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                  Page - 1 of 1                  Record - 1 of 25   [TOP]
Compound ID1354
Compound Structure
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Plant SourceCanscora decussata Schult.     Common Name:Daakuni, Sankhaapushpi, Dandotpala (Sanskrit)
Source FamilyGentaniaceae
OriginIndia
Plant Part UsedMother tinture
ExtractEthanol
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneTube Dilution Test
Positive Control Used (conc.)Streptomycin sulphate (0.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml200 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedMangiferin
PubChem ID   5281647
Ethnomedicinal InformationTuberculosis, leprosy
PubMed ID [Source Literature]807707, 565403
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Phenol, Sugar
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight422.085
Molecular FormulaC19H18O11
SMILESO1[C@H]([C@H](O)[C@@H](O)[C@H](O)[C@H]1CO)c1c(O)c2c(oc3c(c2=O)cc(O)c(O)c3)cc1O
XLogP-2.646
PSA188.140
H-bond Donor8
H-bond Acceptor10
No. of Rotatable Bond Count2
No. of Rings4
No. of N0
No. of O11
No. of S0
Reference(s)1) Ghosal S, Chaudhuri RK.Chemical constituents of Gentianaceae XVI: antitubercular activity of xanthones of Canscora decussata Schult.J Pharm Sci. 1975 May;64(5):888-9

2) Ghosal S, Biswas K, Chaudhuri RK.Chemical constituents of Gentianaceae XXIV: Anti-Mycobacterium tuberculosis activity of naturally occurring xanthones and synthetic analogs.J Pharm Sci. 1978 May;67(5):721-2.

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                  Record - 2 of 25   [TOP]
Compound ID1355
Compound Structure
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Plant SourceCanscora decussata Schult.     Common Name:Daakuni, Sankhaapushpi, Dandotpala (Sanskrit)
Source FamilyGentaniaceae
OriginIndia
Plant Part UsedMother tinture
ExtractEthanol
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneTube Dilution Test
Positive Control Used (conc.)Streptomycin sulphate (0.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml10 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified1,3,5-Trihydroxyxanthone
PubChem ID   25200626
Ethnomedicinal InformationTuberculosis, leprosy
PubMed ID [Source Literature]807707, 565403
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight243.029
Molecular FormulaC13H7O5
SMILESO1c2c(c(=O)c3c1c([O-])ccc3)c(O)cc(O)c2
XLogP0.296
PSA80.590
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count0
No. of Rings3
No. of N0
No. of O5
No. of S0
Reference(s)1) Ghosal S, Chaudhuri RK.Chemical constituents of Gentianaceae XVI: antitubercular activity of xanthones of Canscora decussata Schult.J Pharm Sci. 1975 May;64(5):888-9

2) Ghosal S, Biswas K, Chaudhuri RK.Chemical constituents of Gentianaceae XXIV: Anti-Mycobacterium tuberculosis activity of naturally occurring xanthones and synthetic analogs.J Pharm Sci. 1978 May;67(5):721-2.

Curator

                  Record - 3 of 25   [TOP]
Compound ID1356
Compound Structure
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Plant SourceCanscora decussata Schult.     Common Name:Daakuni, Sankhaapushpi, Dandotpala (Sanskrit)
Source FamilyGentaniaceae
OriginIndia
Plant Part UsedMother tinture
ExtractEthanol
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneTube Dilution Test
Positive Control Used (conc.)Streptomycin sulphate (0.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml10 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified1, 3 - Dihydroxy - 5 - Methoxy - 9H - Xanthen - 9 - One
PubChem ID   12026489
Ethnomedicinal InformationTuberculosis, leprosy
PubMed ID [Source Literature]807707, 565403
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight258.053
Molecular FormulaC14H10O5
SMILESO1c2c(c(=O)c3c1cc(O)cc3O)cccc2OC
XLogP0.815
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) Ghosal S, Chaudhuri RK.Chemical constituents of Gentianaceae XVI: antitubercular activity of xanthones of Canscora decussata Schult.J Pharm Sci. 1975 May;64(5):888-9

2) Ghosal S, Biswas K, Chaudhuri RK.Chemical constituents of Gentianaceae XXIV: Anti-Mycobacterium tuberculosis activity of naturally occurring xanthones and synthetic analogs.J Pharm Sci. 1978 May;67(5):721-2.

Curator

                  Record - 4 of 25   [TOP]
Compound ID1357
Compound Structure
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Plant SourceCanscora decussata Schult.     Common Name:Daakuni, Sankhaapushpi, Dandotpala (Sanskrit)
Source FamilyGentaniaceae
OriginIndia
Plant Part UsedMother tinture
ExtractEthanol
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneTube Dilution Test
Positive Control Used (conc.)Streptomycin sulphate (0.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml10 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified1 - Hydroxy - 3, 5 - Dimethoxyxanthen - 9 - One
PubChem ID   5479773
Ethnomedicinal InformationTuberculosis, leprosy
PubMed ID [Source Literature]807707, 565403
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight272.068
Molecular FormulaC15H12O5
SMILESO1c2c(c(=O)c3c1c(OC)ccc3)c(O)cc(OC)c2
XLogP1.334
PSA55.760
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) Ghosal S, Chaudhuri RK.Chemical constituents of Gentianaceae XVI: antitubercular activity of xanthones of Canscora decussata Schult.J Pharm Sci. 1975 May;64(5):888-9

2) Ghosal S, Biswas K, Chaudhuri RK.Chemical constituents of Gentianaceae XXIV: Anti-Mycobacterium tuberculosis activity of naturally occurring xanthones and synthetic analogs.J Pharm Sci. 1978 May;67(5):721-2.

