Common products:
- Wood for small posts, tool handles, and construction components; bast fiber for cordage, string, and plaited craft items.

Industrial and craft applications:
- Fiber is separated by retting; used as tying cord in agriculture and for general ropework. Wood is fashioned into simple implements and structural elements where moderate mechanical performance and resistance to decay are sufficient.

Food and beverages (non-medicinal):
- No established food or beverage use; seeds contain non-protein amino acids and should not be consumed.

Colorants and tanning:
- Bark is rich in hydrolyzable tannins; historically used in leather tanning to produce light-colored leather. Tannin content and leather quality vary with bark age and local practice.

Wood and fiber:
- Wood: light to medium-hard; reddish-brown sapwood and darker heartwood; fiber is strong and flexible with good knot-holding when twisted into cordage. Sapwood is susceptible to insect attack; heartwood has moderate natural durability.

Fragrance and cosmetics:
- No documented uses.

Properties relevant to use:
- Fiber: strength and flexibility enable knotting and sustained tension; compatibility with natural and synthetic twist constructions. Wood: mechanical properties suitable for light-duty applications; natural decay resistance derived from extractives. Bark tannins: hydrolyzable class supporting leather tanning.

Standards and regulation:
- Timber and fiber marketed locally; quality depends on local grading practices and moisture standards. No specific international standards identified for this species.

Sustainability and sourcing:
- Harvested from wild populations and secondary growth; fiber and bark are renewable but limited by slow bark regeneration and minimal timber size. Sustainable practice includes selective harvesting and Allowing regrowth to maintain supply.

Synonyms Top

Scientific name	Authority	First published in
Millettia cinerea	Benth.	F.A.W.Miquel, Pl. Jungh.: 249 (1852)
Millettia dowardi	Collett & Hemsl.
Millettia gentiliana	H.Lév.
Millettia dielsiana var. heterocarpa	(Chun ex T.C.Chen) Z.Wei	Acta Phytotax. Sin.23: 289 (1985)
Millettia bockii	Harms ex Diels	Bot. Jahrb. Syst.29: 412 (1900)
Millettia cinerea var. yunnansis	Pamp.
Pongamia heterocarpa	Baker	Hort. Suburb. Calcutt. 240, nomen. 1845; Baker, in Hook.f., Fl. Brit. Ind. 2: 106.
Millettia bracteosa	Gagnep.	Notul. Syst. (Paris)2: 352 (1913)
Callerya dielsiana var. heterocarpa	(Chun ex T.C.Chen) X.Y.Zhu ex Z.Wei & Pedley	Fl. China10: 187 (2010)
Callerya dielsiana var. solida	(T.C.Chen ex Z.Wei) X.Y.Zhu ex Z.Wei & Pedley	Fl. China10: 187 (2010)
Phaseoloides cinerea	(Benth.) Kuntze	Revis. Gen. Pl.1: 201 (1891)
Millettia heterocarpa	Chun ex T.C.Chen	Acta Phytotax. Sin.3: 364 (1955)
Millettia dielsiana var. solida	T.C.Chen ex Z.Wei	Acta Phytotax. Sin.23: 289 (1985)
Pongamia heterocarpa	Wall. ex Baker	J.D.Hooker, Fl. Brit. India2: 106 (1876)
Pongamia cinerea	Graham	Numer. List : n.° 5888 (1831)
Pongamia palustris	Graham	Numer. List : n.° 5889 (1831)
Pongamia paniculata	Graham	Numer. List : n.° 5904 (1831)
Pongamia oblonga	Graham	Numer. List : n.° 5893 (1831)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Vietnamese	thàn mát tro
Chinese	香花崖豆藤
Chinese	灰毛崖豆藤
Chinese	冲天果
Chinese	山狗豆
Chinese	灰^鸡血藤*(香花崖豆藤）
Chinese	灰毛鸡血藤
Chinese	锈毛鸡血藤
Chinese	昆明鸡血藤
Chinese	锈毛崖豆藤
Chinese	黔滇崖豆藤
Chinese	灰毛岩豆藤
Chinese	灰^鸡血藤

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

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

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - Nepal
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Malaya

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000193046
Tropicos	50166484
KEW	urn:lsid:ipni.org:names:979778-1
The Plant List	ild-39632
Open Tree Of Life	488055
Observations.org	390960
NCBI Taxonomy	185709
IPNI	979778-1
iNaturalist	604784
GBIF	2952284
EOL	643644
Elurikkus	340350
USDA GRIN	403123
CMAUP	NPO2039

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

Natural Phosphodiesterase-4 Inhibitors with Potential Anti-Inflammatory Activities from Millettia dielsiana

