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2′-Deoxyadenosine 5′-monophosphate - 10mM in DMSO, high purity , CAS No.653-63-4

  • Moligand™
  • 10mM in DMSO
Item Number
D425305
Grouped product items
SKUSizeAvailabilityPrice Qty
D425305-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$169.90

Nucleotide derivative.

Basic Description

Synonyms653-63-4|2'-deoxyadenosine-5'-monophosphate|dAMP|2'-Deoxyadenosine 5'-monophosphate|2'-Deoxyadenylic acid|5'-Adenylic acid, 2'-deoxy-|Deoxyadenylic acid|Deoxy-AMP|2'-Deoxyadenosine 5'-phosphate|2'-Deoxy-AMP|Deoxyadenosine 5'-monophosphate|Deoxyadenosine m
Specifications & PurityMoligand™, 10mM in DMSO
Biochemical and Physiological MechanismsNucleotide derivative, used to study adenosine-based interactions during DNA synthesis, inhibition, and damage.
Storage TempStore at -80°C
Shipped InIce chest + Ice pads
GradeMoligand™

Associated Targets

CBX1 Tbio Chromobox protein homolog 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GMNN Tbio Geminin 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RUNX1 Tbio Runt-related transcription factor 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AK1 Tbio Adenylate kinase isoenzyme 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AK2 Tbio Adenylate kinase 2, mitochondrial 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SNCA Tchem Alpha-synuclein 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

POLI Tchem DNA polymerase iota 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SMPD1 Tchem Sphingomyelin phosphodiesterase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

IDH1 Tclin Isocitrate dehydrogenase [NADP] cytoplasmic 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NFE2L2 Tchem Nuclear factor erythroid 2-related factor 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KDM4A Tchem Lysine-specific demethylase 4A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name [(2R,3S,5R)-5-(6-aminopurin-9-yl)-3-hydroxyoxolan-2-yl]methyl dihydrogen phosphate
INCHI InChI=1S/C10H14N5O6P/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(21-7)2-20-22(17,18)19/h3-7,16H,1-2H2,(H2,11,12,13)(H2,17,18,19)/t5-,6+,7+/m0/s1
InChi Key KHWCHTKSEGGWEX-RRKCRQDMSA-N
Canonical SMILES C1C(C(OC1N2C=NC3=C(N=CN=C32)N)COP(=O)(O)O)O
Isomeric SMILES C1[C@@H]([C@H](O[C@H]1N2C=NC3=C(N=CN=C32)N)COP(=O)(O)O)O
WGK Germany 3
PubChem CID 12599
Molecular Weight 331.22

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

Melt Point(°C)148°C

Safety and Hazards(GHS)

WGK Germany 3

Related Documents

Solution Calculators