Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

GENTIANA ALGIDA (Pall.)

Traditional use of Gentiana algida centers on its intensely bitter roots and herb, which are prepared as digestive teas and decoctions across several cold‑highland systems. In central Tibet, local practitioners macerate the plant in warm water to make a bitter “stomach tea” taken with meals (Johns et al., 1999). In Ladakh, herbalists collect the herb at altitude and prepare a brief decoction of roots and aerial parts to relieve indigestion and general fatigue (Srivastava, 1999). Among high‑altitude herders in the Mongolian Altai, villagers steep chopped roots in hot water for a short infusion used before heavy meals; the infusion is also given as a tonic in cold seasons (Lange, 2004). No poultice or alcoholic tincture traditions for this species are recorded in accessible sources.

A practical and widely cited preparation is the bitter digestive tea. Place 2 g (about 1 teaspoon) of dried, chopped roots into 250 mL boiling water, remove from heat, cover, and steep for 10–15 minutes. Strain, and drink 1 cup 20–30 minutes before meals. A follow‑up cup can be taken after meals if needed. Traditional practice limits daily intake to 2–3 cups. Bitter herbs stimulate appetite and gastric secretions and may worsen reflux; people with gastric ulcers or on anticoagulants should avoid high doses (World Health Organization, 1999; Johns et al., 1999).

Active constituents in Gentiana algida include the bitter secoiridoid gentiopicrin, the intense amarogentin, loganic acid, gentiopicroside, swertiamarin, and related iridoids, together with flavonoids and xanthones. These compounds plausibly account for the digestive‑bitter activity that underlies the traditional tea and decoction preparations (Chassot et al., 1999; Lange, 2004).

Today, the bitter decoction remains in limited use among Tibetan and Himalayan herbalists, and extracts are included in several commercial digestive bitter formulations, while modern pharmacology continues to explore iridoid‑rich Gentiana extracts for hepatoprotective and gastrointestinal effects (Bennett et al., 2021).

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Pneumonanthe algida	F.W.Schmidt	Arch. Bot. (Leipzig) 1(1): 10 (1796)
Dasystephana romanzovii	Rydb.	Bull. Torrey Bot. Club 33: 148 (1906)
Gentiana algida var. romanzovii	(Bunge) Kusn.	Trudy S.-Peterburgsk. Obshch. Estestvoisp., Otd. Bot. 24: 119 (1894)
Gentiana algida var. sibirica	Turcz.	Vestn. Estestv. Nauk Moskovsk. Obshch. Isp. Prir. 1860: 1355 1860
Gentiana frigida var. algida	(Pall.) Froel.	Gentiana 39 1796
Gentiana igarashii	Miyabe & Kudô	Trans. Sapporo Nat. Hist. Soc. 8: 5 (1921)
Gentiana romanzovii	Ledeb. ex Bunge	Nouv. Mém. Soc. Imp. Naturalistes Moscou 1: 215 (1829)
Gentiana romanzovii f. hexaloba	A.Roach	Amer. Midl. Naturalist 50: 510 (1953)
Gentianodes algida	(Pall.) Á.Löve & D.Löve	Bot. Not. 125: 256 (1972)
Gentiana algida var. sibirica	Kusn.
Gentiana frigida var. algida	(Pall.) Ledeb.
Dasystephana algida	(Pall.) Borkh.	Arch. Bot. 1: t. 26 (1796)

Common names Top

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Filter by language:

Language	Common/alternative name
English	whitish gentian
Azerbaijani	soyuq acıçiçək
Japanese	トウヤクリンドウ
Kazakh	Суық көкгүл
Korean	산용담
Chinese	小儿血参
Chinese	苦龙胆
Chinese	高山龙胆
Chinese	白花龙胆
Chinese	高山龍膽

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Gentiana algida var. purdomii	(C.Marquand) T.N.Ho	Worldwide Monogr. Gentiana : 223 (2001)
Gentiana algida var. algida		Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - Qinghai
  - Tibet
  - Xinjiang
- Eastern Asia
  - Japan
  - Korea
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Kamchatka
  - Khabarovsk
  - Magadan
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya
- Indo-China
  - Myanmar

