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T4296MTX-211MTX 211；MTX211
MTX-211, an inhibitor of EGFR and PI3K, is used for the therapy of cancer and other diseases.
价 格：￥电议型 号：T4296产 地：中国大陆
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T4200Sacubitril hemicalcium saltAHU-377 (hemicalcium salt)；AHU377 calcium salt；LCZ696中间体
AHU-377 hemicalcium salt is a potent NEP inhibitor with an IC50 of 5 nM. AHU-377 is a component of the heart failure medicine LCZ696. AHU377 is a prodrug of LBQ657, which is an inhibitor of the zinc metallopeptidase neprilysin. Neprilysin degrades a varie
价 格：￥电议型 号：T4200产 地：中国大陆
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T4196Betahistine EP Impurity CNSC19005
NSC19005 is structurally related to Betahistine. NSC19005 is a dimer of Betahistine.
价 格：￥电议型 号：T4196产 地：中国大陆
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T4135OTS964 hydrochlorideOTS964
OTS964 is a potent and selective TOPK inhibitor with potential anticancer activity.
价 格：￥电议型 号：T4135产 地：中国大陆
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T4133CCT196969
CCT196969 is a novel orally available, pan-RAF inhibitor with anti-SRC activity. It also inhibits SRC, LCK, and the p38 MAPKs.
价 格：￥电议型 号：T4133产 地：中国大陆
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T41256SP-96
SP-96 is a highly effective and selective inhibitor of Aurora B with an IC50 of 0.316 nM. SP-96 shows selective growth inhibition in NCI60 screening, including MDA-MD-468 (GI50=107 nM). SP-96 can be used in triple negative breast cancer studies.
价 格：￥电议型 号：T41256产 地：中国大陆
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T40996Coppersensor 1Coppersensor 1；CS1
Coppersensor-1 (CS1) is a boron dipyrromethene (BODIPY)-based fluorescent sensor for selective and sensitive detection of copper(I) ions (Cu + ) in biological samples, including live cells.
价 格：￥电议型 号：T40996产 地：中国大陆
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T4096Quinolinic acid喹啉酸；pyridine-2,3-dicarboxylic acid；QUIN
Quinolinic acid is an endogenous N-methyl-D-aspartate (NMDA) receptor agonist synthesized from L-tryptophan via the kynurenine pathway.
价 格：￥电议型 号：T4096产 地：中国大陆
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T4091TemuterkibLY3214996
LY-3214996 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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T3S2296Gardenoside羟异栀子苷；栀子苷
Gardenoside has hepatoprotective, pain‑relieving, and anti-mastitis effects. it may be a potential therapeutic herb against NASH by suppressed supernatant inflammatory cytokine production and intracellular NFkB activity. Gardenoside may be considere
价 格：￥电议型 号：T3S2296产 地：中国大陆
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T3S1967(S)-Indoximod相思子碱;相思豆碱；红豆；L-Abrine；N-ME-Tryptophan；Abrine
Abrine exhibits inhibition of rabbit small intestine indoleamine 2, 3-dioxygenase, competitive inhibition of IDO, reduction of Foxp3 protein expression in tumor of C57BL/6 mouse allografted with mouse LLC cells at 200 mg/kg, induction of IDO1 protein expr
价 格：￥电议型 号：T3S1967产 地：中国大陆
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T3S1960Kakuol
1. Kakuol has antifungal activity, it can completely inhibit the mycelial growth of Botrytis cinerea Pers ex Fr and Cladosporium cucumerinum Ellis & Arthur at 5 microg ml(-1) and 3 microg ml(-1), respectively. 2. kakuol and a derivative analogue are able
价 格：￥电议型 号：T3S1960产 地：中国大陆
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T3S1896LindenenolLindeneol；Linderene；乌药醇
1. Linderene, linderalactone and isolinderalactone inhibit the enzymes from both origins to the same extent.
价 格：￥电议型 号：T3S1896产 地：中国大陆
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T3S1196mogroside IV
Mogrosides IV is a sweet minor cucurbitane glycoside, it exhibits maltase inhibitory effect(IC50 : 10 mM), and with antioxidant, antidiabetic and anticancer activities.
价 格：￥电议型 号：T3S1196产 地：中国大陆
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T3996Dapiprazole Hydrochloride盐酸达哌唑；Glamidolo Hydrochloride；Reversil Hydrochloride
Dapiprazole Hydrochloride is an alpha-1-adrenergic antagonist that acts by blocking alpha-adrenergic receptors in the smooth muscle of blood vessels (arteries, arterioles and veins), gastrointestinal tract, and radial smooth muscle of the iris.
价 格：￥电议型 号：T3996产 地：中国大陆
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T3975AZD9496
AZD9496 is an orally available selective estrogen receptor(ERα) antagonist, with potential antineoplastic activity.
价 格：￥电议型 号：T3975产 地：中国大陆
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T39695ARD-2128
ARD-2128 is a highly potent, orally bioavailable PROTAC androgen receptor (AR) degrader. ARD-2128 effectively reduces AR protein, suppresses AR-regulated genes in tumor tissues, and inhibits growth of tumor without signs of toxicity. ARD-2128 has the pote
价 格：￥电议型 号：T39695产 地：中国大陆
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T3969I-CBP112
I-CBP112 is a specific and potent acetyl-lysine competitive protein-protein interaction inhibitor targeting the CBP/p300 bromodomains.
价 格：￥电议型 号：T3969产 地：中国大陆
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