Category: 316-41-6

Hu, Yujie et al. published their research in Nongyao in 2012 | CAS: 316-41-6

9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) (cas: 316-41-6) belongs to isoquinoline derivatives. Quinoline and its derivatives are widely used as fungicides, biological agents, antibiotics, alkaloids, dyes, rubber chemicals and flavoring agents. It protonates to form salts upon treatment with strong acids, such as HCl. It forms adducts with Lewis acids, such as BF3.Application of 316-41-6

Bioactivity evaluation of berberine sulfate on Microcystis aeruginosa was written by Hu, Yujie;Ni, Hanwen. And the article was included in Nongyao in 2012.Application of 316-41-6 This article mentions the following:

The inhibitory effect of berberine sulfate was evaluated on a kind of bloom-forming cyanophyta (Microcystis aeruginosa). The biomass reduction was obtained by measuring the optical d. and the chlorophyll-a content of the algal solution The EC50 values of berberine sulfate on M. aeruginosa were 1.627 and 0.851 mg a. i. /L resp. according to the above two methods. These results indicated that berberine sulfate had effective inhibition on the growth of M. aeruginosa. In the experiment, the researchers used many compounds, for example, 9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) (cas: 316-41-6Application of 316-41-6).

9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) (cas: 316-41-6) belongs to isoquinoline derivatives. Quinoline and its derivatives are widely used as fungicides, biological agents, antibiotics, alkaloids, dyes, rubber chemicals and flavoring agents. It protonates to form salts upon treatment with strong acids, such as HCl. It forms adducts with Lewis acids, such as BF3.Application of 316-41-6

Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem

 

Hu, Yujie et al. published their research in Nongyao in 2012 | CAS: 316-41-6

9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) (cas: 316-41-6) belongs to isoquinoline derivatives. Quinoline and its derivatives are widely used as fungicides, biological agents, antibiotics, alkaloids, dyes, rubber chemicals and flavoring agents. It protonates to form salts upon treatment with strong acids, such as HCl. It forms adducts with Lewis acids, such as BF3.Application of 316-41-6

Bioactivity evaluation of berberine sulfate on Microcystis aeruginosa was written by Hu, Yujie;Ni, Hanwen. And the article was included in Nongyao in 2012.Application of 316-41-6 This article mentions the following:

The inhibitory effect of berberine sulfate was evaluated on a kind of bloom-forming cyanophyta (Microcystis aeruginosa). The biomass reduction was obtained by measuring the optical d. and the chlorophyll-a content of the algal solution The EC50 values of berberine sulfate on M. aeruginosa were 1.627 and 0.851 mg a. i. /L resp. according to the above two methods. These results indicated that berberine sulfate had effective inhibition on the growth of M. aeruginosa. In the experiment, the researchers used many compounds, for example, 9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) (cas: 316-41-6Application of 316-41-6).

9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) (cas: 316-41-6) belongs to isoquinoline derivatives. Quinoline and its derivatives are widely used as fungicides, biological agents, antibiotics, alkaloids, dyes, rubber chemicals and flavoring agents. It protonates to form salts upon treatment with strong acids, such as HCl. It forms adducts with Lewis acids, such as BF3.Application of 316-41-6

Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem

 

Khadzhiolov, A. I. et al. published their research in Archives de l’Union Medicale Balkanique et Bulletin de l’Union Medicale Balkanique in 1974 | CAS: 316-41-6

9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) (cas: 316-41-6) belongs to isoquinoline derivatives. Quinoline is a catabolite of tryptophan, the basic structure of some antihypertensive drugs, such as the peripheral vasodilators prazosin and doxazosin. The Pomeranz鈥揊ritsch reaction provides a method for the preparation of isoquinoline. This reaction uses a benzaldehyde and aminoacetoaldehyde diethyl acetal, which in an acid medium react to form isoquinoline.Quality Control of 9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1)

Fluorescent cytochemistry of nucleus and chromosomes after fluorine chromization with berberine sulfate was written by Khadzhiolov, A. I.;Tsvetkova, E.;Vulkov, I.;Gitsov, L.;Cholakova, I.;Marinov, M.;Tsvetkov, I.. And the article was included in Archives de l’Union Medicale Balkanique et Bulletin de l’Union Medicale Balkanique in 1974.Quality Control of 9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) This article mentions the following:

F chromization with berberine sulfate was performed on blood cells, cells from lymphatic nodes, and chromosome preparations Chromatin acquired a brilliant golden yellow color. There were regions in the nodes or even entire nodes almost completely without fluorescence; these were assumed to be undifferentiated or neoplastic cells containing a large amount of euchromatin. Similar differences in the fluorescence of deoxynucleoprotein complexes were observed in metaphasic and meiotic chromosomes. The regions with an intense golden yellow coloration probably corresponded to the localization of satellite or repetitive DNA. It was possible to distinguish quant. between active and nonactive DNA chromatin. In the experiment, the researchers used many compounds, for example, 9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) (cas: 316-41-6Quality Control of 9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1)).

9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) (cas: 316-41-6) belongs to isoquinoline derivatives. Quinoline is a catabolite of tryptophan, the basic structure of some antihypertensive drugs, such as the peripheral vasodilators prazosin and doxazosin. The Pomeranz鈥揊ritsch reaction provides a method for the preparation of isoquinoline. This reaction uses a benzaldehyde and aminoacetoaldehyde diethyl acetal, which in an acid medium react to form isoquinoline.Quality Control of 9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1)

Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem

 

Szokol, Miklos et al. published their research in Kiserletes Orvostudomany in 1971 | CAS: 316-41-6

9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) (cas: 316-41-6) belongs to isoquinoline derivatives. Being an analog of pyridine, isoquinoline is a weak base, with a pKa of 5.14. Other industrial applications include their use as corrosion inhibitors, preservatives, and as solvents for resins and terpenes.Name: 9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1)

Fluorochrome staining of granular cells of the juxtaglomerular apparatus was written by Szokol, Miklos. And the article was included in Kiserletes Orvostudomany in 1971.Name: 9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) This article mentions the following:

Exptl. results with kidney sections of male and female albino mice and albino Wistar rats showed that in addition to the known Thioflavine T, Aurophosphine, Auramine O, berberine sulfate, acridine orange, and Thioflavine S are also suitable for the fluorochrome staining of granular cells of the juxtaglomerular apparatus. Also, a number of other tested stains were listed which gave weaker effects. Lipofuscin grains in the arterioles of human kidney were stained only very slightly by these fluorochromes, and can thus be sharply distinguished from the intensive secondary fluorescence of the specific juxtaglomerular granules. Optimum staining effect with 1% solutions was obtained in 3-8 min, and with 0.1-0.01% solutions in 15-30 min. Advantage of using fluorochromes over the light microscope is the quickness and simpleness of method, and the visibility of stains even at lower magnification. Further, just the specific juxtaglomerular granules are stained intensively by the tested fluorochromes. In the experiment, the researchers used many compounds, for example, 9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) (cas: 316-41-6Name: 9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1)).

9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1) (cas: 316-41-6) belongs to isoquinoline derivatives. Being an analog of pyridine, isoquinoline is a weak base, with a pKa of 5.14. Other industrial applications include their use as corrosion inhibitors, preservatives, and as solvents for resins and terpenes.Name: 9,10-Dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium sulfate(2:1)

Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem