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Filtered Search Results
TARGETMOL CHEMICALS INC MCU-I4 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. MCU-i4 is a novel negative modulator of the MCU binding MICU1 and impairing muscle cell growth. purity: 99%
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TARGETMOL CHEMICALS INC DBET57 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. dBET57 is heterobifunctional degrader of BRD4 based on the PROTAC technology exhibits significant degradation of BRD4BD1 with a DC50/5h of 500 nM and inactive on BRD4BD2purity: 99%
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eMolecules 13504-85-3 | Z-Hyp-OH | Accela ChemBio265.265 | C13H15NO5 | 97.000 | O[C@@H]1C[C@H](N(C1)C(=O)OCc1ccccc1)C(O)=O | 25g | 135706127
Z-Hyp-OH | Accela ChemBio | 13504-85-3265.265 | C13H15NO5 | 97.000 | O[C@@H]1C[C@H](N(C1)C(=O)OCc1ccccc1)C(O)=O | 25g | 135706127
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eMolecules 1417794-63-8 | Methyl 5-aminopyrazine-2-carboxylate hydrochloride | MFCD18425624 | 1g
Ambeed | Methyl 2-(2-(((6-(trifluoromethyl)pyridin-2-yl)oxy)methyl)phenyl)acetate | 1g | 633657907 | A1482498 | 187327-30-6 | 325.287 | C16H14F3NO3
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TARGETMOL CHEMICALS INC CP 465022 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. CP 465022 hydrochloride is a potent and selective noncompetitive antagonist of AMPA receptor with anticonvulsant activity. CP 465022 hydrochloride inhibits Kainate-induced response with an IC50 of 25 nM in rat cortical neurons. purity: 98%
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TARGETMOL CHEMICALS INC LOFENDAZAM 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. Lofendazam (Bu 1014) is a benzodiazepine derivative that has sedative and anxiolytic effects. purity: 98%
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TARGETMOL CHEMICALS INC ARN25068 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. ARN25068 is a potent inhibitor of GSK-3(beta) FYN and DYRK1A protein kinases exerting its activity in the sub-micromolar range. This compound effectively addresses tau hyperphosphorylation [1]. purity: 99%
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TARGETMOL CHEMICALS INC S1P RECEPTOR AGONIST 1 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. S1p receptor agonist 1 (S1p-receptor-agonist-1) is an S1P receptor agonist. purity: 99%
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TARGETMOL CHEMICALS INC BREVILIN A 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Brevilin A is a sesquiterpene lactone isolated from Centipeda minima inhibits janus kinase activity and blocks STAT3 signaling in cancer cells with anti-tumor activity. Brevilin A is a selective inhibitor of JAK-STAT signal pathway by attenuating the JAKs activity and blocking STAT3 signaling (IC50 = 10.6 uM) in Cancer Cells.Brevilin A induces apoptosis and autophagy via mitochondrial pathway and PI3K/AKT/mTOR inactivation in colon adenocarcinoma cell CT26.antitumourpurity: 99%
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TARGETMOL CHEMICALS INC LFM-A13 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. LFM-A13(IC50=2.5 uM) a specific Bruton's tyrosine kinase (BTK) is more than 100-fold specificity than other protein kinases such as JAK1 JAK2 HCK EGFR and IRK. purity: 99%
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TARGETMOL CHEMICALS INC PRANIDIPINE 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Pranidipine (OPC-13340) is a novel long-acting 14-dihydropyridine calcium channel blocker. It prolongs acetylcholine-induced relaxation in presence of endothelium as well as nitroglycerin-induced relaxation in absence of endothelium. It also has antihypertensive activity. purity: 99%
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TARGETMOL CHEMICALS INC LEXIBULIN 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Lexibulin (CYT-997)(CYT-997) is a potent tubulin polymerization inhibitor (IC50 10-100 nM in Y cell lines). Lexibulin blocks the formation of the mitotic spindle and leading to cell cycle arrest at the G2/M phase; this may result in disruption of the tumor vasculature and tumor blood flow and tumor cell death. purity: 99%
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TARGETMOL CHEMICALS INC TELAGLENASTAT 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 500 mg 1000 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Telaglenastat (CB 839) (IC50 of 24 nM) an effective specific and oral inhibitor which is bioavailable glutaminase for recombinant human GAC. purity: 99%
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eMolecules 218916-64-4 | 3-((tert-Butoxycarbonyl)amino)-2-hydroxypropanoic acid | ChemScene | MFCD08275906 | 205.210 | C8H15NO5 | 97.000 | CC(C)(C)OC(=O)NCC(O)C(O)=O | 5g | 632274290
3-((tert-Butoxycarbonyl)amino)-2-hydroxypropanoic acid | ChemScene | 218916-64-4 | MFCD08275906 | 205.210 | C8H15NO5 | 97.000 | CC(C)(C)OC(=O)NCC(O)C(O)=O | 5g | 632274290
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TARGETMOL CHEMICALS INC TELOTRISTAT ETIPRATE 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Telotristat Etiprate (LX 1606 Hippurate) is an orally bioavailable tryptophan hydroxylase (TPH) inhibitor with potential antiserotonergic activity. purity: 99%
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