Halovir C
AlkaPlorer ID: AK002070
Synonym: None
IUPAC Name: N-[(2S)-1-hydroxy-4-methylpentan-2-yl]-2-[[(2S)-3-methyl-2-[[(2S)-4-methyl-2-[[(2S)-1-[2-methyl-2-(tetradecanoylamino)propanoyl]pyrrolidine-2-carbonyl]amino]pentanoyl]amino]butanoyl]amino]pentanediamide
Structure
SMILES: CCCCCCCCCCCCCC(O)=NC(C)(C)C(=O)N1CCC[C@H]1C(O)=N[C@@H](CC(C)C)C(O)=N[C@H](C(O)=NC(CCC(=N)O)C(O)=N[C@H](CO)CC(C)C)C(C)C
InChI: InChI=1S/C45H83N7O8/c1-10-11-12-13-14-15-16-17-18-19-20-23-38(55)51-45(8,9)44(60)52-26-21-22-36(52)42(58)49-35(28-31(4)5)41(57)50-39(32(6)7)43(59)48-34(24-25-37(46)54)40(56)47-33(29-53)27-30(2)3/h30-36,39,53H,10-29H2,1-9H3,(H2,46,54)(H,47,56)(H,48,59)(H,49,58)(H,50,57)(H,51,55)/t33-,34?,35-,36-,39-/m0/s1
InChIKey: VCAGNEUDNVLWPT-WTPQGBEESA-N
Reference
Halovirs A–E, new antiviral agents from a marine-Derived fungus of the genus Scytalidium
PubChem CID: 139292100
LOTUS: LTS0133189
{NPAtlas: NPA000319
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Scytalidium sp. | Scytalidium | None | None | Leotiomycetes | Ascomycota | Fungi | Eukaryota |
Properties Information
Molecule Weight: 850.1999999999999
TPSA？: 247.57
MolLogP？: 9.769969999999995
Number of H-Donors: 8
Number of H-Acceptors: 8
RingCount: 1
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|