Lynamicin G

AlkaPlorer ID: AK031305

Synonym: 'lynamicin G', 'Lynamicin G'

IUPAC Name: dimethyl 3,4-bis(5-chloro-1H-indol-3-yl)-1-methylpyrrole-2,5-dicarboxylate

Structure

SMILES: COC(=O)C1=C(C2=CNC3=CC=C(Cl)C=C23)C(C2=CNC3=CC=C(Cl)C=C23)=C(C(=O)OC)N1C

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InChI: InChI=1S/C25H19Cl2N3O4/c1-30-22(24(31)33-2)20(16-10-28-18-6-4-12(26)8-14(16)18)21(23(30)25(32)34-3)17-11-29-19-7-5-13(27)9-15(17)19/h4-11,28-29H,1-3H3

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InChIKey: HDSWTZRUKHSYDF-UHFFFAOYSA-N

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Source

Species Genus Family Order Class Phylum Kingdom Domain
None None Streptomycetaceae Kitasatosporales Actinomycetes Actinomycetota None Bacteria

Properties Information

Molecule Weight: 496.35000000000025

TPSA: 89.11000000000001

MolLogP: 6.201700000000004

Number of H-Donors: 2

Number of H-Acceptors: 5

RingCount: 5

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi
Bacillus subtilis Bacillus subtilis MIC 128.0 ug.mL-1 10.1021/np500362p
Bacillus thuringiensis Bacillus thuringiensis MIC 128.0 ug.mL-1 10.1021/np500362p
Candida albicans Candida albicans MIC 128.0 ug.mL-1 10.1021/np500362p
Escherichia coli Escherichia coli MIC 128.0 ug.mL-1 10.1021/np500362p
Homo sapiens HepG2 Inhibition nan % 10.1021/np500362p
Homo sapiens MCF7 IC50 10000.0 nM 10.1021/np500362p
Homo sapiens NCI-H460 Inhibition nan % 10.1021/np500362p
Staphylococcus aureus Staphylococcus aureus MIC 128.0 ug.mL-1 10.1021/np500362p

Metabolism Information