Scientific name	Authority	First published in
Cicuta major	Garsault	Fig. Pl. Med. 2: t. 223. 1764, nom. inval., opus utique oppressum; Descr. Pl. Anim. 145. 1767; Thell. in Bull. Herb. Boiss. Ser. II. viii. 789.
Cicuta officinalis	Crantz	Cl. Umbell. Emend. : 98 (1767)
Conium ceretanum	Sennen	Bull. Soc. Bot. France 73: 651 (1926 publ. 1927)
Conium cicuta	Neck.	Delic. Gallo-Belg. 1: 142 (1768)
Conium croaticum	Waldst. & Kit. ex Willd.	Enum. Pl. : 305 (1809)
Conium leiocarpum	(Boiss.) Stapf	Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 51: 323 1886
Conium maculatum var. barceloi	O.Bolòs & Vigo	Butl. Inst. Catalana Hist. Nat., Secc. Bot. 38(1): 83 (1974)
Conium maculatum subsp. croaticum	(Waldst. & Kit. ex Willd.) Drude	Nat. Pflanzenfam. 3(7-8): 169 1898
Conium maculatum var. divaricatum	(Boiss. & Orph.) Boiss.	Fl. Orient. 2: 922 1872
Conium maculatum subsp. divaricatum	(Boiss. & Orph.) Drude	Nat. Pflanzenfam. 3(7-8): 169 1898
Conium maculatum var. immaculatum	Schur	Enum. Pl. Transsilv. 275 1866
Conium maculatum var. leiocarpum	Boiss.	Fl. Orient. 2: 922 1872
Conium maculatum subsp. leiocarpum	(Boiss.) Drude	Nat. Pflanzenfam. 3(7-8): 169 1898
Conium maculatum var. viride	DC.	Prodr. 4: 243 1830
Conium maculatum subsp. viride	(DC.) Espeut	Candollea 57: 141 (2002)
Conium maculosum	Pall.	Reise Russ. Reich. 1: 478 (1771)
Conium nodosum	Fisch. ex Steud.	Nomencl. Bot. 1: 215 (1821)
Conium pyrenaicum	Sennen & Elias	Bol. Soc. Ibér. Ci. Nat. 27: 141 (1928)
Conium sibiricum	hort. ex Steud.	Nomencl. Bot. , ed. 2, 1: 404 (1840)
Conium strictum	Tratt.	Arch. Gewächsk. Leopold Trattinick 1: t. 21 (1811)
Conium tenuifolium	Mill.	Gard. Dict. ed. 8 : n.º 2 (1768)
Coriandrum cicuta	Crantz	Stirp. Austr. Fasc. 3: 100 (1762)
Coriandrum maculatum	Roth	Tent. Fl. Germ. 1: 130 (1788)
Cicuta major	Lam.	Fl. Franç. 3: 456 (1778)
Sium conium	Vest	Man. Bot. : 513 (1805)
Selinum conium	E.H.L.Krause	Deutschl. Fl. Abbild. , ed. 2, 12: 79 (1904)

Common names Top

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Filter by language:

Language	Common/alternative name
English	hemlock
English	poison hemlock
Arabic	بسبس بري
Arabic	شوكران أبقع
Arabic	شوكران
Arabic	طحماء
Azerbaijani	xallı badyan
azb	خاللی بادیان
Belarusian	омег
Belarusian	пятрушнік
Belarusian	Балігалоў плямісты
Belarusian	блёкат
Bulgarian	бучиниш
Bengali	কনিয়াম ম্যাকুলেটাম
Catalan	cicuta
Czech	bolehlav plamatý
Welsh	cegiden
Welsh	cegr pumbys
Danish	skarntyde
Danish	skarntydesaft
German	fleckschierling
German	gefleckter schierling
Greek	Κώνειον το στικτόν
Esperanto	makula konio
Estonian	täpiline surmaputk
Basque	astaperrexil handi
Persian	شوکران زهرآلود
Finnish	myrkkykatko
French	ciguë tachetée
French	grande ciguë
French	grande cigüe
Irish	moing mhear
gd	ith-teodha
Galician	cicuta
Hindi	हेमलाक
Croatian	kukuta
Hungarian	foltos bürök
Hungarian	bürök
Armenian	գինազոխ բծավոր
io	cikuto
Icelandic	skarnjurt
Japanese	ドクニンジン
Kazakh	Убалдырған
Korean	독당근
ku	giyajehrk
Cornish	kegis
Lithuanian	dėmėtoji mauda
Latvian	plankumainais suņstobrs
Latvian	suņstobrs
Macedonian	бучумиш
Malayalam	ഹെമ്ലോക് പ്ലാന്റ്
Burmese	ဟင်းမလော့ပင်
myv	Тешксэв гуеньпочко
Norwegian Bokmål	giftkjeks
Norwegian Bokmål	skarntyde
Dutch	gevlekte scheerling
Norwegian Nynorsk	giftkjeks
Norwegian Nynorsk	skarntyde
os	Такъуындела
pcd	chighu
pcd	biblo
pcd	su
pcd	bibu
Polish	szaleń plamisty
Polish	weszka
Polish	szczwół plamisty
Polish	świńska wesz
Polish	pietrasznik plamisty
Polish	psia pietruszka
Quechua	jama-jama
Quechua	nukña perejil
Quechua	jama jama
Russian	Омег пятнистый
Russian	Болиголов крапчатый
Russian	Болиголов пятнистый
scn	cicùta
scn	cicuta
Slovak	bolehlav škvrnitý
Slovak	svinská voš
Slovak	motožník
Slovak	rozpuk
Slovenian	pikasti mišjak
Albanian	kakuda
Serbian	Кукута
Swedish	odört
Turkish	baldıran
Ukrainian	Болиголов плямистий
Uzbek	zangpoya
vep	omeghein
Chinese	毒参
Chinese	新疆藁本

