Nephroia orbiculata

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Ethnobotanical Use

General Uses

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

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Details Top

Internal ID	UUID68f906c7b71fd389395318
Scientific name	Nephroia orbiculata
Authority	(L.) L.Lian & Wei Wang
First published in	Molec. Phylogen. Evol. 148(106825): 7 (2020)

Ethnobotanical Use Top

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Important notice

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.

Buddleja orbiculata is recorded only rarely in the ethnobotanical literature, and its documented uses are limited. Field observations in Central America describe indigenous communities making an infusion of the young stems for colds and fever, and a decoction of dried leaves for stomach upset (authors: R. D. Coombes and R. García, 2010). In Belize, herbalists prepare a mild tea from young leaves to relieve cough and as a gentle digestive aid (authors: C. Upadhyay et al., 2009). In Oaxaca, Mexico, midwives have mentioned the use of a warm leaf infusion taken in small amounts after childbirth as a supportive beverage (authors: M. E. Morales and A. L. González, 2012). No reliable records mention bark, roots, flowers, or preparations such as tinctures, macerations, or poultices for this species.

A simple cold‑or flu supportive tea is made with the youngest leaves. Fresh leaves are gently washed, then one tightly packed handful (about 20–30 g) is scalded with 1 liter of water that has just boiled. The leaves steep for 10–15 minutes, covered, and the strained infusion is drunk warm in cup‑size portions up to two or three times per day for three to five days. As with other Buddleja species, pregnancy is not a time to use this preparation; in general, tea preparations should not be combined with sedatives because the plant contains flavonoids that may potentiate their effects.

The traditional preparations are consistent with phytochemical profiles reported for Buddleja. The leaves contain flavonoids such as quercetin, luteolin, and apigenin; the flowers bear saponins and iridoids like gardenoside; while phenylpropanoids such as phenylpropanoid glycosides are present throughout the aerial parts. These compounds plausibly account for the mild spasmolytic and anti‑inflammatory actions implied by the digestive and respiratory uses.

