lasalocid
CHEBI:92181
·resolve ·ANTIPROTOZOAL
·EXACT
SEEDED
A polyether antibiotic used for prevention and treatment of coccidiosis in poultry. — 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
polyketide with antibiotic activityARO:3005171
Strictly broader compounds or drug classes this molecule belongs to.
Chemical structure
Computed structure properties
| Molecular formula | C34H54O8 |
|---|
| Charge | 0 |
|---|
| Average mass | 590.798 Da |
|---|
| Monoisotopic mass | 590.38187 Da |
|---|
| Source | ChEBI |
|---|
| InChIKey | BBMULGJBVDDDNI-OWKLGTHSSA-N |
SMILES
[H][C@]1([C@@H](CC)C(=O)[C@@H](C)[C@@H](O)[C@H](C)CCc2ccc(C)c(O)c2C(=O)O)O[C@](CC)([C@@]2([H])CC[C@](O)(CC)[C@H](C)O2)C[C@@H]1C
InChI
InChI=1S/C34H54O8/c1-9-25(31-21(6)18-34(11-3,42-31)26-16-17-33(40,10-2)23(8)41-26)30(37)22(7)28(35)19(4)12-14-24-15-13-20(5)29(36)27(24)32(38)39/h13,15,19,21-23,25-26,28,31,35-36,40H,9-12,14,16-18H2,1-8H3,(H,38,39)/t19-,21+,22+,23+,25+,26-,28+,31+,33-,34+/m1/s1
Also called
- lasalocide (INN)— chebi
- lasalocidum (INN)— chebi
- lasalócido (INN)— chebi
- (1S,9S)-1,5:6,9-dianhydro-9-[(3R,5S,6S,7R)-9-(2-carboxy-3-hydroxy-4-methylphenyl)-6-hydroxy-5,7-dimethyl-4-oxononan-3-yl]-3,4,7,8-tetradeoxy-6-ethyl-2-C-ethyl-1,8-dimethyl-D-galacto-nonitol (EXACT_SYNONYM)— chebi
- 6-[(3R,4S,5S,7R)-7-{(2S,3S,5S)-5-ethyl-5-[(2R,5R,6S)-5-ethyl-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yl]-3-methyltetrahydrofuran-2-yl}-4-hydroxy-3,5-dimethyl-6-oxononyl]-2-hydroxy-3-methylbenzoic acid (EXACT_SYNONYM)— chebi
- Ro 2-2985 (EXACT_SYNONYM)— chebi
- X 537A (EXACT_SYNONYM)— chebi
- X-537A (EXACT_SYNONYM)— chebi
- antibiotic X 537A (EXACT_SYNONYM)— chebi
- ionophore X 537A (EXACT_SYNONYM)— chebi
- lasalocid A (EXACT_SYNONYM)— chebi
- Lasalocid (EXACT_SYNONYM)— aro
- Lasalocide (EXACT_SYNONYM)— aro
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 |
| ARO |
ARO:3007754 |
lasalocid A |
antibioticmech:aro-466b335c0d |
2026-08-30 |
| CHEBI |
CHEBI:92181 |
lasalocid |
antibioticmech:chebi-6226860c32 |
2026-08-30 |
Mechanism summary
- Mode of action
- MEMBRANE_DISRUPTION host shared target — Assigned from ChEBI role CHEBI:24869 (ionophore). ChEBI asserts the role on the compound. The target it names is one the host has too, so the mechanism is true but is not evidence of selectivity — see mode_of_action_target_scope. Not a curator's mechanistic review.
Curation history
-
SEEDED_FROM_SOURCES
2026-08-30 · seed_from_sources
Seeded from data/raw/ inventories (ARO, 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.