Hydrangea serrata is a deciduous shrub with oval leaves and panicles of blue and pink flowers that is native to mountainous regions of Korea and Japan. It is commonly known as mountain hydrangea or tea of heaven and is widely cultivated as an ornamental shrub in suitable climates. It is similar to H. macrophylla but is smaller and more hardy. It grows best in partial shade and well-drained soil, and its flower color can be affected by soil pH. It is hardy to USDA Zone 6 and can be grown in Zone 5 with protection. Propagation can be done through seeds, cuttings, or layering. It may be susceptible to certain diseases and pests. There are numerous cultivars of H. serrata, many of which have received the Royal Horticultural Society's Award of Garden Merit. The leaves of this plant are also used to make herbal teas in Korea and Japan.

Synonyms Top

Scientific name	Authority	First published in
Platycrater serrata	Makino	Bot. Mag. (Tokyo) 26: 387 (1912)
Hydrangea buergeri	Siebold & Zucc.	Fl. Jap. 1: 111 (1839)
Hydrangea japonica	Siebold	Nova Acta Phys.-Med. Acad. Caes. Leop.-Carol. Nat. Cur. 14(2): 689 (1828)
Hydrangea pubescens	Court.	Syll. Pl. Nov. 2: 45 (1828)
Hydrangea sitsitan	Siebold	Nova Acta Phys.-Med. Acad. Caes. Leop.-Carol. Nat. Cur. 14(2): 692 (1828)
Hydrangea acuminata	Siebold & Zucc.	Fl. Jap. 1: 110 (1839)
Hydrangea serrata f. belladonna	Kitam.	Acta Phytotax. Geobot. 14: 86 (1951)
Hortensia serrata f. belladonna	(Kitam.) H.Ohba & S.Akiyama	J. Jap. Bot. 91: 346 (2016)
Hortensia serrata f. plenidecuris	H.Ohba & S.Akiyama	J. Jap. Bot. 91: 346 (2016)
Hortensia serrata f. prolifera	(Regel) H.Ohba & S.Akiyama	J. Jap. Bot. 91: 347 (2016)
Hortensia serrata	(Thunb.) H.Ohba & S.Akiyama	J. Jap. Bot. 91: 346 (2016)
Hydrangea serrata var. japonica	(Siebold) H.Ohba & S.Akiyama	Bull. Natl. Mus. Nat. Sci., Tokyo, B. 39: 179 (2013)
Hortensia serrata var. acuminata	(Siebold & Zucc.) H.Ohba & S.Akiyama	J. Jap. Bot. 91: 347 (2016)

Common names Top

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Filter by language:

Language	Common/alternative name
English	hydrangea macrophylla subsp. serrata
Hungarian	fűrészeslevelű hortenzia
Japanese	ヤマアジサイ
Korean	산수국
Latvian	robainā hortenzija
Polish	hortensja piłkowana
Chinese	澤八仙花

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Hydrangea serrata var. angustata	(Franch. & Savat.) H.Ohba	J. Jap. Bot. 64: 325 (1989)
Hydrangea serrata var. minamitanii	H.Ohba	J. Jap. Bot. 64: 199 (1989)
Hydrangea serrata var. yesoensis	(Koidz.) H.Ohba	Fl. Japan 2b: 90 (2001)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Eastern Asia
  - Japan
  - Korea

Asia-tropical click to expand
- Indian Subcontinent
  - Assam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001257038
UNII	218VPU9N9U
Tropicos	50182992
INPN	103113
KEW	urn:lsid:ipni.org:names:791682-1
Missouri Botanical Garden	292385
Open Tree Of Life	584050
NCBI Taxonomy	859264
IPNI	791682-1
iNaturalist	452290
GBIF	7319016
Freebase	/m/06w4c4j
EPPO	HYEMS
USDA GRIN	19469
Wikipedia	Hydrangea_serrata
CMAUP	NPO12284

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

Two haplotype-resolved genomes reveal important flower traits in bigleaf hydrangea (Hydrangea macrophylla) and insights into Asterid evolution

Wu X, Simpson SA, Youngblood RC, Liu XF, Scheffler BE, Rinehart TA, Alexander LW, Hulse-Kemp AM

Hortic Res

09-Nov-2023

PMCID:	PMC10734616
doi:	10.1093/hr/uhad217
PMID:	38130599

Plant Extracts as Skin Care and Therapeutic Agents

Michalak M

Int J Mol Sci

22-Oct-2023

PMCID:	PMC10607442
doi:	10.3390/ijms242015444
PMID:	37895122

Extensive characterization of 28 complete chloroplast genomes of Hydrangea species: A perspective view of their organization and phylogenetic and evolutionary relationships

Raman G, Choi KS, Lee EM, Morden CW, Shim H, Kang JS, Yang TJ, Park S

Comput Struct Biotechnol J

10-Oct-2023

PMCID:	PMC10589384
doi:	10.1016/j.csbj.2023.10.010
PMID:	37867966

Analysis of the RNA Editing Sites and Orthologous Gene Function of Transcriptome and Chloroplast Genomes in the Evolution of Five Deutzia Species

Cai H, Ren Y, Du J, Liu L, Long L, Yang M

Int J Mol Sci

19-Aug-2023

PMCID:	PMC10454583
doi:	10.3390/ijms241612954
PMID:	37629135

Re-Examination of Several Elsinoë Species Reported from Japan

Ujat AH, Ono T, Hattori Y, Nakashima C

Mycobiology

15-Jun-2023

PMCID:	PMC10288934
doi:	10.1080/12298093.2023.2219049
PMID:	37359956

Protective effect of Schizonepeta tenuifolia Briq. ethanolic extract against UVB-induced skin aging and photodamage in hairless mice

Gu MJ, Lee HW, Yoo G, Kim D, Choi IW, Kim Y, Ha SK

Front Pharmacol

07-Jun-2023

PMCID:	PMC10283040
doi:	10.3389/fphar.2023.1176073
PMID:	37351505

Hydrangea serrata Hot Water Extract and Its Major Ingredient Hydrangenol Improve Skin Moisturization and Wrinkle Conditions via AP-1 and Akt/PI3K Pathway Upregulation

Yoon JH, Park SH, Yoon SE, Hong SY, Lee JB, Lee J, Cho JY

Nutrients

24-May-2023

PMCID:	PMC10255818
doi:	10.3390/nu15112436
PMID:	37299400

Protective effects of red orange (Citrus sinensis [L.] Osbeck [Rutaceae]) extract against UVA-B radiation-induced photoaging in Skh:HR-2 mice

Kim YH, Lim CY, Jung JI, Kim TY, Kim EJ

Nutr Res Pract

03-Mar-2023

PMCID:	PMC10375325
doi:	10.4162/nrp.2023.17.4.641
PMID:	37529272

Mechanism of action and therapeutic effects of oxidative stress and stem cell-based materials in skin aging: Current evidence and future perspectives

Qian H, Shan Y, Gong R, Lin D, Zhang M, Wang C, Wang L

Front Bioeng Biotechnol

09-Jan-2023

PMCID:	PMC9868183
doi:	10.3389/fbioe.2022.1082403
PMID:	36698629

Efficacy of a Horticultural Therapy Program Designed for Emotional Stability and Career Exploration among Adolescents in Juvenile Detention Centers

Park KH, Kim SY, Park SA

Int J Environ Res Public Health

20-Jul-2022

PMCID:	PMC9319874
doi:	10.3390/ijerph19148812
PMID:	35886667

Effect of Standardized Hydrangea serrata (Thunb.) Ser. Leaves Extract on Body Weight and Body Fat Reduction in Overweight or Obese Humans: A Randomized Double-Blind Placebo-Controlled Study

Han HS, Chung KS, Shin YK, Yu JS, Kang SH, Lee SH, Lee KT

Nutrients

03-Jan-2022

PMCID:	PMC8747274
doi:	10.3390/nu14010208
PMID:	35011083

Molecular targets of exercise mimetics and their natural activators

Jang YJ, Byun S

BMB Rep

31-Dec-2021

PMCID:	PMC8728540
doi:	10.5483/BMBRep.2021.54.12.151
PMID:	34814977

Eisenia bicyclis Extract Repairs UVB-Induced Skin Photoaging In Vitro and In Vivo: Photoprotective Effects

Choi SI, Han HS, Kim JM, Park G, Jang YP, Shin YK, Ahn HS, Lee SH, Lee KT

Mar Drugs

03-Dec-2021

PMCID:	PMC8709268
doi:	10.3390/md19120693
PMID:	34940692

Skin Aging, Cellular Senescence and Natural Polyphenols

Csekes E, Račková L

Int J Mol Sci

23-Nov-2021

PMCID:	PMC8657738
doi:	10.3390/ijms222312641
PMID:	34884444

Standardized Hydrangea serrata (Thunb.) Ser. Extract Ameliorates Obesity in db/db Mice

