Scientific name	Authority	First published in
Robinia uliginosa	Willd.	Sp. Pl., ed. 4, 3: 1133 (1802)
Pongamia madagascariensis	Baker
Deguelia uliginosa	(Willd.) Baill.	Bull. Mens. Soc. Linn. Paris1: 442 (1885)
Deguelia trifoliata	(Lour.) Taub.	Bot. Centralbl.47: 386 (1891)
Derris uliginosa	(Willd.) Benth.	F.A.W.Miquel, Pl. Jungh.: 252 (1852)
Derris heterophylla	(Willd.) Backer ex K.Heyne	Nutt. Pl. Ned.-Ind., ed. 2, 2: 806 (1927)
Dalbergia heterophylla	Willd.	Sp. Pl., ed. 4, 3: 901 (1802)
Derris forsteniana	Blume ex Miq.	Fl. Ned. Ind.1(1): 144 (1855)
Deguelia uliginosa var. loureiri	Benth.
Galedupa uliginosa	(Willd.) Roxb.	Fl. Ind. ed. 1832, 3: 243 (1832)
Pongamia uliginosa	(Willd.) DC.	Prodr.2: 416 (1825)
Pterocarpus uliginosus	Roxb. ex G.Don	Gen. Hist.2: 377 (1832)
Derris multiflora	Benth.	F.A.W.Miquel, Pl. Jungh.: 253 (1852)
Derris heteropylla	(Willd.) Backer
Derris affinis	Benth.	F.A.W.Miquel, Pl. Jungh.: 252 (1852)
Derris floribunda	Prain	Fl. Ned. Ind. i. I. 152; Benth. in Journ. Linn. Soc. iv. Suppl. (1860) 105.
Tephrosia uliginosa	(Willd.) Spreng.	Syst. Veg. ed. 16, 3: 282 (1826)
Pongamia triphylla	Wight	Bot. Misc.3(Suppl.): t. 41 (1833)
Pongamia religiosa	Wight	Bot. Misc.3: 301 (1833)
Pongamia piscatoria	Seem.	Bonplandia (Hannover)9: 255 (1861)
Sweetia uliginosa	(Willd.) G.Don	Gen. Hist.2: 342 (1832)
Brachypterum floribundum	Miq.	Fl. Ned. Ind.1(1): 139 (1855)
Dalbergia acuminata	Hassk.	Flora25(2, Beibl. 1): 53 (1842)
Dalbergia radicans	Zipp. ex Miq.	Fl. Ned. Ind.1(1): 141 (1855)
Dalbergia repens	Span.	Linnaea15: 197 (1841)
Deguelia floribunda	(Miq.) Taub.	Bot. Centralbl.47: 386 (1891)
Deguelia multiflora	(Benth.) Taub.	Bot. Centralbl.47: 386 (1891)
Pterocarpus trifoliatus	Kuntze	Revis. Gen. Pl.1: 203 (1891)
Pterocarpus forstenianus	Kuntze	Revis. Gen. Pl.1: 203 (1891)
Pterocarpus multiflorus	Kuntze	Revis. Gen. Pl.1: 203 (1891)
Derris trifoliata var. macrocarpa	Domin	Biblioth. Bot.22(89): 232 (1926)
Pterocarpus floribundus	(Miq.) Kuntze	Revis. Gen. Pl.1: 203 (1891)
Derris floribunda	(Miq.) Benth.	J. Proc. Linn. Soc., Bot.4(Suppl.): 105 (1860)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	threeleaf derris
Arabic	دريس منقعي
Japanese	シイノキカズラ
Malayalam	പൊന്നുംവള്ളി
szy	sadim
Thai	ถอบแถบทะเล
Vietnamese	cóc kèn
Chinese	三葉魚藤
Chinese	三叶鱼藤
Chinese	毒鱼藤
Chinese	篓藤
Chinese	鱼藤
Chinese	魚藤

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

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
- Northeast Tropical Africa
  - Somalia
- South Tropical Africa
  - Mozambique
- Southern Africa
  - Kwazulu-Natal
  - Swaziland
- Western Indian Ocean
  - Comoros
  - Madagascar
  - Réunion
  - Seychelles

Asia-temperate click to expand
- China
  - China Southeast
  - Hainan
- Eastern Asia
  - Nansei-shoto
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - Bismarck Archipelago
  - New Guinea
  - Solomon Islands

Australasia click to expand
- Australia
  - Northern Territory
  - Queensland

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands
  - Marianas
- South-central Pacific
  - Society Islands
  - Tuamotu
- Southwestern Pacific
  - Fiji
  - Nauru
  - New Caledonia
  - Samoa
  - Tonga
  - Vanuatu
  - Wallis-Futuna Islands

