Alpha 2.0
Login Register
» Authors » Pornthip Boonsri

Pornthip Boonsri

Explore the profile of Pornthip Boonsri including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 11
Citations 26
Followers 0
Related Specialties
Biochemistry
Chemistry
Pharmacology
Top 10 Co-Authors
Koichi Kato
Supa Hannongbua
Arthit Makarasen
Suwicha Patnin
Supanna Techasakul
Sunit Suksamrarn
Maho Yagi-Utsumi
Piyada Jittangprasert
Amornmart Jaratrungtawee
Duckyong Sung
Published In
Biochem Biophys Res Commun
Fitoterapia
J Mol Graph Model
Int Immunol
Sci Rep
Affiliations
Soon will be listed here.
Recent Articles
1.
Identification of potential C1-binding sites in the immunoglobulin CL domains
Yanaka S, Kodama A, Nishiguchi S, Fujita R, Shen J, Boonsri P, et al.
Int Immunol . 2024 Apr; 36(8):405-412. PMID: 38564192
Immunoglobulin G (IgG) molecules that bind antigens on the membrane of target cells spontaneously form hexameric rings, thus recruiting C1 to initiate the complement pathway. However, our previous report indicated...
2.
Multiple spectroscopic and computational studies on binding interaction of 2-phenylamino-4-phenoxyquinoline derivatives with bovine serum albumin
Ngueanngam N, Jityuti B, Patnin S, Boonsri P, Makarasen A, Buranaprapuk A
Spectrochim Acta A Mol Biomol Spectrosc . 2024 Feb; 310:123948. PMID: 38309006
Binding characteristics of potent non-nucleoside HIV-1 reverse transcriptase inhibitors, 4-(2',6'-dimethyl-4'-formylphenoxy)-2-(5″-cyanopyridin-2″ylamino) quinoline (1) and 4-(2',6'-dimethyl-4'-cyanophenoxy)-2-(5″-cyanopyridin-2″ylamino) quinoline (2), to bovine serum albumin (BSA) under simulative physiological conditions were investigated by multiple spectroscopic...
3.
Discovery of Novel Naphthoquinone-Chalcone Hybrids as Potent FGFR1 Tyrosine Kinase Inhibitors: Synthesis, Biological Evaluation, and Molecular Modeling
Leechaisit R, Mahalapbutr P, Boonsri P, Karnchanapandh K, Rungrotmongkol T, Prachayasittikul V, et al.
ACS Omega . 2023 Sep; 8(36):32593-32605. PMID: 37720749
This work presents a flexible synthesis of 10 novel naphthoquinone-chalcone derivatives (-) by nucleophilic substitution of readily accessible aminochalcones and 2,3-dichloro-1,4-naphthoquinone. All compounds displayed broad-spectrum cytotoxic activities against all the...
4.
Stability improvement of UV-filter between methoxy cinnamic acid derivatives and cyclodextrins inclusion complexes based on DFT and TD-DFT investigations
Promkatkaew M, Boonsri P, Suramitr S, Karpkird T, Wolschann P, Hannongbua S
J Mol Graph Model . 2023 Sep; 125:108619. PMID: 37666055
Structures and UV-vis absorption spectra of the host-guest interaction of the methoxy cinnamic acid (MCA) derivatives and cyclodextrins (CDs) were performed by using the density functional theory (DFT) and time-dependent...
5.
Carbon dots derived from citric acid and urea as fluorometric probe for determining melamine contamination in infant formula sample
Phimmasone S, Boonsri P, Siangproh W, Ratanawimarnwong N, Jittangprasert P, Mantim T, et al.
Methods Appl Fluoresc . 2023 Aug; 12(1). PMID: 37647911
Melamine has been intentionally added into food products to increase the protein count at less cost, especially in dairy products for infant resulting in serious adverse effects on health of...
6.
New bioactive cyclopeptide alkaloids with rare terminal unit from the root bark of
Lomchoey N, Panseeta P, Boonsri P, Apiratikul N, Prabpai S, Kongsaeree P, et al.
RSC Adv . 2022 May; 8(33):18204-18215. PMID: 35541146
Six new 14-membered ring cyclopeptide alkaloids, cambodines A-F (1-6), and two known compounds, frangufoline (7) and lotusanine B (8), were isolated from the root bark extract of Pierre. Their structures...
7.
Highly potent cholinesterase inhibition of geranylated xanthones from Garcinia fusca and molecular docking studies
Saenkham A, Jaratrungtawee A, Siriwattanasathien Y, Boonsri P, Chainok K, Suksamrarn A, et al.
Fitoterapia . 2020 May; 146:104637. PMID: 32470371
Three new oxygenated xanthones, fuscaxanthones L-N (1-3), and 14 known xanthones 4-17, together with the other known metabolites 18-20 were isolated from the stem barks of Garcinia fusca Pierre. Their...
8.
Molecular Docking Studies and Synthesis of Amino-oxy-diarylquinoline Derivatives as Potent Non-nucleoside HIV-1 Reverse Transcriptase Inhibitors
Makarasen A, Kuno M, Patnin S, Reukngam N, Khlaychan P, Deeyohe S, et al.
Drug Res (Stuttg) . 2019 Nov; 69(12):671-682. PMID: 31698495
In this study, amino-oxy-diarylquinolines were designed using structure-guided molecular hybridization strategy and fusing of the pharmacophore templates of nevirapine (NVP), efavirenz (EFV), etravirine (ETV, TMC125) and rilpivirine (RPV, TMC278). The...
9.
NMR characterization of HIV-1 reverse transcriptase binding to various non-nucleoside reverse transcriptase inhibitors with different activities
Thammaporn R, Yagi-Utsumi M, Yamaguchi T, Boonsri P, Saparpakorn P, Choowongkomon K, et al.
Sci Rep . 2015 Oct; 5:15806. PMID: 26510386
Human immunodeficiency virus type 1 reverse transcriptase (HIV-1 RT) is an important target for antiviral therapy against acquired immunodeficiency syndrome. However, the efficiency of available drugs is impaired most typically...
10.
Stable isotope-assisted NMR characterization of interaction between lipid A and sarcotoxin IA, a cecropin-type antibacterial peptide
Yagi-Utsumi M, Yamaguchi Y, Boonsri P, Iguchi T, Okemoto K, Natori S, et al.
Biochem Biophys Res Commun . 2013 Jan; 431(2):136-40. PMID: 23313507
Sarcotoxin IA is a 39-residue cecropin-type peptide from Sarcophaga peregrina. This peptide exhibits antibacterial activity against Gram-negative bacteria through its interaction with lipid A, a core component of lipopolysaccharides. To...