Halovir B
AlkaPlorer ID: AK001023
Synonym: None
IUPAC Name: (2S)-N-[(2S)-1-hydroxy-4-methylpentan-2-yl]-2-[[(2S)-2-[[(2S)-2-[[(2S,4R)-4-hydroxy-1-[2-methyl-2-(tetradecanoylamino)propanoyl]pyrrolidine-2-carbonyl]amino]-4-methylpentanoyl]amino]propanoyl]amino]pentanediamide
Structure
SMILES: CCCCCCCCCCCCCC(O)=NC(C)(C)C(=O)N1C[C@H](O)C[C@H]1C(O)=N[C@@H](CC(C)C)C(O)=N[C@@H](C)C(O)=N[C@@H](CCC(=N)O)C(O)=N[C@H](CO)CC(C)C
InChI: InChI=1S/C43H79N7O9/c1-9-10-11-12-13-14-15-16-17-18-19-20-37(54)49-43(7,8)42(59)50-26-32(52)25-35(50)41(58)48-34(24-29(4)5)40(57)45-30(6)38(55)47-33(21-22-36(44)53)39(56)46-31(27-51)23-28(2)3/h28-35,51-52H,9-27H2,1-8H3,(H2,44,53)(H,45,57)(H,46,56)(H,47,55)(H,48,58)(H,49,54)/t30-,31-,32+,33-,34-,35-/m0/s1
InChIKey: FFCLYSVFZQXUHI-XUVLUQBSSA-N
Reference
Halovirs A–E, new antiviral agents from a marine-Derived fungus of the genus Scytalidium
PubChem CID: 139291843
LOTUS: LTS0127392
{NPAtlas: NPA018758
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Scytalidium sp. | Scytalidium | None | None | Leotiomycetes | Ascomycota | Fungi | Eukaryota |
Properties Information
Molecule Weight: 838.145
TPSA？: 267.79999999999995
MolLogP？: 8.104670000000008
Number of H-Donors: 9
Number of H-Acceptors: 9
RingCount: 1
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|