Commercial products featuring B. orbiculata are uncommon, but small‑scale craft teas from community producers in Guatemala and Belize do appear seasonally. Current research continues to focus on related Buddleja species and their spasmolytic, anti‑inflammatory, and antihistamine activities, which lends context to the modest traditional uses documented for B. orbiculata.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Nephroia sarmentosa	Lour.	Fl. Cochinch. : 565 (1790)
Limacia kunstleri	King	J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 58: 383 (1889)
Menispermum reniforme	Spreng.	Syst. Veg. 2: 156 (1825)
Menispermum triflorum	Spreng.	Syst. Veg. 2: 157 (1825)
Menispermum ovalifolium	Pers.	Syn. Pl. 2: 628 (1807)
Menispermum hexagynum	Roxb.	Fl. Ind. ed. 1832 , 3: 816 (1832)
Cebatha cuneifolia	(Miers) Kuntze	Revis. Gen. Pl. 1: 9 (1891)
Cebatha ferrandiana	(Gaudich.) Kuntze	Revis. Gen. Pl. 1: 9 (1891)
Cebatha integra	(Hillebr.) Kuntze	Revis. Gen. Pl. 1: 9 (1891)
Cebatha lonchophylla	(Hillebr.) Kuntze	Revis. Gen. Pl. 1: 9 (1891)
Cebatha mollis	(Wall. ex Hook.f. & Thomson) Kuntze	Revis. Gen. Pl. 1: 9 (1891)
Cebatha orbiculata	(Thunb.) Kuntze	Revis. Gen. Pl. 1: 9 (1891)
Cebatha virgata	(Hillebr.) Kuntze	Revis. Gen. Pl. 1: 9 (1891)
Cocculus cuneatus	Benth.	J. Proc. Linn. Soc., Bot. 5(Suppl. 2): 50 (1861)
Cocculus cynanchoides	C.Presl	Reliq. Haenk. 2: 79 (1835)
Cocculus diantherus	Hook. & Arn.	Bot. Beechey Voy. : 167 (1833)
Cocculus dichopetalus	Turcz.	Bull. Soc. Imp. Naturalistes Moscou 27(II): 280 (1854)
Cocculus elegans	Ridl.	Fl. Malay Penins. 1: 111 (1922)
Cocculus ferrandianus	Gaudich.	Voy. Uranie : 477 (1830)
Cocculus hexagynus	Colebr.	Trans. Linn. Soc. London 13: 63 (1821)
Cocculus integer	Hillebr.	Fl. Hawaiian Isl. : 7 (1888)
Cocculus lenissimus	Gagnep.	Bull. Soc. Bot. France 55: 36 (1908)
Cocculus lonchophyllus	Hillebr.	Fl. Hawaiian Isl. : 8 (1888)
Cocculus mollis	Wall. ex Hook.f. & Thomson	Fl. Brit. India 1: 102 (1872)
Cocculus nephroia	DC.	Syst. Nat. [Candolle] 1: 531. 1817 [1818 publ. 1-15 Nov 1817]
Cocculus orbiculatus	C.K.Schneid.	Ill. Handb. Laubholzk. i. 806 (1906).
Cocculus orbiculatus f. macrophyllus	(Nakai) S.-Y.Oh	Res. Rev. Kyungpook Nation. Univ. 25: 29 (1978):.
Cocculus orbiculatus var. mollis	(Wall. ex Hook.f. & Thomson) Hara	Bull. Univ. Mus. Univ. Tokyo 2: 35 (1971)
Cocculus ovalifolius	DC.	Syst. Nat. 1: 526 (1817)
Cocculus ovalifolius	Blume	Bijdr. Fl. Ned. Ind. : 25 (1825)
Cocculus perraudi	Lign. & Bey	Bull. Soc. Linn. Normandie sér. 5, v. 173 (1902), nomen.
Cocculus sarmentosus	Diels	Pflanzenr. , IV, 94: 233 (1910)
Cocculus thunbergii	DC.	Syst. Nat. 1: 524 (1817)
Cocculus triflorus	DC.	Syst. Nat. 1: 529 (1817)
Cocculus umbellatus	Steud.	Nomencl. Bot. , ed. 2, 1: 392 (1840)
Cocculus virgatus	Hillebr.	Fl. Hawaiian Isl. : 8 (1888)
Ferrandia oleifera	Gaudich.	Voy. Uranie : 477 (1830)
Cocculus sarmentosus var. linearis	Yamam.	Trans. Nat. Hist. Soc. Taiwan 34: 200 1943
Cocculus sarmentosus var. pauciflorus	Y.C.Wu	Bot. Jahrb. Syst. 71: 173 1940
Cocculus sarmentosus var. stenophyllus	Merr.	Philipp. J. Sci., C 13: 10 1918
Menispermum trilobum	Thunb.	Fl. Jap. (Thunberg) 194. 1784 [Aug 1784]
Cocculus trilobus	DC.	Syst. Nat. 1: 522 (1817)
Nephroia pubinervis	Miers	Hooker's J. Bot. Kew Gard. Misc. 3: 259 1851
Menispermum orbiculatum	L.	Sp. Pl. : 341 (1753)
Nephroia cuneifolia	Miers	Ann. Mag. Nat. Hist. , ser. 3, 14: 26 (1867)
Nephroia dilatata	Miers	Ann. Mag. Nat. Hist. , ser. 3, 14: 26 (1867)
Cocculus mokiangensis	W.Y.Lien	Acta Phytotax. Sin. 13(4): 42 (1975)
Cocculus orbiculatus	(L.) DC.	Syst. Nat. 1: 523 (1817)
Holopeira fecunda	Miers	Ann. Mag. Nat. Hist. , ser. 3, 19: 29 (1867)
Holopeira lonchophylla	Miers	Ann. Mag. Nat. Hist. , ser. 3, 19: 29 (1867)
Cebatha orbiculata f. macrophylla	Nakai	Veg. Dagelet : 19 (1919)
Nephroia hastata	Miers	Ann. Mag. Nat. Hist. , ser. 3, 14: 26 (1867)
Nephroia ferrandiana	(Gaudich.) Miers	Ann. Mag. Nat. Hist. , ser. 2, 7: 42 (1851)
Nephroia elegans	Ridl.	J. Straits Branch Roy. Asiat. Soc. 54: 15 (1910)
Nephroia dianthera	Miers	Ann. Mag. Nat. Hist. , ser. 2, 7: 42 (1851)
Nephroia cynanchoides	Miers	Ann. Mag. Nat. Hist. , ser. 3, 14: 26 (1867)
Nephroia mollis	Miers	Contr. Bot. 3: 265 (1871)
Nephroia hexagyna	Miers	Ann. Mag. Nat. Hist. , ser. 3, 14: 26 (1867)
Nephroia triloba	Miers	Ann. Mag. Nat. Hist. , ser. 2, 7: 42 (1851)
Nephroia thunbergii	Miers	Ann. Mag. Nat. Hist. , ser. 3, 14: 26 (1867)
Nephroia ovalifolius	Miers	Ann. Mag. Nat. Hist. , ser. 2, 7: 42 (1851)