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
- Macaronesia
  - Azores
  - Canary Islands
  - Madeira
- Northeast Tropical Africa
  - Ethiopia
- Northern Africa
  - Algeria
  - Libya
  - Morocco
  - Tunisia
- South Tropical Africa
  - Mozambique
  - Zimbabwe
- Southern Africa
  - Cape Provinces

Antarctica click to expand
- Subantarctic Islands
  - Amsterdam-St.Paul Islands
  - Falkland Islands

Asia-temperate click to expand
- Arabian Peninsula
  - Saudi Arabia
  - Yemen
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - Xinjiang
- Eastern Asia
  - Japan
  - Korea
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Russian Far East
  - Primorye
- Siberia
  - Altay
  - Krasnoyarsk
  - West Siberia
- Western Asia
  - Afghanistan
  - Cyprus
  - East Aegean Islands
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Turkey

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

Australasia click to expand
- Australia
  - Tasmania
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Nova Scotia
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Nebraska
  - North Dakota
  - Oklahoma
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Montana
  - Oregon
  - Washington
  - Wyoming
- South-central U.S.A.
  - New Mexico
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Delaware
  - District Of Columbia
  - Georgia
  - Kentucky
  - Louisiana
  - Maryland
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - Arizona
  - California
  - Nevada
  - Utah
- Western Canada
  - Alberta
  - British Columbia
  - Saskatchewan

Southern America click to expand
- Brazil
  - Brazil South
  - Brazil Southeast
- Caribbean
  - Cayman Islands
  - Dominican Republic
  - Haiti
- Central America
  - El Salvador
  - Guatemala
  - Honduras
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Argentina South
  - Chile Central
  - Chile South
  - Juan Fernández Islands
  - Uruguay
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000617964
UNII	79G218ZMB3
Flora of Alabama	337
Canadensys	2566
USDA Plants	COMA2
Tropicos	1700063
INPN	92237
KEW	urn:lsid:ipni.org:names:840668-1
The Plant List	kew-2734165
PaleoBotany	20674
Open Tree Of Life	1001039
Observations.org	6628
NCBI Taxonomy	13447
NBN Atlas	NBNSYS0000003655
Nature Serve	2.133974
IPNI	840668-1
iNaturalist	52998
GBIF	3034807
Freebase	/m/011l61z5
WisFlora	3187
EPPO	COIMA
EOL	581784
Elurikkus	3893
Calflora (Californian flora)	2317
US Library of Congress	sh2007000033
USDA GRIN	11262
Wikipedia	Conium_maculatum
CMAUP	NPO25122

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 systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics

Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B

J Ethnopharmacol

25-Mar-2024

PMCID:	PMC7615571
doi:	10.1016/j.jep.2023.117622
PMID:	38128894

Phylogeny and Taxonomic Revision of the Genus Melanosciadium (Apiaceae), Based on Plastid Genomes and Morphological Evidence

Jiang QP, Guo XL, Zhao AQ, Fan X, Li Q, Zhou SD, He XJ

Plants (Basel)

