Scientific name	Authority	First published in
Simarouba officinalis	DC.	Ann. Mus. Hist. Nat. 17: 423 (1811)
Simarouba medicinalis	Endl.	Med. Pfl. Österr. Pharm. : 528 (1842)
Quassia glauca	Spreng.	Syst. Veg. 2: 319 (1825)
Simarouba glauca var. latifolia	Cronquist	Bull. Torrey Bot. Club 71: 231 (1944)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	paradisetree
Kannada	ಲಕ್ಷ್ಮೀತರು
Marathi	लक्ष्मीतरू

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Southeast
  - Mexico Southwest
- Southeastern U.S.A.
  - Florida

Southern America click to expand
- Caribbean
  - Bahamas
  - Cuba
  - Dominican Republic
  - Haiti
  - Jamaica
- Central America
  - Belize
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000492142
Florida Plant Atlas	606
USDA Plants	SIGL3
Tropicos	29400084
KEW	urn:lsid:ipni.org:names:814130-1
Open Tree Of Life	708255
NCBI Taxonomy	43729
Nature Serve	2.147610
IUCN Red List	150108258
IPNI	814130-1
iNaturalist	169001
GBIF	3190669
Freebase	/m/06wbmxb
EPPO	SMBGL
USDA GRIN	33957
Wikipedia	Simarouba_glauca
CMAUP	NPO20624

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

Engine Performance of High-Acid Oil-Biodiesel through Supercritical Transesterification

Lin CY, Lin YW

ACS Omega

11-Jan-2024

PMCID:	PMC10809246
doi:	10.1021/acsomega.3c06997
PMID:	38284058

Geometric entropy of plant leaves: A measure of morphological complexity

Muraleedharan V, Rajan SC, R J

PLoS One

02-Jan-2024

PMCID:	PMC10760904
doi:	10.1371/journal.pone.0293596
PMID:	38166118

Saponin-Derived Silver Nanoparticles from Phoenix dactylifera (Ajwa Dates) Exhibit Broad-Spectrum Bioactivities Combating Bacterial Infections

Adnan M, Siddiqui AJ, Ashraf SA, Ashraf MS, Alomrani SO, Alreshidi M, Tepe B, Sachidanandan M, Danciu C, Patel M

Antibiotics (Basel)

07-Sep-2023

PMCID:	PMC10525761
doi:	10.3390/antibiotics12091415
PMID:	37760712

Plant Extracts from the Yucatan Peninsula in the In Vitro Control of Curvularia lunata and Antifungal Effect of Mosannona depressa and Piper neesianum Extracts on Postharvest Fruits of Habanero Pepper

Cruz-Cerino P, Cristóbal-Alejo J, Ruiz-Carrera V, Gamboa-Angulo M

Plants (Basel)

09-Aug-2023

PMCID:	PMC10459550
doi:	10.3390/plants12162908
PMID:	37631120

Combined Effect of Operating Parameters and Nanoparticles on the Performance of a Diesel Engine: Response Surface Methodology-Coupled Genetic Algorithm Approach

Dewangan A, Mallick A, Yadav AK, Ahmad A, Alqahtani D, Islam S

ACS Omega

30-Jun-2023

PMCID:	PMC10339400
doi:	10.1021/acsomega.3c02782
PMID:	37457477

Silene uniflora Extracts for Strawberry Postharvest Protection

Buzón-Durán L, Sánchez-Hernández E, Martín-Ramos P, Navas-Gracia LM, García-González MC, Oliveira R, Martín-Gil J

Plants (Basel)

29-Apr-2023

PMCID:	PMC10180817
doi:	10.3390/plants12091846
PMID:	37176904

Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India?

Kumar BM

Agrofor Syst

07-Apr-2023

PMCID:	PMC10081327
doi:	10.1007/s10457-023-00821-7
PMID:	37193256

An insight into endophytic antimicrobial compounds: an updated analysis

Digra S, Nonzom S

Plant Biotechnol Rep

14-Mar-2023

PMCID:	PMC10013304
doi:	10.1007/s11816-023-00824-x
PMID:	37359493

Ecological quality as a coffee quality enhancer. A review

Torrez V, Benavides-Frias C, Jacobi J, Speranza CI

Agron Sustain Dev

02-Feb-2023

PMCID:	PMC9894527
doi:	10.1007/s13593-023-00874-z
PMID:	36748099

A Perspective on Using Organic Molecules Composing Carbon Dots for Cancer Treatment