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil West-central

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000198908
USDA Plants	DETR5
Tropicos	13018261
INPN	447181
KEW	urn:lsid:ipni.org:names:491450-1
The Plant List	ild-4542
Open Tree Of Life	1064460
NCBI Taxonomy	185716
IPNI	491450-1
iNaturalist	354252
GBIF	5350336
Freebase	/m/0fq1kvp
EOL	686038
USDA GRIN	13555
Wikipedia	Derris_trifoliata
CMAUP	NPO5064

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

Acute rotenone poisoning: A scoping review

Tat J, Heskett K, Boss GR

Heliyon

21-Mar-2024

PMCID:	PMC11021885
doi:	10.1016/j.heliyon.2024.e28334
PMID:	38633629

Targeting oxidative stress with natural products: A novel strategy for esophageal cancer therapy

Cao F, Zhang HL, Guo C, Xu XL, Yuan Q

World J Gastrointest Oncol

15-Feb-2024

PMCID:	PMC10900143
doi:	10.4251/wjgo.v16.i2.287
PMID:	38425393

Implementation of machine learning in DNA barcoding for determining the plant family taxonomy

Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA

Heliyon

21-Sep-2023

PMCID:	PMC10520734
doi:	10.1016/j.heliyon.2023.e20161
PMID:	37767518

Biogenic Silver Nanoparticles for Targeted Cancer Therapy and Enhancing Photodynamic Therapy

Kah G, Chandran R, Abrahamse H

Cells

07-Aug-2023

PMCID:	PMC10417642
doi:	10.3390/cells12152012
PMID:	37566091

Recent advances in nanoparticle applications in respiratory disorders: a review

Taghavizadeh Yazdi ME, Qayoomian M, Beigoli S, Boskabady MH

Front Pharmacol

19-Jul-2023

PMCID:	PMC10395100
doi:	10.3389/fphar.2023.1059343
PMID:	37538179

Energy metabolism disturbance in migraine: From a mitochondrial point of view

Wang Y, Wang Y, Yue G, Zhao Y

Front Physiol

13-Apr-2023

PMCID:	PMC10133718
doi:	10.3389/fphys.2023.1133528
PMID:	37123270

The Potassium Channel Blocker β-Bungarotoxin from the Krait Bungarus multicinctus Venom Manifests Antiprotozoal Activity

Osipov AV, Cheremnykh EG, Ziganshin RH, Starkov VG, Nguyen TT, Nguyen KC, Le DT, Hoang AN, Tsetlin VI, Utkin YN

Biomedicines

07-Apr-2023

PMCID:	PMC10136136
doi:	10.3390/biomedicines11041115
PMID:	37189733

Targeting glycolysis in non-small cell lung cancer: Promises and challenges

Xu JQ, Fu YL, Zhang J, Zhang KY, Ma J, Tang JY, Zhang ZW, Zhou ZY

Front Pharmacol

30-Nov-2022

PMCID:	PMC9748442
doi:	10.3389/fphar.2022.1037341
PMID:	36532721

Hydroxyapatite-binding Silver/Titanium Dioxide as a Potential Control Compound Against Mosquito Vectors, Aedes aegypti (Diptera: Culicidae) and Anopheles dirus (Diptera: Culicidae)

Srisawat R, Sriwichai P, Ruangsittichai J, Rotejanaprasert C, Imaizumi N, Yamaki D, Maekawa M, Eshita Y, Okazaki N

J Med Entomol

14-Nov-2022

PMCID:	PMC9835759
doi:	10.1093/jme/tjac175
PMID:	36373613

Potential Focal Adhesion Kinase Inhibitors in Management of Cancer: Therapeutic Opportunities from Herbal Medicine

Chen F, Zhong Z, Zhang C, Lu Y, Chan YT, Wang N, Zhao D, Feng Y

Int J Mol Sci

01-Nov-2022

PMCID:	PMC9659249
doi:	10.3390/ijms232113334
PMID:	36362132

Effect of the physicochemical changes in the antimicrobial durability of green synthesized silver nanoparticles during their long-term storage

Habibullah G, Viktorova J, Ulbrich P, Ruml T

RSC Adv

25-Oct-2022

PMCID:	PMC9594854
doi:	10.1039/d2ra04667a
PMID:	36349158

Stem cambial variants of Taiwan lianas

Yang SZ, Chen PH, Chen JJ

Bot Stud

24-Sep-2022

PMCID:	PMC9509506
doi:	10.1186/s40529-022-00358-5
PMID:	36153445

Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells

Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T

Molecules

09-Sep-2022

PMCID:	PMC9501561
doi:	10.3390/molecules27185858
PMID:	36144591

Distribution Characteristics and Restoration Application of Vegetation in Chengcun Bay Surrounding Areas of Yangjiang City