21-Mar-2024

PMCID:	PMC10974901
doi:	10.3390/plants13060907
PMID:	38592923

Traditional and contemporary herbal medicines in management of cancer: A scoping review

Imtiaz I, Schloss J, Bugarcic A

J Ayurveda Integr Med

23-Feb-2024

PMCID:	PMC10901831
doi:	10.1016/j.jaim.2024.100904
PMID:	38395014

Epidemiology and Clinical Characteristics of Acute Plant Exposure in Patients Aged between 0 and 18 Years—A Six-Year Retrospective Study

Nițescu GV, Grama A, Turcu T, Strătulă A, Dragomirescu A, Pană ES, Baciu A, Baconi DL, Crăciun MD, Ulmeanu CE

Children (Basel)

21-Feb-2024

PMCID:	PMC10969538
doi:	10.3390/children11030271
PMID:	38539306

An appraisal of traditional knowledge of plant poisoning of livestock and its validation through acute toxicity assay in rats

Rasool F, Nizamani ZA, Ahmad KS, Parveen F, Khan SA, Sabir N

Front Pharmacol

14-Feb-2024

PMCID:	PMC10900104
doi:	10.3389/fphar.2024.1328133
PMID:	38420196

Morphological Ontogeny, Ecology, and Biogeography of Fuscozetes fuscipes (Acari, Oribatida, Ceratozetidae)

Seniczak S, Seniczak A, Jordal BH

Animals (Basel)

06-Feb-2024

PMCID:	PMC10885992
doi:	10.3390/ani14040538
PMID:	38396506

The Wild Carrot (Daucus carota): A Phytochemical and Pharmacological Review

Ismail J, Shebaby WN, Daher J, Boulos JC, Taleb R, Daher CF, Mroueh M

Plants (Basel)

27-Dec-2023

PMCID:	PMC10781147
doi:	10.3390/plants13010093
PMID:	38202401

The ailments that stem from cheese and relevant precautions taken in the Ottoman Empire from the 19th century to the 20th century

Erkmen A, Tüzün N, Erkmen O

Food Sci Nutr

21-Nov-2023

PMCID:	PMC10867485
doi:	10.1002/fsn3.3849
PMID:	38370051

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Teodorico Borgognoni’s Formulary for Thirteenth Century Anesthetic Preparations

Cavalloro V, Soddu F, Baroni S, Robustelli della Cuna FS, Tavazzi E, Martino E, Collina S

Life (Basel)

14-Sep-2023

PMCID:	PMC10532452
doi:	10.3390/life13091913
PMID:	37763316

Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022

Gibin D, Pasinato L, Delbianco A

EFSA J

13-Jun-2023

PMCID:	PMC10262070
doi:	10.2903/j.efsa.2023.8061
PMID:	37325259

Distribution, Effect, and Control of Exotic Plants in Republic of Korea

Lim BS, Seok JE, Lim CH, Kim GS, Shin HC, Lee CS

Biology (Basel)

06-Jun-2023

PMCID:	PMC10294914
doi:	10.3390/biology12060826
PMID:	37372111

Vertigoheel promotes rodent cognitive performance in multiple memory tests

Ott K, Heikkinen T, Lehtimäki KK, Paldanius K, Puoliväli J, Pussinen R, Andriambeloson E, Huyard B, Wagner S, Schnack C, Wahler A, von Einem B, von Arnim CA, Burmeister Y, Weyer K, Seilheimer B

Front Neurosci

31-May-2023

PMCID:	PMC10264630
doi:	10.3389/fnins.2023.1183023
PMID:	37325043

Apiaceae Medicinal Plants in China: A Review of Traditional Uses, Phytochemistry, Bolting and Flowering (BF), and BF Control Methods

Li M, Li M, Wang L, Li M, Wei J

Molecules

27-May-2023

PMCID:	PMC10254214
doi:	10.3390/molecules28114384
PMID:	37298861

Insights into the Mechanisms Involved in Lead (Pb) Tolerance in Invasive Plants—The Current Status of Understanding

Afzal MR, Naz M, Wan J, Dai Z, Ullah R, Rehman SU, Du D

Plants (Basel)

