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Hunteria umbellata

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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 UUID643fdf4885da1291496327
Scientific name Hunteria umbellata
Authority Hallier f.
First published in Jahrb. Hamburg. Wiss. Anst. 17: 190 (1899)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hunteria eburnea Pichon Bol. Soc. Brot. , sér. 2, 27: 91 (1953)
Hunteria elliotii (Stapf) Pichon Bol. Soc. Brot. , sér. 2, 27: 97 (1953)
Hunteria mayumbensis Pichon Bol. Soc. Brot. , sér. 2, 27: 95 (1953)
Picralima elliotii Stapf Bull. Misc. Inform. Kew 1908: 302 (1908)
Picralima gracilis A.Chev. Explor. Bot. Afrique Occ. Franç. 1: 427 (1920)
Picralima umbellata Stapf Bull. Misc. Inform. Kew 1908: 302 (1908)
Polyadoa elliotii Stapf Fl. Trop. Afr. 4(1): 104 (1902)
Polyadoa umbellata Stapf Fl. Trop. Afr. 4(1): 103 (1902)
Carpodinus umbellata K.Schum. Bot. Jahrb. Syst. 23: 221 (1896)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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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
  • Africa
    • West Tropical Africa
      • Benin
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Nigeria
      • Senegal
      • Sierra Leone
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000215682
Tropicos 1805274
KEW urn:lsid:ipni.org:names:79368-1
The Plant List kew-100819
Open Tree Of Life 516429
NCBI Taxonomy 141571
IUCN Red List 136108289
IPNI 79368-1
GBIF 5536469
Freebase /m/0wfrhl2
EPPO HUJUM
Wikipedia Hunteria_umbellata

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
Jatonik polyherbal mixture induced rat liver MMPT pore opening in normal Wistar rat: In vitro and in vivo studies Folashade OP, Boyenle ID, Oyedeji TA, Ojeniyi FD, Damilare AA, Ehigie LO, Ehigie AF Chin Herb Med 16-Oct-2023
PMCID:PMC10874763
doi:10.1016/j.chmed.2023.06.002
PMID:38375053
Traditional knowledge of plants used in hunting and fishing practices among Baka hunter-gatherers of eastern Cameroon Fongnzossie EF, Ngansop MT, Oishi T, Biwole AB, Biye EH, Ichikawa M J Ethnobiol Ethnomed 03-Jan-2023
PMCID:PMC9808952
doi:10.1186/s13002-022-00571-3
PMID:36597154
Angiotensin converting enzyme inhibitors from medicinal plants: a molecular docking and dynamic simulation approach Fadahunsi OS, Olorunnisola OS, Adegbola PI, Subair TI, Elegbeleye OE In Silico Pharmacol 13-Oct-2022
PMCID:PMC9561457
doi:10.1007/s40203-022-00135-z
PMID:36245815
Wandering through southwestern Nigeria: An inventory of Yoruba useful angiosperm plants Ajao AA, Mukaila YO, Sabiu S Heliyon 25-Dec-2021
PMCID:PMC8733184
doi:10.1016/j.heliyon.2021.e08668
PMID:35024488
Evaluation of Male Fertility-Enhancing Activities of Water Seed Extract of Hunteria umbellata in Wistar Rats Adeneye AA, Olagunju JA, Murtala BA Evid Based Complement Alternat Med 14-Aug-2019
PMCID:PMC6710732
doi:10.1155/2019/7693010
PMID:31485248
Medicinal plants for the treatment of obesity: ethnopharmacological approach and chemical and biological studies de Freitas Junior LM, de Almeida Jr EB Am J Transl Res 15-May-2017
PMCID:PMC5446492
PMID:28559960
Effects of Natural Products on Fructose-Induced Nonalcoholic Fatty Liver Disease (NAFLD) Chen Q, Wang T, Li J, Wang S, Qiu F, Yu H, Zhang Y, Wang T Nutrients 31-Jan-2017
PMCID:PMC5331527
doi:10.3390/nu9020096
