PlantaeDB Logo
Login Sign-up

Erythrina subumbrans

Erythrina subumbrans - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Erythrina subumbrans - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID643fd952adbdc079634704
Scientific name Erythrina subumbrans
Authority (Hassk.) Merr.
First published in Philipp. J. Sci., C5: 113 (1910)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Erythrina lithosperma Blume ex Miq. Fl. Ned. Ind.1(1): 209 (1855)
Erythrina mysorensis Gamble Fl. Madras: 354 (1918)
Hypaphorus subumbrans Hassk. Hort. Bogor. Descr.: 198 (1858)
Erythrina holosericea Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist.42: 69 (1873)
Erythrina sumatrana Miq. Fl. Ned. Ind., Eerste Bijv.: 304 (1861)
Erythrina lithosperma var. inermis Miq. Fl. Ned. Ind.1(1): 209 (1855)
Erythrina lithosperma var. armata Miq. Fl. Ned. Ind.1(1): 209 (1855)
Hypaphorus subumbrans var. inermis Hassk. Hort. Bogor. Descr.: 199 (1858)
Hypaphorus subumbrans var. aculeata Hassk. Hort. Bogor. Descr.: 205 (1858)
Erythrina hypaphorus Boerl. ex Koord.-Schum. Meded. Lands Plantentuin19: 433 (1898)
Erythrina holoserica Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 42(2): 69 1873
Corallodendron holosericeum (Kurz) Kuntze Revis. Gen. Pl.1: 172 (1891)
Corallodendron lithospermum (Blume ex Miq.) Kuntze Revis. Gen. Pl.1: 173 (1891)
Corallodendron sumatranum (Miq.) Kuntze Revis. Gen. Pl.1: 173 (1891)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
ace reudeup
bjn dadap
Indonesian dadap serep
jv dhadhap srep
Malayalam തണൽമുരിക്ക്
Malay dedap batik
Thai ทองหลางป่า
Chinese 翅果刺桐

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
  • Pacific
    • South-central Pacific
      • Cook Islands
    • Southwestern Pacific
      • Fiji
      • Niue
      • Samoa

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000185021
USDA Plants ERSU15
Tropicos 13043706
INPN 448580
KEW urn:lsid:ipni.org:names:494601-1
The Plant List ild-31147
Open Tree Of Life 80721
NCBI Taxonomy 1288014
IPNI 494601-1
iNaturalist 82770
GBIF 5349636
Freebase /m/0gg9mcb
EOL 643188
USDA GRIN 15769
Wikipedia Erythrina_subumbrans
CMAUP NPO28044

