Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jaraslak Pechwang"'
Autor:
THEERA SRISAWAT, KATESARIN MANEENOON, PATTANA WUTTIPONG, SURAPHON THITITHANAKUL, JARASLAK PECHWANG, KHANCHAI WONGCHANA, PARINUCH CHUMKAEW, WARANYU RATCHAREON
Publikováno v:
Biodiversitas Journal of Biological Diversity. 24
Srisawat T, Maneenoon K, Wuttipong P, Thitithanakul S, Pechwang J, Wongchana K, Chumkaew P, Ratchareon W. 2023. Population structure and distribution of the endangered Vatica diospyroides in Southern Thailand to inform its conservation strategies. Bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::706f705d35184229dd73664eed3bb531
https://doi.org/10.13057/biodiv/d240319
https://doi.org/10.13057/biodiv/d240319
Publikováno v:
Chemistry of Natural Compounds. 57:907-910
Two new aporphine alkaloids, amocurines D and E (1 and 2), together with five known compounds (3–7), were isolated from the stems of Amoora cucullata. The structures of these compounds were elucidated based on their spectroscopic data. Compound 1 s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8798dc53adada992c4837bbc14757829
https://doi.org/10.1007/s10600-021-03508-6
https://doi.org/10.1007/s10600-021-03508-6
Publikováno v:
Records of Natural Products, Vol 13, Iss 6, Pp 491-498 (2019)
Two new oxoprotoberberine alkaloids, amocurine A and B (1 and 2), a new aporphine alkaloid, amocurine C (3), along with three known compounds (4-6) were isolated from the roots of Amoora cucullata. Their structures were determined by analysis of spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7c4098eaa7d9bd45e3f2c3b2c76347e
https://www.acgpubs.org/doc/20190906165204A8-128-RNP-1902-1181.pdf
https://www.acgpubs.org/doc/20190906165204A8-128-RNP-1902-1181.pdf
Autor:
Uraiwan Werapun, Jaraslak Pechwang
Publikováno v:
Journal of Nano Research. 56:28-38
TiO2 and iron-doped TiO2 were synthesized by sol-gel method. TiO2 and 0.5 %mol Fe:TiO2 were calcined at 500 and 800 °C for 3 h. The synthesized particles were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02c3364ddada79c1b79d530aae81976c
https://doi.org/10.4028/www.scientific.net/jnanor.56.28
https://doi.org/10.4028/www.scientific.net/jnanor.56.28
Autor:
Uraiwan Werapun, Atiphon Phatthiya, Parinuch Chumkaew, Seppo Karrila, Jaraslak Pechwang, Warit Werapun
Publikováno v:
Current Nanoscience. 14:273-279
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a51516f35ae27e86c09a90a4e51b87b
https://doi.org/10.2174/1573413714666180115121150
https://doi.org/10.2174/1573413714666180115121150
Publikováno v:
Journal of natural medicines. 71(3)
Phytochemical investigation of the stems from Brucea javanica led to the isolation of two new quassinoids, brujavanol C (1) and brujavanol D (2), together with six known compounds (3–8). The chemical structures were elucidated by means of various s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::925f7e9ee4274b60e7758e177ed65bf0
https://pubmed.ncbi.nlm.nih.gov/28455552
https://pubmed.ncbi.nlm.nih.gov/28455552
Autor:
Patima Permpoonpattana, Amornrat Keawkumpai, Theera Srisawat, Parinuch Chumkaew, Darika Kongrit, Saranyoo Klaiklay, Karnsiree Thimabut, Jaraslak Pechwang
Publikováno v:
Tropical Journal of Pharmaceutical Research; Vol 17, No 5 (2018); 875-882
Purpose : To investigate the antibacterial activity of extracts from C atunaregam tomentosa on Bacillus subtilis and Staphylococcus aureus , and the bacterial responses to the extracts. Methods: The antibacterial activity of fruit, leaf and stem bark
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2dd3946f32acc05a0f3077ffeb2ea33
https://doi.org/10.4314/tjpr.v17i5.18
https://doi.org/10.4314/tjpr.v17i5.18
Autor:
Nongnuj Muangsin, Prakitsin Sihanonth, Alisa S. Vangnai, Jaraslak Pechwang, Surachai Pornpakakul, Jittra Piapukiew, Narongsak Chaichit, Siriporn Chuchawankul, Amorn Petsom
Publikováno v:
Natural product research. 24(10)
Biotranformation of ent-kaur-16-en-19-oic acid (1) using Psilocybe cubensis resulted in hydroxylated products. After two days of incubation, ent-16beta,17-dihydroxy-kauran-19-oic acid (2) was isolated. After further incubation for nine days, two nove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f3af8d5e9026e3173a62c3bfc58d8fc
https://pubmed.ncbi.nlm.nih.gov/20496227
https://pubmed.ncbi.nlm.nih.gov/20496227