Northern America click to expand
- Northwestern U.S.A.
  - Colorado
  - Montana
  - Wyoming
- South-central U.S.A.
  - New Mexico
- Southwestern U.S.A.
  - Utah
- Subarctic America
  - Alaska
  - Aleutian Islands
  - Yukon
- Western Canada
  - British Columbia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000696823
Canadensys	5993
USDA Plants	GEAL2
Tropicos	13800009
KEW	urn:lsid:ipni.org:names:367731-1
The Plant List	kew-2819866
Open Tree Of Life	449120
Observations.org	118186
NCBI Taxonomy	50748
Nature Serve	2.149756
IPNI	367731-1
iNaturalist	118783
GBIF	3170111
Freebase	/m/0nbcnk5
EPPO	GETAG
EOL	581410
USDA GRIN	17347

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

Nose of dog, eye of elk, and wolf’s liver: exploring the interconnectedness of Indigenous health and foraging among the Dukha reindeer herders of Mongolia

Hatcherson J

Int J Circumpolar Health

18-Apr-2024

PMCID:	PMC11028006
doi:	10.1080/22423982.2024.2343454
PMID:	38634711

Tibetan medicine Bang Jian: a comprehensive review on botanical characterization, traditional use, phytochemistry, and pharmacology

Li Y, Zhang J, Fan JY, Zhong SH, Gu R

Front Pharmacol

14-Dec-2023

PMCID:	PMC10757618
doi:	10.3389/fphar.2023.1295789
PMID:	38161696

The Distribution Characteristics of Vegetation in the Subrange of the Altai Mountains, Xinjiang

Cao Q, Wei Y, Li W, Feng Y, Abduraimov OS

Plants (Basel)

20-Nov-2023

PMCID:	PMC10675357
doi:	10.3390/plants12223915
PMID:	38005812

Morphometric Characteristics and Genetic Issr Marker Variability in Rhodiola rosea L. (Crassulaceae) in Different Ecological and Geographic Conditions in the Altai Republic

Dorogina OV, Kuban IN, Achimova AA, Williams N, Lashchinskiy NN, Zhmud EV

Int J Mol Sci

16-Oct-2023

PMCID:	PMC10607822
doi:	10.3390/ijms242015224
PMID:	37894905

Therapeutic potential of plant iridoids in depression: a review

Kou Y, Li Z, Yang T, Shen X, Wang X, Li H, Zhou K, Li L, Xia Z, Zheng X, Zhao Y

Pharm Biol

27-Oct-2022

PMCID:	PMC9621214
doi:	10.1080/13880209.2022.2136206
PMID:	36300881

Decades-long phylogeographic issues: complex historical processes and ecological factors on genetic structure of alpine plants in the Japanese Archipelago

Ikeda H

J Plant Res

15-Feb-2022

PMCID:	PMC8894158
doi:	10.1007/s10265-022-01377-w
PMID:	35166981

Why flowers close at noon? A case study of an alpine species Gentianopsis paludosa (Gentianaceae)

Hou Q, Zhao X, Pang X, Duan M, Ehmet N, Shao W, Sun K

Ecol Evol

15-Jan-2022

PMCID:	PMC8809448
doi:	10.1002/ece3.8490
PMID:	35136551

Current state of populations of Rhodiola rosea L. (Crassulaceae) in East Kazakhstan

Kubentayev SA, Zhumagul MZ, Kurmanbayeva MS, Alibekov DT, Kotukhov JA, Sitpayeva GT, Mukhtubayeva SK, Izbastina KS

Bot Stud

07-Nov-2021

PMCID:	PMC8572951
doi:	10.1186/s40529-021-00327-4
PMID:	34746988

A Review on the Ethnomedicinal Usage, Phytochemistry, and Pharmacological Properties of Gentianeae (Gentianaceae) in Tibetan Medicine

Chi X, Zhang F, Gao Q, Xing R, Chen S

Plants (Basel)

05-Nov-2021

PMCID:	PMC8620629
doi:	10.3390/plants10112383
PMID:	34834747

Morphological Characterization and Transcriptional Regulation of Corolla Closure in Ipomoea purpurea

