Esta buscando: Daunorubicin+hydrochloride

Proveedor: TCI

Descripción: Daunorubicin hydrochloride ≥98.0% (by total nitrogen basis)

Certificados

Numero del catalogo: (ENZOALX380043M010)

Proveedor: ENZO LIFE SCIENCES

Descripción: Antitumor antibiotic.

UOM: 1 * 10 mg

New Product Promoción

Numero del catalogo: (1164700.)

Proveedor: USP

Descripción: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

UOM: 1 * 200 mg

Promoción

Numero del catalogo: (ENZOALX380260M005)

Proveedor: ENZO LIFE SCIENCES

Descripción: More potent, lipophilic and antineoplastic analog of daunorubicin. DNA-damaging effect includes DNA oxidation and methylation, DNA intercalation, inhibition of DNA synthesis, induction of DNA strand breaks and delay of cell cycle progression. Inhibitor of topoisomerase IIα. Produces endonucleolytic cleavage and is a marker of apoptosis.

UOM: 1 * 5 mg

New Product Promoción

Proveedor: MP Biomedicals

Descripción: Soluble in water, methanol, aqueous alcohols. Practically insoluble in chloroform, ether, benzene.

Numero del catalogo: (BOSSBS-7953R-A680)

Proveedor: Bioss

Descripción: Catalyzes the NADPH-dependent reduction of a variety of aromatic and aliphatic aldehydes to their corresponding alcohols. Catalyzes the reduction of mevaldate to mevalonic acid and of glyceraldehyde to glycerol. Has broad substrate specificity. In vitro substrates include succinic semialdehyde, 4-nitrobenzaldehyde, 1,2-naphthoquinone, methylglyoxal, and D-glucuronic acid. Plays a role in the activation of procarcinogens, such as polycyclic aromatic hydrocarbon trans-dihydrodiols, and in the metabolism of various xenobiotics and drugs, including the anthracyclines doxorubicin (DOX) and daunorubicin (DAUN).

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (ENZOBMLPI1100010)

Proveedor: ENZO LIFE SCIENCES

Descripción: A potent irreversible mechanism based serine protease inhibitor. Inhibits granzymes A, B, and H, cathepsin G, neutrophil elastase and proteinase 3. Inhibits activation of neutral sphingomyelinase and apoptosis triggered by daunorubicin as well as camptothecin-induced apoptosis in HL-60 cells. Inhibits migration of eosinophils through basement membrane components in vitro.

UOM: 1 * 10 mg

New Product Promoción

Numero del catalogo: (BOSSBS-7953R-HRP)

Proveedor: Bioss

Descripción: Catalyzes the NADPH-dependent reduction of a variety of aromatic and aliphatic aldehydes to their corresponding alcohols. Catalyzes the reduction of mevaldate to mevalonic acid and of glyceraldehyde to glycerol. Has broad substrate specificity. In vitro substrates include succinic semialdehyde, 4-nitrobenzaldehyde, 1,2-naphthoquinone, methylglyoxal, and D-glucuronic acid. Plays a role in the activation of procarcinogens, such as polycyclic aromatic hydrocarbon trans-dihydrodiols, and in the metabolism of various xenobiotics and drugs, including the anthracyclines doxorubicin (DOX) and daunorubicin (DAUN).

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-7953R-A750)

Proveedor: Bioss

Descripción: Catalyzes the NADPH-dependent reduction of a variety of aromatic and aliphatic aldehydes to their corresponding alcohols. Catalyzes the reduction of mevaldate to mevalonic acid and of glyceraldehyde to glycerol. Has broad substrate specificity. In vitro substrates include succinic semialdehyde, 4-nitrobenzaldehyde, 1,2-naphthoquinone, methylglyoxal, and D-glucuronic acid. Plays a role in the activation of procarcinogens, such as polycyclic aromatic hydrocarbon trans-dihydrodiols, and in the metabolism of various xenobiotics and drugs, including the anthracyclines doxorubicin (DOX) and daunorubicin (DAUN).

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (PRSI79-673)

Proveedor: ProSci Inc.

Descripción: Xenobiotic transporter that may play an important role in the exclusion of xenobiotics from the brain. May be involved in brain-to-blood efflux. Appears to play a major role in the multidrug resistance phenotype of several cancer cell lines. When overexpressed, the transfected cells become resistant to mitoxantrone, daunorubicin and doxorubicin, display diminished intracellular accumulation of daunorubicin, and manifest an ATP-dependent increase in the efflux of rhodamine 123.

UOM: 1 * 100 µG

Promoción

Proveedor: Merck

Descripción: Phenethylbiguanide hydrochloride, Supelco®

Proveedor: Merck

Descripción: 2'-Deoxycytidine hydrochloride, Supelco®

Numero del catalogo: (8.14911.0025)

Proveedor: Merck

Descripción: O-Methylhydroxylamine hydrochloride para síntesis, Sigma-Aldrich®

UOM: 1 * 25 g

MSDS Promoción

Proveedor: Merck

Descripción: O-Methylhydroxylamine hydrochloride 97.5-102.5% (by argentometric titration), LiChropur™ for GC derivatisation, Supelco®

Numero del catalogo: (1.04527.0010)

Proveedor: Merck

Descripción: 3-Methyl-2-benzothiazolinonehydrazone hydrochloride, GR para análisis, Supelco®

UOM: 1 * 10 g

MSDS Certificados Promoción

Numero del catalogo: (43504-10G)

Proveedor: Merck

Descripción: O-Ethylhydroxylamine hydrochloride 99.0-101.0% (by argentometric titration), LiChropur™ for GC derivatisation, Supelco®

UOM: 1 * 10 g

Promoción