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Ajuga parviflora

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440373d79d5e202975815
Scientific name Ajuga parviflora
Authority Benth.
First published in Pl. Asiat. Rar. 1: 59 (1830)

Description Top

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Synonyms Top

Scientific name Authority First published in
Bulga parviflora Kuntze Revis. Gen. Pl. 2: 512 (1891)
Ajuga depressa Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 29: 192 (1883)

Common names Top

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Language Common/alternative name
Arabic عجوقة صغيرة الزهرة

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Nepal
      • Pakistan
      • West Himalaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000934858
Tropicos 17600015
KEW urn:lsid:ipni.org:names:444647-1
The Plant List kew-5361
Open Tree Of Life 5793029
NCBI Taxonomy 1585252
IPNI 444647-1
iNaturalist 874292
GBIF 3886822

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Keeping Healthy in Your Skin—Plants and Fungi Used by Indigenous Himalayan Communities to Treat Dermatological Ailments Haq SM, Khoja AA, Lone FA, Waheed M, Bussmann RW, Casini R, Mahmoud EA, Elansary HO Plants (Basel) 06-Apr-2023
PMCID:PMC10097107
doi:10.3390/plants12071575
PMID:37050200
A Cross-Cultural Analysis of Medicinal Plant Utilization among the Four Ethnic Communities in Northern Regions of Jammu and Kashmir, India Mir TA, Jan M, Jan HA, Bussmann RW, Sisto F, Fadlalla IM Biology (Basel) 27-Oct-2022
PMCID:PMC9687545
doi:10.3390/biology11111578
PMID:36358279
Ethnogynaecological Knowledge of Traditional Medicinal Plants Used by the Indigenous Communities of North Waziristan, Pakistan Rehman S, Iqbal Z, Qureshi R, Ur Rahman I, Khan MA, Elshaer MM, Al Farraj DA, Elshikh MS, Younas M, Sakhi S, Nawaz G, Ali N, Rahim F, Ali H, Khan I, Rahman SU, Abu Bakr Elsaid NM Evid Based Complement Alternat Med 04-Aug-2022
PMCID:PMC9371843
doi:10.1155/2022/6528264
PMID:35966728
A Cross-Cultural Analysis of Plant Resources among Five Ethnic Groups in the Western Himalayan Region of Jammu and Kashmir Haq SM, Hassan M, Bussmann RW, Calixto ES, Rahman IU, Sakhi S, Ijaz F, Hashem A, Al-Arjani AB, Almutairi KF, Abd_Allah EF, Aziz MA, Ali N Biology (Basel) 23-Mar-2022
PMCID:PMC9032642
doi:10.3390/biology11040491
PMID:35453691
Comparison of Herbal Medicines Used for Women’s Menstruation Diseases in Different Areas of the World Jiao M, Liu X, Ren Y, Wang Y, Cheng L, Liang Y, Li Y, Zhang T, Wang W, Mei Z Front Pharmacol 04-Feb-2022
PMCID:PMC8854496
doi:10.3389/fphar.2021.751207
PMID:35185533
Synthesis and Encapsulation of Ajuga parviflora Extract with Zeolitic Imidazolate Framework-8 and Their Therapeutic Action against G+ and G– Drug-Resistant Bacteria Ahanger AM, Kumar S, Arya A, Suryavanshi A, Kain D, Vandana ACS Omega 06-Jan-2022
PMCID:PMC8772321
doi:10.1021/acsomega.1c03984
PMID:35071862
Plants predict the mineral mines – A methodological approach to use indicator plant species for the discovery of mining sites Ahmad Z, Mulk Khan S, Page S, Alamri S, Hashem M J Adv Res 18-Oct-2021
PMCID:PMC9263987
doi:10.1016/j.jare.2021.10.005
PMID:35777902
Phyto-ecological studies and distribution pattern of plant species and communities of Dhirkot, Azad Jammu and Kashmir, Pakistan Mumshad M, Ahmad I, Khan SM, Abdullah, Rehman K, Islam M, Sakhi S, Khan SU, Afridi SG, Shams S, Azam S, Ahmad I, Afza R, Ahmad Z PLoS One 06-Oct-2021
