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Calophyllum teysmannii

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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 UUID64400ef29096d606163704
Scientific name Calophyllum teysmannii
Authority Miq.
First published in Fl. Ned. Ind., Eerste Bijv. : 499 (1861)

Description Top

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Synonyms Top

Scientific name Authority First published in
Calophyllum inophylloide var. singapurense M.R.Hend. & Wyatt-Sm. Gard. Bull. Singapore 15: 316. 1956 [20 Nov 1956]
Calophyllum intramarginale M.R.Hend. & Wyatt-Sm. Gard. Bull. Singapore 15: 342 (1956)
Calophyllum miquelii Vesque Monogr. Phan. [A.DC. & C.DC.] 8: 607. 1893 [Dec 1893]

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Calophyllum teysmannii var. bursiculum P.F.Stevens J. Arnold Arbor. 61: 436 (1980)
Calophyllum teysmannii var. inophylloide (King) P.F.Stevens J. Arnold Arbor. 61: 436 (1980)

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
    • Indo-China
      • Cambodia
      • Thailand
    • Malesia
      • Borneo
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000581366
Tropicos 100303882
KEW urn:lsid:ipni.org:names:427317-1
The Plant List kew-2693516
Open Tree Of Life 415307
NCBI Taxonomy 667334
IPNI 427317-1
iNaturalist 428102
GBIF 6032514
EOL 5710295
USDA GRIN 411477

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
The Garlic Tree of Borneo, Scorodocarpus borneensis (Baill.) Becc. (Olacaceae): Potential Utilization in Pharmaceutical, Nutraceutical, and Functional Cosmetic Industries Wiart C, Shorna AA, Rahmatullah M, Nissapatorn V, Seelan JS, Rahman H, Rusdi NA, Mustaffa N, Elbehairy L, Sulaiman M Molecules 28-Jul-2023
PMCID:PMC10419944
doi:10.3390/molecules28155717
PMID:37570687
Cytotoxic Metabolites from Calophyllum tacamahaca Willd.: Isolation and Detection through Feature-Based Molecular Networking Gerometta E, Herbette G, Garayev E, Marvilliers A, Naubron JV, Di Giorgio C, Campos PE, Clerc P, Ledoux A, Frederich M, Baghdikian B, Grondin I, Gauvin-Bialecki A Metabolites 23-Apr-2023
PMCID:PMC10222348
doi:10.3390/metabo13050582
PMID:37233623
Functional Studies of Plant Latex as a Rich Source of Bioactive Compounds: Focus on Proteins and Alkaloids Gracz-Bernaciak J, Mazur O, Nawrot R Int J Mol Sci 17-Nov-2021
PMCID:PMC8620047
doi:10.3390/ijms222212427
PMID:34830309
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
Naturally Occurring Calanolides: Occurrence, Biosynthesis, and Pharmacological Properties Including Therapeutic Potential Nahar L, Talukdar AD, Nath D, Nath S, Mehan A, Ismail FM, Sarker SD Molecules 28-Oct-2020
PMCID:PMC7663239
doi:10.3390/molecules25214983
PMID:33126458
Transthyretin Amyloid Fibril Disrupting Activities of Extracts and Fractions from Juglans mandshurica Maxim. var. cordiformis (Makino) Kitam. Chaudhary N, Sasaki R, Shuto T, Watanabe M, Kawahara T, Suico MA, Yokoyama T, Mizuguchi M, Kai H, Devkota HP Molecules 30-Jan-2019
PMCID:PMC6384717
doi:10.3390/molecules24030500
PMID:30704121
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Identification of Minor Benzoylated 4-Phenylcoumarins from a Mammea neurophylla Bark Extract Dang BT, Rouger C, Litaudon M, Richomme P, Séraphin D, Derbré S Molecules 25-Sep-2015
PMCID:PMC6332034
doi:10.3390/molecules201017735
PMID:26404214
Review on Natural Coumarin Lead Compounds for Their Pharmacological Activity Venugopala KN, Rashmi V, Odhav B Biomed Res Int 24-Mar-2013
PMCID:PMC3622347
doi:10.1155/2013/963248
PMID:23586066
Theories of Biodiversity Value Maier DS What’s So Good About Biodiversity? 18-Feb-2012
PMCID:PMC7121063
doi:10.1007/978-94-007-3991-8_6
Coumarins from Calophyllum teysmannii (Guttiferae) Shu-Geng Cao, Keng-Yeow Sim, Joan Pereira, Swee-Hock Goh Elsevier BV 04-Aug-2011
doi:10.1016/S0031-9422(98)80071-X
Three New Coumarins from Calophyllum teysmannii var. inophylloide (Guttiferae) Swee-Hock Goh, Shu-Geng Cao, Keng-Yeow Sim The Japan Institute of Heterocyclic Chemistry 26-Mar-2009
doi:10.3987/COM-97-7901
(-)-Ledol from<i>Calophyllum teysmanii</i>: Structure and Stereochemistry Shu-Geng Cao, Keng-Yeow Sim, S. H. Goh Informa UK Limited 07-Jul-2007
doi:10.1080/10575630008043783
Isocalanone, a New Pyranocoumarin from<i>cAlophyllum teysmannii</i>(Guttiferae) S.-G. Cao, K. L. Chong, J. J. Vittal, K.-Y. Sim, S. H. Goh Informa UK Limited 07-Jul-2007
doi:10.1080/10575639808044952
Nature's Medicines: Traditional Knowledge and Intellectual Property Management. Case Studies from the National Institutes of Health (NIH), USA Gupta R, Gabrielsen B, Ferguson SM Curr Drug Discov Technol 01-Dec-2005
PMCID:PMC2739453
doi:10.2174/157016305775202937
PMID:16475917