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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Pharm Biol 22-Dec-2023
PMCID:PMC10763916
doi:10.1080/13880209.2023.2292261
PMID:38131672
Impact of the coronavirus pandemic on financial returns of smallholder coffee plantations in Lao PDR Phimmavong S, Maraseni TN, Keenan RJ, Phongoudome C, Douangphosy B Agrofor Syst 22-Jan-2023
PMCID:PMC9867901
doi:10.1007/s10457-023-00808-4
PMID:36712175
An overview on possible management strategies for coffee white stem borer Xylotrechus quadripes Chevrolat (Coleoptera: Cerambycidae) in Nepal Pandey M, Kayastha P, Khanal S, Shrestha S, Thakur G, Adhikari K, Shah KK, Pant D, Khanal D Heliyon 28-Aug-2022
PMCID:PMC9478357
doi:10.1016/j.heliyon.2022.e10445
PMID:36119870
Pest categorisation of Maconellicoccus hirsutus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Sven Magnusson C, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Gregoire J, Malumphy C, Antonatos S, Kertesz V, Maiorano A, Papachristos D, MacLeod A EFSA J 11-Jan-2022
PMCID:PMC8749475
doi:10.2903/j.efsa.2022.7024
PMID:35035580
Cheminformatic Characterization of Natural Antimicrobial Products for the Development of New Lead Compounds Oselusi SO, Christoffels A, Egieyeh SA Molecules 29-Jun-2021
PMCID:PMC8271829
doi:10.3390/molecules26133970
PMID:34209681
Antidiabetic and antimicrobial flavonoids from the twigs and roots of Erythrina subumbrans (Hassk.) Merr. Phukhatmuen P, Meesakul P, Suthiphasilp V, Charoensup R, Maneerat T, Cheenpracha S, Limtharakul T, Pyne SG, Laphookhieo S Heliyon 28-Apr-2021
PMCID:PMC8102414
doi:10.1016/j.heliyon.2021.e06904
PMID:33997418
The Effect of Steaming and Fermentation on Nutritive Values, Antioxidant Activities, and Inhibitory Properties of Tea Leaves Chupeerach C, Aursalung A, Watcharachaisoponsiri T, Whanmek K, Thiyajai P, Yosphan K, Sritalahareuthai V, Sahasakul Y, Santivarangkna C, Suttisansanee U Foods 08-Jan-2021
PMCID:PMC7827290
doi:10.3390/foods10010117
PMID:33429899
Ethnobotanical study on wild edible plants used by three trans-boundary ethnic groups in Jiangcheng County, Pu’er, Southwest China Cao Y, Li R, Zhou S, Song L, Quan R, Hu H J Ethnobiol Ethnomed 27-Oct-2020
PMCID:PMC7590688
doi:10.1186/s13002-020-00420-1
PMID:33109239
Medicinal Plants for Treating Musculoskeletal Disorders among Karen in Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Plants (Basel) 28-Jun-2020
PMCID:PMC7412036
doi:10.3390/plants9070811
PMID:32605228
Anti-Infectious Plants of the Thai Karen: A Meta-Analysis Phumthum M, Balslev H Antibiotics (Basel) 02-Jun-2020
PMCID:PMC7345792
doi:10.3390/antibiotics9060298
PMID:32498413
Selection of Thai Medicinal Plants with Anti-Obesogenic Potential via In Vitro Methods Ruangaram W, Kato E Pharmaceuticals (Basel) 29-Mar-2020
PMCID:PMC7243097
doi:10.3390/ph13040056
PMID:32235329
Assessing the Identity of Commercial Herbs From a Cambodian Market Using DNA Barcoding Cui X, Li W, Wei J, Qi Y, Li R, Yang Y, Shi Y, Meng X, Mi Y, Huot T, Sun W, Zheng X Front Pharmacol 24-Mar-2020
PMCID:PMC7105672
doi:10.3389/fphar.2020.00244
PMID:32265692
Traditional Uses of Leguminosae among the Karen in Thailand Sutjaritjai N, Wangpakapattanawong P, Balslev H, Inta A Plants (Basel) 13-Dec-2019
PMCID:PMC6963713
doi:10.3390/plants8120600
PMID:31847100
Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD Evid Based Complement Alternat Med 21-Aug-2017
PMCID:PMC5585606
doi:10.1155/2017/5748256
PMID:28904556

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 / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(1S,11R,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,15-diol 162885746 Click to see C1CN2C3C1(C=CC(C3)O)C4=CC5=C(C=C4C2O)OCO5 287.31 unknown https://doi.org/10.1021/NP070506W
> Alkaloids and derivatives / Erythrina alkaloids / Erythrinanes
(2R,13bS)-2,11,12-trimethoxy-1,2,5,6-tetrahydroindolo[7a,1-a]isoquinoline-3,8,9-trione 24770438 Click to see COC1CC23C(=CC1=O)CCN2C(=O)C(=O)C4=CC(=C(C=C34)OC)OC 357.40 unknown https://doi.org/10.1021/NP070506W
10,11-Dioxoepierythratidine 24770439 Click to see COC1CC23C(=CC1O)CCN2C(=O)C(=O)C4=CC(=C(C=C34)OC)OC 359.40 unknown https://doi.org/10.1021/NP070506W
10,11-Dioxoerythratine 24770437 Click to see COC1CC23C(=CC1O)CCN2C(=O)C(=O)C4=CC5=C(C=C34)OCO5 343.30 unknown https://doi.org/10.1021/NP070506W
18-Hydroxy-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,16-tetraene-11,12-dione 162992989 Click to see COC1CC23C(=CC1O)CCN2C(=O)C(=O)C4=CC5=C(C=C34)OCO5 343.30 unknown https://doi.org/10.1021/NP070506W
2,11,12-Trimethoxy-1,2,5,6-tetrahydroindolo[7a,1-a]isoquinoline-3,8,9-trione 162983414 Click to see COC1CC23C(=CC1=O)CCN2C(=O)C(=O)C4=CC(=C(C=C34)OC)OC 357.40 unknown https://doi.org/10.1021/NP070506W
3-hydroxy-2,11,12-trimethoxy-2,3,5,6-tetrahydro-1H-indolo[7a,1-a]isoquinoline-8,9-dione 162974908 Click to see COC1CC23C(=CC1O)CCN2C(=O)C(=O)C4=CC(=C(C=C34)OC)OC 359.40 unknown https://doi.org/10.1021/NP070506W
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Panduratin H 24864449 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)OC)C2=CC=CC=C2 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
[(2R)-7-Hydroxy-5-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-8-yl][(1R,2S,6R)-3-methyl-2-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexenyl]methanone 101855692 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 540.70 unknown via CMAUP database
[(2S)-7-Hydroxy-5-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-8-yl][(1R,2S,6R)-3-methyl-2-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexenyl]methanone 101855694 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 540.70 unknown via CMAUP database
Panduratin D 24864268 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CO3)C4=CC=CC=C4 430.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
CID 429190 429190 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C 458.70 unknown https://doi.org/10.1021/NP070506W
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP070506W
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP070506W
Sophoradiol 9846221 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)C)O)C)C 442.70 unknown https://doi.org/10.1021/NP070506W
Soyasapogenol B 115012 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C 458.70 unknown https://doi.org/10.1021/NP070506W
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
3-(1H-indol-3-yl)-2-(trimethylazaniumyl)propanoate 3861164 Click to see C[N+](C)(C)C(CC1=CNC2=CC=CC=C21)C(=O)[O-] 246.30 unknown https://doi.org/10.1139/V81-400
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Hypaphorine 442106 Click to see C[N+](C)(C)C(CC1=CNC2=CC=CC=C21)C(=O)[O-] 246.30 unknown https://doi.org/10.1021/JA01874A065
https://doi.org/10.1139/V81-400
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Panduratin E 24864269 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)C)C4=CC=CC=C4 472.60 unknown via CMAUP database
> Organoheterocyclic compounds / Coumarans
(6aS,11aR,11bS)-6a,11b-dihydroxy-9-methoxy-10-(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromen-3-one 101995345 Click to see CC(=CCC1=C(C=CC2=C1OC3C2(COC4=CC(=O)C=CC34O)O)OC)C 370.40 unknown https://doi.org/10.1021/NP070506W
6a,11b-Dihydroxy-9-methoxy-10-(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromen-3-one 162999850 Click to see CC(=CCC1=C(C=CC2=C1OC3C2(COC4=CC(=O)C=CC34O)O)OC)C 370.40 unknown https://doi.org/10.1021/NP070506W
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-[(3,3-Dimethyloxiran-2-yl)methoxy]-6,8-dimethoxychromen-2-one 14841895 Click to see CC1(C(O1)COC2=C(C=C3C=CC(=O)OC3=C2OC)OC)C 306.31 unknown https://doi.org/10.1021/NP070506W
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(-)-nicolaioidesin B 637029 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O 406.50 unknown via CMAUP database
(1'R,2'S,6'R)-2-Hydroxyisopanduratin A 23656472 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)O)O 392.50 unknown via CMAUP database
(2-hydroxy-4,6-dimethoxyphenyl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 44444916 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)OC)O)C3=CC=CC=C3 420.50 unknown via CMAUP database
2,6-Dihydroxy-4-methoxyphenyl[2beta-(3-methyl-2-butenyl)-3-methyl-6alpha-phenyl-3-cyclohexene-1beta-yl]methanone 25023021 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
4-hydroxypanduratin A 636530 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=CC=C3 392.50 unknown via CMAUP database
Isopanduratin A 10069916 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
Isopanduratin A1 44444913 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O 406.50 unknown via CMAUP database
Panduratin A 6483648 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
Panduratin C 6483647 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=C(C=C3)O 422.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-6-geranylpinostrobin 44444914 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)OC)C)C 406.50 unknown via CMAUP database
2alpha-Phenyl-6-[(E)-3,7-dimethyl-2,6-octadienyl]-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one 44444915 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C)C 392.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-8-geranylpinostrobin 23656470 Click to see CC(=CCCC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C)C 406.50 unknown via CMAUP database
(2S)-5,7-dihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 124355984 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)C 476.60 unknown https://doi.org/10.1021/NP070506W