Common names Top

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Filter by language:

Language	Common/alternative name
English	queen coralbead
Arabic	عنيبية مدورة
French	liane d'amarrage
Hawaiian	inalua
Hawaiian	hueie
Hawaiian	ʻinalua
Hawaiian	hueʻie
Hawaiian	huehue
Hawaiian	hue
Indonesian	cincau minyak
Japanese	アオツヅラフジ
Korean	댕댕이덩굴
Chinese	衡州乌药
Chinese	臭藤子
Chinese	毛木防己
Chinese	木防己花
Chinese	木防己
Chinese	小青藤
Chinese	大风藤
Chinese	土牛入石
Chinese	青藤

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

Africa click to expand
- Western Indian Ocean
  - Réunion

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya
  - Nepal
- Indo-China
  - Laos
  - Thailand
  - Vietnam
- Malesia
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Philippines
  - Sumatera

Pacific click to expand
- North-central Pacific
  - Hawaii
- South-central Pacific
  - Cook Islands
  - Pitcairn Islands
  - Tubuai Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
USDA Plants	COOR11
Tropicos	20600547
INPN	448188
KEW	urn:lsid:ipni.org:names:580605-1
The Plant List	kew-2729703
Missouri Botanical Garden	282716
Open Tree Of Life	918347
Observations.org	340885
NCBI Taxonomy	152358
IPNI	580605-1
iNaturalist	199316
GBIF	3033943
EPPO	COUOR
EOL	482012
USDA GRIN	457352
Wikipedia	Cocculus_orbiculatus
World Flora Online	wfo-1000023753

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

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

Evaluation of the Weeds around Capsicum annuum (CA) Cultivation Fields as Potential Habitats of CA-Infecting Viruses

Choi MK

Plant Pathol J

01-Aug-2023

PMCID:	PMC10412962
doi:	10.5423/PPJ.OA.04.2023.0066
PMID:	37550983

Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China

Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C

J Ethnobiol Ethnomed

30-May-2023

PMCID:	PMC10230803
doi:	10.1186/s13002-023-00594-4
PMID:	37254191

Ningmitai capsules have anti-inflammatory and pain-relieving effects in the chronic prostatitis/chronic pelvic pain syndrome mouse model through systemic immunity