Le VT, Hung HV, Ha NX, Le CH, Minh PT, Lam DT

Molecules

25-Oct-2023

PMCID:	PMC10650832
doi:	10.3390/molecules28217253
PMID:	37959674

Ethnobotanical study on medicinal plants used by Bulang people in Yunnan, China

Zhou H, Zhang J, Kirbis BS, Mula Z, Zhang W, Kuang Y, Huang Q, Yin L

J Ethnobiol Ethnomed

07-Sep-2023

PMCID:	PMC10486041
doi:	10.1186/s13002-023-00609-0
PMID:	37679773

Oxidative-Stress-Mediated ER Stress Is Involved in Regulating Manoalide-Induced Antiproliferation in Oral Cancer Cells

Peng SY, Tang JY, Lan TH, Shiau JP, Chen KL, Jeng JH, Yen CY, Chang HW

Int J Mol Sci

16-Feb-2023

PMCID:	PMC9965613
doi:	10.3390/ijms24043987
PMID:	36835397

Forest edges increase pollinator network robustness to extinction with declining area

Ren P, Didham RK, Murphy MV, Zeng D, Si X, Ding P

Nat Ecol Evol

30-Jan-2023

PMCID:	PMC9998274
doi:	10.1038/s41559-022-01973-y
PMID:	36717744

Siwalik plant megafossil diversity in the Eastern Himalayas: A review

Khan MA, Mahato S, Spicer RA, Spicer TE, Ali A, Hazra T, Bera S

Plant Divers

17-Dec-2022

PMCID:	PMC10311196
doi:	10.1016/j.pld.2022.12.003
PMID:	37397603

Hepatoprotective Effect of Millettia dielsiana: In Vitro and In Silico Study

Le VT, Hung DV, Quy BM, Minh PT, Lam DT

Molecules

16-Dec-2022

PMCID:	PMC9787921
doi:	10.3390/molecules27248978
PMID:	36558112

Chinese herbal bath therapy for the treatment of Atopic dermatitis in children: A meta-analysis and systematic review

Guo Z, Li Y, Hou Y, Wang Y, Liang Y, Si X, Pan G, Wang Y, Hu Q

Medicine (Baltimore)

25-Nov-2022

PMCID:	PMC9704985
doi:	10.1097/MD.0000000000031923
PMID:	36451483

Diverse diets and low‐fiber, low‐tannin foraging preferences: Foraging criteria of Tibetan macaques (Macaca thibetana) at low altitude in Huangshan

Li B, Li W, Liu C, Yang P, Li J

Ecol Evol

04-Oct-2022

PMCID:	PMC9532248
doi:	10.1002/ece3.9338
PMID:	36225833

Efficacy and Safety of Qiwei Tongbi Oral Liquid in Patients with Stable Long-Standing Rheumatoid Arthritis

Lu W, Fang L, Zhang J

Biomed Res Int

23-Oct-2021

PMCID:	PMC8557082
doi:	10.1155/2021/3930800
PMID:	34725638

An Apriori Algorithm-Based Association Rule Analysis to Identify Herb Combinations for Treating Uremic Pruritus Using Chinese Herbal Bath Therapy

Lu PH, Keng JL, Kuo KL, Wang YF, Tai YC, Kuo CY

Evid Based Complement Alternat Med

23-Nov-2020

PMCID:	PMC7704140
doi:	10.1155/2020/8854772
PMID:	33299462

Hepatoprotective effects of Hovenia dulcis seeds against alcoholic liver injury and related mechanisms investigated via network pharmacology

Meng X, Tang GY, Zhao CN, Liu Q, Xu XY, Cao SY

World J Gastroenterol

28-Jun-2020

PMCID:	PMC7327782
doi:	10.3748/wjg.v26.i24.3432
PMID:	32655267

Seasonal variations in group leaf characteristics in species with red young leaves

Zhang TJ, Tian XS, Liu XT, Huang XD, Peng CL

Sci Rep

11-Nov-2019

PMCID:	PMC6848096
doi:	10.1038/s41598-019-52753-x
PMID:	31712569

Screen for Potential Candidate Alternatives of Sargentodoxa cuneata from Its Six Adulterants Based on Their Phenolic Compositions and Antioxidant Activities

Yang L, Yin P, Cao X, Liu Y

Int J Mol Sci

31-Oct-2019

PMCID:	PMC6862427
doi:	10.3390/ijms20215427
PMID:	31683574

Danshen Formulae for Cancer: A Systematic Review and Meta-Analysis of High-Quality Randomized Controlled Trials

Wang T, Fu X, Wang Z

Evid Based Complement Alternat Med

02-Apr-2019

PMCID:	PMC6466905
doi:	10.1155/2019/2310639
PMID:	31061667

Kampo Therapies and the Use of Herbal Medicines in the Dentistry in Japan

Watanabe S, Toyama T, Sato T, Suzuki M, Morozumi A, Sakagami H, Hamada N

Medicines (Basel)

