0000000001304791

AUTHOR

Stephen S. Nyandoro

showing 19 related works from this author

Modified ent-Abietane Diterpenoids from the Leaves of Suregada zanzibariensis

2022

The leaf extract of Suregada zanzibariensis gave two new modified ent-abietane diterpenoids, zanzibariolides A (1) and B (2), and two known triterpenoids, simiarenol (3) and β-amyrin (4). The structures of the isolated compounds were elucidated based on NMR and MS data analysis. Single-crystal X-ray diffraction was used to establish the absolute configurations of compounds 1 and 2. The crude leaf extract inhibited the infectivity of herpes simplex virus 2 (HSV-2, IC50 11.5 μg/mL) and showed toxicity on African green monkey kidney (GMK AH1) cells at CC50 52 μg/mL. The isolated compounds 1–3 showed no anti-HSV-2 activity and exhibited insignificant toxicity against GMK AH1 cells at ≥100 μM. p…

PharmacologyOrganisk kemibioaktiiviset yhdisteetOrganic ChemistryPharmaceutical SciencemyrkyllisyysluonnonaineetAnalytical ChemistryterpeenitComplementary and alternative medicinetyräkkikasvitDrug DiscoveryMolecular Medicineinhibiittorit
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Polyoxygenated Cyclohexenes and Other Constituents of Cleistochlamys kirkii Leaves.

2016

Thirteen new metabolites, including the polyoxygenated cyclohexene derivatives cleistodiendiol (1), cleistodienol B (3), cleistenechlorohydrins A (4) and B (5), cleistenediols A-F (6-11), cleistenonal (12), and the butenolide cleistanolate (13), 2,5-dihydroxybenzyl benzoate (cleistophenolide, 14), and eight known compounds (2, 15-21) were isolated from a MeOH extract of the leaves of Cleistochlamys kirkii. The purified metabolites were identified by NMR spectroscopic and mass spectrometric analyses, whereas the absolute configurations of compounds 1, 17, and 19 were established by single-crystal X-ray diffraction. The configuration of the exocyclic double bond of compound 2 was revised base…

Double bondStereochemistryCyclohexenesPlasmodium falciparumCyclohexenePharmaceutical ScienceBreast Neoplasms01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundAntimalarialsInhibitory Concentration 50X-Ray DiffractionDrug DiscoveryCyclohexenesHumansta116metabolitesCleistochlamys kirkiiButenolidePharmacologychemistry.chemical_classificationMolecular Structure010405 organic chemistryOrganic Chemistryspectrometric analysesMass spectrometricAntineoplastic Agents Phytogenic3. Good health0104 chemical sciencesPlant Leaves010404 medicinal & biomolecular chemistryCleistophenolideHEK293 CellsComplementary and alternative medicinechemistryMolecular MedicineJournal of natural products
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N-Cinnamoyltetraketide Derivatives from the Leaves of Toussaintia orientalis

2015

Seven N-cinnamoyltetraketides (1−7), including the new Ztoussaintine E (2), toussaintine F (6), and toussaintine G (7), were isolated from the methanol extract of the leaves of Toussaintia orientalis using column chromatography and HPLC. The configurations of E-toussaintine E (1) and toussaintines A (3) and D (5) are revised based on single-crystal X-ray diffraction data from racemic crystals. Both the crude methanol extract and the isolated constituents exhibit antimycobacterial activities (MIC 83.3−107.7 μM) against the H37Rv strain of Mycobacterium tuberculosis. Compounds 1, 3, 4, and 5 are cytotoxic (ED50 15.3−105.7 μM) against the MDA-MB-231 triple negative aggressive breast cancer cel…

kemiaToussaintia orientalismedicine.drug_classAntitubercular AgentsPharmaceutical ScienceAnnonaceaeMicrobial Sensitivity TestsAntimycobacterialchemistry01 natural sciencesHigh-performance liquid chromatographyTanzaniaAnalytical ChemistryMycobacterium tuberculosischemistry.chemical_compoundColumn chromatographyDrug DiscoverymedicineHumansTriple negativeNuclear Magnetic Resonance Biomolecularta116PharmacologyChromatographybiologyStrain (chemistry)Molecular Structure010405 organic chemistryCyclohexanonesOrganic ChemistryMycobacterium tuberculosisbiology.organism_classificationtoussaintia orientalis0104 chemical sciences3. Good healthPlant Leavesn-cinnamoyltetraketide010404 medicinal & biomolecular chemistryComplementary and alternative medicinechemistryCinnamatesMolecular MedicineFemaleMethanolDrug Screening Assays AntitumorJournal of Natural Products
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Crotofolane Diterpenoids and Other Constituents Isolated from Croton kilwae

