Kopsia fruticosa - Unknown
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Internal ID UUID643fe020e7317828207014
Scientific name Kopsia fruticosa
Authority (Roxb.) A.DC.
First published in Prodr. 8: 352 (1844)

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Synonyms Top

Scientific name Authority First published in
Kopsia roxburghii Wehmer Pfl.-Stoffe : 625 (1911)
Kopsia vinciflora Blume Bijdr. Fl. Ned. Ind. : 1030 (1826)
Tabernaemontana longiflora Rusby Descr. S. Amer. Pl. : 82 (1920)
Tabernaemontana rosea Ten. Cat. Ort. Bot. Napoli : 97 (1845)
Calpicarpum roxburghii G.Don Gen. Hist. 4: 100 (1837)
Cerbera fruticosa Roxb. Fl. Ind. 2: 526. 1824 (1824)
Cerbera fruticosa Ker Gawl. Bot. Reg. 5:pl. 391 1819

Common names Top

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Language Common/alternative name
English pink kopsia
English shrub vinca
Afrikaans pienkkopsia
Bengali ডাকুর
Sango gböô
Chinese 红花蕊木

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Distribution (via Powo/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000221361
Tropicos 1802827
INPN 446919
KEW urn:lsid:ipni.org:names:79497-1
The Plant List kew-106327
Open Tree Of Life 22369
NCBI Taxonomy 28505
IPNI 79497-1
iNaturalist 345550
GBIF 5536025
USDA GRIN 21251

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
Finding activity through rigidity: syntheses of natural products containing tricyclic bridgehead carbon centers Xu Z, Li X, Rose JA, Herzon SB Nat Prod Rep 16-Aug-2023
PMCID:PMC10472132
doi:10.1039/d3np00008g
PMID:37140079
Phylogeography of Himalrandia lichiangensis from the dry-hot valleys in Southwest China Qiao Y, Liu J, Gong X Front Plant Sci 17-Oct-2022
PMCID:PMC9618719
doi:10.3389/fpls.2022.1002519
PMID:36325543
Samarium(ii) iodide-mediated reactions applied to natural product total synthesis Heravi MM, Nazari A RSC Adv 30-Mar-2022
PMCID:PMC8965710
doi:10.1039/d1ra08163b
PMID:35424959
Research progress of Chinese herbal medicine compounds and their bioactivities: Fruitful 2020 Gu X, Hao D, Xiao P Chin Herb Med 17-Mar-2022
PMCID:PMC9476823
doi:10.1016/j.chmed.2022.03.004
PMID:36117669
Synthesis of indole derivatives as prevalent moieties present in selected alkaloids Heravi MM, Amiri Z, Kafshdarzadeh K, Zadsirjan V RSC Adv 15-Oct-2021
PMCID:PMC9042329
doi:10.1039/d1ra05972f
PMID:35497516
Proteomic analysis of early salt stress responsive proteins in alfalfa roots and shoots Xiong J, Sun Y, Yang Q, Tian H, Zhang H, Liu Y, Chen M Proteome Sci 30-Oct-2017
PMCID:PMC5663070
doi:10.1186/s12953-017-0127-z
PMID:29093645
Effect of selected local medicinal plants on the asexual blood stage of chloroquine resistant Plasmodium falciparum Mohd Abd Razak MR, Afzan A, Ali R, Amir Jalaluddin NF, Wasiman MI, Shiekh Zahari SH, Abdullah NR, Ismail Z BMC Complement Altern Med 15-Dec-2014
PMCID:PMC4300612
doi:10.1186/1472-6882-14-492
PMID:25510573
Antiproliferative activity of Vallaris glabra Kuntze (Apocynaceae) Wong SK, Lim YY, Ling SK, Chiang Chan EW Pharmacogn Mag 01-Apr-2014
PMCID:PMC4078344
doi:10.4103/0973-1296.133238
PMID:24991097
Caffeoylquinic acids in leaves of selected Apocynaceae species: Their isolation and content Wong SK, Lim YY, Ling SK, Chan EW Pharmacognosy Res 01-Jan-2014
PMCID:PMC3897013
doi:10.4103/0974-8490.122921
PMID:24497746
Enantioselective cyclization of enamide-ynes and application to the synthesis of the kopsifoline core Corkey BK, Heller ST, Wang YM, Toste FD Tetrahedron 01-Mar-2013
PMCID:PMC3678774
doi:10.1016/j.tet.2013.02.091
PMID:23772095

