共 16 条
Hologram QSAR studies on farnesoid X receptor activators
被引:20
作者:

Honorio, Kathia M.
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机构:
Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil

Garratt, Richard C.
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h-index: 0
机构:
Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil

Polikarpov, Igor
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机构:
Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil

Andricopulo, Adriano D.
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机构:
Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil
机构:
[1] Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil
关键词:
hQSAR;
drug design;
FXR;
medicinal chemistry;
cholesterol;
D O I:
10.2174/157018006776743206
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Farsenoid X receptor (FXR) is an attractive drug target due to its role in the regulation of cholesterol and bile acid levels' Hologram quantitative structure-activity relationships (HQSAR) were conducted on a series of FXR activators, and the final model obtained was used to predict the potency of 10 test set compounds. The predicted values were in good agreement with the experimental results.
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页码:261 / 267
页数:7
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[1]
Two- and three-dimensional quantitative structure-activity relationships for a series of purine nucleoside phosphorylase inhibitors
[J].
Castilho, MS
;
Postigo, MP
;
de Paula, CBV
;
Montanari, CA
;
Oliva, G
;
Andricopulo, AD
.
BIOORGANIC & MEDICINAL CHEMISTRY,
2006, 14 (02)
:516-527

Castilho, MS
论文数: 0 引用数: 0
h-index: 0
机构: Univ Sao Paulo, Lab Quim Med & Computac, Ctr Biotecnol Mol Estrutural, Inst Fis Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil

Postigo, MP
论文数: 0 引用数: 0
h-index: 0
机构: Univ Sao Paulo, Lab Quim Med & Computac, Ctr Biotecnol Mol Estrutural, Inst Fis Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil

de Paula, CBV
论文数: 0 引用数: 0
h-index: 0
机构: Univ Sao Paulo, Lab Quim Med & Computac, Ctr Biotecnol Mol Estrutural, Inst Fis Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil

Montanari, CA
论文数: 0 引用数: 0
h-index: 0
机构: Univ Sao Paulo, Lab Quim Med & Computac, Ctr Biotecnol Mol Estrutural, Inst Fis Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil

Oliva, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Sao Paulo, Lab Quim Med & Computac, Ctr Biotecnol Mol Estrutural, Inst Fis Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil

Andricopulo, AD
论文数: 0 引用数: 0
h-index: 0
机构: Univ Sao Paulo, Lab Quim Med & Computac, Ctr Biotecnol Mol Estrutural, Inst Fis Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil
[2]
Regulation of bile acid synthesis: pathways, nuclear receptors, and mechanisms
[J].
Chiang, JYL
.
JOURNAL OF HEPATOLOGY,
2004, 40 (03)
:539-551

Chiang, JYL
论文数: 0 引用数: 0
h-index: 0
机构:
Northeastern Ohio Univ Coll Med & Pharm, Coll Med, Dept Biochem & Mol Pathol, Rootstown, OH 44272 USA Northeastern Ohio Univ Coll Med & Pharm, Coll Med, Dept Biochem & Mol Pathol, Rootstown, OH 44272 USA
[3]
Structure-activity relationship of bile acids and bile acid analogs in regard to FXR activation
[J].
Fujino, T
;
Une, M
;
Imanaka, T
;
Inoue, K
;
Nishimaki-Mogami, T
.
JOURNAL OF LIPID RESEARCH,
2004, 45 (01)
:132-138

Fujino, T
论文数: 0 引用数: 0
h-index: 0
机构: Hiroshima Univ, Grad Sch Biomed Sci, Programs Pharmaceut Sci, Div Med Chem, Hiroshima, Japan

Une, M
论文数: 0 引用数: 0
h-index: 0
机构:
Hiroshima Univ, Grad Sch Biomed Sci, Programs Pharmaceut Sci, Div Med Chem, Hiroshima, Japan Hiroshima Univ, Grad Sch Biomed Sci, Programs Pharmaceut Sci, Div Med Chem, Hiroshima, Japan

Imanaka, T
论文数: 0 引用数: 0
h-index: 0
机构: Hiroshima Univ, Grad Sch Biomed Sci, Programs Pharmaceut Sci, Div Med Chem, Hiroshima, Japan

Inoue, K
论文数: 0 引用数: 0
h-index: 0
机构: Hiroshima Univ, Grad Sch Biomed Sci, Programs Pharmaceut Sci, Div Med Chem, Hiroshima, Japan

