Aconitum violaceum

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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	UUID6440071bda7c7937127044
Scientific name	Aconitum violaceum
Authority	Jacquem. ex Stapf
First published in	Ann. Roy. Bot. Gard. (Calcutta) 10: 144 (1905)

Description Top

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Aconitum violaceum is a species of perennial plant found in the Himalayan region of India, Pakistan, and Nepal. It is found at an altitude range of 3,600–4,800 m (12,000–16,000 ft) and is used in traditional Tibetan medicine. It has a bitter taste and a cooling tendency.

Synonyms Top

Scientific name	Authority	First published in
Aconitum multifidum	Royle	Ill. Bot. Himal. Mts. [Royle] 56. 1834 [Mar 1834]
Aconitum violaceum var. multifidum	(Royle) Qureshi & Chaudhri	Pakistan Syst. 4: 44 (1988)
Aconitum violaceum var. weileri	(Gilli) Riedl	Willdenowia 8: 325 (1978)
Aconitum weileri	Gilli	Oesterr. Bot. Z. 104: 305 (1957)

Common names Top

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Language	Common/alternative name
Nepali	बिख

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

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

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000518301
Tropicos	27103046
KEW	urn:lsid:ipni.org:names:707944-1
The Plant List	kew-2619738
Open Tree Of Life	698587
NCBI Taxonomy	279771
IUCN Red List	50126562
IPNI	707944-1
iNaturalist	499369
GBIF	7278196
Freebase	/m/0k92pct
Wikipedia	Aconitum_violaceum
CMAUP	NPO2458
PFAF	Aconitum violaceum

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

Cross-cultural ethnobotany of the Baltis and Shinas in the Kharmang district, Trans-Himalaya India-Pakistan border

Hussain B, Abbas Z, Alam J, Harun N, Khan SM, Ahmad Z, Han H, Yoo S, Raposo A

Heliyon

27-Mar-2024

PMCID:	PMC10998220
doi:	10.1016/j.heliyon.2024.e28613
PMID:	38586350

The local medicinal plant knowledge in Kashmir Western Himalaya: a way to foster ecological transition via community-centred health seeking strategies

Manzoor M, Ahmad M, Zafar M, Gillani SW, Shaheen H, Pieroni A, Al-Ghamdi AA, Elshikh MS, Saqib S, Makhkamov T, Khaydarov K

J Ethnobiol Ethnomed

30-Nov-2023

PMCID:	PMC10688143
doi:	10.1186/s13002-023-00631-2
PMID:	38037066

The known, unknown, and the intriguing about members of a critically endangered traditional medicinal plant genus Aconitum

Kakkar RA, Haneen MA, Parida AC, Sharma G

Front Plant Sci

28-Jul-2023

PMCID:	PMC10421671
doi:	10.3389/fpls.2023.1139215
PMID:	37575934

Neuropharmacological Potential of Diterpenoid Alkaloids

Salehi A, Ghanadian M, Zolfaghari B, Jassbi AR, Fattahian M, Reisi P, Csupor D, Khan IA, Ali Z

Pharmaceuticals (Basel)

14-May-2023

PMCID:	PMC10223254
doi:	10.3390/ph16050747
PMID:	37242531

A cross-cultural study of high-altitude botanical resources among diverse ethnic groups in Kashmir Himalaya, India

Haq SM, Waheed M, Khoja AA, Amjad MS, Bussmann RW, Ali K

J Ethnobiol Ethnomed

13-Apr-2023

PMCID:	PMC10100632
doi:	10.1186/s13002-023-00582-8
PMID:	37055855

Pattern of β-Diversity and Plant Species Richness along Vertical Gradient in Northwest Himalaya, India

Wani ZA, Khan S, Bhat JA, Malik AH, Alyas T, Pant S, Siddiqui S, Moustafa M, Ahmad AE

Biology (Basel)

18-Jul-2022

PMCID:	PMC9312975
doi:	10.3390/biology11071064
PMID:	36101443

A Cross-Cultural Analysis of Plant Resources among Five Ethnic Groups in the Western Himalayan Region of Jammu and Kashmir

Haq SM, Hassan M, Bussmann RW, Calixto ES, Rahman IU, Sakhi S, Ijaz F, Hashem A, Al-Arjani AB, Almutairi KF, Abd_Allah EF, Aziz MA, Ali N

Biology (Basel)

23-Mar-2022

PMCID:	PMC9032642
doi:	10.3390/biology11040491
PMID:	35453691

High-Frequency Plant Regeneration, Genetic Uniformity, and Flow Cytometric Analysis of Regenerants in Ruta chalepensis L.

