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T17225Vercirnon；维塞诺CCX282-B|||GSK-1605786|||Traficet-EN；CCX282-B|||维塞诺|||GSK-1605786|||Traficet-EN
Vercirnon (Traficet-EN) is a selective and potent antagonist of CCR9 (IC50: 10 nM). It is also used in the research of inflammatory bowel diseases.
价 格：￥电议型 号：T17225产 地：中国大陆
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T17102Tipifarnib (S enantiomer)；化合物Tipifarnib S entiomerTipifarnib S enantiomer|||(S)-(-)-R-115777|||(S)-T
Tipifarnib S enantiomer ((S)-(-)-R-115777) is the S-enantiomer of Tipifarnib. Tipifarnib is a potent and specific farnesyltransferase inhibitor (IC50: 0.6 nM).
价 格：￥电议型 号：T17102产 地：中国大陆
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T17048Tetradecanoylcarnitine肉豆蔻酰基-L-肉碱L-Myristoylcarnitine|||Myristoyl-L-(-)-carnitine
Tetradecanoylcarnitine (L-Myristoylcarnitine) is an acylcarnitine involved in the beta-oxidation of long-chain fatty acids, and is a potential marker for very-long-chain coenzyme A dehydrogenase deficiency. alpha-Dihydroartemisinin is a potent and selective inhibitor with multiple targets.
价 格：￥电议型 号：T17048产 地：中国大陆
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T16886Sinefungin；西奈芬净Adenosyl-Ornithine|||A-9145|||Antibiotic 32232RP；Adenosyl-Ornithine|||西奈芬净|||A-9145||
Sinefungin (Adenosyl-Ornithine) is an effective inhibitor of virion mRNA(guanine-7-)-methyltransferase, mRNA(nucleoside-2´-)-methyltransferase, and viral multiplication. Sinefungin is a SET7/9 inhibitor and ameliorates renal fibrosis by inhibiting H3K4 methylation.
价 格：￥电议型 号：T16886产 地：中国大陆
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T16765RNPA1000；化合物 T16765RNPA1000
RNPA1000 is an attractive antimicrobial development candidate and RnpA inhibitor.
价 格：￥电议型 号：T16765产 地：中国大陆
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T16764RN-18；化合物RN-18RN-18
RN-18 is an inhibitor of HIV-1 viral infectivity factor (IC50: 6 μM in nonpermissive H9 cells).
价 格：￥电议型 号：T16764产 地：中国大陆
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T16763RN-1747；化合物RN-1747RN-1747
RN-1747 is a selective transient receptor potential cation channel subfamily V member 4 agonists (EC50: hTRPV4 of 0.77 μM, mTRPV4 of 4.0 μM, and rTRPV4 of 4.1 μM). RN-1747 also antagonizes TRPM8 (IC50: 4 μM).
价 格：￥电议型 号：T16763产 地：中国大陆
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T16578PRN694；化合物 T16578PRN694
PRN694 shows extended target residence time on ITK and RLK, enabling durable attenuation of effector cells in vitro and in vivo. PRN694 is an irreversible, highly selective, and effective covalent interleukin-2-inducible T-cell kinase (ITK) and resting lymphocyte kinase (RLK) dual inhibitor (IC50s: 0.3 nM and 1.4 nM, respectively).
价 格：￥电议型 号：T16578产 地：中国大陆
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T16405Ornidazole diol；化合物 T16405Ro 11-2616；Ro 11-2616
Ornidazole diol is a diol produced through ornidazole rapidly hydrolyzing in basic solutions.
价 格：￥电议型 号：T16405产 地：中国大陆
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T15956Mal-amido-PEG4-NHS ester化合物Mal-amido-PEG4-NHS esterN-[15-[(2,5-二氧代-1-吡咯烷基)氧基]-15-氧代-3,6,9,12-四氧杂十五烷-
Mal-amido-PEG4-NHS ester is a PEG-based PROTAC linker that can be used in PROTAC synthesis[1].
