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.

Spatholobus suberectus, commonly known in Chinese as “Jin Qian Cao,” has a long history of use in East Asian traditional medicine. Among the Han Chinese, the dried root is boiled as a decoction to treat blood stasis, bruising, and rheumatic pain (Chinese Pharmacopoeia, 2020). In Korean traditional practice, the same root is macerated in alcohol to produce a tincture that is applied topically for joint inflammation and muscle soreness (Korean Pharmacopoeia, 2015). Vietnamese herbalists also prepare a mild infusion of the root to relieve fever and headaches, citing the “Vietnamese Traditional Medicine Journal” (2018). In each case, the root is the primary material, and the preparations are typically decoctions, infusions, or alcohol tinctures that are consumed orally or applied externally.

A simple, safe recipe for a mild root tea is as follows: take 5 g of dried Spatholobus suberectus root, add 200 ml of boiling water, and let steep for 30 minutes. Strain the liquid and drink one cup in the morning and one in the evening. If you are pregnant, nursing, or taking anticoagulants, consult a healthcare professional before use, as the plant’s bioactive compounds may influence blood clotting. The tea can be sweetened with honey or a small amount of sugar if desired.

The therapeutic effects of Spatholobus suberectus are largely attributed to its rich content of isoflavones and flavonoids. Formononetin, biochanin A, and daidzein are the most abundant isoflavones, while quercetin and kaempferol glycosides contribute antioxidant activity. These compounds have been shown in vitro to inhibit inflammatory mediators such as COX‑2 and to scavenge free radicals, providing a biochemical basis for the plant’s traditional use in pain and inflammation.

Modern research continues to validate these traditional claims. Recent pharmacological studies published in the *Journal of Ethnopharmacology* (2022) demonstrate significant anti‑inflammatory and anti‑oxidant effects of Spatholobus suberectus extracts in animal models. The root is also available as a standardized dietary supplement in China and is marketed in specialty health stores in the United States, where it is often sold as a “blood‑circulation tonic.” Thus, Spatholobus suberectus remains a relevant example of how ancient herbal wisdom can inform contemporary health practices.

General Uses Top

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Common products:
Wooden tool handles, whips, and walking sticks are made from the tough, flexible woody stems. Small goods, turnery, and craft items are also reported.

Industrial and craft applications:
Small specialty handles and craft turnery capitalize on the stem’s mechanical properties (dense fiber structure and toughness).

Properties relevant to use:
Stems exhibit high strength-to-weight ratio and durability suitable for small tools and implements.

Synonyms Top

Scientific name	Authority	First published in
Butea suberecta	(Dunn) Blatt.	J. Indian Bot. Soc.8: 138 (1929)
Spatholobus floribundus	Craib	Bull. Misc. Inform. Kew1927: 64 (1927)
Spatholobus laoticus	Gagnep.	Notul. Syst. (Paris)2: 369 (1913)
Butea laotica	(Gagnep.) Blatt.	J. Indian Bot. Soc.8: 136 (1929)

Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	鸡血藤
Chinese	密花豆
Chinese	小豆花
Chinese	紫梗藤
Chinese	马鹿花
Chinese	百骑大栗树
Chinese	一种维管植物

Subspecies (abbr. subsp./ssp.) Top

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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

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya
- Indo-China
  - Laos
  - Thailand
  - Vietnam

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000186508
UNII	J4FRL97E6E
Tropicos	13062433
KEW	urn:lsid:ipni.org:names:519185-1
The Plant List	ild-32974
Open Tree Of Life	122721
NCBI Taxonomy	455371
IPNI	519185-1
GBIF	2977075
EOL	643997
USDA GRIN	423553
CMAUP	NPO25653

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_004329165.1	ASM432916v1	Chromosome	Guangxi Botanical Garden of Medicinal Plants	2019-03-07	79.79	761.48 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

Potential Effects of Traditional Chinese Medicine in Anti-Aging and Aging-Related Diseases: Current Evidence and Perspectives

Ding X, Ma X, Meng P, Yue J, Li L, Xu L

Clin Interv Aging

01-May-2024

PMCID:	PMC11070163
doi:	10.2147/CIA.S447514
PMID:	38706635

Metochalcone induces senescence-associated secretory phenotype via JAK2/STAT3 pathway in breast cancer

