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产品数：86101
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T60904ERCC1-XPF-IN-2
ERCC1-XPF-IN-2 is active in nucleotide excision repair, cisplatin enhancement and γH2AX assays. ERCC1-XPF-IN-2 is a potent inhibitor of ERCC1-XPF endonuclease with an IC 50 value of 0.6 μM [1].
价 格：￥电议型 号：T60904产 地：中国大陆
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T9941STK414603STK414603
STK414603 is a heterocyclic acetamide derivative with potential analgesic, anti-inflammatory, and antimicrobial activities.
价 格：￥电议型 号：T9941产 地：中国大陆
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T60165VB124VB124
VB124 is an orally active, potent, and selective inhibitor of MCT4. VB124 can specifically inhibit lactate efflux with IC 50 s of 8.6 nM and 19 nM for lactate import and export in MDA-MB-231 cells, respectively. VB124 is highly selective for MCT4 over MCT1. VB124 can be used for the research of cardiac hypertrophy, heart failure, and metabolism [1].
价 格：￥电议型 号：T60165产 地：中国大陆
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TN260112-O-Methylcarnosic acid12 O Methylcarnosic acid,5α-reductase,Inhibitor,5 alpha Reductase,inhibit,12
12-O-Methylcarnosic acid is a diterpene carnosic acid isolated from the acetone extract of Salvia microphylla, is an active constituent of 5α-reductase inhibition with an IC50 value of 61.7 μM.12-O-Methylcarnosic acid has antioxidant activity, it is effective preventing gastric lesions. 12-O-Methylcarnosic acid can suppress melanin production with downregulation of tyrosinase expression in HMV-II melanoma cells.12-O-Methylcarnosic acid may have anti-diabetic activity, it is able to significantly
价 格：￥电议型 号：TN2601产 地：中国大陆
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T6014911β-HSD1-IN-1111βHSD1IN11
11β-HSD1-IN-11 is a competitive 11β-HSD1 inhibitor with IC50s of 0.34 μM and 0.13 μM against rat and human 11β-HSD1, respectively.
价 格：￥电议型 号：T60149产 地：中国大陆
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T0161Pantoprazole Sodium HydrateSKF96022 sodium,Inhibitor,stability,orally,Pantoprazole Sodium Hydrate,A4
Pantoprazole is a proton pump inhibitor drug, used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease.
价 格：￥电议型 号：T0161产 地：中国大陆
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TP1419LHAEGTFT acetate(926018-95-3 free base)HAEGTFT acetate(926018 95 3 free base),HAEGTFT acetate(9260189
HAEGTFT acetate is the first N-terminal 1-7 residues of GLP-1 peptide.
价 格：￥电议型 号：TP1419L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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T60022WAY-604116WAY604116,WAY 604116
WAY-604116 has anti-inflammatory, antitumor and antiasthmatic effects.
价 格：￥电议型 号：T60022产 地：中国大陆
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T60218YAP/TAZ inhibitor-2?YAP/TAZinhibitor2?
YAP/TAZ inhibitor-2 is a potent and orally active TEAD-YAP/TAZ inhibitor with an EC 50 value of 3 nM. YAP/TAZ inhibitor-2 shows anti-proliferative and antitumor activity [1].
价 格：￥电议型 号：T60218产 地：中国大陆
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T7760Thalidomide-O-amido-C3-NH2 TFAInhibitor,E3 Ligase Ligand-Linker Conjugates 52,E3 Ligase Ligand-Linke
Thalidomide-O-amido-C3-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate. Thalidomide-O-amido-C3-NH2 TFA incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
价 格：￥电议型 号：T7760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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T63872KU-60019
KU-60019 is a specific inhibitor of ATM kinase (IC50: 6.3 nM).
价 格：￥电议型 号：T63872产 地：中国大陆
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T67752Compound V007-6018CompoundV0076018
Compound V007-6018 is a drug-like compound.
价 格：￥电议型 号：T67752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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T60056Benzonitrile, 4-[[5-cyclopropyl-3-methyl-1-[(methylsulfonyl)methyl]-1H-pyrazol-4-yl]oxy]-2,6-dimethy
Benzonitrile, 4-[[5-cyclopropyl-3-methyl-1-[(methylsulfonyl)methyl]-1H-pyrazol-4-yl]oxy]-2,6-dimethyl- is a progesterone receptor antagonist with antiprogestin effects.
价 格：￥电议型 号：T60056产 地：中国大陆
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T8762SW106065cell,SW 106065,cdk4,Inhibitor,MPNST,cycle,ATP,anticancer,cdk6,cyclin,SW106065,Apoptosis,inhi
SW-106065 is a novel pharmacologic inducer of apoptosis in MPNST (malignant peripheral nerve sheath tumors).SW106065 is an apoptosis inducer in malignant peripheral nerve sheath tumors (MPNST). It inhibits ATP consumption of sMPNST and other models of MPNST with an EC50 of 1 μM. SW106065 can be used for MPNST research
价 格：￥电议型 号：T8762产 地：中国大陆
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T7603Pinaverium bromideInhibitor,Ca channels,Pinaverium bromide,Pinaverium,Calcium Channel,inhibit,Ca2+ c
Pinaverium bromide is an calcium channel blocker with Antispasmodic and effectively relieves pain, diarrhea and intestinal discomfort.
价 格：￥电议型 号：T7603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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T8730BMS986260nuclear translocation,TGFβR1,BMS-986260,FOXP3 expression,MINK,Transforming growth factor be
BMS-986260 is a selective, and orally bioavailable TGFβR1 inhibitor(IC50 = 1.6 nM).
价 格：￥电议型 号：T8730产 地：中国大陆
