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Derris reticulata

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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 UUID643fdc4890bb6758617004
Scientific name Derris reticulata
Authority Craib
First published in Bull. Misc. Inform. Kew1927: 384 (1927)

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-0000200311
Tropicos 13022549
KEW urn:lsid:ipni.org:names:491417-1
The Plant List ild-46775
Open Tree Of Life 925050
NCBI Taxonomy 647089
IPNI 491417-1
GBIF 5350287
EOL 661495
CMAUP NPO15721

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
Advances in Natural Product Extraction Techniques, Electrospun Fiber Fabrication, and the Integration of Experimental Design: A Comprehensive Review Ponphaiboon J, Krongrawa W, Aung WW, Chinatangkul N, Limmatvapirat S, Limmatvapirat C Molecules 02-Jul-2023
PMCID:PMC10343563
doi:10.3390/molecules28135163
PMID:37446825
Prenylated Flavonoids in Topical Infections and Wound Healing Sychrová A, Škovranová G, Čulenová M, Bittner Fialová S Molecules 13-Jul-2022
PMCID:PMC9323352
doi:10.3390/molecules27144491
PMID:35889363
Do Uncommon Plant Phenolic Compounds Have Uncommon Properties? A Mini Review on Novel Flavonoids Carrillo JT, Borthakur D 12-Sep-2021
PMCID:PMC8445810
doi:10.1016/j.jobab.2021.09.001
Ethnobotany and the Role of Plant Natural Products in Antibiotic Drug Discovery Porras G, Chassagne F, Lyles JT, Marquez L, Dettweiler M, Salam AM, Samarakoon T, Shabih S, Farrokhi DR, Quave CL Chem Rev 09-Nov-2020
PMCID:PMC8183567
doi:10.1021/acs.chemrev.0c00922
PMID:33164487
Hypoglycaemic activity of Mathurameha, a Thai traditional herbal formula aqueous extract, and its effect on biochemical profiles of streptozotocin-nicotinamide-induced diabetic rats Chayarop K, Peungvicha P, Temsiririrkkul R, Wongkrajang Y, Chuakul W, Rojsanga P BMC Complement Altern Med 29-Jun-2017
PMCID:PMC5492915
doi:10.1186/s12906-017-1851-8
PMID:28662699
Antioxidant, α-glucosidase inhibitory activity and sub-chronic toxicity of Derris reticulata extract: its antidiabetic potential Kumkrai P, Weeranantanapan O, Chudapongse N BMC Complement Altern Med 27-Feb-2015
PMCID:PMC4354750
doi:10.1186/s12906-015-0552-4
PMID:25887793
Screening for estrogenic and antiestrogenic activities of plants growing in Egypt and Thailand El-Halawany AM, El Dine RS, Chung MH, Nishihara T, Hattori M Pharmacognosy Res 01-Apr-2011
PMCID:PMC3129019
doi:10.4103/0974-8490.81958
PMID:21772754
Two New Pyranoflavanones from the Stems Derris reticulata Somsak Ruchirawat, Chulabhorn Mahidol, Hunsa Prawat, Wirongrong Kaweetripob The Japan Institute of Heterocyclic Chemistry 09-Mar-2009
doi:10.3987/COM-02-9483
Prenylated flavanones from Derris reticulata Chulabhorn Mahidol, Hunsa Prawat, Somsak Ruchirawat, Kittisak Lihkitwitayawuid, Long-Ze Lin, Geoffrey A. Cordell Elsevier BV 04-Mar-2003
doi:10.1016/S0031-9422(97)00001-0
Reinvestigation of derris reticulata. Prawat H, Mahidol C, Ruchirawat S Pharm Biol 01-Jan-2000
doi:10.1076/PHBI.38.6.63.5960
PMID:23531140