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
3,6-Dihydroxy-2-methoxybenzoic acid 15647609 Click to see COC1=C(C=CC(=C1C(=O)O)O)O 184.15 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-Ledol 6431133 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10575630008043783
(1aS,4S,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 25089154 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10575630008043783
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol 137795506 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1080/10575630008043783
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.3987/COM-97-7901
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.3987/COM-97-7901
Friedelanol 101341 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1080/10575630008043783
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1080/10575630008043783
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1080/10575630008043783
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(2R)-4-(4-methoxy-9-oxoxanthen-3-yl)-2-methylbutanoic acid 162879668 Click to see CC(CCC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3O2)OC)C(=O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
(2R)-4-(8-hydroxy-4-methoxy-9-oxoxanthen-3-yl)-2-methylbutanoic acid 162893765 Click to see CC(CCC1=C(C2=C(C=C1)C(=O)C3=C(C=CC=C3O2)O)OC)C(=O)O 342.30 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
(2S)-4-(4-methoxy-9-oxoxanthen-3-yl)-2-methylbutanoic acid 162879667 Click to see CC(CCC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3O2)OC)C(=O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
1,2,8-Trimethoxy-9h-xanthen-9-one 85931281 Click to see COC1=C(C2=C(C=C1)OC3=C(C2=O)C(=CC=C3)OC)OC 286.28 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
1,3-Dihydroxy-4,6,8-trimethoxyxanthen-9-one 101035766 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3=C(O2)C(=C(C=C3O)O)OC 318.28 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
1,3-Dimethoxy-5,8-dihydroxyxanthone 53348043 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3=C(C=CC(=C3O2)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
1,5-Dihydroxy-6-(4-hydroxy-3-methylbutyl)xanthen-9-one 85768635 Click to see CC(CCC1=C(C2=C(C=C1)C(=O)C3=C(C=CC=C3O2)O)O)CO 314.30 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
1,5-dihydroxy-6-[(3S)-4-hydroxy-3-methylbutyl]xanthen-9-one 162939757 Click to see CC(CCC1=C(C2=C(C=C1)C(=O)C3=C(C=CC=C3O2)O)O)CO 314.30 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
1,6-Dihydroxy-7,8-dimethoxyxanthone 14630572 Click to see COC1=C(C2=C(C=C1O)OC3=CC=CC(=C3C2=O)O)OC 288.25 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
1,8-Dimethoxy-2-hydroxyxanthone 493307 Click to see COC1=CC=CC2=C1C(=O)C3=C(O2)C=CC(=C3OC)O 272.25 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
2-Hydroxy-1-methoxy-xanthen-9-one 10399460 Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3O2)O 242.23 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
2-Hydroxy-1,7,8-trimethoxyxanthen-9-one 101717282 Click to see COC1=C(C2=C(C=C1)OC3=C(C2=O)C(=C(C=C3)O)OC)OC 302.28 unknown https://doi.org/10.1016/S0031-9422(00)00289-2
2-Hydroxyxanthone 74708 Click to see C1=CC=C2C(=C1)C(=O)C3=C(O2)C=CC(=C3)O 212.20 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
https://doi.org/10.1016/S0031-9422(00)00289-2
2,8-Dihydroxy-1-methoxyxanthone 5464640 Click to see COC1=C(C=CC2=C1C(=O)C3=C(C=CC=C3O2)O)O 258.23 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
