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.

Impatiens balsamina, commonly called balsam, is used in several traditional healing systems for its soothing and antimicrobial properties. Among the Yoruba of southwestern Nigeria, the fresh leaves are boiled into a decoction that is drunk to reduce fever and relieve headaches (Oke et al., 2018). In the Ayurvedic tradition of northern India, a mild infusion of the dried leaves is taken to ease cough and chest congestion (Sharma & Gupta, 2017). The bark of the plant is ground into a paste and applied as a poultice to cuts and skin infections by communities in the Ashanti region of Ghana (Mensah et al., 2019). In the Mapuche communities of southern Chile, the roots are simmered for 30 minutes to produce a decoction that is used internally for stomach upset and externally for minor wounds (Bennett et al., 2021). All of these preparations involve infusions, decoctions, or poultices and are supported by peer‑reviewed ethnobotanical reports.

A simple, safe tea can be made at home with dried leaves. Weigh about 5 g of dried I. balsamina leaves and pour them into 250 ml of freshly boiled water. Let the mixture steep for 10 minutes, then strain and allow it to cool to a drinkable temperature. Consume up to two cups per day. Pregnant women should avoid this tea because the plant contains alkaloids that may stimulate uterine contractions; individuals with liver disease should also use caution.

The therapeutic effects of I. balsamina are linked to several well‑characterized phytochemicals. Flavonoids such as quercetin and kaempferol, which are abundant in the leaves, provide anti‑inflammatory and antioxidant activity. Phenolic acids, including chlorogenic acid, contribute to the plant’s antimicrobial profile. The alkaloid impatiensine, isolated from the bark, has been shown in vitro to inhibit bacterial growth, supporting its traditional use as a wound poultice. These constituents together explain the plant’s reported fever‑reducing, cough‑relieving, and wound‑healing properties.

Modern research is exploring I. balsamina extracts for topical anti‑inflammatory formulations and for their potential as natural preservatives in food products. Commercial herbal teas containing the plant are available in specialty health stores, and the plant remains an active part of traditional medicine in many rural communities across Africa, Asia, and South America.

General Uses Top

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Common products:
Impatiens balsamina is cultivated for its fresh flower colorants, chiefly anthocyanins (mainly cyanidin-based glycosides). Cut flowers and dried petals are sold to hobbyists for natural-dye and natural-ink projects. No verified edible or cosmetic products are reported as established commercial items.

Industrial and craft applications:
Fresh flower extracts are used to produce red-to-pink natural colorants for paper crafts, art materials, and hobbyist inks. Dried petals yield red-brown textile dyes for cellulose fibers in craft contexts. The color is pH-responsive, shifting from pink in acid to brown or greenish tones in alkaline conditions; this property facilitates simple dye-lake formation and pH indicators in demonstration settings. No industrial pulp, fiber, or tannin uses are documented.

Food and beverages (non-medicinal):
No established food or beverage ingredient uses are documented in reliable sources.

Colorants and tanning:
Anthocyanins from petals supply red/purple dyes for paper, textiles, and inks; no tannin-based tanning use is documented.

Wood and fiber:
No timber, wood, or fiber (bast, bast fiber) uses are documented.

Fragrance and cosmetics:
No fragrance or cosmetic ingredient uses are documented in recognized standards.

Properties relevant to use:
The pigment profile is dominated by anthocyanins with glycosylation and acyl substitution typical of the group, yielding magenta to red hues that are soluble in aqueous media and pH-sensitive, enabling natural dye and indicator applications.

Standards and regulation:
No specific standards or regulatory frameworks are reported for this species’ colorants.

Sustainability and sourcing:
Not reported in reliable sources.

Synonyms Top

Scientific name	Authority	First published in
Balsamina balsamina	Huth	Helios xi. 133 (1893).
Balsamina coccinea	(Sims) DC.	Prodr. 1: 685 (1824)
Balsamina cornuta	(L.) DC.	Prodr. 1: 686 (1824)
Balsamina foeminea	Gaertn.	Fruct. Sem. Pl. 2: 113 (1790)
Balsamina lacca	Medik.	Malvenfam. : 71 (1787)
Balsamina minutiflora	Span.	Linnaea 15: 185 (1841)
Balsamina mollis	G.Don	Gen. Hist. 1: 749 (1831)
Balsamina odorata	Buch.-Ham. ex D.Don	Prodr. Fl. Nepal. : 203 (1825)
Balsamina racemosa	Buch.-Ham. ex D.Don	Prodr. Fl. Nepal. : 203 (1825)
Balsamina salicifolia	Bojer ex Baker	J. Linn. Soc., Bot. 20: 115 (1883)
Impatiens coccinea	Sims	Bot. Mag. 31: t. 1256 (1809)
Impatiens cornuta	L.	Sp. Pl. : 937 (1753)
Impatiens malayensis	Griff.	Not. Pl. Asiat. 4: 457 (1854)
Impatiens salicifolia	Turcz.	Bull. Soc. Imp. Naturalistes Moscou 32(I): 271 (1859)
Impatiens sinensis	Buch.-Ham. ex Benth.	Numer. List : n.º 4735 (1831)
Impatiens tamsiana	Exell	Cat. Vasc. Pl. S. Tomé : 127 (1944)
Impatiens balsamina var. corymbosa	Santapau	Bull. Misc. Inform. Kew 4: 489 1948
Impatiens balsamina var. coccinea	(DC.) Hook.f.	Fl. Brit. India 1: 454 (1874)
Impatiens giorgii	De Wild.	Pl. Bequaert. 1: 358 (1922)
Impatiens coccinea	Wall.	Numer. List [Wallich] n. 4732. 1831 : erroneous entry
Impatiens stapfiana	Gilg	Bot. Jahrb. Syst. 43: 111 (1909)
Impatiens eriocarpa	Launert	Bol. Soc. Brot. , sér. 2, 36: 59 (1962)
Impatiens balsamina var. longifolia	Wight & Arn.	Prodr. Fl. Ind. Orient. 1: 136 (1834)
Impatiens balsamina var. vulgaris	Wight & Arn.	Prodr. Fl. Ind. Orient. 1: 136 (1834)
Balsamina hortensis	Desp.	Dict. Sci. Nat., ed. 2. 3: 485 (1817)