Han HS, Chung KS, Shin YK, Lee SH, Lee KT

Nutrients

16-Oct-2021

PMCID:	PMC8538090
doi:	10.3390/nu13103624
PMID:	34684625

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Thunberginol C	10333412	Click to see C1C(OC(=O)C2=C1C=C(C=C2O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1248/CPB.40.3121
Thunberginol D	188928	Click to see C1C(OC(=O)C2=C1C=C(C=C2O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1248/CPB.40.3121
Thunberginol E	10040569	Click to see COC1=C(C=C(C=C1)C2CC3=C(C(=CC(=C3)O)O)C(=O)O2)O	302.28	unknown	https://doi.org/10.1248/CPB.40.3121
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(3S)-3-(3,4-dimethoxyphenyl)-8-hydroxy-3,4-dihydroisochromen-1-one	162846576	Click to see COC1=C(C=C(C=C1)C2CC3=C(C(=CC=C3)O)C(=O)O2)OC	300.30	unknown	https://doi.org/10.1271/BBB1961.43.653
> Benzenoids / Benzene and substituted derivatives / Styrenes
5-[2-(4-Hydroxyphenyl)ethenyl]cyclohexa-1,3-diene-1,3-diol	122177172	Click to see C1C(C=C(C=C1O)O)C=CC2=CC=C(C=C2)O	230.26	unknown	https://doi.org/10.1248/CPB.40.3121
> Benzenoids / Phenols / Methoxyphenols
Phyllodulcin	146694	Click to see COC1=C(C=C(C=C1)C2CC3=C(C(=CC=C3)O)C(=O)O2)O	286.28	unknown	https://doi.org/10.1248/CPB.40.3121 https://doi.org/10.1016/J.BMCL.2007.06.027
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Tritriacontane	12411	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	464.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid	10467	Click to see CCCCCCCCCCCCCCCCCCCC(=O)O	312.50	unknown	via CMAUP database
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Dehydrosoyasaponin I	656760	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8=O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O	941.10	unknown	via CMAUP database
Soyasaponin I	122097	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O	943.10	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4R,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol	21119301	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C	458.70	unknown	via CMAUP database
Isoarborinol	12305182	Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C	426.70	unknown	https://doi.org/10.1248/CPB.40.3121
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Rubiarbonol B	12019474	Click to see CC(C)C1CC(C2C1(CCC3(C2(CC=C4C3C(CC5C4(CCC(C5(C)C)O)C)O)C)C)C)O	458.70	unknown	https://doi.org/10.1248/CPB.40.3121
Sophoradiol	9846221	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)C)O)C)C	442.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(23Z)-Cycloart-23-ene-3beta,25-diol	101690746	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	442.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[4-acetyloxy-6-(acetyloxymethyl)-2-[[(4R,4aR)-4-ethenyl-4a-hydroxy-8-oxo-3,4,5,6-tetrahydropyrano[3,4-c]pyran-3-yl]oxy]-5-[2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoyl]oxyoxan-3-yl] 2,3-dihydroxybenzoate	6325567	Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C3(CCOC(=O)C3=CO2)O)C=C)OC(=O)C4=C(C(=CC=C4)O)O)OC(=O)C)OC(=O)C5=C(C(=CC=C5)OC6C(C(C(C(O6)CO)O)O)O)O	892.80	unknown	https://doi.org/10.1016/S0031-9422(00)82497-8
[4-acetyloxy-6-(acetyloxymethyl)-2-[[(4R,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-5-[2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoyl]oxyoxan-3-yl] 2,3-dihydroxybenzoate	11968715	Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C3CCOC(=O)C3=CO2)C=C)OC(=O)C4=C(C(=CC=C4)O)O)OC(=O)C)OC(=O)C5=C(C(=CC=C5)OC6C(C(C(C(O6)CO)O)O)O)O	876.80	unknown	https://doi.org/10.1016/S0031-9422(00)82497-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
hydrangenol 8-O-glucoside	13962962	Click to see C1C(OC(=O)C2=C1C=CC=C2OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O	418.40	unknown	https://doi.org/10.1016/J.BMCL.2007.06.027
Phyllodulcin 8-glucoside	44440845	Click to see COC1=C(C=C(C=C1)C2CC3=C(C(=CC=C3)OC4C(C(C(C(O4)CO)O)O)O)C(=O)O2)O	448.40	unknown	https://doi.org/10.1016/J.BMCL.2007.06.027
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
[(3R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 7-methoxy-2,2-dimethylchromene-6-carboxylate	5319171	Click to see CC1(C=CC2=CC(=C(C=C2O1)OC)C(=O)OC3C(C(C(C(O3)CO)O)O)O)C	396.40	unknown	https://doi.org/10.1016/S0031-9422(00)82497-8
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3S)-8-hydroxy-3-(4-methoxyphenyl)-3,4-dihydroisochromen-1-one	101165437	Click to see COC1=CC=C(C=C1)C2CC3=C(C(=CC=C3)O)C(=O)O2	270.28	unknown	https://doi.org/10.1271/BBB1961.43.653
