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T22033ARC 239 dihydrochloride；化合物ARC 239 dihydrochlorideARC 239 dihydrochloride
ARC 239 dihydrochloride is a selective α2B adrenoceptor antagonist (pKD values are 8.8, 6.7 and 6.4 at α2B, α2A, and α2D receptors respectively).
价 格：￥电议型 号：T22033产 地：中国大陆
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T21239Propyl caprate；化合物 T21239Propyl decanoate|||Decanoic acid, propyl ester；Propyl decanoate|||Decanoic
Propyl caprate is a biochemical.
价 格：￥电议型 号：T21239产 地：中国大陆
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T2112Fexinidazole；非昔硝唑HOE 239；非昔硝唑|||HOE 239
Fexinidazole (HOE 239) is an antiparasitic agent. It has activity against Trypanosoma cruzi, Tritrichomonas foetus, Trichomonas vaginalis, Entamoeba histolytica, Trypanosoma brucei, and Leishmania donovani. The biologically relevant active metabolites in vivo are the sulfoxide and sulfone.
价 格：￥电议型 号：T2112产 地：中国大陆
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T20184C.I. 67000；化合物 T20184NSC521239|||NSC-521239|||NSC 521239；NSC521239|||NSC-521239|||NSC 521239
C.I. 67000 is an agent of dye.
价 格：￥电议型 号：T20184产 地：中国大陆
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T20128Ethionine；L-乙硫胺酸NSC 82393|||NSC82393|||NSC-82393|||L-Ethionine|||ETH；NSC 82393|||NSC82393|||L-乙硫胺酸||
Ethionine (NSC-82393) is an antimetabolite and methionine antagonist. It also produces liver neoplasms.
价 格：￥电议型 号：T20128产 地：中国大陆
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T19873Edoxaban M4；化合物 T19873D21-2393|||D21 2393|||UNII-IV344R972X|||Edoxaban 4-Carboxylic Acid；D21-2393|||
D21-2393 subjects received a single-oral-dose of edoxaban 30-90 mg in each study occasion under fasting condition. Serial blood samples were collected to measure the plasma concentrations of edoxaban and its major active metabolite D21-2393. Meanwhile, PT, INR, aPTT were measured pre- and post-dose.
价 格：￥电议型 号：T19873产 地：中国大陆
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T19239Cicloxilic acid；环昔酸Cycloxilic acid；Cycloxilic acid
Cicloxilic acid（Cycloxilic acid） has choleretic activity and inhibits biliary cholesterol output.
价 格：￥电议型 号：T19239产 地：中国大陆
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T18239Mal-amido-PEG16-acid；化合物 T18239Maleimide-NH-PEG16-CH2CH2COOH；Maleimide-NH-PEG16-CH2CH2COOH
Mal-amido-PEG16-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T18239产 地：中国大陆
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T17239VU0155069；化合物VU0155069CAY10593；CAY10593
VU0155069 strongly inhibits the invasive migration of several cancer cell lines in transwell assays. VU0155069 is a selective phospholipase D1 inhibitor (IC50: 46 nM in vitro).
价 格：￥电议型 号：T17239产 地：中国大陆
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T16353Meseclazone；美西拉宗W2395|||NSC297623；美西拉宗|||W2395|||NSC297623
Meseclazone has anti-inflammatory, analgesic, and antipyretic activity. Meseclazone shows inhibitory potency of secondary phase ADP aggregation.
价 格：￥电议型 号：T16353产 地：中国大陆
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T16352NSC23925；化合物 T16352NSC23925
NSC23925 is a selective and effective inhibitor of P-glycoprotein (Pgp).
价 格：￥电议型 号：T16352产 地：中国大陆
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T16239N-Methylisatoic anhydride；N-甲基靛红酸酐NMIA；NMIA|||N-甲基靛红酸酐|||1-甲基苯唑
N-Methylisatoic anhydride is a 2´-OH selective acylation agent of RNAs. It is also widely used for resolving secondary RNA structures using the SHAPE technology.
价 格：￥电议型 号：T16239产 地：中国大陆
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T15803LY223982化合物 T15803SKF107324|||CGS23131
LY223982 is an effective and specific inhibitor of the leukotriene B4 receptor (IC50: 13.2 nM). It also can against [3H]LTB4 binding to LTB4 receptor.
价 格：￥电议型 号：T15803产 地：中国大陆
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T15239Epristeride；爱普列特SKF105657|||ONO-9302；SKF105657|||ONO-9302
Epristeride (ONO-9302) is an orally active, selective and non-competitive steroidal 5-α-reductase isoform 2 inhibitor that inhibits SR isoform 2.Episteride reduces prostate size and improves symptoms in men with BPH.Episteride induces atrophy and apoptosis of the ventral prostate in rats.
价 格：￥电议型 号：T15239产 地：中国大陆
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T14239Amino-PEG4-C2-amine；化合物 T14239Amino-PEG4-C2-amine
Amino-PEG4-C2-amine, a PEG-based linker (4 units) for PROTAC development, facilitates the synthesis of PROTACs.
价 格：￥电议型 号：T14239产 地：中国大陆
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T14087ABT-239；化合物ABT-239ABT-239
ABT-239 is a novel, highly efficacious antagonist belonging to the non-imidazole class of histamine H3 receptor (H3R) antagonists. It also acts as a transient receptor potential vanilloid type 1 (TRPV1) antagonist.
价 格：￥电议型 号：T14087产 地：中国大陆
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T13239T 82；化合物 T13239T 82
T 82 is an antagonist of 5-HT3 and inhibitor of acetylcholinesterase (AChE) and used for the treatment of Alzheimer´s Disease.
价 格：￥电议型 号：T13239产 地：中国大陆
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T131239Compound N051-0046；化合物 N051-0046Compound N051-0046
Compound N051-0046 is a useful organic compound for research related to life sciences and the catalog number is T131239.
价 格：￥电议型 号：T131239产 地：中国大陆
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T12695RBN-2397；化合物RBN-2397RBN-2397
RBN-2397 is a potent, selective and orally active accross species NAD+ competitive PARP7 inhibitor with IC50 less than 3 nM.
价 格：￥电议型 号：T12695产 地：中国大陆
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T12675LPT2399；化合物PT2399PT2399
PT2399 is a first-in-class, orally available, small molecule inhibitor of HIF-2 that selectively disrupts the heterodimerization of HIF-2α with HIF-1β. PT2399 displays potent antitumor activity in vivo
价 格：￥电议型 号：T12675L产 地：中国大陆
