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Citrus lucida

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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
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Details Top

Internal ID UUID64402323d1eed885894502
Scientific name Citrus lucida
Authority (Scheff.) Mabb.
First published in Blumea 55: 73 (2010)

Description Top

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Synonyms Top

Scientific name Authority First published in
Feronia lucida Scheff. Natuurk. Tijdschr. Ned.-Indië 31: 19 (1869)
Feroniella lucida Swingle. Bull. Soc. Bot. France 59: 781 (1912 publ. 1913)
Feroniella oblata Swingle Bull. Soc. Bot. France 59: 777 (1912 publ. 1913)

Common names Top

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Language Common/alternative name
Chinese 酸木苹果

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000746276
KEW urn:lsid:ipni.org:names:77104907-1
The Plant List kew-2899529
IPNI 77104907-1
iNaturalist 1205204
GBIF 7707202
Elurikkus 615789

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
Chemical constituents from the roots of Feroniella lucida. Sripisut T, Cheenpracha S, Laphookhieo S J Asian Nat Prod Res 01-Jun-2011
doi:10.1080/10286020.2011.572878
PMID:21623520
Feroniellic acids A–C, three new isomeric furanocoumarins with highly hydroxylated geranyl derived moieties from Feroniella lucida Preecha Phuwapraisirisan, Chalouyluk Phoopichayanun, Butsarakham Supudompol Elsevier BV 11-Mar-2008
doi:10.1016/J.TETLET.2008.03.027
Feroniellides A and B, apotirucallane triterpenes with novel cyclic acetals from Feroniella lucida Preecha Phuwapraisirisan, Serm Surapinit, Pongpun Siripong, Santi Tip-pyang, Udom Kokpol Elsevier BV 14-Dec-2006
doi:10.1016/J.TETLET.2006.11.132
Feroniellins A–C, novel cytotoxic furanocoumarins with highly oxygenated C10 moieties from Feroniella lucida Preecha Phuwapraisirisan, Serm Surapinit, Sitthidesch Sombund, Pongpun Siripong, Santi Tip-pyang Elsevier BV 18-Apr-2006
doi:10.1016/J.TETLET.2006.03.129