Nishimaki-Mogami, T
论文数: 0 引用数: 0
h-index: 0
机构: Hiroshima Univ, Grad Sch Biomed Sci, Programs Pharmaceut Sci, Div Med Chem, Hiroshima, Japan
[4]
Principles for modulation of the nuclear receptor superfamily
[J].
Gronemeyer, H
;
Gustafsson, JÅ
;
Laudet, V
.
NATURE REVIEWS DRUG DISCOVERY,
2004, 3 (11)
:950-964

Gronemeyer, H
论文数: 0 引用数: 0
h-index: 0
机构: Ecole Normale Super Lyon, Lab Biol Mol Cellule, CNRS UMR 5161, INRA LA 1237, F-69364 Lyon 07, France

Gustafsson, JÅ
论文数: 0 引用数: 0
h-index: 0
机构: Ecole Normale Super Lyon, Lab Biol Mol Cellule, CNRS UMR 5161, INRA LA 1237, F-69364 Lyon 07, France

Laudet, V
论文数: 0 引用数: 0
h-index: 0
机构: Ecole Normale Super Lyon, Lab Biol Mol Cellule, CNRS UMR 5161, INRA LA 1237, F-69364 Lyon 07, France
[5]
Hologram quantitative structure-activity relationships for a series of farnesoid X receptor activators
[J].
Honorio, KM
;
Garratt, RC
;
Andricopulo, AD
.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,
2005, 15 (12)
:3119-3125

Honorio, KM
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil

Garratt, RC
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil

Andricopulo, AD
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil Univ Sao Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrutural, Lab Quim Med & Computac, BR-13560970 Sao Carlos, SP, Brazil
[6]
The farnesoid X receptor (FXR) as modulator of bile acid metabolism
[J].
Kuipers, F
;
Claudel, T
;
Sturm, E
;
Staels, B
.
REVIEWS IN ENDOCRINE & METABOLIC DISORDERS,
2004, 5 (04)
:319-326

Kuipers, F
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Groningen, Univ Med Ctr Groningen, Pediat Lab, Ctr Liver Digest & Metab Dis, Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Pediat Lab, Ctr Liver Digest & Metab Dis, Groningen, Netherlands

Claudel, T
论文数: 0 引用数: 0
h-index: 0
机构: Univ Groningen, Univ Med Ctr Groningen, Pediat Lab, Ctr Liver Digest & Metab Dis, Groningen, Netherlands

Sturm, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Groningen, Univ Med Ctr Groningen, Pediat Lab, Ctr Liver Digest & Metab Dis, Groningen, Netherlands

Staels, B
论文数: 0 引用数: 0
h-index: 0
机构: Univ Groningen, Univ Med Ctr Groningen, Pediat Lab, Ctr Liver Digest & Metab Dis, Groningen, Netherlands
[7]
Identification of a chemical tool for the orphan nuclear receptor FXR
[J].
Maloney, PR
;
Parks, DJ
;
Haffner, CD
;
Fivush, AM
;
Chandra, G
;
Plunket, KD
;
Creech, KL
;
Moore, LB
;
Wilson, JG
;
Lewis, MC
;
Jones, SA
;
Willson, TM
.
JOURNAL OF MEDICINAL CHEMISTRY,
2000, 43 (16)
:2971-2974

Maloney, PR
论文数: 0 引用数: 0
h-index: 0
机构: Glaxo Wellcome Res & Dev Ltd, Dept Med Chem, Res Triangle Pk, NC 27709 USA

Parks, DJ
论文数: 0 引用数: 0
h-index: 0
机构: Glaxo Wellcome Res & Dev Ltd, Dept Med Chem, Res Triangle Pk, NC 27709 USA

Haffner, CD
论文数: 0 引用数: 0
h-index: 0
机构: Glaxo Wellcome Res & Dev Ltd, Dept Med Chem, Res Triangle Pk, NC 27709 USA

Fivush, AM
论文数: 0 引用数: 0
h-index: 0
机构: Glaxo Wellcome Res & Dev Ltd, Dept Med Chem, Res Triangle Pk, NC 27709 USA

Chandra, G
论文数: 0 引用数: 0
h-index: 0
机构: Glaxo Wellcome Res & Dev Ltd, Dept Med Chem, Res Triangle Pk, NC 27709 USA

Plunket, KD
论文数: 0 引用数: 0
h-index: 0
机构: Glaxo Wellcome Res & Dev Ltd, Dept Med Chem, Res Triangle Pk, NC 27709 USA

Creech, KL
论文数: 0 引用数: 0
h-index: 0
机构: Glaxo Wellcome Res & Dev Ltd, Dept Med Chem, Res Triangle Pk, NC 27709 USA

