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Puromycin aminonucleoside - 10mM in DMSO, high purity , CAS No.58-60-6

    Grade & Purity:
  • 10mM in DMSO
  • Cas Number:  58-60-6
  • Molecular Weight:  294.31
  • Beilstein Registry Number:   93902
  • EC Number:   200-388-3
  • PubChem CID: 6020
In stock
Item Number
P424907
Grouped product items
SKU Size
Availability
Price Qty
P424907-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$241.90

Podocyte toxin, induces ROS and oxidant-dependent DNA damage

Basic Description

Synonyms Puromycin aminonucleoside | 58-60-6 | Stylomycin aminonucleoside | 3'-amino-3'-deoxy-n6,n6-dimethyladenosine | Aminonucleoside | 3'-Amino-3'-deoxy-N,N-dimethyladenosine | 6-Dimethylamino-9-(3'-ribosylamine)purine | ADENOSINE, 3'-AMINO-3'-DEOXY-N,N-DIMETHYL- | PANS | CHEBI:
Specifications & Purity 10mM in DMSO
Biochemical and Physiological Mechanisms Puromycin aminonucleoside is used to study human glomerular disease by inducing damage of murine glomerular podocytes1 and is used to study glomerular function and morphology.Podocyte toxin, induces ROS and oxidant-dependent DNA damage in podocytes. Purom
Storage Temp Protected from light,Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Puromycin Aminonucleoside (3'-Amino-3'-deoxy-N6,N6-dimethyladenosine) is the aminonucleoside portion of the antibiotic puromycin. It is a puromycin analog which does not inhibit protein synthesis or induce apoptosis. Used in the study of focal and segmental glomerulosclerosis and in the induction of nephrosis in rats. The excretion of sodium and NOx metabolites in rats with puromycin aminonucleoside-induced nephrotic syndrome has been studied. Used to probe endothelial glycosaminoglycan synthesis in cultured glomerular endothelial cells and their relation to cell permeability
The aminonucleoside portion of the antibiotic puromycin.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Nucleosides, nucleotides, and analogues
Class Purine nucleosides
Subclass Purine 3'-deoxyribonucleosides
Intermediate Tree Nodes Not available
Direct Parent Purine 3'-deoxyribonucleosides
Alternative Parents 6-alkylaminopurines  Glycosylamines  Pentoses  Dialkylarylamines  Aminopyrimidines and derivatives  N-substituted imidazoles  Imidolactams  Tetrahydrofurans  1,3-aminoalcohols  Heteroaromatic compounds  Secondary alcohols  1,2-aminoalcohols  Oxacyclic compounds  Azacyclic compounds  Monoalkylamines  Organopnictogen compounds  Primary alcohols  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Purine 3'-deoxyribonucleoside - 6-alkylaminopurine - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Dialkylarylamine - Aminopyrimidine - Monosaccharide - Imidolactam - N-substituted imidazole - Pyrimidine - 1,3-aminoalcohol - Heteroaromatic compound - Imidazole - Tetrahydrofuran - Azole - 1,2-aminoalcohol - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Primary alcohol - Primary amine - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Alcohol - Primary aliphatic amine - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as purine 3'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 3.
External Descriptors adenosines - 3'-deoxyribonucleoside

Associated Targets(non-human)

Trypanosoma cruzi (99888 Activities)
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

IUPAC Name (2R,3R,4S,5S)-4-amino-2-[6-(dimethylamino)purin-9-yl]-5-(hydroxymethyl)oxolan-3-ol
INCHI InChI=1S/C12H18N6O3/c1-17(2)10-8-11(15-4-14-10)18(5-16-8)12-9(20)7(13)6(3-19)21-12/h4-7,9,12,19-20H,3,13H2,1-2H3/t6-,7-,9-,12-/m1/s1
InChIKey RYSMHWILUNYBFW-GRIPGOBMSA-N
Smiles CN(C)C1=NC=NC2=C1N=CN2C3C(C(C(O3)CO)N)O
Isomeric SMILES CN(C)C1=NC=NC2=C1N=CN2[C@H]3[C@@H]([C@@H]([C@H](O3)CO)N)O
WGK Germany 3
Molecular Weight 294.31
Beilstein 93902
Reaxy-Rn 14439847
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=14439847&ln=

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

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

Chemical and Physical Properties

Sensitivity Light sensitive
Molecular Weight 294.310 g/mol
XLogP3 -0.500
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 8
Rotatable Bond Count 3
Exact Mass 294.144 Da
Monoisotopic Mass 294.144 Da
Topological Polar Surface Area 123.000 Ų
Heavy Atom Count 21
Formal Charge 0
Complexity 373.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 4
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

Solution Calculators

Reviews

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