ZHOU J, WAN F, XIAO B, LI X, PENG C, PENG F

Oncol Res

23-Apr-2024

PMCID:	PMC11055985
doi:	10.32604/or.2023.044775
PMID:	38686052

Progress of medicinal plants and their active metabolites in ischemia-reperfusion injury of stroke: a novel therapeutic strategy based on regulation of crosstalk between mitophagy and ferroptosis

Zhang G, Wang Q, Jiang B, Yao L, Wu W, Zhang X, Wan D, Gu Y

Front Pharmacol

08-Apr-2024

PMCID:	PMC11033413
doi:	10.3389/fphar.2024.1374445
PMID:	38650626

Comprehensive effect of Naoxintong capsule combined with Western medicine on coronary heart disease after percutaneous coronary intervention: a meta-analysis

Yu L, Huang P, Wang M, Li Z, Cai H, Feng Y, Wu L, Peng W, Zeng J, Chen B

Front Pharmacol

25-Mar-2024

PMCID:	PMC11000174
doi:	10.3389/fphar.2024.1274000
PMID:	38590642

Pestalotiopsis jiangsuensis sp. nov. Causing Needle Blight on Pinus massoniana in China

Li H, Peng BY, Xie JY, Bai YQ, Li DW, Zhu LH

J Fungi (Basel)

21-Mar-2024

PMCID:	PMC10970983
doi:	10.3390/jof10030230
PMID:	38535238

Shade responses and resistant mechanisms in Spatholobus suberectus

Qin S, Liang Y, Wei G, Wei F, Wei K, Chen X

Heliyon

12-Mar-2024

PMCID:	PMC10956071
doi:	10.1016/j.heliyon.2024.e28077
PMID:	38515727

Integration of Network Pharmacology and Experimental Validation to Explore Jixueteng - Yinyanghuo Herb Pair Alleviate Cisplatin-Induced Myelosuppression

Liu Y, Dai S, Xu Y, Xiang Y, Zhang Y, Xu Z, Sun L, Zhang GC, Shu Q

Integr Cancer Ther

11-Mar-2024

PMCID:	PMC10929034
doi:	10.1177/15347354241237969
PMID:	38462913

A multi-center cross-sectional study of Chinese Herbal Medicine-Drug adverse reactions using active surveillance in Singapore’s Traditional Chinese Medicine clinics

Ng CY, Zhao Y, Wang N, Chia KL, Teo CH, Peh W, Yeo P, Zhong LL

Chin Med

07-Mar-2024

PMCID:	PMC10918936
doi:	10.1186/s13020-024-00915-z
PMID:	38454483

Mechanism of traditional Chinese medicine in elderly diabetes mellitus and a systematic review of its clinical application

Zhang Q, Hu S, Jin Z, Wang S, Zhang B, Zhao L

Front Pharmacol

06-Mar-2024

PMCID:	PMC10953506
doi:	10.3389/fphar.2024.1339148
PMID:	38510656

Traditional Chinese medicine Qingre Huoxue decoction enhances wound healing in through modulation of angiogenic and inflammatory pathways

Li W, Chen Y, Cai Z, He X, Yang L, Zhu J, Wang W

Int Wound J

04-Mar-2024

PMCID:	PMC10912365
doi:	10.1111/iwj.14724
PMID:	38439195

Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China

Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X

J Ethnobiol Ethnomed

23-Feb-2024

PMCID:	PMC10893717
doi:	10.1186/s13002-024-00656-1
PMID:	38395900

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

Ethnobotanical study on ritual plants used by Hani people in Yunnan, China

Ma X, Luo D, Xiong Y, Huang C, Li G

J Ethnobiol Ethnomed

13-Feb-2024

PMCID:	PMC10865556
doi:	10.1186/s13002-024-00659-y
PMID:	38350958

Correction: Zhang et al. Genotype–Environment Interaction and Horizontal and Vertical Distributions of Heartwood for Acacia melanoxylon R.Br. Genes 2023, 14, 1299

Zhang R, Zeng B, Chen T, Hu B

Genes (Basel)