Curator

                  Record - 5 of 25   [TOP]
Compound ID1358
Compound Structure
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Plant SourceCanscora decussata Schult.     Common Name:Daakuni, Sankhaapushpi, Dandotpala (Sanskrit)
Source FamilyGentaniaceae
OriginIndia
Plant Part UsedMother tinture
ExtractEthanol
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneTube Dilution Test
Positive Control Used (conc.)Streptomycin sulphate (0.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml10 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified1, 3, 5, 6 - Tetrahydroxyxanthen - 9 - One
PubChem ID   5479774
Ethnomedicinal InformationTuberculosis, leprosy
PubMed ID [Source Literature]807707, 565403
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight260.032
Molecular FormulaC13H8O6
SMILESO1c2c(c(=O)c3c1cc(O)cc3O)ccc(O)c2O
XLogP-0.238
PSA97.990
H-bond Donor4
H-bond Acceptor5
No. of Rotatable Bond Count0
No. of Rings3
No. of N0
No. of O6
No. of S0
Reference(s)1) Ghosal S, Chaudhuri RK.Chemical constituents of Gentianaceae XVI: antitubercular activity of xanthones of Canscora decussata Schult.J Pharm Sci. 1975 May;64(5):888-9

2) Ghosal S, Biswas K, Chaudhuri RK.Chemical constituents of Gentianaceae XXIV: Anti-Mycobacterium tuberculosis activity of naturally occurring xanthones and synthetic analogs.J Pharm Sci. 1978 May;67(5):721-2

Curator

                  Record - 6 of 25   [TOP]
Compound ID1359
Compound Structure
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Plant SourceCanscora decussata Schult.     Common Name:Daakuni, Sankhaapushpi, Dandotpala (Sanskrit)
Source FamilyGentaniaceae
OriginIndia
Plant Part UsedMother tinture
ExtractEthanol
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneTube Dilution Test
Positive Control Used (conc.)Streptomycin sulphate (0.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml10 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified1, 3, 6 - Trihydroxy - 5 - Methoxyxanthen - 9 - One
PubChem ID   5493675
Ethnomedicinal InformationTuberculosis, leprosy
PubMed ID [Source Literature]807707, 565403
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight274.048
Molecular FormulaC14H10O6
SMILESO1c2c(c(=O)c3c1cc(O)cc3O)ccc(O)c2OC
XLogP-0.148
PSA86.990
H-bond Donor3
H-bond Acceptor5
No. of Rotatable Bond Count1
No. of Rings3
No. of N0
No. of O6
No. of S0
Reference(s)1) Ghosal S, Chaudhuri RK.Chemical constituents of Gentianaceae XVI: antitubercular activity of xanthones of Canscora decussata Schult.J Pharm Sci. 1975 May;64(5):888-9

2) Ghosal S, Biswas K, Chaudhuri RK.Chemical constituents of Gentianaceae XXIV: Anti-Mycobacterium tuberculosis activity of naturally occurring xanthones and synthetic analogs.J Pharm Sci. 1978 May;67(5):721-2

Curator

                  Record - 7 of 25   [TOP]
Compound ID1360
Compound Structure
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Plant SourceCanscora decussata Schult.     Common Name:Daakuni, Sankhaapushpi, Dandotpala (Sanskrit)
Source FamilyGentaniaceae
OriginIndia
Plant Part UsedMother tinture
ExtractEthanol
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneTube Dilution Test
Positive Control Used (conc.)Streptomycin sulphate (0.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml10 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified1, 3, 5 - Trihydroxy - 6 - Methoxyxanthen - 9 - One
PubChem ID   5479775
Ethnomedicinal InformationTuberculosis, leprosy
PubMed ID [Source Literature]807707, 565403
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight274.048
Molecular FormulaC14H10O6
SMILESO1c2c(c(=O)c3c1cc(O)cc3O)ccc(OC)c2O
XLogP-0.148
PSA86.990
H-bond Donor3
H-bond Acceptor5
No. of Rotatable Bond Count1
No. of Rings3
No. of N0
No. of O6
No. of S0
Reference(s)1) Ghosal S, Chaudhuri RK.Chemical constituents of Gentianaceae XVI: antitubercular activity of xanthones of Canscora decussata Schult.J Pharm Sci. 1975 May;64(5):888-9

2) Ghosal S, Biswas K, Chaudhuri RK.Chemical constituents of Gentianaceae XXIV: Anti-Mycobacterium tuberculosis activity of naturally occurring xanthones and synthetic analogs.J Pharm Sci. 1978 May;67(5):721-2

