Triamterene
Pteridine substituted at positions 2, 4 and 7 with amino groups and at position 6 with a phenyl group. A sodium channel blocker, it is used as a diuretic in the treatment of hypertension and oedema. — ChEBI
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Identity & molecular properties
Source-linked values| CAS number | 396-01-0 | ChEBI ↗ |
| Molecular formula | C12H11N7 | ChEBI ↗ |
| Molar mass | 253.269 g/mol | ChEBI ↗ |
| Monoisotopic mass | 253.10759 Da | ChEBI ↗ |
| Formal charge | 0 | ChEBI ↗ |
| ChEBI identifier | CHEBI:9671 | ChEBI ↗ |
Cross-source molecular data
PubChem| Molar mass | 253.26 g/mol | PubChem ↗ |
| Exact mass | 253.10759338 Da | PubChem ↗ |
| Computed XLogP | 1 | PubChem ↗ |
| Topological polar surface area (Ų) | 130 | PubChem ↗ |
| H-bond donors | 3 | PubChem ↗ |
| H-bond acceptors | 7 | PubChem ↗ |
| Rotatable bonds | 1 | PubChem ↗ |
PubChem computed values are shown separately from the ChEBI record. An exact InChIKey match was used to connect the records. Molecular descriptors do not describe a supplied product’s purity, particle size or performance.
Names & structural identifiers
Copy any identifiertriamterene6-phenylpteridine-2,4,7-triamineFNYLWPVRPXGIIP-UHFFFAOYSA-NNc1nc(N)c2nc(-c3ccccc3)c(N)nc2n1InChI=1S/C12H11N7/c13-9-7(6-4-2-1-3-5-6)16-8-10(14)18-12(15)19-11(8)17-9/h1-5H,(H6,13,14,15,17,18,19)Names & synonyms
Names are supplied by ChEBI. Trade names and related synonyms may describe a broader product context.
Classification & relationships
ChEBI ontologyRoles recorded in ChEBI
Database role annotations describe reported biological or chemical roles; they are not product approvals or recommendations for use.
Mass ↔ amount of substance
Calculated from sourced massUses 253.269 g/mol from ChEBI. Assumes the substance described by this record; no purity or concentration correction is applied.
Elemental composition
Theoretical mass fractionsCNHCalculated theoretical mass fractions from the reported formula and PubChem periodic-table atomic masses. These are not assay or purity results.
Research & patent references
Selected source associationsSources & record history
Checked 27 Sep 2026Release 255, 9 September 2026. ChEBI three-star (manually annotated) source entry. View original record ↗ · CC BY 4.0
PubCAS formats source data, connects references and computes explicitly labelled conversions. CAS cross-references are supplied by ChEBI; they do not constitute CAS verification or endorsement.