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                  Page - 1 of 1                  Record - 1 of 24   [TOP]
Compound ID1738
Compound Structure
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Plant SourceFerula communis     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginSaudi Arabia
Plant Part UsedRhizome
Extract
Target BacteriaMycobacterium intracellulare
Assay / Test Done
Positive Control Used (conc.)Amikacin (0.25 µg/ml), Streptomycin (10 µg/ml), Isoniazid (10 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml1.25 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedFerulenol
PubChem ID   54679300
Ethnomedicinal InformationAnti-mycobacterial
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight366.219
Molecular FormulaC24H30O3
SMILESO1c2c(c(O)c(C/C=C(/CC/C=C(/CCC=C(C)C)C)C)c1=O)cccc2
XLogP8.182
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count8
No. of Rings2
No. of N0
No. of O3
No. of S0
Reference(s)1) Mohammed A. Al-Yahya, Ilias Muhammad, Humayun H. Mirza, Farouk S. El-Feraly.Antibacterial constituents from the rhizomes of Ferula communis.Phytotherapy Research.12/1998;12(5):335-339

2) http://www.pfaf.org/user/Plant.aspx?LatinName=Ferula+communis

Curator

                  Record - 2 of 24   [TOP]
Compound ID1739
Compound Structure
DOWNLOAD:
Plant SourceFerula communis     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginSaudi Arabia
Plant Part UsedRhizome
Extract
Target BacteriaMycobacterium intracellulare
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedFerchromone
PubChem IDNR
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Terpene, Sesquiterpene, Chromone, Prenylated, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight384.230
Molecular FormulaC24H32O4
SMILESC1c2c(ccc1)OC1C(C2=O)CC([C@@](O1)(CC/C=C(/CCC=C(C)C)C)C)O
XLogP5.430
PSA55.760
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count6
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) Mohammed A. Al-Yahya, Ilias Muhammad, Humayun H. Mirza, Farouk S. El-Feraly.Antibacterial constituents from the rhizomes of Ferula communis.Phytotherapy Research.12/1998;12(5):335-339

2) http://www.pfaf.org/user/Plant.aspx?LatinName=Ferula+communis

Curator

                  Record - 3 of 24   [TOP]
Compound ID3074
Compound Structure
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Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium aurum (Pasteur Institute 104482)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (0.5 µg/ml), Isoniazid (2 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml2 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedFerulenol
PubChem ID   54679300
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight366.219
Molecular FormulaC24H30O3
SMILESO1c2c(c(O)c(C/C=C(/CC/C=C(/CCC=C(C)C)C)C)c1=O)cccc2
XLogP8.182
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count8
No. of Rings2
No. of N0
No. of O3
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVsheeba, vikramjitmandal

                  Record - 4 of 24   [TOP]
Compound ID3075
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium fortuitum (ATCC 6841)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (8 µg/ml), Isoniazid (0.5 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml2 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedFerulenol
PubChem ID   54679300
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight366.219
Molecular FormulaC24H30O3
SMILESO1c2c(c(O)c(C/C=C(/CC/C=C(/CCC=C(C)C)C)C)c1=O)cccc2
XLogP8.182
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count8
No. of Rings2
No. of N0
No. of O3
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVsheeba, vikramjitmandal

                  Record - 5 of 24   [TOP]
Compound ID3076
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium phlei (ATCC 11758)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (2 µg/ml), Isoniazid (4 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml2 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedFerulenol
PubChem ID   54679300
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight366.219
Molecular FormulaC24H30O3
SMILESO1c2c(c(O)c(C/C=C(/CC/C=C(/CCC=C(C)C)C)C)c1=O)cccc2
XLogP8.182
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count8
No. of Rings2
No. of N0
No. of O3
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVsheeba, vikramjitmandal

                  Record - 6 of 24   [TOP]
Compound ID3077
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium smegmatis (ATCC 14468)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (0.5 µg/ml), Isoniazid (1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml0.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedFerulenol
PubChem ID   54679300
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight366.219
Molecular FormulaC24H30O3
SMILESO1c2c(c(O)c(C/C=C(/CC/C=C(/CCC=C(C)C)C)C)c1=O)cccc2
XLogP8.182
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count8
No. of Rings2
No. of N0
No. of O3
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVsheeba, vikramjitmandal

                  Record - 7 of 24   [TOP]
Compound ID3078
Compound Structure
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Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium fortuitum (ATCC 6841)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (8 µg/ml), Isoniazid (0.5 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml16 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedE - ω - Benzoyloxyferulenol
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol, Benzoyl
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight486.241
Molecular FormulaC31H34O5
SMILESC1ccc2c(c1)c(c(c(=O)o2)C/C=C(/CC/C=C(/CC/C=C(/COC(=O)c1ccccc1)C)C)C)O
XLogP8.550
PSA63.600
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count12
No. of Rings3
No. of N0
No. of O5
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVikramjitmandal

