Marine natural products
Covering: 2015. Previous review: Nat. Prod. Rep., 2016, 33, 382–431 This review covers the
literature published in 2015 for marine natural products (MNPs), with 1220 citations (792 for …
literature published in 2015 for marine natural products (MNPs), with 1220 citations (792 for …
[PDF][PDF] Natural product reports
JW Blunt, BR Copp, RA Keyzers, MH Munroa… - Nat Prod Rep, 2016 - academia.edu
This review covers the literature published in 2015 for marine natural products (MNPs), with
1220 citations (792 for the period January to December 2015) referring to compounds …
1220 citations (792 for the period January to December 2015) referring to compounds …
Stereoselective amino acid synthesis by synergistic photoredox-pyridoxal radical biocatalysis
Developing synthetically useful enzymatic reactions that are not known in biochemistry and
organic chemistry is an important challenge in biocatalysis. Through the synergistic merger …
organic chemistry is an important challenge in biocatalysis. Through the synergistic merger …
Marine mollusk‐derived agents with antiproliferative activity as promising anticancer agents to overcome chemotherapy resistance
ML Ciavatta, F Lefranc, M Carbone… - Medicinal Research …, 2017 - Wiley Online Library
The chemical investigation of marine mollusks has led to the isolation of a wide variety of
bioactive metabolites, which evolved in marine organisms as favorable adaptations to …
bioactive metabolites, which evolved in marine organisms as favorable adaptations to …
Columbamides D and E: Chlorinated Fatty Acid Amides from the Marine Cyanobacterium Moorea bouillonii Collected in Malaysia
JAV Lopez, JG Petitbois, CS Vairappan… - Organic …, 2017 - ACS Publications
Two new chlorinated fatty acid amides, columbamides D (1) and E (2), along with apratoxins
A and C and wewakazole, were isolated from the organic extract of a Moorea bouillonii …
A and C and wewakazole, were isolated from the organic extract of a Moorea bouillonii …
Serinolamides and Lyngbyabellins from an Okeania sp. Cyanobacterium Collected from the Red Sea
JG Petitbois, LO Casalme, JAV Lopez… - Journal of natural …, 2017 - ACS Publications
NMR-and MS-guided fractionation of an extract of an Okeania sp. marine cyanobacterium,
collected from the Red Sea, led to the isolation of four new metabolites, including …
collected from the Red Sea, led to the isolation of four new metabolites, including …
Residual complexity does impact organic chemistry and drug discovery: the case of rufomyazine and rufomycin
MP Choules, LL Klein, DC Lankin… - The Journal of …, 2018 - ACS Publications
Residual complexity (RC) involves the impact of subtle but critical structural and biological
features on drug lead validation, including unexplained effects related to unidentified …
features on drug lead validation, including unexplained effects related to unidentified …
Network pharmacology reveals the potential of dolastatin 16 as a diabetic wound healing agent
D Luthfiana, DH Utomo - In Silico Pharmacology, 2023 - Springer
Dolastatin 16, a marine cyclic depsipeptide, was initially isolated from the sea hare
Dolabella Auricularia by Pettit et al. Due to the lack of information regarding its bioactivity …
Dolabella Auricularia by Pettit et al. Due to the lack of information regarding its bioactivity …
The genetic origin of evolidine, the first cyclopeptide discovered in plants, and related orbitides
Cyclic peptides are reported to have antibacterial, antifungal, and other bioactivities.
Orbitides are a class of cyclic peptides that are small, head-to-tail cyclized, composed of …
Orbitides are a class of cyclic peptides that are small, head-to-tail cyclized, composed of …
Total synthesis and biological activity of dolastatin 16
LO Casalme, A Yamauchi, A Sato… - Organic & …, 2017 - pubs.rsc.org
The total synthesis of dolastatin 16, a macrocyclic depsipeptide first isolated from the sea
hare Dolabella auricularia as a potential antineoplastic metabolite by Pettit et al., was …
hare Dolabella auricularia as a potential antineoplastic metabolite by Pettit et al., was …