PMCID:PMC8494300
doi:10.1371/journal.pone.0257493
PMID:34614011
Inventorization of traditional ethnobotanical uses of wild plants of Dawarian and Ratti Gali areas of District Neelum, Azad Jammu and Kashmir Pakistan Ajaib M, Ishtiaq M, Bhatti KH, Hussain I, Maqbool M, Hussain T, Mushtaq W, Ghani A, Azeem M, Khan SM, Thind S, Bashir R PLoS One 29-Jul-2021
PMCID:PMC8321310
doi:10.1371/journal.pone.0255010
PMID:34324561
Phytochemical, acute toxicity and renal protective appraisal of Ajuga parviflora hydromethanolic leaf extract against CCl4 induced renal injury in rats Burki S, Burki ZG, Asghar MA, Ali I, Zafar S BMC Complement Med Ther 12-Jul-2021
PMCID:PMC8276434
doi:10.1186/s12906-021-03360-9
PMID:34253216
Ecological restoration of habitats invaded by Leucanthemum vulgare that alters key ecosystem functions Khan MA, Hussain K, Shah MA PLoS One 26-Mar-2021
PMCID:PMC7996977
doi:10.1371/journal.pone.0246665
PMID:33770078
Medicinal plants: Treasure for antiviral drug discovery Ali SI, Sheikh WM, Rather MA, Venkatesalu V, Muzamil Bashir S, Nabi SU Phytother Res 16-Feb-2021
PMCID:PMC8013762
doi:10.1002/ptr.7039
PMID:33590931
Bioactive Natural Antivirals: An Updated Review of the Available Plants and Isolated Molecules Mohan S, Elhassan Taha MM, Makeen HA, Alhazmi HA, Al Bratty M, Sultana S, Ahsan W, Najmi A, Khalid A Molecules 22-Oct-2020
PMCID:PMC7659943
doi:10.3390/molecules25214878
PMID:33105694
Effects of Lonicera japonica Flower Bud Extract on Citrobacter rodentium-Induced Digestive Tract Infection Minami M, Makino T Medicines (Basel) 27-Aug-2020
PMCID:PMC7555260
doi:10.3390/medicines7090052
PMID:32867139
Ethnomedicinal knowledge of a marginal hill community of Central Himalaya: diversity, usage pattern, and conservation concerns Ojha SN, Tiwari D, Anand A, Sundriyal RC J Ethnobiol Ethnomed 24-May-2020
PMCID:PMC7245762
doi:10.1186/s13002-020-00381-5
PMID:32448334

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(4aR,5S,7R,8S,8aR)-5-acetyloxy-7,8-dimethyl-4-methylidene-8-[2-(5-oxo-2H-furan-3-yl)ethyl]-2,3,5,6,7,8a-hexahydro-1H-naphthalen-4a-yl]methyl acetate 102247112 Click to see CC1CC(C2(C(C1(C)CCC3=CC(=O)OC3)CCCC2=C)COC(=O)C)OC(=O)C 418.50 unknown https://doi.org/10.1016/0031-9422(96)00207-5
[(4R,4aR,5S,7R,8S,8aR)-5-acetyloxy-4-(chloromethyl)-4-hydroxy-7,8-dimethyl-8-[2-(5-oxo-2H-furan-3-yl)ethyl]-2,3,5,6,7,8a-hexahydro-1H-naphthalen-4a-yl]methyl acetate 102247113 Click to see CC1CC(C2(C(C1(C)CCC3=CC(=O)OC3)CCCC2(CCl)O)COC(=O)C)OC(=O)C 471.00 unknown https://doi.org/10.1016/0031-9422(96)00207-5
[5-acetyloxy-4-(chloromethyl)-4-hydroxy-7,8-dimethyl-8-[2-(5-oxo-2H-furan-3-yl)ethyl]-2,3,5,6,7,8a-hexahydro-1H-naphthalen-4a-yl]methyl acetate 162919289 Click to see CC1CC(C2(C(C1(C)CCC3=CC(=O)OC3)CCCC2(CCl)O)COC(=O)C)OC(=O)C 471.00 unknown https://doi.org/10.1016/0031-9422(96)00207-5
[5-acetyloxy-7,8-dimethyl-4-methylidene-8-[2-(5-oxo-2H-furan-3-yl)ethyl]-2,3,5,6,7,8a-hexahydro-1H-naphthalen-4a-yl]methyl acetate 163040835 Click to see CC1CC(C2(C(C1(C)CCC3=CC(=O)OC3)CCCC2=C)COC(=O)C)OC(=O)C 418.50 unknown https://doi.org/10.1016/0031-9422(96)00207-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0367-326X(99)00019-2