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
> Alkaloids and derivatives / Aporphines
7,17-Dimethoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),14(19),15,17-hexaene-18-carboxylic acid 74318626 Click to see COC1=C(C2=C(CC3C4=C(CCN3)C(=C5C(=C42)OCO5)OC)C=C1)C(=O)O 369.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
> Alkaloids and derivatives / Aspidofractine alkaloids
(-)-Kopsanone 101289843 Click to see C1CC23CCC45C(C2)C(=O)C6C4(C3N(C1)C6)C7=CC=CC=C7N5 306.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
Kopsanone 433961 Click to see C1CC23CCC45C(C2)C(=O)C6C4(C3N(C1)C6)C7=CC=CC=C7N5 306.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
Kopsine 20054949 Click to see COC(=O)N1C2=CC=CC=C2C34C15CCC67C3N(CCC6)CC4C(=O)C5(C7)O 380.40 unknown https://doi.org/10.1021/JA01178A029
Kopsinine 7069830 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4 338.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
methyl (1R,9R,15S,16S,18S,21S)-15-hydroxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate 162922008 Click to see COC(=O)C1CC23CCC14C5(C2N(CCC3O)CC5)C6=CC=CC=C6N4 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
methyl (1R,9R,16R,18R,20R,21R)-20-hydroxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate 137325361 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3O)NC6=CC=CC=C65)CC4 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
methyl (1R,9R,16R,18R,21S)-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7,14-tetraene-18-carboxylate 821468 Click to see COC(=O)C1CC23CCC14C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4 336.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
methyl (1R,9R,16R,18S,21S)-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7,14-tetraene-18-carboxylate 11877527 Click to see COC(=O)C1CC23CCC14C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4 336.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
methyl (1S,12R,19S,24S)-5,7-dioxa-2,15-diazaheptacyclo[17.2.2.112,15.01,12.03,11.04,8.019,24]tetracosa-3(11),4(8),9,17,20-pentaene-21-carboxylate 21579238 Click to see COC(=O)C1=CC23CCC14C5(C2N(CC5)CC=C3)C6=C(N4)C7=C(C=C6)OCO7 378.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
methyl (1S,4R,12S,13S,16S,18R)-18-hydroxy-17-oxo-5,14-diazaheptacyclo[12.5.3.01,13.04,12.04,18.06,11.012,16]docosa-6,8,10-triene-5-carboxylate 163194769 Click to see COC(=O)N1C2=CC=CC=C2C34C15CCC67C3N(CCC6)CC4C(=O)C5(C7)O 380.40 unknown https://doi.org/10.1039/JR9630000022
methyl (1S,9R,16S,21S)-4-methoxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6,14,17-pentaene-18-carboxylate 21579239 Click to see COC1=CC=CC2=C1NC34C25CCN6C5C(CC3)(C=CC6)C=C4C(=O)OC 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
Methyl 15-hydroxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate 162922005 Click to see COC(=O)C1CC23CCC14C5(C2N(CCC3O)CC5)C6=CC=CC=C6N4 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
Methyl 20-hydroxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate 85296692 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3O)NC6=CC=CC=C65)CC4 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
Methyl 3-hydroxy-22-oxokopsan-1-carboxylate 624835 Click to see COC(=O)N1C2=CC=CC=C2C34C15CCC67C3N(CCC6)CC4C(=O)C5(C7)O 380.40 unknown https://doi.org/10.1039/JR9630000022
https://doi.org/10.1021/JA01178A029
Methyl 4-methoxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6,14,17-pentaene-18-carboxylate 73803959 Click to see COC1=CC=CC2=C1NC34C25CCN6C5C(CC3)(C=CC6)C=C4C(=O)OC 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
Methyl 5,7-dioxa-2,15-diazaheptacyclo[17.2.2.112,15.01,12.03,11.04,8.019,24]tetracosa-3(11),4(8),9,17,20-pentaene-21-carboxylate 73803958 Click to see COC(=O)C1=CC23CCC14C5(C2N(CC5)CC=C3)C6=C(N4)C7=C(C=C6)OCO7 378.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
