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CHEBI:44137 - tiamulin
| Formula | C28H47NO4S |
| Net Charge | 0 |
| Average Mass | 493.754 |
| Monoisotopic Mass | 493.32258 |
| SMILES | [H][C@@]12C(=O)CC[C@]13CC[C@@]([H])(C)[C@@]2(C)[C@H](OC(=O)CSCCN(CC)CC)C[C@@](C)(C=C)[C@@H](O)[C@@H]3C |
| InChI | InChI=1S/C28H47NO4S/c1-8-26(6)17-22(33-23(31)18-34-16-15-29(9-2)10-3)27(7)19(4)11-13-28(20(5)25(26)32)14-12-21(30)24(27)28/h8,19-20,22,24-25,32H,1,9-18H2,2-7H3/t19-,20+,22-,24+,25+,26-,27+,28+/m1/s1 |
| InChIKey | UURAUHCOJAIIRQ-QGLSALSOSA-N |
| Wikipedia |
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| Roles Classification |
|---|
| Chemical Role: | Bronsted base A molecular entity capable of accepting a hydron from a donor (Brønsted acid). |
| Biological Role: | antibacterial drug A drug used to treat or prevent bacterial infections. |
| Application: | antibacterial drug A drug used to treat or prevent bacterial infections. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| tiamulin (CHEBI:44137) has functional parent Pleuromutilin (CHEBI:8269) |
| tiamulin (CHEBI:44137) has role antibacterial drug (CHEBI:36047) |
| tiamulin (CHEBI:44137) is a carbotricyclic compound (CHEBI:38032) |
| tiamulin (CHEBI:44137) is a carboxylic ester (CHEBI:33308) |
| tiamulin (CHEBI:44137) is a cyclic ketone (CHEBI:3992) |
| tiamulin (CHEBI:44137) is a organic sulfide (CHEBI:16385) |
| tiamulin (CHEBI:44137) is a secondary alcohol (CHEBI:35681) |
| tiamulin (CHEBI:44137) is a semisynthetic derivative (CHEBI:72588) |
| tiamulin (CHEBI:44137) is a tertiary amino compound (CHEBI:50996) |
| tiamulin (CHEBI:44137) is a tetracyclic diterpenoid (CHEBI:52557) |
| IUPAC Name |
|---|
| (3aS,4R,5S,6S,8R,9R,9aR,10R)-5-hydroxy-4,6,9,10-tetramethyl-1-oxo-6-vinyldecahydro-3a,9-propanocyclopenta[8]annulen-8-yl {[2-(diethylamino)ethyl]sulfanyl}acetate |
| INNs | Source |
|---|---|
| tiamulinum | WHO MedNet |
| tiamulina | WHO MedNet |
| tiamulin | WHO MedNet |
| tiamuline | WHO MedNet |
| Citations |
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