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0367-326X(99)00019-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(1R,2R,7R,10R,11S,14R,15S,16R)-16-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-7,15-dihydroxy-10,14,16-trimethyl-17-oxapentacyclo[13.2.2.01,14.02,11.05,10]nonadec-4-en-9-one 11798583 Click to see CC1=C(C(=O)OC(C1)C2(C3(CCC4(C3(CCC5C4CC=C6C5(C(=O)CC(C6)O)C)C)O2)O)C)C 470.60 unknown https://doi.org/10.1016/S0031-9422(99)00345-3
(1R,2R,7R,10R,11S,14R,15S,16R)-7-hydroxy-16-[(2R)-5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]-10,14,16-trimethyl-17-oxapentacyclo[13.2.2.01,14.02,11.05,10]nonadec-4-en-9-one 15968792 Click to see CC1=C(C(=O)OC(C1)C2(C3CCC4(C3(CCC5C4CC=C6C5(C(=O)CC(C6)O)C)C)O2)C)CO 470.60 unknown https://doi.org/10.1021/NP990029K
(2R)-2-[(1R)-1-[(4S,8R,9S,10R,13R,14R,17S)-4,14-dihydroxy-10,13-dimethyl-1-oxo-7,8,9,11,12,15,16,17-octahydro-4H-cyclopenta[a]phenanthren-17-yl]-1-hydroxyethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 15411316 Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3(C2(CCC4C3CC=C5C4(C(=O)C=CC5O)C)C)O)O)CO 486.60 unknown https://doi.org/10.1002/(SICI)1522-2675(19990908)82:9<1423::AID-HLCA1423>3.0.CO;2-F
(2R)-2-[(1R)-1-[(8R,9S,10R,13R,14R,17S)-14,17-dihydroxy-10,13-dimethyl-1-oxo-2,3,4,7,8,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 162959997 Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)CCC5)C)C)O)O)CO 472.60 unknown https://doi.org/10.1016/S0031-9422(99)00345-3
(2R)-2-[(1R)-1-[(8R,9S,10R,13S,14R,17R)-14,17-dihydroxy-10,13-dimethyl-1-oxo-2,3,4,7,8,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 101010479 Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)CCC5)C)C)O)O)CO 472.60 unknown https://doi.org/10.1016/S0031-9422(99)00345-3
(2R)-2-[(1R)-1-[(8R,9S,10R,13S,14R,17S)-14,17-dihydroxy-10,13-dimethyl-1-oxo-2,3,4,7,8,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 162959998 Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)CCC5)C)C)O)O)CO 472.60 unknown https://doi.org/10.1016/S0031-9422(99)00345-3
(2R)-2-[(1R)-1-[(8R,9S,10R,13S,14R,17S)-14,17-dihydroxy-10,13-dimethyl-1-oxo-2,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-1-hydroxyethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 101010478 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)CC=C5)C)C)O)O)O)CO 486.60 unknown https://doi.org/10.1016/S0031-9422(99)00345-3
(2R)-2-[(1R)-1-hydroxy-1-[(8R,9S,10R,13R,14R,17S)-14-hydroxy-10,13-dimethyl-1-oxo-3,4,7,8,9,11,12,15,16,17-decahydro-2H-cyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 21668784 Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3(C2(CCC4C3CC=C5C4(C(=O)CCC5)C)C)O)O)CO 472.60 unknown https://doi.org/10.1021/NP990029K
(2R)-2-[(1R)-1-hydroxy-1-[(8R,9S,10R,13R,14R,17S)-14-hydroxy-10,13-dimethyl-1-oxo-7,8,9,11,12,15,16,17-octahydro-2H-cyclopenta[a]phenanthren-17-yl]ethyl]-4-(hydroxymethyl)-5-methyl-2,3-dihydropyran-6-one 21668783 Click to see CC1=C(CC(OC1=O)C(C)(C2CCC3(C2(CCC4C3CC=C5C4(C(=O)CC=C5)C)C)O)O)CO 470.60 unknown https://doi.org/10.1021/NP990029K
(2R)-2-[(1R)-1-hydroxy-1-[(8R,9S,10R,13R,14R,17S)-14-hydroxy-10,13-dimethyl-1-oxo-7,8,9,11,12,15,16,17-octahydro-2H-cyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 21679029 Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3(C2(CCC4C3CC=C5C4(C(=O)CC=C5)C)C)O)O)CO 470.60 unknown https://doi.org/10.1021/NP990029K