Venalstonine 426061 Click to see COC(=O)C1CC23CCC14C5(C2N(CC5)CC=C3)C6=CC=CC=C6N4 336.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
methyl (1R,9R,10R,13S,14R,15R,20S)-9,14,15-trihydroxy-6-methoxy-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2(7),3,5-triene-10-carboxylate 12116553 Click to see COC1=CC=CC2=C1NC3(C24CCN5C4C6(CCC3(C6)C(=O)OC)C(C(C5)O)O)O 416.50 unknown https://doi.org/10.1002/HLCA.200490092
https://doi.org/10.1002/CHIN.200435197
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
methyl (1R,9R,10R,13S,14S,20S)-9,14-dihydroxy-6-methoxy-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2(7),3,5-triene-10-carboxylate 12116552 Click to see COC1=CC=CC2=C1NC3(C24CCN5C4C6(CCC3(C6)C(=O)OC)C(CC5)O)O 400.50 unknown https://doi.org/10.1002/CHIN.200435197
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
https://doi.org/10.1002/HLCA.200490092
Methyl 9,14,15-trihydroxy-6-methoxy-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2(7),3,5-triene-10-carboxylate 85434782 Click to see COC1=CC=CC2=C1NC3(C24CCN5C4C6(CCC3(C6)C(=O)OC)C(C(C5)O)O)O 416.50 unknown https://doi.org/10.1002/HLCA.200490092
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
> Alkaloids and derivatives / Pleiocarpaman alkaloids
methyl (13E,14S,16S,18R)-13-ethylidene-18-(hydroxymethyl)-1,11-diazapentacyclo[12.3.1.02,7.08,17.011,16]octadeca-2,4,6,8(17)-tetraene-18-carboxylate 163187529 Click to see CC=C1CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)(CO)C(=O)OC 352.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
methyl (13E)-13-ethylidene-1,11-diazapentacyclo[12.3.1.02,7.08,17.011,16]octadeca-2,4,6,8(17)-tetraene-18-carboxylate 12314382 Click to see CC=C1CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)C(=O)OC 322.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
methyl (13Z,14S,16S,18R)-13-ethylidene-1,11-diazapentacyclo[12.3.1.02,7.08,17.011,16]octadeca-2,4,6,8(17)-tetraene-18-carboxylate 163087785 Click to see CC=C1CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)C(=O)OC 322.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
Pleiocarpamine 5385014 Click to see CC=C1CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)C(=O)OC 322.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
> Alkaloids and derivatives / Strychnos alkaloids
methyl (1S,9S,14E,15R,17S,18R)-14-ethylidene-2,12-diazapentacyclo[13.2.1.01,9.03,8.012,17]octadeca-3,5,7-triene-18-carboxylate 163186535 Click to see CC=C1CN2CCC3C4=CC=CC=C4NC35C2CC1C5C(=O)OC 324.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
2-Hydroxyheptanoic acid 2750949 Click to see CCCCCC(C(=O)O)O 146.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
https://doi.org/10.1002/HLCA.200490092
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
(+)-Pachysandrine B 12313883 Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4OC(=O)C)N(C)C(=O)C=C(C)C)C)C)N(C)C 500.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Hydroisoflavone B 46879794 Click to see C1CC(CC(C1O)O)(C2=COC3=CC(=CC(=C3C2=O)O)O)O 308.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
> Organoheterocyclic compounds / Indoles and derivatives
(5R,17S)-5-ethyl-17-hydroxy-1,9-diazatetracyclo[8.6.1.05,17.011,16]heptadeca-9,11,13,15-tetraen-2-one 24860012 Click to see CCC12CCCN=C3C1(N(C(=O)CC2)C4=CC=CC=C43)O 284.35 unknown https://doi.org/10.1016/J.TETLET.2004.02.142
5-Ethyl-17-hydroxy-1,9-diazatetracyclo[8.6.1.05,17.011,16]heptadeca-9,11,13,15-tetraen-2-one 74335957 Click to see CCC12CCCN=C3C1(N(C(=O)CC2)C4=CC=CC=C43)O 284.35 unknown https://doi.org/10.1016/J.TETLET.2004.02.142
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
methyl (13E)-13-ethylidene-15-(hydroxymethyl)-18-oxa-8,11-diazapentacyclo[7.6.3.110,14.01,9.02,7]nonadeca-2,4,6-triene-15-carboxylate 6266785 Click to see CC=C1CNC2CC1C(C34C2(NC5=CC=CC=C53)OCC4)(CO)C(=O)OC 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
