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Antonio J. Macías-Sánchez

Universidad de Cádiz

H指数:20

被引数:984

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Exploring novel aromatase cytochrome P450-binding ligands: Molecular docking and QSAR study of phorbol esters as aromatase inhibitors

探索新型芳构酶细胞色素P450结合配体：佛波酯作为芳构酶抑制剂的分子对接与QSAR研究

European Journal of Medicinal Chemistry

IF5.9

2025-12-060

OAAI

Synthesis of Farnesyloxy- and Drimanyloxy-Arene Scaffold-Based Hybrid Molecules as Antifungals against Botrytis cinerea

以法尼氧基-和吉玛氧基-芳烃骨架为基础的杂交分子作为抗灰葡萄孢菌真菌剂的合成

Journal of Agricultural and Food Chemistry

IF6.2

2025-10-270

OAAI

Biocatalyzed and Photochemical Formal [2+2] Cycloaddition of Euphoboetirane A: A Route to a Fused Pentacyclic Diterpene Skeleton

ORGANIC LETTERS

IF5

2025-02-020

PRE

Effect of lathyrane-type diterpenoids in neural stem cell physiology: Microbial transformations, molecular docking and dynamics studies( vol 153 , 107769, 2024)

棒状螺甾烷型二萜类化合物对神经干细胞生理学的影响：微生物转化、分子对接和动力学研究（卷 153，107769，2024）

BIOORGANIC CHEMISTRY

IF4.7

2025-01-010

PRE

A Biomimetic Approach to Premyrsinane-Type Diterpenoids: Exploring Microbial Transformation to Enhance Their Chemical Diversity

IF4.1

2024-03-142

OAAI

Isolation and Identification of 12-Deoxyphorbol Esters from Euphorbia resinifera Berg Latex: Targeted and Biased Non-Targeted Identification of 12-Deoxyphorbol Esters by UHPLC-HRMSE

IF4.1

2023-11-141

OAAI

Phorbol Diesters and 12-Deoxy-16-hydroxyphorbol 13,16-Diesters Induce TGFα Release and Adult Mouse Neurogenesis (vol 64, pg 6070, 2021)

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2022-07-270

OA

Pharmacological Potential of Lathyrane-Type Diterpenoids from Phytochemical Sources

PHARMACEUTICALS

IF4.8

2022-06-2316

OAAI

The complemented mutant complΔBcstc7niaD, in the STC7 of Botrytis cinerea led to the characterization of 11,12,13-tri-nor-eremophilenols derivatives

IF3.4

2022-01-013

OAAI

Phorbol Diesters and 12-Deoxy-16-hydroxyphorbol 13,16-Diesters Induce TGFα Release and Adult Mouse Neurogenesis

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2021-05-0411

OAAI

Effects of classical PKC activation on hippocampal neurogenesis and cognitive performance: mechanism of action

NEUROPSYCHOPHARMACOLOGY

IF7.1

2020-12-1714

OAAI

Bond reactivity indices approach analysis of the [2+2] cycloaddition of jatrophane skeleton diterpenoids from Euphorbia gaditana Coss to tetracyclic gaditanone

IF3.4

2020-12-016

OAAI

A novel PKC activating molecule promotes neuroblast differentiation and delivery of newborn neurons in brain injuries

CELL DEATH & DISEASE

IF9.6

2020-04-2218

OAAI

Structural and biosynthetic studies on eremophilenols related to the phytoalexin capsidiol, produced by Botrytis cinerea

IF3.4

2018-10-0110

PREAI

Gaditanone, a Diterpenoid Based on an Unprecedented Carbon Skeleton Isolated from Euphorbia gaditana

JOURNAL OF NATURAL PRODUCTS

IF3.6

2017-07-0526

OAAI

ELAC (3,12-di-O-acetyl-8-O-tigloilingol), a plant-derived lathyrane diterpene, induces subventricular zone neural progenitor cell proliferation through PKCβ activation

BRITISH JOURNAL OF PHARMACOLOGY

IF7.7

2017-06-1123

OAAI

Chemically Induced Cryptic Sesquiterpenoids and Expression of Sesquiterpene Cyclases in Botrytis cinerea Revealed New Sporogenic (+)-4-Epieremophil-9-en-11-ols

ACS CHEMICAL BIOLOGY

IF3.8

2016-03-0821

OAAI

nor-Mevaldic acid surrogates as selective antifungal agent leads against Botrytis cinerea. Enantioselective preparation of 4-hydroxy-6-(1-phenylethoxy)tetrahydro-2H-pyran-2-one

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2015-07-015

OAAI

The Asymmetric Total Synthesis of Cinbotolide: A Revision of the Original Structure

JOURNAL OF ORGANIC CHEMISTRY

IF3.6

2014-11-1412

OAAI

Phytotoxic Activity and Metabolism of Botrytis cinerea and Structure-Activity Relationships of Isocaryolane Derivatives

JOURNAL OF NATURAL PRODUCTS

IF3.6

2013-06-0310

OA