
Biblioteca dei composti TCM
La Biblioteca dei Composti della Medicina Tradizionale Cinese (TCM) è una raccolta completa di composti bioattivi derivati da piante medicinali cinesi tradizionali. Questa biblioteca include una vasta gamma di composti con varie attività farmacologiche, come proprietà antinfiammatorie, antiossidanti, anticancro e antimicrobiche. I ricercatori utilizzano questa biblioteca per esplorare il potenziale terapeutico dei composti della TCM nella scoperta e nello sviluppo di farmaci. Presso CymitQuimica, offriamo l'accesso a una Biblioteca di Composti TCM di alta qualità per la ricerca in medicina naturale, farmacologia e scoperta di farmaci.
Trovati 507 prodotti di "Biblioteca dei composti TCM"
Ordinare per
Purezza (%)
0
100
|
0
|
50
|
90
|
95
|
100
N-Nitrosopyrrolidine-d8
CAS:Prodotto controllato<p>Applications N-Nitrosopyrrolidine-d8 (CAS# 1219802-09-1) is a useful isotopically labeled research compound.<br>References Persichetti, R. A., et al.: From PCT Int. Appl. (2010), WO 2010132810 A1 20101118<br></p>Formula:C42H8N2OColore e forma:YellowPeso molecolare:108.17N-Nitrosodiphenylamine
CAS:<p>Applications N-Nitrosodiphenylamine is the N-nitroso analogue of diphenylamine that was once used as a rubber additive but is no longer due to undesirable carcinogenic effects (1). N-Nitrosodiphenylamine may have potential carcinogenic activity and is currently classified as a probable carcinogen by EPA with genetic toxicity (2,3). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.<br>References 1. Boyland, D. et al.: Eur. J. Cancer. 1968. May;4(2):233-2342. Iversen, O. et al.: Eur. J. Cancer. 1980 May;16(5):695-8.3. McGregor, D. et al.: Mutat. Res. Rev. Gen. Toxicol. 1994 Jun:317(3):195-211<br></p>Formula:C12H10N2OColore e forma:Light GreenPeso molecolare:198.22N-Ethyl-N-nitroso-2-propanamine
CAS:Prodotto controllato<p>Stability Light Sensitive<br>Applications N-Ethyl-N-nitroso-2-propanamine is a building block used in synthesis of amino acids, peptides, and proteins.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Piotrowska, K., et al.: Synthetic Communications, Vol. 9, Issue 8 (1979);<br></p>Formula:C5H12N2OColore e forma:Light YellowPeso molecolare:116.1616N-Nitrosodipropylamine-d14
CAS:Prodotto controllatoFormula:C62H14N2OColore e forma:Colourless To Light YellowPeso molecolare:144.27Methylpropylnitrosamine
CAS:Prodotto controllato<p>Applications Methylpropylnitrosamine is used in biological studies as human liver microsomal cytochrome P-450 enzymes which are involved in the bioactivation of procarcinogens detected by umu gene response in Salmonella typhimurium TA 1535/pSK1002.<br>References Shimada, T., et al.: Cancer Res., 48, 3218 (1989);<br></p>Formula:C4H10N2OColore e forma:NeatPeso molecolare:102.14N-Nitrosodiisobutylamine
CAS:<p>Applications N-Nitrosodiisobutylamine is a nitrosoamine compound that shows carcinogenic effect.<br>References Scanlan, R., et al.: Cancer Res., 43, 2435 (1983), Spiegelhalder, B., et al.: Carcinogenesis, 4, 1147 (1983), Lijinsky, W., et al.: Mutat. Res., 443, 129 (1999), Robichova, S., et al.: Chem. Biol. Interact., 148, 163 (2004),<br></p>Formula:C8H18N2OColore e forma:NeatPeso molecolare:158.24N-Nitrosodiethylamine-d10 (1 mg/ml in Methanol)
CAS:Prodotto controllatoFormula:C42H10N2OColore e forma:ColourlessPeso molecolare:112.20N-Methyl-N’-nitrosopiperazine
