# Brain Permeable SGK1 Inhibitors: A Promising Therapeutic Strategy for Neurodegenerative Diseases

**Authors:** Enrique Madruga, Alfonso Garcia-Rubia, Carlos Sanchez-Nuñez, Loreto Martinez-Gonzalez, Ana María Fernandez-Escamilla, Isabel Lastres-Becker, Carmen Gil, Ana Martinez

PMC · DOI: 10.1021/acs.jmedchem.5c03050 · 2026-03-16

## TL;DR

Researchers developed brain-penetrant inhibitors for SGK1, a promising target for treating neurodegenerative diseases like Alzheimer's.

## Contribution

A new family of brain-permeable SGK1 inhibitors was developed for potential use in neurological disorders.

## Key findings

- A medicinal chemistry program produced brain-penetrant SGK1 inhibitors.
- These inhibitors serve as chemical probes to study SGK1's role in neurodegeneration.
- SGK1 is highlighted as a potential therapeutic target for Alzheimer's disease.

## Abstract

A major challenge
in modern medicine is developing new therapies
for aging-related diseases such as neurodegenerative disorders, whose
prevalence increases with longer life expectancy. Although kinase
inhibitors have achieved clinical success, their development for central
nervous system (CNS) disorders remains limited due to the complexity
of kinase networks and poor blood–brain barrier (BBB) permeability.
Serum/glucocorticoid-regulated kinase 1 (SGK1) participates in multiple
signaling pathways but remains an underexplored target in neurodegeneration.
Following a mixed ligand- and structure-based virtual screening, we
have previously identified a brain-penetrant SGK1 inhibitor. A medicinal
chemistry program based on hit expansion and optimization for BBB
permeability reported here has generated a new family of SGK1 inhibitors
as chemical probes that enable the investigation of SGK1’s
role in neurological disorders and serve as promising starting points
for drug development. These findings highlight SGK1 as a potential
therapeutic target for neurodegenerative diseases, such as Alzheimer’s
disease.

