相似文献
1
Harnessing Nature's wisdom. Turning to Nature for inspiration and avoiding her follies.
EMBO Rep. 2008 Sep;9(9):838-40. doi: 10.1038/embor.2008.160.
2
Marine natural products: drugs from the deep.
Nature. 2006 Oct 26;443(7114):904-5. doi: 10.1038/443904a.
3
Enabling techniques in the search for new antibiotics: Combinatorial biosynthesis of sugar-containing antibiotics.
Biochem Pharmacol. 2017 Jun 15;134:56-73. doi: 10.1016/j.bcp.2016.10.009. Epub 2016 Oct 26.
4
Natural products for lead identification: nature is a valuable resource for providing tools.
EXS. 2003(93):87-107. doi: 10.1007/978-3-0348-7997-2_5.
5
Natural Product-Based Drug Discovery.
Med Res Rev. 2016 Jan;36(1):3. doi: 10.1002/med.21380.
6
Digital phenotyping approaches and mobile devices enhance CNS biopharmaceutical research and development.
Neuropsychopharmacology. 2018 Dec;43(13):2504-2505. doi: 10.1038/s41386-018-0222-6. Epub 2018 Sep 18.
7
New medicines from nature's armamentarium.
Trends Parasitol. 2006 Feb;22(2):51-4. doi: 10.1016/j.pt.2005.12.009. Epub 2006 Jan 10.
8
Putting nature back into drug discovery.
Nat Biotechnol. 2003 Jun;21(6):602. doi: 10.1038/nbt0603-602.
9
10
ADMET--turning chemicals into drugs.
Nat Biotechnol. 2001 Aug;19(8):722-6. doi: 10.1038/90761.
引用本文的文献
1
Identification of New Lupane-Type Triterpenoids as Inverse Agonists of RAR-Related Orphan Receptor Gamma (RORγ).
J Nat Prod. 2025 Aug 22;88(8):1887-1900. doi: 10.1021/acs.jnatprod.5c00416. Epub 2025 Jul 28.
2
NaCTR: Natural product-derived compound-based drug discovery pipeline from traditional oriental medicine by search space reduction.
Comput Struct Biotechnol J. 2024 Oct 29;23:3869-3877. doi: 10.1016/j.csbj.2024.10.035. eCollection 2024 Dec.
3
Reprogramming the Cyclization Cascade of -Isozizaene Synthase to Generate Alternative Terpene Products.
Biochemistry. 2023 Aug 1;62(15):2301-2313. doi: 10.1021/acs.biochem.3c00247. Epub 2023 Jul 14.
4
Perplexing Polyphenolics: The Isolations, Syntheses, Reappraisals, and Bioactivities of Flavonoids, Isoflavonoids, and Neoflavonoids from 2016 to 2022.
Life (Basel). 2023 Mar 9;13(3):736. doi: 10.3390/life13030736.
5
Natural products regulate mitochondrial function in cognitive dysfunction-A scoping review.
Front Pharmacol. 2023 Mar 7;14:1091879. doi: 10.3389/fphar.2023.1091879. eCollection 2023.
6
Indole-Containing Natural Products 2019-2022: Isolations, Reappraisals, Syntheses, and Biological Activities.
Molecules. 2022 Nov 5;27(21):7586. doi: 10.3390/molecules27217586.
7
Applications of Friedel-Crafts reactions in total synthesis of natural products.
RSC Adv. 2018 Dec 3;8(70):40061-40163. doi: 10.1039/c8ra07325b. eCollection 2018 Nov 28.
8
Click Chemistry in Natural Product Modification.
Front Chem. 2021 Nov 17;9:774977. doi: 10.3389/fchem.2021.774977. eCollection 2021.
9
Natural product biosynthesis: What's next? An introduction to the JBC Reviews Thematic Series.
J Biol Chem. 2020 Jan 10;295(2):335-336. doi: 10.1074/jbc.REV119.011586. Epub 2019 Dec 5.
10
Molecular targets of gambogic acid in cancer: recent trends and advancements.
Tumour Biol. 2016 Oct;37(10):12915-12925. doi: 10.1007/s13277-016-5194-8. Epub 2016 Jul 22.
本文引用的文献
1
The spinning processes for spider silk.
Soft Matter. 2006 May 26;2(6):448-451. doi: 10.1039/b601286h.
2
Direct visualization of spruce budworm antifreeze protein interacting with ice crystals: basal plane affinity confers hyperactivity.
Biophys J. 2008 Jul;95(1):333-41. doi: 10.1529/biophysj.107.125328. Epub 2008 Mar 13.
3
Ex vivo rheology of spider silk.
J Exp Biol. 2006 Nov;209(Pt 21):4355-62. doi: 10.1242/jeb.02516.
4
The core structures of roseophilin and the prodigiosin alkaloids define a new class of protein tyrosine phosphatase inhibitors.
Chembiochem. 2004 Nov 5;5(11):1575-9. doi: 10.1002/cbic.200400135.
5
Mechanism of silk processing in insects and spiders.
Nature. 2003 Aug 28;424(6952):1057-61. doi: 10.1038/nature01809.
Zotero 插件