Pedicularis rex

We don't have an image yet. Upload an image!

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	UUID64404eb19aec9000280595
Scientific name	Pedicularis rex
Authority	C.B.Clarke ex Maxim.
First published in	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 32: 589 (1888)

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
Pedicularis mahoangensis	Bonati	Notes Roy. Bot. Gard. Edinburgh 15: 152 (1926)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Chinese	还阳草根
Chinese	五凤朝阳草
Chinese	四方盒子草
Chinese	大王马先蒿
Chinese	大王马先蒿大王亚种洛氏变种

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Pedicularis rex subsp. lipskyana	(Bonati) Tsoong	Fl. Reipubl. Popularis Sin. 68: 111, pl. 21, f. 1–3 1963
Pedicularis rex subsp. parva	(Bonati) Tsoong	Fl. Reipubl. Popularis Sin. 68: 111 1963
Pedicularis rex subsp. pseudocyathus	(Vaniot ex Bonati) Tsoong	Fl. Reipubl. Popularis Sin. 68: 111–112 1963
Pedicularis rex subsp. zayuensis	H.P.Yang	Acta Phytotax. Sin. 28: 136 (1990)

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Pedicularis rex var. rockii	(Bonati) H.L.Li	Proc. Acad. Nat. Sci. Philadelphia 100: 339. 1948 (1948)

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-temperate click to expand
- China
  - China South-central
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
- Indo-China
  - Myanmar

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001139370
Tropicos	29207126
KEW	urn:lsid:ipni.org:names:807561-1
The Plant List	tro-29207126
Open Tree Of Life	914298
NCBI Taxonomy	321410
IPNI	807561-1
iNaturalist	810566
GBIF	7333098
EOL	2894873
CMAUP	NPO15514

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

A Legume Host Benefits More from Arbuscular Mycorrhizal Fungi Than a Grass Host in the Presence of a Root Hemiparasitic Plant

Sui X, Guan K, Chen Y, Xue R, Li A

Microorganisms

15-Feb-2022

PMCID:	PMC8880661
doi:	10.3390/microorganisms10020440
PMID:	35208894

Integrated analyses of the transcriptome and small RNA of the hemiparasitic plant Monochasma savatieri before and after establishment of parasite-host association

Chen L, Guo Q, Zhu Z, Wan H, Qin Y, Zhang H

BMC Plant Biol

10-Feb-2021

PMCID:	PMC7877053
doi:	10.1186/s12870-021-02861-6
PMID:	33568062

The changes of morphological and physiological characteristics in hemiparasitic Monochasma savatieri before and after attachment to the host plant

Chen L, Zhu Z, Guo Q, Guo J, Huang Z, Zhang H

PeerJ

19-Aug-2020

PMCID:	PMC7443084
doi:	10.7717/peerj.9780
PMID:	32879807

De novo assembling a complete mitochondrial genome of Pedicularis rex (Orobanchaceae) using GetOrganelle toolkit

Li X, Lin CY, Yang JB, Yu WB

Mitochondrial DNA B Resour

03-Feb-2020

PMCID:	PMC7748611
doi:	10.1080/23802359.2020.1722038
PMID:	33366872

Phylogenetic Relationships in Orobanchaceae Inferred From Low-Copy Nuclear Genes: Consolidation of Major Clades and Identification of a Novel Position of the Non-photosynthetic Orobanche Clade Sister to All Other Parasitic Orobanchaceae

Li X, Feng T, Randle C, Schneeweiss GM

Front Plant Sci

16-Jul-2019

PMCID:	PMC6646720
doi:	10.3389/fpls.2019.00902
PMID:	31379896

ContentSnapshots

N/A

Ann Bot

28-Jul-2016

PMCID:	PMC4970373
doi:	10.1093/aob/mcw155

Geographic consistency and variation in conflicting selection generated by pollinators and seed predators

Sun SG, Armbruster WS, Huang SQ

Ann Bot

20-Jun-2016

PMCID:	PMC4970362
doi:	10.1093/aob/mcw097
PMID:	27325896

Cloning and characterization of the CarbcL gene related to chlorophyll in pepper (Capsicum annuum L.) under fruit shade stress

Wang SB, Tian SL, Shah SN, Pan BG, Diao WP, Gong ZH

Front Plant Sci

13-Oct-2015

PMCID:	PMC4602107
doi:	10.3389/fpls.2015.00850
PMID:	26528313

Rainwater in cupulate bracts repels seed herbivores in a bumblebee-pollinated subalpine flower

