
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.
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5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiesta(R)-N-(2-hydroxy-2-phenylethyl)-N-(4-nitrophenethyl) Nitrous Amide
Formula:C16H17N3O4Peso molecolare:315.33Ref: 4Z-N-103068
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-N-103051
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5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaN-Nitroso-N-methyl-4-aminobutyric Acid-d3 (1.25 mg/mL in Methanol)
CAS:Prodotto controllatoFormula:C52H3H9N2OColore e forma:ColourlessPeso molecolare:119.18N-Nitrosodiethylamine-d10
CAS:Prodotto controllato<p>Applications N-Nitrosodiethylamine-d10 is a labelled form of N-Nitrosodiethylamine (N525465) which is a widely occurring nitrosamine that is one of the most important environmental carcinogens primarily inducing tumors of liver.NDMA and NDEA were found as an impurity in generic versions of valsartan, losartan and irbesartan.<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 Oda, Y., et al.: Mutation Research, Genetic Toxicology and Environmental Mutagenesis, 584, 1 (2005); Yamazaki, H., et al.: Carcinogenesis, 13, 1789 (1992);Chem. and Eng. News, p.5, Feb. 25, 2019<br></p>Formula:C42H10N2OColore e forma:Colourless To YellowPeso molecolare:112.20N-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-Nitrosodicyclohexylamine
CAS:<p>Applications A novel anti-androgenic compound. A carcinogenic agent.<br>References Singer, G., et al.: Chem-Biol. Interact.,19, 133 (1977), Chou, J., et al.: J. Med. Chem., 22, 792 (1979), Dunn, W., et al.: Bioorg. Chem., 10, 29 (1981), Basak, S., et al.: J. Pharm. Sci., 73, 429 (1984),<br></p>Formula:C12H22N2OColore e forma:Off WhitePeso molecolare:210.32(4R)-N-Nitroso Thiazolidine-4-carboxylic Acid
CAS:Prodotto controllato<p>Applications A chiral N-nitroso compound formed in smoke food (smoked bacon, smoked Swiss cheese, smoke flavoring). A carcinogenic compound.<br>References Lu, S, et al.: Cancer Res., 46, 1485 (1986), Ikins, W.G., et al.: Food Chem. Toxicol., 26, 15 (1988), Kodama, M., et al.: Anticancer Res. 12, 1671 (1992), Ferguson, L., et al.: Mutat Res., 443, 1 (1999),<br></p>Formula:C4H6N2O3SColore e forma:NeatPeso molecolare:162.17N-Nitrosodibenzylamine
CAS:Prodotto controllato<p>Applications N-Nitrosodibenzylamine (NDBzA) is mutagenic to Salmonella typhimurium and induces DNA strand breaks in isolated rat hepatocytes.<br>References Dunn, W., et al.: Bioorg. Chem., 10, 29 (1981), Rose, S., et al.: J. Med. Chem., 25, 769 (1982), Basak, S., et al.: J. Pharm. Sci., 73, 429 (1984), Zielenska, M., et al.: Mutation Res., 180, 11 (1987),<br></p>Formula:C14H14N2OColore e forma:Light YellowPeso molecolare:226.27N-Nitroso-N-methylaniline
CAS:Prodotto controllato<p>Applications N-Nitroso-N-methylaniline is used in the preparation of resin.<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 Miura, K., et al.: Jpn. Kokai Tokkyo Koho (2020), JP 2020029543 A<br></p>Formula:C7H8N2OColore e forma:YellowPeso molecolare:136.15N-Nitroso-L-hydroxyproline
CAS:Prodotto controllatoFormula:C5H8N2O4Colore e forma:Light BrownPeso molecolare:160.13N-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:162.27N-Nitroso-L-proline
CAS:Prodotto controllato<p>Applications A nitrosoamino acid with oncogenic activity. The LD50 of a single ip dose given to Swiss-Webster mice is 203 +/- 22 mg / kg.<br>References Nagasawa, H.T., et al.: J. Med. Chem., 16 (5), 583-585 (1973)<br></p>Formula:C5H8N2O3Colore e forma:Yellow BrownPeso molecolare:144.13N-Nitroso-di-n-butylamine-d18
CAS:Prodotto controllatoFormula:C82H18N2OColore e forma:Colourless To YellowPeso molecolare:176.351-Nitrosopyrrolidine
CAS:Prodotto controllatoFormula:C4H8N2OColore e forma:Light Yellow To YellowPeso molecolare:100.12N-Nitrososarcosine
CAS:Prodotto controllato<p>Applications A carcinogenic compound.<br>References Lu, S., et al.: Cancer Res., 46, 1485 (1986), Tricker, A., et al.: Eur. J. Cancer Prev., 6, 226 (1997),<br></p>Formula:C3H6N2O3Colore e forma:White To Light YellowPeso molecolare:118.09N-Nitrosopiperidine
CAS:<p>Applications A carcinogenic nitrosocompound.<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 Bos, J., et al.: Cancer Res., 49, 4682 (1989), Wong, H., et al.: Carcinogenesis, 24, 291 (2003), Gonzalez-Mancebo, S., et al.: Mutat. Res., 558, 45 (2004), Gonzalez, M., et al.: Bioorg. Med. Chem., 13, 601 (2005),<br></p>Formula:C5H10N2OColore e forma:Light Yellow To YellowPeso molecolare:114.15N-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-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-tert-Butyl-N-ethylnitrosamine
CAS:Prodotto controllato<p>Applications N-tert-Butyl-N-ethylnitrosamine is a tyrosinase inhibitor and a possible carcinogen.<br>References Yuan, Jintao, et al.: Chem. Res. in Toxic., 24(12), 2269-2279 (2011);Ponce, Yovani M., et al.: QSAR & Combi. Sci., 26(4), 469-487 (2007)<br></p>Formula:C6H14N2OColore e forma:NeatPeso molecolare:130.19N-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-Nitrosodimethylamine-d6 (1 mg/mL in Ethanol)
CAS:Prodotto controllatoFormula:C2D6N2OColore e forma:Single SolutionPeso molecolare:80.12N-Nitrosodiethylamine-d10 (1 mg/ml in Methanol)
CAS:Prodotto controllatoFormula:C42H10N2OColore e forma:ColourlessPeso molecolare:112.20N-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-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
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-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-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-Nitroso-2-methylthiazolidine 4-Carboxylic Acid
CAS:Prodotto controllatoFormula:C5H8N2O3SColore e forma:Light BrownPeso molecolare:176.19N-Nitrosodiethylamine-d4
CAS:Prodotto controllato<p>Stability Light Sensitive<br>Applications Isotope labelled N-Nitrosodiethylamine (N525465) (DEN) is a widely occurring nitrosamine that is one of the most important environmental carcinogens (1) primarily inducing tumors of liver (2,3). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.NDMA and NDEA were found as an impurity in generic versions of valsartan, losartan and irbesartan.<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 1. Farber, E. et al.: Cancer Res. 1984 Oct;44(10):4217-23.2. el-Demerdash, E. et al.: Anticancer Res. 2002 Mar-Apr;22(2A):977-84.3. Kweon, S. et al.: Life Sci. 2003 Sep 26;73(19):2515-26.<br></p>Formula:C42H4H6N2OColore e forma:Colourless To YellowPeso molecolare:106.16



