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Description: DL-2-Amino-4-phosphonobutyric acid 95%
Catalog Number: L17671.MD
UOM: 1 * 250 mg
Supplier: Alfa Aesar


Description: 4-Acetyl-2-fluorobenzeneboronic acid pinacol ester 96%
Catalog Number: H62256.03
UOM: 1 * 1 g
Supplier: Alfa Aesar


Description: 5-Acetyl-2,4-dimethylthiazole ≥99%
Catalog Number: A13741.06
UOM: 1 * 5 g
Supplier: Alfa Aesar


Description: 3-Acetyl-1-methyl-1H-pyrrole 95%
Catalog Number: APOSOR919291-5G
UOM: 1 * 5 g
Supplier: APOLLO SCIENTIFIC


Description: Methyl-4-acetyl-1H-pyrrole-2-carboxylate 95%
Catalog Number: APOSOR32252-1G
UOM: 1 * 1 g
Supplier: APOLLO SCIENTIFIC


Description: Ac-DL-Pra-Oet 95%
Catalog Number: APOSOR963272-1G
UOM: 1 * 1 g
Supplier: APOLLO SCIENTIFIC


Description: 2-Acetyl-6-iodo-2H-indazole
Catalog Number: APOSOR110286-1G
UOM: 1 * 1 g
Supplier: APOLLO SCIENTIFIC


Description: 2-Azidoethyl-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 99% min
Catalog Number: APOSBICL4024-2G
UOM: 1 * 2 g
Supplier: APOLLO SCIENTIFIC


Description: CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Catalog Number: BOSSBS-11822R-FITC
UOM: 1 * 100 µl
Supplier: Bioss


Description: CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Catalog Number: BOSSBS-11822R-HRP
UOM: 1 * 100 µl
Supplier: Bioss


Description: 3-Acetyl-5-bromo-2-fluoropyridine 98%
Catalog Number: APOSPC7516-25G
UOM: 1 * 25 g
Supplier: APOLLO SCIENTIFIC


Description: DL-Glutamic acid monohydrate 98+%
Catalog Number: ACRO119931000
UOM: 1 * 100 g
Supplier: Thermo Scientific


Description: 2-(Trifluoromethyl)-DL-phenylglycine 97%
Catalog Number: APOSPC5438-1G
UOM: 1 * 1 g
Supplier: APOLLO SCIENTIFIC


Description: 2-Acetyl-3-(Boc-amino)pyrazine
Catalog Number: APOSOR471345-250MG
UOM: 1 * 250 mg
Supplier: APOLLO SCIENTIFIC


Description: 4-Chloro-3,5-difluoro-DL-phenylalanine
Catalog Number: APOSPC302576-1G
UOM: 1 * 1 g
Supplier: APOLLO SCIENTIFIC


Description: Methyl-1,2,3,4-tetra-O-acetyl-β-D-glucuronate 98%
Catalog Number: H31888.03
UOM: 1 * 1 g
Supplier: Alfa Aesar

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