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T4451Estramustine phosphate sodium雌莫司汀磷酸钠Ro 21-8837/001|||Estramustine phosphate disodium|||雌莫司汀磷酸钠
Estramustine phosphate sodium (Ro 21-8837/001) is an antimicrotubule chemotherapy agent; arrests prostate cancer cells in the G2/M phase of the cell cycle.
价 格：￥电议型 号：T4451产 地：中国大陆
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T4350Palifosfamide；帕利伐米ZIO-201|||Isophosphamide mustard|||Isophosphoramide mustard；ZIO-201|||Isophosphami
Palifosfamide (Isophosphamide mustard) lysine (ZIO-201) is a stable form of palifosfamide. Palifosfamide lysine has broad activity in sarcoma lines in vitro. The IC50 ranges from 2.25 to 6.75 μM for most cell lines except OS222 (IC50=31.5 μM).
价 格：￥电议型 号：T4350产 地：中国大陆
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T4333Quinine dihydrochloride；盐酸奎宁Quinine bimuriate；盐酸奎宁|||Quinine bimuriate
Quinine dihydrochloride (Quinine bimuriate) is a primary alkaloid of various species of Cinchona (Rubiaceae). It is also an antimalarial and muscle relaxant (skeletal).
价 格：￥电议型 号：T4333产 地：中国大陆
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T4212XMU-MP-1；化合物XMU-MP-1XMU-MP-1
XMU-MP-1 is an inhibitor of the pro-apoptotic, sterile 20-like kinases MST1 and 2.
价 格：￥电议型 号：T4212产 地：中国大陆
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T4191Multi-kinase inhibitor 1；化合物Multi-kinase inhibitor IMulti-kinase inhibitor I；Multi-kinase inhibitor
Multi-kinase inhibitor 1 (Multi-kinase inhibitor I) is a Multi-kinase inhibitor.
价 格：￥电议型 号：T4191产 地：中国大陆
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T4129Arachidonic acid；花生四烯酸Immunocytophyte|||arachidonate|||Immunocytophyt|||Vevodar；Immunocytophyte|||花生
Arachidonic acid (Immunocytophyte) is a naturally occurring, unsaturated essential fatty acid that is a component of animal phospholipids. Arachidonic acid is synthesized from dietary linoleic acid and is a precursor for the biosynthesis of prostaglandins, thromboxanes, and leukotrienes.
价 格：￥电议型 号：T4129产 地：中国大陆
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T41243Tumulosic acid；化合物 Tumulosic acidTumulosic acid
Tumulosic acid is a natural product for research related to life sciences. The catalog number is T41243 and the CAS number is 508-24-7.
价 格：￥电议型 号：T41243产 地：中国大陆
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T41051Chlorimuron-ethyl；Chlorimuron-ethylChlorimuron-ethyl
Chlorimuron-ethyl, an influential herbicide extensively employed in soybean cultivation, exerts its action by inducing oxidative stress.
价 格：￥电议型 号：T41051产 地：中国大陆
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T4091Temuterkib；化合物LY3214996LY3214996；LY3214996
Temuterkib (LY3214996) is a potent and selective, orally available inhibitor of the extracellular signal-regulated kinase (ERK) 1 and 2, with potential antineoplastic activity.
价 格：￥电议型 号：T4091产 地：中国大陆
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T40790ω-Muricholic Acid；ω-Muricholic Acidω-Muricholic Acid
ω-Muricholic acid (ω-MCA) is a murine-specific secondary bile acid.
价 格：￥电议型 号：T40790产 地：中国大陆
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T40272KRAS mutant protein inhibitor 1；KRAS mutant protein inhibitor 1KRAS mutant protein inhibitor 1
KRAS mutant protein inhibitor 1 is a KRAS mutant protein inhibitor for potential treatment in cancer.
价 格：￥电议型 号：T40272产 地：中国大陆
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T3S2340Usaramine；光萼野百合碱(15E)-Retrorsine|||Mucronatine|||NISTC15503874；(15E)-Retrorsine|||Mucronatine|||光萼野百
Usaramine (Mucronatine) demonstrates phytotoxicity against Lactuca sativa var. Carrascoy (lettuce) assessed as inhibition of seed germination at 50 ug/cm2 after 24 hr.
