Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA002944
PROPERTIES
| NPAID | NPA002944 |
|---|---|
| CLUSTER ID | 1690 |
| NODE ID | 1380 |
| NAME | RP-66453 |
| FORMULA | C33H36N4O8 |
| MOLECULAR WEIGHT (Da) | 616.6710 |
| ACCURATE MASS (Da) | 616.2533 |
| ORIGIN ORGANISM TYPE | Bacterium |
| ORIGIN GENUS | Streptomyces |
| ORIGIN SPECIES | sp. |
| InChIKey | LRYMXYNLAMRRTH-UHFFFAOYSA-N |
| InChI | InChI=1S/C33H36N4O8/c1-3-16(2)28-32(42)35-24-14-19-11-22(21-10-18(6-9-26(21)38)12-23(34)30(40)37-28)29(39)27(15-19)45-20-7-4-17(5-8-20)13-25(33(43)44)36-31(24)41/h4-11,15-16,23-25,28,38-39H,3,12-14,34H2,1-2H3,(H,35,42)(H,36,41)(H,37,40)(H,43,44) |
| SMILES | CCC(C)C1C(=O)NC2CC3=CC(=C(C(=C3)C4=C(C=CC(=C4)CC(C(=O)N1)N)O)O)OC5=CC=C(CC(NC2=O)C(=O)O)C=C5 |
ORIGINAL ISOLATION REFERENCE
| CITATION | HELYNCK, GERARD; DUBERTRET, CATHERINE; FRECHET, DENISE; LEBOUL, JEAN Isolation of RP 66453, a New Secondary Peptide Metabolite from Streptomyces sp. Useful as a Lead for Neurotensin Antagonists Journal of Antibiotics 1998 51 (5) 512-514. | ||
|---|---|---|---|
| DOI | 10.7164/antibiotics.51.512 | PMID | 9666181 |
SYNTHESES
| CITATION 1 | Bois-Choussy M; Cristau P; Zhu J Total synthesis of an atropdiastereomer of RP-66453 and determination of its absolute configuration. Angewandte Chemie International Edition 2003 42 (35) 4238-41. DOI: 10.1002/anie.200351996 PMID: 14502745 | ||
|---|---|---|---|
