acibenzolar
CHEBI:73185
·resolve ·ANTIFUNGAL
·EXACT
SEEDED
A benzothiadiazole that is 1,2,3-benzothiadiazole in which the hydrogen at position 7 is replaced by a sulfanylcarbonyl group. It is used (particularly as its S-methyl thioester) as a fungicide and plant activator. — ChEBI
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
Strictly broader compounds or drug classes this molecule belongs to.
Chemical structure
Computed structure properties
| Molecular formula | C7H4N2OS2 |
|---|
| Charge | 0 |
|---|
| Average mass | 196.256 Da |
|---|
| Monoisotopic mass | 195.9765 Da |
|---|
| Source | ChEBI |
|---|
| InChIKey | CGIHPACLZJDCBQ-UHFFFAOYSA-N |
SMILES
O=C(S)c1cccc2nnsc12
InChI
InChI=1S/C7H4N2OS2/c10-7(11)4-2-1-3-5-6(4)12-9-8-5/h1-3H,(H,10,11)
Also called
- 1,2,3-benzothiadiazole-7-carbothioic S-acid (EXACT_SYNONYM)— chebi
- benzo[1,2,3]thiadiazole-7-carbothioic S-acid (EXACT_SYNONYM)— chebi
Cross-references
Equivalent identifiers for this same structure in other resources.
Activity roles
Every antimicrobial role a source asserts for this compound — the
unreduced evidence behind its antimicrobial_class.
Source concepts
Every upstream concept that resolved to this record. The merge is
the product: this is what shows ChEBI and CARD are describing the same structure.
Upstream concepts merged into this record
| Source | Native ID | Label | Minted CURIE | Version |
| CHEBI |
CHEBI:73185 |
acibenzolar |
antibioticmech:chebi-13cd90cb47 |
2026-08-30 |
Curation history
-
SEEDED_FROM_SOURCES
2026-08-30 · seed_from_sources
Seeded from data/raw/ inventories (CHEBI)
-
RESEEDED_FROM_SOURCES
2026-08-30 · seed_from_sources
Re-seeded from updated data/raw/ inventories
-
RESEEDED_FROM_SOURCES
2026-08-30 · seed_from_sources
Re-seeded from updated data/raw/ inventories
Provenance
Seeded by scripts/seed_from_sources.py from the committed
inventories in data/raw/.
View the record.