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                  Page - 1 of 1                  Record - 1 of 4   [TOP]
Compound ID2089
Compound Structure
Plant SourceLumnitzera littorea Voigt     Common Name:
Source FamilyCombretaceae
OriginIndia
Plant Part UsedTwig
ExtractEthanol (95 %)
Target BacteriaMycobacterium smegmatis
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml1000 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationPiles
PubMed ID [Source Literature]
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) Pongpan A, Chumsri P and Taworasate T .The antimicrobial activity of some Thai Medicinal Plants. Mahidol Univ J Pharm Sci 1982; 9 4: 88-91

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                  Record - 2 of 4   [TOP]
Compound ID2170
Compound Structure
Plant SourceMesua ferrea L     Common Name:Ironwood, Mesu (English), Naagakeshara, Naagapushpa (Sanskrit)
Source FamilyClusiaceae
OriginIndia
Plant Part UsedTwig
ExtractEthanol (95 %), petroleum ether
Target BacteriaMycobacterium smegmatis
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml1000 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationSore throat, cough, asthma
PubMed ID [Source Literature]
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) Pongpan A, Chumsri P and Taworasate T .The antimicrobial activity of some Thai Medicinal. Plants. Mahidol Univ J Pharm Sci 1982; 9 4: 88-91

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

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                  Record - 3 of 4   [TOP]
Compound ID2578
Compound Structure
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Plant SourceScleropyrum pentandrum     Common Name:
Source FamilySantalaceae
OriginIndia, Malaysia, Philippines, Singapore, Sri Lanka
Plant Part UsedTwig
ExtractHexane
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampin (0.004 µg/ml), Isoniazid (0.06 µg/ml), Kanamycin sulphate (2.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml25 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedScleropyric acid
PubChem ID   11594149
Ethnomedicinal InformationMalaria, tuberculosis
PubMed ID [Source Literature]16204994
Extract PreparationThe pulverized, dry twigs (1.06 kg) were extracted successively with n - Hexane, CHCl3 and MeOH in a soxhlet extraction apparatus to yield the hexane (7.12 g), CHCl3 (3.50 g), and MeOH (12.42 g) extracts, respectively
Chemical Classification [Active Compound]Aliphatic, Alkene, Alkyne, Fatty acid
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight264.209
Molecular FormulaC17H28O2
SMILESOC(=O)CCCCCCCCCCC#CCCC=C
XLogP6.563
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count12
No. of Rings0
No. of N0
No. of O2
No. of S0
Reference(s)1) Suksamrarn A, Buaprom M, Udtip S, Nuntawong N, Haritakun R, Kanokmedhakul S.Antimycobacterial and antiplasmodial unsaturated carboxylic acid from the twigs of Scleropyrum wallichianum.Chem Pharm Bull (Tokyo). 2005 Oct;53(10):1327-9

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                  Record - 4 of 4   [TOP]
Compound ID3861
Compound Structure
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Plant SourceRhus taitensis Guill.     Common Name:Pumac
Source FamilyAnacardiaceae
OriginPapua New Guinea
Plant Part UsedLeaf, twig
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra (ATCC 25177)
Assay / Test DoneMTT Assay
Positive Control Used (conc.)Rifampin (0.0025 - 0.0079 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml10 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedTetrahydroxysqualene
PubChem ID   25058109
Ethnomedicinal InformationNR
PubMed ID [Source Literature]18710283
Extract PreparationAir - dried leaves and twigs (108.6 g) of Rhus taitensis were ground and extracted with 250 ml MeOH (3 × 24 hours) at room temperature. The crude extract (1.7 g) was filtered and concentrated in vacuo. 5 grams of the crude extract were dissolved in MeOH and mixed with 5 g of HP20SS and dried. The mixture was then poured into a column and fractionated using 100 % water, 75 % H2O / 25 % 2 - propanol, 50 % H2O / 50 % 2 - propanol, 25 % H2O / 75 % 2 - propanol, and 100 % MeOH to yield five fractions designated FW, F1, F2, F3, F4, respectively. The fractions were collected and the solvents evaporated using a centrifugal evaporator
Chemical Classification [Active Compound]Aliphatic, Alkene, Terpene, Triterpene, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]ADC (Remel) supplemented 7H9 medium
Cytotoxicity Assay [AID]Against Human T cells
Molecular Weight474.371
Molecular FormulaC30H50O4
SMILESOCC(=CCC/C(=C/CC/C(=C/CC/C=C(/CC/C=C(/CCC=C(CO)CO)C)C)/C)/C)CO
XLogP5.646
PSA80.920
H-bond Donor4
H-bond Acceptor4
No. of Rotatable Bond Count19
No. of Rings0
No. of N0
No. of O4
No. of S0
Reference(s)1) Noro JC, Barrows LR, Gideon OG, Ireland CM, Koch M, Matainaho T, Piskaut P, Pond CD, Bugni TS.Tetrahdroxysqualene from Rhus taitensis shows antimycobacterial activity against Mycobacterium tuberculosis.J Nat Prod. 2008 Sep;71(9):1623-4. Epub 2008 Aug 19

CuratorKeyaMukherjee, Farzana Shamsudeen, gppreetha


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