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                  Page - 1 of 1                  Record - 1 of 20   [TOP]
Compound ID2949
Compound Structure
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Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 Identified1'-Hydroxytetracosanyl cyclohexane
PubChem ID   49797775
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alkanol, Alicyclic
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight408.433
Molecular FormulaC28H56O
SMILESOCCCCCCCCCCCCCCCCCCCCCCC1CCCCC1
XLogP14.106
PSA20.230
H-bond Donor1
H-bond Acceptor1
No. of Rotatable Bond Count22
No. of Rings1
No. of N0
No. of O1
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 2 of 20   [TOP]
Compound ID2950
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 Identified1'-Hydroxydocasanyl cyclohexane
PubChem ID   49797776
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alkanol, Alicyclic
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight380.402
Molecular FormulaC26H52O
SMILESOCCCCCCCCCCCCCCCCCCCCC1CCCCC1
XLogP12.968
PSA20.230
H-bond Donor1
H-bond Acceptor1
No. of Rotatable Bond Count20
No. of Rings1
No. of N0
No. of O1
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 3 of 20   [TOP]
Compound ID2951
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 Identified24-Ethyl cholesta-3,5-diene
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Steroid, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight426.386
Molecular FormulaC30H50O
SMILESC1=CC(CC2=C1C1C(C3(C(CC1)CCC3C(C)CCCCCCCCCC)C)CC2)O
XLogP12.044
PSA20.230
H-bond Donor1
H-bond Acceptor1
No. of Rotatable Bond Count10
No. of Rings4
No. of N0
No. of O1
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 4 of 20   [TOP]
Compound ID2952
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 Identified24-Nor-12-ursene
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight382.360
Molecular FormulaC28H46
SMILESC1CCC(C2[C@]1(C1[C@@](CC2)(C2C(=CC1)C1[C@@](CC2)(CCC([C@@H]1C)C)C)C)C)C
XLogP12.937
PSA0.000
H-bond Donor0
H-bond Acceptor0
No. of Rotatable Bond Count0
No. of Rings5
No. of N0
No. of O0
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 5 of 20   [TOP]
Compound ID2953
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 Identified24-Hydroxy-4-octacosanone
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Aliphatic, Ketone, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight424.428
Molecular FormulaC28H56O2
SMILESCCCC(=O)CCCCCCCCCCCCCCCCCCCC(CCCC)O
XLogP11.693
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count25
No. of Rings0
No. of N0
No. of O2
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 6 of 20   [TOP]
Compound ID2954
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 IdentifiedLupeol
PubChem ID   44586882
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight426.386
Molecular FormulaC30H50O
SMILESO[C@@H]1C([C@H]2[C@@]([C@@H]3[C@]([C@]4(C([C@@H]5[C@@](CC4)(CC[C@H]5C(=C)C)C)CC3)C)(CC2)C)(CC1)C)(C)C
XLogP11.901
PSA20.230
H-bond Donor1
H-bond Acceptor1
No. of Rotatable Bond Count1
No. of Rings5
No. of N0
No. of O1
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 7 of 20   [TOP]
Compound ID2955
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 IdentifiedLupeol acetate
PubChem ID   92157
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, O-Acetyl
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight468.397
Molecular FormulaC32H52O2
SMILESO([C@@H]1C([C@H]2[C@@]([C@@H]3[C@]([C@]4([C@@H]([C@@H]5[C@@](CC4)(CC[C@H]5C(=C)C)C)CC3)C)(CC2)C)(CC1)C)(C)C)C(=O)C
XLogP12.641
PSA26.300
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count3
No. of Rings5
No. of N0
No. of O2
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 8 of 20   [TOP]
Compound ID2956
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 Identifiedβ-Amyrin
PubChem ID   73145
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene. Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight426.386
Molecular FormulaC30H50O
SMILESO[C@@H]1C([C@H]2[C@@]([C@@H]3[C@]([C@]4(C(=CC3)[C@H]3[C@@](CC4)(CCC(C3)(C)C)C)C)(CC2)C)(CC1)C)(C)C
XLogP11.546
PSA20.230
H-bond Donor1
H-bond Acceptor1
No. of Rotatable Bond Count0
No. of Rings5
No. of N0
No. of O1
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 9 of 20   [TOP]
Compound ID2957
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 Identifiedβ-Amyrin acetate
PubChem ID   5318302
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, O-Acetyl
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight468.397
Molecular FormulaC32H52O2
SMILESO([C@@H]1C(C2[C@@](C3[C@](C4(C(=CC3)C3[C@@](CC4)(CCC(C3)(C)C)C)C)(CC2)C)(CC1)C)(C)C)C(=O)C
XLogP12.286
PSA26.300
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count2
No. of Rings5
No. of N0
No. of O2
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 10 of 20   [TOP]
Compound ID2958
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 Identified7,8-Dimthoxy-6-hydroxy cumarine
PubChem ID   11345068
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Aromatic, Bicyclic, Coumarin, Phenol, Ether
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight222.053
Molecular FormulaC11H10O5
SMILESO1c2c(cc(O)c(OC)c2OC)ccc1=O
XLogP1.168
PSA55.760
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count2
No. of Rings2
No. of N0
No. of O5
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 11 of 20   [TOP]
Compound ID2959
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 IdentifiedUrsolic acid
PubChem ID   64945
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, Acid, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight456.360
Molecular FormulaC30H48O3