(2R)-2-[(1S)-1-[(8R,9S,10R,13S,14R,17S)-14,17-dihydroxy-10,13-dimethyl-1-oxo-2,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-1-hydroxyethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 101494955 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)CC=C5)C)C)O)O)O)CO 486.60 unknown https://doi.org/10.1016/S0031-9422(99)00345-3
(2R)-5-(hydroxymethyl)-2-[(1R)-1-hydroxy-1-[(8S,9R,10R,13S,14S,17S)-8,14,17-trihydroxy-10,13-dimethyl-1-oxo-3,4,7,9,11,12,15,16-octahydro-2H-cyclopenta[a]phenanthren-17-yl]ethyl]-4-methyl-2,3-dihydropyran-6-one 100941096 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3(CC=C5C4(C(=O)CCC5)C)O)C)O)O)O)CO 504.60 unknown https://doi.org/10.1002/(SICI)1522-2675(19990908)82:9<1423::AID-HLCA1423>3.0.CO;2-F
(2R)-5-(hydroxymethyl)-2-[(1S)-1-hydroxy-1-[(8S,9R,10R,13S,14S,17S)-8,14,17-trihydroxy-10,13-dimethyl-1-oxo-3,4,7,9,11,12,15,16-octahydro-2H-cyclopenta[a]phenanthren-17-yl]ethyl]-4-methyl-2,3-dihydropyran-6-one 162915573 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3(CC=C5C4(C(=O)CCC5)C)O)C)O)O)O)CO 504.60 unknown https://doi.org/10.1002/(SICI)1522-2675(19990908)82:9<1423::AID-HLCA1423>3.0.CO;2-F
(2S)-2-[(1S)-1-[(8R,9S,10R,13S,14R,17S)-14,17-dihydroxy-10,13-dimethyl-1-oxo-2,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-1-hydroxyethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 163007687 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)CC=C5)C)C)O)O)O)CO 486.60 unknown https://doi.org/10.1016/S0031-9422(99)00345-3
16-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-7,15-dihydroxy-10,14,16-trimethyl-17-oxapentacyclo[13.2.2.01,14.02,11.05,10]nonadec-4-en-9-one 73106250 Click to see CC1=C(C(=O)OC(C1)C2(C3(CCC4(C3(CCC5C4CC=C6C5(C(=O)CC(C6)O)C)C)O2)O)C)C 470.60 unknown https://doi.org/10.1016/S0031-9422(99)00345-3
2-[1-(14,17-Dihydroxy-10,13-dimethyl-1-oxo-2,3,4,7,8,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-17-yl)ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 85235730 Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)CCC5)C)C)O)O)CO 472.60 unknown https://doi.org/10.1016/S0031-9422(99)00345-3
2-[1-(14,17-Dihydroxy-10,13-dimethyl-1-oxo-2,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl)-1-hydroxyethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 75059748 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)CC=C5)C)C)O)O)O)CO 486.60 unknown https://doi.org/10.1016/S0031-9422(99)00345-3
2-[1-(4,14-dihydroxy-10,13-dimethyl-1-oxo-7,8,9,11,12,15,16,17-octahydro-4H-cyclopenta[a]phenanthren-17-yl)-1-hydroxyethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one 163036823 Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3(C2(CCC4C3CC=C5C4(C(=O)C=CC5O)C)C)O)O)CO 486.60 unknown https://doi.org/10.1002/(SICI)1522-2675(19990908)82:9<1423::AID-HLCA1423>3.0.CO;2-F
5-(hydroxymethyl)-2-[1-hydroxy-1-(8,14,17-trihydroxy-10,13-dimethyl-1-oxo-3,4,7,9,11,12,15,16-octahydro-2H-cyclopenta[a]phenanthren-17-yl)ethyl]-4-methyl-2,3-dihydropyran-6-one 162915572 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3(CC=C5C4(C(=O)CCC5)C)O)C)O)O)O)CO 504.60 unknown https://doi.org/10.1002/(SICI)1522-2675(19990908)82:9<1423::AID-HLCA1423>3.0.CO;2-F
Ajugin 100982555 Click to see CC1=C(C(=O)OC(C1)C2(C3(CCC4(C3(CCC5C4CC=C6C5(C(=O)CC(C6)O)C)C)O2)O)C)C 470.60 unknown https://doi.org/10.1016/S0031-9422(99)00045-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0367-326X(99)00019-2
https://doi.org/10.1021/NP990029K
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP990029K
