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产品数：86101
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TP2131LRac1 Inhibitor W56 acetate(1095179-01-3 free base)Rac1 Inhibitor W56 acetate(1095179013 free base),R
Peptide comprising residues 45-60 of the guanine nucleotide exchange factor (GEF) recognition/activation site of Rac1; selectively inhibits Rac1 interaction with Rac1-specific GEFs TrioN, GEF-H1 and Tiam1.
价 格：￥电议型 号：TP2131L产 地：中国大陆
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T9999Benzamide, N-(3-imidazo[2,1-b]thiazol-6-ylphenyl)-2-methoxySirtuin modulator-2,cardiovascular diseas
Benzamide, N-(3-imidazo[2,1-b]thiazol-6-ylphenyl)-2-methoxy exhibits antidiabetic, anti-inflammatory and antitumor activities.
价 格：￥电议型 号：T9999产 地：中国大陆
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TP1782LCEF3 acetate(199727-62-3 free base)CEF3 acetate(199727623 free base),CEF3 acetate(199727 62 3 free b
CEF3 acetate corresponds to aa 13-21 of the influenza A virus M1 protein. The matrix (M1) protein of influenza A virus is a multifunctional protein that plays essential structural and functional roles in the virus life cycle.
价 格：￥电议型 号：TP1782L产 地：中国大陆
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T60034TH1085Inhibitor,DNA glycosylase 1 (OGG1),TH-10785,TH 10785,DNA oxidative lesions,TH1085,enzyme,pheny
TH1085 is an enhancer of OGG1. TH1085 stimulates DNA repair and protects cells from the environmental hazard paraquat (PQ).
价 格：￥电议型 号：T60034产 地：中国大陆
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T7805GW791343 dihydrochlorideinhibit,depressive disorder,Inhibitor,P2X Receptor,neurological disease,ATP,
GW791343 dihydrochloride is a P2X7 allosteric modulator.
价 格：￥电议型 号：T7805产 地：中国大陆
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T8834EST64454 hydrochloridepain,Inhibitor,EST 64454,EST64454 hydrochloride,nerve,selective,EST-64454 hydr
EST64454 is a highly soluble σ1 receptor antagonist (Ki : 22 nM),has the potential for Pain Management.
价 格：￥电议型 号：T8834产 地：中国大陆
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TQ0137A-484954CaMK,Autophagy,Inhibitor,Calmodulin-dependent protein kinases,A-484954,A484954,inhibit,Calmo
A 484954 is a highly specific eukaryotic elongation factor-2 (eEF2, IC50: 280 nM) inhibitor.
价 格：￥电议型 号：TQ0137产 地：中国大陆
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TQ0065PseudobufarenoginInhibitor,inhibit,Pseudobufarenogin
Pseudobufarenogin, a novel anti-tumor compound, suppresses liver cancer growth by inhibiting receptor tyrosine kinase-mediated signaling.
价 格：￥电议型 号：TQ0065产 地：中国大陆
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T9375IU1-248Deubiquitinase,IU1-248,IU1 248,DUBs,IU-1-248,Inhibitor,inhibit,IU1248
IU1-248 is a derivative of IU1. IU1-248 is a potent and selective USP14 inhibitor with an IC50 of 0.83?μM[1].
价 格：￥电议型 号：T9375产 地：中国大陆
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TP1938LRS09 2TFA (1449566-36-2 free base)RS09 2TFA (1449566362 free base),RS09 2TFA (1449566 36 2 free base
RS09 2TFA is a TLR4 agonist. Promotes NF-κB nuclear translocation and induces inflammatory cytokine secretion in RAW264.7 macrophages in vitro. It acts as an adjuvant in vivo and enhances X-15 specific antibody serum concentrations.
价 格：￥电议型 号：TP1938L产 地：中国大陆
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T7214TEPP-46TEPP46,TEPP 46,Pyruvate Kinase,ML 265,ML-265,Inhibitor,TEPP-46,inhibit
ML265 is a potent PKM2 activator (AC50 : 92 nM) showing little or no effect on PKM1, PKL and PKR,induces tetramerization and reduces tumor formation and size in a mouse xenograft model. .
价 格：￥电议型 号：T7214产 地：中国大陆
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TQ0047DG051DG051,Aminopeptidase,inhibit,DG 051,Inhibitor,DG-051
DG051 is a potent leukotriene A4 hydrolase (LTA4H) inhibitor (IC50: 47 nM).
价 格：￥电议型 号：TQ0047产 地：中国大陆
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T7551Belotecan hydrochlorideBelotecan,Topoisomerase,CKD 602,Inhibitor,Belotecan hydrochloride,CKD602,inhi
Belotecan hydrochloride is a synthetic water-soluble camptothecin derivative and topoisomerase I inhibitor with potential antitumor activity
价 格：￥电议型 号：T7551产 地：中国大陆
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T9094JMJD7-IN-1Inhibitor,Histone Demethylase,cancer,JMJD7,JMJD7 IN 1,inhibit,JMJD7IN1,JMJD-7-IN-1
JMJD7-IN-1 is a potent JMJD7 inhibitor, with an IC50 of 6.62 μM. JMJD7-IN-1 shows good inhibitory activity against cells expressing a high level of JMJD7.
价 格：￥电议型 号：T9094产 地：中国大陆
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T6882LY3009120Raf kinases,DP 4978,inhibit,LY-3009120,DP4978,Autophagy,LY3009120,Raf,LY 3009120,Inhibitor
LY03009120 is a potent pan-Raf inhibitor with IC50 of 44 nM, 31-47 nM, and 42 nM for A-raf, B-Raf, and C-Raf in A375 cells, respectively. Phase 1.
价 格：￥电议型 号：T6882产 地：中国大陆
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T9685DS-1971ahypersensitivity,thermal,Sodium Channel,hyperalgesia,Na channels,inhibit,Na+ channels,Inhibi
DS-1971a is a highly potent and selective NaV1.7 inhibitor. DS-1971a exhibits a favorable toxicological profile and analgesic effects.
价 格：￥电议型 号：T9685产 地：中国大陆
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T8616Fasentinanti-angiogenic,glucose,factor,Glucose transporter,inhibit,phase,necrosis,tumor,Fasentin,tra
Fasentin is an inhibitor of GluT1.
价 格：￥电议型 号：T8616产 地：中国大陆
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T6628PirarubicinTopoisomerase,Bacterial,inhibit,Autophagy,Inhibitor,Antibiotic,Pirarubicin
Pirarubicin is an anthracycline antibiotic. It is also a DNA/RNA synthesis inhibitor that intercalates into DNA and interacts with topoisomerase II, utilized as an antineoplastic agent.
价 格：￥电议型 号：T6628产 地：中国大陆
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T6857HLCL-61 hydrochlorideHistone Methyltransferase,HLCL 61,HLCL-61,inhibit,HLCL 61 hydrochloride,Apoptos
HLCL-61 hydrochloride is a potent and selective PRMT5 inhibitor for the treatment of acute myeloid leukemia.
价 格：￥电议型 号：T6857产 地：中国大陆
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T6791BPTESGlutaminase,inhibit,Inhibitor,BPTES
BPTES(IC50 of 0.16 μM) is an effective and specific GlutamiN/Ase GLS1 (KGA) inhibitor.
价 格：￥电议型 号：T6791产 地：中国大陆
