FE35A
AlkaPlorer ID: AK023203
Synonym: 'FE 35A', '', 'FE35A'
IUPAC Name: N-[(2S,3R,4S,5R,6S)-2-(8-ethenyl-1-hydroxy-10,12-dimethoxy-6-oxonaphtho[1,2-c]isochromen-4-yl)-3,5-dihydroxy-6-methyloxan-4-yl]-N-methylacetamide
Structure
SMILES: C=CC1=CC2=C(C(OC)=C1)C1=C(OC2=O)C2=C([C@@H]3O[C@@H](C)[C@H](O)[C@H](N(C)C(C)=O)[C@H]3O)C=CC(O)=C2C(OC)=C1
InChI: InChI=1S/C30H31NO9/c1-7-15-10-18-22(20(11-15)37-5)17-12-21(38-6)24-19(33)9-8-16(23(24)28(17)40-30(18)36)29-27(35)25(31(4)14(3)32)26(34)13(2)39-29/h7-13,25-27,29,33-35H,1H2,2-6H3/t13-,25-,26-,27+,29-/m0/s1
InChIKey: LFLUKKBCPUVQAB-LAVFYLQISA-N
Reference
New Ravidomycin Analogues, FE35A and FE35B, Apoptosis Inducers Produced by Streptomyces rochei.
PubChem CID: 162971386
LOTUS: LTS0162918
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Streptomyces rochei | Streptomyces | Streptomycetaceae | Kitasatosporales | Actinomycetes | Actinomycetota | None | Bacteria |
Properties Information
Molecule Weight: 549.5760000000001
TPSA？: 138.9
MolLogP？: 3.4937000000000022
Number of H-Donors: 3
Number of H-Acceptors: 9
RingCount: 5
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|