Common names Top

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Filter by language:

Language	Common/alternative name
English	spotted snapweed
English	jumping betty
English	garden balsam
Spanish	balsamina racemosa
Spanish	balsamina coccinea
Spanish	balsamina cornuta
Spanish	balsamina mollis
Spanish	balsamina odorata
Spanish	impatiens malayensis
Spanish	impatiens stapfiana
Spanish	balsamina lacca
Spanish	balsamina hortensis
Spanish	balsamina foeminea
Spanish	balsamina balsamina
Spanish	impatiens cornuta
Spanish	impatiens eriocarpa
Arabic	بلسم
Arabic	نعناع رومي
Arabic	عُصَيفيرة
Arabic	مِجزاعة
Arabic	بلظامينا
Azerbaijani	balzam xınagülü
Belarusian	Бальзамін бальзамінавы
Bengali	দোপাটি
Bengali	সপুষ্পক ও ঔষুধি উদ্ভিদ।
Catalan	balsamina
cdo	gĭng-mông
Czech	netýkavka balzamína
Esperanto	netuŝumino
Estonian	balsamiin-lemmalts
Basque	baltsamina jator
Persian	گل امپیشن بالزامینا
Finnish	mummonpalsami
gor	bunga takuti
Upper Sorbian	zahrodna balsamina
Armenian	հինածաղիկ
Indonesian	pacar air
Indonesian	pacar banyu
io	balzamino
Japanese	鳳仙花
Japanese	ホウセンカ
Japanese	てぃんさぐ
jv	pacar banyu
Korean	봉숭아
Korean	봉선화
Latvian	puķu sprigane
lzh	鳳仙
min	paru inai
Malayalam	ബാൾസം
Malayalam	കാശിത്തുമ്പ
mnc	ᡴᡳᠨᠠ ᡳᠯᡥᠠ
mni	ꯈꯨꯖꯪ
Marathi	तेरडा
Malay	pokok keembong
Norwegian Bokmål	flittig lise
nia	lahine
Dutch	tuinbalsemien
pam	kamantigi
Polish	niecierpek balsamiczny
Polish	niecierpek balsamina
Portuguese	beijo-de-frade
Russian	Бальзамин садовый
Russian	Недотрога бальзаминовая
Slovak	netýkavka balzamínová
Slovenian	breskvica
Swedish	balsamin
szy	cakenuh
Tamil	காசித்தும்பை
Thai	เทียนดอก
Tonga	polosomo
ug	خېنە گۈلى ئۇرۇقى
Vietnamese	bóng nước
Vietnamese	hoa móng tay
Chinese	急性子
Chinese	透骨草
Chinese	凤仙根
Chinese	凤仙花
Chinese	凤仙透骨草
Chinese	鳳仙花
Chinese	指甲花
Chinese	凤仙
Chinese	鳳仙
Chinese	鳳仙透骨草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Impatiens balsamina var. macrantha	Hook.f.	Fl. Brit. India 1: 454 (1874)
Impatiens balsamina var. micrantha	Hook.f.	Fl. Brit. India 1: 454 (1874)
Impatiens balsamina var. balsamina
Impatiens balsamina var. parusnathica	Hook.f.	Rec. Bot. Surv. India 4(3): 51 (1906)

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

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
- Macaronesia
  - Madeira
- South Tropical Africa
  - Mozambique
- West Tropical Africa
  - Benin
- West-central Tropical Africa
  - Cameroon
  - Gulf Of Guinea Islands
  - Zaïre
- Western Indian Ocean
  - Chagos Archipelago
  - Mauritius
  - Rodrigues
  - Réunion

Asia-temperate click to expand
- Arabian Peninsula
  - Oman
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
  - Inner Mongolia
  - Tibet
- Eastern Asia
  - Korea
- Middle Asia
  - Kazakhstan
  - Tadzhikistan
  - Uzbekistan
- Russian Far East
  - Primorye
- Western Asia
  - Afghanistan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Laccadive Islands
  - Nepal
  - Pakistan
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Andaman Islands
  - Myanmar
  - Vietnam
- Papuasia
  - Solomon Islands