SMILESO[C@@H]1C([C@H]2[C@@]([C@@H]3[C@]([C@]4(C(=CC3)[C@H]3[C@@](CC4)(CC[C@H]([C@@H]3C)C)C(=O)O)C)(CC2)C)(CC1)C)(C)C
XLogP8.954
PSA57.530
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count1
No. of Rings5
No. of N0
No. of O3
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 12 of 20   [TOP]
Compound ID2960
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 IdentifiedOlean-12(13) en-3β-hexadecanoate
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, Ester
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight692.647
Molecular FormulaC48H84O2
SMILESC1C[C@@H](C([C@]2([C@]1([C@H]1[C@@](CC2)([C@]2(C(=CC1)[C@]1([C@@](CC2)(CCC(C1)(C)C)C)C)C)C)C)C)(C)C)OC(=O)CCCCCCCCCCCCCCC
XLogP20.954
PSA26.300
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count16
No. of Rings5
No. of N0
No. of O2
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 13 of 20   [TOP]
Compound ID2961
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 IdentifiedStigmasterol
PubChem ID   5280794
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Steroid, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight412.371
Molecular FormulaC29H48O
SMILESO[C@@H]1CC2=CC[C@H]3[C@H]4[C@@]([C@H](CC4)[C@H](C)/C=C/[C@H](C(C)C)CC)(CC[C@@H]3[C@]2(CC1)C)C
XLogP11.071
PSA20.230
H-bond Donor1
H-bond Acceptor1
No. of Rotatable Bond Count5
No. of Rings4
No. of N0
No. of O1
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 14 of 20   [TOP]
Compound ID2962
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 IdentifiedHaloxyline A
PubChem ID   11362138
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Alkene, Piperidine, Alkaloid, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight419.376
Molecular FormulaC27H49NO2
SMILESO=C(N1CCCCC1)/C=CC=C/CCCCCCCCCCCCCCCCCO
XLogP9.460
PSA40.540
H-bond Donor1
H-bond Acceptor3
No. of Rotatable Bond Count20
No. of Rings1
No. of N1
No. of O2
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 15 of 20   [TOP]
Compound ID2963
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 IdentifiedHaloxyline B
PubChem ID   11453345
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Alkene, Pyrrolidine, Amide, Alcohol, Alkaloid
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight435.371
Molecular FormulaC27H49NO3
SMILESO[C@@H]1CCCN(C1)C(=O)/C=CC=C/CCCCCCCCCCCCCCCCCO
XLogP8.430
PSA60.770
H-bond Donor2
H-bond Acceptor4
No. of Rotatable Bond Count20
No. of Rings1
No. of N1
No. of O3
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 16 of 20   [TOP]
Compound ID2964
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 Identified5α-Epidioxyergosta-6,9(11), 22-triene
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Steroid, Peroxy, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight426.313
Molecular FormulaC28H42O3
SMILESC1C[C@@H](C[C@@]23[C@]1(C1=CC[C@@]4(C(CC[C@H]4[C@]1(C=C2)OO3)[C@@H](/C=C/[C@H](C(C)C)C)C)C)C)O
XLogP7.484
PSA38.690
H-bond Donor1
H-bond Acceptor3
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O3
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 17 of 20   [TOP]
Compound ID2965
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 Identifiedα - 8 α Epidioxy Ergost - 6, 22 - Dien - 3β - Ol
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Steroid, Peroxide, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight428.329
Molecular FormulaC28H44O3
SMILESC1C[C@@H](C[C@@]23[C@]1([C@@H]1[C@](C=C2)([C@H]2[C@](CC1)(C(CC2)[C@@H](/C=C/[C@H](C(C)C)C)C)C)OO3)C)O
XLogP8.383
PSA38.690
H-bond Donor1
H-bond Acceptor3
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O3
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 18 of 20   [TOP]
Compound ID2966
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 Identified24β (24S)-Ethyl-cholesta-4-22 E diene 3-O-β-D-glucoside
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Steroid, Sugar
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight588.439
Molecular FormulaC36H60O6
SMILESC1CC(C=C2[C@]1([C@@H]1[C@@](CC2)([C@H]2[C@](CC1)(C(CC2)[C@@H](/C=C/[C@H](C(C)C)CC)C)C)C)C)OC1O[C@@H]([C@H]([C@H](O)[C@H]1O)O)CO
XLogP10.835
PSA99.380
H-bond Donor4
H-bond Acceptor6
No. of Rotatable Bond Count8
No. of Rings5
No. of N0
No. of O6
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 19 of 20   [TOP]
Compound ID2967
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 Identified24β (24S)-Ethyl cholesta-4-22 E diene 3-O-α-L-rhamnoside
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Steroid, Sugar
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight558.428
Molecular FormulaC35H58O5
SMILESC1CC(C=C2[C@]1([C@@H]1[C@@H](CC2)[C@H]2[C@](CC1)(C(CC2)[C@@H](/C=C/[C@H](C(C)C)CC)C)C)C)OC1[C@@H]([C@@H]([C@H]([C@@H](O1)C)O)O)O
XLogP10.932
PSA79.150
H-bond Donor3
H-bond Acceptor5
No. of Rotatable Bond Count7
No. of Rings5
No. of N0
No. of O5
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 20 of 20   [TOP]
Compound ID2968
Compound Structure
DOWNLOAD:
Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 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 IdentifiedStigmasterol-3-O-β-D-glucopyranoside
PubChem ID   44237224
Ethnomedicinal InformationHealing of internal ulcers, insect stings
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Steroid, Sugar
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight574.423
Molecular FormulaC35H58O6
SMILESO([C@@H]1CC2=CCC3C4[C@@](C(CC4)[C@H](C)/C=C/[C@H](C(C)C)CC)(CCC3[C@]2(CC1)C)C)C1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)CO
XLogP9.963
PSA99.380
H-bond Donor4
H-bond Acceptor6
No. of Rotatable Bond Count8
No. of Rings5
No. of N0
No. of O6
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba


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