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T23466TP003；化合物TP 003TP-003|||TP 003|||TP 003|||TP003；0
TP003 is a novel non-selective GABAA receptor benzodiazepine site agonist with affinity for α1β2gam2, α2β3gam2, α3β3gam2, α5β2gam2, EC50 of 20.3, 10.6, 3.24, 5.64 nM, respectively. TP003 has antianxiety and partial anticonvulsant activity via the α2GABAA receptor.
价 格：￥电议型 号：T23466产 地：中国大陆
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T23465Tolbutamide Sodium；化合物 T23465Tolbutamide Sodium
potassium channel blocker
价 格：￥电议型 号：T23465产 地：中国大陆
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T23464Tocrifluor T1117；化合物 T23464Tocrifluor T1117
Fluorescent form of AM 251, CB1 receptor antagonist
价 格：￥电议型 号：T23464产 地：中国大陆
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T23462TMPH hydrochloride；化合物 T23462TMPH hydrochloride
neuronal nicotinic ACh receptors (nAChRs) antagonist
价 格：￥电议型 号：T23462产 地：中国大陆
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T23460Tigecycline mesylate；甲磺酸替加环素Tigecycline mesylate
Tigecycline mesylate is a first-in-class, broad-spectrum antibiotic. It also has activity against antibiotic-resistant organisms.
价 格：￥电议型 号：T23460产 地：中国大陆
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T2346Enasidenib；恩西地平AG-221；恩西地平|||AG-221
Enasidenib (AG-221) is an orally available inhibitor of specific mutant forms of the mitochondrial enzyme isocitrate dehydrogenase type 2 (IDH2), with potential antineoplastic activity.
价 格：￥电议型 号：T2346产 地：中国大陆
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T23346SDZ SER 082 fumarate；化合物 T23346SDZ SER 082 fumarate
5-HT2B/2C receptor antagonist
价 格：￥电议型 号：T23346产 地：中国大陆
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T22671CJ 033466；化合物CJ 033466CJ 033466
CJ 033466 is a selective partial agonist of 5-HT4 receptor (EC50 = 9 nM) with gastroprokinetic effect.
价 格：￥电议型 号：T22671产 地：中国大陆
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T22346Indomethacin sodium hydrate；吲哚美辛钠盐三水合物Indometacin sodium hydrate；Indometacin sodium hydrate
Indomethacin sodium hydrate (Indometacin sodium hydrate) is an orally active, competitive and reversible COX1/2 inhibitor with potential anti-inflammatory activity in induced migraines, induced gastrointestinal injuries, and may be used in studies of increased intracranial pressure secondary to severe traumatic brain injury and rheumatoid arthritis in adults.
价 格：￥电议型 号：T22346产 地：中国大陆
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T22029AL 34662；化合物AL 34662AL 34662
AL 34662 is a selective and potent 5-HT2A receptor agonist with IC50s of 0.77 nM and 1.5 nM for rat and human 5-HT2 receptors, respectively.AL 34662 is also a low affinity α-1D adrenergic agonist, with an EC50 of 0.4 μM.AL 34662 can be used to lower intraocular pressure.
价 格：￥电议型 号：T22029产 地：中国大陆
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T21792CGP 3466B maleate马来酸CGP3466B马来酸CGP3466B|||Omigapil (Maleate)|||Omigapil maleate
CGP 3466B maleate (Omigapil maleate) is an orally bioavailable GAPDH nitrosylation inhibitor. Omigapil maleate abrogates Aβ1-42-induced tau acetylation, memory impairment, and locomotor dysfunction in mice. Omigapil maleate has the potential for the research of Alzheimer´s disease. Omigapil maleate (CGP3446B maleate) is a apoptosis inhibitor. Omigapil maleate can be used for the research of congenital muscular dystrophy (CMD).
价 格：￥电议型 号：T21792产 地：中国大陆
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T20648Dodecyl gallate；没食子酸月桂酯NSC-133463|||Nipagallin LA|||Lauryl gallate|||Progallin LA|||NSC 133463|||NSC
Dodecyl gallate (Progallin LA) is the ester of gallic acid and dodecanol. As a food additive, it is used as a preservative and antioxidant.
价 格：￥电议型 号：T20648产 地：中国大陆
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T20346Salicylaldoxime；水杨醛肟Salicylaldoxime
Salicylaldoxime is a chelating agent sometimes used in the analysis of samples containing transition metal ions, with which it often forms brightly colored coordination complexes.
价 格：￥电议型 号：T20346产 地：中国大陆
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T2024A-803467；化合物A-803467A 803467|||A803467；A 803467|||A803467
A-803467 is a selective NaV1.8 channel blocker.
价 格：￥电议型 号：T2024产 地：中国大陆
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T1967AZD-3463；化合物AZD3463ALK/IGF1R inhibitor；ALK/IGF1R inhibitor
AZD-3463 (ALK/IGF1R inhibitor) , an orally bioavailable ALK inhibitor (Ki: 0.75 nM), can inhibit IGF1R with equivalent potency.
价 格：￥电议型 号：T1967产 地：中国大陆
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T1867Otenaproxesul；化合物ATB 346ATB 346；ATB 346
Otenaproxesul (ATB 346) is a novel hydrogen sulphide-releasing derivative of naproxen with markedly reduced toxicity.
价 格：￥电议型 号：T1867产 地：中国大陆
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T18346Methyltetrazine-PEG24-NHS ester；化合物 T18346Methyltetrazine-PEG24-NHS ester
Methyltetrazine-PEG24-NHS ester is a polyethylene glycol (PEG) derived linker employed in the synthesis of proteolysis targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T18346产 地：中国大陆
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T173469-Decyn-1-ol；化合物 T173469-Decyn-1-ol
9-Decyn-1-ol is an alkyl/ether-based PROTAC linker suitable for synthesizing PROTACs. It serves as a conjugation agent to combine GDC-0068 and Lenalidomide, resulting in the formation of INY-03-041. INY-03-041 is a potent and highly selective pan-Akt degrader that operates through the PROTAC mechanism. It effectively inhibits Akt1, Akt2, and Akt3 with IC50 values of 2.0 nM, 6.8 nM, and 3.5 nM, respectively[1].
价 格：￥电议型 号：T17346产 地：中国大陆
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T16791Rottlerin；粗糠柴苦素Mallotoxin|||NSC 56346|||NSC 94525；Mallotoxin|||NSC 56346|||粗糠柴苦素|||NSC 94525
Rottlerin (NSC-56346) is a natural product purified from Mallotus Philippinensis and is a specific PKC inhibitor (IC50: PKCδ of 3-6 μM, PKCα,β,γ of 30-42 μM, PKCε,η,ζ of 80-100 μM). Rottlerin causes apoptosis via caspase 3 activation.
价 格：￥电议型 号：T16791产 地：中国大陆
