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β-Nicotinamide adenine dinucleotide(NAD) - 97%, high purity , CAS No.53-84-9

Moligand™
≥97%

CAS#: 53-84-9
Formula: C₂₁H₂₇N₇O₁₄P₂ · xH₂O
Molecular Weight: 663.43 (anhydrous basis)
Beilstein Registry Number: 3584133
EC Number: 200-184-4
MDL number: MFCD00036253
PubChem CID: 5892

Item Number

N111609

Grouped product items
SKU	Size	Availability	Price
N111609-1g	1g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$58.90
N111609-5g	5g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$25.90
N111609-10g	10g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$48.90
N111609-25g	25g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$86.90
N111609-50g	50g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$156.90

View related series

Phosphorus compounds Six-Membered Heterocyclic Compounds

Basic Description

Synonyms	nadide\|NAD+\|53-84-9\|coenzyme I\|beta-NAD\|beta-nicotinamide adenine dinucleotide\|Codehydrase I\|Codehydrogenase I\|nicotinamide adenine dinucleotide\|beta-NAD+\|Cozymase I\|diphosphopyridine nucleotide\|beta-Diphosphopyridine nucleotide\|COZYMASE\|Nicotinamide dinu
Specifications & Purity	Moligand™, ≥97%
Biochemical and Physiological Mechanisms	Electron acceptor
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads
Grade	Moligand™
Product Description	NAD+, Free Acid is a major electron acceptor molecule in biological oxidation reactions. A major electron acceptor

Associated Targets

GLUD1 Tbio Glutamate dehydrogenase 1, mitochondrial 0 Activities

Discover Target: GLUD1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

HSD17B1 Tchem Estradiol 17-beta-dehydrogenase 1 0 Activities

Discover Target: HSD17B1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

TRPM2 Tchem Transient receptor potential cation channel subfamily M member 2 0 Activities

Discover Target: TRPM2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

HDAC6 Tclin Histone deacetylase 6 0 Activities

Discover Target: HDAC6

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 0 Activities

Discover Target: SLCO1B1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 0 Activities

Discover Target: SLCO1B3

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SIRT1 Tchem NAD-dependent protein deacetylase sirtuin-1 0 Activities

Discover Target: SIRT1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

LDHB Tchem L-lactate dehydrogenase B chain 0 Activities

Discover Target: LDHB

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

MDH1 Tchem Malate dehydrogenase, cytoplasmic 0 Activities

Discover Target: MDH1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ADH1A Tclin Alcohol dehydrogenase 1A 0 Activities

Discover Target: ADH1A

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CHAT Tchem Choline O-acetyltransferase 0 Activities

Discover Target: CHAT

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

IMPDH2 Tclin Inosine-5'-monophosphate dehydrogenase 2 0 Activities

Discover Target: IMPDH2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

P2RY11 Tchem P2Y purinoceptor 11 0 Activities

Discover Target: P2RY11

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

LDHA Tchem L-lactate dehydrogenase A chain 0 Activities

Discover Target: LDHA

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Names and Identifiers

IUPAC Name	[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate
INCHI	InChI=1S/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 Key	BAWFJGJZGIEFAR-NNYOXOHSSA-N
Canonical SMILES	C1=CC(=C[N+](=C1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)N4C=NC5=C(N=CN=C54)N)O)O)O)O)C(=O)N
Isomeric SMILES	C1=CC(=C[N+](=C1)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)([O-])OP(=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)N4C=NC5=C(N=CN=C54)N)O)O)O)O)C(=O)N
WGK Germany	3
RTECS	UU3450000
PubChem CID	5892
Molecular Weight	663.43 (anhydrous basis)
Beilstein	3584133
Reaxy-Rn	3584133

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

22 results found

Lot Number	Certificate Type	Date	Item
H2423382	Certificate of Analysis	Aug 27, 2024	N111609
H2423383	Certificate of Analysis	Aug 27, 2024	N111609
E2413378	Certificate of Analysis	May 21, 2024	N111609
C2426278	Certificate of Analysis	Apr 08, 2024	N111609
C2426279	Certificate of Analysis	Apr 08, 2024	N111609
C2426280	Certificate of Analysis	Apr 08, 2024	N111609
C2426281	Certificate of Analysis	Apr 08, 2024	N111609
C2426282	Certificate of Analysis	Apr 08, 2024	N111609
C2426283	Certificate of Analysis	Apr 08, 2024	N111609
K2314151	Certificate of Analysis	Nov 17, 2023	N111609
K2314150	Certificate of Analysis	Nov 17, 2023	N111609
J2308655	Certificate of Analysis	Oct 10, 2023	N111609
J2308644	Certificate of Analysis	Oct 10, 2023	N111609
J2308625	Certificate of Analysis	Oct 10, 2023	N111609
G2326309	Certificate of Analysis	Jul 31, 2023	N111609
G2326319	Certificate of Analysis	Jul 31, 2023	N111609
A2312184	Certificate of Analysis	Jan 31, 2023	N111609
A2312194	Certificate of Analysis	Jan 31, 2023	N111609
K2204627	Certificate of Analysis	Nov 09, 2022	N111609
K2204688	Certificate of Analysis	Nov 09, 2022	N111609
G2223287	Certificate of Analysis	Jul 30, 2022	N111609
G2223228	Certificate of Analysis	Jul 30, 2022	N111609

Chemical and Physical Properties

Solubility	Soluble in water (200 mg/ml).
Sensitivity	Moisture sensitive.

Safety and Hazards(GHS)

Pictogram(s)	GHS07
Signal	Warning
Hazard Statements	H315:Causes skin irritation H319:Causes serious eye irritation H335:May cause respiratory irritation
Precautionary Statements	P261:Avoid breathing dust/fume/gas/mist/vapors/spray. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing. P280:Wear protective gloves/protective clothing/eye protection/face protection. P302+P352:IF ON SKIN: wash with plenty of water. P321:Specific treatment (see ... on this label). P405:Store locked up. P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P271:Use only outdoors or in a well-ventilated area. P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing. P403+P233:Store in a well-ventilated place. Keep container tightly closed. P362+P364:Take off contaminated clothing and wash it before reuse. P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes. P337+P317:If eye irritation persists: Get medical help. P332+P317:If skin irritation occurs: Get medical help. P319:Get medical help if you feel unwell.
WGK Germany	3
RTECS	UU3450000
Reaxy-Rn	3584133
Merck Index	6344

References

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