PMID:28146130
Flavonoid C-glucosides Derived from Flax Straw Extracts Reduce Human Breast Cancer Cell Growth In vitro and Induce Apoptosis Czemplik M, Mierziak J, Szopa J, Kulma A Front Pharmacol 31-Aug-2016
PMCID:PMC5006111
doi:10.3389/fphar.2016.00282
PMID:27630565
Antihyperglycemic Profile of Erinidine Isolated from Hunteria Umbellata Seed Adeneye Adejuwon A, Crooks PA, Fadhel-Albayati Z, Miller AF, Zito SW, Adeyemi OO, Agbaje EO Afr J Tradit Complement Altern Med 31-Dec-2012
PMCID:PMC3746566
PMID:24146442
Ikirydinium A: a new indole alkaloid from the seeds of Hunteria umbellata (K. Schum) Olusegun S. Ajala, Andrew M. Piggott, Fabien Plisson, Zeinab Khalil, Xiao-cong Huang, Sunday A. Adesegun, Herbert A.B. Coker, Robert J. Capon Elsevier BV 26-Oct-2011
doi:10.1016/J.TETLET.2011.10.106
The Novel Antihyperglycaemic Action of Hunteria Umbellata Seed Fractions Mediated Via Intestinal Glucose Uptake Inhibition Adeneye AA, Adeyemi OO, Agbaje E, Sofidiya MO Afr J Tradit Complement Altern Med 02-Oct-2011
PMCID:PMC3744210
doi:10.4314/ajtcam.v9i1.3
PMID:23983315
Evaluation of Glycemic and Lipid Profile of Offspring of Diabetic Wistar Rats Treated with Malpighia emarginata Juice Barbalho SM, Damasceno DC, Spada AP, Palhares M, Martuchi KA, Oshiiwa M, Sazaki V, da Silva VS Exp Diabetes Res 23-Jan-2011
PMCID:PMC3034956
doi:10.1155/2011/173647
PMID:21318139
Uterotonic Plants and their Bioactive Constituents Gruber CW, O’Brien M Planta Med 15-Sep-2010
PMCID:PMC3407953
doi:10.1055/s-0030-1250317
PMID:20845261
Evaluation of the Toxicity and Reversibility Profile of the Aqueous Seed Extract of Hunteria Umbellata (K. Schum.) Hallier F. in Rodents Adeneye A, Adeyemi O, Agbaje E, Banjo A Afr J Tradit Complement Altern Med 03-Jul-2010
PMCID:PMC3005394
doi:10.4314/ajtcam.v7i4.56704
PMID:21731167
The Alkaloids of Hunteria eburnea Pichon. III.<sup>1</sup> The Tertiary Bases M. F. Bartlett, R. Sklar, A. F. Smith, W. I. Taylor American Chemical Society (ACS) 29-May-2007
doi:10.1021/JO01044A011

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
(1S,2R,3R,5R,6E,7S,8R,9S,10S)-6-ethylidene-3,5,9-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12,14,16-triene-2-carboxylic acid 163186253 Click to see CC=C1C2C(C(C34C(C2(C(OC1O)O)C(=O)O)(CCN3C)C5=CC=CC=C5N4C)O)C(C)C 458.50 unknown https://doi.org/10.1016/S0031-9422(00)81309-6
(1S,2R,3R,6E,7S,8R,9S,10S)-6-ethylidene-3,9,13-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12(17),13,15-triene-2-carboxylic acid 163190978 Click to see CC=C1COC(C2(C1C(C(C34C2(CCN3C)C5=C(N4C)C(=CC=C5)O)O)C(C)C)C(=O)O)O 458.50 unknown https://doi.org/10.1016/S0031-9422(00)81309-6
(1S,2R,5S,6E,7S,8R,9S,10S)-6-ethylidene-5,9,13-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12(17),13,15-triene-2-carboxylic acid 163186049 Click to see CC=C1C2C(C(C34C(C2(COC1O)C(=O)O)(CCN3C)C5=C(N4C)C(=CC=C5)O)O)C(C)C 458.50 unknown https://doi.org/10.1016/S0031-9422(00)81309-6
(1S,2R,6E,7S,8R,9S,10S)-6-ethylidene-9,13,16-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12,14,16-triene-2-carboxylic acid 163186404 Click to see CC=C1COCC2(C1C(C(C34C2(CCN3C)C5=C(C=CC(=C5N4C)O)O)O)C(C)C)C(=O)O 458.50 unknown https://doi.org/10.1016/S0031-9422(00)81309-6
6-Ethylidene-3,5,9-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12,14,16-triene-2-carboxylic acid 163009831 Click to see CC=C1C2C(C(C34C(C2(C(OC1O)O)C(=O)O)(CCN3C)C5=CC=CC=C5N4C)O)C(C)C 458.50 unknown https://doi.org/10.1016/S0031-9422(00)81309-6
