CSNpharm
CSNpharm
5-bromoindole is an inhibitor of glycogen synthase kinase 3 (GSK-3), it can be used as important pharmaceutical chemical intermediate.
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5-CFDA is membrane-permeant and can be loaded into cells via incubation and hydrolyzed by intracellular esterases to 5-carboxyfluorescein and used for labeling human intervertebral disk cells in vitro for fluorescence microscopy.
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CSNpharm
CSNpharm
5-Ethynyluridine is used to help detect RNA synthesis in cells by its biosynthetic incorporation into newly transcribed RNA. Once fed to cells, it is incorporated during active RNA synthesis and can then be detected using a copper-catalyzed click reaction with fluorescent dyes. The cells can then be analysed by fluorescence imaging, flow cytometry or high […]
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5-FAM
100mg
| ≥99%
CSNpharm
5-FAM contains a carboxylic acid that can be used to react with primary amines via carbodiimide activation of the carboxylic acid.
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5-FAM
25mg
| ≥99%
CSNpharm
5-FAM contains a carboxylic acid that can be used to react with primary amines via carbodiimide activation of the carboxylic acid.
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CSNpharm
5-FAM SE is a single isomer, one of the most popular green fluorescent reagents used for labeling peptides, proteins and nucleotides.
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CSNpharm
5-FAM SE is a single isomer, one of the most popular green fluorescent reagents used for labeling peptides, proteins and nucleotides.
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CSNpharm
5-FAM SE is a single isomer, one of the most popular green fluorescent reagents used for labeling peptides, proteins and nucleotides.
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CSNpharm
CSNpharm
5-Fluorocytidine could replace cytidine and be incorporated into cellular RNAs or tRNAs.The bacterial enzyme cytosine deaminase has been used as a negative selection marker system. Cells that express cytosine deaminase convert 5-fluorocytosine to the toxic compound 5-fluorouracil, and transformed seedlings can thus be identified using medium containing 5-fluorocytosine.
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CSNpharm
5-Fluorocytosine is an antimycotic prodrug which can be converted to 5-fluorouracil, working by inhibiting DNA and RNA synthesis and interfering with ribosomal protein synthesis. It shows both antifungal and antitumor activity.
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CSNpharm
5-Fluorocytosine is an antimycotic prodrug which can be converted to 5-fluorouracil, working by inhibiting DNA and RNA synthesis and interfering with ribosomal protein synthesis. It shows both antifungal and antitumor activity.
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CSNpharm
5-Fluorocytosine is an antimycotic prodrug which can be converted to 5-fluorouracil, working by inhibiting DNA and RNA synthesis and interfering with ribosomal protein synthesis. It shows both antifungal and antitumor activity.
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CSNpharm
5-Fluorocytosine is an antimycotic prodrug which can be converted to 5-fluorouracil, working by inhibiting DNA and RNA synthesis and interfering with ribosomal protein synthesis. It shows both antifungal and antitumor activity.
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CSNpharm
5-Fluorouracil is a potent antitumor agent that affects pyrimidine synthesis by inhibiting thymidylate synthetase thus depleting intracellular dTTP pools.
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CSNpharm
5-Fluorouracil is a potent antitumor agent that affects pyrimidine synthesis by inhibiting thymidylate synthetase thus depleting intracellular dTTP pools.
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CSNpharm
5-Fluorouracil is a potent antitumor agent that affects pyrimidine synthesis by inhibiting thymidylate synthetase thus depleting intracellular dTTP pools.
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CSNpharm
5-Fluorouridine is a metabolite of 5-fluorouracil with anticancer activity and cytotoxic activity. 5-fluorouridine inhibits rRNA synthesis of human colon carcinoma cells. 5-Fluorouridine exhibits cytotoxic effect on growth of L1210 cells with an IC50 of 2 nM. 5-Fluorouridine triphosphate acted as a potent competitive inhibitor of VPg uridylylation, the initial step of viral replication.
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CSNpharm
5-Heptadecylresorcinol is a natural product isolated and purified from the herbs of Mangifera indica with strong inhibitory property against the growth of PC3 cells.
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CSNpharm
CSNpharm
CSNpharm
5-Hydroxy-1,7-diphenyl-6-hepten-3-one is a natural product isolated and purified from the rhizoma of Curcuma longa L. with antioxidant activity.
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CSNpharm
5-Hydroxy-1,7-diphenyl-6-hepten-3-one is a natural product isolated and purified from the rhizoma of Curcuma longa L. with antioxidant activity.
