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                  Page - 1 of 1                  Record - 1 of 12   [TOP]
Compound ID1476
Compound Structure
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Plant SourceClausena excavata Burm. f.     Common Name:Clausena (English)
Source FamilyRutaceae
OriginIndia
Plant Part UsedRhizome
ExtractChloroform
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Isoniazid (0.040 – 0.090 µg/ml), Kanamycin sulphate (2 – 5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml200 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedClausenidin
PubChem ID   5315947
Ethnomedicinal InformationFever, indigestion, malaria, colic, muscular pain, diuretic and as tonic; the allied species C. wampi Blanco for bronchitis, in Thai folk medicine for cold
PubMed ID [Source Literature]12624822
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Coumarin, Chromone, Alkene, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]Against KB and BC - 1 cell lines
Molecular Weight328.131
Molecular FormulaC19H20O5
SMILESO1C(CC(=O)c2c1c(C(C)(C)C=C)c1oc(=O)ccc1c2O)(C)C
XLogP3.411
PSA63.600
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count2
No. of Rings3
No. of N0
No. of O5
No. of S0
Reference(s)1) Sunthitikawinsakul A, Kongkathip N, Kongkathip B, Phonnakhu S, Daly JW, Spande TF, Nimit Y, Rochanaruangrai S.Coumarins and carbazoles from Clausena excavata exhibited antimycobacterial and antifungal activities.Planta Med. 2003 Feb;69(2):155-7

2) Kirtikar, K.R., Basu, B.D., 1935. Indian Medicinal Plants, vols. 1–4. Lalit Mohan Basu, Allahabad, India

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                  Record - 2 of 12   [TOP]
Compound ID1482
Compound Structure
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Plant SourceClausena excavata Burm. f.     Common Name:Clausena (English)
Source FamilyRutaceae
OriginIndia
Plant Part UsedRoot
ExtractChloroform
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Isoniazid (0.040 – 0.090 µg/ml), Kanamycin sulphate (2 – 5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedO - Methylated Clausenidin
PubChem ID   504066
Ethnomedicinal InformationFever, indigestion, malaria, colic, muscular pain, diuretic and as tonic; the allied species C. wampi Blanco for bronchitis, in Thai folk medicine for cold
PubMed ID [Source Literature]12624822
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Coumarin, Chromone, Ether
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight342.147
Molecular FormulaC20H22O5
SMILESO1C(CC(=O)c2c1c(C(C)(C)C=C)c1oc(=O)ccc1c2OC)(C)C
XLogP3.930
PSA52.600
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings3
No. of N0
No. of O5
No. of S0
Reference(s)1) Sunthitikawinsakul A, Kongkathip N, Kongkathip B, Phonnakhu S, Daly JW, Spande TF, Nimit Y, Rochanaruangrai S.Coumarins and carbazoles from Clausena excavata exhibited antimycobacterial and antifungal activities.Planta Med. 2003 Feb;69(2):155-7

2) Kirtikar, K.R., Basu, B.D., 1935. Indian Medicinal Plants, vols. 1–4. Lalit Mohan Basu, Allahabad, India

Curator

                  Record - 3 of 12   [TOP]
Compound ID1739
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.)
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 - 4 of 12   [TOP]
Compound ID3715
Compound Structure
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Plant SourceHarrisonia perforata     Common Name:
Source FamilySimaroubaceae
OriginHainan, Cambodia, Cochin, China, Burma and West Malaysia
Plant Part UsedBranch
ExtractEthanol (95 %)
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Isoniazid (0.04 - 0.09 µg/ml), Kanamycin sulphate (2.0 - 5.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedPeucenin - 7 - Methyl Ether
PubChem IDNR
Ethnomedicinal InformationAntimalarial activity, Tuberculosis
PubMed ID [Source Literature]16394547
Extract PreparationThe branches of Harrisonia perforata (5.1 kg) were extracted with 95 % EtOH at room temperature. The ethanolic extract was filtered and evaporated to a dark brown viscous oil (186.3 g). The extract was partitioned between water (500 ml) and EtOAc (3 x 500 ml) and the water layer was further extracted with n-BuOH (3 x 400 ml). After evaporation, the EtOAc-, n-BuOH- and water - soluble fractions gave a brown viscous oil (69.8 g), a dark brown viscous oil (25.7 g) and a light brown viscous oil (50.8 g), respectively. The ethyl acetate soluble fraction is separated by flash column chromatography using silica gel
Chemical Classification [Active Compound]Aromatic, Bicyclic, Chromone, Prenylated, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight274.121
Molecular FormulaC16H18O4
SMILESC1(c(c(cc2c1c(=O)cc(o2)C)OC)CC=C(C)C)O
XLogP1.989
PSA46.530
H-bond Donor1
H-bond Acceptor3
No. of Rotatable Bond Count3
No. of Rings2
No. of N0
No. of O4
No. of S0
Reference(s)1) Tuntiwachwuttikul P, Phansa P, Pootaeng-On Y, Taylor WC.Chromones from the branches of Harrisonia perforata.Chem Pharm Bull (Tokyo). 2006 Jan;54(1):44-7