2023

Six new crotofolane diterpenoids (1-6) and 13 known compounds (7-19) were isolated from the MeOH- CH2Cl2 (1:1, v/v) extracts of the leaves and stem bark of Croton kilwae. The structures of the new compounds were elucidated by extensive analysis of spectroscopic and mass spectrometric data. The structure of crotokilwaepoxide A (1) was confirmed by single -crystal X-ray diffraction, allowing for the determination of its absolute configuration. The crude extracts and the isolated compounds were investigated for antiviral activity against respiratory syncytial virus (RSV) and human rhinovirus type-2 (HRV-2) in HEp-2 and HeLa cells, respectively, for antibacterial activity against the Gram-posit…

PharmacologyOrganisk kemiaromaattiset yhdisteetbioaktiiviset yhdisteetcarbonOrganic Chemistryinfrared lightPharmaceutical SciencealkylsluonnonaineetAnalytical ChemistryterpeenitComplementary and alternative medicinetyräkkikasvitDrug Discoverycarbon-14Molecular Medicinenuclear magnetic resonance spectroscopy
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A New Benzopyranyl Cadenane Sesquiterpene and Other Antiplasmodial and Cytotoxic Metabolites from Cleistochlamys kirkii

2019

Phytochemical investigations of ethanol root bark and stem bark extracts of Cleistochlamys kirkii (Benth.) Oliv. (Annonaceae) yielded a new benzopyranyl cadinane-type sesquiterpene (cleistonol, 1) alongside 12 known compounds (2&ndash

Organisk kemibenzopyranyl sesquiterpenesyöpähoidotCleistochlamys kirkiiOrganic ChemistrymalariaAnnonaceaecleistonol<i>Cleistochlamys kirkii</i>antiplasmodial activityluonnonaineetArticlelcsh:QD241-441terpeenitlcsh:Organic chemistrylääkekemiacytotoxicityMolecules
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Secoiridoids and Iridoids from Morinda asteroscepa

2020

The new 2,3-secoiridoids morisecoiridoic acids A (1) and B (2), the new iridoid 8-acetoxyepishanzilactone (3), and four additional known iridoids (4–7) were isolated from the leaf and stem bark methanol extracts of Morinda asteroscepa using chromatographic methods. The structure of shanzilactone (4) was revised. The purified metabolites were identified using NMR spectroscopic and mass spectrometric techniques, with the absolute configuration of 1 having been established by single-crystal X-ray diffraction analysis. The crude leaf extract (10 μg/mL) and compounds 1–3 and 5 (10 μM) showed mild antiplasmodial activities against the chloroquine-sensitive malaria parasite Plasmodium falciparum (…

Iridoidmedicine.drug_classMetabolitePharmaceutical Science01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundDrug Discoverymedicineorgaaniset yhdisteetnuclear magnetic resonance spectroscopyPharmacologyantimikrobiset yhdisteetStem barkOrganisk kemiChromatographybiology010405 organic chemistrymatarakasvitOrganic ChemistryAbsolute configurationBiochemistry and Molecular BiologyalkylsPlasmodium falciparumbiology.organism_classificationluonnonaineetMass spectrometric0104 chemical sciences3. Good health010404 medicinal & biomolecular chemistryComplementary and alternative medicinechemistryMorindachemical structureMolecular Medicineorganic compoundsBiokemi och molekylärbiologi
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Flavonoids from Erythrina schliebenii

2017

Prenylated and O-methylflavonoids including one new pterocarpan (1), three new isoflavones (2–4), and nineteen known natural products (5–23) were isolated and identified from the root, stem bark, and leaf extracts of Erythrina schliebenii. The crude extracts and their constituents were evaluated for antitubercular activity against Mycobacterium tuberculosis (H37Rv strain), showing MICs of 32–64 μg mL–1 and 36.9–101.8 μM, respectively. Evaluation of their toxicity against the aggressive human breast cancer cell line MDA-MB-231 indicated EC50 values of 13.0–290.6 μM (pure compounds) and 38.3 to >100 μg mL–1 (crude extracts).