6-Ethylidene-3,9,13-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12(17),13,15-triene-2-carboxylic acid 163034778 Click to see CC=C1COC(C2(C1C(C(C34C2(CCN3C)C5=C(N4C)C(=CC=C5)O)O)C(C)C)C(=O)O)O 458.50 unknown https://doi.org/10.1016/S0031-9422(00)81309-6
6-Ethylidene-5,9,13-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12(17),13,15-triene-2-carboxylic acid 162966476 Click to see CC=C1C2C(C(C34C(C2(COC1O)C(=O)O)(CCN3C)C5=C(N4C)C(=CC=C5)O)O)C(C)C 458.50 unknown https://doi.org/10.1016/S0031-9422(00)81309-6
6-Ethylidene-9,13,16-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12,14,16-triene-2-carboxylic acid 162982973 Click to see CC=C1COCC2(C1C(C(C34C2(CCN3C)C5=C(C=CC(=C5N4C)O)O)O)C(C)C)C(=O)O 458.50 unknown https://doi.org/10.1016/S0031-9422(00)81309-6
> Alkaloids and derivatives / Aspidofractine alkaloids
6H,13aH-3a,5a-Ethano-1H-indolizino[8,1-cd]carbazole, 2,3,4,5,11,12-hexahydro-, [10bR-(10bR*,13aS*)]- 534349 Click to see C1CC23CCC4(CC2)C5(C3N(C1)CC5)C6=CC=CC=C6N4 280.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
Kopsinine 7069830 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4 338.40 unknown https://doi.org/10.1016/S0031-9422(00)89713-7
https://doi.org/10.1016/0031-9422(80)83012-3
Methyl aspidofractinine-3-carboxylate 573380 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4 338.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
Pleiocarpine 101650372 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)N(C6=CC=CC=C65)C(=O)OC)CC4 396.50 unknown https://doi.org/10.1016/0031-9422(76)85107-2
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
(+)-Vincadifformine 811594 Click to see CCC12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC 338.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
Methyl 2,3-didehydroaspidospermidine-3-carboxylate 579873 Click to see CCC12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC 338.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
Vincadifformine 94255 Click to see CCC12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0031-9422(00)89713-7
> Alkaloids and derivatives / Corynanthean-type alkaloids
CID 436036 436036 Click to see CC=C1CN2CCC34C5=CC=CC=C5N(C36C2CC1C4(CO6)C(=O)OC)C 366.50 unknown https://doi.org/10.1016/J.TETLET.2011.10.106
Pseudoakuammigine 90479136 Click to see CC=C1CN2CCC34C5=CC=CC=C5N(C36C2CC1C4(CO6)C(=O)OC)C 366.50 unknown https://doi.org/10.1016/J.TETLET.2011.10.106
> Alkaloids and derivatives / Eburnan-type alkaloids
(15R,17S,19R)-17-ethoxy-15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene 163020494 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)OCC 324.50 unknown https://doi.org/10.1016/0031-9422(80)83012-3
14,15-Didehydro-12-methoxyvincamine 181142 Click to see CCC12CC(N3C4=C(CCN(C41)CC=C2)C5=C3C(=CC=C5)OC)(C(=O)OC)O 382.50 unknown https://doi.org/10.1016/S0031-9422(00)89713-7
17-Ethoxy-15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene 163020493 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)OCC 324.50 unknown https://doi.org/10.1016/0031-9422(80)83012-3
1H-Indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine, 13a-ethyl-2,3,5,6,13a,13b-hexahydro- 610470 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C=C2 278.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