价 格：￥电议型 号：T3S2340产 地：中国大陆
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T39716Mutant IDH1-IN-6Mutant IDH1-IN-6Mutant IDH1-IN-6
Mutant IDH1-IN-6 is an orally active compound that effectively inhibits mutant isocitrate dehydrogenase (IDH) enzymes. It demonstrates potency and selectivity, with IC50 values of 6.27, 3.71, 36.9, and 11.5 nM for IDH1 R132H, IDH1 R132C, IDH2 R140Q, and IDH2 R172K mutants, respectively. Notably, Mutant IDH1-IN-6 exhibits lower activity in inhibiting wild-type IDH enzymes.
价 格：￥电议型 号：T39716产 地：中国大陆
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T39678Multitarget AD inhibitor-1；Multitarget AD inhibitor-1Multitarget AD inhibitor-1
Multitarget AD inhibitor-1 is a reversible and selective inhibitor of butyrylcholinesterase (BuChE) with IC50 values of 7.22 μM and 1.55 μM for human BuChE (hBuChE) and equine serum BuChE (eqBuChE), respectively. Additionally, it exhibits inhibitory activity towards β-secretase (IC50 value of 41.60 μM), amyloid β aggregation (IC50 value of 3.09 μM), and tau aggregation. As a diphenylpropylamine derivative, Multitarget AD inhibitor-1 holds promise for research pertaining to the multifunctional, d
价 格：￥电议型 号：T39678产 地：中国大陆
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T39548Amustaline dihydrochloride；Amustaline dihydrochlorideS-303 dihydrochloride；S-303 dihydrochloride
Amustaline (S-303) dihydrochloride is a nucleic acid-targeted alkylator recognized for its efficacy as a pathogen inactivation agent in blood components containing red blood cells. This compound comprises three key elements: an acridine anchor (a non-covalently bonding intercalator targeting nucleic acids), an effector (a bis-alkylator group that interacts with nucleophiles), and a linker (a flexible carbon chain with a labile ester bond, hydrolyzing at neutral pH to non-reactive products).
价 格：￥电议型 号：T39548产 地：中国大陆
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T39444Upacicalcet sodium；Upacicalcet sodiumUpacicalcet sodium
Upacicalcet (sodium) is an intravenous calcimimetic agent that acts directly on parathyroid cell membrane calcium-sensing receptors to suppress excessive parathyroid hormone (PTH) secretion, thereby lowering blood PTH levels. It is indicated for the research of secondary hyperparathyroidism (SHPT).
价 格：￥电议型 号：T39444产 地：中国大陆
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T39430XMU-MP-3；XMU-MP-3XMU-MP-3
XMU-MP-3 is a robust, non-covalent inhibitor of BTK, exhibiting exceptional potency with IC50 values of 10.7 nM and 17.0 nM for BTK WT and BTK C481S mutation, respectively, in the presence of 10 μM ATP. Moreover, XMU-MP-3 elicits apoptosis.
价 格：￥电议型 号：T39430产 地：中国大陆
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T39138Muscotoxin A；Muscotoxin AMuscotoxin A
Muscotoxin A is an ADC cytotoxin with lipopeptide properties that effectively permeabilizes mammalian cell membranes, ultimately inducing necrotic cell death.
价 格：￥电议型 号：T39138产 地：中国大陆
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T38976MUC1, mucin core；MUC1, mucin coreMUC1, mucin core；MUC1, mucin core
MUC1, mucin core is a type I transmembrane glycoprotein that is characterized by its overexpression and abnormal glycosylation in carcinoma cells. It specifically binds to domain 1 of ICAM-1.
价 格：￥电议型 号：T38976产 地：中国大陆
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T3888Scopolin东莨菪苷Murrayin|||东莨菪甙|||Scopoloside|||东莨菪苷
Scopolin (Scopoloside) formation is increased by the enhanced activity of PAL. Scopolin can reduce the clinical symptoms of rat AIA by inhibiting inflammation and angiogenesis, and this compound may be a potent agent for angiogenesis related diseases and can serve as a structural base for screening more potent synthetic analogs.
价 格：￥电议型 号：T3888产 地：中国大陆
