Source Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...

Structure

InChI Key NFSJHKVQTUQJKL-GNHLHROZSA-N
Smiles CC[C@H](C)[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N
InChI
InChI=1S/C74H126N18O11/c1-9-48(8)63(74(103)91-61(41-47(6)7)71(100)86-55(30-16-21-35-76)66(95)84-57(32-18-23-37-78)68(97)88-59(64(81)93)39-45(2)3)92-70(99)58(33-19-24-38-79)85-67(96)56(31-17-22-36-77)87-73(102)62(42-49-25-11-10-12-26-49)90-72(101)60(40-46(4)5)89-69(98)54(29-15-20-34-75)83-65(94)52(80)43-50-44-82-53-28-14-13-27-51(50)53/h10-14,25-28,44-48,52,54-63,82H,9,15-24,29-43,75-80H2,1-8H3,(H2,81,93)(H,83,94)(H,84,95)(H,85,96)(H,86,100)(H,87,102)(H,88,97)(H,89,98)(H,90,101)(H,91,103)(H,92,99)/t48-,52-,54-,55-,56-,57-,58-,59-,60-,61-,62-,63-/m0/s1

Physicochemical Descriptors

Property Name Value
Molecular Formula C74H126N18O11
Molecular Weight 1443.91
AlogP None
Hydrogen Bond Acceptor None
Hydrogen Bond Donor None
Number of Rotational Bond None
Polar Surface Area None
Molecular species None
Aromatic Rings None
Heavy Atoms None
Assay Description Organism Bioactivity Reference
Antibacterial activity against Pseudomonas syringae pv. syringae EPS94 at 25 to 750 uM after 48 hr by broth dilution method Pseudomonas syringae pv. syringae None
Antibacterial activity against Erwinia amylovora PMV6076 at 25 to 750 uM after 48 hr by broth dilution method Erwinia amylovora None
Antibacterial activity against Xanthomonas vesicatoria 2133-2 at 25 to 750 uM after 48 hr by broth dilution method Xanthomonas vesicatoria None

Cross References

Resources Reference
ChEMBL CHEMBL2252942
PubChem 76315505