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                  Page - 1 of 1                  Record - 1 of 6   [TOP]
Compound ID1280
Compound Structure
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Plant SourceBorrichia frutescens L.     Common Name:Sea Daisy
Source FamilyAsteraceae (Compositae)
OriginSoutheastern USA
Plant Part UsedFlower, leaf, stem
ExtractDichloromethane
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test Done
Positive Control Used (conc.)Fusidic acid (4 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml8 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified(24R)-24,25-epoxycycloartan-3-one
PubChem ID   469544
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]8988597
Extract PreparationN/A
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Terpene, Triterpene, Cycloartane, Ketone, Epoxy
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]Against vero cells
Molecular Weight440.365
Molecular FormulaC30H48O2
SMILESO=C1C([C@H]2[C@@]3([C@@]4(C3)[C@H]([C@]3([C@](CC4)([C@H](CC3)[C@@H](CC[C@H]3OC3(C)C)C)C)C)CC2)CC1)(C)C
XLogP9.983
PSA29.600
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count4
No. of Rings6
No. of N0
No. of O2
No. of S0
Reference(s)1) Cantrell CL, Lu T, Fronczek FR, Fischer NH, Adams LB, Franzblau SG.Antimycobacterial cycloartanes from Borrichia frutescens.J Nat Prod. 1996 Dec;59(12):1131-6

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                  Record - 2 of 6   [TOP]
Compound ID1281
Compound Structure
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Plant SourceBorrichia frutescens L.     Common Name:Sea Daisy
Source FamilyAsteraceae (Compositae)
OriginUSA
Plant Part UsedFlower, leaf, stem
ExtractDichloromethane
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test Done
Positive Control Used (conc.)Fusidic acid (4 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml8 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified(3β, 24R) - 24, 25 - Epoxycycloartan - 3 - Ol
PubChem ID   469545
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]8988597
Extract PreparationN/A
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Terpene, Triterpene, Cycloartane, Epoxy, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]Against Vero cells
Molecular Weight442.381
Molecular FormulaC30H50O2
SMILESO[C@H]1C([C@H]2[C@@]3([C@@]4(C3)[C@H]([C@]3([C@](CC4)([C@H](CC3)[C@@H](CC[C@H]3OC3(C)C)C)C)C)CC2)CC1)(C)C
XLogP10.590
PSA32.760
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count4
No. of Rings6
No. of N0
No. of O2
No. of S0
Reference(s)1) Cantrell CL, Lu T, Fronczek FR, Fischer NH, Adams LB, Franzblau SG.Antimycobacterial cycloartanes from Borrichia frutescens.J Nat Prod. 1996 Dec;59(12):1131-6

Curator

                  Record - 3 of 6   [TOP]
Compound ID1282
Compound Structure
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Plant SourceBorrichia frutescens L.     Common Name:Sea Daisy
Source FamilyAsteraceae (Compositae)
OriginUSA
Plant Part UsedFlower, leaf, stem
ExtractDichloromethane
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test Done
Positive Control Used (conc.)Fusidic acid (4 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml64 - 128 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified(23R)-3-Oxolanosta-8,24-dien-23-Ol
PubChem ID   469546
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]8988597
Extract PreparationN/A
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Steroid, Ketone, Prenylated
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]Against Vero cells
Molecular Weight440.365
Molecular FormulaC30H48O2
SMILESO=C1C([C@H]2[C@@](C3=C([C@]4([C@@]([C@H](CC4)[C@@H](C[C@@H](O)C=C(C)C)C)(CC3)C)C)CC2)(CC1)C)(C)C
XLogP7.784
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count4
No. of Rings4
No. of N0
No. of O2
No. of S0
Reference(s)1) Cantrell CL, Lu T, Fronczek FR, Fischer NH, Adams LB, Franzblau SG.Antimycobacterial cycloartanes from Borrichia frutescens.J Nat Prod. 1996 Dec;59(12):1131-6

Curator

                  Record - 4 of 6   [TOP]
Compound ID1283
Compound Structure
Plant SourceBorrichia frutescens L.     Common Name:Sea Daisy
Source FamilyAsteraceae (Compositae)
OriginUSA
Plant Part UsedFlower
ExtractDichloromethane
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test Done
Positive Control Used (conc.)Fusidic acid (4 µg/ml)
Inhibition [%]100 %
Activity [MIC] µg/ml100 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]8988597
Extract PreparationN/A
Chemical Classification [Active Compound]N/A
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Reference(s)1) Cantrell CL, Lu T, Fronczek FR, Fischer NH, Adams LB, Franzblau SG.Antimycobacterial cycloartanes from Borrichia frutescens.J Nat Prod. 1996 Dec;59(12):1131-6

Curator

                  Record - 5 of 6   [TOP]
Compound ID1284
Compound Structure
Plant SourceBorrichia frutescens L.     Common Name:Sea Daisy
Source FamilyAsteraceae (Compositae)
OriginUSA
Plant Part UsedFlower
ExtractDichloromethane
Target BacteriaMycobacterium avium
Assay / Test Done
Positive Control Used (conc.)Rifampin, Clarithromycin
Inhibition [%]99 %
Activity [MIC] µg/ml1000 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]23195767
Extract PreparationN/A
Chemical Classification [Active Compound]N/A
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Reference(s)1) C.L. Cantrell, N.H. Fischer, L. Urbatsch, M.S. McGuire, S.G. Franzblau.Antimycobacterial crude plant extracts from South, Central, and North America.Phytomedicine, Volume 5, Issue 2, April 1998, Pages 137–145

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                  Record - 6 of 6   [TOP]
Compound ID3359
Compound Structure
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Plant SourceBorrichia frutescens     Common Name:Sea Daisy
Source FamilyAsteraceae (Compositae)
OriginSoutheastern United States
Plant Part UsedFlower
Extract
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneRadiorespirometric Bioassay
Positive Control Used (conc.)Fusidic acid (4 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml8 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified(3-αH, 24R) - 24, 25 - Epoxycycloartan - 3 - Ol
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]8988597
Extract Preparation
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Steroid, Epoxide
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]Against Vero cells
Molecular Weight442.381
Molecular FormulaC30H50O2
SMILESC1C[C@H](C(C2[C@]31[C@]1(C(CC2)[C@]2([C@](CC1)([C@H](CC2)[C@@H](CC[C@@H]1C(C)(C)O1)C)C)C)C3)(C)C)O
XLogP10.590
PSA32.760
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count4
No. of Rings6
No. of N0
No. of O2
No. of S0
Reference(s)1) Cantrell CL, Lu T, Fronczek FR, Fischer NH, Adams LB, Franzblau SG.Antimycobacterial cycloartanes from Borrichia frutescens.J Nat Prod. 1996 Dec;59(12):1131-6

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