Eburnamenin-14-ol, 14,15-dihydro-, (14alpha)- 442066 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
https://doi.org/10.1021/JO01044A011
https://doi.org/10.1016/S0031-9422(00)89713-7
Eburnamenin-14-ol, 14,15-dihydro-, (14beta)- 619344 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
Eburnamenin-14(15H)-one 92112 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(=O)C2 294.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
Eburnamenine 6857502 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C=C2 278.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
https://doi.org/10.1021/JO01044A011
Eburnamine 101699 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
Eburnamonine 3195 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(=O)C2 294.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
> Alkaloids and derivatives / Pleiocarpaman alkaloids
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/10.1016/0031-9422(80)83012-3
Pleiocarpamine 5385014 Click to see CC=C1CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)C(=O)OC 322.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
> Alkaloids and derivatives / Quebrachamine alkaloids
Kamassine 624708 Click to see CCC12CCCN(C1)CCC3=C(CC2)NC4=CC=CC=C34 282.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
Quebrachamine 92990 Click to see CCC12CCCN(C1)CCC3=C(CC2)NC4=CC=CC=C34 282.40 unknown https://doi.org/10.1016/0031-9422(80)83012-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Alepterolic acid 13858188 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCC(C2(C)C)O)C 320.50 unknown https://doi.org/10.1016/0031-9422(80)83012-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-[3-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-8,9a-dihydroxy-3a,5b-dimethyl-2,3,4,5,5a,6,7,8,9,10,10a,10b-dodecahydro-1H-cyclopenta[a]fluoren-10-yl]ethanone 163079701 Click to see CCC(CC(C(C)C1CCC2C1(CCC3C2C(C4(C3(CCC(C4)O)C)O)C(=O)C)C)O)C(C)C 476.70 unknown https://doi.org/10.1016/S0031-9422(00)81309-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
3-ethenyl-4-(2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-ylmethyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid 73806906 Click to see C=CC1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)O)CC3C4=C(CCN3)C5=CC=CC=C5N4 516.50 unknown https://doi.org/10.1016/J.TETLET.2011.10.106
Strictosidinic acid 21586927 Click to see C=CC1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)O)CC3C4=C(CCN3)C5=CC=CC=C5N4 516.50 unknown https://doi.org/10.1016/J.TETLET.2011.10.106
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.TETLET.2011.10.106
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.TETLET.2011.10.106
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Prinoidin 25107461 Click to see CC1C(C(C(C(O1)OC2=CC3=C(C(=C2)O)C(=O)C4=C(C3)C=C(C=C4O)C)OC(=O)C)OC(=O)C)O 486.50 unknown https://doi.org/10.1016/S0031-9422(00)81309-6
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
Daurichromene A 10043035 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)CCC(C(=C)C)O)O 342.50 unknown https://doi.org/10.1016/S0031-9422(00)81309-6
