Common products:
The only documented non-medicinal products derived from Prangos pabularia are as a forage and hay crop for livestock in its native range. Published agronomic reports describe its use as cultivated forage (cut as hay) in parts of Central and West Asia.

Food and beverages (non-medicinal):
No edible products or food ingredients are documented for this taxon; avoid describing seeds, roots, or aerial parts as human foods.

Industrial and craft applications:
No industrial products such as fibers, gums/resins, dyes/inks, timber, paper pulp, adhesives, biofuels, or bioplastics are documented for Prangos pabularia.

Colorants and tanning:
No tannins, natural dyes, or coloring agents are reported for this taxon.

Wood and fiber:
No wood or fiber products are documented.

Fragrance and cosmetics:
No fragrance, essential-oil products, or cosmetic ingredients are documented for this species.

Properties relevant to use:
The forage uses are associated with the plant’s nutritive value (reported crude protein, fiber, and mineral content in hay); these properties support feeding value but no other products.

Standards and regulation:
No standards or regulatory frameworks are documented specifically for products derived from Prangos pabularia. Forage trade or livestock feeding may be governed by regional feed safety regulations, but no product-specific standards are reported.

Sustainability and sourcing:
As a forage, P. pabularia is cultivated for hay and grazed in arid and semi-arid regions; no specific sustainability or sourcing data are documented beyond regional agronomic practice.

Synonyms Top

Scientific name	Authority	First published in
Prangos pachypoda	Korovin	Bot. Mater. Gerb. Glavn. Bot. Sada R.S.F.S.R. 5: 73 (1924)
Prangos scabra	Nábělek	Spisy Prír. Fak. Masarykovy Univ. 35: 126 (1923)
Cachrys lophoptera	(Boiss.) Takht.	Fl. Erevana : 188 (1972)
Koelzella pabularia	(Lindl.) M.Hiroe	Umbell. Asia 1: 147 (1958)
Prangos hissarica	Korovin	Izv. Akad. Nauk Tadzhiksk. S.S.R., Otd. Biol. Nauk 1(50): 18 (1973)
Cachrys pabularia	(Lindl.) Baill.	Hist. Pl. 7: 193 (1879)

Common names Top

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Filter by language:

Language	Common/alternative name
Kazakh	Биік прангос
Russian	Прангос кормовой

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Prangos pabularia subsp. cylindrocarpa	(Korovin) Pimenov & V.N.Tikhom.	Sosud. Rast. SSSR : 28 (1981)
Prangos pabularia subsp. gyrocarpa	(G.A.Kuzjmina) Lyskov & Pimenov	Pl. Syst. Evol. 303(7): 825. 2017 [8 Apr 2017] [epublished]
Prangos pabularia subsp. lamellata	(Korovin) Pimenov & V.N.Tikhom.	Sosud. Rast. SSSR : 28 (1981)
Prangos pabularia subsp. sarawschanica	(Regel & Schmalh.) Lyskov & Pimenov	Pl. Syst. Evol. 303(7): 825. 2017 [8 Apr 2017] [epublished]
Prangos pabularia subsp. pabularia		Unknown

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

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-temperate click to expand
- Caucasus
  - Transcaucasus
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Western Asia
  - Afghanistan
  - Iran
  - Iraq
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan
  - West Himalaya

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001068744
Tropicos	1703110
KEW	urn:lsid:ipni.org:names:847470-1
The Plant List	tro-1703110
Open Tree Of Life	795193
Observations.org	137139
NCBI Taxonomy	52497
IPNI	847470-1
iNaturalist	792743
GBIF	6026426
USDA GRIN	29557
CMAUP	NPO19017

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

Nutrient addition alters plant community productivity but not the species diversity of a mountain meadow in Tajikistan