## Linked entities

- **Genes:** SGK1 (serum/glucocorticoid regulated kinase 1) [NCBI Gene 6446]
- **Diseases:** Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Genes:** PRNP (prion protein (Kanno blood group)) [NCBI Gene 5621] {aka ASCR, AltPrP, CD230, CJD, GSS, KURU}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, ABCB1 (ATP binding cassette subfamily B member 1) [NCBI Gene 5243] {aka ABC20, CD243, CLCS, ENPAT, GP170, MDR1}, GAPDH (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 2597] {aka G3PD, GAPD, HEL-S-162eP}, CACNA1C (calcium voltage-gated channel subunit alpha1 C) [NCBI Gene 775] {aka CACH2, CACN2, CACNA1C-IT2, CACNL1A1, CCHL1A1, CaV1.2}, SGK1 (serum/glucocorticoid regulated kinase 1) [NCBI Gene 6446] {aka SGK}, ROCK2 (Rho associated coiled-coil containing protein kinase 2) [NCBI Gene 9475] {aka ROCK-II}, RPS6KA3 (ribosomal protein S6 kinase A3) [NCBI Gene 6197] {aka CLS, HU-3, ISPK-1, MAPKAPK1B, MRX19, RSK}, GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932], CLK2 (CDC like kinase 2) [NCBI Gene 1196], ABCB1 (ATP binding cassette subfamily B member 1) [NCBI Gene 403879] {aka MDR1, p-gp}, RPS6KA5 (ribosomal protein S6 kinase A5) [NCBI Gene 9252] {aka MSK1, MSPK1, RLPK}, Pgp (phosphoglycolate phosphatase) [NCBI Gene 67078] {aka 1700012G19Rik, AUM, G3PP}, PTPA (protein phosphatase 2 phosphatase activator) [NCBI Gene 5524] {aka PARK25, PP2A, PPP2R4, PR53}, Sgk1 (serum/glucocorticoid regulated kinase 1) [NCBI Gene 20393] {aka Sgk}, KCNH2 (potassium voltage-gated channel subfamily H member 2) [NCBI Gene 3757] {aka ERG-1, ERG1, H-ERG, HERG, HERG1, Kv11.1}, MAPK15 (mitogen-activated protein kinase 15) [NCBI Gene 225689] {aka ERK7, ERK8}, SCN5A (sodium voltage-gated channel alpha subunit 5) [NCBI Gene 6331] {aka CDCD2, CMD1E, CMPD2, HB1, HB2, HBBD}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}
- **Diseases:** cancer (MESH:D009369), neuroblastoma (MESH:D009447), neuronal death (MESH:D009410), ALS (MESH:D000690), inflammatory diseases (MESH:D007249), neurological disorders (MESH:D009461), cardiotoxicity (MESH:D066126), AD (MESH:D000544), OA (MESH:D011015), tauopathies (MESH:D024801), BOP (MESH:C538557), diabetes (MESH:D003920), ECBL (MESH:D004675), CNS diseases (MESH:D002493), Neurodegeneration (MESH:D019636), toxicity (MESH:D064420), cardiovascular diseases (MESH:D002318), neuroinflammation (MESH:D000090862), PD (MESH:D010300)
- **Chemicals:** quinoline (MESH:C037219), promazine (MESH:D011395), CH2Cl2 (MESH:D008752), DMSO (MESH:D004121), indazole (MESH:D007191), penicillin (MESH:D010406), ofloxacin (MESH:D015242), NaH (MESH:C025451), NO2 (MESH:D009585), TEA (MESH:C016162), DIPEA (MESH:C027070), oxazole (MESH:D010080), ethyl acetate (MESH:C007650), PBS (MESH:D007854), ester (MESH:D004952), Na (MESH:D012964), Tideglusib (MESH:C520571), CH3CN (MESH:C032159), caffeine (MESH:D002110), H3 (MESH:C012616), desipramine (MESH:D003891), 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide (MESH:D005022), KI (MESH:C066186), potassium phosphate (MESH:C013216), F (MESH:D005461), alkene (MESH:D000475), Fluo-4 (MESH:C409648), H2O (MESH:D014867), DTT (MESH:D004229), polyacrylamide (MESH:C016679), MTT (MESH:C070243), 5-methyl-3-phenylisoxazole-4-carboxylic acid (MESH:C000602358), TBS-T (MESH:C027647), THF (MESH:C018674), benzimidazole (MESH:C031000), 1-hydroxybenzotriazole (MESH:C011852), argon (MESH:D001128), NaCl (MESH:D012965), indole (MESH:C030374), Verapamil (MESH:D014700), HCl (MESH:D006851), Propranolol (MESH:D011433), NaHCO3 (MESH:D017693), Tween 80 (MESH:D011136), CO2 (MESH:D002245), AMES (MESH:C017501), histidine (MESH:D006639), Solutol HS-15 (MESH:C067028), dodecane (MESH:C007548), naphthalene (MESH:C031721), ATP (MESH:D000255), amine (MESH:D000588), EtOH (MESH:D000431), pyrrole (MESH:D011758), luciferin (MESH:D000090562), Atenolol (MESH:D001262), 3H (MESH:D014316), C (MESH:D002244), sodium carboxymethylcellulose (MESH:D002266), diethyl malonate (MESH:C498810)
- **Species:** Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** SH-SY5Y — Homo sapiens (Human), Neuroblastoma, Cancer cell line (CVCL_0019), HEK293 — Homo sapiens (Human), Transformed cell line (CVCL_0045), /c — Mus musculus (Mouse), Hepatocellular carcinoma of the mouse, Cancer cell line (CVCL_9103), MDCKII — Canis lupus familiaris (Dog), Spontaneously immortalized cell line (CVCL_0424)

## Figures

23 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13036784/full.md

---
Source: https://tomesphere.com/paper/PMC13036784