Sun SG, Huang SQ

AoB Plants

10-Apr-2015

PMCID:	PMC4392828
doi:	10.1093/aobpla/plv019
PMID:	25762460

Chemical Constituents from Pedicularis rex C. B. Clarke

Hong-Biao Chu, Ning-Hua Tan, Yu-Mei Zhanga

Walter de Gruyter GmbH

16-Feb-2015

doi:	10.1515/ZNB-2007-1117

Evidence of a component Allee effect driven by predispersal seed predation in a plant (Pedicularis rex, Orobanchaceae)

Xia J, Sun S, Liu G

Biol Lett

23-Oct-2013

PMCID:	PMC3971674
doi:	10.1098/rsbl.2013.0387
PMID:	23925832

ContentSnapshots

N/A

Ann Bot

01-Oct-2013

PMCID:	PMC3783248
doi:	10.1093/aob/mct225

Nutrient requirements differ in two Pedicularis species in the absence of a host plant: implication for driving forces in the evolution of host preference of root hemiparasitic plants

Li AR, Li YJ, Smith SE, Smith FA, Guan KY

Ann Bot

14-Aug-2013

PMCID:	PMC3783243
doi:	10.1093/aob/mct179
PMID:	23946321

Direct and indirect influences of arbuscular mycorrhizal fungi on phosphorus uptake by two root hemiparasitic Pedicularis species: do the fungal partners matter at low colonization levels?

