Halomethanes
eMolecules 1017030-88-4 | ChemScene | 3-(2-(Difluoromethoxy)phenyl)propanoic acid | 100mg | 794193835 | CS-0365521 | MFCD09951709 | 216.184 | C10H10F2O3
AstaTech | 1-BENZYL-3-(TERT-BUTOXYCARBONYLAMINO)PYRROLIDINE-3-CARBOXYLIC ACID | 0.25g | 454128535 | P10794 | 95.000 | 1027511-74-5 | MFCD09838930 | 320.389 | C17H24N2O4
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eMolecules Building Block Tool
eMolecules 7766-48-5 | 5-Iodo-1-pentene - Stabilized over Cu | Oakwood Chemical | MFCD19688471 | 196.031 | C5H9I | 99.000 | ICCCC=C | 1g | 537709831
5-Iodo-1-pentene - Stabilized over Cu | Oakwood Chemical | 7766-48-5 | MFCD19688471 | 196.031 | C5H9I | 99.000 | ICCCC=C | 1g | 537709831
eMolecules 81502-74-1 | Ambeed | 2-Hydroxybenzene-135-tricarbaldehyde | 250mg | 595927639 | A954938 | MFCD01314207 | 178.143 | C9H6O4
Ambeed | 2-Hydroxybenzene-135-tricarbaldehyde | 250mg | 595927639 | A954938 | 81502-74-1 | MFCD01314207 | 178.143 | C9H6O4
![Medchemexpress LLC 3-[4-[(7-hydroxy-6-methyl-2,3-dihydro-1H-inden-4-yl)methyl]-3,5-dimethylpyrazol-1-yl]propanoic acid | 1092551-88-6 | 99.9% | 328.41 | C19H24N2O3 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000240096.png-250.jpg)
Medchemexpress LLC 3-[4-[(7-hydroxy-6-methyl-2,3-dihydro-1H-inden-4-yl)methyl]-3,5-dimethylpyrazol-1-yl]propanoic acid | 1092551-88-6 | 99.9% | 328.41 | C19H24N2O3 | 25 MG
Omzotirome is a small-molecule thyromimetic research compound and a functional analog of iodothyronines investigated for antihyperlipidaemic activity. It is provided for laboratory research use in solid form or as a DMSO solution, with reported analytical data to support experimental work. Handle per institutional safety procedures and applicable regulations.
Medchemexpress LLC (S)-Enzaplatovir | 1323077-88-8 | 99.7% | 377.40 | 5 G
(S)-Enzaplatovir, also known as (S)-BTA-C585, is a high-purity chemical compound. Identified by its CAS number 1323077-88-8 and with a molecular weight of 377.40, it is supplied as an off-white to yellow solid. This compound demonstrates high purity, verified through LCMS analysis, making it suitable for various laboratory applications.
- High purity of 99.7%
- Stable as a powder at -20°C for up to 3 years
- Structure confirmed by 1H NMR spectrum
- Consistency verified by LCMS analysis
- Off-white to yellow solid appearance
Medchemexpress LLC Ro8191 | 691868-88-9 | 98.8% | 373.21 g/mol | C14H5F6N5O | 100 MG
RO8191 is an orally active small-molecule interferon receptor agonist that binds IFNα/β receptor and activates JAK/STAT signalling, showing antiviral activity in HCV replicon assays.
- Orally active IFN receptor agonist that activates JAK/STAT and ISG expression.
- Shown activity in HCV replicon assays (IC50 ≈ 200 nM) and reported anti-HBV effects.
- Chemical formula C14H5F6N5O; molecular weight 373.21 g/mol; CAS 691868-88-9.
- Purity reported ~98.8% (datasheet); supplier documentation also lists ≥99.0%.
- Store under inert gas at -20°C; in solvent store at -80°C (6 months) or -20°C (1 month) under nitrogen.
- Intended for research use only; not for human or veterinary use.
Medchemexpress LLC Omzotirome | 1092551-88-6 | 99.9% | 328.41 g·mol^-1 | C19H24N2O3 | 50 MG
Omzotirome is a thyromimetic research compound, a functional analog of iodothyronines, used in preclinical studies of lipid metabolism and hyperlipidaemia. It acts as a metabolic modulator that increases energy expenditure and fatty acid oxidation, and is supplied at high chemical purity for laboratory research.
- Used in hyperlipidaemia and metabolic research.
- Acts as a thyromimetic metabolic modulator.
- Increases energy expenditure and fatty acid oxidation in preclinical models.
- Provided in small-scale packaging suitable for bench research.
- Solid form recommended to be stored at 4°C; solutions should be stored frozen.
Medchemexpress LLC N-(4-((4-isopropylpiperazin-1-yl)sulfonylphenyl)-5-pentafluorophenyl)nicotinamide | 1803003-65-7 | 99.9% | 513.54 | 5 MG
RN-1665 is an orally active TRPV4 antagonist that exhibits excellent selectivity for related TRP receptors such as TRPV1, TRPV3, and TRPM8. RN-1665 is a TRPV4 probe for focus screens, with IC50s of 0.26 μM and 0.39 μM for hTRPV4 and rTRPV4 from human and rat, respectively.
- IC50 for human TRPV4 is 0.26 μM.
- IC50 for rat TRPV4 is 0.39 μM.
- Antagonist activity at human TRPV4 receptor expressed in HEK293 cells assessed as inhibition of EC80 of 4alpha-PDD-stimulated calcium flux after 10 minutes.
- Antagonist activity at rat TRPV4 receptor expressed in HEK293 cells assessed as inhibition of EC80 of 4alpha-PDD-stimulated calcium flux after 10 minutes.
- Pharmacokinetic analysis has been performed in Wistar rats.