Chen S, Sun Y, Tang K, Zhang F, Ding W, Wang A

Int J Environ Res Public Health

20-Aug-2022

PMCID:	PMC9408589
doi:	10.3390/ijerph191610399
PMID:	36012034

Green Nano-Biotechnology: A New Sustainable Paradigm to Control Dengue Infection

Zohra T, Khalil AT, Saeed F, Latif B, Salman M, Ikram A, Ayaz M, Murthy HC

Bioinorg Chem Appl

08-Aug-2022

PMCID:	PMC9377959
doi:	10.1155/2022/3994340
PMID:	35979184

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
2-O-(4-Hydroxybenzoyl)-6-O-(galloyl)-beta-D-glucopyranose	102086065	Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(OC2O)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	452.40	unknown	via CMAUP database
2,6-di-O-galloyl-beta-glucose	14034262	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O	484.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)-	67179	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
17alpha-Hydroperoxy-28-norlupa-20(29)-ene-3beta-ol	25136231	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OO	444.70	unknown	via CMAUP database
17beta-Hydroperoxy-28-norlupa-20(29)-ene-3beta-ol	25136233	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OO	444.70	unknown	via CMAUP database
28-Nor-20(29)-lupene-diol	15838686	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)O	428.70	unknown	via CMAUP database
Asiatic Acid	119034	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O	488.70	unknown	via CMAUP database
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	via CMAUP database
Betulinaldehyde	99615	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O	440.70	unknown	via CMAUP database
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	via CMAUP database
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
Ursolic aldehyde	14423521	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C=O	440.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Platanic acid	64980	Click to see CC(=O)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	458.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Pimentol	9917512	Click to see COC1=C(C(=CC(=C1)CC=C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O	494.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(4S)-7,8-dimethoxyspiro[2,3-dihydro-1,5-benzodioxepine-4,2'-furo[2,3-e][1]benzofuran]-3'-one	163007815	Click to see COC1=C(C=C2C(=C1)OCCC3(O2)C(=O)C4=C(O3)C5=C(C=C4)OC=C5)OC	368.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.01.002
7,8-Dimethoxyspiro[2,3-dihydro-1,5-benzodioxepine-4,2'-furo[2,3-e][1]benzofuran]-3'-one	102188215	Click to see COC1=C(C=C2C(=C1)OCCC3(O2)C(=O)C4=C(O3)C5=C(C=C4)OC=C5)OC	368.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.01.002
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(6,7-dimethoxy-3,4-dihydro-2H-chromen-4-yl)-(4-methoxy-1-benzofuran-5-yl)methanone	24756410	Click to see COC1=C(C=C2C(=C1)C(CCO2)C(=O)C3=C(C4=C(C=C3)OC=C4)OC)OC	368.40	unknown	https://doi.org/10.1139/V07-120
[(4S)-6,7-dimethoxy-3,4-dihydro-2H-chromen-4-yl]-(4-methoxy-1-benzofuran-5-yl)methanone	163040373	Click to see COC1=C(C=C2C(=C1)C(CCO2)C(=O)C3=C(C4=C(C=C3)OC=C4)OC)OC	368.40	unknown	https://doi.org/10.1139/V07-120
[(4S)-6,7-dimethoxy-3,4-dihydro-2H-chromen-4-yl]-[(2R)-4-hydroxy-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl]methanone	154497377	Click to see CC(=C)C1CC2=C(O1)C=CC(=C2O)C(=O)C3CCOC4=CC(=C(C=C34)OC)OC	396.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.02.005
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(6,7-dimethoxy-3,4-dihydro-2H-chromen-4-yl)-(5-methoxy-2,2-dimethylchromen-6-yl)methanone	21580517	Click to see CC1(C=CC2=C(O1)C=CC(=C2OC)C(=O)C3CCOC4=CC(=C(C=C34)OC)OC)C	410.50	unknown	https://doi.org/10.1139/V07-120 https://doi.org/10.1016/J.PHYTOCHEM.2005.02.005
[(4R)-6,7-dimethoxy-3,4-dihydro-2H-chromen-4-yl]-(5-methoxy-2,2-dimethylchromen-6-yl)methanone	11418415	Click to see CC1(C=CC2=C(O1)C=CC(=C2OC)C(=O)C3CCOC4=CC(=C(C=C34)OC)OC)C	410.50	unknown	https://doi.org/10.1139/V07-120 https://doi.org/10.1016/J.PHYTOCHEM.2005.02.005
[(4S)-6,7-dimethoxy-3,4-dihydro-2H-chromen-4-yl]-(5-hydroxy-2,2-dimethylchromen-6-yl)methanone	162872260	Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C3CCOC4=CC(=C(C=C34)OC)OC)C	396.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.02.005
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
6,7-Dimethoxychroman-4-one	11469836	Click to see COC1=C(C=C2C(=C1)C(=O)CCO2)OC	208.21	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.01.002
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
17,18-Dimethoxy-7,7-dimethyl-8,21-dioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-1(14),3(12),4(9),5,10,15,17,19-octaen-13-one	162889679	Click to see CC1(C=CC2=C(O1)C=CC3=C2CC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)C	390.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.01.002
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	via CMAUP database
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
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl]Oxy-Chromen-4-one	12304323	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	51402820	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	via CMAUP database
5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	51402816	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O	464.40	unknown	via CMAUP database