                  Record - 8 of 24   [TOP]
Compound ID3079
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium phlei (ATCC 11758)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (2 µg/ml), Isoniazid (4 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml2 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedE - ω - Benzoyloxyferulenol
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol, Benzoyl
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight486.241
Molecular FormulaC31H34O5
SMILESC1ccc2c(c1)c(c(c(=O)o2)C/C=C(/CC/C=C(/CC/C=C(/COC(=O)c1ccccc1)C)C)C)O
XLogP8.550
PSA63.600
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count12
No. of Rings3
No. of N0
No. of O5
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVikramjitmandal

                  Record - 9 of 24   [TOP]
Compound ID3080
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium aurum (Pasteur Institute 104482)
Assay / Test Done
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 IdentifiedE - ω - Benzoyloxyferulenol
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol, Benzoyl
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight486.241
Molecular FormulaC31H34O5
SMILESC1ccc2c(c1)c(c(c(=O)o2)C/C=C(/CC/C=C(/CC/C=C(/COC(=O)c1ccccc1)C)C)C)O
XLogP8.550
PSA63.600
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count12
No. of Rings3
No. of N0
No. of O5
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVikramjitmandal

                  Record - 10 of 24   [TOP]
Compound ID3081
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium smegmatis (ATCC 144680)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (0.5 µg/ml), Isoniazid (1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml2 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedE - ω - Benzoyloxyferulenol
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol, Benzoyl
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight486.241
Molecular FormulaC31H34O5
SMILESC1ccc2c(c1)c(c(c(=O)o2)C/C=C(/CC/C=C(/CC/C=C(/COC(=O)c1ccccc1)C)C)C)O
XLogP8.550
PSA63.600
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count12
No. of Rings3
No. of N0
No. of O5
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVikramjitmandal

                  Record - 11 of 24   [TOP]
Compound ID3082
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium fortuitum (ATCC 6841)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (8 µg/ml), Isoniazid (0.5 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml64 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedE - ω - Hydroxyferulenol
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight382.214
Molecular FormulaC24H30O4
SMILESC1ccc2c(c1)c(c(c(=O)o2)C/C=C(/CC/C=C(/CC/C=C(/CO)C)C)C)O
XLogP5.064
PSA57.530
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count9
No. of Rings2
No. of N0
No. of O4
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVikramjitmandal

                  Record - 12 of 24   [TOP]
Compound ID3083
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium phlei (ATCC 11758)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (2 µg/ml), Isoniazid (4 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml16 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedE - ω - Hydroxyferulenol
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight382.214
Molecular FormulaC24H30O4
SMILESC1ccc2c(c1)c(c(c(=O)o2)C/C=C(/CC/C=C(/CC/C=C(/CO)C)C)C)O
XLogP5.064
PSA57.530
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count9
No. of Rings2
No. of N0
No. of O4
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVikramjitmandal

                  Record - 13 of 24   [TOP]
Compound ID3084
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium aurum (Pasteur Institute 104482)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (0.5 µg/ml), Isoniazid (2 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml32 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedE - ω - Hydroxyferulenol
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight382.214
Molecular FormulaC24H30O4
SMILESC1ccc2c(c1)c(c(c(=O)o2)C/C=C(/CC/C=C(/CC/C=C(/CO)C)C)C)O
XLogP5.064
PSA57.530
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count9
No. of Rings2
No. of N0
No. of O4
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVikramjitmandal

                  Record - 14 of 24   [TOP]
Compound ID3085
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium smegmatis (ATCC 144680)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (0.5 µg/ml), Isoniazid (1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml16 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedE - ω - Hydroxyferulenol
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight382.214
Molecular FormulaC24H30O4
SMILESC1ccc2c(c1)c(c(c(=O)o2)C/C=C(/CC/C=C(/CC/C=C(/CO)C)C)C)O
XLogP5.064
PSA57.530
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count9
No. of Rings2
No. of N0
No. of O4
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVikramjitmandal

                  Record - 15 of 24   [TOP]
Compound ID3086
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium fortuitum (ATCC 6841)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (8 µg/ml), Isoniazid (0.5 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml32 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound Identifiedω - acetoxy derivative of ferulenol
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, O-Acetyl, Phenol
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight424.225
Molecular FormulaC26H32O5
SMILESC1cccc2c1c(c(c(=O)o2)C/C=C(/CC/C=C(/CC/C=C(/COC(=O)C)C)C)C)O
XLogP5.804
PSA63.600
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count11
No. of Rings2
No. of N0
No. of O5
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVikramjitmandal

                  Record - 16 of 24   [TOP]
Compound ID3087
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium phlei (ATCC 11758)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (2 µg/ml), Isoniazid (4 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 Identifiedω - acetoxy derivative of ferulenol
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, O-Acetyl, Phenol
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight424.225
Molecular FormulaC26H32O5
SMILESC1cccc2c1c(c(c(=O)o2)C/C=C(/CC/C=C(/CC/C=C(/COC(=O)C)C)C)C)O
XLogP5.804
PSA63.600
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count11
No. of Rings2
No. of N0
No. of O5
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVikramjitmandal

                  Record - 17 of 24   [TOP]
Compound ID3088
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium aurum (Pasteur Institute 104482)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (0.5 µg/ml), Isoniazid (2 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml16 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound Identifiedω - acetoxy derivative of ferulenol
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, O-Acetyl, Phenol
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight424.225
Molecular FormulaC26H32O5
SMILESC1cccc2c1c(c(c(=O)o2)C/C=C(/CC/C=C(/CC/C=C(/COC(=O)C)C)C)C)O
XLogP5.804
PSA63.600
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count11
No. of Rings2
No. of N0
No. of O5
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVikramjitmandal

                  Record - 18 of 24   [TOP]
Compound ID3089
Compound Structure
DOWNLOAD:
Plant SourceFerula communis L.     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginCagliari, Sardinia, Italy
Plant Part UsedRoot
ExtractAcetone
Target BacteriaMycobacterium smegmatis (ATCC 144680)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (0.5 µg/ml), Isoniazid (1 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 Identifiedω - acetoxy derivative of ferulenol
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]15620264
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, O-Acetyl, Phenol
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton Broth
Cytotoxicity Assay [AID]
Molecular Weight424.225
Molecular FormulaC26H32O5
SMILESC1cccc2c1c(c(c(=O)o2)C/C=C(/CC/C=C(/CC/C=C(/COC(=O)C)C)C)C)O
XLogP5.804
PSA63.600
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count11
No. of Rings2
No. of N0
No. of O5
No. of S0
Reference(s)1) Appendino G, Mercalli E, Fuzzati N, Arnoldi L, Stavri M, Gibbons S, Ballero M, Maxia A.Antimycobacterial coumarins from the sardinian giant fennel (Ferula communis).J Nat Prod. 2004 Dec;67(12):2108-10

CuratorVikramjitmandal

                  Record - 19 of 24   [TOP]
Compound ID3970
Compound Structure
DOWNLOAD:
Plant SourceFerula communis     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginSaudi Arabia
Plant Part UsedRhizome
Extract
Target BacteriaMycobacterium smegmatis
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedFerchromone
PubChem IDNR
Ethnomedicinal InformationAnti-mycobacterial
PubMed ID [Source Literature]
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Tricyclic, Terpene, Sesquiterpene, Chromone, Prenylated, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight384.230
Molecular FormulaC24H32O4
SMILESC1c2c(ccc1)OC1C(C2=O)CC([C@@](O1)(CC/C=C(/CCC=C(C)C)C)C)O
XLogP5.430
PSA55.760
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count6
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) Mohammed A. Al-Yahya, Ilias Muhammad, Humayun H. Mirza, Farouk S. El-Feraly.Antibacterial constituents from the rhizomes of Ferula communis.Phytotherapy Research.12/1998;12(5):335-339

2) http://www.pfaf.org/user/Plant.aspx?LatinName=Ferula+communis

Curator

                  Record - 20 of 24   [TOP]
Compound ID3968
Compound Structure
DOWNLOAD:
Plant SourceFerula communis     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginSaudi Arabia
Plant Part UsedRhizome
Extract
Target BacteriaMycobacterium xenopi
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedFerchromone
PubChem IDNR
Ethnomedicinal InformationAnti-mycobacterial
PubMed ID [Source Literature]
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Tricyclic, Terpene, Sesquiterpene, Chromone, Prenylated, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight384.230
Molecular FormulaC24H32O4
SMILESC1c2c(ccc1)OC1C(C2=O)CC([C@@](O1)(CC/C=C(/CCC=C(C)C)C)C)O
XLogP5.430
PSA55.760
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count6
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) Mohammed A. Al-Yahya, Ilias Muhammad, Humayun H. Mirza, Farouk S. El-Feraly.Antibacterial constituents from the rhizomes of Ferula communis.Phytotherapy Research.12/1998;12(5):335-339