methyl (1R,19S)-5-methoxy-8,16-diazahexacyclo[10.6.1.110,12.01,9.02,7.016,19]icosa-2(7),3,5,13-tetraene-10-carboxylate 101733514 Click to see COC1=CC2=C(C=C1)C34CCN5C3C6(CC(C6)(C4N2)C(=O)OC)C=CC5 352.40 unknown https://doi.org/10.1002/CHIN.200435197
methyl (1R,9R,10R,13R,20S)-9-hydroxy-6-methoxy-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2(7),3,5,14-tetraene-10-carboxylate 12116551 Click to see COC1=CC=CC2=C1NC3(C24CCN5C4C6(CCC3(C6)C(=O)OC)C=CC5)O 382.50 unknown https://doi.org/10.1002/HLCA.200490092
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
https://doi.org/10.1002/CHIN.200435197
methyl (1S,9R,10R,13E,14R,15S)-13-ethylidene-15-(hydroxymethyl)-18-oxa-8,11-diazapentacyclo[7.6.3.110,14.01,9.02,7]nonadeca-2,4,6-triene-15-carboxylate 163194052 Click to see CC=C1CNC2CC1C(C34C2(NC5=CC=CC=C53)OCC4)(CO)C(=O)OC 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
methyl (1S,9R,10R,13E,14S,15S)-13-ethylidene-15-(hydroxymethyl)-18-oxa-8,11-diazapentacyclo[7.6.3.110,14.01,9.02,7]nonadeca-2,4,6-triene-15-carboxylate 163194050 Click to see CC=C1CNC2CC1C(C34C2(NC5=CC=CC=C53)OCC4)(CO)C(=O)OC 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
methyl (1S,9S,10R,13R,20S)-5-methoxy-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2(7),3,5,14-tetraene-10-carboxylate 12116556 Click to see COC1=CC2=C(C=C1)C34CCN5C3C6(CCC(C6)(C4N2)C(=O)OC)C=CC5 366.50 unknown https://doi.org/10.1002/HLCA.200490092
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
Methyl 9-hydroxy-6-methoxy-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2(7),3,5,14-tetraene-10-carboxylate 85434780 Click to see COC1=CC=CC2=C1NC3(C24CCN5C4C6(CCC3(C6)C(=O)OC)C=CC5)O 382.50 unknown https://doi.org/10.1002/HLCA.200490092
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
methyl (1R,10R,13R,20S)-6-methoxy-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2(7),3,5,8,14-pentaene-10-carboxylate 12116555 Click to see COC1=CC=CC2=C1N=C3C24CCN5C4C6(CCC3(C6)C(=O)OC)C=CC5 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
https://doi.org/10.1002/HLCA.200490092
methyl (1R,10R,13R,20S)-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2,4,6,8,14-pentaene-10-carboxylate 12116554 Click to see COC(=O)C12CCC3(C1)C=CCN4C3C5(C2=NC6=CC=CC=C65)CC4 334.40 unknown https://doi.org/10.1002/HLCA.200490092
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
methyl (1R,19S)-6-methoxy-8,16-diazahexacyclo[10.6.1.110,12.01,9.02,7.016,19]icosa-2(7),3,5,8,13-pentaene-10-carboxylate 101733513 Click to see COC1=CC=CC2=C1N=C3C24CCN5C4C6(CC3(C6)C(=O)OC)C=CC5 350.40 unknown https://doi.org/10.1002/CHIN.200435197
methyl (1R,19S)-8,16-diazahexacyclo[10.6.1.110,12.01,9.02,7.016,19]icosa-2,4,6,8,13-pentaene-10-carboxylate 101733512 Click to see COC(=O)C12CC3(C1)C=CCN4C3C5(C2=NC6=CC=CC=C65)CC4 320.40 unknown https://doi.org/10.1002/CHIN.200435197
Methyl 6-methoxy-8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2(7),3,5,8,14-pentaene-10-carboxylate 162889493 Click to see COC1=CC=CC2=C1N=C3C24CCN5C4C6(CCC3(C6)C(=O)OC)C=CC5 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
https://doi.org/10.1002/HLCA.200490092
Methyl 8,17-diazahexacyclo[11.6.1.110,13.01,9.02,7.017,20]henicosa-2,4,6,8,14-pentaene-10-carboxylate 162913872 Click to see COC(=O)C12CCC3(C1)C=CCN4C3C5(C2=NC6=CC=CC=C65)CC4 334.40 unknown https://doi.org/10.1002/HLCA.200490092
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(1R,8R,9S,16S)-8,16-bis(4-hydroxyphenyl)-9-[(1S,8S,9S,16R)-4,6,12-trihydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaen-9-yl]-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol 162891434 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7C(C8=C(C=C(C=C8O)O)C9C(OC1=CC(=CC7=C91)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 906.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.027
https://doi.org/10.1002/HLCA.200490092

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