Chemical Name

Diphosphopyridinnucleotid (C₂₁H₂₆N₇O₁₄P₂)

Compound Descriptions:


Formula:	C₂₁H₂₆N₇O₁₄P₂
Molecular Weight:	662.417 ^g/_mol
Name(s):	Diphosphopyridinnucleotid β-Nicotinamide adenine dinucleotide Adenosine 5'-(trihydrogen diphosphate), P'->5'-ester with 3-(aminocarbonyl)-1β-D-ribofuranosylpyridinium, inner salt Adenosine 5'-(trihydrogen diphosphate), P'->5'-ester with 3-(aminocarbonyl)-1β-D-ribofuranosylpyridinium hydroxide, inner salt Pyridinium, 3-carbamoyl-1β-D-ribofuranosyl-, hydroxide, 5'->5'-ester with adenosine 5'-(trihydrogen pyrophosphate), inner salt β-Diphosphopyridine nucleotide β-NAD Adenine-nicotinamide dinucleotide Codehydrase I Codehydrogenase I Coenzyme I Cozymase I DPN Enzopride NAD+ Nadide Nicotinamide-adenine dinucleotide Oxidized diphosphopyridine nucleotide Adenosine 5'-(trihydrogen diphosphate), 5'->5'-ester with 3-(aminocarbonyl)-1β-D-ribofuranosylpyridinium hydroxide, inner salt nadide (INN) Adenosine 5'-(trihydrogen diphosphate), P'->5'-ester with 3-(aminocarbonyl)-1-β-D-ribofuranosylpyridinium, inner salt diphosphoric acid-1-adenosin-5'-yl ester-2-((1R)-1-(3-carbamoyl-pyridinio)-D-1,4-anhydro-ribitol-5-yl ester)-betaine Adenosine 5'-(trihydrogen diphosphate), 5'->5'-ester with 3-(aminocarbonyl)-1-β-D-ribofuranosylpyridinium hydroxide, inner salt Adenosine 5'-(trihydrogen diphosphate), 5'->5'-ester with 3-(aminocarbonyl)-1β-D-ribofuranosylpyridinium, hydroxide, inner salt CO-I CO-1 Endopride Pyridine, nucleotide diphosphate Pyridinium, 3-carbamoyl-1-β-D-ribofuranosyl-, hydroxide, 5'->5'-ester with adenosine 5'-(trihydrogen pyrophosphate), inner salt 3-Carbamoyl-1β-D-ribofuranosylpyridinium hydroxide, 5'-ester with adenosine 5'-pyrophosphate, inner salt Nicotinamid-adenin-dinucleotid Trihydrat β-Nicotinamide adenine dinucleotide tetrahydrate β-Nicotinamid-adenin-dinucleotid Tetrahydrat Coezym I Diphosphopyridine dinucleotide Nicotinamide adenine dinucleotide trihydrate B-Nicotinamidadenindinucleotid Diphosphopyridindinucleotid NAD freie Saeure Beta-nicotinamide adenine dinucleotide Adenosine 5'-(trihydrogen diphosphate), P'->5'-ester with 3-(aminocarbonyl)-1-β-D-ribofuranosylpyridinium hydroxide, inner salt NSC 20272 ß-Nicotinamide adenine dinucleotide Adenosine 5'-(trihydrogen diphosphate), P'->5'-ester with 3-(aminocarbonyl)-1ß-D-ribofuranosylpyridinium, inner salt Adenosine 5'-(trihydrogen diphosphate), P'->5'-ester with 3-(aminocarbonyl)-1ß-D-ribofuranosylpyridinium hydroxide, inner salt Pyridinium, 3-carbamoyl-1ß-D-ribofuranosyl-, hydroxide, 5'->5'-ester with adenosine 5'-(trihydrogen pyrophosphate), inner salt ß-Diphosphopyridine nucleotide ß-NAD Adenosine 5'-(trihydrogen diphosphate), 5'->5'-ester with 3-(aminocarbonyl)-1ß-D-ribofuranosylpyridinium hydroxide, inner salt Adenosine 5'-(trihydrogen diphosphate), P'->5'-ester with 3-(aminocarbonyl)-1-ß-D-ribofuranosylpyridinium, inner salt Adenosine 5'-(trihydrogen diphosphate), 5'->5'-ester with 3-(aminocarbonyl)-1-ß-D-ribofuranosylpyridinium hydroxide, inner salt Adenosine 5'-(trihydrogen diphosphate), 5'->5'-ester with 3-(aminocarbonyl)-1ß-D-ribofuranosylpyridinium, hydroxide, inner salt Pyridinium, 3-carbamoyl-1-ß-D-ribofuranosyl-, hydroxide, 5'->5'-ester with adenosine 5'-(trihydrogen pyrophosphate), inner salt 3-Carbamoyl-1ß-D-ribofuranosylpyridinium hydroxide, 5'-ester with adenosine 5'-pyrophosphate, inner salt ß-Nicotinamide adenine dinucleotide tetrahydrate ß-Nicotinamid-adenin-dinucleotid Tetrahydrat Adenosine 5'-(trihydrogen diphosphate), P'->5'-ester with 3-(aminocarbonyl)-1-ß-D-ribofuranosylpyridinium hydroxide, inner salt β-NAD+ B-NAD NAD freie Säure
CAS-RN:	53-84-9, 30429-30-2, 159929-29-0
EINECS:	200-184-4	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.125	II/3
	Luminescence of Organic Substances: Vol. II/3 6.6, p.371	II/3

Magnetic Properties

Diamagnetic Susceptibility: Vol. II/27b 7.1.21:2351

II/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

Internet Resource: http://ecb.jrc.ec.europa.eu/esis/index.php?PGM=ein

Publish_Date: 1990/06/15