From literature to label.
In one API.
Publications, genes, molecules, clinical trials, patents, and the full FDA & EMA record — one cross-linked Core graph your models and agents query through a single API.
Click a core for its data at a glance — coverage, breakdowns, and the fields you can filter on
- GeneCore: Genes & targets
- BiomedCore: Publications
- DrugCore: Molecules
- TrialCore: Clinical trials
- RegulatoryCore: FDA + EMA
- PatentCore: Patents
Dozens of upstream feeds, from public registries and agency records to curated reference databases and the patent offices, land behind one schema on a continuous ingest cadence.
BiomedCore
Publications
- PubMed citations, abstracts and MeSH indexing
- PubMed Central open-access full text
- Crossref DOI, journal and publisher metadata
- Reference lists and forward citations
- NLM journal catalogue and ISSN registry
- Retraction, correction and erratum notices
- Databank accessions cited on the record: registries, sequences, structures
GeneCore
Genes & targets
- HGNC approved symbols, aliases and previous names
- Ensembl gene models, biotype and genomic location
- NCBI Gene and RefSeq curated summaries
- UniProt Swiss-Prot function, disease and family annotation
- Gene Ontology terms and Reactome pathway membership
- Target class, tractability buckets and chemical probes
- gnomAD constraint, essentiality screens and safety liabilities
DrugCore
Molecules
- ChEMBL molecule registry: structures, InChI and SMILES
- GSRS substance records from FDA, NCATS, EMA and USP
- INN, USAN, ATC and UNII identifiers
- Trade names and full synonym sets
- Mechanism of action and target assignments
- Parent, salt-form and prodrug relationships
- Modality and highest clinical stage reached
TrialCore
Clinical trials
- ClinicalTrials.gov study records, via the CTTI AACT release
- WHO ICTRP national registries: CTIS, EudraCT, ISRCTN, jRCT, ChiCTR, CTRI, ANZCTR, DRKS and more
- Sponsors, collaborators and cooperative groups
- Conditions, interventions and MeSH browse terms
- Design, arms, eligibility criteria and enrolment
- Reported outcomes, result groups and measurements
- Protocol identifiers and linked publications
RegulatoryCore
FDA + EMA
- Drugs@FDA applications, approval status and dates
- FDA product labels, parsed section by section
- FDA review packages: medical, clinical pharmacology, statistical
- Orphan Drug Product designations
- Expedited programs: breakthrough, fast track, priority review, accelerated approval
- Withdrawal notices from the Federal Register and 21 CFR 216.24
- EMA European public assessment reports (EPARs)
- EMA Summary of Product Characteristics, Annex I
- openFDA marketing status and product listings
PatentCore
PreviewPatents
- USPTO, EPO and WIPO publications: grants and applications
- Full text: title, abstract, claims and description
- CPC and IPC classifications
- Assignees, inventors, priority and grant dates
- DOCDB simple patent families
- SureChEMBL compounds annotated from patent text
- Patent-to-patent and patent-to-literature citations
One query, every source. Ask the Core, not the upstream. The answer arrives in the same shape whichever feed it came from.
Find work by the two scientists most central to GLP-1 biology: Lotte Bjerre Knudsen (Novo Nordisk, designed semaglutide) and Daniel Drucker (Toronto, discovered GLP-1's incretin effect).
{ "data": [ { "amassId": "AMBC_RwzeOtqYiRA2S523v1jL81OgndQ", "pmid": "34626851", "pmcid": "PMC8859548", "doi": "10.1016/j.molmet.2021.101351", "title": "GLP-1 physiology informs the pharmacotherapy of obesity", "abstract": "BACKGROUND: Glucagon-like peptide-1 receptor agonists (GLP1RA) augment glucose-dependent insulin release and reduce glucagon secretion and gastric emptying, enabling their successful development for the treatment of type 2 diabetes (T2D).…", "authors": ["Daniel J. Drucker"], "journal": "Molecular metabolism", "issn": "2212-8778", "volumeIssue": "57", "language": "eng", "publicationDate": "2022-03-01", "publicationTypes": ["Journal Article", "Research Support, Non-U.S. Gov't", "Review"], "isRetracted": false, "citationCount": 423, "journalQualityJufo": 2, "meshTerms": ["Adolescent", "Animals", "Diabetes Mellitus, Type 2", "Glucagon-Like Peptide 1", "Glucagon-Like Peptide-1 Receptor", …], "keywords": ["Brain", "Diabetes", "G protein-coupled receptor", "Hunger", "Obesity", …], "substances": ["Glucagon-Like Peptide-1 Receptor", "Liraglutide", "Glucagon-Like Peptide 1"], "hasFulltext": false, "authorsMetadata": [ { "name": "Daniel J. Drucker", "orcid": "0000-0001-6688-8127", "affiliations": [{ "name": "Lunenfeld-Tanenbaum Research Institute", "ror": "01s5axj25", "countryCode": "CA" }] } ], "meshIds": ["D000293", "D000818", "D003924", "D052216", "D000067757", …], "substanceIds": ["D000067757", "D000069450", "D052216"], "referencesTrialCore": [], "references": ["AMBC_5km7Q541cJN5a8RcTUN2tcgYoRj", "AMBC_WUubCFjk6wfURImFXwtDEvKquIE", "AMBC_3pwzL1urfguQm7s2L8Jlj04onOR", "AMBC_YDNDzsaB3vLPfxW6MNxdJU7vwI0", "AMBC_KH7wBl2Araj9gbLXuQWOHefvkIs", …], "citedBy": ["AMBC_B5CfpHBkdFha6MX0Q2GJpCBMw3o", "AMBC_UAflDqTKZtUAEny8XTtIvPvCWu7", "AMBC_P2sn7qrFvXfd8grl0s5scQ2El3t", "AMBC_5Er4ez0MRO1LsHzGpqflcUlzSFZ", "AMBC_PB5LfnIhIOOXiZLcXAokubVODU8", …] }, { "pmid": "32987188", "title": "Glucagon-like peptide-1 receptor co-agonists for treating metabolic disease", "citationCount": 270, … }, { "pmid": "35907261", "title": "Glucagon-like Peptide-1 Receptor-based Therapeutics for Metabolic Liver Disease", "citationCount": 113, … }, { "pmid": "41654015", "title": "Ectopic, hepatic GLP-1R agonism enhances the weight loss efficacy of GLP-1 analogues", "citationCount": 0, … }, { "pmid": "29317623", "title": "GLP-1 release and vagal afferent activation mediate the beneficial metabolic and chronotherapeutic effects of D-allulose", "citationCount": 181, … } ] }
Cross-linked by design. Follow any paper to its targets, any target to its molecules, any molecule to its trials, and any trial back to the evidence.
Click any core in the graph above to see what's inside.