Mekhrovar O, Li YM, Abdullo M, Sino Y, Fan L

Front Plant Sci

15-Jan-2024

PMCID:	PMC10822985
doi:	10.3389/fpls.2023.1235388
PMID:	38288411

Mechanisms of anti-ulcer actions of Prangos pabularia (L.) in ethanol-induced gastric ulcer in rats

Jabbar AA, Mothana RA, Ameen Abdulla M, Othman Abdullah F, Abdul-Aziz Ahmed K, Rizgar Hussen R, Hawwal MF, Fantoukh OI, Hasson S

Saudi Pharm J

29-Oct-2023

PMCID:	PMC10641563
doi:	10.1016/j.jsps.2023.101850
PMID:	37965491

Wound Healing Effect of Supercritical Carbon Dioxide Datura metel L. Leaves Extracts: An In Vitro Study of Anti-Inflammation, Cell Migration, MMP-2 Inhibition, and the Modulation of the Sonic Hedgehog Pathway in Human Fibroblasts

Ruksiriwanich W, Linsaenkart P, Muangsanguan A, Sringarm K, Jantrawut P, Arjin C, Sommano SR, Phimolsiripol Y, Barba FJ

Plants (Basel)

04-Jul-2023

PMCID:	PMC10346957
doi:	10.3390/plants12132546
PMID:	37447107

Vapor and Liquid Phase Profiles of Essential Oils from Abies, Picea and Pinus Species and Their Phytotoxic Interactions with Weed Growth in Pre- and Post-Emergence Conditions

Garzoli S, Vaglia V, Iriti M, Vitalini S

Plants (Basel)

03-Mar-2023

PMCID:	PMC10007276
doi:	10.3390/plants12051172
PMID:	36904031

In Vitro and In Vivo Studies of Heraclenol as a Novel Bacterial Histidine Biosynthesis Inhibitor against Invasive and Biofilm-Forming Uropathogenic Escherichia coli

Kaur H, Chaudhary N, Modgil V, Kalia M, Kant V, Mohan B, Bhatia A, Taneja N

Antibiotics (Basel)

06-Jan-2023

PMCID:	PMC9854483
doi:	10.3390/antibiotics12010110
PMID:	36671311

Analysis of Primary Liquid Chromatography Mass Spectrometry Data by Neural Networks for Plant Samples Classification

Turova P, Stavrianidi A, Svekolkin V, Lyskov D, Podolskiy I, Rodin I, Shpigun O, Buryak A

Metabolites

19-Oct-2022

PMCID:	PMC9611620
doi:	10.3390/metabo12100993
PMID:	36295895

Synthesis, characterization, and antimicrobial evaluation of polyvinylalcohol-osthol composite films

GOWSIA I, MIR FA, BANDAY JA

Turk J Chem

30-Aug-2022

PMCID:	PMC10446923
doi:	10.55730/1300-0527.3496
PMID:	37621357

Natural Coumarins: Exploring the Pharmacological Complexity and Underlying Molecular Mechanisms

Sharifi-Rad J, Cruz-Martins N, López-Jornet P, Lopez EP, Harun N, Yeskaliyeva B, Beyatli A, Sytar O, Shaheen S, Sharopov F, Taheri Y, Docea AO, Calina D, Cho WC

Oxid Med Cell Longev

23-Aug-2021

PMCID:	PMC8440074
doi:	10.1155/2021/6492346
PMID:	34531939

Oxypeucedanin: Chemotaxonomy, Isolation, and Bioactivities

Mottaghipisheh J

Plants (Basel)

30-Jul-2021

PMCID:	PMC8401860
doi:	10.3390/plants10081577
PMID:	34451622

Dihydropyrimidinones: efficient one-pot green synthesis using Montmorillonite-KSF and evaluation of their cytotoxic activity