Curator

                  Record - 8 of 25   [TOP]
Compound ID1361
Compound Structure
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Plant SourceCanscora decussata Schult.     Common Name:Daakuni, Sankhaapushpi, Dandotpala (Sanskrit)
Source FamilyGentaniaceae
OriginIndia
Plant Part UsedMother tinture
ExtractEthanol
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneTube Dilution Test
Positive Control Used (conc.)Streptomycin sulphate (0.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml10 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified3, 5 - Dimethoxy - 1, 6 - Dihydroxyxanthone
PubChem ID   5281630
Ethnomedicinal InformationTuberculosis, leprosy
PubMed ID [Source Literature]807707, 565403
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight288.063
Molecular FormulaC15H12O6
SMILESO1c2c(c(=O)c3c1cc(OC)cc3O)ccc(O)c2OC
XLogP0.371
PSA75.990
H-bond Donor2
H-bond Acceptor5
No. of Rotatable Bond Count2
No. of Rings3
No. of N0
No. of O6
No. of S0
Reference(s)1) Ghosal S, Chaudhuri RK.Chemical constituents of Gentianaceae XVI: antitubercular activity of xanthones of Canscora decussata Schult.J Pharm Sci. 1975 May;64(5):888-9

2) Ghosal S, Biswas K, Chaudhuri RK.Chemical constituents of Gentianaceae XXIV: Anti-Mycobacterium tuberculosis activity of naturally occurring xanthones and synthetic analogs.J Pharm Sci. 1978 May;67(5):721-2

Curator

                  Record - 9 of 25   [TOP]
Compound ID1362
Compound Structure
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Plant SourceCanscora decussata Schult.     Common Name:Daakuni, Sankhaapushpi, Dandotpala (Sanskrit)
Source FamilyGentaniaceae
OriginIndia
Plant Part UsedMother tinture
ExtractEthanol
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneTube Dilution Test
Positive Control Used (conc.)Streptomycin sulphate (0.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml10 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified1, 3, 5, 6, 7 - Pentahydroxyxanthen - 9 - One
PubChem ID   10333643
Ethnomedicinal InformationTuberculosis, leprosy
PubMed ID [Source Literature]807707, 565403
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight276.027
Molecular FormulaC13H8O7
SMILESO1c2c(c(=O)c3c1cc(O)cc3O)cc(O)c(O)c2O
XLogP-0.772
PSA118.220
H-bond Donor5
H-bond Acceptor6
No. of Rotatable Bond Count0
No. of Rings3
No. of N0
No. of O7
No. of S0
Reference(s)1) Ghosal S, Chaudhuri RK.Chemical constituents of Gentianaceae XVI: antitubercular activity of xanthones of Canscora decussata Schult.J Pharm Sci. 1975 May;64(5):888-9

2) Ghosal S, Biswas K, Chaudhuri RK.Chemical constituents of Gentianaceae XXIV: Anti-Mycobacterium tuberculosis activity of naturally occurring xanthones and synthetic analogs.J Pharm Sci. 1978 May;67(5):721-2

Curator

                  Record - 10 of 25   [TOP]
Compound ID1363
Compound Structure
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Plant SourceCanscora decussata Schult.     Common Name:Daakuni, Sankhaapushpi, Dandotpala (Sanskrit)
Source FamilyGentaniaceae
OriginIndia
Plant Part UsedMother tinture
ExtractEthanol
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneTube Dilution Test
Positive Control Used (conc.)Streptomycin sulphate (0.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml10 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified1, 6, 7 - Trihydroxy - 3, 5 - Dimethoxyxanthen - 9 - One
PubChem ID   5479777
Ethnomedicinal InformationTuberculosis, leprosy
PubMed ID [Source Literature]807707, 565403
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight304.058
Molecular FormulaC15H12O7
SMILESO1c2c(c(=O)c3c1cc(OC)cc3O)cc(O)c(O)c2OC
XLogP-0.163
PSA96.220
H-bond Donor3
H-bond Acceptor6
No. of Rotatable Bond Count2
No. of Rings3
No. of N0
No. of O7
No. of S0
Reference(s)1) Ghosal S, Chaudhuri RK.Chemical constituents of Gentianaceae XVI: antitubercular activity of xanthones of Canscora decussata Schult.J Pharm Sci. 1975 May;64(5):888-9

2) Ghosal S, Biswas K, Chaudhuri RK.Chemical constituents of Gentianaceae XXIV: Anti-Mycobacterium tuberculosis activity of naturally occurring xanthones and synthetic analogs.J Pharm Sci. 1978 May;67(5):721-2