CuratorVikramjitmandal, Reshmi

                  Record - 5 of 12   [TOP]
Compound ID3717
Compound Structure
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Plant SourceHarrisonia perforata     Common Name:
Source FamilySimaroubaceae
OriginHainan, Cambodia, Cochin, China, Burma and West Malaysia
Plant Part UsedBranch
ExtractEthanol (95 %)
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Isoniazid (0.04 - 0.09 µg/ml), Kanamycin sulphate (2.0 - 5.3 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml200 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedPerforamone A
PubChem ID   11572850
Ethnomedicinal InformationAntimalarial activity
PubMed ID [Source Literature]16394547
Extract PreparationThe branches of Harrisonia perforata (5.1 kg) were extracted with 95 % EtOH at room temperature. The ethanolic extract was filtered and evaporated to a dark brown viscous oil (186.3 g). The extract was partitioned between water (500 ml) and EtOAc (3 x 500 ml) and the water layer was further extracted with n-BuOH (3 x 400 ml). After evaporation, the EtOAc-, n-BuOH- and water - soluble fractions gave a brown viscous oil (69.8 g), a dark brown viscous oil (25.7 g) and a light brown viscous oil (50.8 g), respectively. The ethyl acetate soluble fraction is separated by flash column chromatography using silica gel
Chemical Classification [Active Compound]Aromatic, Bicyclic, Chromone, Epoxy, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight290.115
Molecular FormulaC16H18O5
SMILESO1C(C1Cc1c2oc(cc(=O)c2c(O)cc1OC)C)(C)C
XLogP1.056
PSA59.060
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings3
No. of N0
No. of O5
No. of S0
Reference(s)1) Tuntiwachwuttikul P, Phansa P, Pootaeng-On Y, Taylor WC.Chromones from the branches of Harrisonia perforata.Chem Pharm Bull (Tokyo). 2006 Jan;54(1):44-7

CuratorVikramjitmandal, Reshmi

                  Record - 6 of 12   [TOP]
Compound ID3718
Compound Structure
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Plant SourceHarrisonia perforata     Common Name:
Source FamilySimaroubaceae
OriginHainan, Cambodia, Cochin, China, Burma and West Malaysia
Plant Part UsedBranch
ExtractEthanol (95 %)
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Isoniazid (0.04 - 0.09 µg/ml), Kanamycin sulphate (2.0 - 5.4 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedPerforamone B
PubChem ID   11608981
Ethnomedicinal InformationAntimalarial activity
PubMed ID [Source Literature]16394547
Extract PreparationThe branches of Harrisonia perforata (5.1 kg) were extracted with 95 % EtOH at room temperature. The ethanolic extract was filtered and evaporated to a dark brown viscous oil (186.3 g). The extract was partitioned between water (500 ml) and EtOAc (3 x 500 ml) and the water layer was further extracted with n-BuOH (3 x 400 ml). After evaporation, the EtOAc-, n-BuOH- and water - soluble fractions gave a brown viscous oil (69.8 g), a dark brown viscous oil (25.7 g) and a light brown viscous oil (50.8 g), respectively. The ethyl acetate soluble fraction is separated by flash column chromatography using silica gel
Chemical Classification [Active Compound]Aromatic, Bicyclic, Chromone, Ether, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight290.115
Molecular FormulaC16H18O5
SMILESO1c2c(C(O)CC(=C)C)c(OC)cc(O)c2c(=O)cc1C
XLogP0.558
PSA66.760
H-bond Donor2
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings2
No. of N0
No. of O5
No. of S0
Reference(s)1) Tuntiwachwuttikul P, Phansa P, Pootaeng-On Y, Taylor WC.Chromones from the branches of Harrisonia perforata.Chem Pharm Bull (Tokyo). 2006 Jan;54(1):44-7

CuratorVikramjitmandal, Reshmi

                  Record - 7 of 12   [TOP]
Compound ID3719
Compound Structure
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Plant SourceHarrisonia perforata     Common Name:
Source FamilySimaroubaceae
OriginChina
Plant Part UsedBranch
ExtractEthanol (95 %)
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Isoniazid (0.04 - 0.09 µg/ml), Kanamycin sulphate (2.0 - 5.5 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml200 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedPerforamone C
PubChem IDNR
Ethnomedicinal InformationAntimalarial activity
PubMed ID [Source Literature]16394547
Extract PreparationThe branches of Harrisonia perforata (5.1 kg) were extracted with 95 % EtOH at room temperature. The ethanolic extract was filtered and evaporated to a dark brown viscous oil (186.3 g). The extract was partitioned between water (500 ml) and EtOAc (3 x 500 ml) and the water layer was further extracted with n-BuOH (3 x 400 ml). After evaporation, the EtOAc-, n-BuOH- and water - soluble fractions gave a brown viscous oil (69.8 g), a dark brown viscous oil (25.7 g) and a light brown viscous oil (50.8 g), respectively. The ethyl acetate soluble fraction is separated by flash column chromatography using silica gel
Chemical Classification [Active Compound]Aromatic, Bicyclic, Chromone, Ether, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight290.115
Molecular FormulaC16H18O5
SMILESC1(cc(c(c2c1c(=O)cc(o2)C)CC(C(=C)C)O)OC)O
XLogP0.756
PSA66.760
H-bond Donor2
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings2
No. of N0
No. of O5
No. of S0
Reference(s)1) Tuntiwachwuttikul P, Phansa P, Pootaeng-On Y, Taylor WC.Chromones from the branches of Harrisonia perforata.Chem Pharm Bull (Tokyo). 2006 Jan;54(1):44-7