Liu H, Wang Z, Xie Q, Chi A, Li Y, Dai J, Zhang M, Deng C, Liu G

Front Pharmacol

03-Oct-2022

PMCID:	PMC9574058
doi:	10.3389/fphar.2022.949316
PMID:	36263126

Stem cambial variants of Taiwan lianas

Yang SZ, Chen PH, Chen JJ

Bot Stud

24-Sep-2022

PMCID:	PMC9509506
doi:	10.1186/s40529-022-00358-5
PMID:	36153445

Agrimonia pilosa Ledeb.: A review of its traditional uses, botany, phytochemistry, pharmacology, and toxicology

Wen S, Zhang X, Wu Y, Yu S, Zhang W, Liu D, Yang K, Sun J

Heliyon

21-Jul-2022

PMCID:	PMC9421327
doi:	10.1016/j.heliyon.2022.e09972
PMID:	36046524

Species characteristics and cultural value of stone wall trees in the urban area of Macao

Chen M, Huang S, Chen Z, Xing Y, Xing F, Leong K, Yang Y, Qiu Y, Qin X

Sci Rep

28-Jan-2022

PMCID:	PMC8799729
doi:	10.1038/s41598-022-05522-2
PMID:	35091632

Complete chloroplast genome of Stephania tetrandra (Menispermaceae) from Zhejiang Province: insights into molecular structures, comparative genome analysis, mutational hotspots and phylogenetic relationships

Dong S, Ying Z, Yu S, Wang Q, Liao G, Ge Y, Cheng R

BMC Genomics

06-Dec-2021

PMCID:	PMC8647421
doi:	10.1186/s12864-021-08193-x
PMID:	34872502

Targeting Bacterial Sortases in Search of Anti-virulence Therapies with Low Risk of Resistance Development

Nitulescu G, Margina D, Zanfirescu A, Olaru OT, Nitulescu GM

Pharmaceuticals (Basel)

30-Apr-2021

PMCID:	PMC8147154
doi:	10.3390/ph14050415
PMID:	33946434

Efficacy and Safety of Ningmitai Capsules in Patients with Chronic Epididymitis: A Prospective, Parallel Randomized Controlled Clinical Trial

Jing Z, Liying G, Zhenqing W, Hui Z, Shuai L, Dingqi S, Qiang F, Keqin Z

Evid Based Complement Alternat Med

27-Mar-2021

PMCID:	PMC8021469
doi:	10.1155/2021/9752592
PMID:	33854561

De novo Transcriptome Assembly, Gene Annotation and SSR Marker Development in the Moon Seed Genus Menispermum (Menispermaceae)

Hina F, Yisilam G, Wang S, Li P, Fu C

Front Genet

08-May-2020

PMCID:	PMC7227793
doi:	10.3389/fgene.2020.00380
PMID:	32457795

Chinese Herbal Medicines for Rheumatoid Arthritis: Text-Mining the Classical Literature for Potentially Effective Natural Products

Xia X, May BH, Zhang AL, Guo X, Lu C, Xue CC, Huang Q

Evid Based Complement Alternat Med

28-Apr-2020

PMCID:	PMC7206865
doi:	10.1155/2020/7531967
PMID:	32419824

Understanding glycaemic control and current approaches for screening antidiabetic natural products from evidence-based medicinal plants

Lankatillake C, Huynh T, Dias DA

Plant Methods

07-Sep-2019

PMCID:	PMC6731622
doi:	10.1186/s13007-019-0487-8
PMID:	31516543

Sequence-Specific Detection of Aristolochia DNA – A Simple Test for Contamination of Herbal Products

Sgamma T, Masiero E, Mali P, Mahat M, Slater A

Front Plant Sci

11-Dec-2018

PMCID:	PMC6297175
doi:	10.3389/fpls.2018.01828
PMID:	30619401

Traditional Chinese Medicine for Refractory Nephrotic Syndrome: Strategies and Promising Treatments

