Phenelfamycin G is produced by Streptomyces albospinus strain Acta 3619. Phenelfamycin G and H are isomeric and similar to phenelfamycin E and F only with the addition of a hydroxyl group at position C-30. Phenelfamycin G and H have a narrow antibacterial spectrum with potent activity against Cutibacterium acnes.
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.
elfamycin antibioticARO:3001219
ARO:3001219| Molecular formula | C66H96O22 |
|---|---|
| Charge | 0 |
| Average mass | 1241.5 Da |
| Monoisotopic mass | 1240.63932469 Da |
| Source | PubChem · retrieved 2026-08-29 |
| InChIKey | VQOMZALHTLFROE-JUDPNWICSA-N |
C[C@H]1[C@H]([C@H](C[C@@H](O1)O[C@H]2[C@@H](O[C@@H](C[C@H]2OC)O[C@@H]3[C@@H](O[C@H](C[C@@H]3OC)OC[C@@H](C(=O)CC/C=C/C=C(\C)/[C@H]([C@@H](C)[C@H]4C[C@@H]([C@@H](O4)/C=C/C=C/C=C/C(=O)O)O)OC)[C@@]5([C@@H]([C@@H](C([C@@H](O5)/C=C/C=C\CO)(C)C)O)OC(=O)CC6=CC=CC=C6)O)C)C)OC)O
InChI=1S/C66H96O22/c1-39(60(79-11)40(2)49-34-47(69)48(84-49)29-21-12-13-23-31-54(70)71)25-17-14-20-28-46(68)45(66(75)64(85-55(72)33-44-26-18-15-19-27-44)63(74)65(6,7)53(88-66)30-22-16-24-32-67)38-80-56-36-51(77-9)61(42(4)82-56)87-58-37-52(78-10)62(43(5)83-58)86-57-35-50(76-8)59(73)41(3)81-57/h12-19,21-27,29-31,40-43,45,47-53,56-64,67,69,73-75H,20,28,32-38H2,1-11H3,(H,70,71)/b13-12+,17-14+,24-16-,29-21+,30-22+,31-23+,39-25+/t40-,41-,42-,43-,45-,47-,48-,49+,50-,51-,52+,53-,56+,57-,58+,59+,60+,61+,62-,63-,64+,66+/m0/s1
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| ARO | ARO:3001322 |
phenelfamycin G | antibioticmech:aro-7086196093 |
2026-08-30 |
Seeded from data/raw/ inventories (ARO)
Re-seeded from updated data/raw/ inventories
Re-seeded from updated data/raw/ inventories