Li AR, Guan KY, Stonor R, Smith SE, Smith FA

Ann Bot

14-Aug-2013

PMCID:	PMC3783241
doi:	10.1093/aob/mct177
PMID:	23946322

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 / Aporphines
(+)-1,2-Methylenedioxy-5,6,6aalpha,7-tetrahydro-4H-dibenzo[de,g]quinoline	26202781	Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5	265.31	unknown	via CMAUP database
(R)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo(de,g)quinoline	1078819	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC	355.40	unknown	via CMAUP database
1-[(12R)-16-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-11-yl]ethanone	10246449	Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5)OC)OCO3	337.40	unknown	via CMAUP database
7H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline-7-carboxaldehyde,5,6,7a,8-tetrahydro-, (7aR)-	158516	Click to see C1CN(C2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5)C=O	293.30	unknown	via CMAUP database
Anonaine	160597	Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5	265.31	unknown	via CMAUP database
Lanuginosine	97622	Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O	305.30	unknown	via CMAUP database
Liriodenine	10144	Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53	275.26	unknown	via CMAUP database
N-acetylanonaine	6453733	Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	307.30	unknown	via CMAUP database
Roemerine	119204	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	279.30	unknown	via CMAUP database
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
(12R,13S)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaen-13-ol	15560530	Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O	281.30	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
[1,1'-Biphenyl]-4-ol, 2'-methoxy-3,5'-di-2-propenyl-	11857938	Click to see COC1=C(C=C(C=C1)CC=C)C2=CC(=C(C=C2)O)CC=C	280.40	unknown	via CMAUP database
4-O-Methylhonokiol	155160	Click to see COC1=C(C=C(C=C1)C2=C(C=CC(=C2)CC=C)O)CC=C	280.40	unknown	via CMAUP database
Caryolanemagnolol	21726647	Click to see CC1(CC2C1CCC3(CC2(CCC3O)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C)C	486.70	unknown	via CMAUP database
Honokiol	72303	Click to see C=CCC1=CC(=C(C=C1)O)C2=CC(=C(C=C2)O)CC=C	266.30	unknown	via CMAUP database
Magnaldehyde E	5319190	Click to see C=CCC1=C(C=CC(=C1)C2=C(C=CC(=C2)C=O)O)O	254.28	unknown	via CMAUP database
Magnolol	72300	Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC=C)O	266.30	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
2,3,4-Trihydroxy-5-(4-prop-2-enylphenoxy)benzaldehyde	71812224	Click to see C=CCC1=CC=C(C=C1)OC2=C(C(=C(C(=C2)C=O)O)O)O	286.28	unknown	via CMAUP database
3-[3,4-Dihydroxy-5-(4-prop-2-enylphenoxy)phenyl]prop-2-enal	134367	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O	296.30	unknown	via CMAUP database
3,4-Dihydroxy-5-(4-prop-2-enylphenoxy)benzaldehyde	23259953	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=O	270.28	unknown	via CMAUP database
5-[(E)-3-methoxyprop-1-enyl]-3-(4-prop-2-enylphenoxy)benzene-1,2-diol	71812222	Click to see COCC=CC1=CC(=C(C(=C1)OC2=CC=C(C=C2)CC=C)O)O	312.40	unknown	via CMAUP database
Obovatal	6439677	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O	296.30	unknown	via CMAUP database
Obovatol	100771	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)CC=C	282.30	unknown	via CMAUP database
Phenol, 2-[3-hydroxy-4-(2-propenyl)phenoxy]-5-(2-propenyl)-	10016628	Click to see C=CCC1=CC(=C(C=C1)OC2=CC(=C(C=C2)CC=C)O)O	282.30	unknown	via CMAUP database
Phenol, 4-(2-propenyl)-2-(4-(2-propenyl)phenoxy)-	159137	Click to see C=CCC1=CC=C(C=C1)OC2=C(C=CC(=C2)CC=C)O	266.30	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Allylphenol	68148	Click to see C=CCC1=CC=C(C=C1)O	134.17	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
[(2R,3R,4R,5R,6R)-5-hydroxy-2-(hydroxymethyl)-6-[(E)-3-(4-hydroxyphenyl)prop-2-enoxy]-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	101453903	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCC=CC4=CC=C(C=C4)O)O)O)O)O	634.60	unknown	https://doi.org/10.1515/ZNB-2007-1117
[5-Hydroxy-2-(hydroxymethyl)-6-[3-(4-hydroxyphenyl)prop-2-enoxy]-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	162880986	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCC=CC4=CC=C(C=C4)O)O)O)O)O	634.60	unknown	https://doi.org/10.1515/ZNB-2007-1117
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	via CMAUP database
(-)-Camphene	440966	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
Bornyl acetate, (-)-	93009	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	via CMAUP database
Cadalene	10225	Click to see CC1=CC2=C(C=CC(=C2C=C1)C)C(C)C	198.30	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Clovanemagnolol	10323149	Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C	486.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
[2R-cis]-1,2,3,4,4a,5,6,7-Octahydro-alpha,alpha,4a,8-tetramethyl-2-naphthalenemethanol	91730386	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	via CMAUP database
2-[(2R,4aS,8aR)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-ol	118976561	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	via CMAUP database
alpha-Eudesmol	92762	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	via CMAUP database
beta-EUDESMOL	91457	Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O	222.37	unknown	via CMAUP database
Eudeshonokiol A	14587421	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)C4=C(C=CC(=C4)CC=C)O)CC=C	488.70	unknown	via CMAUP database
Eudeshonokiol B	21726646	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)CC=C)C4=CC(=C(C=C4)O)CC=C	488.70	unknown	via CMAUP database
Eudesmagnolol	14587417	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)CC=C)C4=C(C=CC(=C4)CC=C)O	488.70	unknown	via CMAUP database
Eudesobovatol A	442837	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=CC(=CC(=C3O)OC4=CC=C(C=C4)CC=C)CC=C	504.70	unknown	via CMAUP database
