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Fragment-based identification of Hsp90 inhibitors
scientific article
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title
Fragment-based identification of Hsp90 inhibitors
(English)
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author
Saverio Minucci
series ordinal
18
object named as
Saverio Minucci
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author name string
John J Barker
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1
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Oliver Barker
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2
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Roberto Boggio
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3
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Viddhata Chauhan
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4
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Robert K Y Cheng
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5
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Vincent Corden
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6
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Stephen M Courtney
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7
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Neil Edwards
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8
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Virginie M Falque
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9
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Fulvia Fusar
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10
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Mihaly Gardiner
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11
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Estelle M N Hamelin
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12
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Thomas Hesterkamp
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13
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Osamu Ichihara
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14
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Richard S Jones
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15
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Owen Mather
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16
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Ciro Mercurio
series ordinal
17
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Christian A G N Montalbetti
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19
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Annett Müller
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20
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Deepti Patel
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21
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Banu G Phillips
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22
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Mario Varasi
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23
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Mark Whittaker
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24
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Dirk Winkler
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25
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Christopher J Yarnold
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26
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publication date
June 2009
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published in
ChemMedChem
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volume
4
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issue
6
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page(s)
963-6
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cites work
A high-affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
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7 January 2021
based on heuristic
inferred from DOI database lookup
Targeting the molecular chaperone heat shock protein 90 provides a multifaceted effect on diverse cell signaling pathways of cancer cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure, function, and mechanism of the Hsp90 molecular chaperone
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The heat shock protein 90 antagonist novobiocin interacts with a previously unrecognized ATP-binding domain in the carboxyl terminus of the chaperone
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The heat shock protein 90-targeting drug cisplatin selectively inhibits steroid receptor activation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structural and functional analysis of the middle segment of hsp90: implications for ATP hydrolysis and client protein and cochaperone interactions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Development and application of Hsp90 inhibitors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hsp90 as a target for drug development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adenine derived inhibitors of the molecular chaperone HSP90-SAR explained through multiple X-ray structures
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
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7 January 2021
based on heuristic
inferred from DOI database lookup
Structure-based discovery of a new class of Hsp90 inhibitors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The benzoquinone ansamycin 17-allylamino-17-demethoxygeldanamycin binds to HSP90 and shares important biologic activities with geldanamycin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Development of 17-allylamino-17-demethoxygeldanamycin hydroquinone hydrochloride (IPI-504), an anti-cancer agent directed against Hsp90.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
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7 January 2021
based on heuristic
inferred from DOI database lookup
Phase I pharmacokinetic and pharmacodynamic study of 17-allylamino, 17-demethoxygeldanamycin in patients with advanced malignancies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
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7 January 2021
based on heuristic
inferred from DOI database lookup
Phase I trial of 17-allylamino-17-demethoxygeldanamycin in patients with advanced cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phase I pharmacokinetic and pharmacodynamic study of 17-N-allylamino-17-demethoxygeldanamycin in pediatric patients with recurrent or refractory solid tumors: a pediatric oncology experimental therapeutics investigators consortium study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phase I and pharmacodynamic study of 17-(allylamino)-17-demethoxygeldanamycin in adult patients with refractory advanced cancers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phase I trial of 17-allylamino-17-demethoxygeldanamycin in patients with advanced cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A phase I study of 17-allylaminogeldanamycin in relapsed/refractory pediatric patients with solid tumors: a Children's Oncology Group study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
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7 January 2021
based on heuristic
inferred from DOI database lookup
SNX2112, a synthetic heat shock protein 90 inhibitor, has potent antitumor activity against HER kinase-dependent cancers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
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7 January 2021
based on heuristic
inferred from DOI database lookup
4,5-diarylisoxazole Hsp90 chaperone inhibitors: potential therapeutic agents for the treatment of cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
NVP-AUY922: a novel heat shock protein 90 inhibitor active against xenograft tumor growth, angiogenesis, and metastasis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragment-based activity space: smaller is better
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragment based drug discovery using fluorescence correlation: spectroscopy techniques: challenges and solutions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular recognition of receptor sites using a genetic algorithm with a description of desolvation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCMDC.200900011
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/CMDC.200900011
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3863387
OpenCitations bibliographic resource ID
3863387
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3863387
PubMed publication ID
19301319
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3863387
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