CAS:Prodotto controllato<p>Stability Light Sensitive<br>Applications N-Methyl-N’-nitrosopiperazine was used as a reagent in the organic synthesis of several compounds including that of (4-methoxyphenoxy)acetic and (3,4,5-trimethoxyphenoxy)acetic acid amides and hydrazides which display antimicrobial and anthelmintic properties and may act as potential neurotropic and cardiovascular agents. N-Methyl-N’-nitrosopiperazine also diplayed strong nasal carcinogenity and genotoxicity toward nasal cells.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Valenta, V., et al.: Collect. Czech. Chem. C., 52, 3013 (1987); Klein, R., et al.: Carcinogenesis, 20, 1629 (1999);<br></p>Formula:C5H11N3OColore e forma:Colourless To Light YellowPeso molecolare:129.16N-Nitrosoethylmethylamine
CAS:Prodotto controllato<p>Applications One of the N-nitrosamines found in the water sources and water treatment process. Carcinogen.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Raska, I., et al.: Bioorg. Med. Chem., 13, 6830 (2005), Puzyn, T., et al.: Environ. Sci. Technol., 42, 5189 (2008),<br></p>Formula:C3H8N2OColore e forma:Colourless To Light YellowPeso molecolare:88.11N-Methyl-N’-nitrosopiperazine-d4
CAS:Prodotto controllato<p>Applications N-Methyl-N’-nitrosopiperazine-d4 is the isotope labelled analog of N-Methyl-N’-nitrosopiperazine (M325800), which is used as a reagent in the organic synthesis of several compounds including that of (4-methoxyphenoxy)acetic and (3,4,5-trimethoxyphenoxy)acetic acid amides and hydrazides which display antimicrobial and anthelmintic properties and may act as potential neurotropic and cardiovascular agents. N-Methyl-N’-nitrosopiperazine also diplayed strong nasal carcinogenity and genotoxicity toward nasal cells.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Valenta, V., et al.: Collect. Czech. Chem. C., 52, 3013 (1987); Klein, R., et al.: Carcinogenesis, 20, 1629 (1999);<br></p>Formula:C52H4H7N3OColore e forma:Light Yellow To OrangePeso molecolare:133.185N-Nitroso-Di-N-butylamine
CAS:Prodotto controllato<p>Stability Light Sensitive<br>Applications N-Nitroso-di-n-butylamine (cas# 924-16-3) is a compound useful in organic synthesis.<br></p>Formula:C8H18N2OColore e forma:Yellow-OrangePeso molecolare:158.24N-Nitrosoethylmethylamine-d3 (Major)
CAS:Prodotto controllato<p>Applications Labelled NEMA (N525950). One of the N-nitrosamines found in the water sources and water treatment process. Carcinogen.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Raska, I., et al.: Bioorg. Med. Chem., 13, 6830 (2005), Puzyn, T., et al.: Environ. Sci. Technol., 42, 5189 (2008),<br></p>Formula:C3D3H5N2OColore e forma:Light YellowPeso molecolare:91.13N-Nitrosodimethylamine-d6 (1 mg/mL in Methanol)
CAS:Prodotto controllato<p>Applications N-Nitrosodimethylamine-d6 (1.0 mg/mL in Methanol) is a highly toxic semi-volatile organic compound and a suspected human carcinogen. It induces liver tumors in rats after chronic exposure to low doses (1,2). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA). Environmental contaminants; Food contaminants.<br>References Chem. and Eng. News, p.5, Feb. 25, 2019<br></p>Formula:C2D6N2OColore e forma:Single SolutionPeso molecolare:80.12N-Nitrosopiperazine
CAS:<p>Stability Light Sensitive<br>Applications A carcinogenic nitrosocompound.<br>References Wong, H., et al.: Carcinogenesis, 24, 291<br></p>Formula:C4H9N3OColore e forma:Light YellowPeso molecolare:115.13N-Nitrosodiisobutylamine-d4
CAS:Prodotto controllato<p>Applications Labelled N-Nitrosodiisobutylamine (N525610). N-Nitrosodiisobutylamine is a nitrosoamine compound that shows carcinogenic effect.<br>References Scanlan, R., et al.: Cancer Res., 43, 2435 (1983), Spiegelhalder, B., et al.: Carcinogenesis, 4, 1147 (1983), Lijinsky, W., et al.: Mutat. Res., 443, 129 (1999), Robichova, S., et al.: Chem. Biol. Interact., 148, 163 (2004),<br></p>Formula:C8H14D4N2OColore e forma:NeatPeso molecolare:162.27