2) http://www.pfaf.org/user/Plant.aspx?LatinName=Ferula+communis

Curator

                  Record - 21 of 24   [TOP]
Compound ID3969
Compound Structure
DOWNLOAD:
Plant SourceFerula communis     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginSaudi Arabia
Plant Part UsedRhizome
Extract
Target BacteriaMycobacterium chelonei
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedFerchromone
PubChem IDNR
Ethnomedicinal InformationAnti-mycobacterial
PubMed ID [Source Literature]
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Tricyclic, Terpene, Sesquiterpene, Chromone, Prenylated, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight384.230
Molecular FormulaC24H32O4
SMILESC1c2c(ccc1)OC1C(C2=O)CC([C@@](O1)(CC/C=C(/CCC=C(C)C)C)C)O
XLogP5.430
PSA55.760
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count6
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) Mohammed A. Al-Yahya, Ilias Muhammad, Humayun H. Mirza, Farouk S. El-Feraly.Antibacterial constituents from the rhizomes of Ferula communis.Phytotherapy Research.12/1998;12(5):335-339

2) http://www.pfaf.org/user/Plant.aspx?LatinName=Ferula+communis

Curator

                  Record - 22 of 24   [TOP]
Compound ID3967
Compound Structure
DOWNLOAD:
Plant SourceFerula communis     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginSaudi Arabia
Plant Part UsedRhizome
Extract
Target BacteriaMycobacterium smegmatis
Assay / Test Done
Positive Control Used (conc.)Amikacin (0.25 µg/ml), Streptomycin (10 µg/ml), Isoniazid (10 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml1.25 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedFerulenol
PubChem ID   54679300
Ethnomedicinal InformationAnti-mycobacterial
PubMed ID [Source Literature]
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight366.219
Molecular FormulaC24H30O3
SMILESO1c2c(c(O)c(C/C=C(/CC/C=C(/CCC=C(C)C)C)C)c1=O)cccc2
XLogP8.182
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count8
No. of Rings2
No. of N0
No. of O3
No. of S0
Reference(s)1) Mohammed A. Al-Yahya, Ilias Muhammad, Humayun H. Mirza, Farouk S. El-Feraly.Antibacterial constituents from the rhizomes of Ferula communis.Phytotherapy Research.12/1998;12(5):335-339

2) http://www.pfaf.org/user/Plant.aspx?LatinName=Ferula+communis

Curator

                  Record - 23 of 24   [TOP]
Compound ID3966
Compound Structure
DOWNLOAD:
Plant SourceFerula communis     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginSaudi Arabia
Plant Part UsedRhizome
Extract
Target BacteriaMycobacterium chelonei
Assay / Test Done
Positive Control Used (conc.)Amikacin (0.25 µg/ml), Streptomycin (10 µg/ml), Isoniazid (10 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml1.25 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedFerulenol
PubChem ID   54679300
Ethnomedicinal InformationAnti-mycobacterial
PubMed ID [Source Literature]
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight366.219
Molecular FormulaC24H30O3
SMILESO1c2c(c(O)c(C/C=C(/CC/C=C(/CCC=C(C)C)C)C)c1=O)cccc2
XLogP8.182
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count8
No. of Rings2
No. of N0
No. of O3
No. of S0
Reference(s)1) Mohammed A. Al-Yahya, Ilias Muhammad, Humayun H. Mirza, Farouk S. El-Feraly.Antibacterial constituents from the rhizomes of Ferula communis.Phytotherapy Research.12/1998;12(5):335-339

2) http://www.pfaf.org/user/Plant.aspx?LatinName=Ferula+communis

Curator

                  Record - 24 of 24   [TOP]
Compound ID3965
Compound Structure
DOWNLOAD:
Plant SourceFerula communis     Common Name:Giant Fennel
Source FamilyApiaceae (Umbelliferae)
OriginSaudi Arabia
Plant Part UsedRhizome
Extract
Target BacteriaMycobacterium xenopi
Assay / Test Done
Positive Control Used (conc.)Amikacin (0.25 µg/ml), Streptomycin (10 µg/ml), Isoniazid (10 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml1.25 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedFerulenol
PubChem ID   54679300
Ethnomedicinal InformationAnti-mycobacterial
PubMed ID [Source Literature]
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Bicyclic, Alkyl, Alkene, Coumarin, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight366.219
Molecular FormulaC24H30O3
SMILESO1c2c(c(O)c(C/C=C(/CC/C=C(/CCC=C(C)C)C)C)c1=O)cccc2
XLogP8.182
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count8
No. of Rings2
No. of N0
No. of O3
No. of S0
Reference(s)1) Mohammed A. Al-Yahya, Ilias Muhammad, Humayun H. Mirza, Farouk S. El-Feraly.Antibacterial constituents from the rhizomes of Ferula communis.Phytotherapy Research.12/1998;12(5):335-339

2) http://www.pfaf.org/user/Plant.aspx?LatinName=Ferula+communis

Curator


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