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1S,2R,3R,6Z,7S,9S,10S)-6-ethylidene-3-hydroxy-11,20-dimethyl-4,21-dioxa-11,20-diazahexacyclo[8.7.3.22,9.01,10.02,7.012,17]docosa-12,14,16-trien-22-one 163189027 Click to see CC=C1COC(C23C1CC(C45C2(CCN4C)C6=CC=CC=C6N5C)OC3=O)O 382.50 unknown https://doi.org/10.1016/0040-4020(67)80028-0
1H,9H-1,4-Ethano-9a,4a-(iminoethano)pyrano[3,4-b]indole-13-acetic acid, alpha-ethylidene-3,4-dihydro-4-(hydroxymethyl)-9,10-dimethyl-3-oxo-, methyl ester, (alphaE,1R,4R,4aR,9aR)- 162944240 Click to see CC=C(C1CC2C34C(C1(C(=O)O2)CO)(CCN3C)C5=CC=CC=C5N4C)C(=O)OC 412.50 unknown https://doi.org/10.1002/HLCA.19680510627
6-Ethylidene-3-hydroxy-11,20-dimethyl-4,21-dioxa-11,20-diazahexacyclo[8.7.3.22,9.01,10.02,7.012,17]docosa-12,14,16-trien-22-one 604323 Click to see CC=C1COC(C23C1CC(C45C2(CCN4C)C6=CC=CC=C6N5C)OC3=O)O 382.50 unknown https://doi.org/10.1016/0040-4020(67)80028-0
Dihydrocorymine, epi-3 6038603 Click to see CC=C1CN2CCC34C2(C(CC1C3(CO)C(=O)OC)O)N(C5=CC=CC=C45)C 384.50 unknown https://doi.org/10.1016/S0031-9422(00)89713-7
methyl (1R,2S,10S,15E,16S,17R,18R)-18-acetyloxy-15-ethylidene-3-methyl-19-oxa-3,13-diazahexacyclo[14.3.1.02,10.02,13.04,9.010,17]icosa-4,6,8-triene-17-carboxylate 163186250 Click to see CC=C1CN2CCC34C2(C5CC1C3(C(O5)OC(=O)C)C(=O)OC)N(C6=CC=CC=C46)C 424.50 unknown https://doi.org/10.1016/0040-4020(67)80028-0
methyl (1R,2S,10S,15E,16S,17R,18S)-15-ethylidene-18-hydroxy-3-methyl-19-oxa-3,13-diazahexacyclo[14.3.1.02,10.02,13.04,9.010,17]icosa-4,6,8-triene-17-carboxylate 163186533 Click to see CC=C1CN2CCC34C2(C5CC1C3(C(O5)O)C(=O)OC)N(C6=CC=CC=C46)C 382.50 unknown https://doi.org/10.1016/0040-4020(67)80028-0
methyl (1R,2S,10S,16S,17R,18R)-18-acetyloxy-15-ethylidene-3-methyl-19-oxa-3,13-diazahexacyclo[14.3.1.02,10.02,13.04,9.010,17]icosa-4,6,8-triene-17-carboxylate 163100971 Click to see CC=C1CN2CCC34C2(C5CC1C3(C(O5)OC(=O)C)C(=O)OC)N(C6=CC=CC=C46)C 424.50 unknown https://doi.org/10.1016/0040-4020(67)80028-0
methyl (1R,2S,10S,16S,17R,18S)-15-ethylidene-18-hydroxy-3-methyl-19-oxa-3,13-diazahexacyclo[14.3.1.02,10.02,13.04,9.010,17]icosa-4,6,8-triene-17-carboxylate 162937613 Click to see CC=C1CN2CCC34C2(C5CC1C3(C(O5)O)C(=O)OC)N(C6=CC=CC=C46)C 382.50 unknown https://doi.org/10.1016/0040-4020(67)80028-0
methyl (1S,9S,10R,12S,13E,18R)-13-ethylidene-10-hydroxy-18-(hydroxymethyl)-8-methyl-8,15-diazapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-triene-18-carboxylate 163186985 Click to see CC=C1CN2CCC34C2(C(CC1C3(CO)C(=O)OC)O)N(C5=CC=CC=C45)C 384.50 unknown https://doi.org/10.1016/S0031-9422(00)89713-7
methyl (1S,9S,10S,12S,13E,18R)-13-ethylidene-10-hydroxy-18-(hydroxymethyl)-8-methyl-8,15-diazapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-triene-18-carboxylate 163186986 Click to see CC=C1CN2CCC34C2(C(CC1C3(CO)C(=O)OC)O)N(C5=CC=CC=C45)C 384.50 unknown https://doi.org/10.1016/S0031-9422(00)89713-7
methyl (E)-2-[(1S,9S,10R,13S,17S)-13-(hydroxymethyl)-8,16-dimethyl-12-oxo-11-oxa-8,16-diazapentacyclo[7.4.3.210,13.01,9.02,7]octadeca-2,4,6-trien-17-yl]but-2-enoate 163193264 Click to see CC=C(C1CC2C34C(C1(C(=O)O2)CO)(CCN3C)C5=CC=CC=C5N4C)C(=O)OC 412.50 unknown https://doi.org/10.1002/HLCA.19680510627
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
1,7-Bis(3,4-dihydroxyphenyl)heptan-3-one 11573476 Click to see C1=CC(=C(C=C1CCCCC(=O)CCC2=CC(=C(C=C2)O)O)O)O 330.40 unknown https://doi.org/10.1016/S0031-9422(00)81309-6

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