Synthesis and SAR studies of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives as potent inhibitors of Bloom helicase

Research output: Contribution to journal › Journal article › Research › peer-review

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Synthesis and SAR studies of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives as potent inhibitors of Bloom helicase. / Rosenthal, Andrew S; Dexheimer, Thomas S; Gileadi, Opher; Nguyen, Giang H; Chu, Wai Kit; Hickson, Ian D; Jadhav, Ajit; Simeonov, Anton; Maloney, David J.

In: Bioorganic & Medicinal Chemistry Letters, Vol. 23, No. 20, 15.10.2013, p. 5660-6.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Rosenthal, AS, Dexheimer, TS, Gileadi, O, Nguyen, GH, Chu, WK, Hickson, ID, Jadhav, A, Simeonov, A & Maloney, DJ 2013, 'Synthesis and SAR studies of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives as potent inhibitors of Bloom helicase', Bioorganic & Medicinal Chemistry Letters, vol. 23, no. 20, pp. 5660-6. https://doi.org/10.1016/j.bmcl.2013.08.025

APA

Rosenthal, A. S., Dexheimer, T. S., Gileadi, O., Nguyen, G. H., Chu, W. K., Hickson, I. D., Jadhav, A., Simeonov, A., & Maloney, D. J. (2013). Synthesis and SAR studies of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives as potent inhibitors of Bloom helicase. Bioorganic & Medicinal Chemistry Letters, 23(20), 5660-6. https://doi.org/10.1016/j.bmcl.2013.08.025

Vancouver

Rosenthal AS, Dexheimer TS, Gileadi O, Nguyen GH, Chu WK, Hickson ID et al. Synthesis and SAR studies of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives as potent inhibitors of Bloom helicase. Bioorganic & Medicinal Chemistry Letters. 2013 Oct 15;23(20):5660-6. https://doi.org/10.1016/j.bmcl.2013.08.025

Author

Rosenthal, Andrew S ; Dexheimer, Thomas S ; Gileadi, Opher ; Nguyen, Giang H ; Chu, Wai Kit ; Hickson, Ian D ; Jadhav, Ajit ; Simeonov, Anton ; Maloney, David J. / Synthesis and SAR studies of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives as potent inhibitors of Bloom helicase. In: Bioorganic & Medicinal Chemistry Letters. 2013 ; Vol. 23, No. 20. pp. 5660-6.

Bibtex

@article{1c6f215ad6094e3c92d877785117a258,
title = "Synthesis and SAR studies of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives as potent inhibitors of Bloom helicase",
abstract = "Human cells utilize a variety of complex DNA repair mechanisms in order to combat constant mutagenic and cytotoxic threats from both exogenous and endogenous sources. The RecQ family of DNA helicases, which includes Bloom helicase (BLM), plays an important function in DNA repair by unwinding complementary strands of duplex DNA as well as atypical DNA structures such as Holliday junctions. Mutations of the BLM gene can result in Bloom syndrome, an autosomal recessive disorder associated with cancer predisposition. BLM-deficient cells exhibit increased sensitivity to DNA damaging agents indicating that a selective BLM inhibitor could be useful in potentiating the anticancer activity of these agents. In this work, we describe the medicinal chemistry optimization of the hit molecule following a quantitative high-throughput screen of >355,000 compounds. These efforts lead to the identification of ML216 and related analogs, which possess potent BLM inhibition and exhibit selectivity over related helicases. Moreover, these compounds demonstrated cellular activity by inducing sister chromatid exchanges, a hallmark of Bloom syndrome.",
author = "Rosenthal, {Andrew S} and Dexheimer, {Thomas S} and Opher Gileadi and Nguyen, {Giang H} and Chu, {Wai Kit} and Hickson, {Ian D} and Ajit Jadhav and Anton Simeonov and Maloney, {David J}",
note = "Published by Elsevier Ltd.",
year = "2013",
month = oct,
day = "15",
doi = "10.1016/j.bmcl.2013.08.025",
language = "English",
volume = "23",
pages = "5660--6",
journal = "Bioorganic & Medicinal Chemistry Letters",
issn = "0960-894X",
publisher = "Pergamon Press",
number = "20",

}

RIS

TY - JOUR

T1 - Synthesis and SAR studies of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives as potent inhibitors of Bloom helicase

AU - Rosenthal, Andrew S

AU - Dexheimer, Thomas S

AU - Gileadi, Opher

AU - Nguyen, Giang H

AU - Chu, Wai Kit

AU - Hickson, Ian D

AU - Jadhav, Ajit

AU - Simeonov, Anton

AU - Maloney, David J

N1 - Published by Elsevier Ltd.

PY - 2013/10/15

Y1 - 2013/10/15

N2 - Human cells utilize a variety of complex DNA repair mechanisms in order to combat constant mutagenic and cytotoxic threats from both exogenous and endogenous sources. The RecQ family of DNA helicases, which includes Bloom helicase (BLM), plays an important function in DNA repair by unwinding complementary strands of duplex DNA as well as atypical DNA structures such as Holliday junctions. Mutations of the BLM gene can result in Bloom syndrome, an autosomal recessive disorder associated with cancer predisposition. BLM-deficient cells exhibit increased sensitivity to DNA damaging agents indicating that a selective BLM inhibitor could be useful in potentiating the anticancer activity of these agents. In this work, we describe the medicinal chemistry optimization of the hit molecule following a quantitative high-throughput screen of >355,000 compounds. These efforts lead to the identification of ML216 and related analogs, which possess potent BLM inhibition and exhibit selectivity over related helicases. Moreover, these compounds demonstrated cellular activity by inducing sister chromatid exchanges, a hallmark of Bloom syndrome.

AB - Human cells utilize a variety of complex DNA repair mechanisms in order to combat constant mutagenic and cytotoxic threats from both exogenous and endogenous sources. The RecQ family of DNA helicases, which includes Bloom helicase (BLM), plays an important function in DNA repair by unwinding complementary strands of duplex DNA as well as atypical DNA structures such as Holliday junctions. Mutations of the BLM gene can result in Bloom syndrome, an autosomal recessive disorder associated with cancer predisposition. BLM-deficient cells exhibit increased sensitivity to DNA damaging agents indicating that a selective BLM inhibitor could be useful in potentiating the anticancer activity of these agents. In this work, we describe the medicinal chemistry optimization of the hit molecule following a quantitative high-throughput screen of >355,000 compounds. These efforts lead to the identification of ML216 and related analogs, which possess potent BLM inhibition and exhibit selectivity over related helicases. Moreover, these compounds demonstrated cellular activity by inducing sister chromatid exchanges, a hallmark of Bloom syndrome.

U2 - 10.1016/j.bmcl.2013.08.025

DO - 10.1016/j.bmcl.2013.08.025

M3 - Journal article

C2 - 24012121

VL - 23

SP - 5660

EP - 5666

JO - Bioorganic & Medicinal Chemistry Letters

JF - Bioorganic & Medicinal Chemistry Letters

SN - 0960-894X

IS - 20

ER -

ID: 108666272