Farooq S, Alharthi FA, Alsalme A, Hussain A, Dar BA, Hamid A, Koul S

RSC Adv

23-Nov-2020

PMCID:	PMC9057999
doi:	10.1039/d0ra09072g
PMID:	35516739

Imperatorin–pharmacological meaning and analytical clues: profound investigation

Kozioł E, Skalicka-Woźniak K

Phytochem Rev

20-Feb-2016

PMCID:	PMC4939159
doi:	10.1007/s11101-016-9456-2
PMID:	27453708

Preserving a Comprehensive Vegetation Knowledge Base – An Evaluation of Four Historical Soviet Vegetation Maps of the Western Pamirs (Tajikistan)

Vanselow KA, Samimi C, Breckle SW

PLoS One

16-Feb-2016

PMCID:	PMC4755548
doi:	10.1371/journal.pone.0148930
PMID:	26881428

Correction: Isolation, Cytotoxicity Evaluation and HPLC-Quantification of the Chemical Constituents from Prangos pabularia

N/A

PLoS One

03-Dec-2014

PMCID:	PMC4255031
doi:	10.1371/journal.pone.0115110

Isolation, Cytotoxicity Evaluation and HPLC-Quantification of the Chemical Constituents from Prangos pabularia

Farooq S, Shakeel-u-Rehman, Dangroo NA, Priya D, Banday JA, Sangwan PL, Qurishi MA, Koul S, Saxena AK

PLoS One

14-Oct-2014

PMCID:	PMC4196845
doi:	10.1371/journal.pone.0108713
PMID:	25314269

Influence of UV-radiation on the photosynthesis and photosynthetic carbon metabolism in high mountainous plants