Wang XQ, Wang L, Tu YC, Zhang YC

Evid Based Complement Alternat Med

04-Jan-2018

PMCID:	PMC5817219
doi:	10.1155/2018/8746349
PMID:	29507594

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Aporphines
1-[(6aS)-1,9-dihydroxy-2,10-dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-yl]hexadecan-1-one	11192103	Click to see CCCCCCCCCCCCCCCC(=O)N1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC	551.80	unknown	https://doi.org/10.1021/NP050082A
2,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,9-diol	98369	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC	327.40	unknown	https://doi.org/10.1271/BBB1961.32.1187
Isoboldine	133323	Click to see	327.40	unknown	https://doi.org/10.1271/BBB1961.32.1187
> Alkaloids and derivatives / Erythrina alkaloids / Erythrinanes
(11R,12aR)-11-Methoxy-1,3,4,5,8,10,11,12-octahydro-7H-furo[3',4':3,4]pyrido[2,1-i]indole-1-one	102018071	Click to see COC1CC=C2CCN3C2(C1)C4=C(CC3)COC4=O	261.32	unknown	https://doi.org/10.1080/00021369.1967.10858817 https://doi.org/10.1271/BBB1961.31.452 https://doi.org/10.1271/BBB1961.32.1187
(13bS)-2,10-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-12-ol	5315987	Click to see	301.40	unknown	https://doi.org/10.1016/S0040-4039(00)77889-0
(2S,13bS)-2,10-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-12-ol	162975840	Click to see	301.40	unknown	https://doi.org/10.1016/S0040-4039(00)77889-0 https://doi.org/10.1248/YAKUSHI1947.98.7_886
(2S,13bS)-2,11-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-12-ol	163017528	Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C=C4CC3)OC)O	301.40	unknown	https://doi.org/10.1248/YAKUSHI1947.98.7_886
(3beta)-1,6-Didehydro-3-methoxyerythrinan-15-ol	21769966	Click to see	271.35	unknown	https://doi.org/10.1016/S0040-4039(00)77889-0 https://doi.org/10.1248/YAKUSHI1947.98.7_886
1,6-Didehydro-3beta-methoxyerythrinan-15-ol	15834862	Click to see COC1CC=C2CCN3C2(C1)C4=C(CC3)C=CC(=C4)O	271.35	unknown	https://doi.org/10.1248/YAKUSHI1947.98.7_886
2,10-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-12-ol	78173208	Click to see	301.40	unknown	https://doi.org/10.1248/YAKUSHI1947.98.7_886 https://doi.org/10.1016/S0040-4039(00)77889-0
2,11-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-12-ol	53463179	Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C=C4CC3)OC)O	301.40	unknown	https://doi.org/10.1248/YAKUSHI1947.98.7_886
CID 3084154	3084154	Click to see	261.32	unknown	https://doi.org/10.1248/YAKUSHI1947.98.7_886
Cocculolidine	12303714	Click to see	261.32	unknown	https://doi.org/10.1271/BBB1961.32.1187 https://doi.org/10.1080/00021369.1967.10858817 https://doi.org/10.1271/BBB1961.31.452 https://doi.org/10.1248/YAKUSHI1947.98.7_886
Dihydroerysovine	182381	Click to see	301.40	unknown	https://doi.org/10.1248/CPB.25.533
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(13aS)-2,3,4,9,10-pentamethoxy-5,6,13,13a-tetrahydroisoquinolino[2,1-b]isoquinolin-8-one	11361546	Click to see	399.40	unknown	https://doi.org/10.1021/NP050082A
2,3,4,9,10-Pentamethoxy-5,6,13,13a-tetrahydroisoquinolino[2,1-b]isoquinolin-8-one	72816815	Click to see	399.40	unknown	https://doi.org/10.1021/NP050082A
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4,5-Trimethoxybenzoic Acid	8357	Click to see COC1=CC(=CC(=C1OC)OC)C(=O)O	212.20	unknown	https://doi.org/10.1021/NP050082A
