Compounds
ID | Spectrum Quality | Annotated Name |
---|
COMPOUND NPA005324
PROPERTIES
NPAID | NPA005324 |
---|---|
CLUSTER ID | 1368 |
NODE ID | 1150 |
NAME | Saptomycin H |
FORMULA | C33H35NO9 |
MOLECULAR WEIGHT (Da) | 589.6410 |
ACCURATE MASS (Da) | 589.2312 |
ORIGIN ORGANISM TYPE | Bacterium |
ORIGIN GENUS | Streptomyces |
ORIGIN SPECIES | sp. HP530 Parent |
InChIKey | DLWNUUQBCVPEHS-LUNSBOQASA-N |
InChI | InChI=1S/C33H35NO9/c1-14-11-20-26(30-24(14)21(36)12-23(42-30)33(6)16(3)43-33)29(39)25-19(27(20)37)10-9-18(28(25)38)22-13-32(5,34(7)8)31(15(2)40-22)41-17(4)35/h9-12,15-16,22,31,38H,13H2,1-8H3/t15-,16?,22+,31+,32-,33?/m0/s1 |
SMILES | CC(=O)O[C@@H]1[C@H](C)O[C@@H](C2=C(O)C3=C(C=C2)C(=O)C2=C(C3=O)C3=C(C(C)=C2)C(=O)C=C(C2(C)OC2C)O3)C[C@]1(C)N(C)C |
ORIGINAL ISOLATION REFERENCE
CITATION | Abe, N; Nakakita, Y; Nakamura, T; Enoki, N; Uchida, H; Munekata, M Novel antitumor antibiotics, saptomycins. I. Taxonomy of the producing organism, fermentation, HPLC analysis and biological activities. Journal of Antibiotics 1993 46 (10) 1530-1535. | ||
---|---|---|---|
DOI | 10.7164/antibiotics.46.1530 | PMID | 8244880 |
REVISIONS
VERSION | SMILES | CITATION | ||
---|---|---|---|---|
Original Isolation | C/C=C\C1C(O1)(C)C2=CC(=O)C3=C(C=C4C(=C3O2)C(=O)C5=C(C4=O)C=CC(=C5O)[C@H]6C[C@]([C@@H]([C@@H](O6)C)OC(=O)C)(C)N(C)C)C | Abe, N; Nakakita, Y; Nakamura, T; Enoki, N; Uchida, H; Munekata, M Novel antitumor antibiotics, saptomycins. I. Taxonomy of the producing organism, fermentation, HPLC analysis and biological activities. Journal of Antibiotics 1993 46 (10) 1530-1535. DOI: 10.7164/antibiotics.46.1530 PMID: 8244880 | ||
2 | CC(=O)O[C@@H]1[C@H](C)O[C@@H](C2=C(O)C3=C(C=C2)C(=O)C2=C(C3=O)C3=C(C(C)=C2)C(=O)C=C(C2(C)OC2C)O3)C[C@]1(C)N(C)C | Shimura, Jun; Ando, Yoshio; Ohmori, Ken; Suzuki, Keisuke Total Synthesis and Structure Assignment of Saptomycin H. Organic Letters 2022 24 (7) 1439-1443. DOI: 10.1021/acs.orglett.1c04306 PMID: 35147030 |