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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
21 Results for "
trans-to-cis photoisomerization
" in MedChemExpress (MCE) Product Catalog:
Products (21)
21 Results for "trans-to-cis 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
Target:
1
1 Cited Publications
Cat. No.: HY-D0823
CAS No.: 146368-16-3
Synonyms: Sulfo-Cy3 NHS ester; Sulfo Cyanine3 NHS ester
1
1 Cited Publications
Synonyms: trans-10,cis-12 CLA2
Research Areas:
(10E,12Z)-Octadeca-10,12-dienoic acid (trans-10,cis-12 CLA2) is an orally active PPARα activator and inhibits adipocyte differentiation. (10E,12Z)-Octadeca-10,12-dienoic acid and its downstream metabolites have various antioxidant and antitumor activities. (10E,12Z)-Octadeca-10,12-dienoic acid can induce proinflammatory cytokines and chemokines, which would lead to decreased adipogenesis and insulin resistance in adipose tissue. (10E,12Z)-Octadeca-10,12-dienoic acid can affect many aspects of milk fat synthesis. (10E,12Z)-Octadeca-10,12-dienoic acid reduces expression of lipogenic enzymes and inhibits the desaturation of fatty acids. (10E,12Z)-Octadeca-10,12-dienoic acid can reduce lipoprotein lipase (LPL) activity in cultured 3T3-L1 adipocytes and enhance triacylglycerol release from these cells. (10E,12Z)-Octadeca-10,12-dienoic acid decreases the expression of hepatic stearoyl-CoA desatyrase mRNA in mice. (10E,12Z)-Octadeca-10,12-dienoic acid is associated with changes in mucosal NF-κB and Cyclin D1 protein levels in mice .
Cat. No.: HY-W127515
CAS No.: 557-48-2
Synonyms: Violet leaf aldehyde
Cat. No.: HY-117583A
CAS No.: 1628784-54-2
Target:
Research Areas:
BG47 is a prototypical histone deacetylases HDAC1 and HDAC2 selective, optoepigenetic probe. BG47 can bind to and competitively inhibits the deacetylase activity of HDAC targets upon a light-induced trans-to-cis isomerization, and increases Histone Methyltransferase H3K9 acetylation. BG47 can be used for neurological disease research .
Cat. No.: HY-117583
Purity: 98.02%
Target:
Research Areas:
cis-BG47 is an cis-isomer of BG47, BG47 is a prototypical histone deacetylases HDAC1 and HDAC2 selective, optoepigenetic probe. BG47 can bind to and competitively inhibits the deacetylase activity of HDAC targets upon a light-induced trans-to-cis isomerization, and increases Histone Methyltransferase H3K9 acetylation. cis-BG47 can be used for neurological disease research .
Cat. No.: HY-W127515S
CAS No.: 1083053-38-6
Synonyms: Violet leaf aldehyde-13C2
Cat. No.: HY-167579
CAS No.: 955920-48-6
Cat. No.: HY-CE00760
CAS No.: 79315-17-6
Synonyms: 2,4-Decadienoyl-coenzyme A
Target:
Research Areas:
2-trans-4-cis-Decadienoyl-CoA (2,4-Decadienoyl-coenzyme A) is an unsaturated fatty acyl-CoA.
Cat. No.: HY-126749
CAS No.: 2223027-70-9
Target:
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
Target:
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-W127515R
CAS No.: 557-48-2
Synonyms: Violet leaf aldehyde (Standard)
Cat. No.: HY-W769547
Cat. No.: HY-CE02001
Synonyms: trans,cis,cis-2,11,14-Eicosatrienoyl-coenzyme A
Target:
Research Areas:
trans,cis,cis-2,11,14-Eicosatrienoyl-CoA (trans,cis,cis-2,11,14-Eicosatrienoyl-coenzyme A) is a coenzyme A derivative .
Cat. No.: HY-CE02000
Synonyms: trans,cis,cis,cis-2,10,13,16-Docosatetraenoyl-coenzyme A
Target:
Research Areas:
trans,cis,cis,cis-2,10,13,16-Docosatetraenoyl-CoA (trans,cis,cis,cis-2,10,13,16-Docosatetraenoyl-coenzyme A) is a coenzyme A derivative .
Cat. No.: HY-CE01929
Synonyms: trans,cis,cis,cis,cis-2,10,13,16,19-Docosapentaenoyl-coenzyme A
Target:
Research Areas:
trans,cis,cis,cis,cis-2,10,13,16,19-Docosapentaenoyl-CoA (trans,cis,cis,cis,cis-2,10,13,16,19-Docosapentaenoyl-coenzyme A) is a coenzyme A derivative .
Cat. No.: HY-CE01999
Synonyms: trans,cis,cis,cis,cis-2,12,15,18,21-Tetracosapentaenoyl-coenzyme A
Target:
Research Areas:
trans,cis,cis,cis,cis-2,12,15,18,21-Tetracosapentaenoyl-CoA (trans,cis,cis,cis,cis-2,12,15,18,21-Tetracosapentaenoyl-coenzyme A) is a coenzyme A derivative .
Cat. No.: HY-CE00008
Synonyms: (2-trans,6-cis)-dodeca-2,6-dienoyl-coenzyme A
Target:
Research Areas:
(2-Trans,6-cis)-dodeca-2,6-dienoyl-CoA ((2-Trans,6-cis)-dodeca-2,6-dienoyl-coenzyme A) is an unsaturated fatty acyl-CoA.
Cat. No.: HY-E72040
Target:
Research Areas:
Abequosyltransferase (EC 2.4.1.60) is a transferase that can convert CDP-alpha-D-abequose and alpha-D-Man-(1->4)-alpha-L-Rha-(1->3)-alpha-D-Gal-di-trans,octa-cis-undecaprenyl diphosphate into alpha-D-Abe-(1->3)-alpha-D-Man-(1->4)-alpha-L-Rha-(1->3)-alpha-D-Gal-di-trans,octa-cis-undecaprenyl diphosphate, CDP and H +.
Cat. No.: HY-Z1074
CAS No.: 21307-05-1
Target:
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.
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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