Eudesobovatol B	10346031	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3OC4=CC=C(C=C4)CC=C)CC=C)O	504.70	unknown	via CMAUP database
gamma-EUDESMOL	6432005	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	via CMAUP database
Proximadiol	165258	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O	240.38	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(E)-4-[(4R,6S)-4-hydroxy-2,6-dimethyl-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohexen-1-yl]but-3-en-2-one	101453904	Click to see CC1=C(C(CC(C1)O)(C)COC2C(C(C(C(O2)CO)O)O)O)C=CC(=O)C	386.40	unknown	https://doi.org/10.1515/ZNB-2007-1117
4-[4-Hydroxy-2,6-dimethyl-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohexen-1-yl]but-3-en-2-one	163026980	Click to see CC1=C(C(CC(C1)O)(C)COC2C(C(C(C(O2)CO)O)O)O)C=CC(=O)C	386.40	unknown	https://doi.org/10.1515/ZNB-2007-1117
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(2S,3R,4S,5S,6R)-2-[[(1S,4aR,5R,7aS)-5-ethoxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101453906	Click to see CCOC1C=C(C2C1C=COC2OC3C(C(C(C(O3)CO)O)O)O)CO	374.40	unknown	https://doi.org/10.1515/ZNB-2007-1117
(2S,3R,4S,5S,6R)-2-[[(1S,4aR,5S,7aS)-5-ethoxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101453905	Click to see CCOC1C=C(C2C1C=COC2OC3C(C(C(C(O3)CO)O)O)O)CO	374.40	unknown	https://doi.org/10.1515/ZNB-2007-1117
2-[[5-Ethoxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162935349	Click to see CCOC1C=C(C2C1C=COC2OC3C(C(C(C(O3)CO)O)O)O)CO	374.40	unknown	https://doi.org/10.1515/ZNB-2007-1117
2-[[5-Hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	348157	Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	346.33	unknown	https://doi.org/10.1515/ZNB-2007-1117
4a,7-Dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carbaldehyde	14589172	Click to see CC1(CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)O	376.36	unknown	https://doi.org/10.1515/ZNB-2007-1117
5-chloro-2-(4-(2-(2-hydroxyethoxy)ethyl)piperazin-1-yl)-N-(6-(3-methoxybenzamido)pyridin-3-yl)isonicotinamide	13848072	Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O	390.40	unknown	https://doi.org/10.1515/ZNB-2007-1117
Aucubin	91458	Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	346.33	unknown	https://doi.org/10.1515/ZNB-2007-1117
Euphroside	14589173	Click to see CC1(CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)O	376.36	unknown	https://doi.org/10.1515/ZNB-2007-1117
Mussaenoside	182423	Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O	390.40	unknown	https://doi.org/10.1515/ZNB-2007-1117
Plantarenaloside	155882	Click to see CC1CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O	360.36	unknown	https://doi.org/10.1515/ZNB-2007-1117
Yuheinoside	13890717	Click to see CC1CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O	360.36	unknown	https://doi.org/10.1515/ZNB-2007-1117
> 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
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	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B	5316860	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
Magnolianin	9918938	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC3=C2OC(C(O3)C4=CC(=C(C(=C4)OC5=CC=C(C=C5)CC=C)O)O)COC6=C(C=C(C=C6)CC=C)C7=C(C=CC(=C7)CC=C)O)CC=C	827.00	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-7-ol	6093330	Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C	314.40	unknown	via CMAUP database
Magnocurarine	53266	Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C	314.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	21629882	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O	624.60	unknown	via CMAUP database
Acteoside;Kusaginin;TJC160	354009	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1515/ZNB-2007-1117
beta-D-Glucopyranoside, 2-(3-hydroxy-4-methoxyphenyl)ethyl 3-O-(6-deoxy-alpha-L-mannopyranosyl)-, 4-[3-(4-hydroxy-3-methoxyphenyl)-2-propenoate], (E)-	72725940	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O	652.60	unknown	https://doi.org/10.1515/ZNB-2007-1117
beta-D-Glucopyranoside, 2-(3-hydroxy-4-methoxyphenyl)ethyl 3-O-(6-deoxy-alpha-L-mannopyranosyl)-, 6-[3-(4-hydroxy-3-methoxyphenyl)-2-propenoate], (E)-	124222280	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)OC)O)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O)O)O	652.60	unknown	https://doi.org/10.1515/ZNB-2007-1117
Isomartynoside	91895373	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)OC)O)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O)O)O	652.60	unknown	https://doi.org/10.1515/ZNB-2007-1117
Martynoside	5319292	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O	652.60	unknown	https://doi.org/10.1515/ZNB-2007-1117
Verbascoside	5281800	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1515/ZNB-2007-1117
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumanolignan	24796112	Click to see C=CCC1=CC(=C(C=C1)O)C2=C3C(=CC(=C2)CC=C)C=CC(=O)O3	318.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1515/ZNB-2007-1117
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1515/ZNB-2007-1117
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl butanoate	162891610	Click to see CCCC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)OC)O)O)O)O	532.50	unknown	https://doi.org/10.1515/ZNB-2007-1117
3'-Methoxy-4',5-dihydroxy-7-[(6-O-butyryl-beta-D-glucopyranosyl)oxy]flavone	101453901	Click to see CCCC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)OC)O)O)O)O	532.50	unknown	https://doi.org/10.1515/ZNB-2007-1117
Luteolin 7-galactoside	5291488	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1515/ZNB-2007-1117
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1515/ZNB-2007-1117
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1515/ZNB-2007-1117

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.

Pedicularis rex

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