https://doi.org/10.1016/S0367-326X(99)00019-2
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0367-326X(99)00019-2
https://doi.org/10.1021/NP990029K
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1S)-2-[(1S,2R,4S,4aR,5R,8aR)-4-acetyloxy-4a-(acetyloxymethyl)-1,2-dimethylspiro[3,4,6,7,8,8a-hexahydro-2H-naphthalene-5,2'-oxirane]-1-yl]-1-(5-oxo-2H-furan-3-yl)ethyl] (2R)-2-methylbutanoate 124708185 Click to see CCC(C)C(=O)OC(CC1(C(CC(C2(C1CCCC23CO3)COC(=O)C)OC(=O)C)C)C)C4=CC(=O)OC4 534.60 unknown https://doi.org/10.1016/0031-9422(96)00207-5
[2-[4-acetyloxy-4a-(acetyloxymethyl)-1,2-dimethylspiro[3,4,6,7,8,8a-hexahydro-2H-naphthalene-5,2'-oxirane]-1-yl]-1-(5-oxo-2H-furan-3-yl)ethyl] 2-methylbutanoate 14356989 Click to see CCC(C)C(=O)OC(CC1(C(CC(C2(C1CCCC23CO3)COC(=O)C)OC(=O)C)C)C)C4=CC(=O)OC4 534.60 unknown https://doi.org/10.1016/0031-9422(96)00207-5
Ajugamarin F 4 180117 Click to see CCC(C)C(=O)OC(CC1(C(CC(C2(C1CCCC23CO3)COC(=O)C)OC(=O)C)C)C)C4=CC(=O)OC4 534.60 unknown https://doi.org/10.1016/0031-9422(96)00207-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,2S,3R,4aR,5S,6R,8S,8aR)-5-[(2S,3aS,5R,6aR)-5-ethoxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl]-8-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-5,6-dimethylspiro[3,4,4a,6,7,8-hexahydro-2H-naphthalene-1,2'-oxirane]-2-yl] (2R)-2-methylbutanoate 162882718 Click to see CCC(C)C(=O)OC1C(CC2C(C(CC(C2(C13CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5CC(OC5O4)OCC)O 596.70 unknown https://doi.org/10.1016/0031-9422(96)00207-5
[(1R,2S,3R,4aR,5S,6R,8S,8aR)-5-[(2S,3aS,5S,6aR)-5-ethoxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl]-8-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-5,6-dimethylspiro[3,4,4a,6,7,8-hexahydro-2H-naphthalene-1,2'-oxirane]-2-yl] (2R)-2-methylbutanoate 162882719 Click to see CCC(C)C(=O)OC1C(CC2C(C(CC(C2(C13CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5CC(OC5O4)OCC)O 596.70 unknown https://doi.org/10.1016/0031-9422(96)00207-5
[3,5-diacetyloxy-8-(5-ethoxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 162890163 Click to see CCOC1CC2CC(OC2O1)C3(C(CC(C4(C3CCC(C45CO5)OC(=O)C)COC(=O)C)OC(=O)C)C)C 538.60 unknown https://doi.org/10.1016/0031-9422(96)00207-5
[5-acetyloxy-7,8-dimethyl-8-[2-(5-oxo-2H-furan-3-yl)ethyl]spiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 5088205 Click to see CC1CC(C2(C(C1(C)CCC3=CC(=O)OC3)CCCC24CO4)COC(=O)C)OC(=O)C 434.50 unknown https://doi.org/10.1016/0031-9422(96)00207-5
[8-acetyloxy-8a-(acetyloxymethyl)-5-(5-ethoxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl)-3-hydroxy-5,6-dimethylspiro[3,4,4a,6,7,8-hexahydro-2H-naphthalene-1,2'-oxirane]-2-yl] 2-methylbutanoate 13966154 Click to see CCC(C)C(=O)OC1C(CC2C(C(CC(C2(C13CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5CC(OC5O4)OCC)O 596.70 unknown https://doi.org/10.1016/0031-9422(96)00207-5
3beta-Acetoxyclerodinin C 102247114 Click to see CCOC1CC2CC(OC2O1)C3(C(CC(C4(C3CCC(C45CO5)OC(=O)C)COC(=O)C)OC(=O)C)C)C 538.60 unknown https://doi.org/10.1016/0031-9422(96)00207-5
Ajugarin I 173866 Click to see CC1CC(C2(C(C1(C)CCC3=CC(=O)OC3)CCCC24CO4)COC(=O)C)OC(=O)C 434.50 unknown https://doi.org/10.1016/0031-9422(96)00207-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Jacaranone 73307 Click to see COC(=O)CC1(C=CC(=O)C=C1)O 182.17 unknown https://doi.org/10.1016/S0367-326X(99)00019-2