Curator

                  Record - 11 of 25   [TOP]
Compound ID1364
Compound Structure
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Plant SourceCanscora decussata Schult.     Common Name:Daakuni, Sankhaapushpi, Dandotpala (Sanskrit)
Source FamilyGentaniaceae
OriginIndia
Plant Part UsedMother tinture
ExtractEthanol
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneTube Dilution Test
Positive Control Used (conc.)Streptomycin sulphate (0.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml10 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified1, 7 - Dihydroxy - 3, 5, 6 - Trimethoxyxanthen - 9 - One
PubChem ID   5491588
Ethnomedicinal InformationTuberculosis, leprosy
PubMed ID [Source Literature]807707, 565403
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight318.074
Molecular FormulaC16H14O7
SMILESO1c2c(c(=O)c3c1cc(OC)cc3O)cc(O)c(OC)c2OC
XLogP-0.073
PSA85.220
H-bond Donor2
H-bond Acceptor6
No. of Rotatable Bond Count3
No. of Rings3
No. of N0
No. of O7
No. of S0
Reference(s)1) Ghosal S, Chaudhuri RK.Chemical constituents of Gentianaceae XVI: antitubercular activity of xanthones of Canscora decussata Schult.J Pharm Sci. 1975 May;64(5):888-9

2) Ghosal S, Biswas K, Chaudhuri RK.Chemical constituents of Gentianaceae XXIV: Anti-Mycobacterium tuberculosis activity of naturally occurring xanthones and synthetic analogs.J Pharm Sci. 1978 May;67(5):721-2

Curator

                  Record - 12 of 25   [TOP]
Compound ID1798
Compound Structure
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Plant SourceGarcinia mangostana     Common Name:Mangosteen
Source FamilyClusiaceae
OriginThailand, Malaysia
Plant Part UsedFruit
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampicin (0.003 - 0.0047 µg/ml), Isoniazid (0.025 - 0.05 µg/ml), Kanamycin sulfate (1.25 - 2.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml6.25 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedGarcinone B
PubChem ID   5495928
Ethnomedicinal InformationTreatment of diarrhea and dysentery and for skin diseases, to lower fever and for urinary disorders
PubMed ID [Source Literature]12843596
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tetracyclic, Xanthonoid, Benzopyran, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight394.142
Molecular FormulaC23H22O6
SMILESO1C(C=Cc2c3c(oc4c(c3=O)c(O)c(c(O)c4)CC=C(C)C)cc(O)c12)(C)C
XLogP2.203
PSA86.990
H-bond Donor3
H-bond Acceptor5
No. of Rotatable Bond Count2
No. of Rings4
No. of N0
No. of O6
No. of S0
Reference(s)1) Suksamrarn S, Suwannapoch N, Phakhodee W, Thanuhiranlert J, Ratananukul P, Chimnoi N, Suksamrarn A.Antimycobacterial activity of prenylated xanthones from the fruits of Garcinia mangostana.Chem Pharm Bull (Tokyo). 2003 Jul;51(7):857-9

2) http://www.montosogardens.com/garcinia_mangostana.htm

Curator

                  Record - 13 of 25   [TOP]
Compound ID1796
Compound Structure
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Plant SourceGarcinia mangostana     Common Name:Mangosteen
Source FamilyClusiaceae
OriginThailand, Malaysia
Plant Part UsedFruit
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampicin (0.003 - 0.0047 µg/ml), Isoniazid (0.025 - 0.05 µg/ml), Kanamycin sulfate (1.25 - 2.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml25 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedGarcinone D
PubChem ID   5495926
Ethnomedicinal InformationTreatment of diarrhea and dysentery and for skin diseases, to lower fever and for urinary disorders
PubMed ID [Source Literature]12843596
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Prenylated, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight428.184
Molecular FormulaC24H28O7
SMILESOC(CCc1c2c(oc3c(c2=O)c(O)c(c(O)c3)CC=C(C)C)cc(O)c1OC)(C)C
XLogP1.895
PSA107.220
H-bond Donor4
H-bond Acceptor6
No. of Rotatable Bond Count6
No. of Rings3
No. of N0
No. of O7
No. of S0
Reference(s)1) Suksamrarn S, Suwannapoch N, Phakhodee W, Thanuhiranlert J, Ratananukul P, Chimnoi N, Suksamrarn A.Antimycobacterial activity of prenylated xanthones from the fruits of Garcinia mangostana.Chem Pharm Bull (Tokyo). 2003 Jul;51(7):857-9

2) http://www.montosogardens.com/garcinia_mangostana.htm

Curator

                  Record - 14 of 25   [TOP]
Compound ID3573
Compound Structure
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Plant SourceGarcinia mangostana     Common Name:Mangosteen
Source FamilyClusiaceae
OriginSoutheast Asian countries (Thailand, Malaysia)
Plant Part UsedFruit hull, fresh aril, seed
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampin (0.003 - 0.0047 µg/ml), Isoniazid (0.025 - 0.05 µg/ml), Kanamycin sulphate (1.25 - 2.5 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml6.25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)
Active Compound Identifiedα - Mangostin
PubChem ID   5281650
Ethnomedicinal InformationSkin infections, wounds and diarrhea, to lower fever and for urinary disorders
PubMed ID [Source Literature]12843596
Extract Preparation MeOH extract were obtained from the fresh green fruit hulls of Garcinia mangostana. Pulverized, fresh arils and seeds were extracted throroughly with MeOH and evaporation of the solvent gave crude extract. The crude extract was partitioned between CHCl3 and H2O to afford CHCl3 extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Prenylated, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]7H9GC medium
Cytotoxicity Assay [AID]NR
Molecular Weight410.173
Molecular FormulaC24H26O6
SMILESO1c2c(c(CC=C(C)C)c(OC)c(O)c2)c(=O)c2c1cc(O)c(c2O)CC=C(C)C
XLogP2.792
PSA86.990
H-bond Donor3
H-bond Acceptor5
No. of Rotatable Bond Count5
No. of Rings3
No. of N0
No. of O6
No. of S0
Reference(s)1) Suksamrarn S, Suwannapoch N, Phakhodee W, Thanuhiranlert J, Ratananukul P, Chimnoi N, Suksamrarn A.Antimycobacterial activity of prenylated xanthones from the fruits of Garcinia mangostana.Chem Pharm Bull (Tokyo). 2003 Jul;51(7):857-9