Abdullaev A, Djumaev B, Karimov KK

BMC Plant Biol

31-May-2005

PMCID:	PMC1810255
doi:	10.1186/1471-2229-5-S1-S1
PMID:	15927007

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonacosane	12409	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC	408.80	unknown	https://doi.org/10.1007/BF00568353
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Himeic Acid A	11774903	Click to see	435.50	unknown	via CMAUP database
himeic acid B	21579676	Click to see	321.40	unknown	via CMAUP database
himeic acid C	21777983	Click to see	434.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Hexadecanoic Acid Propylamide	10379895	Click to see	297.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Alloxanthin	6443740	Click to see	564.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(16R)-ent-kauran-16-ol	21593607	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)C	290.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Kauran-16-ol	623309	Click to see	290.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	13854258	Click to see	220.35	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	97032059	Click to see	220.35	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see	220.35	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
beta-Spathulenol	522266	Click to see	220.35	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Spathulenol	92231	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
6-(3,7-Dimethylocta-2,6-dienyl)-7-hydroxychromen-2-one	5357655	Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C)C	298.40	unknown	via CMAUP database
7-[(2E,6E)-8-hydroxy-3,7-dimethylocta-2,6-dienoxy]chromen-2-one	13819674	Click to see	314.40	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene	5280489	Click to see	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R)-3,5,5-trimethyl-4-[(3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohex-2-en-1-yl]octadeca-3,5,7,9,11,13,15,17-octaen-1-ynyl]cyclohex-3-en-1-ol	101289802	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(=CCCC2(C)C)C)C)C	550.90	unknown	via CMAUP database
(2Z,4E,6E,8E,10E,12E,14E,16E)-3-Hydroxy-19-((4R)-4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-1-((1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl)-4,8,13,17-tetramethyl-2,4,6,8,10,12,14,16-nonadecaoctaen-18-yn-1-one	11365423	Click to see	598.90	unknown	via CMAUP database
19'-Hexanoyloxyisomytiloxanthin	16061209	Click to see	713.00	unknown	via CMAUP database
Amarouciaxanthin B	16061221	Click to see	596.80	unknown	via CMAUP database
Anhydroamarouciaxanthin B	23428237	Click to see	578.80	unknown	via CMAUP database
cis-(4R,5R)-4-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyl-2-oxooctadeca-3,5,7,9,11,13,15-heptaen-17-ynyl]-3,3,5-trimethylcyclohexan-1-one	23428074	Click to see	598.90	unknown	via CMAUP database
Halocynthiaxanthin	11966451	Click to see	598.90	unknown	via CMAUP database
NV766Twa77	102146782	Click to see	600.90	unknown	via CMAUP database
Pectenol A/(Pectenol)	16061215	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(C(C(CC2(C)C)O)O)C)C)C	582.90	unknown	via CMAUP database
Pfaffic acid	441936	Click to see	440.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
7-Dehydrocholesterol	439423	Click to see	384.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Brassicasterol	5281327	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	398.70	unknown	via CMAUP database
Ergosterol	444679	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
Notoamide J	25180709	Click to see CC(C)(C=C)C1(C2=C(C=C(C=C2)O)NC1=O)CC3C(=O)N4CCCC4C(=O)N3	383.40	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
Betaine	247	Click to see	117.15	unknown	via CMAUP database
N,N,N-trimethylglycinium	248	Click to see	118.15	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 / L-alpha-amino acids
L-Arginine	6322	Click to see	174.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
3,3'-Methylenebis(tyrosine)	3082144	Click to see	374.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Kainoids
CID 17753955	17753955	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
Domoic acid C5'-diastereomer	5311075	Click to see	311.33	unknown	via CMAUP database
Isodomoic acid F	101790920	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
> Organic acids and derivatives / Organic sulfonic acids and derivatives / Organosulfonic acids and derivatives / Organosulfonic acids
Taurine	1123	Click to see	125.15	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols / N-acylethanolamines
