Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about CERAMIDE: its mechanistic relationships (Knowledge Graph edges), hypotheses targeting it, analyses mentioning it, and supporting scientific papers. The interactive graph below shows its immediate neighbors. All content is AI-synthesized from peer-reviewed literature.
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| Name | CERAMIDE |
| Key Genes/Proteins | ACSL4, AKT, ALPHA-SYNUCLEIN, ALZHEIMER, AMYLOID, APOE |
| Related Diseases | AGING, Alzheimer'S Disease, ALZHEIMER'S DISEASE |
Knowledge base pages for this entity
flowchart TD
N0["CERAMIDE"]
N1["SMPD1"]
N1 -->|"produces"| N0
N2["APOE"]
N2 -->|"treats"| N0
N3["NEUROINFLAMMATION"]
N0 -->|"activates"| N3
N4["ENDOPLASMIC RETICULUM"]
N0 -->|"regulates"| N4
N5["TAU"]
N0 -->|"activates"| N5
N6["MITOCHONDRIAL DYSFUNCTION"]
N0 -->|"causes"| N6
N7["APP"]
N0 -->|"inhibits"| N7
N8["AXONAL TRANSPORT"]
N0 -->|"inhibits"| N8
N9["INSULIN RESISTANCE"]
N0 -->|"activates"| N9
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classDef protein fill:#1a2a3a,stroke:#4fc3f7,color:#e0e0e0
classDef disease fill:#3a1a1a,stroke:#ef5350,color:#e0e0e0
classDef pathway fill:#2a1a3a,stroke:#ce93d8,color:#e0e0e0
classDef mechanism fill:#2a2a1a,stroke:#ffd54f,color:#e0e0e0
classDef drug fill:#1a2a2a,stroke:#26c6da,color:#e0e0e0
classDef cell_type fill:#2a1a2a,stroke:#ab47bc,color:#e0e0e0
classDef phenotype fill:#2a2a1a,stroke:#ffa726,color:#e0e0e0
classDef process fill:#1a2a2a,stroke:#66bb6a,color:#e0e0e0
classDef biological_process fill:#1a2a2a,stroke:#66bb6a,color:#e0e0e0
classDef concept fill:#1a1a2a,stroke:#7986cb,color:#e0e0e0
classDef entity fill:#1a2a3a,stroke:#4fc3f7,color:#e0e0e0
classDef therapeutic fill:#1a2a2a,stroke:#26c6da,color:#e0e0e0
classDef index fill:#1a1a2a,stroke:#7986cb,color:#e0e0e0
class N0 concept
class N1 gene
class N2 gene
class N3 phenotype
class N5 protein
class N6 phenotype
class N7 gene
class N8 phenotype
class N9 phenotype| Target | Relation | Type | Str |
|---|---|---|---|
| Alzheimer's disease | contributes_to | disease | 0.90 |
| adipogenesis | suppresses | process | 0.90 |
| Tau Phosphorylation | promotes | process | 0.90 |
| tau phosphorylation | promotes | process | 0.90 |
| amyloid-beta | contributes_to | protein | 0.90 |
| Adipose Tissue Function | associated_with | process | 0.90 |
| Neuronal Apoptosis | promotes | process | 0.90 |
| Amyloid-Β | contributes_to | compound | 0.90 |
| SMS1 | substrate_of | enzyme | 0.90 |
| Cerebral Ischemia/Reperfusion Injury | associated_with | disease | 0.90 |
| Ischemic Stroke | associated_with | disease | 0.85 |
| SMSR | binds | enzyme | 0.85 |
| neuronal apoptosis | promotes | process | 0.85 |
| AMYLOID-BETA | contributes_to | protein | 0.85 |
| Neuronal apoptosis | causes | process | 0.85 |
| Tau hyperphosphorylation | contributes_to | process | 0.85 |
| Alzheimer's Disease | biomarker_for | disease | 0.80 |
| Glucose Homeostasis | associated_with | process | 0.80 |
| Adipose Tissue Function | regulates | process | 0.80 |
| Neuroapoptosis | contributes_to | process | 0.80 |
