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Cat. No. Product Name Field of Application Chemical Structure
DC20488 OxPAPC 4
DC20487 OxPAPC 3
DC20486 OxPAPC 2
DC10396 (Z)-Mutagenic Impurity of Tenofovir Disoproxil
(Z)-Mutagenic Impurity of Tenofovir Disoproxil is a mutagenic impurity in tenofovir disoproxil fumarate. Tenofovir is an antiretroviral drug known as nucleotide analogue reverse transcriptase (NtART) inhibitor, which blocks reverse transcriptase, a crucia
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DC24129 (S)-Willardiine
(S)-Willardiine is a potent agonist of AMPA/kainate receptors with EC50 of 44.8 uM..
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DC12085 (S)-Metolachor
(S)-Metolachor, a derivative of aniline, is a major pesticide in use.
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DC20595 (S)-FQI1
(S)-FQI1 is a small-molecule inhibitor of transcription factor LSF with IC50 of 0.93 uM, approximately 2-fold more active than the racemate FQI-1.
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DC23811 (S)-BAY-293(BAY293 S-enantiomer)
(S)-BAY-293 (BAY293 S-enantiomer) is the S-enantiomer of BAY-293 as a negative control compound..
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DC26029 (S)-4CPG
(S)-4CPG, also known as (S)-4-Carboxyphenylglycine, is a novel orally active metabotropic glutamate receptor 1 antagonist.
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DCAPI1481 Sulpiride
(RS)-(±)-Sulpiride is a selective postsynaptic D2DR inhibitor.
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DC9092 (R)-Lansoprazole
(R)-Lansoprazole is a proton pump inhibitor which prevents the stomach from producing acid.
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DC20290 (R)-HZ05
(R)-HZ05 is a potent DHODH inhibitor with IC50 of 11 nM, accumulates cancer cells in S-phase, increases p53 synthesis, and synergizes with an inhibitor of p53 degradation (Nutlin-3a) to reduce tumor growth in vivo..
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DC23692 (R)-DNMDP
(R)-DNMDP (DNMDP R-form) is the R-form of is DNMDP, which is a potent and selective cancer cell cytotoxic agent that binds to PDE3A, promotes an interaction between PDE3A and Schlafen 12 (SLFN12)..
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DC20882 (R)-CE3F4
(R)-CE3F4 is a more potent, selective EPAC1 antagonist than the racemic CE3F4 and (S)-CE3F4, displays 10-fold selectivity for EPAC1 over EPAC2..
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DC22808 (R)-9bMS
(R)-9bMS is a potent and selective ACK1 (TNK2) inhibitor with IC50 of 48 nM.
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DC9533 (R)-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid
(R)-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid is a constrained Phe analogue which can fold into a beta-bend and a helical structure, and to adopt a preferred side-chain disposition in the peptide.
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DC10426 (E)-[6]-Dehydroparadol
(E)-[6]-Dehydroparadol, extracted from patent US 9272994, compound M15, shows growth inhibition and induction of apoptosis against human cancer cells with IC50 values of 43.02 μM in HCT-116 cell and 41.59 μM in H-1299 cell, respectively.
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DC12268 (3-Carboxypropyl)trimethylammonium chloride (γ-Butyrobetaine hydrochloride)
(3-Carboxypropyl)trimethylammonium chloride is angiopathic substance produced as an intermediary metabolite by gut microbiota that feed on carnitine in dietary red meat.
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DC11321 (+)-Muscarine (chloride)
(+)-Muscarine is an agonist of muscarinic acetylcholine receptors that was originally found in A. muscaria.
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