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T18540Phe-Lys(Trt)-PAB
Phe-Lys(Trt)-PAB is a cathepsin cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T18540产 地：中国大陆
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T1854MS436
MS436 is a selective, small-molecule inhibitor for the BRD4 bromodomains.
价 格：￥电议型 号：T1854产 地：中国大陆
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T18537Pentaethylene glycol di(p-toluenesulfonate)Penta(ethylene glycol) bis(p-toluenesulfonate)；Bis-Tos-PE
Pentaethylene glycol di(p-toluenesulfonate) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T18537产 地：中国大陆
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T1853NMS-873NMS 873
NMS-873 is a potent, selective allosteric VCP/p97 inhibitor.
价 格：￥电议型 号：T1853产 地：中国大陆
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T18529PDEC-NB4-Nitrophenyl 2-(Pyridin-2-Yldisulfanyl)Ethyl Carbonate
PDEC-NB is a disulfide cleavable linker used for the antibody-drug conjugate?(ADC).
价 格：￥电议型 号：T18529产 地：中国大陆
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T1852BelinostatNSC726630；PXD101；PX-105684
Belinostat is a novel hydroxamic acid-type histone deacetylase (HDAC) inhibitor with antineoplastic activity. Belinostat targets HDAC enzymes, thereby inhibiting tumor cell proliferation, inducing apoptosis, promoting cellular differentiation, and inhibit
价 格：￥电议型 号：T1852产 地：中国大陆
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T18513OTs-C6-OBn
OTs-C6-OBn is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTAC SGK3 degrader-1[1].
价 格：￥电议型 号：T18513产 地：中国大陆
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T1851ZM 336372Zinc00581684
ZM 336372 is a potent and selective c-Raf inhibitor.
价 格：￥电议型 号：T1851产 地：中国大陆
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T1850Balicatib巴利卡替；AAE581
Balicatib is a potent and selective inhibitor of cathepsin K, used in trials studying the treatment of osteoporosis.
价 格：￥电议型 号：T1850产 地：中国大陆
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T15185Lucitanib德立替尼；E-3810
Lucitanib is a novel VEGFR and FGFR inhibitor. It potently and selectively inhibits VEGFR1, VEGFR2, VEGFR3, FGFR1 and FGFR2 (IC50s: 7 nM, 25 nM, 10 nM, 17.5 nM, and 82.5 nM, respectively).
价 格：￥电议型 号：T15185产 地：中国大陆
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T14185Alkynyl Palmitic Acid
Alkynyl Palmitic Acid is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T14185产 地：中国大陆
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T11857LIT-001
LIT-001 improves social interaction in a mouse model of autism.It is the first nonpeptide oxytocin receptor agonist with EC50 of 55 nM and Ki of 226 nM.
价 格：￥电议型 号：T11857产 地：中国大陆
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T11855LipopolysaccharidesLPS
Lipopolysaccharide is a highly immunogenic antigen which can enhance immune responses.Lipopolysaccharides is an endotoxin derived from the outer leaflet of the outer membrane of Gram-negative bacteria. Lipopolysaccharide consists of an antigen O-specific
价 格：￥电议型 号：T11855产 地：中国大陆
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T11854Lipofermata
Lipofermata is a fatty acid transport protein (FATP) inhibitor that prevents lipid transport to melanoma cells and reduces melanoma growth and invasion.
价 格：￥电议型 号：T11854产 地：中国大陆
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T11852Linaclotide
Linaclotide developed for the treatment of constipation-predominant irritable bowel syndrome (IBS-C) and chronic constipation, and is a potent and selective guanylate cyclase C agonist.
价 格：￥电议型 号：T11852产 地：中国大陆
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T11851Lin28-let-7a antagonist 1
Lin28-let-7a antagonist 1, with an IC50 of 4.03 μM for Lin28A-let-7a-1 interaction，and shows a clear antagonistic effect against the Lin28-let-7a interaction.
价 格：￥电议型 号：T11851产 地：中国大陆
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T11850LIN28 inhibitor LI71
LIN28 inhibitor LI71 is a potent and cell-permeable LIN28 inhibitor, which abolishes LIN28-mediated oligouridylation with an IC50 of 7 uM.
价 格：￥电议型 号：T11850产 地：中国大陆
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T1185RofecoxibMK 966；MK-0966；罗非昔布；罗非考昔
Rofecoxib binds to and inhibits the enzyme cyclooxygenase-2 (COX-2), resulting in an inhibition of the conversion of arachidonic acid to prostaglandins. Rofecoxib is a synthetic, nonsteroidal derivative of phenyl-furanone with anti-inflammatory, antipyret
价 格：￥电议型 号：T1185产 地：中国大陆
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T11607ICI 118,551 hydrochlorideICI 118551 hydrochloride
ICI 118,551 is a highly selective β2 adrenergic receptor antagonist (Kis: 0.7, 49.5, and 611 nM for β2, β1, and β3 receptors).
价 格：￥电议型 号：T11607产 地：中国大陆
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T1147Chlorhexidine dihydrochloride盐酸氯己定；Chlorhexidine 2HCl；NSC-185；Chlorhexidine hydrochloride
Chlorhexidine hydrochloride is a disinfectant and topical anti-infective agent used also as mouthwash to prevent oral plaque.
价 格：￥电议型 号：T1147产 地：中国大陆
