U heeft gezocht op: Daunorubicin+hydrochloride

Leverancier: TCI

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

Catalogus nummer: (ENZOALX380043M010)

Leverancier: ENZO LIFE SCIENCES

Omschrijving: Antitumor antibiotic.

UOM: 1 * 10 mg

New Product Sale

Catalogus nummer: (1164700.)

Leverancier: USP

Omschrijving: 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

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Catalogus nummer: (ENZOALX380260M005)

Leverancier: ENZO LIFE SCIENCES

Omschrijving: 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 Sale

Leverancier: MP Biomedicals

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

Certificaten

Catalogus nummer: (BOSSBS-7953R-A680)

Leverancier: Bioss

Omschrijving: 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

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Catalogus nummer: (ENZOBMLPI1100010)

Leverancier: ENZO LIFE SCIENCES

Omschrijving: 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 Sale

Catalogus nummer: (BOSSBS-7953R-HRP)

Leverancier: Bioss

Omschrijving: 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

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Catalogus nummer: (BOSSBS-7953R-A750)

Leverancier: Bioss

Omschrijving: 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

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Catalogus nummer: (PRSI79-673)

Leverancier: ProSci Inc.

Omschrijving: 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 * 1 EA

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Leverancier: Merck

Omschrijving: Ethanolamine hydrochloride

Catalogus nummer: (47862.)

Leverancier: Merck

Omschrijving: Pyridoxine hydrochloride

UOM: 1 * 1 ST

Certificaten Sale

Catalogus nummer: (33656-100MG-R)

Leverancier: Merck

Omschrijving: Semicarbazide hydrochloride, Supelco®

UOM: 1 * 100 mg

Sale

Leverancier: Merck

Omschrijving: AEBSF hydrochloride (4-(2-aminoethyl)benzenesulphonylfluoride hydrochloride), Sigma-Aldrich®

MSDS

Catalogus nummer: (8.22101.0250)

Leverancier: Merck

Omschrijving: Morpholine hydrochloride

UOM: 1 * 250 g

MSDS Sale

Leverancier: Merck

Omschrijving: 2'-Deoxycytidine hydrochloride, Supelco®