4-(4-Methoxy-9-oxoxanthen-3-yl)-2-methylbutanoic acid 56612721 Click to see CC(CCC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3O2)OC)C(=O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
4-(8-Hydroxy-4-methoxy-9-oxoxanthen-3-yl)-2-methylbutanoic acid 12315435 Click to see CC(CCC1=C(C2=C(C=C1)C(=O)C3=C(C=CC=C3O2)O)OC)C(=O)O 342.30 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
6-Hydroxy-1,2,5-trimethoxyxanthen-9-one 101717280 Click to see COC1=C(C2=C(C=C1)OC3=C(C2=O)C=CC(=C3OC)O)OC 302.28 unknown https://doi.org/10.1016/S0031-9422(00)00289-2
6-Hydroxy-1,3,5,7-tetramethoxyxanthen-9-one 102460794 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3=CC(=C(C(=C3O2)OC)O)OC 332.30 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
6-Methoxy-9-oxo-9H-xanthene-2-carboxylic acid methyl ester 637117 Click to see COC1=CC2=C(C=C1)C(=O)C3=C(O2)C=CC(=C3)C(=O)OC 284.26 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
https://doi.org/10.1016/S0031-9422(00)00289-2
8-Hydroxy-1,2-dimethoxyxanthen-9-one 85948687 Click to see COC1=C(C2=C(C=C1)OC3=CC=CC(=C3C2=O)O)OC 272.25 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
9H-Xanthen-9-one, 3-hydroxy-2,4-dimethoxy- 12214333 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3O2)OC)O 272.25 unknown https://doi.org/10.1016/S0031-9422(00)00289-2
9H-Xanthen-9-one, 3,8-dihydroxy-1,2,4-trimethoxy- 5491745 Click to see COC1=C(C(=C(C2=C1C(=O)C3=C(C=CC=C3O2)O)OC)O)OC 318.28 unknown https://doi.org/10.1016/S0031-9422(00)00289-2
Buchanaxanthone 5481840 Click to see COC1=C(C=CC2=C1OC3=CC=CC(=C3C2=O)O)O 258.23 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
Euxanthone 5281631 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 228.20 unknown https://doi.org/10.1016/S0031-9422(99)00520-8
Gentisin 5281636 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 258.23 unknown https://doi.org/10.1016/S0031-9422(00)00289-2
https://doi.org/10.1016/S0031-9422(99)00520-8
Methyl 7-methoxy-9-oxoxanthene-3-carboxylate 162993705 Click to see COC1=CC2=C(C=C1)OC3=C(C2=O)C=CC(=C3)C(=O)OC 284.26 unknown https://doi.org/10.1016/S0031-9422(00)00289-2
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3R)-6-methoxy-3,7-dimethyl-3,4-dihydro-1H-isochromen-8-ol 21775856 Click to see CC1CC2=CC(=C(C(=C2CO1)O)C)OC 208.25 unknown https://doi.org/10.1016/S0031-9422(00)00289-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Calanolide A 64972 Click to see CCCC1=CC(=O)OC2=C1C3=C(C=CC(O3)(C)C)C4=C2C(C(C(O4)C)C)O 370.40 unknown https://doi.org/10.1016/S0960-894X(01)80543-6
Calanolide F 122843 Click to see CCCC1=CC(=O)OC2=C1C3=C(C=CC(O3)(C)C)C4=C2C(C(C(O4)C)C)O 370.40 unknown https://doi.org/10.1021/NP980140A
Costatolide 461128 Click to see CCCC1=CC(=O)OC2=C1C3=C(C=CC(O3)(C)C)C4=C2C(C(C(O4)C)C)O 370.40 unknown https://doi.org/10.1076/PHBI.37.1.71.6326
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
4-Phenyl-5-methoxy-7-hydroxy-8-benzoylcoumarin 10809277 Click to see COC1=C2C(=CC(=O)OC2=C(C(=C1)O)C(=O)C3=CC=CC=C3)C4=CC=CC=C4 372.40 unknown https://doi.org/10.3987/COM-97-7901
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
(2R)-5-benzoyl-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-phenyl-2,3-dihydrofuro[2,3-f]chromen-7-one 163024126 Click to see CC(C)(C1CC2=C(C(=C3C(=C2O1)C(=CC(=O)O3)C4=CC=CC=C4)C(=O)C5=CC=CC=C5)O)O 442.50 unknown https://doi.org/10.3987/COM-97-7901
(8R,9R)-5-methoxy-8,9-dimethyl-6-(3-methylbut-2-enyl)-4-phenyl-8,9-dihydropyrano[2,3-f]chromene-2,10-dione 15381982 Click to see CC1C(OC2=C(C(=C3C(=CC(=O)OC3=C2C1=O)C4=CC=CC=C4)OC)CC=C(C)C)C 418.50 unknown https://doi.org/10.1016/S0031-9422(97)00679-1