Ahmad MA, Aung YY, Widati AA, Sakti SC, Sumarsih S, Irzaman I, Yuliarto B, Chang JY, Fahmi MZ

Nanotheranostics

22-Jan-2023

PMCID:	PMC9925355
doi:	10.7150/ntno.80076
PMID:	36793348

Below-ground traits mediate tree survival in a tropical dry forest restoration

Werden LK, Averill C, Crowther TW, Calderón-Morales E, Toro L, Alvarado JP, Gutiérrez LM, Mallory DE, Powers JS

Philos Trans R Soc Lond B Biol Sci

14-Nov-2022

PMCID:	PMC9661956
doi:	10.1098/rstb.2021.0067
PMID:	36373912

Complementary and alternative therapies in skin cancer: A literature review of biologically active compounds.

Hidalgo L, Saldías-Fuentes C, Carrasco K, Halpern AC, Mao JJ, Navarrete-Dechent C

Dermatol Ther

27-Sep-2022

PMCID:	PMC10481428
doi:	10.1111/dth.15842
PMID:	36124923

Nematicidal Screening of Aqueous Extracts from Plants of the Yucatan Peninsula and Ecotoxicity

Aviles-Gomez J, Cristóbal-Alejo J, Andrés MF, González-Coloma A, Carnevali G, Pérez-Brito D, Moo-Koh FA, Gamboa-Angulo M

Plants (Basel)

17-Aug-2022

PMCID:	PMC9416186
doi:	10.3390/plants11162138
PMID:	36015441

Eco-biochemical responses, phytoremediation potential and molecular genetic analysis of Alhagi maurorum grown in metal-contaminated soils

