Scientific name	Authority	First published in
Sophora chrysophylla subsp. glabrata	(A.Gray) Chock	Pacific Sci.10: 143 (1956)
Edwardsia chrysophylla	Salisb.	Trans. Linn. Soc. London9: 299 (1808)
Sophora grisea	O.Deg. & Sherff	Bot. Leafl.5: 24 (1951)
Sophora unifoliata	(Rock) O.Deg. & Sherff	Bot. Leafl.5: 24 (1951)
Sophora unifoliata var. elliptica	(Chock) O.Deg. & I.Deg.	Phytologia21: 415 (1971)
Sophora unifoliata var. kanaioensis	(Chock) O.Deg. & I.Deg.	Phytologia21: 415 (1971)
Edwardsia unifoliata	(Rock) O.Deg.	Fl. Hawaiiensis169c: s.p. (1932)
Sophora lanaiensis	(Chock) O.Deg. & I.Deg.	Phytologia21: 411 (1971)
Sophora chrysophylla var. lanaiensis	Chock	Pacific Sci.10: 147 (1956)
Sophora chrysophylla var. unifoliata	Rock	Bull. Div. Forest. Board Commiss. Agric. Forest. Hawaii5: 44 (1919)
Sophora chrysophylla subsp. unifoliata	(Rock) Chock	Pacific Sci.10: 155 (1956)
Sophora chrysophylla var. elliptica	Chock	Pacific Sci.10: 156 (1956)
Sophora chrysophylla var. kanaioensis	Chock	Pacific Sci.10: 156 (1956)
Edwardsia chrysophylla var. glabrata	A.Gray	C.Wilkes, U.S. Expl. Exped., Phan.1: 459 (1854)
Sophora chrysophylla var. glabrata	(A.Gray) Rock	Bull. Div. Forest. Board Commiss. Agric. Forest. Hawaii5: 42 (1919)
Sophora chrysophylla f. haleakalaensis	Chock	Pacific Sci.10: 142 (1956)
Sophora chrysophylla f. obovata	Chock	Pacific Sci.10: 142 (1956)
Sophora chrysophylla f. makuaensis	Chock	Pacific Sci.10: 143 (1956)
Edwardsia chrysophylla var. lanaiensis	Chock	Pacific Sci.10: 147 (1956)

Common names Top

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Filter by language:

Language	Common/alternative name
English	mamani
Arabic	صفيراء ذهبية الأوراق
French	māmame
French	māmane
Russian	Софора золотистолистная

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

Pacific click to expand
- North-central Pacific
  - Hawaii

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000185582
USDA Plants	SOCH
Tropicos	13032950
KEW	urn:lsid:ipni.org:names:518815-1
The Plant List	ild-31857
Open Tree Of Life	437451
NCBI Taxonomy	171561
Nature Serve	2.161269
IPNI	518815-1
iNaturalist	70036
GBIF	2958996
Freebase	/m/026vqwn
EOL	643519
USDA GRIN	34951
Wikipedia	Sophora_chrysophylla

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

Hawaiian Treeline Ecotones: Implications for Plant Community Conservation under Climate Change

Ainsworth A, Drake DR

Plants (Basel)

31-Dec-2023

PMCID:	PMC10780311
doi:	10.3390/plants13010123
PMID:	38202431

Antimicrobial and Antioxidant Activities of Endophytic Fungi Associated with Arrabidaea chica (Bignoniaceae)

Gurgel RS, de Melo Pereira DÍ, Garcia AV, Fernandes de Souza AT, Mendes da Silva T, de Andrade CP, Lima da Silva W, Nunez CV, Fantin C, de Lima Procópio RE, Albuquerque PM

J Fungi (Basel)

21-Aug-2023

PMCID:	PMC10455555
doi:	10.3390/jof9080864
PMID:	37623634

From Plants to Psycho-Neurology: Unravelling the Therapeutic Benefits of Bioactive Compounds in Brain Disorders

