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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
69 Results for "
singlet
" in MedChemExpress (MCE) Product Catalog:
Products (69)
69 Results for "singlet" in MCE Product Catalog:
30
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22
8
8
8 Cited Publications
Cat. No.: HY-15930A
CAS No.: 64285-73-0
Synonyms: BM blue dihydrochloride; Sure Blue TMB dihydrochloride
8
8 Cited Publications
Cat. No.: HY-15930B
CAS No.: 207738-08-7
Synonyms: Sure Blue TMB dihydrochloride x.hydrate
8
8 Cited Publications
Cat. No.: HY-15930C
CAS No.: 54827-18-8
Synonyms: BM blue monosulfate; Sure Blue TMB monosulfate
4
3
3
3 Cited Publications
Hematoporphyrin monomethyl ether, second generation of porphyrin-related photosensitizer, is characterized by its single form, high yield of singlet oxygen, high selectivity, and low toxicity, which has been widely used in the diagnosis and research of various tumors, including lung cancer, bladder cancer, and nevus flammeus and brain glioma .
2
2 Cited Publications
Synonyms: 4',7-Dimethoxy-5-Hydroxyflavone
Category:
other families Flavonoids Monophenols Flavones Phenols Plants Disease Research Fields Inflammation/Immunology
Target:
1
1 Cited Publications
Cat. No.: HY-B2130S1
CAS No.: 62948-75-8
Cat. No.: HY-169798
CAS No.: 23481-50-7
Target:
Research Areas:
1,9-Dimethylmethylene blue is a photosensitizer, virus inactivator and hemoglobin oxidant derived from methylene blue. When activated, 1,9-Dimethylmethylene blue generates reactive oxygen species including singlet oxygen, and acts as a metachromatic dye. When activated in monomeric or dimeric form, 1,9-Dimethylmethylene blue induces photoinactivation of R17 phage and vesicular stomatitis virus and oxidizes hemoglobin via non-singlet oxygen reactive oxygen species or singlet oxygen-mediated pathways, respectively. The monomeric form, with higher nucleic acid affinity, achieves virus inactivation under specific conditions without forming methemoglobin. 1,9-Dimethylmethylene blue binds to substances such as glycosaminoglycans to produce color changes. Although it is susceptible to interference from non-glycosaminoglycan components in urine, it is still applicable to spectrophotometric analysis for glycosaminoglycan quantification. With these unique photochemical and binding properties, 1,9-Dimethylmethylene blue is widely used in studies of viral infections and related biochemical analyses .
Cat. No.: HY-126956
CAS No.: 70579-26-9
Cat. No.: HY-W014423S2
CAS No.: 201740-88-7
Synonyms: H-His-OH-13C6 hydrochloride hydrate
Cat. No.: HY-B2130S
CAS No.: 2421217-23-2
Cat. No.: HY-W021358
CAS No.: 100-22-1
Target:
Research Areas:
N,N,N′,N′-Tetramethyl-p-phenylenediamine is an electron-donating aromatic diamine with a low ionization potential. N,N,N′,N′-Tetramethyl-p-phenylenediamine is a classic electron donor model compound for photochemical electron transfer studies .
Cat. No.: HY-W038786
CAS No.: 527-60-6
Cat. No.: HY-W014423S3
CAS No.: 202468-43-7
Synonyms: H-His-OH-13C6,15N3 hydrochloride hydrate
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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