Antitubercular AgentsPharmaceutical ScienceMicrobial Sensitivity TestsPlant RootsTanzania01 natural sciencesErythrina schliebeniiAnalytical ChemistryMycobacterium tuberculosischemistry.chemical_compoundDrug DiscoveryBotanyHumansta116Nuclear Magnetic Resonance BiomolecularErythrinaEC50FlavonoidsPharmacologyStem barkMolecular StructureTraditional medicinebiology010405 organic chemistryOrganic ChemistryErythrina schliebeniiPterocarpanMycobacterium tuberculosisIsoflavonesbiology.organism_classification0104 chemical sciences3. Good health010404 medicinal & biomolecular chemistryComplementary and alternative medicinechemistryToxicityPlant BarkMolecular MedicineDrug Screening Assays AntitumorCancer cell linesJournal of Natural Products
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CCDC 1497772: Experimental Crystal Structure Determination

2017

Related Article: Stephen S. Nyandoro, Joan J. E. Munissi, Amra Gruhonjic, Sandra Duffy, Fangfang Pan, Rakesh Puttreddy, John P. Holleran, Paul A. Fitzpatrick, Jerry Pelletier, Vicky M. Avery, Kari Rissanen, Máté Erdélyi|2017|J.Nat.Prod.|80|114|doi:10.1021/acs.jnatprod.6b00759

Space GroupCrystallographyCrystal SystemCrystal Structure2-acetoxy-3-(5-oxofuran-2(5H)-ylidene)propyl benzoateCell ParametersExperimental 3D Coordinates
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CCDC 1963302: Experimental Crystal Structure Determination

2020

Related Article: Linda Zandi, Marco Makungu, Joan J. E. Munissi, Sandra Duffy, Rakesh Puttreddy, Daniel von der Heiden, Kari Rissanen, Vicky M. Avery, Stephen S. Nyandoro, Máté Erdélyi|2020|J.Nat.Prod.|83|2641|doi:10.1021/acs.jnatprod.0c00447

Space GroupCrystallographyCrystal SystemCrystal Structure24-dihydroxy-5-(3-hydroxy-1-methoxy-1-oxopropan-2-yl)-2-methylcyclopentane-1-carboxylic acidCell ParametersExperimental 3D Coordinates
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CCDC 1937081: Experimental Crystal Structure Determination

2019

Related Article: Stephen S. Nyandoro, Gasper Maeda, Joan J.E. Munissi, Amra Gruhonjic, Paul A. Fitzpatrick, Sofia Lindblad, Sandra Duffy, Jerry Pelletier, Fangfang Pan, Rakesh Puttreddy, Vicky M. Avery, Máté Erdélyi|2019|Molecules|24|2746|doi:10.3390/molecules24152746

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters5-hydroxy-6-[(2-hydroxyphenyl)methyl]-7-methoxy-2-phenyl-23-dihydro-4H-1-benzopyran-4-oneExperimental 3D Coordinates
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CCDC 1498874: Experimental Crystal Structure Determination

2017

Related Article: Stephen S. Nyandoro, Joan J. E. Munissi, Msim Kombo, Clarence A. Mgina, Fangfang Pan, Amra Gruhonjic, Paul Fitzpatrick, Yu Lu, Bin Wang, Kari Rissanen, Máté Erdélyi|2017|J.Nat.Prod.|80|377|doi:10.1021/acs.jnatprod.6b00839

3-(34-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl)-57-dihydroxy-4H-chromen-4-oneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1497770: Experimental Crystal Structure Determination

2017

Related Article: Stephen S. Nyandoro, Joan J. E. Munissi, Amra Gruhonjic, Sandra Duffy, Fangfang Pan, Rakesh Puttreddy, John P. Holleran, Paul A. Fitzpatrick, Jerry Pelletier, Vicky M. Avery, Kari Rissanen, Máté Erdélyi|2017|J.Nat.Prod.|80|114|doi:10.1021/acs.jnatprod.6b00759

