Statistics
Data distribution across ADMETatlas
Sealed release totals and live diagnostic distributions for the atlas database.
Sealed release at a glance
These headline totals come only from the checksum-sealed release manifest used by the download files, paper, and overview artwork. The detailed charts below are live diagnostic views and state their own denominators; they do not redefine the citable release totals.
Molecular composition
Live diagnostic view of sequence length, residue makeup, and chemical topology in the current atlas database. These denominators may change after the sealed release and are not citable release totals.
Peptide length distribution
Residue counts for canonical standard amino-acid sequences. Cyclic peptides and other modified forms are summarized separately, below.
Amino-acid composition
Residues tallied across all standard amino-acid sequences, colored by side-chain class.
Topology classes
Topology class summarizes sequence/form representation, not developability quality.
Cyclic peptide monomer length
Monomer count for cyclic peptides, using the source's authoritative monomer length. A further 5,162 modified or text-encoded forms from other sources use heterogeneous residue notations and are not length-binned.
Formal ADMET distribution
Live diagnostic endpoint evidence grouped by the five formal ADMET modules used across the site. The sunburst shows module-to-endpoint hierarchy, while the ranking shows where current evidence volume is concentrated.
ADMET module to endpoint
Outer slices are endpoints; inner slices are the five formal modules.
Largest endpoint evidence sets
Top 12 of 17 formal endpoints by record count. Labels link to endpoint pages below.
Endpoint value distributions
How the actual measured values are distributed for the highest-volume numeric endpoints. Each histogram is binned within a single coherent unit; endpoints whose values mix incomparable units are deliberately not shown here.
Permeability
Reported values in log permeability (source-reported). Shaded band marks High permeability ≥ −6.0.
Hemolysis percent observation
Reported values in % hemolysis.
Cytotoxicity percent observation
Reported values in % cytotoxicity.
Cytotoxicity metric
Reported values in µM (log scale).
Hemolysis metric
Reported values in µM (log scale).
Evidence assay context
The experimental conditions under which the endpoint evidence was measured, normalized to controlled scientific vocabularies. Each measurement is comparable only within a matching organism, biological matrix, and route — these distributions show the assay landscape behind the numbers. Counts cover measurements where the source recorded the field; bars omit measurements with no recorded value.
Evidence by species
Organism (or organism-derived system) in which each endpoint measurement was made.
Evidence by matrix
The biological material the peptide was measured in (plasma, cell culture, tissue, buffer, …). Values are only comparable within the same matrix.
Evidence by route
Administration route for in-vivo / dosing studies. 'Multiple routes' marks measurements that report more than one route.
Product context
How the marketed and tracked peptide products in the atlas are described, kept separate from endpoint evidence.
Product route distribution
Routes are product descriptors and should not be interpreted as endpoint evidence.
Product record bands
Priority bands help orient flagship examples versus broader catalog records.
Provenance & corroboration
How traceable the evidence is by source type, and how broadly each endpoint is independently corroborated across distinct external datasets. Individual upstream database names are kept out of the charts and listed in references and downloads instead.
Evidence provenance by source type
Each reference carries one scientific source class. ADMETatlas standardizes curated datasets and directly-extracted primary literature into one comparable evidence model, so every value keeps a traceable origin.
Endpoints by dataset coverage
Bands group endpoints by how many distinct external datasets contain records for them. This describes source coverage, not concordance, independence, or evidence quality. The same primary study can appear through more than one dataset.
High-volume endpoint context
Evidence & curation detail
Curation mechanics behind the numbers: how measurements are classed by scientific role and value form, and how context signals attach. These support traceability and are collapsed by default to keep the page science-forward.
Show curation & evidence-shape charts▾
Formal evidence and reported observations
Stacked bars show how each of the top 12 of 17 endpoints is composed.
How endpoint values are represented
Numeric values, ranges, categorical values, and text observations remain separate.
Context signals by type
Context signals support interpretation around trials, product identity, and reviews; they are not formal endpoint measurements.
Where context attaches
Signals attach at the product level, to the linked peptide identity, or — when identity is not yet resolved — to the source record alone.