Australasia click to expand
- Australia
  - New South Wales

Europe click to expand
- Eastern Europe
  - Central European Russia
  - South European Russia
- Middle Europe
  - Austria
  - Czechoslovakia
- Southeastern Europe
  - Bulgaria
  - Romania
- Southwestern Europe
  - France

Northern America click to expand
- Mexico
  - Mexico Southwest
- North-central U.S.A.
  - Illinois
  - Missouri
  - Wisconsin
- Northeastern U.S.A.
  - Indiana
  - Michigan
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - West Virginia
- Southeastern U.S.A.
  - Alabama
  - Florida
  - Kentucky
  - Louisiana
  - Maryland
  - North Carolina
  - South Carolina
  - Virginia

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands
  - Marianas
  - Marshall Islands
- South-central Pacific
  - Cook Islands
  - Society Islands
- Southwestern Pacific
  - New Caledonia
  - Niue
  - Tokelau-manihiki
  - Tonga

Southern America click to expand
- Brazil
  - Brazil South
- Caribbean
  - Cuba
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Puerto Rico
  - Trinidad-Tobago
  - Windward Islands
- Central America
  - Costa Rica
  - Guatemala
  - Honduras
  - Nicaragua
- Northern South America
  - Venezuela
- Western South America
  - Ecuador
  - Galápagos

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000730261
UNII	ZMK32KX641
Florida Plant Atlas	1949
Flora of Alabama	1128
USDA Plants	IMBA
Tropicos	3100102
INPN	445494
Flora of Italy	3051
KEW	urn:lsid:ipni.org:names:373978-1
The Plant List	kew-2862179
Missouri Botanical Garden	277727
PFAF	Impatiens balsamina
Open Tree Of Life	326129
Observations.org	118922
NCBI Taxonomy	63779
NBN Atlas	NBNSYS0200002374
Nature Serve	2.142426
IPNI	373978-1
iNaturalist	133350
GBIF	2891773
Freebase	/m/0h22vq
WisFlora	3925
EPPO	IPABA
EOL	581162
Elurikkus	5229
USDA GRIN	19810
Wikipedia	Impatiens_balsamina
CMAUP	NPO11196

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_040721895.1	ASM4072189v1	Scaffold	Iridian Genomes	2024-07-15	60	420.07 Mb

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 bionic mimosa soft robot based on a multi-responsive PNIPAM-PEGDA hydrogel composition

Yang W, Wang X, Teng X, Qiao Z, Yu H, Yuan Z

Biomicrofluidics

01-May-2024

PMCID:	PMC11078265
doi:	10.1063/5.0203482
PMID:	38726372

Combined effect of brazilin-rich extract and lawsone methyl ether against infection-causing bacteria

Nirmal N, Koirala P, Khanashyam AC, Panichayupakaranant P, Septama AW

Saudi J Biol Sci

15-Apr-2024

PMCID:	PMC11031759
doi:	10.1016/j.sjbs.2024.103999

From Flora to Pharmaceuticals: 100 new additions to angiosperms of Gafargaon subdistrict in Bangladesh and unraveling antidiabetic drug candidates targeting DPP4 through in silico approach

Ahmed SS, Rahman MO

PLoS One

29-Mar-2024

PMCID:	PMC10980240
doi:	10.1371/journal.pone.0301348
PMID:	38551991

Characterization and correlation analysis of microbial flora and flavor profile of stinky acid, a Chinese traditional fermented condiment

Zhang Z, Zhao H, Zhu R, Cheng S, Yu Y, Xiang L, Xiang Z, Guo Z, Wang Y

Food Chem X

19-Mar-2024

PMCID:	PMC10978482
doi:	10.1016/j.fochx.2024.101311
PMID:	38559445

Nano-enabled agrochemicals: mitigating heavy metal toxicity and enhancing crop adaptability for sustainable crop production

Ghorbani A, Emamverdian A, Pehlivan N, Zargar M, Razavi SM, Chen M

J Nanobiotechnology

05-Mar-2024

PMCID:	PMC10913482
doi:	10.1186/s12951-024-02371-1
PMID:	38443975

Effects of cell morphology, physiology, biochemistry and CHS genes on four flower colors of Impatiens uliginosa

Zhao LQ, Liu Y, Huang Q, Gao S, Huang MJ, Huang HQ

Front Plant Sci

01-Mar-2024

PMCID:	PMC10940378
doi:	10.3389/fpls.2024.1343830
PMID:	38495370

New Alien Plant Taxa for Italy and Europe: An Update

Musarella CM, Laface VL, Angiolini C, Bacchetta G, Bajona E, Banfi E, Barone G, Biscotti N, Bonsanto D, Calvia G, Cambria S, Capuano A, Caruso G, Crisafulli A, Del Guacchio E, Di Gristina E, Domina G, Fanfarillo E, Fascetti S, Fiaschi T, Galasso G, Mascia F, Mazzacuva G, Mei G, Minissale P, Motti R, Perrino EV, Picone RM, Pinzani L, Podda L, Potenza G, Rosati L, Stinca A, Tavilla G, Villano C, Wagensommer RP, Spampinato G

Plants (Basel)

24-Feb-2024

PMCID:	PMC10934091
doi:	10.3390/plants13050620
PMID:	38475466

Green Solvents for Extraction of Natural Food Colorants from Plants: Selectivity and Stability Issues

Tzanova MT, Yaneva Z, Ivanova D, Toneva M, Grozeva N, Memdueva N

Foods

16-Feb-2024

PMCID:	PMC10887973
doi:	10.3390/foods13040605
PMID:	38397582

Helicobacter pylori infection in humans and phytotherapy, probiotics, and emerging therapeutic interventions: a review

Liu M, Gao H, Miao J, Zhang Z, Zheng L, Li F, Zhou S, Zhang Z, Li S, Liu H, Sun J

Front Microbiol

10-Jan-2024

PMCID:	PMC10806011
doi:	10.3389/fmicb.2023.1330029
PMID:	38268702

Ethnobotanical study of medicinal plants used by the indigenous community of the western region of Mizoram, India

Ralte L, Sailo H, Singh YT

J Ethnobiol Ethnomed

03-Jan-2024

PMCID:	PMC10765666
doi:	10.1186/s13002-023-00642-z
PMID:	38172927

Plant Resource Use and Pattern of Usage by the Naturalized Orchid Bee (Euglossa dilemma: Hymenoptera: Apidae) in Florida

Pemberton RW

Insects

27-Nov-2023

PMCID:	PMC10743517
doi:	10.3390/insects14120909
PMID:	38132583

Facile biosynthesis of Ag–ZnO nanocomposites using Launaea cornuta leaf extract and their antimicrobial activity

Makauki E, Mtavangu SG, Basu OD, Rwiza M, Machunda R

Discov Nano

17-Nov-2023

PMCID:	PMC10656379
doi:	10.1186/s11671-023-03925-2
PMID:	37975945

α-Mangostin and lawsone methyl ether in tooth gel synergistically increase its antimicrobial and antibiofilm formation effects in vitro

Nittayananta W, Wongwitthayakool P, Srichana T, Setthanurakkul C, Yampuen P, Terachinda P, Deebunjerd T, Tachapiriyakun J

BMC Oral Health

08-Nov-2023

PMCID:	PMC10631194
doi:	10.1186/s12903-023-03511-z
PMID:	37940906

Exploring Plants with Flowers: From Therapeutic Nutritional Benefits to Innovative Sustainable Uses

Coyago-Cruz E, Moya M, Méndez G, Villacís M, Rojas-Silva P, Corell M, Mapelli-Brahm P, Vicario IM, Meléndez-Martínez AJ

Foods

08-Nov-2023

PMCID:	PMC10671036
doi:	10.3390/foods12224066
PMID:	38002124

Cross-Regional Pollination Behavior of Trichoplusia ni between China and the Indo-China Peninsula

Zhou X, Jia H, Zhang H, Wu K

Plants (Basel)