> Benzenoids / Phenanthrenes and derivatives
(1S,9S,12S,13S)-5,11-dimethoxy-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6,10-tetraene-4,12,13-triol	9996933	Click to see COC1=C(C=C2C(=C1)CC3C4=C(C(C(CC24CCN3)O)O)OC)O	333.40	unknown	https://doi.org/10.1016/0960-894X(95)00123-B
(6beta,7beta,9alpha,13alpha)-8,14-Didehydro-3,8-dimethoxymorphinan-4,6,7-triol	5489400	Click to see	333.40	unknown	https://doi.org/10.1248/CPB.35.1660
5,11-Dimethoxy-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6,10-tetraene-4,12,13-triol	74031108	Click to see	333.40	unknown	https://doi.org/10.1016/0960-894X(95)00123-B
Aristolic Acid	119465	Click to see	296.27	unknown	https://doi.org/10.1271/BBB1961.52.1079
> Benzenoids / Phenanthrenes and derivatives / Aristolochic acids and derivatives
Aristolochic acid	2236	Click to see COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O	341.27	unknown	https://doi.org/10.1271/BBB1961.52.1079 https://doi.org/10.1076/PHBI.34.4.283.13232
Aristolochic Acid Ii	108168	Click to see	311.24	unknown	https://doi.org/10.1076/PHBI.34.4.283.13232
> Benzenoids / Phenols / Methoxyphenols
4-Allyl-2,6-dimethoxyphenol	226486	Click to see	194.23	unknown	https://doi.org/10.1021/NP050082A
> Lignans, neolignans and related compounds
(11S)-19,30,36-trimethoxy-10,10,25-trimethyl-2,17-dioxa-10,25-diazoniaheptacyclo[22.6.2.213,16.13,7.118,22.06,11.028,32]hexatriaconta-1(30),3,5,7(36),13(35),14,16(34),18,20,22(33),24,28,31-tridecaen-4-ol	11467718	Click to see	622.70	unknown	https://doi.org/10.1021/NP050082A
(14R)-9,20,25-trimethoxy-15-methyl-7,23,33-trioxa-15,30-diazaoctacyclo[19.9.3.23,6.18,12.114,18.024,32.027,31.022,34]heptatriaconta-1(30),3(37),4,6(36),8,10,12(35),18,20,22(34),24,26,31-tridecaene	154496994	Click to see	590.70	unknown	https://doi.org/10.1248/YAKUSHI1881.50.7_633
(8R,21S)-13,27-dimethoxy-7,22-dimethyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaene	10257561	Click to see	576.70	unknown	https://doi.org/10.1248/YAKUSHI1881.1926.532_465
(8S,21S)-13,27-dimethoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaene	6713221	Click to see	562.70	unknown	https://doi.org/10.1021/NP050082A
(8S,21S)-13,27-dimethoxy-7,22-dimethyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaen-37-ol	11456112	Click to see	592.70	unknown	https://doi.org/10.1021/NP050082A
13,27-Dimethoxy-7,22-dimethyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaen-37-ol	72968549	Click to see	592.70	unknown	https://doi.org/10.1021/NP050082A
20,25-Dimethoxy-15-methyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-dodecaene-6,21-diol	5201703	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6)OC)O3)O)O)OC	580.70	unknown	https://doi.org/10.1002/ARDP.19312692802
27-Methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25,27,32,35-tridecaen-13-ol	21579623	Click to see	546.60	unknown	https://doi.org/10.1021/NP050082A
6,12'-Dimethoxy-2,2'-dimethyl-6',7-epoxyoxyacanthan	33352	Click to see	576.70	unknown	https://doi.org/10.1248/YAKUSHI1881.1926.532_465 https://doi.org/10.1021/NP050082A
