1 | Experimental and Theoretical Exploration of Aryl Substituent Effects on the Electronic Properties of Asymmetric 4,7-Di(thiophene-2-yl)-benzo[c][2,1,5]thiadiazole Compounds | Coautor: García de la Mora G.A., Sifuentes-Vazquez, Luis Daniel, Martinez-Gonzalez, Eduardo, Toscano, Ruben A., et al. | 2022 | POLYCYCLIC AROMATIC COMPOUNDS | WoS-id: 000526876000001 Scopus-id: 2-s2.0-85083561050
| 3 | 2 |
2 | Glycosylation of Stannyl Ceramides Promoted by Modified Montmorillonite in Supercritical Carbon Dioxide | Coautor: Garcia de la Mora, Gustavo, Antonio Morales-Serna, Jose, Nguyen, Bao N., Garcia-Rios, Erendira, et al. | 2018 | Synthesis-Stuttgart | WoS-id: 000422936300015 Scopus-id: 2-s2.0-85033398322
| 3 | 3 |
3 | Orcinol derivative compound with antioxidant properties protects Langerhans islets against streptozotocin damage | Coautor: Garcia de la Mora, Gustavo, Sanchez-Lira, Nancy M. V., Morales-Miranda, Angelica, Leon Contreras, Juan Carlos, et al. | 2017 | JOURNAL OF PHARMACY AND PHARMACOLOGY | WoS-id: 000395189200009 Scopus-id: 2-s2.0-85011295891
| 4 | 3 |
4 | A New Method for the Synthesis of Symmetrical Disubstituted Pyrazines | Coautor: de la Mora, GG, Rojas, N, Grillasca, Y, Acosta, A, et al. | 2013 | JOURNAL OF HETEROCYCLIC CHEMISTRY | WoS-id: 000325924800040 Scopus-id: 2-s2.0-84880927331
| 7 | 7 |
5 | Facile and efficient addition of terminal alkynes to benzotriazole esters: Synthesis of d-erythro-sphingosine using ynones as the key intermediate | Coautor: de la Mora, GG, Morales-Serna, JA, Sauza, A, de Jesus, GP, et al. | 2013 | TETRAHEDRON LETTERS | WoS-id: 000327805800006 Scopus-id: 2-s2.0-84888131838
| 15 | 15 |
6 | Using Benzotriazole Esters as a Strategy in the Esterification of Tertiary Alcohols | Coautor: de la Mora, GG, Morales-Serna, JA, Vera, A, Paleo, E, et al. | 2010 | Synthesis-Stuttgart | WoS-id: 000286479200016 Scopus-id: 2-s2.0-78650154886
| 16 | 17 |
7 | Synthesis of New Optically Active D-Glucosamine-Pyrrole Derivatives | Coautor: de la Mora, GAG, Frontana-Uribe, BA, Escarcega-Bobadilia, MV, Juarez-Lagunas, J, et al. | 2009 | Synthesis-Stuttgart | WoS-id: 000264895300016 Scopus-id: 2-s2.0-67649440692
| 2 | 4 |
8 | Oxygen and Carbon Dioxide Transport Through High Barrier Polyester Blends | 2ᵒ autor: De La Mora G.G., Hernández-Rivera M.A., Likhatchev D., De La Cruz-Guerra C., et al. | 2009 | POLYMER ENGINEERING AND SCIENCE | WoS-id: 000268533400021 Scopus-id: 2-s2.0-67749086416
| 10 | 10 |
9 | The effects of synthetic 19-noprogestins on osteoblastic cell function are mediated by their non-phenolic reduced metabolites | Coautor: García G.A., Enrírquez J., Lemus A.E., Chimal-Monroy J., et al. | 2007 | JOURNAL OF ENDOCRINOLOGY | WoS-id: 000247430600016 Scopus-id: 2-s2.0-34447101313
| 14 | 12 |
10 | Inhibition of the acrosome reaction (AR) and fertilization capacity of mouse spermatozoa by norethisterone A-ring reduced metabolite (5a-NET) | Coautor: De La Mora Gustavo G., Héctor F.-H., Paola D.C., Arturo B.G., et al. | 2005 | Andrologia | WoS-id: 000231900500005 Scopus-id: 2-s2.0-33644663377
| 2 | 4 |
11 | Vasodilating effect of norethisterone and its 5a metabolites: A novel nongenomic action | Coautor: García G.A., Perusquía M., Villalón C.M., Navarrete E., et al. | 2003 | EUROPEAN JOURNAL OF PHARMACOLOGY | WoS-id: 000185274900020 Scopus-id: 2-s2.0-0041880642
| 7 | 7 |
12 | Norethisterone is bioconverted to oestrogenic compounds that activate both the oestrogen receptor a and oestrogen receptor ß in vitro | Coautor: García de la Mora G., Pasapera A.M., Gutiérrez-Sagal R., Herrera J., et al. | 2002 | EUROPEAN JOURNAL OF PHARMACOLOGY | WoS-id: 000178530100012 Scopus-id: 2-s2.0-0037064233
| 10 | 11 |
13 | Effect of norethisterone and its A-ring reduced metabolites on the acrosome reaction in porcine spermatozoa | Coautor: Garcia G.A., Martinez G., Zayas H., Ducolomb Y., et al. | 2002 | Andrologia | WoS-id: 000178672300002 Scopus-id: 2-s2.0-0036423594
| 4 | 5 |
14 | In vitro metabolism of gestodene in target organs: Formation of A-ring reduced derivatives with oestrogenic activity | Coautor: García G.A., Lemus A.E., Santillán R., Damián-Matsumura P., et al. | 2001 | EUROPEAN JOURNAL OF PHARMACOLOGY | WoS-id: 000168203200012 Scopus-id: 2-s2.0-0035853441