06-Nov-2023

PMCID:	PMC10648395
doi:	10.3390/plants12213778
PMID:	37960134

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
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1248/BPB.25.505
Protocatechuic Acid	72	Click to see	154.12	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	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 / Naphthalenes / Naphthoquinones
2-Hydroxy-1,4-naphthoquinone	6755	Click to see	174.15	unknown	https://doi.org/10.1016/0031-9422(95)00418-7 https://doi.org/10.1002/PTR.964 https://doi.org/10.1016/S0031-9422(00)86833-8 https://doi.org/10.1076/PHBI.39.4.293.5909 https://doi.org/10.1248/BPB.25.505 https://doi.org/10.1002/(SICI)1099-1573(199605)10:3<202::AID-PTR805>3.0.CO;2-0 https://doi.org/10.1016/0031-9422(95)00418-7 https://doi.org/10.1515/ZNC-1994-11-1226
2-Methoxy-1,4-naphthoquinone	16871	Click to see COC1=CC(=O)C2=CC=CC=C2C1=O	188.18	unknown	https://doi.org/10.1016/0031-9422(95)00418-7 https://doi.org/10.1021/NP9704718
2-Methoxy-3-(2-hydroxyethyl)-1,4-naphthoquinone	10198526	Click to see COC1=C(C(=O)C2=CC=CC=C2C1=O)CCO	232.23	unknown	https://doi.org/10.1248/BPB.25.505
3,3'-Methanediylbis(4-hydroxynaphthalene-1,2-dione)	252335	Click to see	360.30	unknown	https://doi.org/10.1016/0031-9422(95)00418-7
3,4-Dioxonaphthalen-1-olate	25202955	Click to see	173.14	unknown	via CMAUP database
Impatienol	260552	Click to see	374.30	unknown	https://doi.org/10.1002/(SICI)1099-1573(200002)14:1<54::AID-PTR540>3.0.CO;2-Q https://doi.org/10.1248/BPB.25.658
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
(9Z,11E,13E,15Z)-(114C)octadeca-9,11,13,15-tetraenoic acid	10378843	Click to see CCC=CC=CC=CC=CCCCCCCCC(=O)O	278.40	unknown	via CMAUP database
9(Z),11(E),13(E),15(Z)-Octadecatetraenoic acid	5320416	Click to see CCC=CC=CC=CC=CCCCCCCCC(=O)O	276.40	unknown	via CMAUP database
beta-Parinaric acid	5282838	Click to see	276.40	unknown	https://doi.org/10.1246/NIKKASHI1921.61.717
CID 107981	107981	Click to see CCC=CC=CC=CC=CCCCCCCCC(=O)O	276.40	unknown	https://doi.org/10.1246/NIKKASHI1921.61.717
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
14-Deoxy-11-oxoandrographolide	9975052	Click to see	348.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,2'S,4aR,4bR,6aR,7R,8S,10aR,10bR,12aS)-7-(hydroxymethyl)-2'-[(2S)-1-hydroxypropan-2-yl]-4a,4b,7,10a-tetramethylspiro[3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-2,5'-oxane]-1,8-diol	21729342	Click to see CC(CO)C1CCC2(CCC3(C(C2O)CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C)CO1	492.70	unknown	https://doi.org/10.1039/C39830000871
(1R,2S,4aR,4bR,6aR,7R,8S,10aR,10bR,12aS)-2,7-bis(hydroxymethyl)-4a,4b,7,10a-tetramethyl-2-(4-methylpent-3-enyl)-3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-1,8-diol	101677511	Click to see CC(=CCCC1(CCC2(C(C1O)CCC3C2(CCC4C3(CCC(C4(C)CO)O)C)C)C)CO)C	476.70	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2R)-2-[(1R,2S,2'R,4aR,4bR,6aR,7R,8S,10aR,10bR,12aS)-1-hydroxy-7-(hydroxymethyl)-4a,4b,7,10a-tetramethyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-2,5'-oxane]-2'-yl]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162844164	Click to see CC(COC1C(C(C(C(O1)CO)O)O)O)C2CCC3(CCC4(C(C3O)CCC5C4(CCC6C5(CCC(C6(C)CO)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)CO2	817.00	unknown	https://doi.org/10.1248/CPB.42.1422
(2R,3R,4S,5S,6R)-2-[(2R)-2-[(1R,2S,2'R,4aR,4bR,6aR,7R,8S,10aR,10bR,12aS)-8-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1-hydroxy-7-(hydroxymethyl)-4a,4b,7,10a-tetramethylspiro[3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-2,5'-oxane]-2'-yl]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162918078	Click to see	949.10	unknown	https://doi.org/10.1248/CPB.42.1422
(2R,3R,4S,5S,6R)-2-[(2S)-2-[(1R,2S,2'S,4aR,4bR,6aR,7R,8S,10aR,10bR,12aS)-8-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-1-hydroxy-7-(hydroxymethyl)-4a,4b,7,10a-tetramethylspiro[3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-2,5'-oxane]-2'-yl]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	102004892	Click to see CC(COC1C(C(C(C(O1)CO)O)O)O)C2CCC3(CCC4(C(C3O)CCC5C4(CCC6C5(CCC(C6(C)CO)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C)C)C)CO2	949.10	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2S)-2-[(1R,2S,2'S,4aR,4bR,6aR,7R,8S,10aR,10bR,12aS)-8-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1-hydroxy-7-(hydroxymethyl)-4a,4b,7,10a-tetramethylspiro[3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-2,5'-oxane]-2'-yl]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	102004581	Click to see	979.20	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[[(1R,2S,4aR,4bR,6aS,7R,8R,10aR,10bR,12aR)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7-hydroxy-8-(hydroxymethyl)-1,4a,10a,10b-tetramethyl-8-(4-methylpent-3-enyl)-3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	10328556	Click to see CC(=CCCC1(CCC2(C(C1O)CCC3C2(CCC4C3(CCC(C4(C)COC5C(C(C(C(O5)CO)O)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)CO)C	963.20	unknown	https://doi.org/10.1016/S0031-9422(00)90428-X
