dehydroemetine
A pyridoisoquinoline which was developed in response to the cardiovascular toxicity associated with emetine and results from the dehydrogenation of the heterotricylic ring of emetine. It is an antiprotozoal agent and displays antimalarial, antiamoebic, and antileishmanial properties.
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
| Charge | |
|---|---|
| Source | ChEBI |
| InChIKey | XXLZPUYGHQWHRN-RPBOFIJWSA-N |
[H][C@@]12CC(C[C@H]3NCCc4cc(OC)c(OC)cc43)=C(CC)CN1CCc1cc(OC)c(OC)cc12
InChI=1S/C29H38N2O4/c1-6-18-17-31-10-8-20-14-27(33-3)29(35-5)16-23(20)25(31)12-21(18)11-24-22-15-28(34-4)26(32-2)13-19(22)7-9-30-24/h13-16,24-25,30H,6-12,17H2,1-5H3/t24-,25+/m1/s1
Also called
- Dametin
- Mebadin
- Mebadine
- dehidroemetina
- dehydroemetinum
- déhydroémétine
- 6',7',10,11-tetramethoxy-2,3-didehydroemetan
- (−)-2,3-dehydroemetine
- (−)-R,S-dehydroemetine
- 2,3-didehydro-6',7',10,11-tetramethoxyemetan
- 2,3-didehydroemetine
- 2-dehydroemetine
- BT 436
- Ro 1-9334
- Ro 1-9334/19
- Ro-1-9334/19
- Ro-1933419
Cross-references
Drug registries
Patents and articles
Activity roles
- antiprotozoal drug
CHEBI:35820 - antimalarial
CHEBI:38068 - antileishmanial agent
CHEBI:70868
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:149634 |
dehydroemetine | antibioticmech:chebi-18a3a93b5d |
2026-08-30 |
Curation history
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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
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories