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                  Page - 1 of 1                  Record - 1 of 5   [TOP]
Compound ID3975
Compound Structure
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Plant SourceAllium neapolitanum     Common Name:
Source FamilyAmaryllidaceae
OriginLincolnshire, UK
Plant Part UsedBulb
ExtractChloroform
Target BacteriaMycobacterium abcessus (ATCC 19977)
Assay / Test DoneColumbia Blood Agar
Positive Control Used (conc.)Ethambutol (128 µg/ml), Isoniazid (128 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml16 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedCanthin-6-one
PubChem ID   97176
Ethnomedicinal Information
PubMed ID [Source Literature]17421058
Extract Preparation6.3 kg of macerated bulb material underwent cold extraction with hexane, chloroform and methanol (3 l)
Chemical Classification [Active Compound]Aromatic, Tetracyclic, Alkaloid, Carbazole, Quinoline, Amide
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight220.064
Molecular FormulaC14H8N2O
SMILESO=c1n2c3c(c4c2cccc4)ccnc3cc1
XLogP2.809
PSA34.890
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count0
No. of Rings4
No. of N2
No. of O1
No. of S0
Reference(s)1) O'Donnell G, Gibbons S.Antibacterial activity of two canthin-6-one alkaloids from Allium neapolitanum.Phytother Res. 2007 Jul;21(7):653-7

Curator

                  Record - 2 of 5   [TOP]
Compound ID3974
Compound Structure
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Plant SourceAllium neapolitanum     Common Name:
Source FamilyAmaryllidaceae
OriginLincolnshire, UK
Plant Part UsedBulb
ExtractChloroform
Target BacteriaMycobacterium fortuitum (ATCC 6841)
Assay / Test DoneColumbia Blood Agar
Positive Control Used (conc.)Ethambutol (4 µg/ml), Isoniazid (0.25 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml16 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedCanthin-6-one
PubChem ID   97176
Ethnomedicinal Information
PubMed ID [Source Literature]17421058
Extract Preparation6.3 kg of macerated bulb material underwent cold extraction with hexane, chloroform and methanol (3 l)
Chemical Classification [Active Compound]Aromatic, Tetracyclic, Alkaloid, Carbazole, Quinoline, Amide
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight220.064
Molecular FormulaC14H8N2O
SMILESO=c1n2c3c(c4c2cccc4)ccnc3cc1
XLogP2.809
PSA34.890
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count0
No. of Rings4
No. of N2
No. of O1
No. of S0
Reference(s)1) O'Donnell G, Gibbons S.Antibacterial activity of two canthin-6-one alkaloids from Allium neapolitanum.Phytother Res. 2007 Jul;21(7):653-7

Curator

                  Record - 3 of 5   [TOP]
Compound ID3796
Compound Structure
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Plant SourceAllium neapolitanum     Common Name:NR
Source FamilyAmaryllidaceae
OriginLincolnshire, UK
Plant Part UsedBulb
ExtractChloroform
Target BacteriaMycobacterium phlei (ATCC 11758)
Assay / Test DoneColumbia Blood Agar
Positive Control Used (conc.)Ethambutol (0.5 µg/ml), Isoniazid (2 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml8 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCanthin-6-one
PubChem ID   97176
Ethnomedicinal InformationNR
PubMed ID [Source Literature]17421058
Extract Preparation6.3 kg of macerated bulb material underwent cold extraction with hexane, chloroform and methanol (3 l)
Chemical Classification [Active Compound]Aromatic, Tetracyclic, Alkaloid, Carbazole, Quinoline, Amide
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]NR
Molecular Weight220.064
Molecular FormulaC14H8N2O
SMILESO=c1n2c3c(c4c2cccc4)ccnc3cc1
XLogP2.809
PSA34.890
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count0
No. of Rings4
No. of N2
No. of O1
No. of S0
Reference(s)1) O'Donnell G, Gibbons S.Antibacterial activity of two canthin-6-one alkaloids from Allium neapolitanum.Phytother Res. 2007 Jul;21(7):653-7

CuratorNajiya-beegum, vikramjitmandal

                  Record - 4 of 5   [TOP]
Compound ID3799
Compound Structure
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Plant SourceAllium neapolitanum     Common Name:NR
Source FamilyAmaryllidaceae
OriginLincolnshire, UK
Plant Part UsedBulb
ExtractChloroform
Target BacteriaMycobacterium smegmatis (ATCC 14468)
Assay / Test DoneColumbia Blood Agar
Positive Control Used (conc.)Ethambutol (0.25 µg/ml), Isoniazid (2 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml8 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCanthin-6-one
PubChem ID   97176
Ethnomedicinal InformationNR
PubMed ID [Source Literature]17421058
Extract Preparation6.3 kg of macerated bulb material underwent cold extraction with hexane, chloroform and methanol (3 l)
Chemical Classification [Active Compound]Aromatic, Tetracyclic, Alkaloid, Carbazole, Quinoline, Amide
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]NR
Molecular Weight220.064
Molecular FormulaC14H8N2O
SMILESO=c1n2c3c(c4c2cccc4)ccnc3cc1
XLogP2.809
PSA34.890
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count0
No. of Rings4
No. of N2
No. of O1
No. of S0
Reference(s)1) O'Donnell G, Gibbons S.Antibacterial activity of two canthin-6-one alkaloids from Allium neapolitanum.Phytother Res. 2007 Jul;21(7):653-7

CuratorNajiya-beegum, vikramjitmandal

                  Record - 5 of 5   [TOP]
Compound ID3800
Compound Structure
DOWNLOAD:
Plant SourceAllium neapolitanum     Common Name:NR
Source FamilyAmaryllidaceae
OriginLincolnshire, UK
Plant Part UsedBulb
ExtractChloroform
Target BacteriaMycobacterium smegmatis (mc2 2700)
Assay / Test DoneColumbia Blood Agar
Positive Control Used (conc.)Ethambutol (0.25 µg/ml), Isoniazid (2 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml8 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCanthin-6-one
PubChem ID   97176
Ethnomedicinal InformationNR
PubMed ID [Source Literature]17421058
Extract Preparation6.3 kg of macerated bulb material underwent cold extraction with hexane, chloroform and methanol (3 l)
Chemical Classification [Active Compound]Aromatic, Tetracyclic, Alkaloid, Carbazole, Quinoline, Amide
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]NR
Molecular Weight220.064
Molecular FormulaC14H8N2O
SMILESO=c1n2c3c(c4c2cccc4)ccnc3cc1
XLogP2.809
PSA34.890
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count0
No. of Rings4
No. of N2
No. of O1
No. of S0
Reference(s)1) O'Donnell G, Gibbons S.Antibacterial activity of two canthin-6-one alkaloids from Allium neapolitanum.Phytother Res. 2007 Jul;21(7):653-7

CuratorNajiya-beegum, vikramjitmandal


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