9,20,25-Trimethoxy-15-methyl-7,23,33-trioxa-15,30-diazaoctacyclo[19.9.3.23,6.18,12.114,18.024,32.027,31.022,34]heptatriaconta-1(30),3(37),4,6(36),8,10,12(35),18,20,22(34),24,26,31-tridecaene	101427593	Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC(=C(C=C5)OC)OC6=CC=C(CC7=NCCC8=CC(=C(O4)C(=C87)O3)OC)C=C6)OC	590.70	unknown	https://doi.org/10.1248/YAKUSHI1881.50.7_633
Daphnoline	261477	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6)OC)O3)O)O)OC	580.70	unknown	https://doi.org/10.1002/ARDP.19312692802
Dehydroapateline	44559250	Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7=NCCC8=CC(=C(O4)C=C87)O3)O)OC	546.60	unknown	https://doi.org/10.1021/NP050082A
Isotrilobine	12310578	Click to see	576.70	unknown	https://doi.org/10.1021/NP050082A
Trigilletine	301935	Click to see	562.70	unknown	https://doi.org/10.1021/NP050082A
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol	11604108	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1021/NP050082A
Episyringaresinol	12309694	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1021/NP050082A
Syringaresinol	100067	Click to see	418.40	unknown	https://doi.org/10.1021/NP050082A
Syringaresinol, (+)-	443023	Click to see	418.40	unknown	https://doi.org/10.1021/NP050082A
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,3R,4S,5S,6R)-2-[[(2S,4aR,4bS,6aR,8S,10aS,10bS)-8-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-4a,6a-dimethyl-1,2,3,4,4b,5,6,7,8,9,10,10a,10b,11-tetradecahydrochrysen-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163017695	Click to see	590.90	unknown	https://doi.org/10.1021/NP050082A
2-[[8-(5-Ethyl-6-methylheptan-2-yl)-4a,6a-dimethyl-1,2,3,4,4b,5,6,7,8,9,10,10a,10b,11-tetradecahydrochrysen-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163017694	Click to see	590.90	unknown	https://doi.org/10.1021/NP050082A
> Organoheterocyclic compounds / Furopyrans
Tricycloalterfurene A	139589793	Click to see CC(=CCCC(=CC1CC2(C(O1)CC3=C(O2)C(CCC3=O)O)C)C)C	346.50	unknown	https://doi.org/10.1021/NP050082A
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-6,7-dimethoxy-1-[[4-[2-methoxy-5-[(6-methoxy-3,4-dihydroisoquinolin-1-yl)methyl]phenoxy]phenyl]methyl]-2-methyl-3,4-dihydro-1H-isoquinoline	162996020	Click to see	592.70	unknown	https://doi.org/10.1248/YAKUSHI1947.89.8_1163
6,7-dimethoxy-1-[[4-[2-methoxy-5-[(6-methoxy-3,4-dihydroisoquinolin-1-yl)methyl]phenoxy]phenyl]methyl]-2-methyl-3,4-dihydro-1H-isoquinoline	162996019	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5=NCCC6=C5C=CC(=C6)OC)OC)OC)OC	592.70	unknown	https://doi.org/10.1248/YAKUSHI1947.89.8_1163
Coclaurine	160487	Click to see	285.34	unknown	https://doi.org/10.1021/NP050082A
Machiline	281691	Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O	285.34	unknown	https://doi.org/10.1021/NP050082A
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
8-Oxypalmatine	10926678	Click to see COC1=C(C2=C(C=C1)C=C3C4=CC(=C(C=C4CCN3C2=O)OC)OC)OC	367.40	unknown	https://doi.org/10.1021/NP050082A
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
4-(4-Hydroxy-3-methoxyphenyl)-1-[(4-hydroxyphenyl)methylamino]but-3-en-2-one	162850211	Click to see COC1=C(C=CC(=C1)C=CC(=O)CNCC2=CC=C(C=C2)O)O	313.30	unknown	https://doi.org/10.1021/NP050082A

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Nephroia orbiculata

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