Zhang P, Sun M, Wang X, Guo R, Sun Y, Gui M, Li J, Wang T, Zhang L

Front Plant Sci

07-Sep-2021

PMCID:	PMC8453026
doi:	10.3389/fpls.2021.697764
PMID:	34557209

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

Phytochemical studies on traditional herbal medicines based on the ethnopharmacological information obtained by field studies

Tanaka N, Kashiwada Y

J Nat Med

13-Jul-2021

PMCID:	PMC8397699
doi:	10.1007/s11418-021-01545-7
PMID:	34255289

Chemistry, Pharmacology and Therapeutic Potential of Swertiamarin – A Promising Natural Lead for New Drug Discovery and Development

Muhamad Fadzil NS, Sekar M, Gan SH, Bonam SR, Wu YS, Vaijanathappa J, Ravi S, Lum PT, Dhadde SB

Drug Des Devel Ther

21-Jun-2021

PMCID:	PMC8233004
doi:	10.2147/DDDT.S299753
PMID:	34188450

Effects of ambient climate and three warming treatments on fruit production in an alpine, subarctic meadow community

Alatalo JM, Jägerbrand AK, Dai J, Mollazehi MD, Abdel‐Salam AG, Pandey R, Molau U

Am J Bot

31-Mar-2021

PMCID:	PMC8251864
doi:	10.1002/ajb2.1631
PMID:	33792046

Prevalence and phenology of fine root endophyte colonization across populations of Lycopodiella inundata

