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ce 1

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  • Inhibitors & Agonists
    8
    TargetMol | Inhibitors_Agonists
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1-(2'-Deoxy-5'-O-DMT-2'-fluoro-b-D-arabinofuranosyl)thymine 3'-CE phosphoramidite
TNU1420208193-48-0
1-(2'-Deoxy-5'-O-DMT-2'-fluoro-b-D-arabinofuranosyl)thymine 3'-CE phosphoramidite is a nucleoside phosphoramidite.
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7-10 days
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CE-245677
T14921717899-97-3
CE-245677 is a potent, reversible inhibitor of Tie2 and TrkA B kinases, with cellular IC50 values of 4.7 nM and 1 nM, respectively.
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TargetMol | Inhibitor Sale
CE3F4 analog 1
T396062141967-43-1
CE3F4 analog 1 is an analogue of CE3F4. It is a chemical compound utilized in various [scientific applications] due to its unique properties, notably in (radical scavenging) and (oxidation-reduction) processes. It plays a significant role in advanced (catalysis), (pharmaceutical) research, and (material science) due to its stability and reactivity.
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7-10 days
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CE-326597
T68482870615-40-0
CE-326597 is a potent and selective CCK1R agonist. The type 1 cholecystokinin receptor (CCK1R) has multiple physiologic roles relating to nutrient homeostasis,including mediation of postcibal satiety. The type 1 cholecystokinin (CCK) receptor (CCK1R) is a key mediator of postcibal satiety and a potential target for drugs that may be useful to prevent and or treat obesity.
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6-8 weeks
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DMT-5Me-dC(Bz)-CE Phosphoramidite
T75269105931-57-5
DMT-5Me-dC(Bz)-CE Phosphoramidite is employed in the synthesis of locked nucleic acids (LNAs) to improve the spectral properties and target affinity of fluorescent oligonucleotide probes [1].
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Tanshinone IIA anhydride
T7554161077-78-9
Tanshinone IIA anhydride is a potent, irreversible inhibitor of human carboxylesterase (CE), exhibiting inhibitory constants (K i values) of 1.9 nM for human CE1 and 1.4 nM for human intestinal CE (hiCE), respectively [1].
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Cholesteryl Palmitoleate
Cholesterol Palmitoleate, CE(16:1), 16:1(9Z) Cholesterol ester, 16:1(9Z) CE
T8521716711-66-3
Cholesteryl palmitoleate, a cholesterol ester, exhibits elevated plasma levels in ApoE- - mice following exposure to cigarette smoke and in pediatric patients diagnosed with biliary atresia. It serves as a standard for identifying cholesterol esters in human meibomian gland secretions.
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6-8 weeks
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(S)-CE-123
T853632378384-49-5
(S)-CE-123 is an innovative and highly selective atypical dopamine transporter (DAT) inhibitor, exhibiting an EC 50 of 2.76 μM in uptake inhibition assays performed in HEK293 cells with stable expression of human DAT isoforms. As a Modafinil analogue, (S)-CE-123 can cross the blood–brain barrier and enhances cognitive and motivational functions in experimental animals [1] [2].
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10-14 weeks
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