| Metabolic Health | associated_with | phenotype | 0.80 |
| APP | inhibits | gene | 0.70 |
| AXONAL TRANSPORT | inhibits | phenotype | 0.70 |
| NEUROINFLAMMATION | biomarker_for | phenotype | 0.70 |
| INSULIN RESISTANCE | activates | phenotype | 0.70 |
| INSULIN RESISTANCE | regulates | phenotype | 0.70 |
| Insulin Resistance | causes | phenotype | 0.70 |
| AGING | regulates | phenotype | 0.70 |
| MITOCHONDRIAL DYSFUNCTION | causes | phenotype | 0.70 |
| AGING | activates | phenotype | 0.70 |
| TAU | activates | protein | 0.70 |
| Apoptosis | associated_with | entity | 0.70 |
| Apoptosis | interacts_with | entity | 0.70 |
| Apoptosis | activates | entity | 0.70 |
| NEUROINFLAMMATION | activates | phenotype | 0.70 |
| AMYLOID | associated_with | protein | 0.70 |
| ALZHEIMER'S DISEASE | interacts_with | disease | 0.65 |
| NEUROINFLAMMATION | interacts_with | phenotype | 0.65 |
| ALPHA-SYNUCLEIN | regulates | protein | 0.65 |
| AMYLOID | causes | protein | 0.65 |
| INSULIN RESISTANCE | produces | phenotype | 0.65 |
| NEURODEGENERATION | regulates | disease | 0.65 |
| NEURODEGENERATION | interacts_with | disease | 0.65 |
| PYROPTOSIS | activates | phenotype | 0.65 |
| ALZHEIMER'S DISEASE | causes | disease | 0.65 |
| LYSOSOMAL DYSFUNCTION | activates | phenotype | 0.65 |
| NEURODEGENERATION | activates | disease | 0.65 |
| OXIDATIVE STRESS | interacts_with | phenotype | 0.65 |
| PINK1 | interacts_with | gene | 0.65 |
| CTSD | regulates | gene | 0.65 |
| Source | Relation | Type | Str |
|---|---|---|---|
| Myriocin | associated_with | drug | 0.95 |
| CERS5 | associated_with | gene | 0.90 |
| Myriocin | downregulates | drug | 0.90 |
| SPT | catalyzes | enzyme | 0.90 |
| CERS2 | associated_with | gene | 0.90 |
| SMSR | regulates | enzyme | 0.85 |
| Neutral sphingomyelinase inhibitors | inhibits | drug | 0.85 |
| Neutral Sphingomyelinase Inhibitors | inhibits | drug | 0.85 |
| APOE | regulates | gene | 0.85 |
| neutral sphingomyelinase inhibitors | inhibits | drug | 0.85 |
| serine palmitoyltransferase inhibitors | inhibits | drug | 0.85 |
| APOE4 | exacerbates | gene | 0.80 |
| LDL | interacts_with | protein | 0.80 |
| VLDL | interacts_with | protein | 0.80 |
| VLDL | transports | protein | 0.80 |
| LDL | transports | protein | 0.80 |
| liver-gut-brain axis | regulates | pathway | 0.75 |
| AMYLOID | produces | protein | 0.70 |
| APP | treats | gene | 0.70 |
| CANCER | destabilizes | disease | 0.70 |
| OXIDATIVE STRESS | activates | phenotype | 0.70 |
| APP | activates | gene | 0.70 |
| Apoptosis | interacts_with | entity | 0.70 |
| Apoptosis | associated_with | entity | 0.70 |
| APOE | causes | gene | 0.70 |
| APOE | regulates | gene | 0.70 |
| ENDOPLASMIC RETICULUM STRESS | causes | phenotype | 0.70 |
| APOE | treats | gene | 0.70 |
| APOE | activates | gene | 0.70 |
| APOE | inhibits | gene | 0.70 |
| GOLGI APPARATUS | regulates | organelle | 0.65 |
| LRRK2 | regulates | gene | 0.65 |
| AKT | regulates | gene | 0.65 |
| MITOPHAGY | exacerbates | phenotype | 0.65 |
| MITOPHAGY | interacts_with | phenotype | 0.65 |