Grosso C, Santos M, Barroso MF

Antioxidants (Basel)

11-Aug-2023

PMCID:	PMC10451187
doi:	10.3390/antiox12081603
PMID:	37627598

Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity

Cely-Veloza W, Kato MJ, Coy-Barrera E

ACS Omega

28-Jul-2023

PMCID:	PMC10413377
doi:	10.1021/acsomega.3c02179
PMID:	37576649

Combined transcriptome and metabolome analysis of Nerium indicum L. elaborates the key pathways that are activated in response to witches’ broom disease

Wang S, Wang S, Li M, Su Y, Sun Z, Ma H

BMC Plant Biol

14-Jun-2022

PMCID:	PMC9199210
doi:	10.1186/s12870-022-03672-z
PMID:	35701735

The Biological Activity of Natural Alkaloids against Herbivores, Cancerous Cells and Pathogens

Thawabteh A, Juma S, Bader M, Karaman D, Scrano L, Bufo SA, Karaman R

Toxins (Basel)

11-Nov-2019

PMCID:	PMC6891610
doi:	10.3390/toxins11110656
PMID:	31717922

Seed freeze sensitivity and ex situ longevity of 295 species in the native Hawaiian flora

Chau MM, Chambers T, Weisenberger L, Keir M, Kroessig TI, Wolkis D, Kam R, Yoshinaga AY

Am J Bot

09-Sep-2019

PMCID:	PMC6856683
doi:	10.1002/ajb2.1351
PMID:	31502257

Facilitating adaptation to climate change while restoring a montane plant community

Leopold CR, Hess SC

PLoS One

20-Jun-2019

PMCID:	PMC6586318
doi:	10.1371/journal.pone.0218516
PMID:	31220135

Quantitative Analysis of Pedogenic Thresholds and Domains in Volcanic Soils

Bateman JB, Chadwick OA, Vitousek PM

Ecosystems

01-Apr-2019

PMCID:	PMC7079697
doi:	10.1007/s10021-019-00361-1
PMID:	32189991

Genetic Variation and Hybridisation among Eight Species of kōwhai (Sophora: Fabaceae) from New Zealand Revealed by Microsatellite Markers

Heenan P, Mitchell C, Houliston G

Genes (Basel)

20-Feb-2018

PMCID:	PMC5852607
doi:	10.3390/genes9020111
PMID:	29461510

The sentinel tree nursery as an early warning system for pathway risk assessment: Fungal pathogens associated with Chinese woody plants commonly shipped to Europe

Vettraino AM, Li HM, Eschen R, Morales-Rodriguez C, Vannini A

PLoS One

29-Nov-2017

PMCID:	PMC5706704
doi:	10.1371/journal.pone.0188800
PMID:	29186190

UV Screening in Native and Non-native Plant Species in the Tropical Alpine: Implications for Climate Change-Driven Migration of Species to Higher Elevations

Barnes PW, Ryel RJ, Flint SD

Front Plant Sci

22-Aug-2017

PMCID:	PMC5572244
doi:	10.3389/fpls.2017.01451
PMID:	28878792

More than one fungus in the pepper pot: Integrative taxonomy unmasks hidden species within Myriostoma coliforme (Geastraceae, Basidiomycota)

Sousa JO, Suz LM, García MA, Alfredo DS, Conrado LM, Marinho P, Ainsworth AM, Baseia IG, Martín MP

PLoS One

07-Jun-2017

PMCID:	PMC5462367
doi:	10.1371/journal.pone.0177873
PMID:	28591150

The Genera of Fungi – G 4: Camarosporium and Dothiora

Crous PW, Groenewald JZ

IMA Fungus

23-May-2017

PMCID:	PMC5493531
doi:	10.5598/imafungus.2017.08.01.10
PMID:	28824845

Diversity and Distribution of Phenol Oxidase Producing Fungi from Soda Lake and Description of Curvularia lonarensis sp. nov.