Heikal YM, El-Esawi MA, Naidu R, Elshamy MM

BMC Plant Biol

01-Aug-2022

PMCID:	PMC9341119
doi:	10.1186/s12870-022-03768-6
PMID:	35909101

Endophytes in Lignin Valorization: A Novel Approach

Mattoo AJ, Nonzom S

Front Bioeng Biotechnol

19-Jul-2022

PMCID:	PMC9343868
doi:	10.3389/fbioe.2022.895414
PMID:	35928943

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 / Indolonaphthyridine alkaloids
Canthin-6-one	97176	Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3	220.23	unknown	https://doi.org/10.1002/PTR.1642
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
(1R,9R,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	15939858	Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O	260.33	unknown	via CMAUP database
Anagyrine	5351589	Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O	244.33	unknown	via CMAUP database
Thermospine	638234	Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O	244.33	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
Caulophylline	670971	Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2	204.27	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
Mamanine	3085182	Click to see C1CCN2CC(CC(C2C1)CO)C3=CC=CC(=O)N3	262.35	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(+)-12alpha-Hydroxysophocarpine	44408595	Click to see C1CC2CN3C(C4C2N(C1)CCC4)C(C=CC3=O)O	262.35	unknown	via CMAUP database
(1R,2R,5S,9S,17S)-5-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	10659287	Click to see C1CC2CN3C(CCC(C3=O)O)C4C2N(C1)CCC4	264.36	unknown	via CMAUP database
(1R,2R,9R,13R,17S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	21586634	Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-]	264.36	unknown	via CMAUP database
(1R,2R,9R,17S)-7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one	21763818	Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4	246.35	unknown	via CMAUP database
(5beta,6beta,7beta,11alpha)-Matridin-15-one	638232	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	via CMAUP database
5,9-Dihydroxymatrine	14274649	Click to see C1CC2C3CC(CN4C3C(CCC4)(CN2C(=O)C1)O)O	280.36	unknown	via CMAUP database
5alpha-Hydroxysophocarpine	15385686	Click to see C1CC2C3CC=CC(=O)N3CC4(C2N(C1)CCC4)O	262.35	unknown	via CMAUP database
9alpha-Hydroxy-13,14-didehydromatridine-15-one	12133310	Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CC(C4)O	262.35	unknown	via CMAUP database
9alpha-Hydroxymatrine	15385684	Click to see C1CC2C3CC(CN4C3C(CCC4)CN2C(=O)C1)O	264.36	unknown	via CMAUP database
Allomatrine	7000681	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	via CMAUP database
Isomatrine	5271984	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	via CMAUP database
Matridin-15-one, 12,13-didehydro-	3041752	Click to see C1CC2CN3C(C=CCC3=O)C4C2N(C1)CCC4	246.35	unknown	via CMAUP database
Matrine	91466	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	via CMAUP database
Sophocarpine	115269	Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4	246.35	unknown	via CMAUP database
Sophoranol	12442899	Click to see C1CC2C3CCCN4C3C(CCC4)(CN2C(=O)C1)O	264.36	unknown	via CMAUP database
Sophoridine	165549	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
Lupanine	91471	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O	248.36	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate	21636205	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)CO)O)O)O)(C)C)C)C)C)C)C(=O)OC)O)O)CO)O)O)O)O)O	1251.40	unknown	via CMAUP database
Soyasaponin I	122097	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O	943.10	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
[(1S,4R,5R,6R,7S,8R,11R,13S,17S,18S,19R)-4,5,17-Trihydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] 2-hydroxy-2-methylbutanoate	12310232	Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C)O	494.50	unknown	https://doi.org/10.1016/S0021-9673(01)95055-1
[(1S,4S,5R,6R,7S,8R,11R,13S,16S,17S,18S,19R)-4,5,16,17-tetrahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] (2S)-2-hydroxy-2-methylbutanoate	90469735	Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(C=C5C)O)O)C)OC1=O)O)O)C)O	496.50	unknown	https://doi.org/10.1016/S0021-9673(01)95055-1
Glaucarubin	3321199	Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(C=C5C)O)O)C)OC1=O)O)O)C)O	496.50	unknown	https://doi.org/10.1021/JA01652A060
Glaucarubinone	441796	Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C)O	494.50	unknown	https://doi.org/10.1016/S0021-9673(01)95055-1
Glaucarubol 15-O-beta-D-glucopyranoside	435280	Click to see CC1C2C(C(=O)OC3C24COC(C1O)(C4C5(C(C3)C(=CC(C5O)O)C)C)O)OC6C(C(C(C(O6)CO)O)O)O	558.60	unknown	https://doi.org/10.1016/S0040-4039(00)99867-8
Glaucarubolone 15-O-beta-D-glucopyranoside	435281	Click to see CC1C2C(C(=O)OC3C24COC(C1O)(C4C5(C(C3)C(=CC(=O)C5O)C)C)O)OC6C(C(C(C(O6)CO)O)O)O	556.60	unknown	https://doi.org/10.1016/S0040-4039(00)99867-8
Simarubaceae	441794	Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(C=C5C)O)O)C)OC1=O)O)O)C)O	496.50	unknown	https://doi.org/10.1021/JA01652A060 https://doi.org/10.1016/S0021-9673(01)95055-1
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid	9476	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
Neochlorogenic acid	5280633	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
> Organoheterocyclic compounds / Azoles / Imidazoles
2,4-Dimethylimidazole	70259	Click to see CC1=CN=C(N1)C	96.13	unknown	via CMAUP database
4-Methylimidazole	13195	Click to see CC1=CN=CN1	82.10	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Kushecarpin B	10831417	Click to see COC1C2C(C3(CCC(=O)C=C3O1)OC)OC4=CC5=C(C=C24)OCO5	346.30	unknown	via CMAUP database
Kushecarpin C	10496772	Click to see COC1C2C(C3(CCC(=O)C=C3O1)O)OC4=CC5=C(C=C24)OCO5	332.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Coumarans
Kushecarpin A	10495761	Click to see COC1C2C(C3(CCC(=O)C=C3O1)O)OC4=C2C=CC(=C4)OC	318.32	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
