Molecule

Nocardimicin D

AlkaPlorer ID: AK056869

Synonym: '(-)-Nocardimicin D', 'Nocardimicin D'

IUPAC Name: [(2R,3R)-1-[[(3S)-1-hydroxy-2-oxoazepan-3-yl]amino]-2-methyl-1-oxohexadecan-3-yl] (2R)-6-[acetyl(hydroxy)amino]-2-[[2-(2-hydroxyphenyl)-1,3-oxazole-4-carbonyl]amino]hexanoate

Structure

SMILES: CCCCCCCCCCCCC[C@@H](OC(=O)[C@@H](CCCCN(O)C(C)=O)N=C(O)C1=COC(C2=CC=CC=C2O)=N1)[C@@H](C)C(O)=N[C@H]1CCCCN(O)C1=O

InChI: InChI=1S/C41H63N5O10/c1-4-5-6-7-8-9-10-11-12-13-14-25-36(29(2)37(49)42-32-22-17-20-27-46(54)40(32)51)56-41(52)33(23-18-19-26-45(53)30(3)47)43-38(50)34-28-55-39(44-34)31-21-15-16-24-35(31)48/h15-16,21,24,28-29,32-33,36,48,53-54H,4-14,17-20,22-23,25-27H2,1-3H3,(H,42,49)(H,43,50)/t29-,32+,33-,36-/m1/s1

InChIKey: CILDOHPTQUQJJM-QHDIWBMLSA-N

Reference

Nocardimicins A, B, C, D, E, and F, Siderophores with Muscarinic M3 Receptor Inhibiting Activity from <i>Nocardia</i> sp. TP-A0674

PubChem CID: 163030841

LOTUS: LTS0241886

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
None	None	Nocardiaceae	Mycobacteriales	Actinomycetes	Actinomycetota	None	Bacteria

Properties Information

Molecule Weight: 785.98

TPSA？: 218.82

MolLogP？: 8.10420000000001

Number of H-Donors: 5

Number of H-Acceptors: 11

RingCount: 3

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi