Scientific name	Authority	First published in
Ochradenus rostratus	Ehrenb. ex Müll.Arg.	Neue Denkschr. Allg. Schweiz. Ges. Gesammten Naturwiss. 16: 95 (1858)
Asparagus deltae	Blatt.	J. Indian Bot. Soc. 6: 70 (1927)

Common names Top

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Filter by language:

Language	Common/alternative name
English	ochradenus jagodowy
Spanish	ochradenus jagodowy
Arabic	جردى توتية
Arabic	كرد
Arabic	علندرة
Arabic	قرضي
Bulgarian	ochradenus jagodowy
German	ochradenus jagodowy
French	ochradenus jagodowy
Hebrew	רכפתן מדברי
Italian	ochradenus jagodowy
Russian	ochradenus jagodowy

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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

Africa click to expand
- Northeast Tropical Africa
  - Chad
  - Djibouti
  - Eritrea
  - Ethiopia
  - Somalia
  - Sudan
- Northern Africa
  - Egypt
  - Libya

Asia-temperate click to expand
- Arabian Peninsula
  - Gulf States
  - Kuwait
  - Oman
  - Saudi Arabia
  - Yemen
- Western Asia
  - Iran
  - Palestine
  - Sinai

Asia-tropical click to expand
- Indian Subcontinent
  - India
  - Pakistan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000388341
Tropicos	27300078
KEW	urn:lsid:ipni.org:names:715387-1
The Plant List	kew-2396575
Open Tree Of Life	706047
NCBI Taxonomy	264972
IPNI	715387-1
iNaturalist	185344
GBIF	7275957
EOL	2900349
CMAUP	NPO4204

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

Genome-wide transcriptome profiling reveals molecular response pathways of Trichoderma harzianum in response to salt stress

Yang Q, Mao Z, Hao Y, Zheng S, Zhao J, Li Y, Yang Y, Xie B, Ling J, Li Y

Front Microbiol

01-Feb-2024

PMCID:	PMC10867199
doi:	10.3389/fmicb.2024.1342584
PMID:	38362502

Potential of Halophytes as Sustainable Fodder Production by Using Saline Resources: A Review of Current Knowledge and Future Directions

Hasnain M, Abideen Z, Ali F, Hasanuzzaman M, El-Keblawy A

Plants (Basel)

29-May-2023

PMCID:	PMC10255648
doi:	10.3390/plants12112150
PMID:	37299129

Bacterial detoxification of plant defence secondary metabolites mediates the interaction between a shrub and frugivorous birds

Trabelcy B, Shteindel N, Lalzar M, Izhaki I, Gerchman Y

Nat Commun

31-Mar-2023

PMCID:	PMC10066296
doi:	10.1038/s41467-023-37525-6
PMID:	37002264

Glucosinolates in Wild-Growing Reseda spp. from Croatia

Đulović A, Tomaš J, Blažević I

Molecules

12-Feb-2023

PMCID:	PMC9959328
doi:	10.3390/molecules28041753
PMID:	36838744

Saudi Arabian Plants: A Powerful Weapon against a Plethora of Diseases

El-Seedi HR, Kotb SM, Musharraf SG, Shehata AA, Guo Z, Alsharif SM, Saeed A, Hamdi OA, Tahir HE, Alnefaie R, Verpoorte R, Khalifa SA

Plants (Basel)

08-Dec-2022

PMCID:	PMC9783889
doi:	10.3390/plants11243436
PMID:	36559548

The Life Cycle of the Xylophagous Beetle, Steraspis speciosa (Coleoptera, Buprestidae), Feeding on Acacia Trees in Saudi Arabia

Alanazi NA, Ghorbel M, Brini F, Mseddi K

Life (Basel)

02-Dec-2022

PMCID:	PMC9782656
doi:	10.3390/life12122015
PMID:	36556380

Fuel exploitation and environmental degradation at the Iron Age copper industry of the Timna Valley, southern Israel

Cavanagh M, Ben-Yosef E, Langgut D

Sci Rep

21-Sep-2022

PMCID:	PMC9492654
doi:	10.1038/s41598-022-18940-z
PMID:	36130974

Synergistic action of Trichoderma koningiopsis and T. asperellum mitigates salt stress in paddy

Anshu A, Agarwal P, Mishra K, Yadav U, Verma I, Chauhan S, Srivastava PK, Singh PC

Physiol Mol Biol Plants

02-Jun-2022

PMCID:	PMC9203646
doi:	10.1007/s12298-022-01192-6
PMID:	35722516

Wild Egyptian medicinal plants show in vitro and in vivo cytotoxicity and antimalarial activities

Abdou AM, Seddek AL, Abdelmageed N, Badry MO, Nishikawa Y

BMC Complement Med Ther

12-May-2022

PMCID:	PMC9101831
doi:	10.1186/s12906-022-03566-5
PMID:	35550108

Pest categorisation of Plicosepalus acaciae

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Fejer Justesen A, 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, Dehnen‐Schmutz K, Migheli Q, Vloutoglou I, Maiorano A, Streissl F, Reignault PL

EFSA J

10-Mar-2022

PMCID:	PMC8913038
doi:	10.2903/j.efsa.2022.7142
PMID:	35311013

Floristic composition of Jandaf Mountain as biodiversity hotspot area in southwestern Saudi Arabia

Al-Namazi AA, Algarni SM, Wan JS, Al Mosallam MS, Alotaibi F

Saudi J Biol Sci

05-Mar-2022

PMCID:	PMC9280213
doi:	10.1016/j.sjbs.2022.03.003
PMID:	35844416

A novel salt-tolerant strain Trichoderma atroviride HN082102.1 isolated from marine habitat alleviates salt stress and diminishes cucumber root rot caused by Fusarium oxysporum

Zhang C, Wang W, Hu Y, Peng Z, Ren S, Xue M, Liu Z, Hou J, Xing M, Liu T

BMC Microbiol

01-Mar-2022

PMCID:	PMC8887007
doi:	10.1186/s12866-022-02479-0
PMID:	35232373

Climate change and hydrological regime in arid lands: Impacts of dams on the plant diversity, vegetation structure and soil in Saudi Arabia

Al-Munqedhi BM, El-Sheikh MA, Alfarhan AH, Alkahtani AM, Arif IA, Rajagopal R, Alharthi ST

Saudi J Biol Sci

25-Jan-2022

PMCID:	PMC9280318
doi:	10.1016/j.sjbs.2022.01.043
PMID:	35844430

Heavy Metal Effects on Biodiversity and Stress Responses of Plants Inhabiting Contaminated Soil in Khulais, Saudi Arabia

Alsherif EA, Al-Shaikh TM, AbdElgawad H

Biology (Basel)

20-Jan-2022

PMCID:	PMC8869145
doi:	10.3390/biology11020164
PMID:	35205031

The first complete chloroplast genome sequences in Resedaceae: Genome structure and comparative analysis