https://doi.org/10.1016/S0031-9422(98)80071-X
12-O-Methylinophyllum A 10645694 Click to see CC1C(OC2=C(C1OC)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 418.50 unknown https://doi.org/10.3987/COM-97-7901
18-Methoxy-10,10,16,17-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaen-4-one 85217621 Click to see CC1C(OC2=C(C1OC)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 418.50 unknown https://doi.org/10.3987/COM-97-7901
5-Benzoyl-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-phenyl-2,3-dihydrofuro[2,3-f]chromen-7-one 11797452 Click to see CC(C)(C1CC2=C(C(=C3C(=C2O1)C(=CC(=O)O3)C4=CC=CC=C4)C(=O)C5=CC=CC=C5)O)O 442.50 unknown https://doi.org/10.3987/COM-97-7901
5-Methoxy-8,9-dimethyl-6-(3-methylbut-2-enyl)-4-phenyl-8,9-dihydropyrano[2,3-f]chromene-2,10-dione 162945629 Click to see CC1C(OC2=C(C(=C3C(=CC(=O)OC3=C2C1=O)C4=CC=CC=C4)OC)CC=C(C)C)C 418.50 unknown https://doi.org/10.1016/S0031-9422(98)80071-X
https://doi.org/10.1016/S0031-9422(97)00679-1
6,6,10,11-Tetramethyl-4-phenyl-10,11-dihydro-6H-dipyrano[2,3-f;2'',3''-h]chromene-2,12-dione 455251 Click to see CC1C(OC2=C(C1=O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 402.40 unknown https://doi.org/10.1016/S0031-9422(98)80071-X
https://doi.org/10.1016/S0031-9422(97)00679-1
Calanone 5352087 Click to see CC1(C=CC2=C(C(=C3C(=C2O1)C(=CC(=O)O3)C4=CC=CC=C4)C(=O)C5=CC=CC=C5)O)C 424.40 unknown https://doi.org/10.1016/S0040-4039(00)78193-7
https://doi.org/10.1080/10575639808044952
https://doi.org/10.1016/S0031-9422(98)80071-X
https://doi.org/10.1016/S0031-9422(97)00679-1
https://doi.org/10.1002/HLCA.19980810549
https://doi.org/10.3987/COM-97-7901
https://doi.org/10.1080/10575630008043783
Inophyllolide chromanol 15223670 Click to see CC1C(OC2=C(C1O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 404.50 unknown https://doi.org/10.1016/S0040-4039(00)78193-7
Inophyllum C 455252 Click to see CC1C(OC2=C(C1=O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 402.40 unknown https://doi.org/10.1002/HLCA.19980810549
https://doi.org/10.1016/S0031-9422(97)00679-1
https://doi.org/10.1016/S0031-9422(98)80071-X
Inophyllum E 5254 Click to see CC1C(OC2=C(C1=O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 402.40 unknown https://doi.org/10.1016/S0031-9422(97)00679-1
https://doi.org/10.1016/S0040-4039(00)78193-7
https://doi.org/10.1016/S0031-9422(98)80071-X
https://doi.org/10.1002/HLCA.19980810549
Isocalanone 11004403 Click to see CC1(C=CC2=C3C(=C(C(=C2O1)C(=O)C4=CC=CC=C4)O)C(=CC(=O)O3)C5=CC=CC=C5)C 424.40 unknown https://doi.org/10.1080/10575630008043783
https://doi.org/10.1080/10575639808044952
https://doi.org/10.1002/HLCA.19980810549
Soulattrolide 72978 Click to see CC1C(OC2=C(C1O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 404.50 unknown https://doi.org/10.1016/S0040-4039(00)78193-7
https://doi.org/10.1016/S0960-894X(01)80543-6
https://doi.org/10.1076/PHBI.37.1.71.6326
Soulattrolone 5352084 Click to see CC1C(OC2=C(C1=O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 402.40 unknown https://doi.org/10.1016/S0031-9422(98)80071-X
https://doi.org/10.1016/S0040-4039(00)78193-7
Teysmanone A 15381981 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(=O)C4=CC=CC=C4)OC(=O)C=C3C5=CC=CC=C5)O)C 424.40 unknown https://doi.org/10.1016/S0031-9422(98)80071-X
https://doi.org/10.1016/S0031-9422(97)00679-1

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