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CSNpharm
CSNpharm
5-Hydroxy-3′,4′,7-trimethoxyflavone, a natural product isolated and purified fromt Lippia nodiflora L., shows prominent inhibitory activity against soybean lipoxygenase.
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CSNpharm
5-Hydroxy-4-methoxycanthin-6-one, a natural product isolated and purified from the barks of Picrasma quassioides (D.Don) Benn with anti-inflammatory effect and protective effect on dextran sulfate sodium -induced rat colitis, exhibits significant cytotoxic activity against CNE2 cell line, reduces the development of carrageenan-induced paw edema and complete Freund’s adjuvant (CFA)-induced chronic arthritis in rats.
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CSNpharm
5-Hydroxy-7-acetoxy-8-methoxyflavone is a natural product isolated and purified from the root of Scutellaria baicalensis Georgi.
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CSNpharm
5-Hydroxy-7-acetoxy-8-methoxyflavone is a natural product isolated and purified from the root of Scutellaria baicalensis Georgi.
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CSNpharm
CSNpharm
CSNpharm
5-Hydroxyindole-3-acetic acid (5-HIAA), the major metabolite of serotonin, is a histamine H1 receptor antagonist and can be used to treat allergies.
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CSNpharm
5-Hydroxymethyl-2-furancarboxylic acid is the main metabolite of 5-hydroxymethyl-2-furfural, a product of acid-catalyzed degradation of sugars during the heating and storage of foods that influences taste and physiological functions in the body.
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CSNpharm
5-Hydroxymethylfurfural (2-Hydroxymethyl-5-furfural), derived from lignocellulosic biomass, inhibits yeast growth and fermentation as stressors.
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CSNpharm
5-Hydroxymethyluracil (5hmU) is a thymine base modification found in the genomic DNA of diverse organisms ranging from bacteriophages to mammals
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CSNpharm
5-Hydroxymethyluracil (5hmU) is a thymine base modification found in the genomic DNA of diverse organisms ranging from bacteriophages to mammals
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CSNpharm
5-Hydroxypyrazine-2-Carboxylic acid, a metabolite of pyrazinamide, is versatile building block for synthesis of antituberculous agents.
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CSNpharm
5-Hydroxypyrazine-2-Carboxylic acid, a metabolite of pyrazinamide, is versatile building block for synthesis of antituberculous agents.
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CSNpharm
CSNpharm
CSNpharm
5-Iodotubercidin is a potent inhibitor (IC50 = 26 nM). It also inhibits nucleoside transporter, CK1, insulin receptor tyrosine kinase, phosphorylase kinase, PKA, CK2 and PKC.
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CSNpharm
5-Iodotubercidin is a potent inhibitor (IC50 = 26 nM). It also inhibits nucleoside transporter, CK1, insulin receptor tyrosine kinase, phosphorylase kinase, PKA, CK2 and PKC.
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CSNpharm
5-Iodotubercidin is a potent inhibitor (IC50 = 26 nM). It also inhibits nucleoside transporter, CK1, insulin receptor tyrosine kinase, phosphorylase kinase, PKA, CK2 and PKC.
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CSNpharm
5-Iodotubercidin is a potent inhibitor (IC50 = 26 nM). It also inhibits nucleoside transporter, CK1, insulin receptor tyrosine kinase, phosphorylase kinase, PKA, CK2 and PKC.
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CSNpharm
5-Iodotubercidin is a potent inhibitor (IC50 = 26 nM). It also inhibits nucleoside transporter, CK1, insulin receptor tyrosine kinase, phosphorylase kinase, PKA, CK2 and PKC.
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CSNpharm
5-iodouridine has been shown to promote bacterial cell lethality when combined with gamma-irradiation in Chinese hamster cells.
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CSNpharm
5-Methyl-2’-O-methyluridine is one of three oligonucleotide in platinum-derivatized homopyrimidine triplex-forming oligonucleotides (Pt-TFOs) useful in crosslinking to the transcribed strand in the human androgen receptor (AR) gene. It shows inhibitory activity against M. bovis and M. avium.
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CSNpharm
5-Methoxyflavone, belonged to Flavonoid family, is a DNA polymerase-beta inhibitor and neuroprotective agent against beta-amyloid toxicity. possess central nervous system (CNS) depressant effect mediated through the ionotropic GABAA receptors.
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