Sharma R, Prakash O, Sonawane MS, Nimonkar Y, Golellu PB, Sharma R

Front Microbiol

22-Nov-2016

PMCID:	PMC5118452
doi:	10.3389/fmicb.2016.01847
PMID:	27920761

Phytochemical Profile Top

Add a new one!

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 / Lupin alkaloids / Anagyrine-type alkaloids
(1R,9R,10S,12S)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	162941576	Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O	260.33	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
12-Hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	621307	Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O	260.33	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
Anagyrine	5351589	Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O	244.33	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5 https://doi.org/10.1039/JR9420000507
CID 10246	10246	Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O	244.33	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
Thermopsine	92768	Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O	244.33	unknown	https://doi.org/10.1039/JR9420000507 https://doi.org/10.1016/S0031-9422(00)85050-5
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(-)-Cytisine	22407	Click to see C1C2CNCC1C3=CC=CC(=O)N3C2	190.24	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one	1747617	Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2	204.27	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
(1S,9R)-11-but-3-enyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one	7067420	Click to see C=CCCN1CC2CC(C1)C3=CC=CC(=O)N3C2	244.33	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
1,2,3,4,5,6-Hexahydro-1,5-methano-pyrido[1,2-a][1,5]diazocin-8-one	683511	Click to see C1C2CNCC1C3=CC=CC(=O)N3C2	190.24	unknown	https://doi.org/10.1016/0040-4020(76)85049-1
1,5-Methano-8H-pyrido[1,2-a][1,5]diazocin-8-one, 3-(3-butenyl)-1,2,3,4,5,6-hexahydro-, (1R)-	547355	Click to see C=CCCN1CC2CC(C1)C3=CC=CC(=O)N3C2	244.33	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
Caulophylline	670971	Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2	204.27	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
Cytisine, N-formyl-	589870	Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O	218.25	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
Cytisinicline	10235	Click to see C1C2CNCC1C3=CC=CC(=O)N3C2	190.24	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
N-Formylcytisine	179619	Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O	218.25	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
N-Methylcytisine	234566	Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2	204.27	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
Rhombifoline	92795	Click to see C=CCCN1CC2CC(C1)C3=CC=CC(=O)N3C2	244.33	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
(-)-Mamanine N-oxide	163184400	Click to see C1CC[N+]2(CC(CC(C2C1)CO)C3=CC=CC(=O)N3)[O-]	278.35	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
(6S)-6-[(1S,3R,9aR)-1-(hydroxymethyl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-3-yl]piperidin-2-one	163035603	Click to see C1CCN2CC(CC(C2C1)CO)C3CCCC(=O)N3	266.38	unknown	https://doi.org/10.1016/0040-4020(76)85049-1 https://doi.org/10.1016/S0031-9422(00)85050-5
6-[(1S,3R,5R,9aR)-1-(hydroxymethyl)-5-oxido-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-5-ium-3-yl]-1H-pyridin-2-one	163186471	Click to see C1CC[N+]2(CC(CC(C2C1)CO)C3=CC=CC(=O)N3)[O-]	278.35	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
6-[1-(hydroxymethyl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-3-yl]-1H-pyridin-2-one	323274	Click to see C1CCN2CC(CC(C2C1)CO)C3=CC=CC(=O)N3	262.35	unknown	https://doi.org/10.1016/0040-4020(76)85049-1 https://doi.org/10.1016/S0031-9422(00)85050-5
6-[1-(hydroxymethyl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-3-yl]piperidin-2-one	78177132	Click to see C1CCN2CC(CC(C2C1)CO)C3CCCC(=O)N3	266.38	unknown	https://doi.org/10.1016/0040-4020(76)85049-1 https://doi.org/10.1016/S0031-9422(00)85050-5
Mamanine	3085182	Click to see C1CCN2CC(CC(C2C1)CO)C3=CC=CC(=O)N3	262.35	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5 https://doi.org/10.1016/0040-4020(76)85049-1
