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CAS Number


 

Dihydro-diphospho-pyridinnucleotid Σ (C21H27N7O14P2)

Compound Descriptions:

Structure Drawing
Formula:C21H27N7O14P2
Molecular Weight:663.425 g/mol
Name(s):Dihydro-diphospho-pyridinnucleotid Σ
1,4-Dihydronicotinamide adenine dinucleotide
Adenosine 5'-(trihydrogen diphosphate), P'->5'-ester with 1,4-dihydro-1β-D-ribofuranosyl-3-pyridinecarboxamide
Adenosine 5'-(trihydrogen pyrophosphate), 5'->5'-ester with 1,4-dihydro-1β-D-ribofuranosylnicotinamide
Adenosine pyrophosphate, 5'->5'-ester with 1,4-dihydro-1β-D-ribofuranosylnicotinamide
β-DPNH
β-NADH
Codehydrase I, reduced
Codehydrogenase I, reduced
Coenzyme I, reduced
Cozymase I, reduced
Dihydrocodehydrogenase I
Dihydrocozymase
Dihydronicotinamide mononucleotide
NADH2
Nicotinamide-adenine dinucleotide, reduced
Reduced codehydrogenase I
Reduced diphosphopyridine nucleotide
Reduced nicotinamide adenine diphosphate
Reduced nicotinamide-adenine dinucleotide
Adenosine 5'-(trihydrogen diphosphate), 5'->5'-ester with 1,4-dihydro-1β-D-ribofuranosyl-3-pyridinecarboxamide
dihydrodiphosphopyridine nucleotide
Adenosine 5'-(trihydrogen diphosphate), P'->5'-ester with 1,4-dihydro-1-β-D-ribofuranosyl-3-pyridinecarboxamide
O5'-[2-(1-(3-carbamoyl-4H-pyridin-1-yl)-β-D-1-deoxy-ribofuranos-5-yloxy)-1,2-dihydroxy-phosphoryl]-adenosine
O5'-(2-(1-(3-carbamoyl-4H-pyridin-1-yl)-β-D-1-deoxy-ribofuranos-5-yloxy)-1,2-dihydroxy-phosphoryl)-adenosine
reduced nicotinamide adenine dinucleotide
Adenosine 5'-(trihydrogen pyrophosphate), 5'->5'-ester with 1,4-dihydro-1-β-D-ribofuranosylnicotinamide
Adenosine pyrophosphate, 5'->5'-ester with 1,4-dihydro-1-β-D-ribofuranosylnicotinamide
ENADA
Adenosine 5'-(trihydrogen diphosphate), P'->5'-ester with 1,4-dihydro-1ß-D-ribofuranosyl-3-pyridinecarboxamide
Adenosine 5'-(trihydrogen pyrophosphate), 5'->5'-ester with 1,4-dihydro-1ß-D-ribofuranosylnicotinamide
Adenosine pyrophosphate, 5'->5'-ester with 1,4-dihydro-1ß-D-ribofuranosylnicotinamide
ß-DPNH
ß-NADH
Adenosine 5'-(trihydrogen diphosphate), 5'->5'-ester with 1,4-dihydro-1ß-D-ribofuranosyl-3-pyridinecarboxamide
Adenosine 5'-(trihydrogen diphosphate), P'->5'-ester with 1,4-dihydro-1-ß-D-ribofuranosyl-3-pyridinecarboxamide
O5'-[2-(1-(3-carbamoyl-4H-pyridin-1-yl)-ß-D-1-deoxy-ribofuranos-5-yloxy)-1,2-dihydroxy-phosphoryl]-adenosine
O5'-(2-(1-(3-carbamoyl-4H-pyridin-1-yl)-ß-D-1-deoxy-ribofuranos-5-yloxy)-1,2-dihydroxy-phosphoryl)-adenosine
Adenosine 5'-(trihydrogen pyrophosphate), 5'->5'-ester with 1,4-dihydro-1-ß-D-ribofuranosylnicotinamide
Adenosine pyrophosphate, 5'->5'-ester with 1,4-dihydro-1-ß-D-ribofuranosylnicotinamide
dihydronicotinamide-adenine dinucleotide
CAS-RN:58-68-4, 443892-10-2
EINECS:200-393-0 EINECS
Classification:charged; oxygen heterocycle; nitrogen heterocycle; aromatic; alicycle; large ring; fused rings; 5ring; 6ring; 9ring; amide; alcohol; chiral; 1fragment; ionic

European Regulations

1 matching entries in european regulations: ECHA-pre

Landolt-Börnstein Citations:

Acoustical and Optical Properties

 Luminescence of Organic Substances: Vol. II/3 2.1, p.125II/3

Magnetic Properties

 Diamagnetic Susceptibility: Vol. II/27b 7.1.21:2355II/27B

References

II/27B
Short: II/27B
Title: Diamagnetic Susceptibility of Organic Compounds, Oils, Paraffins and Polyethylenes
Author: Kumar, M.; Gupta, R.
Editor: Gupta, Radha Raman
Source: Landolt-Börnstein, New Series
Volume: II/27B
Year: 2008
Keyword: diamagnetic susceptibility; organic compounds
ISBN: 978-3-540-44359-9 (print)
ISBN: 978-3-540-45860-9 (online)
Internet Resource: doi:10.1007/978-3-540-45860-9
RefComment: VIII, 503 p. With CD-ROM., Hardcover
RefComment: Written for: Scientists and researchers in the fields of physics, chemistry, materials science
RefComment: Supplement and Revised Editon to II/16
Abstract: The volume II/27 has been divided into three subvolumes according to the classes of compounds: Subvolume A: Diamagnetic susceptibility and magnetic anisotropy of inorganic and organometallic compounds; Subvolume B: Diamagnetic susceptibility of organic compounds, oils, paraffins and polyethylenes; Subvolume C: Diamagnetic susceptibility and magnetic anisotropy of organic compounds. The data presented in this volume are based on the literature survey of the chemical abstracts up to 2005. The calculated values of diamagnetic susceptibility of organic compounds in the present subvolume II/27B are presented along with their experimental values. They have been calculated with the use of structural parameters in structural formula by using different theoretical methods available in the literature.
II/3
Short: II/3
Title: Luminescence of Organic Substances
Author: Schmillen, A.; Legler, R.
Editor: Hellwege, K.-H.; Hellwege, A.M.
Source: Landolt-Börnstein, New Series
Volume: II/3
Year: 1967
ISBN: 3-540-03895-7
ISBN: 978-3-540-03895-5
Internet Resource: DOI:10.1007/b86158
RefComment: 270 figs., VIII, 416 pages. Hardcover
Abstract: For more than 1000 luminescent organic substances the most important data are represented as wave numbers of absorption and emission bands, decay times and quantum efficiencies. Additional tables contain further information for restricted groups of substances (figures on typical spectra, wave numbers of sharp single bands, influence of surrounding molecules, etc.).
EINECS
Short: EINECS
Title: EINECS (European Inventory of Existing Commercial Chemical Substances)
Source: Official Journal of the European Communities
Volume: C 146 A (15.06.1990)
Page: 1
Year: 1990
Publish_Date: 1990/06/15

  File created on 2009/18/08 by LCI Publisher GmbH (Gaja Peters, Inga Thede, Volkmar Vill, Ron Zenczykowski)
  © 2009   Landolt Börnstein,   Springer-Verlag Berlin Heidelberg