Detalhe da pesquisa
1.
A-ring and E-ring modifications of the cytotoxic alkaloid Luotonin A: Synthesis, computational and biological studies.
Bioorg Med Chem
; 28(9): 115443, 2020 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32201190
2.
How Full-Length FVIII Benefits from Its Heterogeneity - Insights into the Role of the B-Domain.
Pharm Res
; 36(5): 77, 2019 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30937539
3.
Position-Selective Synthesis and Biological Evaluation of Four Isomeric A-Ring Amino Derivatives of the Alkaloid Luotonin A.
Molecules
; 24(4)2019 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-30781470
4.
A Facile Oxidative Opening of the C-Ring in Luotonin A and Derivatives.
Molecules
; 22(9)2017 Sep 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28895937
5.
The Forty-Sixth Euro Congress on Drug Synthesis and Analysis: Snapshot .
Molecules
; 22(11)2017 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-29143778
6.
Extended Functional Groups (EFG): An Efficient Set for Chemical Characterization and Structure-Activity Relationship Studies of Chemical Compounds.
Molecules
; 21(1): E1, 2015 Dec 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-26703557
7.
In-line warming reduces in-line pressure of subcutaneous infusion of concentrated immunoglobulins.
Drug Deliv Transl Res
; 13(9): 2367-2377, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36920736
8.
Fingerprint-based in silico models for the prediction of P-glycoprotein substrates and inhibitors.
Bioorg Med Chem
; 20(18): 5388-95, 2012 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22595422
9.
Weinreb amidation as the cornerstone of an improved synthetic route to A-ring-modified derivatives of luotonin A.
Molecules
; 17(10): 11363-78, 2012 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-23011278
10.
Synthesis of ortho-functionalized 4-aminomethylpyridazines as substrate-like semicarbazide-sensitive amine oxidase inhibitors.
Chem Pharm Bull (Tokyo)
; 58(7): 964-70, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20606348
11.
Functionality pattern matching as an efficient complementary structure/reaction search tool: an open-source approach.
Molecules
; 15(8): 5079-92, 2010 Jul 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-20714286
12.
The Mu.Ta.Lig. Chemotheca: A Community-Populated Molecular Database for Multi-Target Ligands Identification and Compound-Repurposing.
Front Chem
; 6: 130, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29725591
13.
Synthesis and in-vitro antitumor activity of 1-[3-(indol-1-yl)prop-1-yn-1-yl]phthalazines and related compounds.
Molecules
; 12(8): 1900-9, 2007 Aug 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-17960095
14.
CO: A chemical ontology for identification of functional groups and semantic comparison of small molecules.
FEBS Lett
; 579(21): 4685-91, 2005 Aug 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-16098521
15.
Unexpected hydrazinolysis behaviour of 1-chloro-4-methyl-5H-pyridazino[4,5-b]indole and a convenient synthesis of new [1,2,4]-triazolo[4',3':1,6]pyridazino[4,5-b]indoles.
Molecules
; 9(10): 849-59, 2004 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-18007485
16.
European initiative towards quality standards in education and training for discovery, development and use of medicines.
Eur J Pharm Sci
; 45(5): 515-20, 2012 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-22178534
17.
FlaME: Flash Molecular Editor - a 2D structure input tool for the web.
J Cheminform
; 3(1): 6, 2011 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21284863
18.
1,5-dimethyl-6H-pyridazino[4,5-b]carbazole, a 3-aza bioisoster of the antitumor alkaloid olivacine.
Chem Pharm Bull (Tokyo)
; 50(11): 1479-83, 2002 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-12419913