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(+)-Matrine	285698	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
Matrine	91466	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
Oxymatrine	114850	Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-]	264.36	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,2R,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one	92143189	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O	248.36	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
(1R,9R,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one	14379239	Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O	246.35	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
(1R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one	51018075	Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O	246.35	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
(1R,9R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one	163185252	Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O	246.35	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
(1S,2S,9R,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane-6,16-dione	163032815	Click to see C1CCN2C(C1)C3CC(C2=O)C4CCCC(=O)N4C3	262.35	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
2,17-Dioxosparteine	521208	Click to see C1CCN2C(C1)C3CC(C2=O)C4CCCC(=O)N4C3	262.35	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
5,6-Dehydrolupanine	520559	Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O	246.35	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
alpha-Isolupahine	6101749	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O	248.36	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
alpha-Isolupanine	119201	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O	248.36	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Ethanone, 1-[4-hydroxy-3-(4-hydroxy-3-methyl-2-butenyl)phenyl]-	604558	Click to see CC(=CCC1=C(C=CC(=C1)C(=O)C)O)CO	220.26	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
> Organoheterocyclic compounds / Isobenzofurans
[(1S,5R,6R)-5-[[(1R,3aR,7R,7aS)-7-hydroxy-3a,7-dimethyl-3-oxo-4,5,6,7a-tetrahydro-1H-2-benzofuran-1-yl]methyl]-7-methylidene-4-oxo-6-bicyclo[3.2.1]oct-2-enyl] acetate	162904392	Click to see CC(=O)OC1C(=C)C2CC1(C(=O)C=C2)CC3C4C(CCCC4(C)O)(C(=O)O3)C	388.50	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Pyridinones
6-[5-(hydroxymethyl)-1-methylpiperidin-3-yl]-1H-pyridin-2-one	6325429	Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO	222.28	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
Kuraramine	11447394	Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO	222.28	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
Ammodendrine	442625	Click to see CC(=O)N1CCCC(=C1)C2CCCCN2	208.30	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
Pyridine, 1-acetyl-1,2,3,4-tetrahydro-5-(2-piperidinyl)-	108191	Click to see CC(=O)N1CCCC(=C1)C2CCCCN2	208.30	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
> Organoheterocyclic compounds / Quinolizines
1-[[(1R,5R,9aS)-5-oxido-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-5-ium-1-yl]methyl]piperidine-2,6-dione	163188138	Click to see C1CC[N+]2(CCCC(C2C1)CN3C(=O)CCCC3=O)[O-]	280.36	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
1-[[(1R,8AR)-2,3,4,5,6,7,8,8A-Octahydro-1H-quinolizin-1-YL]methyl]pipe ridine-2,6-dione	586638	Click to see C1CCN2CCCC(C2C1)CN3C(=O)CCCC3=O	264.36	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
1-[[(1R,9aS)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl]piperidine-2,6-dione	21681276	Click to see C1CCN2CCCC(C2C1)CN3C(=O)CCCC3=O	264.36	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
1-[[(1R,9aS)-5-oxido-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-5-ium-1-yl]methyl]piperidine-2,6-dione	101667015	Click to see C1CC[N+]2(CCCC(C2C1)CN3C(=O)CCCC3=O)[O-]	280.36	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
2,6-Piperidinedione, 1-[(octahydro-2H-quinolizin-1-yl)methyl]-, (1R-cis)-	91715880	Click to see C1CCN2CCCC(C2C1)CN3C(=O)CCCC3=O	264.36	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