09-Feb-2024

PMCID:	PMC10887675
doi:	10.3390/genes15020221
PMID:	38397249

Non‐immunosuppressive treatment for IgA nephropathy

Tunnicliffe DJ, Reid S, Craig JC, Samuels JA, Molony DA, Strippoli GF

Cochrane Database Syst Rev

01-Feb-2024

PMCID:	PMC10832348
doi:	10.1002/14651858.CD003962.pub3
PMID:	38299639

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 / Harmala alkaloids
(1S,2R,4R,5Z,12R,13S,16Z)-25-[(1R)-8-hydroxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl]-11,22-diazapentacyclo[11.11.2.12,22.02,12.04,11]heptacosa-5,16,25-trien-13-ol	10793134	Click to see	568.80	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Sparteine	7014	Click to see	234.38	unknown	via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
1,8-Dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]anthracene-9,10-dione	14211228	Click to see	416.40	unknown	https://doi.org/10.1002/HLCA.200690121
1,8-dihydroxy-3-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]anthracene-9,10-dione	14211230	Click to see	416.40	unknown	https://doi.org/10.1002/HLCA.200690121
Aloe emodin	10207	Click to see	270.24	unknown	https://doi.org/10.1002/HLCA.200690121
Physcion	10639	Click to see	284.26	unknown	via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin	3220	Click to see	270.24	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives
Npc112006	21965192	Click to see	124.18	unknown	via CMAUP database
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	via CMAUP database
> 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	via CMAUP database
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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see	170.12	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 / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethyl 3,4-Dihydroxybenzoate	77547	Click to see CCOC(=O)C1=CC(=C(C=C1)O)O	182.17	unknown	https://doi.org/10.1016/S1875-5364(12)60007-7
> Benzenoids / Phenol ethers / Anisoles
Anethole	637563	Click to see	148.20	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenetriols and derivatives / Phloroglucinols and derivatives
Phloroglucinol	359	Click to see C1=C(C=C(C=C1O)O)O	126.11	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2,6-Dimethoxyphenol	7041	Click to see	154.16	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aR,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol	332425	Click to see	388.40	unknown	via CMAUP database
4-[3-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol	4546425	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC	388.40	unknown	https://doi.org/10.1016/S1875-5364(12)60007-7
Medioresinol, (+)-	181681	Click to see	388.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Prestegane B	146425	Click to see	358.40	unknown	https://doi.org/10.1016/S1875-5364(12)60007-7
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl Dodecanoate	7800	Click to see	228.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
2-Dodecyl-3-Methylbutanedioic Acid	99891	Click to see CCCCCCCCCCCCC(C(C)C(=O)O)C(=O)O	300.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hexacosanoic Acid	10469	Click to see	396.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(R)-oct-1-en-3-ol	6992244	Click to see	128.21	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-Pinene, (+)-	82227	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol	94221	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	via CMAUP database
(+)-Limonene	440917	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Eucarvone	136330	Click to see CC1=CC=CC(CC1=O)(C)C	150.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Farnesene	5281517	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	via CMAUP database
Bisabolol	1549992	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	via CMAUP database
Caryophyllene oxide	1742210	Click to see	220.35	unknown	via CMAUP database
gamma-Cadinene	6432404	Click to see	204.35	unknown	via CMAUP database
Vomifoliol, (+)-	5280462	Click to see	224.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Ilexolide A	441931	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(O6)CO)O)O)C)C)C2=C1C)C)C(=O)O	586.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulinic Acid	64971	Click to see	456.70	unknown	via CMAUP database
Epifriedelanol	119242	Click to see	428.70	unknown	via CMAUP database
Friedelin	91472	Click to see	426.70	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
(3s,8s,9s,10r,13r,14s,17r)-10,13-Dimethyl-17-[(2r,5s)-5-propan-2-yloctan-2-yl]2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-ol	15976101	Click to see	428.70	unknown	via CMAUP database
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	via CMAUP database
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	via CMAUP database
7alpha-Hydroxysitosterol	161816	Click to see	430.70	unknown	via CMAUP database
Npc29	6432744	Click to see	414.70	unknown	via CMAUP database
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
Stigmasterol	5280794	Click to see	412.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
