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TN1511Cleomiscosin ACleomiscosin A
Cleomiscosin A is derived from Acer okamotoanum leaf and twig and shows inhibitory activity to TNF-α secretion of the mouse peritoneal macrophages. Cleomiscosin A can be used in studies about the prevention of LDL oxidation in atherosclerotic lesions.
价 格：￥电议型 号：TN1511产 地：中国大陆
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TQ0253PLX51107PLX 51107,Epigenetic Reader Domain,PLX51107,inhibit,PLX-51107,Inhibitor
PLX51107 is a potent and selective BET inhibitor (Kds: 1.6, 2.1, 1.7, and 5 nM for BRD2-BD1, BRD3-BD1, BRD4-BD1, and BRDT-BD1).
价 格：￥电议型 号：TQ0253产 地：中国大陆
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T11492GSK2983559 free acidinhibit,THP-1 cell,RIP kinase,GSK 2983559,GSK2983559 free acid,Inhibitor,GSK-298
GSK2983559 free acid is an effective and selective inhibitor of receptor-interacting protein 2 (RIP2). GSK2983559 free acid shows excellent activity in blocking many proinflammatory cytokine responses in human inflammatory bowel disease explant samples an
价 格：￥电议型 号：T11492产 地：中国大陆
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T8384Gatifloxacin hydrochlorideAM-1155,Antibiotic,PD 135432,BMS 206584,E. coli,?Pseudomonas aeruginosa,?M
Gatifloxacin hydrochloride is an antibiotic of the fourth-generation fluoroquinolone family, which can inhibit the bacterial enzyme DNA rotase and topoisomerase IV.
价 格：￥电议型 号：T8384产 地：中国大陆
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TQ0035FulacimstatFulacimstat,inhibit,BAY 1142524,Inhibitor,BAY-1142524
Fulacimstat (BAY1142524) is a chymase inhibitor, with IC50s of 3, 4 nM for hamster and human chymase enzyme, respectively.
价 格：￥电议型 号：TQ0035产 地：中国大陆
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T11029hDHODH-IN-5
hDHODH-IN-5 is an inhibitor of human dihydroorotate dehydrogenase (hDHODH, IC50 = 0.91 μM).
价 格：￥电议型 号：T11029产 地：中国大陆
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T9976OBX02-011
OBX02-011 is an effective and reversible inhibitor of EGFR tyrosine kinase with IC50s of 0.134 and 2.09 nM for triple mutants Del19/T790M/C797S and L858R/T790M/C797S.
价 格：￥电议型 号：T9976产 地：中国大陆
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TN1115Pseudolaric acid A-O-β-D-glucopyranosideinhibit,Inhibitor,Pseudolaric acid AOβDglucopyranoside,Pseud
Pseudolaric acid A-O-beta-D-glucopyranoside is a natural product with antibacterial, anticancer
价 格：￥电议型 号：TN1115产 地：中国大陆
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T61111UCB-5307
UCB-5307 is a TNF signaling inhibitor with a K D of 9 nM. UCB-5307 can penetrate the preformed hTNF/hTNFR1 complex [1].
价 格：￥电议型 号：T61111产 地：中国大陆
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T7611ODM-203anti-tumor immunity,ODM-203,FGFR,HUVEC,H1581,Inhibitor,cancer,Vascular endothelial growth fac
ODM-203, a Selective Inhibitor of FGFR and VEGFR, Shows Strong Antitumor Activity, and Induces Antitumor Immunity
价 格：￥电议型 号：T7611产 地：中国大陆
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TN7112(25R)-3β,17α-dihydroxy-5α- spirostan-6-one3-O-α-L- rhamnopyranosyl-(1→2)-β- D-glucopyranoside(25R)3β
(25R)-3β,17α-dihydroxy-5α- spirostan-6-one3-O-α-L- rhamnopyranosyl-(1→2)-β- D-glucopyranoside is a natural product isolated from the bulbs of Lilium brownii var. viridulum.
价 格：￥电议型 号：TN7112产 地：中国大陆
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TN4562Oleoside 11-methyl esterOleoside 11-methyl ester,glucoside,Oleoside 11methyl ester,Inhibitor,secoiri
Methyloleoside is a natural product.
价 格：￥电议型 号：TN4562产 地：中国大陆
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T9303MRTX1133KRAS,Ras,MRTX 1133,G12D,cells,active,wild-type,phosphorylation,mutant,MRTX1133,inactive,ERK,
MRTX1133 is a potent, selective, and noncovalent inhibitor of KRAS G12D. MRTX1133 exhibits an estimated KD against KRAS G12D of 0.2 pM. MRTX1133 inhibits mutant KRAS-dependent signal transduction by preventing SOS1-catalyzed nucleotide exchange and/or formation of the KRAS G12D/GTP/RAF1 complex. MRTX1133 selectively inhibits KRAS G12D mutant tumor cells with no effect on KRAS wild-type. MRTX1133 exhibits single digit nanomolar activity in cellular assays and marked in vivo efficacy in tumor mode
价 格：￥电议型 号：T9303产 地：中国大陆
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T28118MSP3MSP3
MSP3 is an agonist of TRPV1 (EC50 = 0.87 μM) and shows antinociceptive and neuroprotective effects.
价 格：￥电议型 号：T28118产 地：中国大陆
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T11962MC3482MC3482,MC-3482
MC3482 is a specific inhibitor of sirtuin5 (SIRT5).
价 格：￥电议型 号：T11962产 地：中国大陆
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T9960MCU-i11MCUi11,MCU i11
MCU-i11 is a novel negative modulator of the MCU, binding MICU1 and impairing muscle cell growth.
价 格：￥电议型 号：T9960产 地：中国大陆
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T11134DZ2002DZ-2002,DZ2002
DZ2002 is an orally active, reversible and low-cytotoxic type III SAHH inhibitor (Ki=17.9 nM), with good immunosuppressive activity. DZ2002 prevents the development of experimental dermal fibrosis by reversing the profibrotic phenotype of various cell types. DZ2002 can be used in studies of autoimmune diseases such as lupus syndrome and systemic sclerosis.
价 格：￥电议型 号：T11134产 地：中国大陆
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T20711HemipyocyanineHemipyocyanine
Hemipyocyanine is the virulence factor of Gram-negative, aerobic rod bacterium Pseudomonas aeruginosa. Hemipyocyanine is an α-Amylase inhibitor.
价 格：￥电议型 号：T20711产 地：中国大陆
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TN1111ArnidiolInhibitor,inhibit,Arnidiol
Arnidiol is a pentacyclic triterpene isolated from Barleria Longiflora Linn FArnidiol has anti-inflammatory activity, it possesses marked inhibitory activity against 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced inflammation in mice.
价 格：￥电议型 号：TN1111产 地：中国大陆
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T101153-Nitrocoumarin
3-Nitrocoumarin (3-NC) is a potent and selective Phospholipase C-γ (PLCγ) inhibitor.
价 格：￥电议型 号：T10115产 地：中国大陆
