Tabernaemontana pachysiphon - Unknown
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Internal ID UUID643fee8296c7b299473938
Scientific name Tabernaemontana pachysiphon
Authority Stapf
First published in Bull. Misc. Inform. Kew 1894: 22 (1894)

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Synonyms Top

Scientific name Authority First published in
Sarcopharyngia angolensis (Stapf) L.Allorge Mém. Mus. Natl. Hist. Nat., B, Bot. 30: 180 (1985)
Tabernaemontana angolensis Stapf Bull. Misc. Inform. Kew 1894: 23 (1894)
Tabernaemontana holstii K.Schum. Pflanzenw. Ost-Afrikas , C: 317 (1895)
Voacanga dichotoma K.Schum. Pflanzenw. Ost-Afrikas , C: 317 (1895)
Tabernaemontana pachysiphon var. cumminsii (Stapf) H.Huber Kew Bull. 15: 438. 1962
Conopharyngia angolensis Stapf Fl. Trop. Afr. 4(1): 146 (1902)
Conopharyngia cumminsii Stapf Fl. Trop. Afr. 4(1): 145 (1902)
Conopharyngia holstii Stapf Fl. Trop. Afr. 4(1): 146 (1902)
Conopharyngia pachysiphon Stapf Fl. Trop. Afr. 4(1): 146 (1902)

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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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Zambia
    • West Tropical Africa
      • Benin
      • Ghana
      • Nigeria
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000320031
Tropicos 1805687
KEW urn:lsid:ipni.org:names:82263-1
The Plant List kew-200853
Open Tree Of Life 94846
NCBI Taxonomy 403125
IUCN Red List 146206475
IPNI 82263-1
iNaturalist 132899
GBIF 3615365
Freebase /m/0wjtl53
USDA GRIN 464351
Wikipedia Tabernaemontana_pachysiphon

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
Tree species composition along environmental and disturbance gradients in tropical sub-montane forests, Tanzania Lolila NJ, Shirima DD, Mauya EW PLoS One 08-Mar-2023
PMCID:PMC9994703
doi:10.1371/journal.pone.0282528
PMID:36888683
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Environmental Factors Regulate Plant Secondary Metabolites Qaderi MM, Martel AB, Strugnell CA Plants (Basel) 18-Jan-2023
PMCID:PMC9920071
doi:10.3390/plants12030447
PMID:36771531
Indole-Containing Natural Products 2019–2022: Isolations, Reappraisals, Syntheses, and Biological Activities Umer SM, Solangi M, Khan KM, Saleem RS Molecules 05-Nov-2022
PMCID:PMC9655573
doi:10.3390/molecules27217586
PMID:36364413
Floristic composition and turnover analysis in Dahomey Gap and the surrounding sub‐humid Togolese mountain minor forest refuges: Importance for biogeography and biodiversity conservation in sub‐Saharan Africa Adjossou K, Kokou K, Deconchat M Ecol Evol 04-Oct-2022
PMCID:PMC9532220
doi:10.1002/ece3.9304
PMID:36225837
Repellent activity against Anopheles gambiae of the leaves of nesting trees in the Sebitoli chimpanzee community of Kibale National Park, Uganda Lacroux C, Pouydebat E, Rossignol M, Durand S, Aleeje A, Asalu E, Chandre F, Krief S Malar J 27-Sep-2022
PMCID:PMC9513939
doi:10.1186/s12936-022-04291-7
PMID:36163024
Effects of Light on Secondary Metabolite Biosynthesis in Medicinal Plants Zhang S, Zhang L, Zou H, Qiu L, Zheng Y, Yang D, Wang Y Front Plant Sci 10-Dec-2021
PMCID:PMC8702564
doi:10.3389/fpls.2021.781236
PMID:34956277
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465
Major Bioactive Alkaloids and Biological Activities of Tabernaemontana Species (Apocynaceae) Naidoo CM, Naidoo Y, Dewir YH, Murthy HN, El-Hendawy S, Al-Suhaibani N Plants (Basel) 05-Feb-2021
PMCID:PMC7915066
doi:10.3390/plants10020313
PMID:33562893
Effects of Nutrient Fertility on Growth and Alkaloidal Content in Mitragyna speciosa (Kratom) Zhang M, Sharma A, León F, Avery B, Kjelgren R, McCurdy CR, Pearson BJ Front Plant Sci 21-Dec-2020
PMCID:PMC7779599
doi:10.3389/fpls.2020.597696
PMID:33408731
On the hunt for the alternate host of Hemileia vastatrix Koutouleas A, Jørgen Lyngs Jørgensen H, Jensen B, Lillesø JB, Junge A, Ræbild A Ecol Evol 23-Nov-2019
PMCID:PMC6912922
doi:10.1002/ece3.5755
PMID:31871671
Indole alkaloids and anti-nociceptive mechanisms of Tabernaemontana divaricata (L.) R. Br. flower methanolic extract. Ali Khan MS, Misbah, Ahmed N, Arifuddin M, Rehman A, Ling MP Food Chem Toxicol 01-Aug-2018
doi:10.1016/J.FCT.2018.06.007
PMID:29883785
Formation and Change of Chloroplast-Located Plant Metabolites in Response to Light Conditions Chen Y, Zhou B, Li J, Tang H, Tang J, Yang Z Int J Mol Sci 26-Feb-2018
PMCID:PMC5877515
doi:10.3390/ijms19030654
PMID:29495387
Traditional knowledge on wild and cultivated plants in the Kilombero Valley (Morogoro Region, Tanzania) Salinitro M, Vicentini R, Bonomi C, Tassoni A J Ethnobiol Ethnomed 09-Mar-2017
PMCID:PMC5345176
doi:10.1186/s13002-017-0146-y
PMID:28279174
Chimpanzees (Pan troglodytes) Flexibly Use Introduced Species for Nesting and Bark Feeding in a Human-Dominated Habitat McCarthy MS, Lester JD, Stanford CB Int J Primatol 16-Sep-2016
PMCID:PMC5422490
doi:10.1007/s10764-016-9916-y
PMID:28546652