Levodopa	6047	Click to see C1=CC(=C(C=C1CC(C(=O)O)N)O)O	197.19	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 21952380	21952380	Click to see	118.09	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(3-hydroxy-5-methoxyphenoxy)oxane-3,4,5-triol	101405537	Click to see COC1=CC(=CC(=C1)O)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O	434.40	unknown	https://doi.org/10.1002/HLCA.200690121
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(3-hydroxy-5-methoxyphenoxy)oxane-3,4,5-triol	162966498	Click to see	434.40	unknown	https://doi.org/10.1002/HLCA.200690121
5-[(2S,3R,4S,5R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2-hydroxybenzoic acid	101405538	Click to see C1C(C(C(C(O1)OC2=CC(=C(C=C2)O)C(=O)O)OC3C(C(CO3)(CO)O)O)O)O	418.30	unknown	https://doi.org/10.1002/HLCA.200690121
5-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2-hydroxybenzoic acid	162880080	Click to see	418.30	unknown	https://doi.org/10.1002/HLCA.200690121
> Organoheterocyclic compounds / Furans / Furoic acid and derivatives / Furoic acids
2-Furancarboxylic acid	6919	Click to see	112.08	unknown	via CMAUP database
> Organoheterocyclic compounds / Piperidines
4-Methylpiperidine	69381	Click to see	99.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-cis-Feruloyl tyramine	6440659	Click to see	313.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(-)-Praeruptorin B	25717254	Click to see	426.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	101228664	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C(C(=CC(=C56)O)O)C7C(C(OC8=CC(=CC(=C78)O)O)C9=CC(=C(C=C9)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O	1155.00	unknown	via CMAUP database
Proanthocyanidin B2	5320711	Click to see	578.50	unknown	via CMAUP database
Procyanidin B2, (+)-	122738	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	via CMAUP database
Procyanidin C1	169853	Click to see	866.80	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol	73160	Click to see	290.27	unknown	via CMAUP database
(+)-Epicatechin	182232	Click to see	290.27	unknown	via CMAUP database
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol	1203	Click to see	290.27	unknown	via CMAUP database
Catechin	9064	Click to see	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Gallocatechin	9882981	Click to see	306.27	unknown	via CMAUP database
(+)-Epigallocatechin	10425234	Click to see	306.27	unknown	via CMAUP database
Epigallocatechin	72277	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	via CMAUP database
Gallocatechin	65084	Click to see	306.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Eriodictyol	11095	Click to see	288.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
(+-)-Naringenin	932	Click to see	272.25	unknown	via CMAUP database
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one	667495	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	via CMAUP database
(2S)-2-(3,4-Dihydroxyphenyl)-6,7-dihydroxy-2,3-dihydrochromen-4-one	102196479	Click to see C1C(OC2=CC(=C(C=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
2-(3,4-dihydroxyphenyl)-6,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-one	12314367	Click to see	288.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
3',4',7-Trihydroxyflavaonone	3496769	Click to see	272.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
4',7-Dihydroxyflavanone	1889	Click to see	256.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
Butin	92775	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O	272.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
Eriodictyol	440735	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
Liquiritigenin	114829	Click to see	256.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
Naringenin	439246	Click to see	272.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin	471	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
(2R,3R)-3,7-Dihydroxyflavanone	14730799	Click to see	256.25	unknown	via CMAUP database
(2R,3S)-2-(3,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-2,3-Dihydrochromen-4-One	712318	Click to see	304.25	unknown	via CMAUP database
(2R)-2-(3,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-2,3-Dihydrochromen-4-One	10185	Click to see	304.25	unknown	via CMAUP database
(2S,3R)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one	11449086	Click to see	288.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
(3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydro-4H-chromen-4-one	12309272	Click to see	304.25	unknown	via CMAUP database
3,5,7-Trihydroxy-2-(4-Hydroxyphenyl)Chroman-4-One	662	Click to see	288.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
Aromadendrin	122850	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
Taxifolin	439533	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
Taxifolin, (-)-	712316	Click to see	304.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7,3',4'-Trihydroxyflavone	5322065	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O)O	270.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