2) http://www.montosogardens.com/garcinia_mangostana.htm

CuratorGppreetha, vikramjitmandal, reshmi

                  Record - 15 of 25   [TOP]
Compound ID3575
Compound Structure
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Plant SourceGarcinia mangostana L.     Common Name:Mangosteen
Source FamilyClusiaceae
OriginSoutheast Asia
Plant Part UsedFruit hull
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampin (0.003 - 0.0047 µg/ml), Isoniazid (0.025 - 0.05 µg/ml), Kanamycin sulphate (1.25 - 2.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedDemethylcalabaxanthone
PubChem ID   509270
Ethnomedicinal InformationSkin infections, wounds and diarrhea
PubMed ID [Source Literature]12843596
Extract PreparationMeOH extract were obtained from the fresh green fruit hulls of Garcinia mangostana. Pulverized, fresh arils and seeds were extracted throroughly with MeOH and evaporation of the solvent gave crude extract. The crude extract was partitioned between CHCl3 and H2O to afford CHCl3 extract
Chemical Classification [Active Compound]Aromatic, Tetracyclic, Xanthonoid, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]NR
Molecular Weight378.147
Molecular FormulaC23H22O5
SMILESO1C(C=Cc2c1cc1oc3c(c(=O)c1c2O)c(CC=C(C)C)c(O)cc3)(C)C
XLogP3.163
PSA66.760
H-bond Donor2
H-bond Acceptor4
No. of Rotatable Bond Count2
No. of Rings4
No. of N0
No. of O5
No. of S0
Reference(s)1) Suksamrarn S, Suwannapoch N, Phakhodee W, Thanuhiranlert J, Ratananukul P, Chimnoi N, Suksamrarn A.Antimycobacterial activity of prenylated xanthones from the fruits of Garcinia mangostana.Chem Pharm Bull (Tokyo). 2003 Jul;51(7):857-9

2) http://www.montosogardens.com/garcinia_mangostana.htm

CuratorGppreetha, vikramjitmandal, reshmi

                  Record - 16 of 25   [TOP]
Compound ID3577
Compound Structure
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Plant SourceGarcinia mangostana L.     Common Name:Mangosteen
Source FamilyClusiaceae
OriginSoutheast Asia
Plant Part UsedFruit hull
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampin (0.003 - 0.0047 µg/ml), Isoniazid (0.025 - 0.05 µg/ml), Kanamycin sulphate (1.25 - 2.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedTrapezifolixanthone
PubChem ID   188341
Ethnomedicinal InformationSkin infections, wounds and diarrhea
PubMed ID [Source Literature]12843596
Extract PreparationMeOH extract were obtained from the fresh green fruit hulls of Garcinia mangostana. Pulverized, fresh arils and seeds were extracted throroughly with MeOH and evaporation of the solvent gave crude extract. The crude extract was partitioned between CHCl3 and H2O to afford CHCl3 extract
Chemical Classification [Active Compound]Aromatic, Tetracyclic, Xanthonoid, Benzopyran, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]NR
Molecular Weight378.147
Molecular FormulaC23H22O5
SMILESO1C(C=Cc2c1c(c1oc3c(c(=O)c1c2O)cccc3O)CC=C(C)C)(C)C
XLogP3.166
PSA66.760
H-bond Donor2
H-bond Acceptor4
No. of Rotatable Bond Count2
No. of Rings4
No. of N0
No. of O5
No. of S0
Reference(s)1) Suksamrarn S, Suwannapoch N, Phakhodee W, Thanuhiranlert J, Ratananukul P, Chimnoi N, Suksamrarn A.Antimycobacterial activity of prenylated xanthones from the fruits of Garcinia mangostana.Chem Pharm Bull (Tokyo). 2003 Jul;51(7):857-9