5,7,4'-Trihydroxy-3',8-diprenylflavanone 10319282 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)C 408.50 unknown https://doi.org/10.1021/NP070506W
Euchrestaflavanone A 484588 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)C 408.50 unknown https://doi.org/10.1021/NP070506W
Hydroxysophoranone 42607927 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)C 476.60 unknown https://doi.org/10.1021/NP070506W
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 2-prenylated flavones
vogelin C 44448192 Click to see CC(=CCC1=C(C=C(C=C1O)O)C2=CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)C 422.50 unknown https://doi.org/10.1021/NP070506W
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
5-O-Methylnaringenin 182315 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
Alpinetin 154279 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-5,7-Dimethoxyflavanone 689012 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
3,5,7-Trimethoxyflavone 117900 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(=C(O2)C3=CC=CC=C3)OC 312.30 unknown via CMAUP database
3',4',5,7-Tetramethoxyflavone 631170 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-phenyl- 5748697 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O 298.29 unknown via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
5,7-Dimethoxyflavone 88881 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 282.29 unknown via CMAUP database
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 unknown via CMAUP database
Apigenin trimethyl ether 79730 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC 312.30 unknown via CMAUP database
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
Quercetin pentamethyl ether 97332 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC)OC 372.40 unknown via CMAUP database
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown via CMAUP database
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown via CMAUP database
Tetramethylkaempferol 631095 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
1-methoxy-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 162857633 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C(=C(C(=C4)O)CC=C(C)C)OC)O)C 422.50 unknown https://doi.org/10.1021/NP070506W
1-Methoxyerythrabyssin Ii 24761044 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C(=C(C(=C4)O)CC=C(C)C)OC)O)C 422.50 unknown https://doi.org/10.1021/NP070506W
3,6a-Dihydroxy-9-methoxy-10-prenylpterocarpan 3559400 Click to see CC(=CCC1=C(C=CC2=C1OC3C2(COC4=C3C=CC(=C4)O)O)OC)C 354.40 unknown https://doi.org/10.1021/NP070506W
4-Prenylphaseollidin 21141346 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)O)C 392.50 unknown https://doi.org/10.1021/NP070506W
9-Methoxy-2,10-bis(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a-diol 85135193 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3(C2OC4=C3C=CC(=C4CC=C(C)C)OC)O)C 422.50 unknown https://doi.org/10.1021/NP070506W
CID 10408212 10408212 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1021/NP070506W
Cristacarpin 126540 Click to see CC(=CCC1=C(C=CC2=C1OC3C2(COC4=C3C=CC(=C4)O)O)OC)C 354.40 unknown https://doi.org/10.1021/NP070506W
Erybraedin A 362562 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)O)C 392.50 unknown https://doi.org/10.1021/NP070506W
Erycristagallin 10362969 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3=C2OC4=C3C=CC(=C4CC=C(C)C)O)C 390.50 unknown https://doi.org/10.1021/NP070506W
Erystagallin A 10410005 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3(C2OC4=C3C=CC(=C4CC=C(C)C)OC)O)C 422.50 unknown https://doi.org/10.1021/NP070506W
Erythrabyssin II 5086400 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1021/NP070506W
eryvarin A 44448173 Click to see CC1(C(CC2=C(O1)C=CC3=C2OC4C3(COC5=C4C=CC(=C5)OC)O)O)C 370.40 unknown https://doi.org/10.1021/NP070506W
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
3-[2,4-Dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-8-(3-methylbut-2-enyl)chromen-4-one 73946815 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=COC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C 422.50 unknown https://doi.org/10.1021/NP070506W
> Phenylpropanoids and polyketides / Kavalactones
2H-Pyran-2-one, 4-methoxy-6-(2-phenylethyl)- 160673 Click to see COC1=CC(=O)OC(=C1)CCC2=CC=CC=C2 230.26 unknown via CMAUP database
Demethoxyyangonin 5273621 Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
4,2',4'-Trihydroxy-6'-methoxydihydrochalcone 42607705 Click to see COC1=CC(=CC(=C1C(=O)CCC2=CC=C(C=C2)O)O)O 288.29 unknown via CMAUP database
Phloretin 4788 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O)O)O)O 274.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(1R,4S,13R)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl]-3-phenylprop-2-en-1-one 101306880 Click to see CC1(C2CCC3(CC2C4=C(O3)C=C(C(=C4O1)C(=O)C=CC5=CC=CC=C5)O)C)C 390.50 unknown via CMAUP database
2',4-Dihydroxy-4',6'-dimethoxychalcone 6293081 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)O)O 300.30 unknown via CMAUP database
Cardamonin 641785 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown via CMAUP database
CID 460718 460718 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O 256.25 unknown via CMAUP database
Helichrysetin 6253344 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
2',4'-Dihydroxy-3'-[(2E)-3,7-dimethyl-2,6-octadienyl]-6'-methoxychalcone 23656471 Click to see CC(=CCCC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=CC=C2)O)C)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
1-[(1R,2R,3R)-2-(3,5-Dihydroxy-phenyl)-4,6-dihydroxy-3-(4-hydroxy-phenyl)-indan-1-yl]-1-(4-hydroxy-phenyl)-methanone 484754 Click to see C1=CC(=CC=C1C2C(C(C3=C2C(=CC(=C3)O)O)C(=O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 470.50 unknown https://doi.org/10.1021/NP070506W
2,4-Dihydroxy-6-phenethylbenzoic acid (2E)-3,7-dimethyl-2,6-octadienyl ester 23656469 Click to see CC(=CCCC(=CCOC(=O)C1=C(C=C(C=C1O)O)CCC2=CC=CC=C2)C)C 394.50 unknown via CMAUP database

Biological Material Top ebay Auctions

Please wait .. loading items ..

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.