28-Feb-2019

PMCID:	PMC6473445
doi:	10.3390/medicines6010034
PMID:	30823475

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 / Ergoline and derivatives / Clavines and derivatives
Penniclavine	115247	Click to see CN1CC(C=C2C1CC3=CNC4=CC=CC2=C34)(CO)O	270.33	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
1,2,3-Trimethoxybenzene	12462	Click to see COC1=C(C(=CC=C1)OC)OC	168.19	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid	21635582	Click to see	957.10	unknown	via CMAUP database
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-carboxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid	101923141	Click to see	795.00	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aR,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylate	11803947	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CCC7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O	941.10	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-6-(acetyloxymethyl)-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aR,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylate	10819773	Click to see	983.10	unknown	via CMAUP database
Calenduloside E	176079	Click to see	632.80	unknown	via CMAUP database
chikusetsusaponin IV	10079497	Click to see	927.10	unknown	via CMAUP database
Chikusetsusaponin Iva	13909684	Click to see	795.00	unknown	via CMAUP database
Glycoside ST-J	101720880	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(C(O9)C(=O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O	1103.20	unknown	via CMAUP database
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
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylate	21669007	Click to see	971.10	unknown	via CMAUP database
Narcissiflorine	162878	Click to see	764.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,6aS,6bR,8aR,10R,12aS)-3,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid	101277261	Click to see	470.70	unknown	via CMAUP database
(3R,4aR,6aR,6aS,6bR,8aR,12aS)-3-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12-decahydro-1H-picene-4a-carboxylic acid	101277260	Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)C)C	468.70	unknown	via CMAUP database
(3R,4R,4aS,6aR,6aS,6bR,8aR,10R,12aS)-3,4,10-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid	16112781	Click to see	486.70	unknown	via CMAUP database
(4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	15379012	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(CO6)O)O)O)C)C(=O)O)C	604.80	unknown	via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylic acid	102239749	Click to see	470.70	unknown	via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10S,12aS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,6a,7,8,8a,10,11,12-decahydro-1H-picene-4a-carboxylic acid	16112782	Click to see	468.70	unknown	via CMAUP database
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	10395290	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C	751.00	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aR,6aR,6bS,8aR,10R,12aS,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,7,8,8a,10,11,12,14b-decahydro-1H-picene-4a-carboxylate	10605857	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CC=C7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O	939.10	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aR,6aR,6bS,8aR,12aS,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-3,10-dioxo-1,4,5,6,7,8,8a,11,12,14b-decahydropicene-4a-carboxylate	10748397	Click to see	937.10	unknown	via CMAUP database
asperosaponin C	13878127	Click to see	588.80	unknown	via CMAUP database
Papyriogenin A	3081523	Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)C)C	466.70	unknown	via CMAUP database
Papyriogenin C	3081568	Click to see	468.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
7alpha-Hydroxysitosterol	161816	Click to see	430.70	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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4aR,6aR,6bS,14aR,14bS)-4,4,6a,6b,11,11,14b-heptamethyl-2,4a,5,6,7,8,12,14a-octahydro-1H-picene-3,10-dione	102588576	Click to see	420.60	unknown	via CMAUP database
3alpha-Hydroxy-28-noroleana-11,13(18),17(22)-triene-21-one	102588575	Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2=CC1=O)C)C)(C)C)O)C)C	422.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
1-Benzofuran-5-carbaldehyde	2773875	Click to see C1=CC2=C(C=CO2)C=C1C=O	146.14	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Beta propiolactones
(1S,2R,5R,7R,10S,11R,18S,19S,22S)-7,18-dihydroxy-1,2,6,6,10,17,17-heptamethyl-20-oxahexacyclo[12.10.0.02,11.05,10.015,22.019,22]tetracosa-12,14-dien-21-one	101967008	Click to see	468.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
Dihydrocoumarin	660	Click to see	148.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3-Phenylprop-2-En-1-Ol	308	Click to see	134.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin	323	Click to see	146.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
3,7,4'-Tri-O-Acetyl Kaempferol	44584293	Click to see	412.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin	5316673	Click to see	432.40	unknown	via CMAUP database
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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 7-O-(2-E-p-coumaroyl-alpha-L-rhamnopyranoside)	11678667	Click to see	578.50	unknown	via CMAUP database
kaempferol 7-O-(2,3-di-E-p-coumaroyl-alpha-L-rhamnopyranoside)	11607311	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O)O	724.70	unknown	via CMAUP database
> 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 / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin	5280448	Click to see	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afromosin	5281704	Click to see	298.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids
2,3-dimethoxy-6-(7-methoxy-4H-chromen-3-yl)phenol	5318605	Click to see	314.30	unknown	via CMAUP database
Isosativan	591624	Click to see	286.32	unknown	via CMAUP database

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Callerya cinerea

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