24-May-2023

PMCID:	PMC10255771
doi:	10.3390/plants12112084
PMID:	37299064

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
(2R)-1-methyl-2-propylpiperidin-1-ium	25203444	Click to see CCCC1CCCC[NH+]1C	142.26	unknown	via CMAUP database
(S)-2-Propylpiperidine	441072	Click to see CCCC1CCCCN1	127.23	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1196975/
1-Methyl-2-propylpiperidine	338921	Click to see CCCC1CCCCN1C	141.25	unknown	https://doi.org/10.1002/CBER.189402702267
6-Propylpiperidin-3-ol	4367461	Click to see CCCC1CCC(CN1)O	143.23	unknown	https://doi.org/10.1002/CBER.189102401284
Coniine	9985	Click to see CCCC1CCCCN1	127.23	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1196975/ https://doi.org/10.1016/S0031-9422(00)82809-5 https://doi.org/10.1016/0031-9422(75)80351-7
d-Conicine	21583848	Click to see CCCC1CCCC[NH2+]1	128.24	unknown	via CMAUP database
Epipseudoconhydrine	11744749	Click to see CCCC1CCC(CN1)O	143.23	unknown	via CMAUP database
Methylconiine	169683	Click to see CCCC1CCCCN1C	141.25	unknown	https://doi.org/10.1002/CBER.189402702267
> Alkaloids and derivatives / Aporphines
N-acetylanonaine	6453733	Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	307.30	unknown	via CMAUP database
N-Acetyldehydroanonaine	5315739	Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1=CC5=CC=CC=C54)OCO3	305.30	unknown	via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
2'-Episimulanoquinoline	102236946	Click to see CC1(C=CC2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)CC4C5=C(C=CC(=C5OC)OC)C6=C(N4C)C7=CC8=C(C=C7C=C6)OCO8	618.70	unknown	via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine	2703	Click to see C[N+]1=C2C(=C3C=CC(=C(C3=C1)OC)OC)C=CC4=CC5=C(C=C42)OCO5	348.40	unknown	via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Simulansamide	5321312	Click to see CN(C=O)C1=C(C=CC2=CC(=C(C=C21)OC)OC)C3=C(C(=C(C=C3)OC)OC)O	397.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
(-)-Pseudoephedrine	62946	Click to see CC(C(C1=CC=CC=C1)O)NC	165.23	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
5-(Hydroxymethyl)-1-[2-(4-hydroxyphenyl)ethyl]pyrrole-2-carbaldehyde	636825	Click to see C1=CC(=CC=C1CCN2C(=CC=C2C=O)CO)O	245.27	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Sinapaldehyde	5280802	Click to see COC1=CC(=CC(=C1O)OC)C=CC=O	208.21	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol	11604108	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
Pinoresinol	73399	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2Z,6E,8E,10E)-N-(2-methylpropyl)dodeca-2,6,8,10-tetraenamide	5321101	Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)C	247.38	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4R,9R,10S,13R,16R)-16-hydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	10614344	Click to see CC1(CCCC2(C1CCC34C2CCC(C3O)C(=C)C4=O)C)C	302.50	unknown	https://doi.org/10.2298/JSC110206128R
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalyl acetate, (-)-	442474	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
Abscisic acid	5280896	Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C	264.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(14-Acetyloxy-2,3-dihydroxy-4,9,13,18-tetramethyl-5-oxo-6,17-dioxatetracyclo[11.5.0.03,7.016,18]octadec-8-en-12-yl) acetate	73837071	Click to see CC1C(=O)OC2C1(C(C3C(C(CCC(=C2)C)OC(=O)C)(C(CC4C3(O4)C)OC(=O)C)C)O)O	466.50	unknown	https://doi.org/10.1002/CBER.189102401284
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24S)-Ergost-4-en-3-one	14537343	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C	398.70	unknown	https://doi.org/10.2298/JSC110206128R
(24xi)-Ergosta-5,7,9(11),22-tetraen-3-ol	3593510	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CC=C3C2=CC=C4C3(CCC(C4)O)C)C	394.60	unknown	https://doi.org/10.2298/JSC110206128R
(3S,9S,10R,13R,14R,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	247705	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	https://doi.org/10.2298/JSC110206128R
17-(5,6-dimethylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	314387	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C	398.70	unknown	https://doi.org/10.2298/JSC110206128R
17-(5,6-dimethylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	632418	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3=C2CC=C4C3(CCC(C4)O)C)C	396.60	unknown	https://doi.org/10.2298/JSC110206128R
17-(5,6-Dimethylheptan-2-yl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one	14537342	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C	398.70	unknown	https://doi.org/10.2298/JSC110206128R
22,23-Dihydrobrassicasterol	5283637	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.2298/JSC110206128R
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.2298/JSC110206128R
Dehydroergosterol	6436660	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CC=C3C2=CC=C4C3(CCC(C4)O)C)C	394.60	unknown	https://doi.org/10.2298/JSC110206128R
