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N6-Methyl-2'-deoxyadenosine - 99%, high purity , CAS No.2002-35-9

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N6-Methyl-2'-deoxyadenosine - 99%, high purity , CAS No.2002-35-9

COA

Grade & Purity:

≥99%

Cas Number: 2002-35-9
Molecular Weight: 265.27
MDL number: MFCD00055999
PubChem CID: 168948
PubChem SID: 504757626

In stock

Item Number

M122955

Grouped product items
SKU	Size	Availability	Price
M122955-10mg	10mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$35.90
M122955-50mg	50mg	5	$138.90
M122955-250mg	250mg	2	$412.90
M122955-1g	1g	2	$1,477.90

View related series

Cell Cycle (2830)

Basic Description

Synonyms	Q27107487 \| Adenosine, 2'-deoxy-N-methyl- \| N(6)-Methyl-2'-deoxyadenosine \| NSC 66392 \| n6-methyldeoxyadenosine \| 6-(METHYLAMINO)PURINE DEOXYRIBOSIDE \| AKOS024260286 \| hydrogen phosphorus, PH3 \| SCHEMBL548569 \| N(sup 6)-Isopentenyladenosine \| (2R,3S,5R)-2
Specifications & Purity	≥99%
Biochemical and Physiological Mechanisms	N6-Methyl-2′-deoxyadenosine (N6-Me-dAdo) is a precursor of N6-methyl 2′-deoxyadenosine 3′,5′-bisphosphate (N6MABP), a competitive and selective inhibitor of P2Y1 receptors. It is located at the transcription start site and plays a role in increased gene e
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	N6-Methyl-2′-deoxyadenosine (N6-Me-dAdo) is a precursor of N6-methyl 2′-deoxyadenosine 3′,5′-bisphosphate (N6MABP), a competitive and selective inhibitor of P2Y1 receptors.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
  - Class Purine nucleosides
    - Subclass Purine 2'-deoxyribonucleosides

Kingdom	Organic compounds
Superclass	Nucleosides, nucleotides, and analogues
Class	Purine nucleosides
Subclass	Purine 2'-deoxyribonucleosides
Intermediate Tree Nodes	Not available
Direct Parent	Purine 2'-deoxyribonucleosides
Alternative Parents	6-alkylaminopurines Secondary alkylarylamines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Purine 2'-deoxyribonucleoside - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Secondary aliphatic/aromatic amine - N-substituted imidazole - Pyrimidine - Imidolactam - Tetrahydrofuran - Heteroaromatic compound - Azole - Imidazole - Secondary alcohol - Secondary amine - Oxacycle - Organoheterocyclic compound - Azacycle - Alcohol - Organonitrogen compound - Organic nitrogen compound - Organopnictogen compound - Organooxygen compound - Primary alcohol - Organic oxygen compound - Hydrocarbon derivative - Amine - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.
External Descriptors	purine 2'-deoxyribonucleoside
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504757626
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504757626
IUPAC Name	(2R,3S,5R)-2-(hydroxymethyl)-5-[6-(methylamino)purin-9-yl]oxolan-3-ol
INCHI	InChI=1S/C11H15N5O3/c1-12-10-9-11(14-4-13-10)16(5-15-9)8-2-6(18)7(3-17)19-8/h4-8,17-18H,2-3H2,1H3,(H,12,13,14)/t6-,7+,8+/m0/s1
InChIKey	DYSDOYRQWBDGQQ-XLPZGREQSA-N
Smiles	CNC1=C2C(=NC=N1)N(C=N2)C3CC(C(O3)CO)O
Isomeric SMILES	CNC1=C2C(=NC=N1)N(C=N2)[C@H]3C[C@@H]([C@H](O3)CO)O
WGK Germany	3
Molecular Weight	265.27
Reaxy-Rn	58374180
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=58374180&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot Number	Certificate Type	Date	Item
F1515026	Certificate of Analysis	Mar 08, 2023	M122955
H2330048	Certificate of Analysis	Jun 21, 2022	M122955
I2207902	Certificate of Analysis	Jun 21, 2022	M122955
I2207904	Certificate of Analysis	Jun 21, 2022	M122955
I2207923	Certificate of Analysis	Jun 21, 2022	M122955

Chemical and Physical Properties

Solubility	Miscible in water
Sensitivity	Heat sensitive
Molecular Weight	265.270 g/mol
XLogP3	-0.200
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	7
Rotatable Bond Count	3
Exact Mass	265.117 Da
Monoisotopic Mass	265.117 Da
Topological Polar Surface Area	105.000 Å²
Heavy Atom Count	19
Formal Charge	0
Complexity	321.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	3
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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