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T23493UCL 1684 dibromide;化合物 T23493UCL 1684;UCL 1684
apamin-sensitive Ca2+-activated K+ channel (KCa2.1) blocker
价 格:¥电议型 号:T23493产 地:中国大陆
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T23146PHA 568487 free base;化合物PHA 568487PHA 568487;PHA 568487
The quinuclidine PHA 568487 free base is an agonist of the alpha 7 nicotinic acetylcholine receptor that was designed to mitigate the bioactivation associated with the core scaffold and subsequently remove associated liabilities with in vivo tolerability.
价 格:¥电议型 号:T23146产 地:中国大陆
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T22684CP 339818 hydrochloride;化合物 T22684CP 339818 hydrochloride
KV1.3 channel antagonist
价 格:¥电议型 号:T22684产 地:中国大陆
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T2251NVP-TAE 684;化合物TAE684TAE684;TAE684|||5-氯-N2-[2-甲氧基-4-[4-(4-甲基-1-哌嗪基)-1-哌啶基]苯基]-N4-[2-[(1-甲基乙基)磺酰基]苯基
NVP-TAE 684 (TAE684) is a excellently effective and specific ALK inhibitor(IC50=3 nM).
价 格:¥电议型 号:T2251产 地:中国大陆
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T21684Bufuralol (hydrochloride);化合物 T21684Bufuralol (hydrochloride)
Bufuralol hydrochloride (Ro 3-4787 hydrochloride) is a potent non-selective, orally active β-adrenoreceptor antagonist with partial agonist activity, which is also a CYP2D6 probe substrate [1] [2].
价 格:¥电议型 号:T21684产 地:中国大陆
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T21130Precocene II;早熟素ⅡAI3-36847|||Ageratochromene|||BRN 0160683;早熟素Ⅱ|||AI3-36847|||Ageratochromene|||BRN
Precocene II (Ageratochromene), an antiallotropin compound, inhibits juvenile hormone biosynthesis. Precocene II has insecticidal, antifungal, antibacterial, and antioxidant activities.
价 格:¥电议型 号:T21130产 地:中国大陆
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T206842’,7’-Dichlorofluorescein diacetate;双氯荧光黄乙酸乙酯Diacetyldichlorofluorescein|||Leuco-dcf diacetate|||Dcf
2´,7´-Dichlorofluorescein diacetate (Diacetyldichlorofluorescein), a cell-permeable fluorogenic probe, is useful for the detection of nitric oxide (NO) and reactive oxygen species (ROS) and for the determination of the degree of overall oxidative stress.
价 格:¥电议型 号:T20684产 地:中国大陆
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T19653CPI-268456;化合物 T19653CPI-268456
CPI-268456 is a compound which has bioactive.
价 格:¥电议型 号:T19653产 地:中国大陆
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T18684SNIPER(ABL)-013;化合物 T18684SNIPER(ABL)-013
SNIPER(ABL)-013, a compound that links GNF5 (ABL inhibitor) with Bestatin (IAP ligand) via a linker, effectively reduces BCR-ABL protein levels with a DC50 of 20 μM[1].
价 格:¥电议型 号:T18684产 地:中国大陆
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T1852Rac-Belinostat;化合物BelinostatNSC726630|||PXD101|||PX-105684;NSC726630|||PXD101|||PX-105684
Rac-Belinostat (PX-105684) 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 inhibiting angiogenesis. This agent may sensitize drug-resistant tumor cells to other antineoplastic agents, possibly through a mechanism involving the down-regulation of thymidylate synthase.
价 格:¥电议型 号:T1852产 地:中国大陆
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T1851ZM 336372;化合物ZM 336372Zinc00581684;Zinc00581684
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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T17684Boc-NH-PEG8-CH2CH2NH2叔丁氧羰基八聚乙二醇胺叔丁氧羰基八聚乙二醇胺
Boc-NH-PEG8-CH2CH2NH2 is a PEG-based PROTAC linker that can be used in PROTAC synthesis.
价 格:¥电议型 号:T17684产 地:中国大陆
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T16879LSHU 9119 acetate;化合物SHU 9119 acetateSHU 9119 acetate (168482-23-3 free base);SHU 9119 acetate (16848
SHU 9119 acetate is a well-known antagonist of human melanocortin 3 and 4 (hMC3R, hMC4R) receptors and a partial hMC5R agonist. The IC50 values of human MC3R, MC4R and MC5R is 0.23, 0.06, and 0.09 nM respectively.
价 格:¥电议型 号:T16879L产 地:中国大陆
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T16849SB-222200;化合物SB-222200SB-222200
SB-222200 is a selective, reversible, and competitive antagonist of the human NK-3 receptor(Ki=4.4 nM).
价 格:¥电议型 号:T16849产 地:中国大陆
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T16848SB-218078;化合物 T16848SB-218078
SB-218078 is less potently inhibits Cdc2 (IC50: 250 nM) and PKC (IC50: 1000 nM). SB-218078 is a potent, ATP-competitive, and cell-permeable checkpoint kinase 1 inhibitor that inhibits Chk1 phosphorylation of cdc25C (IC50: 15 nM).
价 格:¥电议型 号:T16848产 地:中国大陆
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T16847SA 47;化合物 T16847SA 47
SA 47 is a selective and effective inhibitor of fatty acid amide hydrolase and carbamate.
价 格:¥电议型 号:T16847产 地:中国大陆
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T16846Sauristolactam;化合物 T16846Saurolactam;Saurolactam
Sauristolactam inhibits the receptor activator of nuclear factor-κB ligand (RANKL)-induced osteoclastogenesis and has the potential to inhibit osteoclast differentiation. Sauristolactam, a natural aristolactam isolated from aerial portions of Saururus Chinensis. Sauristolactam has significant neuroprotective activity against glutamate-induced toxicity in primary cultured rat cortical cells.
价 格:¥电议型 号:T16846产 地:中国大陆
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T16845Sarolaner;化合物SarolanerPF-6450567;PF-6450567
Sarolaner (PF-6450567) is an orally active and broad-spectrum ectoparasiticide (LC80: 0.3 μg/mL against C. felis and an LC100: 0.003 μg/mL against O. turicata).
价 格:¥电议型 号:T16845产 地:中国大陆