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Lutein 5281243 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C 568.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Super Squalene; trans-Squalene;AddaVax 1105 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
4-Aminobutanoate 6992099 Click to see C(CC(=O)[O-])C[NH3+] 103.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
4-Allyloxycoumarin 5133468 Click to see C=CCOC1=CC(=O)OC2=CC=CC=C21 202.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Daphnin 439499 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(8S)-10-[(2R)-2,3-dihydroxy-3-methylbutyl]-5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 163034879 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC(C(C)(C)O)O)OC(CC3=O)C4=CC=C(C=C4)O)O)C 440.50 unknown https://doi.org/10.3987/COM-02-9483
(8S)-10-[(2S)-2,3-dihydroxy-3-methylbutyl]-5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 163034880 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC(C(C)(C)O)O)OC(CC3=O)C4=CC=C(C=C4)O)O)C 440.50 unknown https://doi.org/10.3987/COM-02-9483
(8S)-10-[(R)-[(2S)-3,3-dimethyloxiran-2-yl]-hydroxymethyl]-5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 163106540 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C4C(O4)(C)C)O)OC(CC3=O)C5=CC=C(C=C5)O)O)C 438.50 unknown https://doi.org/10.1076/PHBI.38.6.63.5960
(8S)-10-[[(2S)-3,3-dimethyloxiran-2-yl]methyl]-5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 162933197 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC4C(O4)(C)C)OC(CC3=O)C5=CC=C(C=C5)O)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(97)00001-0
(8S)-5-hydroxy-10-[(2R)-2-hydroxy-3-methylbut-3-enyl]-8-(4-hydroxyphenyl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 163072889 Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)O 422.50 unknown https://doi.org/10.1016/S0031-9422(97)00001-0
(8S)-5-hydroxy-10-[(2S)-2-hydroxy-3-methylbut-3-enyl]-8-(4-hydroxyphenyl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 163072890 Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)O 422.50 unknown https://doi.org/10.1016/S0031-9422(97)00001-0
10-(2,3-Dihydroxy-3-methylbutyl)-5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 85379880 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC(C(C)(C)O)O)OC(CC3=O)C4=CC=C(C=C4)O)O)C 440.50 unknown https://doi.org/10.3987/COM-02-9483
10-[(3,3-Dimethyloxiran-2-yl)methyl]-5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 73082308 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC4C(O4)(C)C)OC(CC3=O)C5=CC=C(C=C5)O)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(97)00001-0
2-(4-Hydroxyphenyl)-5-hydroxy-2,3-dihydro-10-(3-methyl-2-butenyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:5,4-b']dipyran-4-one 13846826 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1016/S0031-9422(97)00001-0
5-Hydroxy-10-(2-hydroxy-3-methylbut-3-enyl)-8-(4-hydroxyphenyl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 74819380 Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)O 422.50 unknown https://doi.org/10.1016/S0031-9422(97)00001-0
Dereticulatin 42607939 Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)O 422.50 unknown https://doi.org/10.1016/S0031-9422(97)00001-0
Lupinifolin 10250777 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1016/S0031-9422(97)00001-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
8-(2-O-beta-D-Xylopyranosyl-beta-D-glucopyranosyl)-4',5,7-trihydroxy-3'-methoxyflavone 101429641 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)OC5C(C(C(CO5)O)O)O)O 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3',4',5,7-Tetrahydroxy-6-(beta-D-glucopyranosyloxy)flavone 5459939 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
4',5-Dihydroxy-3',8-dimethoxy-7-(beta-D-glucopyranosyloxy)flavone 14825846 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)O)OC)O 492.40 unknown via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxy-phenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one 86573698 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O)O 608.50 unknown via CMAUP database
Luteolin 7-rutinoside 10461109 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 594.50 unknown via CMAUP database
Thermopsoside 11294177 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown via CMAUP database
Tricin 7-(6-rhamnosyl)glucoside 100925474 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C(=C5)OC)O)OC)O)O)O)O)O)O)O 638.60 unknown via CMAUP database
Tricin 7-glucoside 5322022 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 492.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
4',5,7-Trihydroxy-8-(beta-D-glucopyranosyloxy)flavone 6420079 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
8-(beta-D-Glucopyranosyloxy)-4',5,7-trihydroxy-3'-methoxyflavone 101288288 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Hypolaetin-8-glucoside 5318255 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Vitexin-4invertedexclamationmarka-o-glucoside 57387656 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(2S)-4',5-Dihydroxy-8-hydroxymethyl-6'',6''-dimethylpyrano[2'',3'':7,6]flavanone 10970624 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CO)OC(CC3=O)C4=CC=C(C=C4)O)O)C 368.40 unknown https://doi.org/10.3987/COM-02-9483
5-Hydroxy-10-(hydroxymethyl)-8-(4-hydroxyphenyl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 21597569 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CO)OC(CC3=O)C4=CC=C(C=C4)O)O)C 368.40 unknown https://doi.org/10.3987/COM-02-9483

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