geissoschizoline
CHEBI:5283
·resolve ·ANTIPROTOZOAL
·EXACT
SEEDED
An indole alkaloid that is (16α)-curan substituted by a hydroxy group at position 17. — 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 | C19H26N2O |
|---|
| Charge | 0 |
|---|
| Average mass | 298.43 Da |
|---|
| Monoisotopic mass | 298.20451 Da |
|---|
| Source | ChEBI |
|---|
| InChIKey | FAQGZHFLASTWAV-RWANUPMISA-N |
|---|
SMILES
[H][C@@]12C[C@]3([H])N(CC[C@@]34c3ccccc3N[C@@]4([H])[C@H]1CO)C[C@H]2CC
InChI
InChI=1S/C19H26N2O/c1-2-12-10-21-8-7-19-15-5-3-4-6-16(15)20-18(19)14(11-22)13(12)9-17(19)21/h3-6,12-14,17-18,20,22H,2,7-11H2,1H3/t12-,13+,14+,17+,18+,19-/m1/s1
Also called
- (16α)-curan-17-ol (EXACT_SYNONYM)— chebi
- Geissoschizoline (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:5283 |
geissoschizoline |
antibioticmech:chebi-66d6caa709 |
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.