Lamprolobine	87752	Click to see C1CCN2CCCC(C2C1)CN3C(=O)CCCC3=O	264.36	unknown	https://doi.org/10.1016/S0031-9422(00)85050-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones
4',7-Dihydroxyflavone	5282073	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O	254.24	unknown	https://doi.org/10.1248/CPB.38.1712
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Medicagol	5319322	Click to see C1OC2=C(O1)C=C3C(=C2)C4=C(O3)C5=C(C=C(C=C5)O)OC4=O	296.23	unknown	https://doi.org/10.1248/CPB.38.1712
Sophoracoumestan A	14630492	Click to see CC1(C=CC2=CC3=C(C=C2O1)OC4=C3C(=O)OC5=C4C=CC(=C5)O)C	334.30	unknown	https://doi.org/10.1248/CPB.38.1712
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(1R,13R)-7,7-Dimethyl-8,12,20-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-2(11),3,5,9,14(19),15,17-heptaene-1,17-diol	5318770	Click to see CC1(C=CC2=CC3=C(C=C2O1)OC4C3(COC5=C4C=CC(=C5)O)O)C	338.40	unknown	https://doi.org/10.1248/CPB.38.1712
(1S,13S)-7,7-dimethyl-8,12,20-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-2(11),3,5,9,14(19),15,17-heptaene-1,17-diol	14630496	Click to see CC1(C=CC2=CC3=C(C=C2O1)OC4C3(COC5=C4C=CC(=C5)O)O)C	338.40	unknown	https://doi.org/10.1248/CPB.38.1712
3-Hydroxy-8,9-methylenedioxypterocarpane	363863	Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5	284.26	unknown	https://doi.org/10.1248/CPB.38.1712
Maackiain	91510	Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5	284.26	unknown	https://doi.org/10.1248/CPB.38.1712
Tuberosin	14630495	Click to see CC1(C=CC2=CC3=C(C=C2O1)OC4C3(COC5=C4C=CC(=C5)O)O)C	338.40	unknown	https://doi.org/10.1248/CPB.38.1712
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
(3R)-3-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-4-hydroxyphenyl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	162897376	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1)C2COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)C)C	476.60	unknown	https://doi.org/10.1248/CPB.38.1712
(3S)-3-[5-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxyphenyl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	163194946	Click to see CC(=CCCC(=CCC1=CC(=C(C=C1O)O)C2COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)C)C	492.60	unknown	https://doi.org/10.1248/CPB.38.1712
(3S)-5,7-dihydroxy-3-[4-hydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	92469183	Click to see CC(=CCC1=C(C=CC(=C1OC)C2COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)C	438.50	unknown	https://doi.org/10.1248/CPB.38.1712
3-[3-(3,7-Dimethylocta-2,6-dienyl)-4-hydroxyphenyl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	72733691	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1)C2COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)C)C	476.60	unknown	https://doi.org/10.1248/CPB.38.1712
3-[5-(3,7-Dimethylocta-2,6-dienyl)-2,4-dihydroxyphenyl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	72733692	Click to see CC(=CCCC(=CCC1=CC(=C(C=C1O)O)C2COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)C)C	492.60	unknown	https://doi.org/10.1248/CPB.38.1712
Isosophoranone	10478290	Click to see CC(=CCC1=C(C=CC(=C1OC)C2COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)C	438.50	unknown	https://doi.org/10.1248/CPB.38.1712
Sophoraisoflavanone C	14630493	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1)C2COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)C)C	476.60	unknown	https://doi.org/10.1016/0305-1978(95)00056-9 https://doi.org/10.1248/CPB.38.1712
Sophoraisoflavanone D	14630494	Click to see CC(=CCCC(=CCC1=CC(=C(C=C1O)O)C2COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)C)C	492.60	unknown	https://doi.org/10.1385/BTER:80:2:139 https://doi.org/10.1002/PTR.869 https://doi.org/10.1248/CPB.38.1712
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
GU17;ISL;Isoliquiritigen	425	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O	256.25	unknown	https://doi.org/10.1248/CPB.38.1712
Trihydroxychalcone	638278	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O	256.25	unknown	https://doi.org/10.1248/CPB.38.1712

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Sophora chrysophylla

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