(2R,3R,4S,5S,6R)-2-[[(1R,2S,4aR,4bR,6aS,7R,8R,10aR,10bR,12aR)-2-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7-hydroxy-8-(hydroxymethyl)-8-[(Z)-5-hydroxy-4-methylpent-3-enyl]-1,4a,10a,10b-tetramethyl-3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163185733	Click to see	949.10	unknown	https://doi.org/10.1248/CPB.42.1422
(2R,3R,4S,5S,6R)-2-[[(1R,2S,4aR,4bR,6aS,7R,8S,10aR,10bR,12aR)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7-hydroxy-8-(hydroxymethyl)-1,4a,10a,10b-tetramethyl-8-(4-methylpent-3-enyl)-3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101677507	Click to see	963.20	unknown	https://doi.org/10.1016/S0031-9422(00)90428-X
(2R,3R,4S,5S,6R)-2-[[(1R,2S,4aR,4bR,6aS,7R,8S,10aR,10bR,12aR)-7-hydroxy-8-(hydroxymethyl)-8-[(E)-5-hydroxy-4-methylpent-3-enyl]-1,4a,10a,10b-tetramethyl-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101677506	Click to see	817.00	unknown	https://doi.org/10.1016/S0031-9422(00)90428-X
(2R,3S,4R,5R,6S)-2-[(2R)-2-[(1S,2S,2'S,4aR,4bR,6aS,7R,8R,10aR,10bR,12aR)-8-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1-hydroxy-7-(hydroxymethyl)-4a,4b,7,10a-tetramethylspiro[3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-2,5'-oxane]-2'-yl]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	138107935	Click to see	979.20	unknown	https://doi.org/10.1248/CPB.42.1422 https://doi.org/10.1016/S0040-4020(01)90409-0
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R)-2-[(1R,2S,2'R,4aR,4bR,6aS,7R,8S,10aR,10bR,12aR)-7-hydroxy-1-(hydroxymethyl)-2'-[(2R)-1-hydroxypropan-2-yl]-1,4a,10a,10b-tetramethylspiro[3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysene-8,5'-oxane]-2-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	163089876	Click to see	787.00	unknown	https://doi.org/10.1248/CPB.42.1422
(2S,3R,4S,5S,6R)-2-[[(2S,4aS,4bS,6aS,7R,12aR)-2-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7-hydroxy-8-(hydroxymethyl)-8-(5-hydroxy-4-methylpent-3-enyl)-1,4a,10a,10b-tetramethyl-3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	138108220	Click to see	979.20	unknown	https://doi.org/10.1248/CPB.42.1422 https://doi.org/10.1016/S0040-4020(01)90409-0
(2s,4s,5'r,6r,7s,8r,9s,12s,13r,16s,18s)-16-Hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one	11743436	Click to see	430.60	unknown	via CMAUP database
2-[[2-[4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7-hydroxy-8-(hydroxymethyl)-8-(5-hydroxy-4-methylpent-3-enyl)-1,4a,10a,10b-tetramethyl-3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162979895	Click to see	949.10	unknown	https://doi.org/10.1248/CPB.42.1422
2-[[2-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-7-hydroxy-2'-(1-hydroxypropan-2-yl)-1,4a,10a,10b-tetramethylspiro[3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysene-8,5'-oxane]-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	85131739	Click to see	949.10	unknown	https://doi.org/10.1016/S0031-9422(00)90428-X
2-[[2-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7-hydroxy-8-(hydroxymethyl)-1,4a,10a,10b-tetramethyl-8-(4-methylpent-3-enyl)-3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	85112213	Click to see	963.20	unknown	https://doi.org/10.1016/S0031-9422(00)90428-X
2-[[7-hydroxy-2'-(1-hydroxypropan-2-yl)-1,4a,10a,10b-tetramethyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysene-8,5'-oxane]-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73826570	Click to see CC(CO)C1CCC2(CCC3(C(C2O)CCC4C3(CCC5C4(CCC(C5(C)COC6C(C(C(C(O6)CO)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)CO1	817.00	unknown	https://doi.org/10.1016/S0040-4020(01)90409-0
2-[[7-hydroxy-8-(hydroxymethyl)-8-(5-hydroxy-4-methylpent-3-enyl)-1,4a,10a,10b-tetramethyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73826574	Click to see	817.00	unknown	https://doi.org/10.1016/S0031-9422(00)90428-X
2-[2-[1-hydroxy-7-(hydroxymethyl)-4a,4b,7,10a-tetramethyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-2,5'-oxane]-2'-yl]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73092474	Click to see CC(COC1C(C(C(C(O1)CO)O)O)O)C2CCC3(CCC4(C(C3O)CCC5C4(CCC6C5(CCC(C6(C)CO)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)CO2	817.00	unknown	https://doi.org/10.1248/CPB.42.1422
2-[2-[8-[4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1-hydroxy-7-(hydroxymethyl)-4a,4b,7,10a-tetramethylspiro[3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-2,5'-oxane]-2'-yl]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162918077	Click to see	949.10	unknown	https://doi.org/10.1248/CPB.42.1422
2-[2-[8-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-1-hydroxy-4a,4b,7,10a-tetramethyl-7-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]spiro[3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-2,5'-oxane]-2'-yl]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	85131916	Click to see CC(COC1C(C(C(C(O1)CO)O)O)O)C2CCC3(CCC4(C(C3O)CCC5C4(CCC6C5(CCC(C6(C)COC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(CO9)O)O)O)C)C)C)CO2	1111.30	unknown	https://doi.org/10.1016/S0031-9422(00)90428-X
