EDCtox

Mechanistic evidence atlas. Scores summarise biological direction and magnitude. They are not a toxicity rank or a human-risk number.

Compounds

Olanzapine

Olanzapine

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Category
pharmaceutical · Atypical antipsychotic
Record
specific compound · in current use
Identifiers
CAS 132539-06-1
Aliases
—

Atypical antipsychotic. Metabolic disruption at therapeutic doses is recorded separately from dopamine pharmacology and from mitochondrial hypotheses.

Flags: pharmaceutical

Phase-1 numbers are seed hypotheses. They are not curated consensus, not a toxicity total, and not a statement of human risk. Association is not written as causation.
REP
Reproductive
+2
DEV
Developmental
+2
NEUROENDO
Neuroendocrine / HPA
+3
IMM
Immune
—
MET
Metabolic
+4
MITO
Mitochondrial
+3
REDOX
Redox
+3

Left of the centre line is protective or restorative. Right is disruptive. Physiological activity is labelled and is not drawn as disruption. Domains are not added together.

Pathway notes

  • Olanzapine metabolic, mitochondrial, and redox chain is tagged across MET, MITO, REDOX. Those domain signals are shown as a profile and are not added together.

REP · Reproductive

+2

Headline +2 is the strongest independent cluster (HPG_AXIS: Prolactin). Other clusters and child mechanisms were not added. Human relevance is the relevance of the headline cluster, not the maximum relevance anywhere in the domain, and it is not multiplied into the score. No curated scientific findings are linked yet. The number is a seed assessment, not a literature count. Direction DISRUPTIVE. Confidence MODERATE. Human relevance H3. Supporting findings 0. Contradictory findings 0. Curation SEED_HYPOTHESIS.

Direction: Disruptive signal
Confidence: Moderate
Human relevance: H3 · substantial human observation plus biology
Findings 0 supporting / 0 contradictory · 0 capped

DEV · Developmental

+2

Headline +2 is the strongest independent cluster (DEVELOPMENTAL_PROGRAMMING: Developmental metabolic programming). Other clusters and child mechanisms were not added. Human relevance is the relevance of the headline cluster, not the maximum relevance anywhere in the domain, and it is not multiplied into the score. No curated scientific findings are linked yet. The number is a seed assessment, not a literature count. Direction DISRUPTIVE. Confidence LOW. Human relevance H1. Supporting findings 0. Contradictory findings 0. Curation SEED_HYPOTHESIS.

Direction: Disruptive signal
Confidence: Low
Human relevance: H1 · mechanistic, cellular, or high-dose animal
Findings 0 supporting / 0 contradictory · 0 capped

NEUROENDO · Neuroendocrine / HPA

+3

Headline +3 is the strongest independent cluster (DOPAMINE: Dopamine). Other clusters and child mechanisms were not added. Human relevance is the relevance of the headline cluster, not the maximum relevance anywhere in the domain, and it is not multiplied into the score. No curated scientific findings are linked yet. The number is a seed assessment, not a literature count. Direction CONTEXT_DEPENDENT. Confidence HIGH. Human relevance H4. Supporting findings 0. Contradictory findings 0. Curation SEED_HYPOTHESIS.

Direction: Context-dependent
Confidence: High
Human relevance: H4 · established at relevant human exposure
Findings 0 supporting / 0 contradictory · 0 capped

IMM · Immune

—

No quantitative mechanistic score is stored for this domain.

Direction: Direction uncertain
Confidence: —
Human relevance: —
Findings 0 supporting / 0 contradictory · 0 capped

MET · Metabolic

+4

Headline +4 is the strongest independent cluster (INSULIN_SIGNALING: Insulin resistance). Other clusters and child mechanisms were not added. 1 same-pathway observation capped. Human relevance is the relevance of the headline cluster, not the maximum relevance anywhere in the domain, and it is not multiplied into the score. No curated scientific findings are linked yet. The number is a seed assessment, not a literature count. Capped same-pathway nodes: IRS1. Direction DISRUPTIVE. Confidence HIGH. Human relevance H4. Supporting findings 0. Contradictory findings 0. Curation SEED_HYPOTHESIS.

Direction: Disruptive signal
Confidence: High
Human relevance: H4 · established at relevant human exposure
Findings 0 supporting / 0 contradictory · 1 capped

MITO · Mitochondrial

+3

Headline +3 is the strongest independent cluster (BIOENERGETIC_OUTPUT: ATP production). Other clusters and child mechanisms were not added. Human relevance is the relevance of the headline cluster, not the maximum relevance anywhere in the domain, and it is not multiplied into the score. No curated scientific findings are linked yet. The number is a seed assessment, not a literature count. Direction DISRUPTIVE. Confidence LOW. Human relevance H1. Supporting findings 0. Contradictory findings 0. Curation SEED_HYPOTHESIS.

Direction: Disruptive signal
Confidence: Low
Human relevance: H1 · mechanistic, cellular, or high-dose animal
Findings 0 supporting / 0 contradictory · 0 capped

REDOX · Redox

+3

Headline +3 is the strongest independent cluster (ROS_GENERATION: ROS (total)). Other clusters and child mechanisms were not added. Human relevance is the relevance of the headline cluster, not the maximum relevance anywhere in the domain, and it is not multiplied into the score. No curated scientific findings are linked yet. The number is a seed assessment, not a literature count. Direction DISRUPTIVE. Confidence LOW. Human relevance H1. Supporting findings 0. Contradictory findings 0. Curation SEED_HYPOTHESIS.

Direction: Disruptive signal
Confidence: Low
Human relevance: H1 · mechanistic, cellular, or high-dose animal
Findings 0 supporting / 0 contradictory · 0 capped