Sophoramine	169014	Click to see C1CC2CN3C(=O)C=CC=C3C4C2N(C1)CCC4	244.33	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(3S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate	6920044	Click to see C1C([NH2+]CC2=C1C3=CC=CC=C3N2)C(=O)[O-]	216.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Pyridinones
(+)-Isokuraramine	101665417	Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO	222.28	unknown	via CMAUP database
(+)-Kuraramine	46187187	Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO	222.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(2,4-Dihydroxy-5-prenylphenyl)-5,6-methylenedioxybenzofuran	15953774	Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=CC3=CC4=C(C=C3O2)OCO4)C	338.40	unknown	via CMAUP database
2'-Hydroxy-4'-methoxy-5,6-methylenedioxy-2-phenylbenzofuran	44260109	Click to see COC1=CC(=C(C=C1)C2=CC3=CC4=C(C=C3O2)OCO4)O	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid	2518	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid	709	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	via CMAUP database
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S,2''S)-6-lavandulyl-5,7,2',4'-tetrahydroxylflavanone	118975901	Click to see CC(=CCC(CC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C(=C)C)C	424.50	unknown	via CMAUP database
(2S)-2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one	38351420	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)OC)O)C	370.40	unknown	via CMAUP database
Kushenol V	10572194	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3O)O)OC)O)C	386.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R,3R)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-5-methoxy-2,3-dihydrochromen-4-one	44584091	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O	472.50	unknown	via CMAUP database
(2R,3S)-2-(2,4-Dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-((R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl)chroman-4-one	102004822	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C	454.50	unknown	via CMAUP database
(2S)-2-(2,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-(1-methylethenyl)hexyl]-4H-1-benzopyran-4-one	44563159	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O	442.50	unknown	via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	6565899	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C	424.50	unknown	via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-7-hydroxy-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	26209050	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C	438.50	unknown	via CMAUP database
(2S)-2'-methoxykurarinone	11982641	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C	452.50	unknown	via CMAUP database
(2S)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	14258999	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC(=C(C=C3)O)OC)C	370.40	unknown	via CMAUP database
(2S)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2-(2-hydroxyphenyl)-2,3-dihydrochromen-4-one	44563122	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O	426.50	unknown	via CMAUP database
(2S)-7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	60039901	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C	452.50	unknown	via CMAUP database
(2S)-7,2'-dihydroxy-8-lavandulyl-5-methoxyflavanone	42607847	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C	422.50	unknown	via CMAUP database
(2S)-7,4'-dihydroxy-8-lavandulyl-5-methoxyflavanone	42608062	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=C(C=C3)O)C(=C)C)C	422.50	unknown	via CMAUP database
(2S)-euchrenone a7	44593508	Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C	340.40	unknown	via CMAUP database
(2S)-Isoxanthohumol	9928523	Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=C(C=C3)O)C	354.40	unknown	via CMAUP database
7,2',4'-Trihydroxy-8-lavandulyl-5-methoxyflavanone	11982640	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C	438.50	unknown	via CMAUP database
8-Prenylnaringenin	480764	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C	340.40	unknown	via CMAUP database
CID 102004745	102004745	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC(CC=C(C)C)C(=C)C)O)C	492.60	unknown	via CMAUP database
Flavenochromane A	11351168	Click to see CC1(CCC2=CC(=C(C=C2O1)O)C3C(C(=O)C4=C(O3)C5=C(C=C4O)OC(CC5)(C)C)O)C	440.50	unknown	via CMAUP database
Isobavachin	193679	Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C	324.40	unknown	via CMAUP database
Kurarinol	44563198	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O	456.50	unknown	via CMAUP database
Kushenol A	44563121	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C	408.50	unknown	via CMAUP database
Kushenol E	127234	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)O)C	424.50	unknown	via CMAUP database
Kushenol I	20832634	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C	454.50	unknown	via CMAUP database
Kushenol L	21721878	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC=C(C)C)O)C	440.50	unknown	via CMAUP database
Kushenol M	180948	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC(CC=C(C)C)C(=C)C)O)C	508.60	unknown	via CMAUP database
Kushenol S	10854625	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O)C	340.40	unknown	via CMAUP database
KushenolK	44428630	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O	472.50	unknown	via CMAUP database
leachianone A	44593449	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C	438.50	unknown	via CMAUP database
Leachianone G	5275227	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C	356.40	unknown	via CMAUP database
Sophoraflavanone G	72936	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C	424.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Licoflavonol	5481964	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)C	354.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
8-Prenylkaempferol	5318624	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C	354.40	unknown	via CMAUP database
