EN
0
Home > Products > Pharmaceuticals & Life Science > Biotechnology & Diagnostics > beta-Diphosphopyridine nucleotide
beta-Diphosphopyridine nucleotide structure, CAS 53-84-9

beta-Diphosphopyridine nucleotide

CAS Number53-84-9

Synonymsb-Diphosphopyridine Nucleotide; DPN; beta-Diphosphopyrid; MFCD00036253; Coenzyme I Hydrate,oxidized form; Diphosphopyridine nucleotide; Cozymase Hydrate,oxidized form; β-Nicotinamide adenine dinucleotide; EINECS 200-184-4; β-Diphosphopyridine Nucleotide Hydrate,oxidized form; β-NAD Hydrate,oxidized form; Adenine-D-ribose-phosphate-phosphate-D-ribose-nicotinamide; b-Nicotinamide Adenine Dinucleotide; β-DPN Hydrate,oxidized form; Codehydrogenase; β-Nicotinamide Adenine Dinucleotide Hydrate,oxidized form; ARPPRN; b-NAD; Cozymase; beta-Diphosphopyridine nucleotide; β-NAD; β-Nicotinamide adenine dinucleotide hydrate; NAD; β-DPN; NAD+

Molecular FormulaC21H27N7O14P2

Molecular Weight663.43 (anhydrous basis)

Purity≥96.5 (HPLC)%

Density

Boiling Point

Melting Point140 - 142ºC

Flash Point

Appearancepowder

EINECS

MSDSChineseEnglish

SymbolTransport

Signal WordWarning

Cat. No.: 2A-9009378 Purity: ≥96.5 (HPLC)%
Change View

Please Login or Create an Account to: See VlP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