Qahtan AA, Faisal M, Alatar AA, Abdel-Salam EM

Plants (Basel)

20-Dec-2021

PMCID:	PMC8704675
doi:	10.3390/plants10122820
PMID:	34961291

Plant Resources Utilization among Different Ethnic Groups of Ladakh in Trans-Himalayan Region

Haq SM, Yaqoob U, Calixto ES, Rahman IU, Hashem A, Abd_Allah EF, Alakeel MA, Alqarawi AA, Abdalla M, Hassan M, Bussmann RW, Abbasi AM, Ur Rahman S, Ijaz F

Biology (Basel)

26-Aug-2021

PMCID:	PMC8468708
doi:	10.3390/biology10090827
PMID:	34571704

Methods of green synthesis of Au NCs with emphasis on their morphology: A mini-review

Sayadi K, Akbarzadeh F, Pourmardan V, Saravani-Aval M, Sayadi J, Chauhan NP, Sargazi G

Heliyon

09-Jun-2021

PMCID:	PMC8220187
doi:	10.1016/j.heliyon.2021.e07250
PMID:	34189304

Status and consolidated list of threatened medicinal plants of India

Gowthami R, Sharma N, Pandey R, Agrawal A

Genet Resour Crop Evol

25-May-2021

PMCID:	PMC8148398
doi:	10.1007/s10722-021-01199-0
PMID:	34054223

Comparative Assessment of Medicinal Plant Utilization among Balti and Shina Communities in the Periphery of Deosai National Park, Pakistan

Abbas Z, Kousar S, Aziz MA, Pieroni A, Aldosari AA, Bussmann RW, Raza G, Abbasi AM

Biology (Basel)

14-May-2021

PMCID:	PMC8153600
doi:	10.3390/biology10050434
PMID:	34068859

Micropropagation of Tricholepis roylei Hook. F.—a point endemic species of the Western Himalaya

Panwar GS, Joshi B

J Genet Eng Biotechnol

10-Aug-2020

PMCID:	PMC7415789
doi:	10.1186/s43141-020-00051-9
PMID:	32776183

Quantitative Ethnobotanical Study of Indigenous Knowledge on Medicinal Plants Used by the Tribal Communities of Gokand Valley, District Buner, Khyber Pakhtunkhwa, Pakistan

Sulaiman, Shah S, Khan S, Bussmann RW, Ali M, Hussain D, Hussain W

Plants (Basel)

06-Aug-2020

PMCID:	PMC7463859
doi:	10.3390/plants9081001
PMID:	32781736

Ecology, distribution mapping and conservation implications of four critically endangered endemic plants of Kashmir Himalaya