2) http://www.montosogardens.com/garcinia_mangostana.htm

CuratorGppreetha, vikramjitmandal, reshmi

                  Record - 17 of 25   [TOP]
Compound ID3578
Compound Structure
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Plant SourceGarcinia mangostana L.     Common Name:Mangosteen
Source FamilyClusiaceae
OriginSoutheast Asia
Plant Part UsedFruit hull
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampin (0.003 - 0.0047 µg/ml), Isoniazid (0.025 - 0.05 µg/ml), Kanamycin sulphate (1.25 - 2.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml6.25 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identifiedβ - mangostin
PubChem IDNR
Ethnomedicinal InformationSkin infections, wounds and diarrhea
PubMed ID [Source Literature]12843596
Extract PreparationMeOH extract were obtained from the fresh green fruit hulls of Garcinia mangostana. Pulverized, fresh arils and seeds were extracted throroughly with MeOH and evaporation of the solvent gave crude extract. The crude extract was partitioned between CHCl3 and H2O to afford CHCl3 extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Prenylated, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]NR
Molecular Weight424.189
Molecular FormulaC25H28O6
SMILESO1c2c(c(CC=C(C)C)c(c(O)c2)OC)c(=O)c2c1cc(c(c2O)CC=C(C)C)OC
XLogP3.311
PSA75.990
H-bond Donor2
H-bond Acceptor5
No. of Rotatable Bond Count6
No. of Rings3
No. of N0
No. of O6
No. of S0
Reference(s)1) Suksamrarn S, Suwannapoch N, Phakhodee W, Thanuhiranlert J, Ratananukul P, Chimnoi N, Suksamrarn A.Antimycobacterial activity of prenylated xanthones from the fruits of Garcinia mangostana.Chem Pharm Bull (Tokyo). 2003 Jul;51(7):857-9

2) http://www.montosogardens.com/garcinia_mangostana.htm

CuratorGppreetha, vikramjitmandal, reshmi

                  Record - 18 of 25   [TOP]
Compound ID3579
Compound Structure
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Plant SourceGarcinia mangostana L.     Common Name:Mangosteen
Source FamilyClusiaceae
OriginSoutheast Asia
Plant Part UsedFruit hull
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampin (0.003 - 0.0047 µg/ml), Isoniazid (0.025 - 0.05 µg/ml), Kanamycin sulphate (1.25 - 2.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml25 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identifiedγ - Mangostin
PubChem ID   5464078
Ethnomedicinal InformationSkin infections, wounds and diarrhea
PubMed ID [Source Literature]12843596
Extract PreparationMeOH extract were obtained from the fresh green fruit hulls of Garcinia mangostana. Pulverized, fresh arils and seeds were extracted throroughly with MeOH and evaporation of the solvent gave crude extract. The crude extract was partitioned between CHCl3 and H2O to afford CHCl3 extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]NR
Molecular Weight396.157
Molecular FormulaC23H24O6
SMILESO1c2c(c(CC=C(C)C)c(O)c(O)c2)c(=O)c2c1cc(O)c(c2O)CC=C(C)C
XLogP2.702
PSA97.990
H-bond Donor4
H-bond Acceptor5
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O6
No. of S0
Reference(s)1) Suksamrarn S, Suwannapoch N, Phakhodee W, Thanuhiranlert J, Ratananukul P, Chimnoi N, Suksamrarn A.Antimycobacterial activity of prenylated xanthones from the fruits of Garcinia mangostana.Chem Pharm Bull (Tokyo). 2003 Jul;51(7):857-9

2) http://www.montosogardens.com/garcinia_mangostana.htm

CuratorGppreetha, vikramjitmandal, reshmi

                  Record - 19 of 25   [TOP]
Compound ID3581
Compound Structure
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Plant SourceGarcinia mangostana L.     Common Name:Mangosteen
Source FamilyClusiaceae
OriginSoutheast Asia
Plant Part UsedFruit hull
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampin (0.003 - 0.0047 µg/ml), Isoniazid (0.025 - 0.05 µg/ml), Kanamycin sulphate (1.25 - 2.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml100 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedMangostenol
PubChem IDNR
Ethnomedicinal InformationSkin infections, wounds and diarrhea
PubMed ID [Source Literature]12843596
Extract PreparationMeOH extract were obtained from the fresh green fruit hulls of Garcinia mangostana. Pulverized, fresh arils and seeds were extracted throroughly with MeOH and evaporation of the solvent gave crude extract. The crude extract was partitioned between CHCl3 and H2O to afford CHCl3 extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Ether, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]NR
Molecular Weight426.168
Molecular FormulaC24H26O7
SMILESO1c2c(c(O)c(c(c2)O)CC(C(=C)C)O)c(=O)c2c1cc(O)c(c2CC=C(C)C)OC
XLogP1.226
PSA107.220
H-bond Donor4
H-bond Acceptor6
No. of Rotatable Bond Count6
No. of Rings3
No. of N0
No. of O7
No. of S0
Reference(s)1) Suksamrarn S, Suwannapoch N, Phakhodee W, Thanuhiranlert J, Ratananukul P, Chimnoi N, Suksamrarn A.Antimycobacterial activity of prenylated xanthones from the fruits of Garcinia mangostana.Chem Pharm Bull (Tokyo). 2003 Jul;51(7):857-9