Anandamide	5281969	Click to see	347.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2,3,4-trimethylphenyl)methoxy]oxane-3,4,5-triol	101010854	Click to see	312.36	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
(5S)-2,4,4-trimethyl-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one	162846349	Click to see CC1=CC(C(CC1=O)COC2C(C(C(C(O2)CO)O)O)O)(C)C	330.37	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(2-methyl-4-oxopyran-3-yl)oxyoxan-2-yl]methyl acetate	11088814	Click to see CC1=C(C(=O)C=CO1)OC2C(C(C(C(O2)COC(=O)C)O)O)O	330.29	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
[3,4,5-Trihydroxy-6-(2-methyl-4-oxopyran-3-yl)oxyoxan-2-yl]methyl acetate	85394544	Click to see	330.29	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
2-(Hydroxymethyl)-6-(propan-2-yloxy)oxane-3,4,5-triol	15613266	Click to see	222.24	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
2-(Hydroxymethyl)-6-[(2,3,4-trimethylphenyl)methoxy]oxane-3,4,5-triol	163039315	Click to see	312.36	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
2,4,4-trimethyl-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohexa-2,5-dien-1-one	101010853	Click to see CC1=CC(C(=CC1=O)COC2C(C(C(C(O2)CO)O)O)O)(C)C	328.36	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
2,4,4-Trimethyl-5-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one	162846347	Click to see	330.37	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
2,4,4-Trimethyl-5-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohexa-2,5-dien-1-one	163074771	Click to see	328.36	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Isopropyl beta-D-glucopyranoside	21572943	Click to see CC(C)OC1C(C(C(C(O1)CO)O)O)O	222.24	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
Aspermytin A	9993091	Click to see	266.38	unknown	via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
CID 101396440	101396440	Click to see CC1CC2C3C(CC4(O3)C(CC(CN4)C)C)OC(C1)(O2)CC(=C)C5C(CC(C(O5)(C(C6CC7C(O6)CC(C8(O7)CCC9(O8)C=CCC(O9)C=CCCC(=O)O)C)O)O)C)C	842.10	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodiazepines / 1,4-benzodiazepines
(3R,3'R)-3'-(3-hydroxyphenyl)-4-methylspiro[1H-1,4-benzodiazepine-3,2'-oxirane]-2,5-dione	92278353	Click to see CN1C(=O)C2=CC=CC=C2NC(=O)C13C(O3)C4=CC(=CC=C4)O	310.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
6-Hydroxy-4,4,7a-trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one	14334	Click to see	196.24	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Loliolide	100332	Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C	196.24	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(3S,8aS)-3-[[(3R)-7,7-dimethyl-3-(2-methylbut-3-en-2-yl)-2-oxo-1H-pyrano[2,3-g]indol-3-yl]methyl]-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione	16127840	Click to see	449.50	unknown	via CMAUP database
Notoamide A	16128040	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	463.50	unknown	via CMAUP database
Notoamide B	16127923	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	447.50	unknown	via CMAUP database
Notoamide H	25180895	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)O)C	479.50	unknown	via CMAUP database
Notoamide O	102043608	Click to see	479.50	unknown	via CMAUP database
Notoamide Q	46919487	Click to see	479.60	unknown	via CMAUP database
Sclerotiamide	10647785	Click to see	463.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
Notoamide D	16127841	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3(CC5N4C(=O)C6CCCN6C5=O)O)C(C)(C)C=C)C	449.50	unknown	via CMAUP database
Notoamide K	25180896	Click to see	465.50	unknown	via CMAUP database
Notoamide P	46919486	Click to see CC1(C=CC2=C3C(=CC(=C2O1)Br)C4(CC5(C(=O)N6CCCC6C(=O)N5C4(N3)C(C)(C)C=C)O)O)C	544.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
Viridicatol	115033	Click to see C1=CC=C2C(=C1)C(=C(C(=O)N2)O)C3=CC(=CC=C3)O	253.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
(+)-Stephacidin A	16127922	Click to see	431.50	unknown	via CMAUP database
Notoamide F	25180710	Click to see	461.60	unknown	via CMAUP database
Notoamide G	25180707	Click to see	477.60	unknown	via CMAUP database
Notoamide I	25180708	Click to see	445.50	unknown	via CMAUP database
Notoamide R	46919488	Click to see	447.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
(S)-Auraptenol	13343540	Click to see	260.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
6-(2-Hydroxy-3-methylbut-3-enyl)-7-methoxychromen-2-one	14886049	Click to see CC(=C)C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC)O	260.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