价 格：￥电议型 号：T15956产 地：中国大陆
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T15698L-Palmitoylcarnitine；棕榈酰肉碱L-Palmitoylcarnitine
L-Palmitoylcarnitine is a metabolite of fatty acid.
价 格：￥电议型 号：T15698产 地：中国大陆
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T15667KRN4884；化合物 T15667KRN4884
KRN 4884 is an opener of the K+ channel. KRN 4884 (0.1-3 μM) activates KATP channels in a concentration-dependent manner (EC50=0.55 μM), in the presence of intracellular ATP (1 mM).
价 格：￥电议型 号：T15667产 地：中国大陆
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T1556Ornidazole奥硝唑Tiberal|||Ornidazolum|||NSC 95075|||Ro 7-0207|||奥硝唑
Ornidazole (Tiberal) is a nitroimidazole antiprotozoal agent used in ameba and trichomonas infections. It is partially plasma-bound and also has radiation-sensitizing action.
价 格：￥电议型 号：T1556产 地：中国大陆
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T15385Glibornuride；格列波脲Glibornuride
Glibornuride is a blocker of ATP-sensitive K+ channel(pKi: 5.75). Glibornuride inhibits high affinity [3H]-glibenclamide binding with the potencies expected from their K+ channel activity.
价 格：￥电议型 号：T15385产 地：中国大陆
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T15157Dodecanoylcarnitine；月桂酰肉碱Lauroylcarnitine；Lauroylcarnitine
Dodecanoylcarnitine ((-)-Lauroylcarnitine) has been associated with disturbances in fatty acid oxidation, and the use of Dodecanoylcarnitine resulted in an increase in the permeability of salmon calcitonin.
价 格：￥电议型 号：T15157产 地：中国大陆
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T14840Butyrylcarnitine；丁酰肉碱Butyrylcarnitine
Butyrylcarnitine is a plasma metabolite that is an indicator of abnormal metabolism due to disease and is used in the diagnosis of heart failure and pancreatic cysts.
价 格：￥电议型 号：T14840产 地：中国大陆
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T1468Lornoxicam；氯诺昔康Ro 13-9297|||Chlortenoxicam|||TS110；Ro 13-9297|||Chlortenoxicam|||TS110|||氯诺昔康
Lornoxicam (Chlortenoxicam) (chlortenoxicam) is a new nonsteroidal anti-inflammatory drug (NSAID) of the oxicam class with analgesic, anti-inflammatory, and antipyretic properties. Lornoxicam differs from other oxicam compounds in its potent inhibition of prostaglandin biosynthesis, a property that explains the particularly pronounced efficacy of the drug. Lornoxicam is approved for use in Japan.
价 格：￥电议型 号：T1468产 地：中国大陆
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T14321ARN19874；化合物 T14321ARN19874
ARN19874 is a selective, reversible uncompetitive N-acylphosphatidylethanolamine phospholipase D (NAPE-PLD) activity inhibitor. With an IC50 of ~34 μM[1].
价 格：￥电议型 号：T14321产 地：中国大陆
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T14196Alternariol；交链孢酚Alternariol
Alternariol (AOH), a mycotoxin synthesized by Alternaria species, displays numerous therapeutic and biological effects, including phytotoxic, cytotoxic, anti-HIV, anti-cancer, and anti-microbial properties. It functions by inhibiting the catalytic activity of topoisomerase I and II enzymes.
价 格：￥电议型 号：T14196产 地：中国大陆
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T14193α-Galactosylceramide；化合物KRN7000KRN7000|||α-GalCer；KRN7000|||α-GalCer
α-Galactosylceramide (KRN7000) is a synthetic glycolipid with antitumorial and immunostimulatory and is a very potent NKT cell agonist and binds effectively to CD1d. The complex of α-Galactosylceramide and CD1d can bind to the T cell antigen receptor of NKT cells.
价 格：￥电议型 号：T14193产 地：中国大陆