2) http://www.montosogardens.com/garcinia_mangostana.htm

CuratorGppreetha, vikramjitmandal, reshmi

                  Record - 20 of 25   [TOP]
Compound ID3585
Compound Structure
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Plant SourceGarcinia mangostana L.     Common Name:Mangosteen
Source FamilyClusiaceae
OriginSoutheast Asia
Plant Part UsedFruit hull
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampin (0.003 - 0.0047 µg/ml), Isoniazid (0.025 - 0.05 µg/ml), Kanamycin sulphate (1.25 - 2.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml25 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedMangostenone A
PubChem ID   509267
Ethnomedicinal InformationSkin infections, wounds and diarrhea
PubMed ID [Source Literature]12843596
Extract PreparationMeOH extract were obtained from the fresh green fruit hulls of Garcinia mangostana. Pulverized, fresh arils and seeds were extracted throroughly with MeOH and evaporation of the solvent gave crude extract. The crude extract was partitioned between CHCl3 and H2O to afford CHCl3 extract
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Xanthonoid, Benzopyran, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]NR
Molecular Weight460.189
Molecular FormulaC28H28O6
SMILESO1C(C=Cc2c3oc4c(c(=O)c3c(c(O)c12)CC=C(C)C)c(O)c1c(OC(C=C1)(C)C)c4)(C)C
XLogP3.603
PSA75.990
H-bond Donor2
H-bond Acceptor5
No. of Rotatable Bond Count2
No. of Rings5
No. of N0
No. of O6
No. of S0
Reference(s)1) Suksamrarn S, Suwannapoch N, Phakhodee W, Thanuhiranlert J, Ratananukul P, Chimnoi N, Suksamrarn A.Antimycobacterial activity of prenylated xanthones from the fruits of Garcinia mangostana.Chem Pharm Bull (Tokyo). 2003 Jul;51(7):857-9

2) http://www.montosogardens.com/garcinia_mangostana.htm

CuratorGppreetha, vikramjitmandal, reshmi

                  Record - 21 of 25   [TOP]
Compound ID3586
Compound Structure
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Plant SourceGarcinia mangostana L.     Common Name:Mangosteen
Source FamilyClusiaceae
OriginSoutheast Asia
Plant Part UsedFruit hull
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampin (0.003 - 0.0047 µg/ml), Isoniazid (0.025 - 0.05 µg/ml), Kanamycin sulphate (1.25 - 2.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml25 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedTovophyllin B
PubChem ID   509268
Ethnomedicinal InformationSkin infections, wounds and diarrhea
PubMed ID [Source Literature]12843596
Extract PreparationMeOH extract were obtained from the fresh green fruit hulls of Garcinia mangostana. Pulverized, fresh arils and seeds were extracted throroughly with MeOH and evaporation of the solvent gave crude extract. The crude extract was partitioned between CHCl3 and H2O to afford CHCl3 extract
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Xanthonoid, Benzopyran, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]NR
Molecular Weight460.189
Molecular FormulaC28H28O6
SMILESO1C(C=Cc2c3c(oc4c(c3=O)c(O)c3c(OC(C=C3)(C)C)c4)c(c(O)c12)CC=C(C)C)(C)C
XLogP3.603
PSA75.990
H-bond Donor2
H-bond Acceptor5
No. of Rotatable Bond Count2
No. of Rings5
No. of N0
No. of O6
No. of S0
Reference(s)1) Suksamrarn S, Suwannapoch N, Phakhodee W, Thanuhiranlert J, Ratananukul P, Chimnoi N, Suksamrarn A.Antimycobacterial activity of prenylated xanthones from the fruits of Garcinia mangostana.Chem Pharm Bull (Tokyo). 2003 Jul;51(7):857-9

2) http://www.montosogardens.com/garcinia_mangostana.htm

CuratorGppreetha, vikramjitmandal, reshmi

                  Record - 22 of 25   [TOP]
Compound ID3587
Compound Structure
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Plant SourceGarcinia mangostana L.     Common Name:Mangosteen
Source FamilyClusiaceae
OriginSoutheast Asia
Plant Part UsedFruit hull
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampin (0.003 - 0.0047 µg/ml), Isoniazid (0.025 - 0.05 µg/ml), Kanamycin sulphate (1.25 - 2.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml200 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedMangostanol
PubChem ID   10048103
Ethnomedicinal InformationSkin infections, wounds and diarrhea
PubMed ID [Source Literature]12843596
Extract PreparationMeOH extract were obtained from the fresh green fruit hulls of Garcinia mangostana. Pulverized, fresh arils and seeds were extracted throroughly with MeOH and evaporation of the solvent gave crude extract. The crude extract was partitioned between CHCl3 and H2O to afford CHCl3 extract
Chemical Classification [Active Compound]Aromatic, Tetracyclic, Xanthonoid, Benzopyran, Prenylated, Phenol, Ether
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]NR
Molecular Weight426.168
Molecular FormulaC24H26O7
SMILESO1C(C(O)Cc2c1cc1oc3c(c(=O)c1c2O)c(CC=C(C)C)c(OC)c(O)c3)(C)C
XLogP1.883
PSA96.220
H-bond Donor3
H-bond Acceptor6
No. of Rotatable Bond Count3
No. of Rings4
No. of N0
No. of O7
No. of S0
Reference(s)1) Suksamrarn S, Suwannapoch N, Phakhodee W, Thanuhiranlert J, Ratananukul P, Chimnoi N, Suksamrarn A.Antimycobacterial activity of prenylated xanthones from the fruits of Garcinia mangostana.Chem Pharm Bull (Tokyo). 2003 Jul;51(7):857-9