Inquiry

Quality Control of [ 53-84-9 ] Purity: ≥96.5 (HPLC)% SDS Specification MoL

COA NMR CNMR HPLC LC-MS
Chemical & Physical Properties
CAS Number53-84-9
Catalog No.2A-9009378
Chinese Name辅酶I
Synonymsb-Diphosphopyridine Nucleotide; DPN; beta-Diphosphopyrid; MFCD00036253; Coenzyme I Hydrate,oxidized form; Diphosphopyridine nucleotide; Cozymase Hydrate,oxidized form; β-Nicotinamide adenine dinucleotide; EINECS 200-184-4; β-Diphosphopyridine Nucleotide Hydrate,oxidized form; β-NAD Hydrate,oxidized form; Adenine-D-ribose-phosphate-phosphate-D-ribose-nicotinamide; b-Nicotinamide Adenine Dinucleotide; β-DPN Hydrate,oxidized form; Codehydrogenase; β-Nicotinamide Adenine Dinucleotide Hydrate,oxidized form; ARPPRN; b-NAD; Cozymase; beta-Diphosphopyridine nucleotide; β-NAD; β-Nicotinamide adenine dinucleotide hydrate; NAD; β-DPN; NAD+
Molecular FormulaC21H27N7O14P2
Molecular Weight663.43 (anhydrous basis)
Purity≥96.5 (HPLC)
Melting Point140 - 142ºC
Appearancepowder
Storage ConditionThis product should be sealed and stored dry at 4°
ApplicationNAD+, nicotinamide adenine dinucleotide, is a coenzyme that transfers hydrogen ions. NAD+ is the oxidized form of NADH.
HTC29349990
PubChem ID24897803
MDL NumberMFCD00036253
SMILESNC1=NC=NC2=C1N=CN2.O[C@@H]3[C@@H](COP(O)(OP(OC[C@@H](O4)[C@@H](O)[C@@H](O)[C@H]4[N+]5=CC=CC(C(N)=O)=C5)([O-])=O)=O)OC[C@@H]3O
InChI1S/C21H27N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChI KeyBAWFJGJZGIEFAR-NNYOXOHSSA-N
NACRES CodeNA.55
eCl@ss39200202
UNSPSC41106305
Hazard SymbolsTransport
MSDSmsds/9378_1_53_84_9.pdf
BioactivityNAD+ is a coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage. Related Catalog Research Areas >> Metabolic Disease Natural Products >> Saccharides and Glycosides Target Human Endogenous Metabolite In Vitro NAD+ is a coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage. NAD+ is the oxidized form of NADH[1]. NAD+ is found widely in nature and is involved in numerous enzymatic reactions in which it serves as an electron carrier by being alternately oxidized (NAD+) and reduced (Nadide) [2]. In Vivo Oral NAD+ supplementation has been used to combat simple fatigue as well as such mysterious and energy-sapping disorders as chronic fatigue syndrome and fibromyalgia[3]. References [1]. Viollet, B., et al., Cellular and molecular mechanisms of metformin: an overview. Clin Sci (Lond), 2012. 122(6): p. 253-70. [2]. Brandt, U., Energy converting NADH:quinone oxidoreductase (complex I). Annu Rev Biochem, 2006. 75: p. 69-92. [3]. Kussmaul, L. and J. Hirst, The mechanism of superoxide production by NADH:ubiquinone oxidoreductase (complex I) from bovine heart mitochondria. Proc Natl Acad Sci U S A, 2006. 103(20): p. 7607-12. Chemical & Physical Properties Melting Point 140 - 142ºC Molecular Formula C21H27N7O14P2 Molecular Weight 663.425 Exact Mass 663.109131 PSA 340.71000 LogP -5.72 InChIKey BAWFJGJZGIEFAR-NNYOXOHSSA-O SMILES NC(=O)c1ccc[n+](C2OC(COP(=O)(O)OP(=O)(O)OCC3OC(n4cnc5c(N)ncnc54)C(O)C3O)C(O)C2O)c1
Use ofNAD+ is a coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage. Properties Articles286 Name NAD zwitterion Synonym More Synonyms NAD+ Biological Activity Description NAD+ is a coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage. Related Catalog Research Areas >> Metabolic Disease Natural Products >> Saccharides and Glycosides Human Endogenous Metabolite In Vitro NAD+ is a coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage. NAD+ is the oxidized form of NADH[1]. NAD+ is found widely in nature and is involved in numerous enzymatic reactions in which it serves as an electron carrier by being alternately oxidized (NAD+) and reduced (Nadide) [2]. In Vivo Oral NAD+ supplementation has been used to combat simple fatigue as well as such mysterious and energy-sapping disorders as chronic fatigue syndrome and fibromyalgia[3]. References [1]. Viollet, B., et al., Cellular and molecular mechanisms of metformin: an overview. Clin Sci (Lond), 2012. 122(6): p. 253-70. [2]. Brandt, U., Energy converting NADH:quinone oxidoreductase (complex I). Annu Rev Biochem, 2006. 75: p. 69-92. [3]. Kussmaul, L. and J. Hirst, The mechanism of superoxide production by NADH:ubiquinone oxidoreductase (complex I) from bovine heart mitochondria. Proc Natl Acad Sci U S A, 2006. 103(20): p. 7607-12. Chemical & Physical Properties Molecular Formula C21H27N7O14P2 Exact Mass 663.109131 PSA 340.71000 LogP -5.72 InChIKey BAWFJGJZGIEFAR-NNYOXOHSSA-O
Transport InfoShipping Name: UN
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available
Related Products in Biotechnology & Diagnostics
Uridine 5'-triphosphate63-39-82A-9008898
3-Deazauridine23205-42-72A-9008981
6-Azauridine54-25-12A-9009006
7-Allyl-7,8-dihydro-8-oxoguanosine121288-39-92A-9009013
Barium dibutyacyladenosine cyclphosphate18837-96-22A-9009305
Cyclocytidine hydrochloride10212-25-62A-9009944
Dapiprazole72822-12-92A-9010003
Dapiprazole hydrochloride72822-13-02A-9010004
Elisartan158682-68-92A-9010298
Odapipam131796-63-92A-9011745
Browse all Biotechnology & Diagnostics products »
Contact Us

Phone:

630-322-8886

630-322-8887

Email:

[email protected]

Office Locations:

Chicago, IL, USA

San Francisco, CA, USA