| 17 | 18 |
15 | A-ring reduced metabolites of 19-nor synthetic progestins as subtype selective agonists for ERa | Coautor: García G.A., Larrea F., García-Becerra R., Lemus A.E., et al. | 2001 | Endocrinology | WoS-id: 000170689500009 Scopus-id: 2-s2.0-17944364190
| 57 | 57 |
16 | Assessment of the oestrogenic activity of the contraceptive progestin levonorgestrel and its non-phenolic metabolites | Coautor: García G.A., Santillán R., Pérez-Palacios G., Reyes M., et al. | 2001 | EUROPEAN JOURNAL OF PHARMACOLOGY | WoS-id: 000171149300013 Scopus-id: 2-s2.0-0035860446
| 12 | 16 |
17 | The oestrogenic effects of gestodene, a potent contraceptive progestin, are mediated by its A-ring reduced metabolites | Coautor: García G.A., Lemus A.E., Zaga V., Santillán R., et al. | 2000 | JOURNAL OF ENDOCRINOLOGY | WoS-id: 000087699900018 Scopus-id: 2-s2.0-0034125796
| 21 | 25 |
18 | The androgenic effect of norethisterone and 5a-norethisterone on the contractile response of the rat vas deferens to methoxamine and serotonin | Coautor: Garcia G.A., Campos M.G., Oropeza M.V., Lemus A.E., et al. | 1999 | LIFE SCIENCES | WoS-id: 000079849300011 Scopus-id: 2-s2.0-0033538067
| 3 | 4 |
19 | Variations of progesterone receptor and c-fos gene expression in the rat uterus after treatment with norethisterone and its A-ring reduced metabolites | Coautor: García G.A., Mendoza-Rodríguez C.A., Camacho-Arroyo I., Cerbón M.A. | 1999 | Contraception | WoS-id: 000082378000009 Scopus-id: 2-s2.0-0344980406
| 10 | 10 |
20 | Kinetic study and simulation of the precopolytransesterification step in the copoly(ethylene-polyoxyethylene terephthalate) production process | 2ᵒ autor: García-De La Mora G.A., De La Cruz-Guerra C., Cruz-Gómez M.J. | 1999 | POLYMER ENGINEERING AND SCIENCE | Scopus-id: 2-s2.0-0343893678
| 0 | 1 |
21 | A-ring reduced derivatives of two synthetic progestins induce anxiolytic effects in ovariectomized rats | Coautor: García G.A., Picazo O., Fernández-Guasti A., Lemus A.E. | 1998 | BRAIN RESEARCH | WoS-id: 000074784000006 Scopus-id: 2-s2.0-0032527053
| 17 | 16 |
22 | Differential effects of 5a-norethisterone on the histomorphology of the oviduct and uterus of the pregnant rabbit | Coautor: García G.A., Anzaldua S.R., Camacho-Arroyo I., Cerbón M.A. | 1998 | Contraception | Scopus-id: 2-s2.0-0031816070
| 4 | 5 |
23 | 5a-Reduction of norethisterone enhances its binding affinity for androgen receptors but diminishes its androgenic potency | Coautor: García G.A., Lemus A.E., Enríquez J., Grillasca I., et al. | 1997 | JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY | WoS-id: A1997XC69600015 Scopus-id: 2-s2.0-0030609851
| 28 | 31 |
24 | In situ free radical and carbocation reactions between alkylbenzenes promoted by a bentonite clay | Coautor: García De La Mora G., Salmón M., Moreno E., Angeles E., et al. | 1996 | JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL | WoS-id: A1996UW53800002 Scopus-id: 2-s2.0-0030601042
| 1 | 1 |
25 | Separation of 'triplet' zoapatanol and montanol obtained from Montanoa tomentosa s.s.p. tomentosa by reverse-phase high performance liquid chromatography | Coautor: Garcia-De La Mora G., Guzman A., Gallegos A.J., Flores-Moreno J.M. | 1985 | Archivos De Investigación Médica | WoS-id: A1985ATH9900009 Scopus-id: 2-s2.0-0021828682
| 2 | 0 |
26 | Bisabolene derivatives from Stevia salicifolia | Coautor: García de la Mora G.A., Calderón J.S., Angeles E., Salmón M. | 1984 | Phytochemistry | WoS-id: A1984SA42700042 Scopus-id: 2-s2.0-48749136049
| 6 | 6 |
27 | A diterpenic acid from Stevia lucida | Coautor: de la Mora G.G., Salmón M., Ortega A., Angeles E. | 1983 | Phytochemistry | WoS-id: A1983QV46800045 Scopus-id: 2-s2.0-0010415823
| 11 | 12 |
28 | Long-acting contraceptive agents: Norethisterone esters of monoalkenyl and monoalkynyl acids | Coautor: Garcia De La Mora G.A., Francisco C.G., Freire R., Hernandez R., et al. | 1983 | Steroids | WoS-id: A1983SC60600003 Scopus-id: 2-s2.0-0021080471
| 3 | 3 |