Ergosterol	444679	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	https://doi.org/10.2298/JSC110206128R
Lichesterol	5281329	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3=C2CC=C4C3(CCC(C4)O)C)C	396.60	unknown	https://doi.org/10.2298/JSC110206128R
Stellasterol	5283628	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C	398.70	unknown	https://doi.org/10.2298/JSC110206128R
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(22e)-Stigmasta-4,22-diene-3,6-dione	10455054	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(=O)CCC34C)C)C(C)C	424.70	unknown	https://doi.org/10.2298/JSC110206128R
(5alpha,22E)-Stigmast-22-ene-3,6-dione	163195002	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CCC(=O)C4)C)C)C(C)C	426.70	unknown	https://doi.org/10.2298/JSC110206128R
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one	12943207	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C)C(C)C	410.70	unknown	https://doi.org/10.2298/JSC110206128R
17-(5-Ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-1,2,4,5,6,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one	543613	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(=O)C4)C)C)C(C)C	410.70	unknown	https://doi.org/10.2298/JSC110206128R
17-(5-Ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one	255607	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	410.70	unknown	https://doi.org/10.2298/JSC110206128R
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol	72576472	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.2298/JSC110206128R
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	521229	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.2298/JSC110206128R
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.2298/JSC110206128R
17-(5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	12442813	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(=O)C4)C)C)C(C)C	414.70	unknown	https://doi.org/10.2298/JSC110206128R
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol	6743	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C	416.70	unknown	https://doi.org/10.2298/JSC110206128R
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.2298/JSC110206128R
22,23-Dihydro-alpha-spinasterone	14160308	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(=O)C4)C)C)C(C)C	412.70	unknown	https://doi.org/10.2298/JSC110206128R
3-Hydroxystigmast-5-en-7-one	160608	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C	428.70	unknown	https://doi.org/10.2298/JSC110206128R
3beta-Hydroxyporiferast-5-en-7-one	14779505	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C	428.70	unknown	https://doi.org/10.2298/JSC110206128R
5a-Stigmast-22-en-3,6-dion	129650926	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CCC(=O)C4)C)C)C(C)C	426.70	unknown	https://doi.org/10.2298/JSC110206128R
5alpha-Stigmasta-7,16-dien-3beta-ol	22295562	Click to see CCC(CCC(C)C1=CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.2298/JSC110206128R
5alpha-Stigmastan-3-one	5491512	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(=O)C4)C)C)C(C)C	414.70	unknown	https://doi.org/10.2298/JSC110206128R
5alpha-Stigmastane-3,6-dione	13992092	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CCC(=O)C4)C)C)C(C)C	428.70	unknown	https://doi.org/10.2298/JSC110206128R
alpha-Spinasterin	5281331	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.2298/JSC110206128R
alpha-Spinasterone	21159864	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(=O)C4)C)C)C(C)C	410.70	unknown	https://doi.org/10.2298/JSC110206128R
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.2298/JSC110206128R
beta-Sitosterone	9801811	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C	412.70	unknown	via CMAUP database
delta7Stigmastenol	521367	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.2298/JSC110206128R
Schottenol	441837	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.2298/JSC110206128R
Schottenone	129681578	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(=O)C4)C)C)C(C)C	412.70	unknown	https://doi.org/10.2298/JSC110206128R
Sitostenone	579897	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	https://doi.org/10.2298/JSC110206128R
Stigmast-22E-en-3beta-ol	5283650	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.2298/JSC110206128R
Stigmast-4-ee-3,6-dione	14308881	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(=O)CCC34C)C)C(C)C	426.70	unknown	https://doi.org/10.2298/JSC110206128R
Stigmast-4-en-3-one	5484202	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	https://doi.org/10.2298/JSC110206128R
Stigmast-4-ene-3,6-dione	5490007	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(=O)CCC34C)C)C(C)C	426.70	unknown	https://doi.org/10.2298/JSC110206128R
Stigmasta-4,22-dien-3-one	6442194	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	410.70	unknown	https://doi.org/10.2298/JSC110206128R
Stigmasta-4,6-dien-3-one	12943206	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C)C(C)C	410.70	unknown	https://doi.org/10.2298/JSC110206128R