6-(2,3-Dihydroxy-3-methylbutyl)-7-methoxycoumarin	605103	Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC)O)O	278.30	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-7-methoxychromen-2-one	71721987	Click to see	260.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
7-methoxy-2-oxo-2H-chromene-8-carbaldehyde	11275724	Click to see COC1=C(C2=C(C=C1)C=CC(=O)O2)C=O	204.18	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-7-methoxychromen-2-one	13343542	Click to see	260.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Auraptenol	13343541	Click to see	260.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Osthol	10228	Click to see	244.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7 https://doi.org/10.1007/BF00568353
Suberosin	68486	Click to see CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)OC)C	244.28	unknown	https://doi.org/10.1007/BF00564139
Ulopterol	176475	Click to see	278.30	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(8R)-8-prop-1-en-2-yl-8,9-dihydrofuro[2,3-h]chromen-2-one	51520705	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3	228.24	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
8-Prop-1-en-2-yl-8,9-dihydrofuro(2,3-h)chromen-2-one	5318874	Click to see	228.24	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Angenomalin	51520704	Click to see	228.24	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Linear furanocoumarins
4-[(2R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(2-methyl-4-oxopyran-3-yl)oxyoxan-3-yl]oxy-2-hydroxy-3-methylbutoxy]furo[2,3-g]chromen-6-one	163105905	Click to see	574.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
9-[(2R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(2-methyl-4-oxopyran-3-yl)oxyoxan-3-yl]oxy-2-hydroxy-3-methylbutoxy]furo[2,3-g]chromen-6-one	163079185	Click to see	574.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
9-[3-[4,5-Dihydroxy-6-(hydroxymethyl)-2-(2-methyl-4-oxopyran-3-yl)oxyoxan-3-yl]oxy-2-hydroxy-3-methylbutoxy]furo[2,3-g]chromen-6-one	163079184	Click to see	574.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(-)-Heraclenol	40429858	Click to see	304.29	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
(+)-4-[(R)-2-Hydroxy-3-methoxy-3-methylbutoxy]-7H-furo[3,2-g][1]benzopyran-7-one	15945061	Click to see	318.32	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
(+)-Oxypeucedanin	928465	Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C	286.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
[(2S)-3-hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-4-yl)oxybutan-2-yl] acetate	163193611	Click to see	346.30	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
[3-Hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-4-yl)oxybutan-2-yl] acetate	14481789	Click to see	346.30	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
4-((3,3-Dimethyloxiran-2-Yl)Methoxy)Furo(3,2-G)Chromen-7-One	160544	Click to see	286.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
4-(2-Hydroxy-3-methoxy-3-methyl-butoxy)-furo[3,2-g][1]benzopyran-7-one	483514	Click to see	318.32	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
4-(2,3-Dihydroxy-3-methylbutoxy)furo(3,2-g)chromen-7-one	483513	Click to see	304.29	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
4-[(2R)-2-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(2-methyl-4-oxopyran-3-yl)oxyoxan-3-yl]oxy-3-hydroxy-3-methylbutoxy]furo[3,2-g]chromen-7-one	162852254	Click to see CC1=C(C(=O)C=CO1)OC2C(C(C(C(O2)CO)O)O)OC(COC3=C4C=CC(=O)OC4=CC5=C3C=CO5)C(C)(C)O	574.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
4-[(2R)-2-hydroxy-3-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutoxy]furo[3,2-g]chromen-7-one	97538132	Click to see	466.40	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
4-[(2R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(2-methyl-4-oxopyran-3-yl)oxyoxan-3-yl]oxy-2-hydroxy-3-methylbutoxy]furo[3,2-g]chromen-7-one	163083972	Click to see CC1=C(C(=O)C=CO1)OC2C(C(C(C(O2)CO)O)O)OC(C)(C)C(COC3=C4C=CC(=O)OC4=CC5=C3C=CO5)O	574.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
4-[(2S)-2-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(2-methyl-4-oxopyran-3-yl)oxyoxan-3-yl]oxy-3-hydroxy-3-methylbutoxy]furo[3,2-g]chromen-7-one	162852255	Click to see	574.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
4-[(2S)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(2-methyl-4-oxopyran-3-yl)oxyoxan-3-yl]oxy-2-hydroxy-3-methylbutoxy]furo[3,2-g]chromen-7-one	163083971	Click to see	574.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
4-[2-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(2-methyl-4-oxopyran-3-yl)oxyoxan-3-yl]oxy-3-hydroxy-3-methylbutoxy]furo[3,2-g]chromen-7-one	11124670	Click to see	574.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
