Prenol lipids
Selleck Chemical LLC Linalool S4957-25mg
Linalool (Phantol) a monoterpene compound commonly found as major component of essential oils of several aromatic species is a competitive antagonist of NMDA receptors
Sigma Aldrich Fine Chemicals Biosciences L-Linalool natural, >=95%, FG | 126-91-0 | MFCD00135469 | 9KG
L-Linalool natural, >=95%, FG | Purity: >=95% | Mol Wt: 154.25 | 126-91-0 | MFCD00135469 | 9KG
Apexbio Technology LLC Linalool 78-70-6 20mg
Linalool (CAS 78-70-6) is a naturally occurring monoterpene alcohol predominantly isolated from Cinnamomum camphora (L ) Presl It exhibits modulatory effects on the central nervous system including interactions with neurotransmitter receptors such as GABA sub A /sub contributing to its observed anxiolytic and neuroprotective properties in preclinical studies Linalool is widely investigated for its potential anti-inflammatory antimicrobial and antioxidant activities Due to these diverse bioactivities it is utilized in biomedical research exploring therapeutic strategies for neurological disorders inflammation and microbial infections Store under sealed cool and dry conditions
Accela Chembio Inc MF: C33H49P | MW: 476.72 | ?97% | Flash Point: 317.7 celsius | BP: 569.8 celsius at 760 mmHg.
MF: C33H49P | MW: 476.72 | ?97% | Flash Point: 317.7 celsius | BP: 569.8 celsius at 760 mmHg.
Medchemexpress LLC (S)-Flurbiprofen | 51543-39-6 | C15H13FO2 | 100 MG
(S)-Flurbiprofen is an active enantiomer of Flurbiprofen, demonstrating IC50 values of 0.48 μM for COX-1 and 0.47 μM for COX-2. It effectively suppresses basal and stimulated PGE2 release in rat skin.
- Active enantiomer of Flurbiprofen
- COX inhibitor
- Inhibits COX-1 with an IC50 of 0.48 μM
- Inhibits COX-2 with an IC50 of 0.47 μM
- Suppresses PGE2 release
- Purity: 99.88%
- Ee.: 99.08%
- Appearance: Solid
- Color: White to off-white
Medchemexpress LLC (S)-Flurbiprofen | 51543-39-6 | C15H13FO2 | 500 MG
(S)-Flurbiprofen is an active enantiomer of Flurbiprofen, functioning as a COX inhibitor with IC50 values of 0.48 μM for COX-1 and 0.47 μM for COX-2.
- Purity of 99.88%
- Enantiomeric excess (ee.) of 99.08%
- Appears as a white to off-white solid
- Soluble in DMSO: 100 mg/mL (409.40 mM)
- Melting point: 109-110 °C
- Boiling point: 376.2 °C at 760 mmHg
- Suppresses basal and stimulated PGE2 release in rat skin
eMolecules 2-Isopropylbenzaldehyde | 6502-22-3 | MFCD06201222 | 25g
Oakwood Chemical | 2-Isopropylbenzaldehyde | 25g | 537680111 | 022363 | | 6502-22-3 | MFCD06201222 | 148.205 | C10H12O
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eMolecules Medchem Express / (S)-Flurbiprofen / 100mg / 532149379 / HY-15123 / / 51543-39-6 / MFCD00866152 / 244.265 / C15H13FO2
Medchem Express / (S)-Flurbiprofen / 100mg / 532149379 / HY-15123 / / 51543-39-6 / MFCD00866152 / 244.265 / C15H13FO2
![Strem, An Ascensus Company CAS# 52462-29-0. Di-μ-chlorobis[(p-cymene)chlororuthenium(II)], min. 98%. MFCD00064793. 25G.](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00009818-44-0190.25.JPG-250.jpg)
Strem, An Ascensus Company CAS# 52462-29-0. Di-μ-chlorobis[(p-cymene)chlororuthenium(II)], min. 98%. MFCD00064793. 25G.
CAS# 52462-29-0. 25G. Di-μ-chlorobis[(p-cymene)chlororuthenium(II)], min. 98%. MFCD00064793. Molecular Formula: C20H28Cl4Ru2. Molecular Weight: 612.39. Color/Form: brown pwdr. Strem#: 44-0190 www.strem.com/catalog/v3/44-0190/
eMolecules Ambeed / 2-Isopropylbenzoic Acid / 250mg / 515725949 / A921812 / / 2438-04-2 / MFCD00045836 / 164.204 / C10H12O2
Ambeed / 2-Isopropylbenzoic Acid / 250mg / 515725949 / A921812 / / 2438-04-2 / MFCD00045836 / 164.204 / C10H12O2
Medchemexpress LLC Genipin (Standard) | 6902-77-8 | 97.51% | 226.23 | 100 MG
Genipin (Standard) is the analytical standard of Genipin. This product is intended for research and analytical applications. Genipin is a natural crosslinking reagent derived from *Gardenia jasminoides* Ellis fruits. It inhibits UCP2 (uncoupling protein 2) in cells and has a variety of bioactivities, including modulation on proteins, antitumor, anti-inflammation, immunosuppression, antithrombosis, and protection of hippocampal neurons. It can also be used for type 2 diabetes research.
- Used as an analytical standard for qualitative, quantitative and methodological research experiments.
- Commonly used in HPLC, GC and MS.
Medchemexpress LLC Genipin | 6902-77-8 | MFCD00888600 | >98.0% | 226.23 | C11H14O5 | 10 MG
Genipin is a natural crosslinking reagent derived from Gardenia jasminoides fruits, commonly used in biochemical and materials research. It inhibits uncoupling protein 2 (UCP2) and displays bioactivities including protein modulation, anti-inflammatory, antitumor, immunosuppressive, and neuroprotective effects. Supplied as a high-purity solid suitable for analytical and research applications.
- Natural crosslinking reagent derived from Gardenia jasminoides.
- Inhibits uncoupling protein 2 (UCP2).
- Useful in research areas such as autophagy, metabolic, and neurological disease.
- Purity >98.0%.
- Molecular weight 226.23 g/mol.
- Light yellow to yellow solid powder appearance.
- Storage: powder -20°C (3 years) or 4°C (2 years).
- Available in small pack sizes including 10 mg for analytical use.
eMolecules Medchem Express / Ajugol / 5mg / 446275542 / HY-N0914 / / 52949-83-4 / MFCD28902296 / 348.348 / C15H24O9
Medchem Express / Ajugol / 5mg / 446275542 / HY-N0914 / / 52949-83-4 / MFCD28902296 / 348.348 / C15H24O9
Apexbio Technology LLC Catalpol 2415-24-9 20mg
Catalpol (2415-24-9) is a small-molecule modulator targeting adrenal cortical cells It is designed to stimulate steroidogenic pathways thereby promoting androgen hormone secretion Catalpol exerts its biological activity primarily through upregulation of steroid biosynthesis and inhibition of inflammatory mediators In in vitro experiments evaluating steroid hormone biosynthesis catalpol demonstrates an inhibitory activity profile against inflammatory mediators with an IC50 value ranging approximately from 10 to 50 M depending on assay conditions and cell models used Based on these pharmacological properties catalpol holds research potential in adrenal cortex function studies regulation of androgen synthesis pathways and investigations of anti-inflammatory mechanisms