Moore, LB
论文数: 0 引用数: 0
h-index: 0
机构: Glaxo Wellcome Res & Dev Ltd, Dept Med Chem, Res Triangle Pk, NC 27709 USA

Wilson, JG
论文数: 0 引用数: 0
h-index: 0
机构: Glaxo Wellcome Res & Dev Ltd, Dept Med Chem, Res Triangle Pk, NC 27709 USA

Lewis, MC
论文数: 0 引用数: 0
h-index: 0
机构: Glaxo Wellcome Res & Dev Ltd, Dept Med Chem, Res Triangle Pk, NC 27709 USA

Jones, SA
论文数: 0 引用数: 0
h-index: 0
机构: Glaxo Wellcome Res & Dev Ltd, Dept Med Chem, Res Triangle Pk, NC 27709 USA

Willson, TM
论文数: 0 引用数: 0
h-index: 0
机构: Glaxo Wellcome Res & Dev Ltd, Dept Med Chem, Res Triangle Pk, NC 27709 USA
[8]
Structural basis for bile acid binding and activation of the nuclear receptor FXR
[J].
Mi, LZ
;
Devarakonda, S
;
Harp, JM
;
Han, C
;
Pellicciari, R
;
Willson, TM
;
Khorasanizadeh, S
;
Rastinejad, F
.
MOLECULAR CELL,
2003, 11 (04)
:1093-1100

Mi, LZ
论文数: 0 引用数: 0
h-index: 0
机构: Univ Virginia, Hlth Syst, Dept Pharmacol, Charlottesville, VA 22908 USA

Devarakonda, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Virginia, Hlth Syst, Dept Pharmacol, Charlottesville, VA 22908 USA

Harp, JM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Virginia, Hlth Syst, Dept Pharmacol, Charlottesville, VA 22908 USA

Han, C
论文数: 0 引用数: 0
h-index: 0
机构: Univ Virginia, Hlth Syst, Dept Pharmacol, Charlottesville, VA 22908 USA

Pellicciari, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Virginia, Hlth Syst, Dept Pharmacol, Charlottesville, VA 22908 USA

Willson, TM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Virginia, Hlth Syst, Dept Pharmacol, Charlottesville, VA 22908 USA

Khorasanizadeh, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Virginia, Hlth Syst, Dept Pharmacol, Charlottesville, VA 22908 USA

Rastinejad, F
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Virginia, Hlth Syst, Dept Pharmacol, Charlottesville, VA 22908 USA Univ Virginia, Hlth Syst, Dept Pharmacol, Charlottesville, VA 22908 USA
[9]
Discovery of novel nuclear receotor modulating ligands: an for peptide interaction integral role profiling
[J].
Pearce, KH
;
Iannone, MA
;
Simmons, CA
;
Gray, JG
.
DRUG DISCOVERY TODAY,
2004, 9 (17)
:741-751

Pearce, KH
论文数: 0 引用数: 0
h-index: 0
机构:
GlaxoSmithKline, Dept Gene Express & Prot Biochem, Discovery Res, Res Triangle Pk, NC 27709 USA GlaxoSmithKline, Dept Gene Express & Prot Biochem, Discovery Res, Res Triangle Pk, NC 27709 USA

Iannone, MA
论文数: 0 引用数: 0
h-index: 0
机构:
GlaxoSmithKline, Dept Gene Express & Prot Biochem, Discovery Res, Res Triangle Pk, NC 27709 USA GlaxoSmithKline, Dept Gene Express & Prot Biochem, Discovery Res, Res Triangle Pk, NC 27709 USA

Simmons, CA
论文数: 0 引用数: 0
h-index: 0
机构:
GlaxoSmithKline, Dept Gene Express & Prot Biochem, Discovery Res, Res Triangle Pk, NC 27709 USA GlaxoSmithKline, Dept Gene Express & Prot Biochem, Discovery Res, Res Triangle Pk, NC 27709 USA

Gray, JG
论文数: 0 引用数: 0
h-index: 0
机构:
GlaxoSmithKline, Dept Gene Express & Prot Biochem, Discovery Res, Res Triangle Pk, NC 27709 USA GlaxoSmithKline, Dept Gene Express & Prot Biochem, Discovery Res, Res Triangle Pk, NC 27709 USA
[10]
Farnesoid X receptor: From structure to potential clinical applications
[J].
Pellicciari, R
;
Costantino, G
;
Fiorucci, S
.
JOURNAL OF MEDICINAL CHEMISTRY,
2005, 48 (17)
:5383-5403

Pellicciari, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Perugia, Dipartimento Chim & tecnol Farmaco, I-06123 Perugia, Italy

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