Stigmastane-3,6-dione	543599	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CCC(=O)C4)C)C)C(C)C	428.70	unknown	https://doi.org/10.2298/JSC110206128R
Stigmastanol	241572	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C	416.70	unknown	https://doi.org/10.2298/JSC110206128R
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.2298/JSC110206128R
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(Z)-3-hydroxy(2,3-13C2)prop-1-enyl]-2-methoxyphenoxy]oxane-3,4,5-triol	11602622	Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O	344.33	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Ganodine	126543	Click to see C1=CC=C(C=C1)CCN2C(=CC=C2C=O)CO	229.27	unknown	via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
(5S,9R,13R,16S)-N,6,13-trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-16-amine	5316046	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)CN1	328.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Piperidines
(+)-Conhydrine	11744748	Click to see CCC(C1CCCCN1)O	143.23	unknown	https://doi.org/10.1002/JLAC.18561000311
Conhydrine	10314	Click to see CCC(C1CCCCN1)O	143.23	unknown	https://doi.org/10.1002/JLAC.18561000311
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
3,5-Dimethoxy-2-methyl-pyran-4-one	10419590	Click to see CC1=C(C(=O)C(=CO1)OC)OC	170.16	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
gamma-Coniceine	442632	Click to see CCCC1=NCCCC1	125.21	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1199726/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1196975/ https://doi.org/10.1007/BF00267647
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
1,2-Dimethoxy-13-methyl-[1,3]benzodioxolo[5,6-c]phenanthridine	101673185	Click to see CC1=C2C(=C3C=CC4=CC5=C(C=C4C3=N1)OCO5)C=CC(=C2OC)OC	347.40	unknown	via CMAUP database
Oxychelerythrine	147279	Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=C(C1=O)C(=C(C=C5)OC)OC	363.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine	68085	Click to see COC1=C2C=COC2=NC3=CC=CC=C31	199.20	unknown	via CMAUP database
gamma-Fagarine	107936	Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3	229.23	unknown	via CMAUP database
Robustine	164950	Click to see COC1=C2C=COC2=NC3=C1C=CC=C3O	215.20	unknown	via CMAUP database
Skimmianine	6760	Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC	259.26	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Hydroxyquinolines
Zanthobisquinolone	54688597	Click to see CN1C2=CC=CC=C2C(=C(C1=O)CC3=C(C4=CC=CC=C4N(C3=O)C)O)O	362.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methylquinolin-2-one	182073	Click to see CN1C2=CC=CC=C2C(=CC1=O)OC	189.21	unknown	via CMAUP database
4-Methoxy-1H-quinolin-2-one	600167	Click to see COC1=CC(=O)NC2=CC=CC=C21	175.18	unknown	via CMAUP database
N-Methylschinifoline	101652163	Click to see CC(=C)C=CC1=C(C2=CC=CC=C2N(C1=O)C)OC	255.31	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
6,6,12-Trimethylisochromeno[4,3-c]quinolin-11-one	10017165	Click to see CC1(C2=CC=CC=C2C3=C(O1)C4=CC=CC=C4N(C3=O)C)C	291.30	unknown	via CMAUP database
7-Methoxyflindersine	101995295	Click to see CC1(C=CC2=C(O1)C3=C(C=C(C=C3)OC)NC2=O)C	257.28	unknown	via CMAUP database
Benzosimuline	5321951	Click to see CC1=CC2=C(C=C1)C(OC3=C2C(=O)N(C4=CC=CC=C43)C)(C)C	305.40	unknown	via CMAUP database
Flindersine	68230	Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3NC2=O)C	227.26	unknown	via CMAUP database
N-Acetoxymethylflindersine	11289552	Click to see CC(=O)OCN1C2=CC=CC=C2C3=C(C1=O)C=CC(O3)(C)C	299.32	unknown	via CMAUP database
Rel-zanthodioline	5315424	Click to see CC1(C(C(C2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)O)O)C	305.32	unknown	via CMAUP database
Ribalinine	932818	Click to see CC1(C(CC2=C(O1)N(C3=CC=CC=C3C2=O)C)O)C	259.30	unknown	via CMAUP database
Zanthobungeanine	5315422	Click to see CC1(C=CC2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)C	271.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-Balanophonin	23252258	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O	356.40	unknown	via CMAUP database
(+)-Simulanol	52918181	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)OC)C=CCO	388.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(Z)-3,4-Dimethoxycinnamic acid	1585026	Click to see COC1=C(C=C(C=C1)C=CC(=O)O)OC	208.21	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
cis-Caffeic acid	1549111	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone	8417	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC	206.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Isofraxidin	5318565	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)O	222.19	unknown	via CMAUP database
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	via CMAUP database

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Conium maculatum

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