Design and synthesis of non-hydrolyzable homoisoprenoid α-monofluorophosphonate inhibitors of PPAPDC family integral membrane lipid phosphatases

Thangaiah Subramanian; Hongmei Ren; Karunai Leela Subramanian; Manjula Sunkara; Fredrick O. Onono; Andrew J. Morris; H. Peter Spielmann

doi:10.1016/j.bmcl.2014.08.013

Design and synthesis of non-hydrolyzable homoisoprenoid α-monofluorophosphonate inhibitors of PPAPDC family integral membrane lipid phosphatases

Thangaiah Subramanian
, Hongmei Ren
, Karunai Leela Subramanian
, Manjula Sunkara
, Fredrick O. Onono
, Andrew J. Morris
, H. Peter Spielmann

Producción científica: Article › revisión exhaustiva

3 Citas (Scopus)

Resumen

An efficient, diversity oriented synthesis of homoisoprenoid α-monofluorophosphonates utilizing electrophilic fluorination is presented along with their activity as inhibitors of PPAPDC2 family integral membrane lipid phosphatases. These novel phosphatase-resistant analogues of isoprenoid monophosphates are a platform for further structure-activity relationship studies and provide access to other isoprenoid family members where the phosphate ester oxygen is replaced by a α-monofluoromethylene moiety.

Idioma original	English
Páginas (desde-hasta)	4414-4417
Número de páginas	4
Publicación	Bioorganic and Medicinal Chemistry Letters
Volumen	24
N.º	18
DOI	https://doi.org/10.1016/j.bmcl.2014.08.013
Estado	Published - sept 15 2014

Nota bibliográfica

Publisher Copyright:
© 2014 Elsevier Ltd. All rights reserved.

Financiación

We thank Drs. Jing Chen and Haining Zhu for assistance obtaining some of the mass spectra. This work was supported by NIH grants R01 GM66152 to H.P.S., R01 GM50388 , P20 GM103527 and with resources provided by the Lexington Veterans Affairs Medical Center to A.J.M.

Financiadores	Número del financiador
Lexington Veterans Affairs Medical Center
National Institutes of Health (NIH)	R01 GM50388, R01 GM66152
National Institute of General Medical Sciences	P20GM103527

ASJC Scopus subject areas

Biochemistry
Molecular Medicine
Molecular Biology
Pharmaceutical Science
Drug Discovery
Clinical Biochemistry
Organic Chemistry

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10.1016/j.bmcl.2014.08.013

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title = "Design and synthesis of non-hydrolyzable homoisoprenoid α-monofluorophosphonate inhibitors of PPAPDC family integral membrane lipid phosphatases",

abstract = "An efficient, diversity oriented synthesis of homoisoprenoid α-monofluorophosphonates utilizing electrophilic fluorination is presented along with their activity as inhibitors of PPAPDC2 family integral membrane lipid phosphatases. These novel phosphatase-resistant analogues of isoprenoid monophosphates are a platform for further structure-activity relationship studies and provide access to other isoprenoid family members where the phosphate ester oxygen is replaced by a α-monofluoromethylene moiety.",

keywords = "Farnesyl diphosphate, Isoprenol, Mevalonate pathway, Phosphatase inhibitor, Phosphonate",

author = "Thangaiah Subramanian and Hongmei Ren and Subramanian, \{Karunai Leela\} and Manjula Sunkara and Onono, \{Fredrick O.\} and Morris, \{Andrew J.\} and Spielmann, \{H. Peter\}",

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doi = "10.1016/j.bmcl.2014.08.013",

language = "English",

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T1 - Design and synthesis of non-hydrolyzable homoisoprenoid α-monofluorophosphonate inhibitors of PPAPDC family integral membrane lipid phosphatases

AU - Subramanian, Thangaiah

AU - Ren, Hongmei

AU - Subramanian, Karunai Leela

AU - Sunkara, Manjula

AU - Onono, Fredrick O.

AU - Morris, Andrew J.

AU - Spielmann, H. Peter

PY - 2014/9/15

Y1 - 2014/9/15

N2 - An efficient, diversity oriented synthesis of homoisoprenoid α-monofluorophosphonates utilizing electrophilic fluorination is presented along with their activity as inhibitors of PPAPDC2 family integral membrane lipid phosphatases. These novel phosphatase-resistant analogues of isoprenoid monophosphates are a platform for further structure-activity relationship studies and provide access to other isoprenoid family members where the phosphate ester oxygen is replaced by a α-monofluoromethylene moiety.

AB - An efficient, diversity oriented synthesis of homoisoprenoid α-monofluorophosphonates utilizing electrophilic fluorination is presented along with their activity as inhibitors of PPAPDC2 family integral membrane lipid phosphatases. These novel phosphatase-resistant analogues of isoprenoid monophosphates are a platform for further structure-activity relationship studies and provide access to other isoprenoid family members where the phosphate ester oxygen is replaced by a α-monofluoromethylene moiety.

KW - Farnesyl diphosphate

KW - Isoprenol

KW - Mevalonate pathway

KW - Phosphatase inhibitor

KW - Phosphonate

UR - https://www.scopus.com/pages/publications/84906965211

UR - https://www.scopus.com/pages/publications/84906965211#tab=citedBy

U2 - 10.1016/j.bmcl.2014.08.013

DO - 10.1016/j.bmcl.2014.08.013

M3 - Article

C2 - 25150376

AN - SCOPUS:84906965211

SN - 0960-894X

VL - 24

SP - 4414

EP - 4417

JO - Bioorganic and Medicinal Chemistry Letters

JF - Bioorganic and Medicinal Chemistry Letters

IS - 18

ER -

Design and synthesis of non-hydrolyzable homoisoprenoid α-monofluorophosphonate inhibitors of PPAPDC family integral membrane lipid phosphatases

Resumen

Nota bibliográfica

Financiación

ASJC Scopus subject areas

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