| INSULIN RESISTANCE | interacts_with | phenotype | 0.65 |
| MINOCYCLINE | activates | drug | 0.65 |
| FINGOLIMOD | encodes | drug | 0.65 |
| GBA | encodes | gene | 0.65 |
| OXIDATIVE STRESS | degrades | phenotype | 0.60 |
| APOE | expressed_in | gene | 0.60 |
| SPHINGOMYELIN | participates_in | phenotype | 0.55 |
| inflammation | regulates | pathway | 0.50 |
| inflammation | interacts_with | pathway | 0.50 |
| IL-10 | interacts_with | protein | 0.50 |
| IL-10 | activates | protein | 0.50 |
| CERS2 | interacts_with | gene | 0.50 |
| SPTLC1 | inhibits | gene | 0.50 |
| SPTLC1 | activates | gene | 0.50 |
| ALZHEIMER | inhibits | gene | 0.50 |
Hypotheses where this entity is a therapeutic target
| Hypothesis | Score | Disease | Analysis |
|---|---|---|---|
| SMPD1 (Acid Sphingomyelinase) Inhibition for Ceramide Reduct | 0.732 | neurodegeneration | How do sphingomyelin/ceramide ratios spe |
Scientific analyses that reference this entity
No analyses mention this entity
Experimental studies targeting or related to this entity
| Experiment | Type | Disease | Score | Feasibility | Model | Status | Est. Cost |
|---|---|---|---|---|---|---|---|
| No experiments found | |||||||
Scientific publications cited in analyses involving this entity
| Title & PMID | Authors | Journal | Year | Citations |
|---|---|---|---|---|
| Pathogenic Variants and Olipudase Alfa Treatment of Patients With Acid Sphingomy [PMID:41692468] | ["Hsu-Heng Lin", "Hui-An Chen", "Shyh-Je | Molecular genetics & genom | 2026 | 0 |
| Multi-omics analysis identifies SMPD1 as a key contributor in sphingolipid pathw [PMID:41428198] | ["Aron Park", "Baeki E Kang", "Eun-Ju Ji | Genes & genomics | 2026 | 0 |
| A multi-dimensional bioinformatic dissection of the molecular mechanisms in high [PMID:41191606] | Yu X MD, Lei J MSc, Du X MSc, He Y MSc, | Int J Surg | 2026 | 0 |
| Plasma metabolites may inhibit childhood obesity by regulating ferroptosis throu [PMID:41249848] | Wang JG, Pan XH, Li Y | Int J Obes (Lond) | 2026 | 0 |
| Multi-omics analysis identifies SMPD1 as a key contributor in sphingolipid pathw [PMID:41428198] | Park A, Kang BE, Jin EJ, Kim HJ, Lee CW | Genes Genomics | 2026 | 0 |
| AXL Promotes Ischemic Myelin Repair Through Alleviating Myelin Debris Deposition [PMID:41524160] | Jia J, Gan Y, Li J, Li L, Meng H et al. | Adv Sci (Weinh) | 2026 | 0 |
| Pathogenic Variants and Olipudase Alfa Treatment of Patients With Acid Sphingomy [PMID:41692468] | Lin HH, Chen HA, Lin SJ, Hsu RH, Lee NC | Mol Genet Genomic Med | 2026 | 0 |
| AXL Promotes Ischemic Myelin Repair Through Alleviating Myelin Debris Deposition [PMID:41524160] | Jia J, Gan Y, Li J, Li L, Meng H, Sun M, | Advanced science (Weinheim, Ba | 2026 | 0 |
| A multi-dimensional bioinformatic dissection of the molecular mechanisms in high [PMID:41191606] | Yu X, Lei J, Du X, He Y, Peng W, Yang R, | International journal of surge | 2026 | 0 |
Multi-agent debates referencing this entity
No debates reference this entity
Hypotheses and analyses mentioning CERAMIDE in their description or question text
No additional research found