Amythiamicin A is a cyclic thiazolyl peptide antibiotic with a structure similar to GE2270A. Amythiamicin B, C, and D also exist, but are not discussed further here. Amythiamicin A was shown to have the highest activity in cell free protein synthesis assays.
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 | C50H51N15O8S6 |
|---|---|
| Charge | 0 |
| Average mass | 1182.4 Da |
| Monoisotopic mass | 1181.23693069 Da |
| Source | PubChem · retrieved 2026-08-29 |
| InChIKey | BAGBLRBLZUISAJ-UHFFFAOYSA-N |
CC1=C2C(=O)NC(C3=NC(=CS3)C(=O)NCC(=O)NC(C4=NC(=CS4)C5=NC(=CS5)C6=C(C=CC(=N6)C7=NC(=CS7)C8=NC(CO8)C(=O)N9CCCC9C(=O)N)C3=NC(=CS3)C(=O)NC(C(=N2)S1)CC(=O)NC)C(C)C)C(C)C
InChI=1S/C50H51N15O8S6/c1-20(2)35-48-61-31(19-78-48)46-57-27(15-75-46)38-23(9-10-24(54-38)45-60-30(18-76-45)43-56-26(14-73-43)50(72)65-11-7-8-32(65)39(51)68)44-58-29(17-74-44)41(70)55-25(12-33(66)52-6)47-64-37(22(5)79-47)42(71)63-36(21(3)4)49-59-28(16-77-49)40(69)53-13-34(67)62-35/h9-10,15-21,25-26,32,35-36H,7-8,11-14H2,1-6H3,(H2,51,68)(H,52,66)(H,53,69)(H,55,70)(H,62,67)(H,63,71)
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| ARO | ARO:3001260 |
amythiamicin A | antibioticmech:aro-b0e6c47827 |
2026-08-30 |
Seeded from data/raw/ inventories (ARO)
Re-seeded from updated data/raw/ inventories
Re-seeded from updated data/raw/ inventories