4-[2-[4,5-Dihydroxy-6-(hydroxymethyl)-2-(2-methyl-4-oxopyran-3-yl)oxyoxan-3-yl]oxy-3-hydroxy-3-methylbutoxy]furo[3,2-g]chromen-7-one	22297213	Click to see	574.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
4-[2-Hydroxy-3-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutoxy]furo[3,2-g]chromen-7-one	74096942	Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)OC4C(C(C(C(O4)CO)O)O)O	466.40	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
4-[3-[4,5-Dihydroxy-6-(hydroxymethyl)-2-(2-methyl-4-oxopyran-3-yl)oxyoxan-3-yl]oxy-2-hydroxy-3-methylbutoxy]furo[3,2-g]chromen-7-one	85302719	Click to see CC1=C(C(=O)C=CO1)OC2C(C(C(C(O2)CO)O)O)OC(C)(C)C(COC3=C4C=CC(=O)OC4=CC5=C3C=CO5)O	574.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
5-[[(2S)-3,3-dimethyloxiran-2-yl]methoxy]furo[3,2-g]chromen-7-one	53316971	Click to see CC1(C(O1)COC2=CC(=O)OC3=C2C=C4C=COC4=C3)C	286.28	unknown	via CMAUP database
9-((2-Hydroxy-3-methylbut-3-en-1-yl)oxy)-7H-furo(3,2-g)(1)benzopyran-7-one	148619	Click to see	286.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
9-(2-Hydroxy-3-methoxy-3-methylbutoxy)furo[3,2-g]chromen-7-one	483515	Click to see	318.32	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
9-(2,3-Dihydroxy-3-methylbutoxy)furo(3,2-g)chromen-7-one	328236	Click to see	304.29	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
9-[(2R)-2-hydroxy-3-methoxy-3-methylbutoxy]furo[3,2-g]chromen-7-one	163186678	Click to see	318.32	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
9-[(2R)-2-hydroxy-3-methylbut-3-enoxy]furo[3,2-g]chromen-7-one	131636642	Click to see CC(=C)C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O	286.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
9-[[(2R)-2-Hydroxy-3-methyl-3-buten-1-yl]oxy]-7H-furo[3,2-g][1]benzopyran-7-one; (+)-Isogospherol	91895301	Click to see CC(=C)C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O	286.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
9-[2-Hydroxy-3-[2-hydroxy-2-methyl-1-[(7-oxofuro[3,2-g]chromen-9-yl)oxymethyl]propoxy]-3-methyl-butoxy]furo[3,2-g]chromen-7-one	85228420	Click to see	590.60	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Heraclenin	458010	Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C	286.28	unknown	via CMAUP database
Heraclenol	73253	Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)O	304.29	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Heraclenol 3'-O-beta-D-glucopyranoside	21573687	Click to see	466.40	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Imperatorin	10212	Click to see	270.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Isoimperatorin	68081	Click to see	270.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Oxyimperatorin	182251	Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C	286.28	unknown	via CMAUP database
Oxypeucedanin	33306	Click to see	286.28	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Oxypeucedanin hydrate	17536	Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O	304.29	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Pabularin B	10886325	Click to see CC1=C(C(=O)C=CO1)OC2C(C(C(C(O2)CO)O)O)OC(C)(C)C(COC3=C4C=CC(=O)OC4=CC5=C3C=CO5)O	574.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Pabularin C	11082393	Click to see CC1=C(C(=O)C=CO1)OC2C(C(C(C(O2)CO)O)O)OC(C)(C)C(COC3=C4C(=CC5=C3OC=C5)C=CC(=O)O4)O	574.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
Peucedanin	8616	Click to see	258.27	unknown	via CMAUP database
Rivulobirin E	10674926	Click to see	590.60	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-hydroxypsoralens
Alloimperatorin	69502	Click to see	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Pelargonidin 3-O-sophoroside	23724704	Click to see	595.50	unknown	https://doi.org/10.1016/S0031-9422(02)00023-7
> Phenylpropanoids and polyketides / Saxitoxins, gonyautoxins, and derivatives
[(3aS,4R,10aS)-2,6-diamino-9,9,10,10-tetrahydroxy-3,3a,4,8-tetrahydropyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid	102411283	Click to see	411.35	unknown	via CMAUP database
[(3aS,4R,9S,10aS)-2,6-diamino-9,10,10-trihydroxy-3a,4,8,9-tetrahydro-3H-pyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid	44587284	Click to see	395.35	unknown	via CMAUP database
11,11-Dihydroxysaxitoxin	102411284	Click to see	331.29	unknown	via CMAUP database
11beta-Hydroxysaxitoxin	60135304	Click to see C1C(C(C23N1C(=NC(C2N=C(N3)N)COC(=O)N)N)(O)O)O	315.29	unknown	via CMAUP database

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Prangos pabularia

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