Pyrroles
eMolecules 4-Bromo-2-chloro-5-fluoropyridine | 884495-10-7 | MFCD06659500 | 1g
Ambeed | 4-Bromo-2-chloro-5-fluoropyridine | 1g | 552602397 | A161528 | | 884495-10-7 | MFCD06659500 | 210.430 | C5H2BrClFN
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eMolecules Building Block Tool
Medchemexpress LLC (3S,5S)-atorvastatin | 501121-34-2 | MFCD09839951 | 95.0% | 558.64 g/mol | C33H35FN2O5 | 10 MG
(3S,5S)-atorvastatin is the inactive stereoisomer of atorvastatin provided for research use. It is reported to act as a pregnane X receptor (PXR) agonist and is used in pharmacology and metabolic-disease studies. Supplied as a high-purity solid for in vitro and analytical applications.
- Inactive enantiomer of atorvastatin
- Acts as pregnane X receptor (PXR) agonist
- Supplied with reported purity of 95.0%
- Available in a 10 mg quantity for laboratory use
- Suitable for in vitro and analytical research; not for human use
eMolecules ChemScene / (S)-1-(4-Bromo-3-fluorophenyl)ethanamine hydrochloride / 100mg / 632324132 / CS-0158622 / 0.000 / 2109874-10-2 / MFCD24428137 / 254.530 / C8H10BrClFN
ChemScene / (S)-1-(4-Bromo-3-fluorophenyl)ethanamine hydrochloride / 100mg / 632324132 / CS-0158622 / 0.000 / 2109874-10-2 / MFCD24428137 / 254.530 / C8H10BrClFN
Medchemexpress LLC 4-amino-N-(1-benzylpiperidin-4-yl)-5-chloro-2-methoxybenzamide;2-hydroxybutanedioic acid | 57645-91-7 | MFCD01743960 | 99.4% | 507.96 | C24H30ClN3O7 | 10 MG
Clebopride malate is the malate salt of clebopride, an orally active dopamine D2 receptor antagonist supplied as a research-grade analytical standard for laboratory pharmacology and analytical studies. It is provided as a high-purity solid intended for controlled experimental use and should be stored sealed and away from moisture; solutions may be frozen for extended storage.
- Malate salt form of clebopride.
- Orally active dopamine D2 receptor antagonist.
- High purity suitable for analytical applications.
- Supplied in a small research-grade pack for laboratory use.
- Stable when stored sealed and away from moisture; follow refrigerated or frozen conditions for solutions.
Medchemexpress LLC 4-(4,5-diphenyl-1H-imidazol-2-yl)benzoyl chloride | 162756-62-9 | 98.0% | 358.82 | C22H15ClN2O | 10 MG
4-(4,5-diphenyl-1H-imidazol-2-yl)benzoyl chloride is a benzoyl chloride derivative used as a labeling reagent for amines and for HPLC derivatization in analytical and research workflows. Supplied as a solid with high purity suitable for laboratory use.
- Used to derivatize amines for HPLC analysis
- Fluorescent imidazolyl moiety aids sensitive detection
- High purity (98.0%) suitable for analytical work
- Available in small, controlled package sizes for research use
- Stable solid form for convenient storage and handling
Medchemexpress LLC Ethyl 2-amino-4-methyl-5-((3-nitrophenyl)carbamoyl)-thiophene-3-carboxylate | 303141-21-1 | 99.7% | 10 MG
DC-S239 is a selective inhibitor of histone methyltransferase SET7 with reported in vitro activity (IC50 = 4.59 μM); supplied as a high-purity solid for research use.
- Selective SET7 inhibitor with IC50 = 4.59 μM.
- Reported antiproliferative activity in MCF7 and HL60 cells.
- High purity suitable for biochemical and cellular studies.
- Soluble in DMSO (125 mg/mL) for in vitro experiments.
- Stable as a powder at -20°C for long-term storage.
