Candicidin D; 26E,28E-Isomer, 18-decarboxy, 18-methyl, 3ξ-alcohol
AlkaPlorer ID: AK291534
Synonym: Antibiotic CS 103-I, CS 103-I
IUPAC Name: None
Structure
SMILES: CC1C=CC=CC=CC=CC=CC=CC=CC(OC2OC(C)C(O)C(N)C2O)CC2OC(O)(CC(O)CC(O)CC(O)CC(=O)CCCC(O)CC(=O)OC1C(C)CC(C)C(O)CC(=O)C1=CC=C(N)C=C1)CC(O)C2C
InChI: InChI=1S/C59H88N2O16/c1-36-19-16-14-12-10-8-6-7-9-11-13-15-17-22-48(75-58-56(72)54(61)55(71)40(5)74-58)32-52-39(4)51(69)35-59(73,77-52)34-47(66)30-46(65)29-45(64)28-43(62)20-18-21-44(63)31-53(70)76-57(36)38(3)27-37(2)49(67)33-50(68)41-23-25-42(60)26-24-41/h6-17,19,22-26,36-40,44-49,51-52,54-58,63-67,69,71-73H,18,20-21,27-35,60-61H2,1-5H3
InChIKey: OMUDFQHNXYWYRC-UHFFFAOYSA-N
Reference
CAS: 1155336-44-9
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Streptomyces sp. FR-008 | Streptomyces | Streptomycetaceae | Kitasatosporales | Actinomycetes | Actinomycetota | None | Bacteria |
Properties Information
Molecule Weight: 1081.3509999999997
TPSA？: 322.23999999999995
MolLogP？: 4.496900000000005
Number of H-Donors: 11
Number of H-Acceptors: 18
RingCount: 4
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|