Hydrangenol	119199	Click to see C1C(OC(=O)C2=C1C=CC=C2O)C3=CC=C(C=C3)O	256.25	unknown	https://doi.org/10.1248/CPB.40.3121
> Organoheterocyclic compounds / Isocoumarans / Isobenzofuranones
Thunberginol F	6439493	Click to see C1=CC2=C(C(=C1)O)C(=O)OC2=CC3=CC(=C(C=C3)O)O	270.24	unknown	https://doi.org/10.1248/CPB.40.3121 https://doi.org/10.1016/J.BMCL.2007.06.027
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	https://doi.org/10.1248/CPB.40.3121
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2S,3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one	98049813	Click to see C1=CC(=C(C=C1O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	304.25	unknown	via CMAUP database
Aromadendrin	122850	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin	114776	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
Isoscoparin	442611	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O	462.40	unknown	via CMAUP database
Isovitexin	162350	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Isoschaftoside	3084995	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	564.50	unknown	via CMAUP database
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	via CMAUP database
Schaftoside	442658	Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O	564.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	via CMAUP database
Isoquercetin	5280804	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
Thunberginol A	5321948	Click to see C1=CC2=C(C(=C1)O)C(=O)OC(=C2)C3=CC(=C(C=C3)O)O	270.24	unknown	https://doi.org/10.1248/CPB.40.3121 https://doi.org/10.1016/J.PHYMED.2007.09.010
Thunberginol B	5473310	Click to see C1=CC(=C(C=C1C2=CC3=CC(=CC(=C3C(=O)O2)O)O)O)O	286.24	unknown	https://doi.org/10.1248/CPB.40.3121 https://doi.org/10.1016/J.PHYMED.2007.09.010
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
3,9-Dihydroxypterocarpan	162933	Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4)O	256.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
1,3,8-Trihydroxy-9-methoxy-11H-benzofuro[2,3-b][1]benzopyran-11-one	15126297	Click to see COC1=C(C=C2C(=C1)C3=C(O2)OC4=CC(=CC(=C4C3=O)O)O)O	314.25	unknown	via CMAUP database
2'-Hydroxygenistein	5282074	Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O	286.24	unknown	via CMAUP database
Genistein	5280961	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O	270.24	unknown	via CMAUP database
Lupinalbin A	5324349	Click to see C1=CC2=C(C=C1O)OC3=C2C(=O)C4=C(C=C(C=C4O3)O)O	284.22	unknown	via CMAUP database
Orobol	5281801	Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Ambocin	5491738	Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC=C(C4=O)C5=CC=C(C=C5)O)O)O)O)O)O)(CO)O	564.50	unknown	via CMAUP database
Ambonin	20055730	Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C(=CO4)C5=CC=C(C=C5)O)O)O)O)O)(CO)O	548.50	unknown	via CMAUP database
Genistin	5281377	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-Methoxydaidzein	5319422	Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3S)-3-(2,4-dimethoxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one	92143157	Click to see COC1=CC(=C(C=C1)C2COC3=CC(=CC(=C3C2=O)O)O)OC	316.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
5,7-Dihydroxy-3',4',5'-trimethoxyisoflavone	21676203	Click to see COC1=CC(=CC(=C1OC)OC)C2=COC3=CC(=CC(=C3C2=O)O)O	344.30	unknown	via CMAUP database
Formononetin	5280378	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Dihydroresveratrol	185914	Click to see C1=CC(=CC=C1CCC2=CC(=CC(=C2)O)O)O	230.26	unknown	https://doi.org/10.1248/CPB.40.3121
Hydrangeic acid	5318116	Click to see C1=CC(=C(C(=C1)O)C(=O)O)C=CC2=CC=C(C=C2)O	256.25	unknown	https://doi.org/10.1248/CPB.40.3121 https://doi.org/10.1016/J.BMCL.2007.06.027
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
2-[(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoic acid	162989278	Click to see C1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)O)CC(C3=CC=C(C=C3)O)O	436.40	unknown	https://doi.org/10.1248/CPB.20.1755
2-hydroxy-6-[(2R)-2-(4-hydroxyphenyl)-2-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]benzoic acid	162923880	Click to see C1=CC(=C(C(=C1)O)C(=O)O)CC(C2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O	436.40	unknown	https://doi.org/10.1248/CPB.20.1755

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Hydrangea serrata

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