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 / Aspidospermatan-type alkaloids
Lochnericine 11382599 Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=CC=CC=C6N3)C(=O)OC 352.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
> Alkaloids and derivatives / Corynanthean-type alkaloids
Epiisositsirikine 6442570 Click to see CC=C1CN2CCC3=C(C2CC1C(CO)C(=O)OC)NC4=CC=CC=C34 354.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
Isositsirikine 6436828 Click to see CC=C1CN2CCC3=C(C2CC1C(CO)C(=O)OC)NC4=CC=CC=C34 354.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
methyl (2R)-2-[(2R,3Z,12bS)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]-3-hydroxypropanoate 6504264 Click to see CC=C1CN2CCC3=C(C2CC1C(CO)C(=O)OC)NC4=CC=CC=C34 354.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
> Alkaloids and derivatives / Ibogan-type alkaloids
(1R,10R,15R,17S,18S)-17-ethyl-6,7-dimethoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2,4,6,8-tetraene 163106244 Click to see CCC1CC2CC3C1N(C2)CCC4C3=NC5=CC(=C(C=C45)OC)OC 340.50 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
12,13-Dimethoxyibogamine 193302 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)OC 340.50 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
Conodurine B640243K102 5477056 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC 704.90 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
Ibogamine-18-carboxylic acid, 12-methoxy-, methyl ester 363270 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1016/J.FCT.2018.06.007
Ibogamine-18-carboxylic acid, 13-methoxy-, methyl ester 99199 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
Isovoacangine 44393473 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1055/S-2006-957393
https://doi.org/10.1016/S0031-9422(00)83488-3
methyl (1R,15S,17R,18R)-17-ethyl-7-[(1S,12R,14R,15E,18R)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 162846696 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC 704.90 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
methyl (1S,10S,15R,17S,18S)-17-ethyl-10-hydroxy-6,7-dimethoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2,4,6,8-tetraene-1-carboxylate 101930203 Click to see CCC1CC2CC3(C1N(C2)CCC4(C3=NC5=CC(=C(C=C54)OC)OC)O)C(=O)OC 414.50 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
methyl (1S,15R,17S,18S)-17-(1-hydroxyethyl)-6,7-dimethoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 138114025 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)OC)C(=O)OC)O 414.50 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
methyl (1S,15R,17S,18S)-17-ethyl-14-oxo-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 131878933 Click to see CCC1CC2CC3(C1N(C2=O)CCC4=C3NC5=CC=CC=C45)C(=O)OC 352.40 unknown https://doi.org/10.1002/JPS.2600660821
methyl (1S,15R,17S,18S)-17-ethyl-6-[(1R,15E,18S)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 137628555 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)C(=O)OC 704.90 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
methyl (1S,15R,17S,18S)-17-ethyl-7-[(1S,12R,14R,15Z,18S)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 101603227 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC 704.90 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
methyl (1S,15R,18S)-17-ethyl-6,7-dimethoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 137706033 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)OC)C(=O)OC 398.50 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
methyl (1S,15S,17R,18R)-17-ethyl-7-[(1S,12S,14R,15Z,18S)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-hydroxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 163068193 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)O)C(=O)OC 690.90 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
methyl (1S,15S,17S,18S)-17-ethyl-5-[(1S,12R,14S,15E)-15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl]-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 134714950 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=CC(=C5C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)OC)C(=O)OC 704.90 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
