Muestra la distribución de la producción WoS, Scopus y SciELO del autor.
Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.
| Firmas del autor | |
| Nombre | FAUNDES, JUDITH |
| Género | Mujer |
| Área Principal WOS | Chemistry, Multidisciplinary; Biochemistry & Molecular Biology; Chemistry, Organic; |
| Afiliación Principal | Universidad De Santiago De Chile |
| ORCID
|
0000-0001-8063-7885 |
Publicaciones en Chile
Citas Totales
Afiliaciones Chilenas
| WOS | #Pub |
|---|---|
| Chemistry, Multidisciplinary | 4 |
| Biochemistry & Molecular Biology | 2 |
| Chemistry, Organic | 2 |
| Engineering, Chemical | 1 |
| Scopus | #Pub |
|---|
| SciELO | #Pub |
|---|
| Autor | Género | # Pub |
|---|---|---|
| ZUNIGA-LOYOLA, CESAR | Hombre | 2 |
| MONTOYA-K, MARGARITA | Mujer | 1 |
| MEJIAS, SOPHIA | Mujer | 1 |
| FAUNDEZ, MARIO A. | Hombre | 1 |
| RECIO-CORTES, FRANCISCO JAVIER | Hombre | 1 |
| MUNOZ-OSSES, MICHELLE | Mujer | 1 |
| TASCA, FEDERICO | Hombre | 1 |
| MASCAYANO-COLLADO, CAROLINA LORENA | Mujer | 1 |
| VALDERRAMA-GUERRERO, JAIME ADOLFO | Hombre | 2 |
| DANIMANN, ALEX | Hombre | 1 |
| MEZA, PAULINA | Mujer | 1 |
| VACCARO, SILVANA | Mujer | 1 |
| IBACACHE, JUANA A. | Mujer | 4 |
| MORALES, PILAR | - | 1 |
| SEGURA-DEL RIO, RODRIGO | Hombre | 1 |
| Año | Firma | Institución (Incites asoc.) | H Index | Average Percentile | Impact Citation | Impact Relative World | Impact Journal Normalized Citation | Impact Category Normalized Citation | Percentage Cited | Percentage Top 1 | Percentage Top 10 | Percentage Journal Q1 | Percentage Journal Q2 | Percentage Journal Q3 | Percentage Journal Q4 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2019 | Faundes, Judith | Universidad de Santiago de Chile | 0.0 | 100.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 100.0 | 0.0 | 0.0 |
| Título | Año | Citas | Tipo | Revista | Indexada |
|---|---|---|---|---|---|
| Preparation Of Novel Homodimers Derived From Cytotoxic Isoquinolinequinones. A Twin Drug Approach | 2018 | 14 | artículo de investigación | Molecules | WoS Scopus |
| Green Synthesis And Electrochemical Properties Of Mono And Dimers Derived From Phenylaminoisoquinolinequinones | 2019 | 4 | artículo de investigación | Molecules | WoS Scopus |
| Short And Improved Synthesis Of Cytotoxic Homodimers With An Isoquinoline Structure | 2020 | 0 | Revista De Chimie | Scopus WoS | |
| Effect Of Substituents And Chain Length In Amino 1,4 Naphthoquinones On Glutathione S Transferase Inhibition: Molecular Docking And Electrochemical Perspectives: A Structure Activity Study | 2022 | 0 | artículo de investigación | New Journal Of Chemistry | WoS Scopus |
| Palabra Clave | #Pub |
|---|---|
| amination reaction | 2 |
| antiproliferative activity | 2 |
| twin drugs | 2 |
| cancer-cells | 2 |
| naphthoquinones | 2 |
| reduction | 1 |
| induction | 1 |
| isoquınolınequınones | 1 |
| mechanism | 1 |
| mıcrowave | 1 |
| progression | 1 |
| quinones | 1 |
| redox | 1 |
| homodimers | 1 |
| reduction potentials | 1 |
| ultrasound | 1 |
| vitro cytotoxic evaluation | 1 |
| homodımers | 1 |
| 1,4-naphthoquinone | 1 |
| heterodimers | 1 |
| half-wave potential | 1 |
| green synthesis | 1 |
| ethacrynic-acid | 1 |
| enzyme | 1 |
| cytotoxic activity | 1 |
| cyclic voltammetry | 1 |
| cancer-cell lines | 1 |
| apoptosis | 1 |
| anilinoisoquinolinequinones | 1 |
| activation | 1 |