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Filtered Search Results
Ambeed AMBEED
5000889051 26-DICHLORO-9-ETHYL-9H-P 100MG
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Aobchem AOBCHEM
5000871544 7-CHLORO-9 9-DIMETHYL-9H-FLUO
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Chemscene CHEMSCENE
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5000576385 S-3- 9H-FLUOREN-9-YL METHOX 5G
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Chemscene CHEMSCENE
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5000578727 R-2- 9H-FLUOREN-9-YL METHO 10G
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Chemscene CHEMSCENE
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5000578869 S-2- 9H-FLUOREN-9-YL METHOX 5G
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Chemscene CHEMSCENE
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5000578073 R-2- 9H-FLUOREN-9-YL METHO 25G
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eMolecules EMOLECULES INC
5000841495 R-2-9H-FLUOREN-9-YL 25G
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Aobchem AOBCHEM
5000872831 9- 2- METHYLTHIO PHENYL -9H-CA
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eMolecules 330795-57-8 | (S)-tert-Butyl 6-(((9H-fluoren-9-yl)methoxy)carbonylamino)-2-aminohexanoate hydrochloride | Combi-Blocks, Inc. | MFCD26131502 | 461.000 | C25H33ClN2O4 | 98.000 | Cl.CC(C)(C)OC(=O)[C@@H](N)CCCCNC(=O)OCC1c2ccccc2-c2ccccc12 | 25g | 703124436
(S)-tert-Butyl 6-(((9H-fluoren-9-yl)methoxy)carbonylamino)-2-aminohexanoate hydrochloride | Combi-Blocks, Inc. | 330795-57-8 | MFCD26131502 | 461.000 | C25H33ClN2O4 | 98.000 | Cl.CC(C)(C)OC(=O)[C@@H](N)CCCCNC(=O)OCC1c2ccccc2-c2ccccc12 | 25g | 703124436
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Apexbio Technology LLC N-(3-pyridyl)-Indomethacin amide 261766-29-4 50mg
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N-3-pyridyl-Indomethacin amide is a small-molecule inhibitor targeting cyclooxygenase-2 (COX-2) It is designed to selectively inhibit the COX-2 isoform thereby modulating inflammatory responses mediated by this enzyme N-3-pyridyl-Indomethacin amide exerts its biological activity primarily through reversible inhibition of COX-2 In studies with recombinant human COX-2 N-3-pyridyl-Indomethacin amide demonstrates potent inhibition with an IC50 value of approximately 0 052 M Based on these pharmacological properties N-3-pyridyl-Indomethacin amide holds research potential in the investigation of COX-2-related pathways in inflammation pain and associated cellular signaling events
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eMolecules 2098497-06-2 | tert-Butyl (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-aminopropanoate hydrochloride | ChemScene | MFCD21363165 | 418.920 | C22H27ClN2O4 | 98.000 | Cl.CC(C)(C)OC(=O)[C@H](CN)NC(=O)OCC1c2ccccc2-c2ccccc12 | 250mg | 632309692
tert-Butyl (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-aminopropanoate hydrochloride | ChemScene | 2098497-06-2 | MFCD21363165 | 418.920 | C22H27ClN2O4 | 98.000 | Cl.CC(C)(C)OC(=O)[C@H](CN)NC(=O)OCC1c2ccccc2-c2ccccc12 | 250mg | 632309692
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Medchemexpress LLC 2S,4R-4-(Fmoc-amino)-1-(Boc)-pyrrolidine-2-carboxylic acid | 176486-63-8 | 452.50 | 10 G
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This proline derivative is a beneficial ergogenic dietary substance. Amino acids and amino acid derivatives, such as this product, are commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, fuel supply during exercise, mental performance during stress-related tasks, and prevent exercise-induced muscle damage.
- Proline derivative
- Used as an ergogenic supplement
- Influences the secretion of anabolic hormones
- Aids in fuel supply during exercise
- Improves mental performance during stress-related tasks
- Prevents exercise-induced muscle damage
- Recognized as a beneficial ergogenic dietary substance
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Cayman Chemical IndomethacIn heptyl ester 50mg
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A potent, non-selective COX-2 inhibitor (IC50 = 0.04 µM); >1,700 times more potent as an inhibitor of COX-2 than COX-1
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Sigma Aldrich Fine Chemicals Biosciences Indomethacin Related Compo50MG
Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
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Cayman Chemical IndomethacIn N-octyl amIde 1mg
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Indomethacin is a potent but non-selective inhibitor of both COX-1 and COX-2 in sheep and humans.{1286} Structurally, indomethacin is a substituted indole acetic acid, wherein the carboxylate can be derivitized as an ester or amide. These derivatives show enhanced selectivity for the COX-2 isoform. For example, the IC50 values of indomethacin N-octyl amide for the inhibition of ovine COX-1 and human recombinant COX-2 are 66 µM and 40 nM, respectively, making it 1,650 times more potent as an inhibitor of COX-2 than COX-1.{8243} While indomethacin itself has an IC50 of 0.05 µM for the inhibition of COX-2, it also inhibits COX-1 with a corresponding IC50 of 0.67 µM.
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