Quinolacetic acid 6453213 Click to see C1=CC(C=CC1=O)(CC(=O)O)O 168.15 unknown https://doi.org/10.1515/ZNB-2001-0819
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(4R)-2-Hydroxy-4alpha-(beta-D-glucopyranosyloxy)-4-methyl-2,5-cyclohexadiene-1-one 101122456 Click to see CC1(C=CC(=O)C(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 302.28 unknown https://doi.org/10.1515/ZNB-2001-0819
2-Hydroxy-4-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexa-2,5-dien-1-one 162981841 Click to see CC1(C=CC(=O)C(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 302.28 unknown https://doi.org/10.1515/ZNB-2001-0819
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
Methyl 2-(2,2-dimethyl-6-oxo-7,7a-dihydro-1,3-benzodioxol-3a-yl)acetate 163033791 Click to see CC1(OC2CC(=O)C=CC2(O1)CC(=O)OC)C 240.25 unknown https://doi.org/10.1515/ZNB-2001-0819
methyl 2-[(3aS,7aR)-2,2-dimethyl-6-oxo-7,7a-dihydro-1,3-benzodioxol-3a-yl]acetate 101122457 Click to see CC1(OC2CC(=O)C=CC2(O1)CC(=O)OC)C 240.25 unknown https://doi.org/10.1515/ZNB-2001-0819
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
4-[2-[(1R)-8aalpha-Acetoxymethyl-3,4,4abeta,5,6,7,8,8a-octahydro-8alpha-hydroxy-5alpha,6alpha-dimethylspiro[naphthalene-1(2H),2'-oxiran]-5-yl]ethyl]furan-2(5H)-one 78302589 Click to see CC1CC(C2(C(C1(C)CCC3=CC(=O)OC3)CCCC24CO4)COC(=O)C)O 392.50 unknown https://doi.org/10.1016/0031-9422(96)00207-5
Ajugarin II 3085250 Click to see CC1CC(C2(C(C1(C)CCC3=CC(=O)OC3)CCCC24CO4)COC(=O)C)O 392.50 unknown https://doi.org/10.1016/0031-9422(96)00207-5
> Organoheterocyclic compounds / Furofurans
[(4R,4aR,5S,7R,8S,8aR)-8-[(2S,3aS,5R,6aR)-5-ethoxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl]-5-acetyloxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 10600777 Click to see CCOC1CC2CC(OC2O1)C3(C(CC(C4(C3CCCC45CO5)COC(=O)C)OC(=O)C)C)C 480.60 unknown https://doi.org/10.1016/0031-9422(96)00207-5
[(4R,4aR,5S,7R,8S,8aR)-8-[(2S,3aS,5S,6aR)-5-ethoxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl]-5-acetyloxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 10719524 Click to see CCOC1CC2CC(OC2O1)C3(C(CC(C4(C3CCCC45CO5)COC(=O)C)OC(=O)C)C)C 480.60 unknown https://doi.org/10.1016/0031-9422(96)00207-5
[5-acetyloxy-8-(5-ethoxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 14543113 Click to see CCOC1CC2CC(OC2O1)C3(C(CC(C4(C3CCCC45CO5)COC(=O)C)OC(=O)C)C)C 480.60 unknown https://doi.org/10.1016/0031-9422(96)00207-5
[8-(2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl)-5-acetyloxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 13559425 Click to see CC1CC(C2(C(C1(C)C3CC4CCOC4O3)CCCC25CO5)COC(=O)C)OC(=O)C 436.50 unknown https://doi.org/10.1016/0031-9422(96)00207-5
14,15-Dihydroclerodin 11812163 Click to see CC1CC(C2(C(C1(C)C3CC4CCOC4O3)CCCC25CO5)COC(=O)C)OC(=O)C 436.50 unknown https://doi.org/10.1016/0031-9422(96)00207-5
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4E,7R,11S,17R)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadecane-3,8-dione 133568461 Click to see CC=C1CC(C(C(=O)OCC2CCN3C2C(CC3)OC1=O)(C)O)C 337.40 unknown https://doi.org/10.1021/NP990029K
(1S,4Z,7S,17S)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 133562009 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1515/ZNB-2000-0116
Senecionine 5280906 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1515/ZNB-2000-0116

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