
Acetyl hexapeptide 38 Acetate, breast enhancement peptide, is a kind of acetylated hexapeptide, can significantly stimulate the use of the site of fat synthesis, increase the volume of the chest or cheek, shape the perfect body
价 格：￥电议型 号：T8953L产 地：中国大陆
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TQ0050NCGC00244536NCGC 00244536,inhibit,Histone Demethylase,NCGC00244536,Inhibitor,NCGC-00244536
NCGC00244536 is a potent KDM4B inhibitor (IC50: 10 nM).
价 格：￥电议型 号：TQ0050产 地：中国大陆
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T6879LLY-507protein,inhibit,methyltransferase,methylation,breast,cancer,SMYD2,LLY-507,p53,Inhibitor,Histo
LLY-507 is an effective, cell-active, and specific inhibitor of protein-lysine Methyltransferase SMYD2.
价 格：￥电议型 号：T6879产 地：中国大陆
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T6530HC-030031HC-030031,HC 030031,TRP Channel,Transient receptor potential channels,Inhibitor,inhibit
HC-030031 is a potent TRPA1 inhibitor, which antagonizes AITC- and formalin-evoked calcium influx with IC50s of 6.2±0.2 and 5.3±0.2 μM, respectively.
价 格：￥电议型 号：T6530产 地：中国大陆
