MST-312
A member of the class of benzamides that results from the formal condensation of the two amino groups of benzene-1,3-diamine with the carboxylic acid groups of two molar equivalents of 2,3-dihydroxybenzoic acid. It is telomerase inhibitor (IC50 = 0.67 μM in a TRAP assay) and exhibits antineoplastic activity.
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
Classification
Chemical structure
| Molecular formula | C20H16N2O6 |
|---|---|
| Charge | 0 |
| Average mass | 380.356 Da |
| Monoisotopic mass | 380.10084 Da |
| Source | ChEBI |
| InChIKey | MIQUEZGHEJGPJB-UHFFFAOYSA-N |
O=C(Nc1cccc(NC(=O)c2cccc(O)c2O)c1)c1cccc(O)c1O
InChI=1S/C20H16N2O6/c23-15-8-2-6-13(17(15)25)19(27)21-11-4-1-5-12(10-11)22-20(28)14-7-3-9-16(24)18(14)26/h1-10,23-26H,(H,21,27)(H,22,28)
Also called
- N,N'-benzene-1,3-diylbis(2,3-dihydroxybenzamide)
- MST 312
- MST312
- N,N'-(1,3-phenylene)bis(2,3-dihydroxybenzamide)
- N,N'-bis(2,3-dihydroxybenzoyl)-1,3-phenylenediamine
- N-[3-[[(2,3-dihydroxyphenyl)-oxomethyl]amino]phenyl]-2,3-dihydroxybenzamide
- telomerase inhibitor IX
Cross-references
Activity roles
- EC 2.7.7.49 (RNA-directed DNA polymerase) inhibitor
CHEBI:59897
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:95003 |
MST-312 | antibioticmech:chebi-b6a5e7b03e |
2026-08-30 |
Mechanism summary
- Mode of action
- VIRAL_POLYMERASE_INHIBITION host shared target
Curation history
-
SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories