Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Guang ping Cao"'
Publikováno v:
Journal of Functional Foods, Vol 17, Iss , Pp 632-639 (2015)
To potentiate activities of angiotensin-I converting enzyme (ACE) inhibitory peptides VK, YA, KY and TAY from oyster hydrolysate, four novel tripeptides VKW, YAW, KYW and TAW were designed by modification with Trp at the C-terminus. The tripeptides w
Externí odkaz:
https://doaj.org/article/481c3d83fa264d0192d11b044e8a17ae
Autor:
Guang-Ping Cao, Jia-Lang Xia, Long-Yan Zhao, Zhen-Zhou Tang, Xiao Lin, Yong-Hong Liu, Cheng-Hai Gao, Kai Liu, Meng Bai
Publikováno v:
The Journal of antibiotics. 75(9)
One new xanthene derivative, named penicixanthene E (1), together with one known compound 2, was isolated from the EtOAc extract of the endophytic fungus Penicillium sp. GXIMD 03101, which was identified from the mangrove Acanthus ilicifolius L. coll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f2718108f6f6ed8297fd4c1af22f1f1
https://pubmed.ncbi.nlm.nih.gov/35918478
https://pubmed.ncbi.nlm.nih.gov/35918478
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e59278 (2013)
Sirtuin belongs to a family of typical histone deacetylase which regulates the fundamental cellular biological processes including gene expression, genome stability, mitosis, nutrient metabolism, aging, mitochondrial function, and cell motility. Mich
Externí odkaz:
https://doaj.org/article/97adc6d4150a49918c07c8e1dc0684cd
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e62740 (2013)
Human chymase catalyzes the hydrolysis of peptide bonds. Three chymase inhibitors with very similar chemical structures but highly different inhibitory profiles towards the hydrolase function of chymase were selected with the aim of elucidating the o
Externí odkaz:
https://doaj.org/article/2f23b9d7814844bd846741ffd7dab454
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e60470 (2013)
Due to the diligence of inherent redundancy and robustness in many biological networks and pathways, multitarget inhibitors present a new prospect in the pharmaceutical industry for treatment of complex diseases. Nevertheless, to design multitarget i
Externí odkaz:
https://doaj.org/article/9d96da46daa7420db84f87b392067997
Autor:
Ayoung Baek, Guang Ping Cao, Rabia Mukthar Rana, Seok Ju Park, Shailima Rampogu, Amir Zeb, Raj Kumar, Keun Woo Lee, Chanin Park, Rohit Bavi, Minky Son
Publikováno v:
IEEE/ACM transactions on computational biology and bioinformatics. 17(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5978dc49b1e24916b6bf8ed65f0e470f
https://pubmed.ncbi.nlm.nih.gov/30334765
https://pubmed.ncbi.nlm.nih.gov/30334765
Autor:
Keun Woo Lee, Yongseong Kim, Sundarapandian Thangapandian, Yeung-Joon Choi, Raj Kumar, Guang Ping Cao, Minky Son, Yong Jung Kwon, Jung-Keun Suh, Hyong-Ha Kim
Publikováno v:
Archives of Pharmacal Research. 39:1356-1369
HDAC8 inhibitors have become an attractive treatment for cancer. This study aimed to facilitate the identification of potential chemical scaffolds for the selective inhibition of histone deacetylase 8 (HDAC8) using in silico approaches. Non-linear QS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddec4f8d0a12c7a7f634ff36280d3460
https://doi.org/10.1007/s12272-015-0705-5
https://doi.org/10.1007/s12272-015-0705-5
Autor:
Keun Woo Lee, Minky Son, Shailima Rampogu, Seok Ju Park, Amir Zeb, Guang Ping Cao, Rabia Mukthar Rana, Chanin Park, Raj Kumar, Ayoung Baek, Rohit Bavi
Publikováno v:
IEEE/ACM transactions on computational biology and bioinformatics. 16(5)
Aromatase inhibitors with an $\mathrm{IC}_{50}$ IC 50 value ranging from 1.4 to 49.7 µM are known to act as antiepileptic drugs besides being potential breast cancer inhibitors. The aim of the present study is to identify novel antiepileptic aromata
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6a516a53229fb531975a0667d59984d
https://pubmed.ncbi.nlm.nih.gov/32031923
https://pubmed.ncbi.nlm.nih.gov/32031923
Publikováno v:
Journal of Functional Foods, Vol 17, Iss, Pp 632-639 (2015)
To potentiate activities of angiotensin-I converting enzyme (ACE) inhibitory peptides VK, YA, KY and TAY from oyster hydrolysate, four novel tripeptides VKW, YAW, KYW and TAW were designed by modification with Trp at the C-terminus. The tripeptides w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db6feafad84d2ea90bfbd45661fea78d
https://doi.org/10.1016/j.jff.2015.06.016
https://doi.org/10.1016/j.jff.2015.06.016
Autor:
Sudhir Singh, Yuno Lee, Hyun Suk Jung, Keun Woo Lee, Bhumi Nath Tripathi, Sung Hyun Hong, Jae-Young Cho, Sang Yeol Lee, Eun Mi Lee, Seung Sik Lee, Guang Ping Cao, Byung Yeoup Chung
Publikováno v:
Annals of Botany. 116:713-725
Background and aims The 2-Cys peroxiredoxin (Prx) A protein of Arabidopsis thaliana performs the dual functions of a peroxidase and a molecular chaperone depending on its conformation and the metabolic conditions. However, the precise mechanism respo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b8b68848fd342485c93801ade1da0db
https://doi.org/10.1093/aob/mcv094
https://doi.org/10.1093/aob/mcv094