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 / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(+/-)-6-Acetonyldihydrochelerythrine 443700 Click to see CC(=O)CC1C2=C(C=CC(=C2OC)OC)C3=C(N1C)C4=CC5=C(C=C4C=C3)OCO5 405.40 unknown https://doi.org/10.1080/10286020.2011.572878
Acetonylchelerythrine 185516 Click to see CC(=O)CC1C2=C(C=CC(=C2OC)OC)C3=C(N1C)C4=CC5=C(C=C4C=C3)OCO5 405.40 unknown https://doi.org/10.1080/10286020.2011.572878
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
N-[(2R)-2-hydroxy-2-(4-methoxyphenyl)ethyl]benzamide 10084553 Click to see COC1=CC=C(C=C1)C(CNC(=O)C2=CC=CC=C2)O 271.31 unknown https://doi.org/10.1080/10286020.2011.572878
Tembamide 177583 Click to see COC1=CC=C(C=C1)C(CNC(=O)C2=CC=CC=C2)O 271.31 unknown https://doi.org/10.1080/10286020.2011.572878
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aphidicolane and stemodane diterpenoids
5'-Hydroxy-2,2,2',6'-tetramethylspiro[1,3-dioxolane-4,13'-tetracyclo[10.3.1.01,10.02,7]hexadecane]-6'-carboxylic acid 162814124 Click to see CC1(OCC2(O1)CCC34CC2CC3CCC5C4(CCC(C5(C)C(=O)O)O)C)C 392.50 unknown https://doi.org/10.1080/10286020.2011.572878
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(E,4R,6R,7S)-4,6,7-trihydroxy-2,6-dimethyl-8-(7-oxofuro[3,2-g]chromen-4-yl)oxyoct-2-enoic acid 101852053 Click to see CC(=CC(CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O)O)C(=O)O 418.40 unknown https://doi.org/10.1016/J.TETLET.2008.03.027
(E,4R,6S,7R)-4,6,7-trihydroxy-2,6-dimethyl-8-(7-oxofuro[3,2-g]chromen-4-yl)oxyoct-2-enoic acid 101852054 Click to see CC(=CC(CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O)O)C(=O)O 418.40 unknown https://doi.org/10.1016/J.TETLET.2008.03.027
(E,4R,6S,7S)-4,6,7-trihydroxy-2,6-dimethyl-8-(7-oxofuro[3,2-g]chromen-4-yl)oxyoct-2-enoic acid 101852052 Click to see CC(=CC(CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O)O)C(=O)O 418.40 unknown https://doi.org/10.1016/J.TETLET.2008.03.027
4,6,7-Trihydroxy-2,6-dimethyl-8-(7-oxofuro[3,2-g]chromen-4-yl)oxyoct-2-enoic acid 162956677 Click to see CC(=CC(CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O)O)C(=O)O 418.40 unknown https://doi.org/10.1016/J.TETLET.2008.03.027
5-Geranoxypsoralen;Bergamottin; Bergaptin 119057 Click to see CC(=CCCC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C)C 338.40 unknown https://doi.org/10.1080/10286020.2011.572878
8-(3,7-Dimethylocta-2,6-dienoxy)-7-hydroxychromen-2-one 163029749 Click to see CC(=CCCC(=CCOC1=C(C=CC2=C1OC(=O)C=C2)O)C)C 314.40 unknown https://doi.org/10.1080/10286020.2011.572878
9-[(3,7-Dimethyl-2,6-octadien-1-yl)oxy]-7H-furo[3,2-g][1]benzopyran-7-one 155658 Click to see CC(=CCCC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C)C 338.40 unknown https://doi.org/10.1080/10286020.2011.572878
Bergamottin 5471349 Click to see CC(=CCCC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C)C 338.40 unknown https://doi.org/10.1080/10286020.2011.572878
Xanthotoxol geranyl ether 5317564 Click to see CC(=CCCC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C)C 338.40 unknown https://doi.org/10.1080/10286020.2011.572878
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,5R,7R,8R,9R,10S,13S,17S)-7-hydroxy-17-[(1S,2S,4S,5S)-2-hydroxy-7,7-dimethyl-6,8-dioxabicyclo[3.2.1]octan-4-yl]-4,4,8,10,13-pentamethyl-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] 2-(methylamino)benzoate 163190139 Click to see CC1(C(CCC2(C1CC(C3(C2CCC4(C3=CCC4C5CC(C6C(OC5O6)(C)C)O)C)C)O)C)OC(=O)C7=CC=CC=C7NC)C 621.80 unknown https://doi.org/10.1016/J.TETLET.2006.11.132
[7-hydroxy-17-(2-hydroxy-7,7-dimethyl-6,8-dioxabicyclo[3.2.1]octan-4-yl)-4,4,8,10,13-pentamethyl-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] 2-(methylamino)benzoate 162946527 Click to see CC1(C(CCC2(C1CC(C3(C2CCC4(C3=CCC4C5CC(C6C(OC5O6)(C)C)O)C)C)O)C)OC(=O)C7=CC=CC=C7NC)C 621.80 unknown https://doi.org/10.1016/J.TETLET.2006.11.132
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(1S,2R,3R,5R,7S,10S,11R,14R,15S)-15-[(2R,3S,5R)-5-[(1S)-1,2-dihydroxy-2-methylpropyl]-2-methoxyoxolan-3-yl]-3-hydroxy-2,6,6,10-tetramethyl-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] 2-(methylamino)benzoate 21668675 Click to see CC1(C(CCC2(C1CC(C3(C2CCC45C3(C4)CCC5C6CC(OC6OC)C(C(C)(C)O)O)C)O)C)OC(=O)C7=CC=CC=C7NC)C 653.90 unknown https://doi.org/10.1016/J.TETLET.2006.11.132