Alzahrani D, Albokhari E, Abba A, Yaradua S

Sci Prog

06-Dec-2021

PMCID:	PMC10450604
doi:	10.1177/00368504211059973
PMID:	34870493

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 / Phenols / Methoxyphenols
4-Amino-3-methoxyphenol	19818056	Click to see COC1=C(C=CC(=C1)O)N	139.15	unknown	via CMAUP database
N-Trans-feruloyltramine	5280537	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O	313.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
(6'S)-beta,epsilon-carotene	6419724	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Acetobetulinic acid	10300534	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O	498.70	unknown	via CMAUP database
Diosgenin	99474	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	via CMAUP database
Tigogenin	99516	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1	416.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-beta-hydroxysteroids
(1R,2S,4S,6R,7S,8R,9S,10R,12S,13R,16S)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-10,16-diol	46833330	Click to see CC1C2C(CC3C2(C(CC4C3CC=C5C4(CCC(C5)O)C)O)C)OC16CCCCO6	416.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Physalins and derivatives
(1R,2R,4R,5R,8S,11R,13S,14S,15R,16S,19S,22S,23R,25S)-2,19-dihydroxy-13,16,23-trimethyl-6,10,17,26,27,30-hexaoxanonacyclo[23.2.2.15,14.15,15.01,23.04,22.08,13.011,16.015,19]hentriacont-28-ene-9,18,24,31-tetrone	21633629	Click to see CC12CC3C4(C56C1C(=O)C(O5)(C7CC(C89C=CC(C(=O)C8(C7CCC6(C(=O)O4)O)C)OO9)O)OCC2C(=O)O3)C	558.50	unknown	via CMAUP database
(1R,2S,5S,8S,9R,15S,17R,18R,21S,24R,26S,27S)-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.118,27.01,5.02,24.08,17.09,14.021,26]nonacosa-11,13-diene-4,10,22,29-tetrone	56683730	Click to see CC12CC3C4(C56C1C(=O)C(O5)(C7CC(C8=CC=CC(=O)C8(C7CCC6(C(=O)O4)O)C)O)OCC2C(=O)O3)C	526.50	unknown	via CMAUP database
(1R,2S,5S,8S,9S,14R,15R,17R,18R,21S,24R,26S,27S)-14-chloro-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.118,27.01,5.02,24.08,17.09,14.021,26]nonacos-11-ene-4,10,22,29-tetrone	10769263	Click to see CC12CC3C4(C56C1C(=O)C(O5)(C7CC(C8(CC=CC(=O)C8(C7CCC6(C(=O)O4)O)C)Cl)O)OCC2C(=O)O3)C	563.00	unknown	via CMAUP database
5,6-Epxoyphysalin B	49864133	Click to see CC12CC3C4(C56C1C(=O)C(O5)(C7CC8C9(O8)CC=CC(=O)C9(C7CCC6(C(=O)O4)O)C)OCC2C(=O)O3)C	526.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
Solanidine	65727	Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C	397.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
(1R,2S,3'R,4S,6R,7S,8R,9S,10R,12S,13R,16S)-10,16-dihydroxy-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,6'-piperidine]-3'-carboxylic acid	21573758	Click to see CC1C2C(CC3C2(C(CC4C3CC=C5C4(CCC(C5)O)C)O)C)OC16CCC(CN6)C(=O)O	459.60	unknown	via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-10,16-diol	21573757	Click to see CC1C2C(CC3C2(C(CC4C3CC=C5C4(CCC(C5)O)C)O)C)OC16CCC(CN6)CO	445.60	unknown	via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-10,16-diol	21573755	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)O)C)O)C)C)NC1	429.60	unknown	via CMAUP database
N-Methylsolasodine	21573751	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)N(C1)C	427.70	unknown	via CMAUP database
Solasodine	442985	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1	413.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
12-Hydroxysolasonine	21573761	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)NC1	900.10	unknown	via CMAUP database
CID 21573759	21573759	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)NC1	721.90	unknown	via CMAUP database
Degalactotigonin	162401	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)C)OC1	1035.20	unknown	via CMAUP database
Nigrumnin I	10820113	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1	1151.30	unknown	via CMAUP database
Nigrumnin II	10630134	Click to see CC1CCC2(C(C3(C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1	1181.30	unknown	via CMAUP database
Solamargine	73611	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1	868.10	unknown	via CMAUP database
Solanigroside C	16083118	Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)O)C)OC1=O)O	1111.20	unknown	via CMAUP database
Solanigroside D	16083121	Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1=O)O	1181.30	unknown	via CMAUP database
Solanigroside E	16083119	Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1=O)O	1197.30	unknown	via CMAUP database
Solanigroside G	16083120	Click to see CC1CCC2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)O)C)OC1	1051.20	unknown	via CMAUP database
Solanigroside H	16083123	Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1	1047.20	unknown	via CMAUP database