Hussain Mir A, Tyub S, Kamili AN

Saudi J Biol Sci

11-May-2020

PMCID:	PMC7451753
doi:	10.1016/j.sjbs.2020.05.006
PMID:	32884420

Phytochemical Profile Top

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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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate	7428	Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O	184.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol	14529	Click to see CC1=CC=C(C=C1)C(C)(C)O	150.22	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
2-Naphthol	8663	Click to see C1=CC=C2C=C(C=CC2=C1)O	144.17	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
3,4-Dehydrolarreatricin	25775479	Click to see CC1=C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C	282.30	unknown	via CMAUP database
4-[(2S,3R,5S)-5-(4-hydroxyphenyl)-3-methyl-4-methylideneoxolan-2-yl]phenol	73213070	Click to see CC1C(OC(C1=C)C2=CC=C(C=C2)O)C3=CC=C(C=C3)O	282.30	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
4,4'-(3,4-Dimethyl-2,5-dihydrofuran-2alpha,5beta-diyl)bis(2-methoxyphenol)	73213069	Click to see CC1=C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC)C	342.40	unknown	via CMAUP database
4,4'-(3alpha-Methyl-4-methylenetetrahydrofuran-2alpha,5beta-diyl)bis(2-methoxyphenol)	73213151	Click to see CC1C(OC(C1=C)C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC	342.40	unknown	via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol	10393	Click to see C1=CC(=CC=C1CCO)O	138.16	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Larreatricin	26389403	Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C	284.30	unknown	via CMAUP database
Meso-3,3'-Didemethoxynectandrin B	14213224	Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C	284.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(6R,9S)-Roseoside	11165077	Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	386.40	unknown	via CMAUP database
[(E)-2-cyano-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	11972424	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(=CCOC2C(C(C(C(O2)CO)O)O)O)C#N)O	451.40	unknown	via CMAUP database
[(E)-2-cyano-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	11972423	Click to see C1=CC(=CC=C1C=CC(=O)OCC(=CCOC2C(C(C(C(O2)CO)O)O)O)C#N)O	421.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
[R,(+)]-3,7-Dimethyl-7-octen-1-ol acetate	36690979	Click to see CC(CCCC(=C)C)CCOC(=O)C	198.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
7-Octen-1-ol, 3,7-dimethyl-, (S)-	81263	Click to see CC(CCCC(=C)C)CCO	156.26	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
[8-Acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate	5100366	Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=CC=C7)O)OC)OC(=O)C)OC)OC)O)COC	629.70	unknown	https://doi.org/10.1016/S0031-9422(00)97417-X
Acetylbenzoylpseudaconine	60208143	Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=CC=C7)O)OC)OC(=O)C)OC)OC)O)COC	629.70	unknown	https://doi.org/10.1016/S0031-9422(00)97417-X
Bikhaconitine	441713	Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC(=C(C=C7)OC)OC)O)OC)OC(=O)C)OC)OC)COC	673.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	via CMAUP database
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Sabinene	11051711	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	via CMAUP database
(+)-3-Carene	443156	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-beta-Phellandrene	442484	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
(+)-Terpinen-4-ol	2724161	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Humulene	5318102	Click to see CC1=CCC(C=CCC(=C)CCC1)(C)C	204.35	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron	88113319	Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O	192.12	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-Propenoic acid, 3-(4-hydroxyphenyl)-, methyl ester	92203	Click to see COC(=O)C=CC1=CC=C(C=C1)O	178.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Gallocatechin-(4alpha->8)-epigallocatechin	442682	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	610.50	unknown	via CMAUP database
Gallocatechin-(4alpha->8)-gallocatechin-(4alpha->8)-gallocatechin	71664720	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C(=C7)O)O)O)O)C8=CC(=C(C(=C8)O)O)O)O)O)O)C9=CC(=C(C(=C9)O)O)O)O	914.80	unknown	via CMAUP database
Prodelphinidin B3	13831068	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	via CMAUP database
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-1-benzopyran-1-ium-3-yl 6-O-[(2Z)-3-(4-hydroxyphenyl)prop-2-enoyl]-beta-D-glucopyranoside	118797966	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	595.50	unknown	via CMAUP database
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenium-3-yl 6-O-[(2Z)-3-(4-hydroxyphenyl)prop-2-enoyl]-beta-D-glucopyranoside	72193639	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O	611.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
3-[(6-O-alpha-L-Rhamnopyranosyl-beta-D-glucopyranosyl)oxy]-4',5,7-trihydroxy-3',5'-dimethoxyflavylium	101942241	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)OC)O)OC)O)O)O)O)O)O)O)O	639.60	unknown	via CMAUP database
Delphinidin 3-O-glucoside cation	443650	Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	465.40	unknown	via CMAUP database
Keracyanin cation	441674	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O	595.50	unknown	via CMAUP database
Kuromanin	441667	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	449.40	unknown	via CMAUP database
Oenin	443652	Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	493.40	unknown	via CMAUP database
Pelargonidin 3-glucoside ion	443648	Click to see C1=CC(=CC=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O	433.40	unknown	via CMAUP database
Pelargonidin 3-O-rutinoside	443917	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC=C(C=C5)O)O)O)O)O)O)O)O)O	579.50	unknown	via CMAUP database
Peonidin 3-O-rutinoside	90470732	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O)O)O	609.60	unknown	via CMAUP database
Peonidin-3-glucoside	443654	Click to see COC1=C(C=CC(=C1)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O	463.40	unknown	via CMAUP database
Petunidin 3-glucoside	443651	Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	479.40	unknown	via CMAUP database
Petunidin 3-rutinoside	101949843	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)OC)O)O)O)O)O)O)O)O)O)O	625.60	unknown	via CMAUP database
Tulipanin	5492231	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O)O)O	611.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Cannabiscitrin	5486615	Click to see C1=C(C=C(C(=C1O)O)OC2C(C(C(C(O2)CO)O)O)O)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)O	480.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-beta-D-Arabinopyranosyloxy-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-1-benzopyrylium	101603499	Click to see C1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O	435.40	unknown	via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	12358426	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	via CMAUP database
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	via CMAUP database
Hyperoside	5281643	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	via CMAUP database
Isoquercetin	5280804	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	via CMAUP database
kaempferol 3-O-beta-L-glucopyranoside	9911508	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	via CMAUP database
myricetin 3-O-alpha-L-glucopyranoside	72551451	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	via CMAUP database
myricetin 3-O-beta-D-glucopyranoside	5318606	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	via CMAUP database
Pyranocyanin D	101198724	Click to see C1=CC(=CC=C1C2=CC3=C4C(=CC(=[OH+])C=C4OC(=C3OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O2)O	565.50	unknown	via CMAUP database
Pyranodelphinin D	101198725	Click to see C1=CC(=CC=C1C2=CC3=C4C(=CC(=[OH+])C=C4OC(=C3OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C(=C6)O)O)O)O2)O	581.50	unknown	via CMAUP database

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Aconitum violaceum

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