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 / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin	114776	Click to see	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Apigenin 6,8-di-c-alpha-l-arabinopyranoside	21576179	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(CO5)O)O)O)O)O)O)O	534.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(E)-3-(4-hydroxyphenyl)-1-[2-hydroxy-4-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one	161786848	Click to see	418.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
3-(4-Hydroxyphenyl)-1-[2-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one	73981690	Click to see	418.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
Neoisoliquiritine	5320092	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O	418.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Hesperetin	72281	Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O	302.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
(S)-2-(3,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-6-methoxy-4H-1-benzopyran-4-one	90477819	Click to see	318.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
6-Methoxyeriodictyol	14034285	Click to see COC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)O)O	318.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
7,3',4'-Trihydroxy-6-methoxy flavanone	5321538	Click to see COC1=C(C=C2C(=C1)C(=O)CC(O2)C3=CC(=C(C=C3)O)O)O	302.28	unknown	https://doi.org/10.1016/J.CHROMA.2011.06.091
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Medicagol	5319322	Click to see C1OC2=C(O1)C=C3C(=C2)C4=C(O3)C5=C(C=C(C=C5)O)OC4=O	296.23	unknown	https://doi.org/10.1016/J.CHROMA.2011.06.091
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein	5281708	Click to see	254.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
Genistein	5280961	Click to see	270.24	unknown	https://doi.org/10.3184/174751918X15386515371813
Pseudobaptigenin	5281805	Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O	282.25	unknown	https://doi.org/10.3184/174751918X15386515371813
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavanquinones
5-[(3R)-7-hydroxy-3,4-dihydro-2H-chromen-3-yl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione	10403457	Click to see COC1=C(C(=O)C(=CC1=O)C2CC3=C(C=C(C=C3)O)OC2)OC	316.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
Puerarin	5281807	Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O	416.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
7-[(2S,4S,6R)-3-[(2S,3R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(4-methoxyphenyl)chromen-4-one	6325281	Click to see	562.50	unknown	https://doi.org/10.1016/S1875-5364(12)60007-7
Formononetin 7-O-apiosyl-(1->2)-glucoside	44257223	Click to see	562.50	unknown	via CMAUP database
Genistin	5281377	Click to see	432.40	unknown	via CMAUP database
Ononin	442813	Click to see	430.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(+)-Vestitol	177149	Click to see	272.29	unknown	via CMAUP database
3-(2,4-Dimethoxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-ol	596401	Click to see	286.32	unknown	https://doi.org/10.3184/174751918X15386515371813
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin	5280448	Click to see	284.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008 https://doi.org/10.1016/J.CHROMA.2011.06.091
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
3-(3,4-dimethoxyphenyl)-7-hydroxy-4H-chromen-4-one	5748605	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)OC	298.29	unknown	via CMAUP database
8-O-Methylretusin	5319771	Click to see	298.29	unknown	via CMAUP database
Afromosin	5281704	Click to see	298.29	unknown	https://doi.org/10.1016/J.CHROMA.2011.06.091
Biochanin A	5280373	Click to see	284.26	unknown	via CMAUP database
biochanin A(1-)	25203224	Click to see	283.25	unknown	via CMAUP database
Formononetin	5280378	Click to see	268.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.008
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids
CID 14058036	14058036	Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)OC)OC2)O	286.32	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Cajanin	5281706	Click to see	300.26	unknown	via CMAUP database
Prunetin	5281804	Click to see	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(Z)-1-(2,4-dihydroxyphenyl)-3-(3,4-dihydroxyphenyl)prop-2-en-1-one	5315562	Click to see	272.25	unknown	via CMAUP database
(Z)-1-(6-hydroxy-2,3,4-trimethoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one	86820664	Click to see	344.40	unknown	via CMAUP database
Butein	5281222	Click to see	272.25	unknown	https://doi.org/10.1016/J.CHROMA.2011.06.091
Isoliquiritigenin	638278	Click to see	256.25	unknown	via CMAUP database
Lopac-I-3766	6603886	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O	256.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retrochalcones
Licochalcone a	5318998	Click to see CC(C)(C=C)C1=C(C=C(C(=C1)C=CC(=O)C2=CC=C(C=C2)O)OC)O	338.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(9S,10R)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-9-ol	10024925	Click to see	416.50	unknown	via CMAUP database
5,6,7,8-Tetrahydro-1,2,3,10,11,12-hexamethoxydibenzo[a,c]cyclooctene	19020980	Click to see	388.50	unknown	via CMAUP database

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Spatholobus suberectus

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