Solasonine	119247	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1	884.10	unknown	via CMAUP database
Uttronin B	102058012	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
Uttroside B	44566638	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)C)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)O	1215.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-Azaniumylacetate	5257127	Click to see C(C(=O)[O-])[NH3+]	75.07	unknown	via CMAUP database
> 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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Ethyl 4-O-(3-O-methyl-6-deoxy-beta-D-glucopyranosyl)-3-O-methyl-2,6-dideoxy-alpha-D-glucopyranoside	101490302	Click to see CCOC1CC(C(C(O1)C)OC2C(C(C(C(O2)C)O)OC)O)OC	350.40	unknown	via CMAUP database
Ethyl 4-O-(3-O-methyl-6-deoxy-beta-D-glucopyranosyl)-3-O-methyl-2,6-dideoxy-beta-D-glucopyranoside	101490301	Click to see CCOC1CC(C(C(O1)C)OC2C(C(C(C(O2)C)O)OC)O)OC	350.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
2-(1H-Indol-3-yl)ethyl acetate	588705	Click to see CC(=O)OCCC1=CNC2=CC=CC=C21	203.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
4-Hydroxy-3-methoxycinnamic Acid Ethyl Ester	65133	Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)OC	222.24	unknown	via CMAUP database
Ethyl caffeate	5317238	Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O	208.21	unknown	via CMAUP database
Methyl 4-hydroxy-3,5-dimethoxycinnamate; Sinapic acid methyl ester	159894	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC	238.24	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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Petunidin 3-(p-coumaroylrutinoside) 5-glucoside	101243377	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC(=C(C(=C6)OC)O)O)O)O)O)O)O)OC(=O)C=CC7=CC=C(C=C7)O	933.80	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one	5353915	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	https://doi.org/10.1016/0031-9422(91)80109-E
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	51402807	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	https://doi.org/10.1016/0031-9422(91)80109-E
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	https://doi.org/10.1016/0031-9422(91)80109-E
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	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	https://doi.org/10.1016/0031-9422(91)80109-E
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	90657242	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O	626.50	unknown	https://doi.org/10.1016/0031-9422(91)80109-E
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5462193	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/0031-9422(91)80109-E
Afzelin	5316673	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	432.40	unknown	https://doi.org/10.1016/0031-9422(91)80109-E
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/0031-9422(91)80109-E
kaempferol-3-O-alpha-L-rhamnoside	15558501	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	432.40	unknown	https://doi.org/10.1016/0031-9422(91)80109-E
Kaempferol-3-O-rhamnoside	5835713	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	432.40	unknown	https://doi.org/10.1016/0031-9422(91)80109-E
Quercetin 3-gentiobioside	5320834	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O	626.50	unknown	https://doi.org/10.1016/0031-9422(91)80109-E
Quercetin-3-gentiobioside	13915961	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O	626.50	unknown	https://doi.org/10.1016/0031-9422(91)80109-E
Quercitrin	5280459	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	https://doi.org/10.1016/0031-9422(91)80109-E
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2S,3S,4S,5S,6R)-6-[[(2R,3S,4R,5S,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-7-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	163003417	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)COC(=O)C=CC6=CC=C(C=C6)O)O)O)O)O)O)O)C7=CC(=C(C=C7)O)O)O)O)O)O	918.80	unknown	https://doi.org/10.1016/0031-9422(91)80109-E
3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	101616682	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O	756.70	unknown	https://doi.org/10.1016/0031-9422(91)80109-E
3-[(2S,3S,4R,5R,6R)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	162965900	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O	756.70	unknown	https://doi.org/10.1016/0031-9422(91)80109-E
3-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one	74978204	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O	756.70	unknown	https://doi.org/10.1016/0031-9422(91)80109-E

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Ochradenus baccatus

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