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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
9 Results for "
photoisomerization
" in MedChemExpress (MCE) Product Catalog:
Products (9)
9 Results for "photoisomerization" in MCE Product Catalog:
3
3 Cited Publications
Cat. No.: HY-W004500
CAS No.: 116-31-4
Category:
Human Gut Microbiota Metabolites Microorganisms Terpenoids Other Diseases Diterpenoids Endogenous metabolite Disease Research Fields
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1
1 Cited Publications
Cat. No.: HY-D0823
CAS No.: 146368-16-3
Synonyms: Sulfo-Cy3 NHS ester; Sulfo Cyanine3 NHS ester
Cat. No.: HY-D0485
CAS No.: 12224-02-1
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Research Areas:
Fluorescent brightener 24 is a stilbene-type fluorescent brightener and fading regulator .
Cat. No.: HY-126749
CAS No.: 2223027-70-9
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Research Areas:
VUF14738 (compound 28) is a bidirectional photoswitch antagonist that can rapidly and reversibly photoisomerize at the histamine H3 receptor, with binding affinity increased or decreased upon illumination, and can be used in real-time electrophysiological experiments to study the activity of dynamic light modulation of receptor activation.
Cat. No.: HY-121143
CAS No.: 73711-18-9
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Research Areas:
Bis-Q is an acetylcholine (ACh) agonist that targets voltage-clamped muscle fibers of the fish Xenomystus nigris. Bis-Q exists in two forms: cis-Bis-Q (non-agonist) and trans-Bis-Q (agonist). Photoisomerization converts cis-Bis-Q to trans-Bis-Q, which induces agonist-induced currents. Channels activated by trans-Bis-Q and ACh have similar conductances and open times. Flashes increase the ratio of trans-Bis-Q to cis-Bis-Q until light equilibrium is reached. Further flashes transiently increase agonist-induced currents, indicating binding of trans-Bis-Q to desensitized receptors. Higher concentrations of cis-Bis-Q produce larger agonist-induced currents that decay exponentially. .
Cat. No.: HY-Z1074
CAS No.: 21307-05-1
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Research Areas:
Previtamin D2 is a precursor to Vitamin D2 (ergocalciferol) , formed through the photoisomerization of ergosterol, a compound found in fungi and some plants. Exposure to ultraviolet (UV) light triggers the conversion of ergosterol to previtamin D2, which then rapidly isomerizes to vitamin D2.
Cat. No.: HY-W753500
CAS No.: 54664-98-1
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Cat. No.: HY-N17441
CAS No.: 78259-41-3
Target:
Cat. No.: HY-N21835
CAS No.: 11096-49-4
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
