메뉴 건너뛰기




Volumn 19, Issue 7, 2009, Pages 2053-2058

Exploring the pharmacokinetic properties of phosphorus-containing selective HDAC 1 and 2 inhibitors (SHI-1:2)

Author keywords

Pharmacokinetics; Phosphorus containing therapeutic; Selective histone deacetylase inhibitor; Xenograft; Zolinza

Indexed keywords

HISTONE DEACETYLASE 1; HISTONE DEACETYLASE 2; HISTONE DEACETYLASE INHIBITOR; PHOSPHINE DERIVATIVE; PHOSPHONIC ACID DERIVATIVE;

EID: 61849130717     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2009.02.009     Document Type: Article
Times cited : (19)

References (30)
  • 19
    • 61849178283 scopus 로고    scopus 로고
    • note
    • Diethyl(4-carboxylphenyl)phosphonate, CAS 1527-34-0, ABCR, catalog number AB147504.
  • 22
    • 33947087939 scopus 로고
    • Methoxy-substituted examples saponified with superior results than the corresponding ethoxy examples, putatively as a result of the mechanism of alkaline hydrolysis. For a discussion of alkaline mechanism, see
    • Methoxy-substituted examples saponified with superior results than the corresponding ethoxy examples, putatively as a result of the mechanism of alkaline hydrolysis. For a discussion of alkaline mechanism, see. Cook R.D., Diebert C.E., Schwarz W., Turley P.C., and Haake P. J. Am. Chem. Soc. 95 (1973) 8088
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 8088
    • Cook, R.D.1    Diebert, C.E.2    Schwarz, W.3    Turley, P.C.4    Haake, P.5
  • 23
    • 11444265188 scopus 로고
    • Acidic hydrolysis is more facile, but incompatible with our BOC protecting group. For a discussion of acidic mechanism, see
    • Acidic hydrolysis is more facile, but incompatible with our BOC protecting group. For a discussion of acidic mechanism, see. Abbas K., and Cook R.D. Tetrahedron Lett. 41 (1975) 3559
    • (1975) Tetrahedron Lett. , vol.41 , pp. 3559
    • Abbas, K.1    Cook, R.D.2
  • 24
    • 61849091069 scopus 로고    scopus 로고
    • note
    • 1H-Benzotriazol-1-yl-oxytris(dimethylamino) phosphonium hexofluorophoshate (BOP), CAS 056602-33-6. It is worth noting that the dehydration reaction yields inferior results with diimides such as EDC.
  • 25
    • 0037059912 scopus 로고    scopus 로고
    • Commercially available from Acros Organics, CAS 117196-73-3. For a preparation, see
    • Commercially available from Acros Organics, CAS 117196-73-3. For a preparation, see. Steere J.A., Sampson P.B., and Honek J.F. Bioorg. Med. Chem. Lett. 12 (2002) 457
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 457
    • Steere, J.A.1    Sampson, P.B.2    Honek, J.F.3
  • 26
    • 61849150724 scopus 로고    scopus 로고
    • note
    • For assay details, see Ref. 7b.
  • 27
    • 61849127961 scopus 로고    scopus 로고
    • note
    • 50 = 0.460 μM) substituents.
  • 28
    • 61849097458 scopus 로고    scopus 로고
    • note
    • Statistical significance was demonstrated via t-test analysis looking for a P-value of <0.05 relative to vehicle.
  • 30
    • 61849157934 scopus 로고    scopus 로고
    • The compounds described in this paper are the topic of a patent application. The reader is directed to this publication for experimental information: Close, J, Grimm, J, Heidebrecht, R. W, Kattar, S, Miller, T. A, Otte, K. M, Peterson, S, Siliphaivanh, P, Tempest, P, Wilson, K. J, Witter, D. J, WO 2008010985
    • The compounds described in this paper are the topic of a patent application. The reader is directed to this publication for experimental information: Close, J.; Grimm, J.; Heidebrecht, R. W.; Kattar, S.; Miller, T. A.; Otte, K. M.; Peterson, S.; Siliphaivanh, P.; Tempest, P.; Wilson, K. J.; Witter, D. J.; WO 2008010985.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.