Methyl 17-ethyl-7-(15-ethylidene-18-methoxycarbonyl-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-yl)-6-hydroxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 163068192 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)O)C(=O)OC 690.90 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
Voacamine 11953931 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC(=C(C=C45)OC)C6CC7C(C(CC8=C6NC9=CC=CC=C89)N(CC7=CC)C)C(=O)OC)C(=O)OC 704.90 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
> Alkaloids and derivatives / Macroline alkaloids
(E)-16-Epi-normacusine B 5460548 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)CO 294.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
methyl (12R,14R)-15-ethylidene-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 129317237 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
methyl (1S,12R,13R,14S,15E)-15-ethylidene-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 163189580 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
methyl (1S,14S,15E)-15-ethylidene-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 6436185 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
Normacusine B 5318845 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)CO 294.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
> Alkaloids and derivatives / Strychnos alkaloids
Dihydrocondylocarpine 100004 Click to see CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC 324.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
https://doi.org/10.1055/S-2006-957393
methyl (1S,17R,18S)-18-ethyl-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate 134716702 Click to see CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC 324.40 unknown https://doi.org/10.1055/S-2006-957393
https://doi.org/10.1016/S0031-9422(00)83488-3
Tubotaiwin 9973540 Click to see CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC 324.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
Tubotaiwine N-oxide 431067 Click to see CCC1C2CC[N+]3(C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC)[O-] 340.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
https://doi.org/10.1055/S-2006-957393
> Alkaloids and derivatives / Vallesaman alkaloids
CID 6912322 6912322 Click to see CC=C1CN2CCC1C(=C)C3=C(C2)C4=CC=CC=C4N3 264.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
https://doi.org/10.1211/0022357991777092
https://doi.org/10.1055/S-2006-957393
> Alkaloids and derivatives / Vobasan alkaloids
(1S,14R,15E,18R)-15-ethylidene-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-one 163015309 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2CO)NC4=CC=CC=C34)C 324.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
(1S,14R,15Z,18R)-15-ethylidene-18-(hydroxymethyl)-17-methyl-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraen-12-one 101926661 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2CO)NC4=CC=CC=C34)C 324.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
Affinine 5281345 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2CO)NC4=CC=CC=C34)C 324.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
methyl (1S,14R,15E,18R)-15-ethylidene-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 6436182 Click to see CC=C1CNC2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34 338.40 unknown https://doi.org/10.1002/JPS.2600660821
methyl (1S,14R,15Z,18S)-15-ethylidene-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.03,11.04,9]octadeca-3(11),4,6,8-tetraene-18-carboxylate 101281359 Click to see CC=C1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C 352.40 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Penipacid A 139585900 Click to see CC(=NCC(C)(C)O)NC1=CC=CC=C1C(=O)O 250.29 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/S0031-9422(00)83488-3
> 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/S0031-9422(00)83488-3
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/10.1016/S0031-9422(00)83488-3
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/S0031-9422(00)83488-3

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