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates(2-acetoxy-56-dihydroxycyclohex-3-en-1-ylidene)methyl benzoate
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CCDC 1498877: Experimental Crystal Structure Determination

2017

Related Article: Stephen S. Nyandoro, Joan J. E. Munissi, Msim Kombo, Clarence A. Mgina, Fangfang Pan, Amra Gruhonjic, Paul Fitzpatrick, Yu Lu, Bin Wang, Kari Rissanen, Máté Erdélyi|2017|J.Nat.Prod.|80|377|doi:10.1021/acs.jnatprod.6b00839

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates567-trimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one
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CCDC 1498873: Experimental Crystal Structure Determination

2017

Related Article: Stephen S. Nyandoro, Joan J. E. Munissi, Msim Kombo, Clarence A. Mgina, Fangfang Pan, Amra Gruhonjic, Paul Fitzpatrick, Yu Lu, Bin Wang, Kari Rissanen, Máté Erdélyi|2017|J.Nat.Prod.|80|377|doi:10.1021/acs.jnatprod.6b00839

Space GroupCrystallography57-dihydroxy-2-(4-methoxy-35-bis(3-methylbut-2-en-1-yl)phenyl)-23-dihydro-4H-chromen-4-oneCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1498875: Experimental Crystal Structure Determination

2017

Related Article: Stephen S. Nyandoro, Joan J. E. Munissi, Msim Kombo, Clarence A. Mgina, Fangfang Pan, Amra Gruhonjic, Paul Fitzpatrick, Yu Lu, Bin Wang, Kari Rissanen, Máté Erdélyi|2017|J.Nat.Prod.|80|377|doi:10.1021/acs.jnatprod.6b00839

Space GroupCrystallography57-dihydroxy-3-(4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl)-4H-chromen-4-oneCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1498876: Experimental Crystal Structure Determination

2017

Related Article: Stephen S. Nyandoro, Joan J. E. Munissi, Msim Kombo, Clarence A. Mgina, Fangfang Pan, Amra Gruhonjic, Paul Fitzpatrick, Yu Lu, Bin Wang, Kari Rissanen, Máté Erdélyi|2017|J.Nat.Prod.|80|377|doi:10.1021/acs.jnatprod.6b00839

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters567-trimethoxy-2-(4-methoxyphenyl)-23-dihydro-4H-chromen-4-oneExperimental 3D Coordinates
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CCDC 1498878: Experimental Crystal Structure Determination

2017

Related Article: Stephen S. Nyandoro, Joan J. E. Munissi, Msim Kombo, Clarence A. Mgina, Fangfang Pan, Amra Gruhonjic, Paul Fitzpatrick, Yu Lu, Bin Wang, Kari Rissanen, Máté Erdélyi|2017|J.Nat.Prod.|80|377|doi:10.1021/acs.jnatprod.6b00839

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters1-(6-hydroxy-234-trimethoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-oneExperimental 3D Coordinates
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CCDC 1497771: Experimental Crystal Structure Determination

2017

Related Article: Stephen S. Nyandoro, Joan J. E. Munissi, Amra Gruhonjic, Sandra Duffy, Fangfang Pan, Rakesh Puttreddy, John P. Holleran, Paul A. Fitzpatrick, Jerry Pelletier, Vicky M. Avery, Kari Rissanen, Máté Erdélyi|2017|J.Nat.Prod.|80|114|doi:10.1021/acs.jnatprod.6b00759

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(1S2R3R4S)-2-((benzoyloxy)methyl)cyclohex-5-en-1234-tetrol 14-diacetateExperimental 3D Coordinates
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CCDC 1937082: Experimental Crystal Structure Determination

2019

Related Article: Stephen S. Nyandoro, Gasper Maeda, Joan J.E. Munissi, Amra Gruhonjic, Paul A. Fitzpatrick, Sofia Lindblad, Sandra Duffy, Jerry Pelletier, Fangfang Pan, Rakesh Puttreddy, Vicky M. Avery, Máté Erdélyi|2019|Molecules|24|2746|doi:10.3390/molecules24152746

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters2-(38-dimethyl-12345678-octahydroazulen-5-yl)propan-2-olExperimental 3D Coordinates
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