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CAS 14047-27-9

:

(αS)-6-Amino-α-methyl-9H-purine-9-ethanol

Description:
(αS)-6-Amino-α-methyl-9H-purine-9-ethanol, with the CAS number 14047-27-9, is a purine derivative characterized by its structural features that include an amino group and an ethanol side chain. This compound is a member of the purine family, which plays a crucial role in various biological processes, including nucleic acid metabolism and energy transfer. The presence of the amino group contributes to its potential as a building block for nucleotides, while the α-methyl group may influence its biological activity and solubility. The ethanol moiety can enhance its interaction with biological systems, potentially affecting its pharmacokinetics and pharmacodynamics. This compound may exhibit properties such as being a substrate or inhibitor for specific enzymes, making it of interest in biochemical research and pharmaceutical applications. Its stereochemistry, indicated by the (αS) designation, suggests specific spatial arrangements that can significantly impact its biological function and interactions. Overall, this compound's unique characteristics make it a valuable subject for further study in medicinal chemistry and biochemistry.
Formula:C8H11N5O
InChI:InChI=1S/C8H11N5O/c1-5(14)2-13-4-12-6-7(9)10-3-11-8(6)13/h3-5,14H,2H2,1H3,(H2,9,10,11)/t5-/m0/s1
InChI key:InChIKey=MJZYTEBKXLVLMY-YFKPBYRVSA-N
SMILES:C([C@H](C)O)N1C=2C(N=C1)=C(N)N=CN2
Synonyms:
  • (S)-(-)-9-(2-Hydroxypropyl)Adenine
  • (S)-1-(6-amino-9H-purin-9-yl)propan-2-ol
  • (αS)-6-Amino-α-methyl-9H-purine-9-ethanol
  • 1-(6-Amino-9H-purin-9-yl)-2-propanol
  • 9-[(2S)-2-Hydroxypropyl]adenine
  • 9H-Purine-9-ethanol, 6-amino-α-methyl-, (S)-
  • 9H-Purine-9-ethanol, 6-amino-α-methyl-, (αS)-
  • 9H-Purine-9-ethanol, 6-amino-α-methyl-, <span class="text-smallcaps">L</span>-
  • <span class="text-smallcaps">L</span>-(+)-9-(2-Hydroxypropyl)adenine
  • 9H-Purine-9-ethanol, 6-amino-α-methyl-, L-
  • L-(+)-9-(2-Hydroxypropyl)adenine
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