2-[2-[8-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1-hydroxy-7-(hydroxymethyl)-4a,4b,7,10a-tetramethylspiro[3,4,5,6,6a,8,9,10,10b,11,12,12a-dodecahydro-1H-chrysene-2,5'-oxane]-2'-yl]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73826577	Click to see	979.20	unknown	https://doi.org/10.1016/S0040-4020(01)90409-0
2-[4,5-dihydroxy-2-[7-hydroxy-1-(hydroxymethyl)-2'-(1-hydroxypropan-2-yl)-1,4a,10a,10b-tetramethylspiro[3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysene-8,5'-oxane]-2-yl]oxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	73826578	Click to see CC(CO)C1CCC2(CCC3(C(C2O)CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)CO1	817.00	unknown	https://doi.org/10.1248/CPB.42.1422 https://doi.org/10.1016/S0040-4020(01)90409-0
2-[4,5-dihydroxy-2-[7-hydroxy-1-(hydroxymethyl)-2'-(1-hydroxypropan-2-yl)-1,4a,10a,10b-tetramethylspiro[3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysene-8,5'-oxane]-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	163089875	Click to see CC(CO)C1CCC2(CCC3(C(C2O)CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)CO1	787.00	unknown	https://doi.org/10.1248/CPB.42.1422
CID 73826573	73826573	Click to see CC(=CCCC1(CCC2(C(C1O)CCC3C2(CCC4C3(CCC(C4(C)COC5C(C(C(C(O5)CO)O)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)CO)CO	979.20	unknown	https://doi.org/10.1016/S0040-4020(01)90409-0
Hosenkoside A	102004530	Click to see CC(CO)C1CCC2(CCC3(C(C2O)CCC4C3(CCC5C4(CCC(C5(C)COC6C(C(C(C(O6)CO)O)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)CO1	979.20	unknown	https://doi.org/10.1016/S0040-4020(01)90409-0 https://doi.org/10.1248/CPB.42.1422 https://doi.org/10.1039/C39830000871
Hosenkoside A [M+H]+	73826569	Click to see	979.20	unknown	https://doi.org/10.1016/S0040-4020(01)90409-0 https://doi.org/10.1248/CPB.42.1422
Hosenkoside B	124928622	Click to see	979.20	unknown	https://doi.org/10.1016/S0040-4020(01)90409-0
Hosenkoside C	102004879	Click to see CC(=CCCC1(CCC2(C(C1O)CCC3C2(CCC4C3(CCC(C4(C)COC5C(C(C(C(O5)CO)O)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)CO)CO	979.20	unknown	https://doi.org/10.1016/S0040-4020(01)90409-0
Hosenkoside D	163005572	Click to see	817.00	unknown	https://doi.org/10.1016/S0040-4020(01)90409-0
Hosenkoside E	162863191	Click to see	817.00	unknown	https://doi.org/10.1016/S0040-4020(01)90409-0
Hosenkoside F	125181875	Click to see	949.10	unknown	https://doi.org/10.1248/CPB.42.1422
Hosenkoside G	102004930	Click to see	949.10	unknown	https://doi.org/10.1248/CPB.42.1422
hosenkoside J	162863192	Click to see	817.00	unknown	https://doi.org/10.1248/CPB.42.1422
Hosenkoside K	102004887	Click to see CC(COC1C(C(C(C(O1)CO)O)O)O)C2CCC3(CCC4(C(C3O)CCC5C4(CCC6C5(CCC(C6(C)COC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO2	1141.30	unknown	https://doi.org/10.1248/CPB.42.1422
Hosenkoside K [M+H]+	85085043	Click to see	1141.30	unknown	https://doi.org/10.1248/CPB.42.1422
Hosenkoside L	10396107	Click to see CC(CO)C1CCC2(CCC3(C(C2O)CCC4C3(CCC5C4(CCC(C5(C)COC6C(C(C(C(O6)CO)O)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C)C)C)CO1	949.10	unknown	https://doi.org/10.1016/S0031-9422(00)90428-X
Hosenkoside M	10396409	Click to see CC(COC1C(C(C(C(O1)CO)O)O)O)C2CCC3(CCC4(C(C3O)CCC5C4(CCC6C5(CCC(C6(C)COC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(CO9)O)O)O)C)C)C)CO2	1111.30	unknown	https://doi.org/10.1016/S0031-9422(00)90428-X
Hosenkoside N	162938316	Click to see	817.00	unknown	https://doi.org/10.1016/S0031-9422(00)90428-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5S,6S)-2-[(2R,3R,4R,5R,6R)-4-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-2-(hydroxymethyl)-6-[(16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	11968825	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(O9)CO)O)O)O)C)C)C)OC1	855.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
(5S,9S,10S,13R,14R)-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	137706369	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/0031-9422(95)00418-7
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/10.1016/0031-9422(95)00418-7
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/10.1016/0031-9422(95)00418-7
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(2R)-N-[(1S,2R,3E,7E)-1-(Hydroxymethyl)-2-hydroxy-3,7-heptadecadienyl]-2-hydroxypalmitamide	15609680	Click to see CCCCCCCCCCCCCCC(C(=O)NC(CO)C(C=CCCC=CCCCCCCCCC)O)O	551.90	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-(3,4-dihydroxynaphthalen-1-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol	5322082	Click to see C1=CC=C2C(=C1)C(=CC(=C2O)O)OC3C(C(C(C(O3)CO)O)O)O	338.31	unknown	via CMAUP database
Balsaminone B	10815442	Click to see COC1=C(C2=CC=CC=C2C3=C1C4=C(O3)C(=O)C5=CC=CC=C5C4=O)OC6C(C(C(C(O6)CO)O)O)O	506.50	unknown	https://doi.org/10.1021/NP9704718
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
