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Myrtopsis sellingii

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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 UUID643ffe74688b5125315126
Scientific name Myrtopsis sellingii
Authority Guillaumin
First published in Acta Horti Gothob. 19: 19 (1952)

Description Top

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Synonyms Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000453237
INPN 673759
KEW urn:lsid:ipni.org:names:774460-1
Open Tree Of Life 6126499
IPNI 774460-1
GBIF 5594524
CMAUP NPO9572

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)!
Title Authors Publication Released IDs
Produits neutres et alcaloides de Myrtopsis macrocarpa, M. myrtoidea, M. novae-caledoniae et M. sellingii Mohamed Saïd Hifnawy, Jacqueline Vaquette, Thierry Sévenet, Jean-Louis Pousset, André Cavé Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)86717-5
[Neutral products of Myrtopsis sellingii: two new coumarins, myrsellin and myrsellinol (author's transl)]. Hifnawy MS, Vaquette J, Pousset JL, Cavé A Planta Med 01-Feb-1977
doi:10.1055/S-0028-1097509
PMID:854544
[Alkaloids of Myrtopsis sellingii; a new alkaloid, myrtopsine (author's transl)]. Hifnawy MS, Vaquette J, Sévenet T, Pousset JL, Cavé A Planta Med 01-Jun-1976
doi:10.1055/S-0028-1097674
PMID:959375

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 / Steroids and steroid derivatives
(1S,3aR,5aS,5bR,7aR,9R,11aS,11bS,13aR,13bS)-3a,5a,5b,8,8-pentamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,9,10,11,11a,11b,12,13,13a,13b-hexadecahydro-1H-cyclopenta[a]chrysen-9-ol 163008201 Click to see CC(=C)C1CCC2(C1C3CCC4C5CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C 412.70 unknown https://doi.org/10.1055/S-0028-1097509
3a,5a,5b,8,8-pentamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,9,10,11,11a,11b,12,13,13a,13b-hexadecahydro-1H-cyclopenta[a]chrysen-9-ol 14888883 Click to see CC(=C)C1CCC2(C1C3CCC4C5CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C 412.70 unknown https://doi.org/10.1055/S-0028-1097509
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
24-epi-Pterosterone 11027254 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)O 480.60 unknown via CMAUP database
25S-Inokosterone 12358616 Click to see CC(CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)CO 480.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
Ponasterone A 115127 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O 464.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
22,23-Dihydrobrassicasterol 5283637 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
[(2R,3S,4S,5R,6R)-6-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-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-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl hexadecanoate 13051627 Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(C)C(C)C)C)C)O)O)O 801.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
(3S,8R,9S,10R,13R,14R,17S)-17-[(2R,5R)-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 162965368 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)86717-5
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Sitoindoside I 9832350 Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 815.30 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
(2S,3S)-2-(2-hydroxypropan-2-yl)-4-methoxy-2,3-dihydrofuro[2,3-b]quinolin-3-ol 163024601 Click to see CC(C)(C1C(C2=C(C3=CC=CC=C3N=C2O1)OC)O)O 275.30 unknown https://doi.org/10.1055/S-0028-1097674
https://doi.org/10.1016/S0031-9422(00)86717-5
2-(2-Hydroxypropan-2-yl)-4-methoxy-2,3-dihydrofuro[2,3-b]quinolin-3-ol 21769979 Click to see CC(C)(C1C(C2=C(C3=CC=CC=C3N=C2O1)OC)O)O 275.30 unknown https://doi.org/10.1055/S-0028-1097674
https://doi.org/10.1016/S0031-9422(00)86717-5
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
4-Methoxyfuro(2,3-b)quinolin-7-ol 135438120 Click to see COC1=C2C=COC2=NC3=C1C=CC(=C3)O 215.20 unknown https://doi.org/10.1055/S-0028-1097674
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown https://doi.org/10.1055/S-0028-1097674
Gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown https://doi.org/10.1055/S-0028-1097674
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1055/S-0028-1097674
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methylquinolin-2-one 182073 Click to see CN1C2=CC=CC=C2C(=CC1=O)OC 189.21 unknown https://doi.org/10.1055/S-0028-1097674
4-Methoxy-1H-quinolin-2-one 600167 Click to see COC1=CC(=O)NC2=CC=CC=C21 175.18 unknown https://doi.org/10.1016/S0031-9422(00)86717-5
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3R)-4-[(E)-2-carboxyethenyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid 10316325 Click to see C1=CC(=C(C=C1C2C(C3=C(C=CC(=C3O2)O)C=CC(=O)O)C(=O)O)O)O 358.30 unknown via CMAUP database
(3R,4R,5R)-5-[(2S,3R)-4-[(E)-2-carboxyethenyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carbonyl]oxy-3,4-dihydroxycyclohexene-1-carboxylic acid 10436502 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C2C(OC3=C(C=CC(=C23)C=CC(=O)O)O)C4=CC(=C(C=C4)O)O 514.40 unknown via CMAUP database
Przewalskinic acid A 9975641 Click to see C1=CC(=C(C=C1C2C(C3=C(C=CC(=C3O2)O)C=CC(=O)O)C(=O)O)O)O 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Woodorien 192694 Click to see COC(=O)C1=CC(=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O 330.29 unknown via CMAUP database

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