Flavenochromane B	11327657	Click to see CC1(CCC2=C3C(=C4C(=C2O1)CCC(O4)(C)C)C(=O)C(=C(O3)C5=CC=C(C=C5)O)O)C	422.50	unknown	via CMAUP database
Flavenochromane C	11451469	Click to see CC1(CCC2=C3C(=C(C=C2O1)OC)C(=O)C(=C(O3)C4=CC=C(C=C4)O)O)C	368.40	unknown	via CMAUP database
Isoanhydroicaritin	5322079	Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC)C	368.40	unknown	via CMAUP database
Kushenol C	5481237	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C	438.50	unknown	via CMAUP database
Kushenol G	44259516	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)O	456.50	unknown	via CMAUP database
Sophoflavescenol	9929189	Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C	368.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	13093776	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	5318902	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O	562.50	unknown	via CMAUP database
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one	12304095	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain-3-O-glucosyl-6''-O-malonate	23724669	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)OC5=CC6=C(C=C25)OCO6	532.40	unknown	via CMAUP database
(-)-Variabilin	442828	Click to see COC1=CC2=C(C=C1)C3C(CO2)(C4=C(O3)C=C(C=C4)OC)O	300.30	unknown	via CMAUP database
(+)-Maackiain	161298	Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5	284.26	unknown	via CMAUP database
(+)-Medicarpin	73067	Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O	270.28	unknown	via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,12S)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol	6326060	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6	446.40	unknown	via CMAUP database
(6aR,11aR)-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-8,9-diol	361910	Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC(=C(C=C4O3)O)O	286.28	unknown	via CMAUP database
(6aR,11aR)-8-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol	21676223	Click to see COC1=C(C=C2C(=C1)C3COC4=C(C3O2)C=CC(=C4)O)O	286.28	unknown	via CMAUP database
(6aS,12aS)-6abeta,12abeta-Dihydro-3-methoxy-6H-[1,3]dioxolo[5,6]benzofuro[3,2-c][1]benzopyran	373519	Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5	298.29	unknown	via CMAUP database
CID 44428627	44428627	Click to see COC1=CC2=C(C=C1)C3C(CO2)(C4=C(O3)C=C(C=C4)OC)O	300.30	unknown	via CMAUP database
Maackiain	91510	Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5	284.26	unknown	via CMAUP database
Pterocarpin	1715306	Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5	298.29	unknown	via CMAUP database
Trifolirhizin	442827	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6	446.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
3',4',7-Trihydroxyisoflavone	5284648	Click to see C1=CC(=C(C=C1C2=COC3=C(C2=O)C=CC(=C3)O)O)O	270.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
Flavescenone A	101238023	Click to see CC(=CCC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC4=C(C=C3O)OCO4)O)C	384.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
Alpinumisoflavone	5490139	Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C	336.30	unknown	via CMAUP database
Flavescenone B	101238024	Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC4=C(C=C3O)OCO4)O)C	382.40	unknown	via CMAUP database
Lupalbigenin	10001388	Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)C	406.50	unknown	via CMAUP database
Luteone	5281797	Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=C(C=C(C=C3)O)O)O)C	354.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3'-Hydroxy-4'-methoxy-7-(6-O-(beta-D-xylopyranosyl)-beta-D-glucopyranosyloxy)isoflavone	73603980	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O	578.50	unknown	via CMAUP database
3'-Hydroxy-4'-methoxy-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone	73603978	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O	578.50	unknown	via CMAUP database
3'-Hydroxydaidzin	68607439	Click to see C1=CC(=C(C=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	via CMAUP database
3'-Methoxy-4'-hydroxy-7-(6-O-(beta-D-xylopyranosyl)-beta-D-glucopyranosyloxy)isoflavone	73603979	Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O	578.50	unknown	via CMAUP database
3'-Methoxy-4'-hydroxy-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone	102131642	Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O	578.50	unknown	via CMAUP database
3',4'-(Epoxymethanoxy)-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone	102131643	Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C(=CO4)C5=CC6=C(C=C5)OCO6)O)O)O)O)(CO)O	576.50	unknown	via CMAUP database
Ambonin	20055730	Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C(=CO4)C5=CC=C(C=C5)O)O)O)O)O)(CO)O	548.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin	5280448	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O	284.26	unknown	via CMAUP database
Koparin	5318834	Click to see COC1=C(C(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A	5280373	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O	284.26	unknown	via CMAUP database
Formononetin	5280378	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Kuraridine	44428631	Click to see CC(=CCC(CC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=C(C=C(C=C2)O)O)O)C(=C)C)C	438.50	unknown	via CMAUP database
Xanthohumol	639665	Click to see CC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=C(C=C2)O)O)C	354.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
Sophodibenzoside A	73603983	Click to see COC1=C(C=C(C=C1)C(=O)C(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)O)O	582.50	unknown	via CMAUP database
Sophodibenzoside B	73603972	Click to see COC1=C(C=C(C=C1)C(=O)C(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)O)O	582.50	unknown	via CMAUP database

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Simarouba glauca

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top