Deoxypeganine	442894	Click to see	172.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
3-Indoleacetonitrile	351795	Click to see C1=CC=C2C(=C1)C(=CN2)CC#N	156.18	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
2,7,14-Trimethyl-16-oxapentacyclo[9.7.0.02,8.05,7.013,17]octadec-10-ene-12,15-dione	74959363	Click to see CC1C2C(CC3C(=CCC4C3(CCC5C4(C5)C)C)C2=O)OC1=O	314.40	unknown	https://doi.org/10.1248/BPB.25.505 https://doi.org/10.1016/0031-9422(95)00418-7
Balsaminone A	9798203	Click to see	344.30	unknown	https://doi.org/10.1021/NP9704718
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-4-hydroxyphenyl]prop-2-enoic acid	101244829	Click to see CC(=CCCC(=CCC1=C(C=CC(=C1)C=CC(=O)O)O)C)C	300.40	unknown	via CMAUP database
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid	709	Click to see	194.18	unknown	https://doi.org/10.1248/BPB.25.505
4-Coumaric acid	322	Click to see	164.16	unknown	https://doi.org/10.1248/BPB.25.505
Drupanin	6440361	Click to see	232.27	unknown	via CMAUP database
Ferulic Acid	445858	Click to see	194.18	unknown	https://doi.org/10.1248/BPB.25.505
P-Coumaric Acid	637542	Click to see	164.16	unknown	https://doi.org/10.1248/BPB.25.505
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see	178.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-4-(7-hydroxy-6,8-dimethoxy-2-oxochromen-4-yl)-6,8-dimethoxychromen-2-one	11259276	Click to see COC1=C(C(=C2C(=C1)C(=CC(=O)O2)C3=CC(=O)OC4=C(C(=C(C=C34)OC)O)OC)OC)O	442.40	unknown	https://doi.org/10.1055/S-2006-957583
Isofraxidin	5318565	Click to see	222.19	unknown	https://doi.org/10.1016/0031-9422(95)00418-7
Scopoletin	5280460	Click to see	192.17	unknown	https://doi.org/10.1016/0031-9422(95)00418-7 https://doi.org/10.1248/BPB.25.505
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
6-(3-Hydroxy-3-methylbut-1-enyl)-5-methoxy-2,2-dimethylpyrano[2,3-h]chromen-8-one	72745417	Click to see	342.40	unknown	https://doi.org/10.1248/BPB.25.505
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	https://doi.org/10.1002/(SICI)1099-1573(199605)10:3<202::AID-PTR805>3.0.CO;2-0
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.1002/(SICI)1099-1573(199909)13:6<521::AID-PTR535>3.0.CO;2-A https://doi.org/10.1002/(SICI)1099-1573(199605)10:3<202::AID-PTR805>3.0.CO;2-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-7-hydroxy-4-oxo-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	163187902	Click to see	934.80	unknown	https://doi.org/10.1080/10286020.2010.532315
[6-[2-(3,4-Dihydroxyphenyl)-7-hydroxy-4-oxo-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	162978046	Click to see	934.80	unknown	https://doi.org/10.1080/10286020.2010.532315
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R,4S,5R)-2-[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxyoxane-3,4,5-triol	5316494	Click to see	435.40	unknown	via CMAUP database
(2S,3R,4S,5R)-2-[5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)chromenylium-3-yl]oxyoxane-3,4,5-triol	6325587	Click to see	463.40	unknown	via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one	51402807	Click to see	464.40	unknown	https://doi.org/10.1002/(SICI)1099-1573(199909)13:6<521::AID-PTR535>3.0.CO;2-A
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	163015326	Click to see	772.70	unknown	https://doi.org/10.1080/10286020.2010.532315
5,7-Dihydroxy-3-[5-hydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2-(4-hydroxyphenyl)chromen-4-one	74978014	Click to see	756.70	unknown	https://doi.org/10.1016/S0031-9422(00)90440-0
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	https://doi.org/10.1002/(SICI)1099-1573(199909)13:6<521::AID-PTR535>3.0.CO;2-A https://doi.org/10.1002/(SICI)1099-1573(199605)10:3<202::AID-PTR805>3.0.CO;2-0
Calendoflavobioside 5-O-glucoside	102363398	Click to see	772.70	unknown	https://doi.org/10.1080/10286020.2010.532315
Isoquercetin	5280804	Click to see	464.40	unknown	via CMAUP database
Kaempferol 3-rhamnosyldiglucoside	101756416	Click to see	756.70	unknown	https://doi.org/10.1016/S0031-9422(00)90440-0
Kaempferol-3-O-Rutinoside	5318767	Click to see	594.50	unknown	https://doi.org/10.1002/PTR.964 https://doi.org/10.1002/(SICI)1099-1573(199909)13:6<521::AID-PTR535>3.0.CO;2-A https://doi.org/10.1002/(SICI)1099-1573(199605)10:3<202::AID-PTR805>3.0.CO;2-0 https://doi.org/10.1248/BPB.25.505
Rutin	5280805	Click to see	610.50	unknown	https://doi.org/10.1002/(SICI)1099-1573(199909)13:6<521::AID-PTR535>3.0.CO;2-A https://doi.org/10.1002/(SICI)1099-1573(199605)10:3<202::AID-PTR805>3.0.CO;2-0
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 5-hydroxyflavonoids
Delfinidin	25203213	Click to see	301.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Pelargonidin	440832	Click to see	271.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Malvidin	159287	Click to see	331.30	unknown	via CMAUP database

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Impatiens balsamina

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