Kowal J, Arrigoni E, Serra J, Bidartondo M

Mycorrhiza

30-Jul-2020

PMCID:	PMC7392370
doi:	10.1007/s00572-020-00979-3
PMID:	32734329

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(3S,4R)-3-(hydroxymethyl)-4-[(2R)-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-3-en-2-yl]oxan-2-one	95224521	Click to see	362.37	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
1-O-beta-D-Glucopyranosylamplexine	101273519	Click to see	362.37	unknown	https://doi.org/10.1016/0031-9422(95)00599-4 https://doi.org/10.1021/NP010358O
3-(Hydroxymethyl)-4-[1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-3-en-2-yl]oxan-2-one	72820992	Click to see	362.37	unknown	https://doi.org/10.1016/0031-9422(95)00599-4 https://doi.org/10.1021/NP010358O
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/0031-9422(95)00599-4
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/10.1016/0031-9422(95)00599-4
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/10.1016/0031-9422(95)00599-4
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
Stigmasterol	5280794	Click to see	412.70	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-2-(acetyloxymethyl)-6-[[(3R,4R,4aR)-4-ethenyl-4a-hydroxy-8-oxo-3,4,5,6-tetrahydropyrano[3,4-c]pyran-3-yl]oxy]oxan-3-yl] 2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate	162877915	Click to see	798.70	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-2-(acetyloxymethyl)-6-[[(3R,4R,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]oxan-3-yl] 2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate	102143856	Click to see	782.70	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
[4,5-Diacetyloxy-2-(acetyloxymethyl)-6-[(4-ethenyl-4a-hydroxy-8-oxo-3,4,5,6-tetrahydropyrano[3,4-c]pyran-3-yl)oxy]oxan-3-yl] 2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate	75144806	Click to see	798.70	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
[4,5-diacetyloxy-2-(acetyloxymethyl)-6-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]oxan-3-yl] 2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate	74029859	Click to see	782.70	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
Rindoside	46174003	Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C3(CCOC(=O)C3=CO2)O)C=C)OC(=O)C)OC(=O)C)OC(=O)C4=C(C(=CC=C4)OC5C(C(C(C(O5)CO)O)O)O)O	798.70	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
Trifloroside	101688128	Click to see	782.70	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(-)-Sweroside	161036	Click to see	358.34	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
(3R,4R,4aS)-4-ethenyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one	131704891	Click to see	358.34	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
(3S,4R,4aS)-4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one	354447	Click to see	358.34	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
[(2R,3S,4S,5R,6S)-6-[[(3S,4R,4aR)-4-ethenyl-4a-hydroxy-8-oxo-3,4,5,6-tetrahydropyrano[3,4-c]pyran-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 2,3-dihydroxybenzoate	102094444	Click to see	510.40	unknown	https://doi.org/10.1055/S-2006-957770
[(2R,3S,4S,5R,6S)-6-[[(3S,4R,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 2,3-dihydroxybenzoate	102094443	Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)COC(=O)C4=C(C(=CC=C4)O)O)O)O)O	494.40	unknown	https://doi.org/10.1055/S-2006-957770
[(2S,3R,4S,5S,6R)-2-[[(3S,4R,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 2,3-dihydroxybenzoate	101687152	Click to see	494.40	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
[2-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 2,3-dihydroxybenzoate	78407175	Click to see	494.40	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
[6-[(4-Ethenyl-4a-hydroxy-8-oxo-3,4,5,6-tetrahydropyrano[3,4-c]pyran-3-yl)oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 2,3-dihydroxybenzoate	162950404	Click to see C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)COC(=O)C4=C(C(=CC=C4)O)O)O)O)O	510.40	unknown	https://doi.org/10.1055/S-2006-957770
[6-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 2,3-dihydroxybenzoate	162932637	Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)COC(=O)C4=C(C(=CC=C4)O)O)O)O)O	494.40	unknown	https://doi.org/10.1055/S-2006-957770
4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one	581257	Click to see	358.34	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
Gentiopicroside	88708	Click to see	356.32	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Gentianose	117678	Click to see	504.40	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Anofinic acid	5319235	Click to see	204.22	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
Methyl 2,2-dimethylchromene-6-carboxylate	5316881	Click to see CC1(C=CC2=C(O1)C=CC(=C2)C(=O)OC)C	218.25	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,5-dihydroxy-3-methoxy-8-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one	44144324	Click to see COC1=CC(=C2C(=C1)OC3=C(C=CC(=C3C2=O)OC4C(C(C(C(O4)CO)O)O)O)O)O	436.40	unknown	https://doi.org/10.1007/BF00630190
1,5-Dihydroxy-3-methoxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one	5858086	Click to see	436.40	unknown	https://doi.org/10.1007/BF00630190
1,5,8-Trihydroxy-3,4-dimethoxyxanthone	86183532	Click to see	304.25	unknown	https://doi.org/10.1007/BF00629661
Bellidifolin	5281623	Click to see COC1=CC(=C2C(=C1)OC3=C(C=CC(=C3C2=O)O)O)O	274.22	unknown	https://doi.org/10.1055/S-2004-832632 https://doi.org/10.1007/BF00630190
Chiratol	10356746	Click to see	288.25	unknown	https://doi.org/10.1007/BF00630190
Isobellidifolin	5322042	Click to see COC1=C2C(=C(C=C1)O)C(=O)C3=C(C=C(C=C3O2)O)O	274.22	unknown	https://doi.org/10.1007/BF00629661
Swerchirin	5281660	Click to see	288.25	unknown	https://doi.org/10.1007/BF00629661
Swertianolin	5281662	Click to see	436.40	unknown	https://doi.org/10.1007/BF00630190
> Organoheterocyclic compounds / Coumarans
(2R)-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-carboxylic acid	162964493	Click to see CC(=C)C1CC2=C(O1)C=CC(=C2)C(=O)O	204.22	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
(2S)-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-carboxylic acid	131405161	Click to see	204.22	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
2-Isopropenyl-2,3-dihydrobenzofuran-5-carboxylic acid	5317368	Click to see	204.22	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
methyl (2S)-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-carboxylate	162858985	Click to see	218.25	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
Methyl 2-isopropenyl-2,3-dihydrobenzofuran-5-carboxylate	5316729	Click to see CC(=C)C1CC2=C(O1)C=CC(=C2)C(=O)OC	218.25	unknown	https://doi.org/10.1016/0031-9422(95)00599-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
5-Hydroxy-2-(4-Hydroxyphenyl)-7-Methoxy-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Chromen-4-One	369636	Click to see	446.40	unknown	https://doi.org/10.1007/BF00630190
Swertisin	124034	Click to see	446.40	unknown	https://doi.org/10.1007/BF00630190
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin	5281675	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/0031-9422(95)00599-4

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Gentiana algida

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