2) http://www.montosogardens.com/garcinia_mangostana.htm

CuratorGppreetha, vikramjitmandal, reshmi

                  Record - 23 of 25   [TOP]
Compound ID3758
Compound Structure
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Plant SourceArtcarpus rigidus BLUME subsp. rigidus     Common Name:NR
Source FamilyMoraceae
OriginNR
Plant Part UsedNR
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)NR
Inhibition [%]NR
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedArtoindonesianin C
PubChem ID   10552003
Ethnomedicinal InformationNR
PubMed ID [Source Literature]17015984
Extract PreparationThe dried root bark (1.5 kg) was milled and extracted successively with n - hexane, CHCl3 and MeOH in a Soxhlet extraction apparatus. The extracts were evaporated to dryness under reduced pressure at about 40°C. The hexane extract (brownish syrup, 8.4 g), the CHCl3 extract (dark brownish sticky solid, 16.1 g) and the methanolic extract (dark brownish mass, 45.6 g) were obtained, respectively
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Xanthonoid, Benzopyran, Phenol, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]Against human epidermoid carcinoma in the mouth (KB), human breast cancer cells (BC), human lung cancer cells (NCI - H187)
Molecular Weight462.131
Molecular FormulaC26H22O8
SMILESO1c2c3c(C(O)(CC3=O)C(=O)OC)c(cc2c(=O)c2c1c1c(OC(C=C1)(C)C)cc2O)C(=C)C
XLogP1.501
PSA110.130
H-bond Donor2
H-bond Acceptor7
No. of Rotatable Bond Count3
No. of Rings5
No. of N0
No. of O8
No. of S0
Reference(s)1) Namdaung U, Aroonrerk N, Suksamrarn S, Danwisetkanjana K, Saenboonrueng J, Arjchomphu W, Suksamrarn A.Bioactive constituents of the root bark of Artocarpus rigidus subsp. rigidus.Chem Pharm Bull (Tokyo). 2006 Oct;54(10):1433-6

CuratorReshmi, vikramjitmandal, rachanake

                  Record - 24 of 25   [TOP]
Compound ID1805
Compound Structure
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Plant SourceGarcinia mangostana     Common Name:Mangosteen
Source FamilyClusiaceae
OriginThailand, Malaysia
Plant Part UsedFruit
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampicin (0.003 - 0.0047 µg/ml), Isoniazid (0.025 - 0.05 µg/ml), Kanamycin sulfate (1.25 - 2.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml200 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedMangostinone
PubChem ID   6478778
Ethnomedicinal InformationTreatment of diarrhea and dysentery and for skin diseases, lower fever and for urinary disorders
PubMed ID [Source Literature]12843596
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Prenylated, Phenol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight380.162
Molecular FormulaC23H24O5
SMILESO1c2c(c(O)c(C/C=C(/CCC=C(C)C)C)c(O)c2)c(=O)c2c1c(O)ccc2
XLogP3.588
PSA77.760
H-bond Donor3
H-bond Acceptor4
No. of Rotatable Bond Count5
No. of Rings3
No. of N0
No. of O5
No. of S0
Reference(s)1) Suksamrarn S, Suwannapoch N, Phakhodee W, Thanuhiranlert J, Ratananukul P, Chimnoi N, Suksamrarn A.Antimycobacterial activity of prenylated xanthones from the fruits of Garcinia mangostana.Chem Pharm Bull (Tokyo). 2003 Jul;51(7):857-9

2) http://www.montosogardens.com/garcinia_mangostana.htm

Curator

                  Record - 25 of 25   [TOP]
Compound ID4074
Compound Structure
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Plant SourceGarcinia mangosta     Common Name:
Source FamilyGuttiferae
Origin
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml15.24 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identifiedα-Mangostin
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Tricyclic, Xanthonoid, Prenylated, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight408.194
Molecular FormulaC25H28O5
SMILESCC(=CCc1c(O)c2c(cc1O)Cc1cc(O)c(OC)c(CC=C(C)C)c1C2=O)C
XLogP3.755
PSA86.990
H-bond Donor3
H-bond Acceptor5
No. of Rotatable Bond Count5
No. of Rings3
No. of N0
No. of O5
No. of S0
Reference(s)1) In silico Comparison of Antimycobacterial Natural Products with Known Antituberculosis Drugs. Marlene Espinoza-Moraga, Nicholas M. Njuguna, Grace Mugumbate, Julio Caballero, and Kelly Chibale. Journal of Chemical Information and Modeling 2013 53 (3), 649-660

2) García, A., Bocanegra-García, V., Palma-Nicolás, J. P., Rivera, G. Vennerstrom, J. L. Recent Advances in Antitubercular Natural Products. Eur. J. Med. Chem. 2012, 49, 1-23

Curator


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