[15-[5-(1,2-Dihydroxy-2-methylpropyl)-2-methoxyoxolan-3-yl]-3-hydroxy-2,6,6,10-tetramethyl-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] 2-(methylamino)benzoate 162851405 Click to see CC1(C(CCC2(C1CC(C3(C2CCC45C3(C4)CCC5C6CC(OC6OC)C(C(C)(C)O)O)C)O)C)OC(=O)C7=CC=CC=C7NC)C 653.90 unknown https://doi.org/10.1016/J.TETLET.2006.11.132
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
1-[(13S)-2,3-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl]propan-2-one 124350708 Click to see CC(=O)CC1C2=CC(=C(C=C2C3=C(N1C)C4=CC5=C(C=C4C=C3)OCO5)OC)OC 405.40 unknown https://doi.org/10.1080/10286020.2011.572878
8-Acetonyldihydronitidine 10740045 Click to see CC(=O)CC1C2=CC(=C(C=C2C3=C(N1C)C4=CC5=C(C=C4C=C3)OCO5)OC)OC 405.40 unknown https://doi.org/10.1080/10286020.2011.572878
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one 604512 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1080/10286020.2011.572878
4-[(2R,3R)-2,3-dihydroxy-3-methyl-4-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]butoxy]furo[3,2-g]chromen-7-one 163060369 Click to see CC1=CC(OC1=O)CC(C)(C(COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)O)O 400.40 unknown https://doi.org/10.1080/10286020.2011.572878
4-[(2S)-2-hydroxy-2-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]ethoxy]furo[3,2-g]chromen-7-one 11646755 Click to see CC1(CCC(O1)C(C)(C)O)C(COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)O 388.40 unknown https://doi.org/10.1016/J.TETLET.2006.03.129
4-[(3,6-Dihydroxy-3,7,7-trimethyloxepan-2-yl)methoxy]furo[3,2-g]chromen-7-one 73065263 Click to see CC1(C(CCC(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)(C)O)O)C 388.40 unknown https://doi.org/10.1016/J.TETLET.2006.03.129
4-[(E)-3-methyl-4-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]but-2-enoxy]furo[3,2-g]chromen-7-one 163190072 Click to see CC1=CC(OC1=O)CC(=CCOC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 366.40 unknown https://doi.org/10.1080/10286020.2011.572878
4-[[(2R,3S,6R)-3,6-dihydroxy-3,7,7-trimethyloxepan-2-yl]methoxy]furo[3,2-g]chromen-7-one 11696741 Click to see CC1(C(CCC(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)(C)O)O)C 388.40 unknown https://doi.org/10.1016/J.TETLET.2006.03.129
4-[[(2S,3S,6R)-3-hydroxy-6-(2-hydroxypropan-2-yl)-3-methyloxan-2-yl]methoxy]furo[3,2-g]chromen-7-one 11675450 Click to see CC1(CCC(OC1COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C(C)(C)O)O 388.40 unknown https://doi.org/10.1016/J.TETLET.2006.03.129
4-[[(2S,3S)-3-methyl-3-(4-methylpent-3-enyl)oxiran-2-yl]methoxy]furo[3,2-g]chromen-7-one 162916201 Click to see CC(=CCCC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C)C 354.40 unknown https://doi.org/10.1080/10286020.2011.572878
4-[[3-Hydroxy-6-(2-hydroxypropan-2-yl)-3-methyloxan-2-yl]methoxy]furo[3,2-g]chromen-7-one 73050517 Click to see CC1(CCC(OC1COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C(C)(C)O)O 388.40 unknown https://doi.org/10.1016/J.TETLET.2006.03.129
4-[2-Hydroxy-2-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]ethoxy]furo[3,2-g]chromen-7-one 73040943 Click to see CC1(CCC(O1)C(C)(C)O)C(COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)O 388.40 unknown https://doi.org/10.1016/J.TETLET.2006.03.129
4-[3-methyl-4-(4-methyl-5-oxo-2H-furan-2-yl)but-2-enoxy]furo[3,2-g]chromen-7-one 163031237 Click to see CC1=CC(OC1=O)CC(=CCOC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 366.40 unknown https://doi.org/10.1080/10286020.2011.572878
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 270.28 unknown https://doi.org/10.1080/10286020.2011.572878
Marmesin 334704 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1080/10286020.2011.572878
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown https://doi.org/10.1080/10286020.2011.572878
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1080/10286020.2011.572878
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1080/10286020.2011.572878
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Demethylsuberosin 5316525 Click to see CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C 230.26 unknown https://doi.org/10.1080/10286020.2011.572878
Osthenol 5320318 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)C 230.26 unknown https://doi.org/10.1080/10286020.2011.572878
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown https://doi.org/10.1080/10286020.2011.572878

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