Dmitry Pitushkin

Dr. Dmitry Pitushkin

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Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2018 in Bioorganic & Medicinal Chemistry Letters
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Journal Article
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VBVladimir Burmistrov
Vladimir Burmistrov
CMChristophe Morisseau
Christophe Morisseau
DPDmitry Pitushkin
Dmitry Pitushkin
DKDmitry Karlov
Dmitry Karlov
Robert R. FayzullinRobert R. Fayzullin
Robert R. Fayzullin
BHBruce Hammock
Bruce Hammock

1 July 2015 in Russian Chemical Bulletin
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Journal Article
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GBGennady Butov
Gennady Butov
VBV. V. Burmistrov
V. V. Burmistrov
DDD. V. Danilov
D. V. Danilov
DPDmitry Pitushkin
Dmitry Pitushkin
CMC. Morisseau
C. Morisseau
BHB. D. Hammock
B. D. Hammock

Verified
Journal Article
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Vladimir BurmistrovVladimir Burmistrov
Vladimir Burmistrov
Christophe MorisseauChristophe Morisseau
Christophe Morisseau
Denis BabkovDenis Babkov
Denis Babkov
TGTatiana Golubeva
Tatiana Golubeva
DPDmitry Pitushkin
Dmitry Pitushkin
BHBruce Hammock
Bruce Hammock
The inhibitory potency of the series of inhibitors of the soluble epoxide hydrolase (sEH) based on the selenourea moiety and containing adamantane and aromatic lipophilic groups ranges from 34.3 nM to 1.2 μM. The most active compound 5d possesses aliphatic spacers between the selenourea group and lipophilic fragments. Synthesized compounds were tested against the LPS-induced activation of primary murine macrophages. The most prominent anti-inflammatory activity, defined as a suppression of nitric oxide synthesis by LPS-stimulated macrophages, was demonstrated for compounds 4a and 5b. The cytotoxicity of the obtained substances was studied using human neuroblastoma and fibroblast cell cultures. Using these cell assays, the cytotoxic concentration for 4a was 4.7–18.4 times higher than the effective anti-inflammatory concentration. The genotoxicity and the ability to induce oxidative stress was studied using bacterial lux-biosensors. Substance 4a does not exhibit genotoxic properties, but it can cause oxidative stress at concentrations above 50 µM. Put together, the data showed the efficacy and safety of compound 4a.

1 May 2017 in Russian Journal of Organic Chemistry
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Journal Article
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GBGennady Butov
Gennady Butov
VBV. V. Burmistrov
V. V. Burmistrov
DPDmitry Pitushkin
Dmitry Pitushkin
One-step preparation method was developed for adamantyl-containing isocyanates obtained by Curtius reaction from adamantanecarboxylic and acetic acids. Synthesis of isocyanate was performed without the isolation of intermediate acid chloride which solution was added to sodium azide in boiling toluene. In the reactor the acid azide formation and its rearrangement in isocyanate occurred simultaneously. Yields of target products were 83–94% with respect to the acid.

1 September 2014 in Russian Journal of Organic Chemistry
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Journal Article
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GBGennady Butov
Gennady Butov
VMV. M. Mokhov
V. M. Mokhov
Vladimir BurmistrovVladimir Burmistrov
Vladimir Burmistrov
KSK. R. Saad
K. R. Saad
DPDmitry Pitushkin
Dmitry Pitushkin
A convenient and efficient procedure has been developed for the synthesis of 1-azidoadamantane, 1-adamantyl isocyanate, and 1-adamantyl isothiocyanate by reaction of 1,3-dehydroadamantane with...

16 March 2017 in SynOpen
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Vladimir BurmistrovVladimir Burmistrov
Vladimir Burmistrov
DPDmitry Pitushkin
Dmitry Pitushkin
GBGennady Butov
Gennady Butov
A series of adamantyl isothiocyanates containing different substituents in the nodal positions of adamantane or spacers between the adamantane and isothiocyanate group have been synthesised by using the reaction of the corresponding adamantyl amines with phenyl isothiocyanate.