![Medchemexpress LLC [2-chloro-3-(trifluoromethyl)phenyl]-[(4R)-1-(5-fluoropyrimidin-2-yl)-4-methyl-6,7-dihydro-4H-triazolo... | 1627902-21-9 | MFCD31556312 | 99.3% | 440.78 g/mol | C18H13ClF4N6O | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000227025.png-250.jpg)
Medchemexpress LLC [2-chloro-3-(trifluoromethyl)phenyl]-[(4R)-1-(5-fluoropyrimidin-2-yl)-4-methyl-6,7-dihydro-4H-triazolo... | 1627902-21-9 | MFCD31556312 | 99.3% | 440.78 g/mol | C18H13ClF4N6O | 10 MG
JNJ-54175446 is a brain-penetrant, selective purine P2X7 receptor antagonist used in central nervous system research and clinical investigations of neuroinflammation and mood disorders. It is characterized by high potency at human and rat P2X7 receptors and is available in both solid and solution formats across multiple package sizes.
- Brain-penetrant P2X7 receptor antagonist.
- High potency: pIC50 8.46 (human), 8.81 (rat).
- Available as solid and DMSO solution; multiple package sizes from 1 mg to 500 mg.
- High reported purity of 99.3%.
- Suitable for in vitro and in vivo CNS pharmacology studies.
![Medchemexpress LLC 2H-Cyclopenta[b]furan-2-one, 5-(benzoyloxy)hexahydro-4-(hydroxymethyl)-, (3aR,4S,5R,6aS)- | 39746-00-4 | 98.0% | 276.28 | 10 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000404186-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 2H-Cyclopenta[b]furan-2-one, 5-(benzoyloxy)hexahydro-4-(hydroxymethyl)-, (3aR,4S,5R,6aS)- | 39746-00-4 | 98.0% | 276.28 | 10 G
(-)-Corey lactone benzoate is a building block in the chemical synthesis of corey aldehyde. It is for research use only and not sold to patients. It appears as a solid with a white to off-white color.
- Building block in the chemical synthesis of corey aldehyde.
- For research use only.
- Appears as a solid.
- White to off-white color.
Cayman Chemical SBromoenol lactone
A selective iPLA2β inhibitor; inhibits vasopressin-induced release of arachidonate from cultured rat aortic smooth muscle (A10) cells (IC50 = 2 µM); >1,000-fold selective for iPLA2 versus cPLA2 and 10-fold selective for iPLA2β versus iPLA2γ
Cayman Chemical SBromoenol lactone
A selective iPLA2β inhibitor; inhibits vasopressin-induced release of arachidonate from cultured rat aortic smooth muscle (A10) cells (IC50 = 2 µM); >1,000-fold selective for iPLA2 versus cPLA2 and 10-fold selective for iPLA2β versus iPLA2γ
Selleck Chemical LLC Quisinostat (JNJ-26481585) 2HCl S1096-5mg
Quisinostat (JNJ-26481585) 2HCl is a novel second-generation HDAC inhibitor with highest potency for HDAC1 with IC50 of 0 11 nM in a cell-free assay modest potent to HDACs 2 4 10 and 11 greater than 30-fold selectivity against HDACs 3 5 8 and 9 and lowest potency to HDACs 6 and 7 Phase 2
Cayman Chemical SBromoenol lactone
A selective iPLA2β inhibitor; inhibits vasopressin-induced release of arachidonate from cultured rat aortic smooth muscle (A10) cells (IC50 = 2 µM); >1,000-fold selective for iPLA2 versus cPLA2 and 10-fold selective for iPLA2β versus iPLA2γ
TARGETMOL CHEMICALS INC 2-HYDROXY ATORVASTATIN C 5MG
Also available in 1 mg 50 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. 2-Hydroxy atorvastatin calcium salt is a hydroxy metabolite of Atorvastatin calcium salt which is a potent HMG-CoA reductase inhibitor (IC50 = 8 nM). purity: 97%
TARGETMOL CHEMICALS INC Atorvastatin lactone 25MG
Also available in 1 mL, 2 mg, 5 mg, 10 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Atorvastatin lactone is a prodrug form of atorvastatin. Which is an orally active 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor. Purity 98.16%
Medchemexpress LLC HY-15816A 5mg Medchemexpress, Ulixertinib (hydrochloride) CAS:1956366-10-1 Purity:>98%
Medchemexpress, HY-15816A 5mg Ulixertinib (hydrochloride) CAS:1956366-10-1 Ulixertinib hydrochloride is a potent, orally active, highly selective, ATP-competitive and reversible covalent inhibitor of ERK1/2 kinases, with an IC 50 of <0.3 nM against ERK2. Ulixertinib hydrochloride inhibits the phosphorylated ERK2 (pERK) and downstream kinase RSK (pRSK) in an A375 melanoma cell line [1] [2] . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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