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
Leucoside	44566720	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O	580.50	unknown	via CMAUP database
O-Quercetin 3-(2-O-xylopyranosylglucopyranoside)	101138141	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O	596.50	unknown	via CMAUP database
Rhamnetin-O(3)-neohesperidoside	5487094	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC(=C(C=C5)O)O)O)O)O)O)O	624.50	unknown	https://doi.org/10.1021/NP50046A032
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(-)-Deguelin;(-)-cis-Deguelin	606171	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C	394.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.02.005 https://doi.org/10.1139/V07-120 https://doi.org/10.1055/S-2004-815447
(1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(12H)-one, 1,2-dihydro-8,9-dimethoxy-2-(1-methylethenyl)-, (R)-	99190	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC	392.40	unknown	https://doi.org/10.1139/V07-120
(1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(6aH)-one,12,12a-dihydro-6a-hydroxy-8,9-dimethoxy-, (6aR-cis)-	184294	Click to see COC1=C(C=C2C(=C1)C3(C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)O)OC	368.30	unknown	https://doi.org/10.1139/V07-120
(1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(6aH)-one,12,12a-dihydro-6a-hydroxy-8,9-dimethoxy-, (6aS-cis)-	183157	Click to see COC1=C(C=C2C(=C1)C3(C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)O)OC	368.30	unknown	https://doi.org/10.1055/S-2004-815447
(Rac)-Tephrosin	4485131	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C	410.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268681/ https://doi.org/10.1139/V07-120 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.002 https://doi.org/10.1055/S-2004-815447
13-Hydroxy-16,17-dimethoxy-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),5,9,14,16,18-heptaen-12-one	13846201	Click to see COC1=C(C=C2C(=C1)C3(C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)O)OC	368.30	unknown	https://doi.org/10.1055/S-2004-815447 https://doi.org/10.1139/V07-120
5'beta-Rotenone	5102	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC	394.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.02.005 https://doi.org/10.1139/V07-120 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.002 https://doi.org/10.1055/S-2004-815447
6-Hydroxy-9,10-dimethoxy-3,3-dimethyl-13,13a-dihydro-3H,7aH-pyrano[2,3-c:6,5-f']dichromen-7-one	243723	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C	410.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.02.005 https://doi.org/10.1139/V07-120 https://doi.org/10.1055/S-2004-815447
alpha-Toxicarol	442826	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C	410.40	unknown	https://doi.org/10.1055/S-2004-815447 https://doi.org/10.1139/V07-120 https://doi.org/10.1016/J.PHYTOCHEM.2005.02.005
CID 303992	303992	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC	410.40	unknown	https://doi.org/10.1139/V07-120
Deguelin	107935	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C	394.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.02.005 https://doi.org/10.1055/S-2004-815447 https://doi.org/10.1139/V07-120
Dehydrodeguelin	3083803	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)C	392.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.01.002 https://doi.org/10.1139/V07-120
Dehydrorotenone	303993	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC	392.40	unknown	https://doi.org/10.1139/V07-120
Dehydrotoxicarol	5491616	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)O)C	408.40	unknown	https://doi.org/10.1139/V07-120
Derride	13846199	Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)OC	352.30	unknown	https://doi.org/10.1055/S-2004-815447
Elliptone	160477	Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)OC	352.30	unknown	https://doi.org/10.1055/S-2004-815447
Rotenolone	68184	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC	410.40	unknown	https://doi.org/10.1139/V07-120
Rotenone	6758	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC	394.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.01.002 https://doi.org/10.1016/S0031-9422(00)98664-3 https://doi.org/10.1055/S-2004-815447 https://doi.org/10.1016/J.PHYTOCHEM.2005.02.005 https://doi.org/10.1139/V07-120
Tephrosin	114909	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C	410.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.01.002 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268681/ https://doi.org/10.1055/S-2004-815447 https://doi.org/10.1139/V07-120
> Phenylpropanoids and polyketides / Tannins
1,6-bis-O-galloyl-beta-D-glucose	440221	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	484.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3-O-Methylellagic acid 4-O-rhamnoside	16720461	Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)OC)O)O)O	462.40	unknown	via CMAUP database
3,3'-Di-O-methylellagic acid	5488919	Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)OC)O)O	330.24	unknown	via CMAUP database
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	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.

Derris trifoliata

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