CuratorVikramjitmandal, Reshmi

                  Record - 8 of 12   [TOP]
Compound ID3720
Compound Structure
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Plant SourceHarrisonia perforata     Common Name:
Source FamilySimaroubaceae
OriginChina
Plant Part UsedBranch
ExtractEthanol (95 %)
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Isoniazid (0.04 - 0.09 µg/ml) and Kanamycin sulphate (2.0 - 5.6 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml100 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedEugenin
PubChem ID   10189
Ethnomedicinal InformationAntimalarial activity
PubMed ID [Source Literature]16394547
Extract PreparationThe branches of Harrisonia perforata (5.1 kg) were extracted with 95 % EtOH at room temperature. The ethanolic extract was filtered and evaporated to a dark brown viscous oil (186.3 g). The extract was partitioned between water (500 ml) and EtOAc (3 x 500 ml) and the water layer was further extracted with n-BuOH (3 x 400 ml). After evaporation, the EtOAc-, n-BuOH- and water - soluble fractions gave a brown viscous oil (69.8 g), a dark brown viscous oil (25.7 g) and a light brown viscous oil (50.8 g), respectively. The ethyl acetate soluble fraction is separated by flash column chromatography using silica gel
Chemical Classification [Active Compound]Aromatic, Bicyclic, Chromone, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight206.058
Molecular FormulaC11H10O4
SMILESO1c2c(c(O)cc(OC)c2)c(=O)cc1C
XLogP0.495
PSA46.530
H-bond Donor1
H-bond Acceptor3
No. of Rotatable Bond Count1
No. of Rings2
No. of N0
No. of O4
No. of S0
Reference(s)1) Tuntiwachwuttikul P, Phansa P, Pootaeng-On Y, Taylor WC.Chromones from the branches of Harrisonia perforata.Chem Pharm Bull (Tokyo). 2006 Jan;54(1):44-7

CuratorVikramjitmandal, Reshmi

                  Record - 9 of 12   [TOP]
Compound ID3721
Compound Structure
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Plant SourceHarrisonia perforata     Common Name:
Source FamilySimaroubaceae
OriginChina
Plant Part UsedBranch
ExtractEthanol (95 %)
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Isoniazid (0.04 - 0.09 µg/ml) and Kanamycin sulphate (2.0 - 5.7 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedPerforamone D
PubChem IDNR
Ethnomedicinal InformationAntimalarial activity
PubMed ID [Source Literature]16394547
Extract PreparationThe branches of Harrisonia perforata (5.1 kg) were extracted with 95 % EtOH at room temperature. The ethanolic extract was filtered and evaporated to a dark brown viscous oil (186.3 g). The extract was partitioned between water (500 ml) and EtOAc (3 x 500 ml) and the water layer was further extracted with n-BuOH (3 x 400 ml). After evaporation, the EtOAc-, n-BuOH- and water - soluble fractions gave a brown viscous oil (69.8 g), a dark brown viscous oil (25.7 g) and a light brown viscous oil (50.8 g), respectively. The ethyl acetate soluble fraction is separated by flash column chromatography using silica gel
Chemical Classification [Active Compound]Aromatic, Tricyclic, Chromone, Benzopyran, Phenol, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight274.084
Molecular FormulaC15H14O5
SMILESC12OC(C=Cc1c1c(c(c2)O)c(=O)cc(o1)CO)(C)C
XLogP0.339
PSA66.760
H-bond Donor2
H-bond Acceptor4
No. of Rotatable Bond Count1
No. of Rings3
No. of N0
No. of O5
No. of S0
Reference(s)1) Tuntiwachwuttikul P, Phansa P, Pootaeng-On Y, Taylor WC.Chromones from the branches of Harrisonia perforata.Chem Pharm Bull (Tokyo). 2006 Jan;54(1):44-7

CuratorVikramjitmandal, Reshmi

                  Record - 10 of 12   [TOP]
Compound ID3970
Compound Structure
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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 - 11 of 12   [TOP]
Compound ID3968
Compound Structure
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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 - 12 of 12   [TOP]
Compound ID3969
Compound Structure
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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


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