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Chemical Compound Review

NSC-508     hexane-1,6-diol

Synonyms: AGN-PC-0CRI4T, NSC508, CHEMBL458616, ACMC-1AWZJ, CCRIS 8982, ...
 
 
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Disease relevance of Hexamethylene glycol

 

High impact information on Hexamethylene glycol

 

Anatomical context of Hexamethylene glycol

 

Associations of Hexamethylene glycol with other chemical compounds

  • The synthesis of three hydrophobic peptides, which are partial sequences of thioredoxin, on a newly developed, flexible 1,6-hexanediol diacrylate cross-linked polystyrene, in good yield and purity, is described [9].
  • 0. The glass transition temperature of the poly (ortho esters) can be continuously and predictably varied between 115 and 20 degrees Celsius by using an appropriate ratio of 1,6-hexanediol, and trans-cyclohexanedimethanol in the condensation reaction with the diketene acetal [10].
  • The purpose of the present study was to evaluate the safety of ethylene glyco (EG) and 1,6-hexanediol (HD) solutions as experimental dentin primers when subjected to the guinea pig maximization test (GPMT), primary irritation test, cumulative skin irritation test and human patch test [11].
 

Gene context of Hexamethylene glycol

References

  1. Lactate dehydrogenase isoenzyme 1 as determined by inhibition with 1,6-hexanediol and by two other methods in patients with myocardial infarction or cardiac-bypass surgery. Shamberger, R.J. Clin. Chem. (1987) [Pubmed]
  2. 1,6-hexanediol diacrylate: a rapid and potent sensitizer in the printing industry. Morgan, V.A., Fewings, J.M. Australas. J. Dermatol. (2000) [Pubmed]
  3. Metabolism of N-nitrosohexamethyleneimine to give 1,6-hexanediol bound to rat liver nucleic acids. Ross, A.E., Mirvish, S.S. J. Natl. Cancer Inst. (1977) [Pubmed]
  4. Comparison of the in vitro metabolism of N-nitrosohexamethyleneimine by rat liver and lung microsomal fractions. Hecker, L.I., McClusky, G.A. Cancer Res. (1982) [Pubmed]
  5. Direct evidence for the formation of a complex between 1-cysteine peroxiredoxin and glutathione S-transferase pi with activity changes in both enzymes. Ralat, L.A., Manevich, Y., Fisher, A.B., Colman, R.F. Biochemistry (2006) [Pubmed]
  6. Hexahydrocarbon effects on intermediate filament organization in human fibroblasts. Durham, H.D., Peña, S.D., Ecobichon, D.J. Muscle Nerve (1988) [Pubmed]
  7. Ultrastructural studies of the dying-back process. V. Axonal neurofilaments accumulate at sites of 2,5-hexanedione application: evidence for nerve fibre dysfunction in experimental hexacarbon neuropathy. Politis, M.J., Pellegrino, R.G., Spencer, P.S. J. Neurocytol. (1980) [Pubmed]
  8. Optimum concentration and application time of 1,6-hexanediol as a dentin primer. Rahman, M.A., Tani, C., Itoh, K., Wakumoto, S., Hisamitsu, H. Dental materials journal. (1995) [Pubmed]
  9. Solid phase synthesis of hydrophobic peptides on 1,6-hexanediol diacrylate cross-linked polystyrene resin. Varkey, J.T., Pillai, V.N. J. Pept. Sci. (1999) [Pubmed]
  10. Controlled release of contraceptive steroids from biodegradable poly (ortho esters). Heller, J., Penhale, D.W., Fritzinger, B.K., Rose, J.E., Helwing, R.F. Contraceptive delivery systems. (1983) [Pubmed]
  11. Evaluation of skin irritation and sensitization of two diol solutions used as experimental dentin primers in humans and guinea pigs. Kurihara, A., Manabe, A., Katsuno, K., Itoh, K., Hisamitsu, H., Wakumoto, S., Yoshida, T. Dental materials journal. (1996) [Pubmed]
  12. Synthesis of thioredoxin partial sequences on 1,6-hexanediol diacrylate (HDODA)-cross-linked polystyrene resin. Varkey, J.T., Pillai, V.N. J. Pept. Res. (1998) [Pubmed]
 
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