Oxazoles
Medchemexpress LLC 4-Methoxyphenyl 3 4- | 5mg
4-Methoxyphenyl 3 4-O-isopropylidene- -d-Galactopyranoside is a class of biochemical reagents used for the study of glycobiology Glycobiology studies the structure synthesis biology and evolution of sugars It deals with carbohydrate chemistry glycan formation and degradation enzymology protein-glycan recognition and the role of glycans in biological systems The field is closely related to basic research biomedicine and biotechnology[1]
Apexbio Technology LLC Y-27632 146986-50-7 200mg
Y-27632 (CAS 146986-50-7) is a selective inhibitor of Rho-associated protein kinases (ROCK) specifically targeting ROCK1 and ROCK2 isoforms It competitively binds to the ATP-binding site inhibiting ROCK1 and ROCK2 with Ki values of 0 22 M and 0 30 M respectively Compared to other kinases such as citron kinase PKN and PKC Y-27632 exhibits significantly higher selectivity toward ROCK isoforms In cellular assays Y-27632 at 10 M concentration effectively disrupts stress fiber formation in Swiss 3T3 fibroblast cells It is widely used in cell biology research to study ROCK signaling pathways and cytoskeletal dynamics
Medchemexpress LLC Y-27632 dihydrochloride | 129830-38-2 | MFCD03490488 | 99.9% | 320.26 g/mol | C14H23Cl2N3O | 50 MG
Y-27632 dihydrochloride is an ATP-competitive inhibitor of Rho-associated protein kinases (ROCK I and II) used in cellular and pharmacological research to modulate ROCK signaling. Supplied as a high-purity solid, it is commonly used in cell signaling studies, pharmacodynamic assays, and stem cell culture applications that require ROCK pathway inhibition.
- ATP-competitive inhibitor of ROCK I and II with reported activity in the low hundreds of nanomolar range.
- High purity suitable for research applications.
- Solid form for easy handling and storage.
- Available in research-scale package sizes for laboratory use.
- Applicable to cell signaling, pharmacology, and stem cell culture studies.
Medchemexpress LLC Y-27632 dihydrochloride | 129830-38-2 | MFCD03490488 | 99.9% | 320.26 | C14H23Cl2N3O | 100 MG
Y-27632 dihydrochloride is an ATP-competitive inhibitor of Rho-associated kinases (ROCK) used as a research reagent in cell biology and pharmacology studies. It is orally active and has documented kinase selectivity and potency.
- ATP-competitive inhibitor of ROCK-I and ROCK-II.
- Orally active compound with reported antiepileptic effects.
- Reported Ki values: ROCK-I 220 nM, ROCK-II 300 nM.
- High reported purity (≈99.94%).
- Available in multiple solid pack sizes and bulk by inquiry.
BIOHIPPO AAV-hSyn-XCaMP-Y-WPRE-hGH-polyA
Recombinant adeno associated virus expressing XCaMP-Y under the hSyn promoter with WPRE and hGH polyA elements. Offered under the Biohippo AAVX Series with multiple serotypes available including AAV2/1, AAV2/2, AAV2/5, AAV2/6, AAV2/6m, AAV2/6.2FF, AAV2/7m8, AAV2/8, AAV2/9, AAV2/DJ, AAV2/DJ8, AAV2/Retro, AAV2/PHP.eB, AAV2/PHP.B, AAV2/rh10, AAV2/PHP.S, AAV2/anc80, AAV2/B10, AAV2/olig001, AAV2/BI30, AAV2/BR1, AAV2/MG1.2, AAV1/2, AAV2/MaCPNS1, and AAV2/MaCPNS2. Regular titer is greater than or equal to 2.00E+12 vg per mL, with high titer greater than or equal to 1.00E+13 vg per mL available upon request at no additional cost. Customers may specify preferred serotype and titer when placing orders.
![Medchemexpress LLC 5-[(3S)-3-hydroxy-4-phenyl-1-buten-1-yl]1-[6-(2H-tetrazol-5R-yl)hexyl]-2-pyrrolidinone | 346673-06-1 | MFCD18384961 | >98.0% | 383.5 g/mol | C21H29N5O2 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000263817.png-250.jpg)
Medchemexpress LLC 5-[(3S)-3-hydroxy-4-phenyl-1-buten-1-yl]1-[6-(2H-tetrazol-5R-yl)hexyl]-2-pyrrolidinone | 346673-06-1 | MFCD18384961 | >98.0% | 383.5 g/mol | C21H29N5O2 | 5 MG
CAY10598 (TCS 2510) is a potent, selective agonist of the prostaglandin E2 EP4 receptor supplied for research use only. It activates EP4 signaling and elevates intracellular cAMP, making it a useful pharmacological tool to probe EP4-mediated pathways in inflammation, metabolic disease, bone healing, and cardiovascular research. Reported properties include Ki ≈ 1.2 nM, molecular weight 383.5 g/mol, and typical purity ≥98%.
- Selective EP4 receptor agonist.
- Potent EP4 binding (Ki ≈ 1.2 nM).
- High purity ≥98%.
- Elevates intracellular cAMP in target cells.
- Useful for inflammation and metabolic disease research.
- Supplied as a solid for in vitro and in vivo studies; store at -20 °C.
Medchemexpress LLC 2-Methoxyphenyl dihydrouracil | 2377643-33-7 | 95.1% | 264.23 g/mol | C12H12N2O5 | 5 G
2-Methoxyphenyl dihydrouracil is a small-molecule cereblon (CRBN) ligand used as a synthetic building block in targeted protein degradation research. It is supplied as a purified solid with characterized molecular formula C12H12N2O5 and molecular weight 264.23 g/mol, and is accompanied by analytical documentation and recommended cold, light-protected storage to preserve stability.
- CRBN ligand useful for PROTAC synthesis
- High purity for research applications
- Available in multiple quantities including 5 g
- Supplied with certificate of analysis
- Stable when stored refrigerated and protected from light