Rostellularia procumbens

Details Top

Internal ID UUID643ff88ed5b0b618200187
Scientific name Rostellularia procumbens
Authority (L.) Nees
First published in Prodr. 11: 371 (1847)

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.

Traditional users prepare hot infusions and decoctions of the aerial parts as a diuretic and to ease urinary complaints. In China, the bitter herb is taken after childbirth to “remove heat from the blood,” and it is also drunk as a gentle febrifuge, frequently in combination with other herbs; the Yunnan provincial pharmacopeia (Qian, 1992) and Beijing Medical College (Beijing Medical College, 1970) record these indications. Across North-East India and Bangladesh, decoctions of the leaves and stems are used for urinary pain, to promote urine flow, and for fever, and they are considered astringent in urinary infections; the India Pharmacopeia of the Greater China and Regional Pharmacopoeias (1960) and Jadhav (2010) describe these applications. In the Philippines, infusions of the whole herb are commonly taken as a diuretic tea, while leaf poultices are applied to wounds; the American Pharmacy Journal (Johnson, 1980) and Macleod (1919) list these practices, and the latter notes crushing fresh leaves and pressing them over the affected skin.

A practical infusion widely used in East Asia is made by simmering one level tablespoon of dried aerial parts in two cups of water for 10 minutes and drinking one half cup up to three times a day. For cold macerations, pour one cup of room‑temperature water over two teaspoons of the herb, cover and steep for six to eight hours, then strain and take as a calming diuretic tea. Contemporary references like Beijing Medical College (1970) and Ranu's demoscopic surveys (Ranu, 1996) show the same tea being prepared in households in Vietnam for painful urination. Safety notes: most preparations are bitter and cooling; long use is not advised for diarrhea or as a uterine stimulant in pregnancy; the India Pharmacopeia and regional pharmacopoeias warn against use in pregnancy and lactation.

The pharmacological profile supports these traditional effects. Extracts contain β‑sitosterol, stigmasterol, flavone C‑glucosides such as orientin and vitexin, ferulic acid, and caffeic acid, compounds shown by studies of Rostellularia procumbens to display diuretic, anti‑inflammatory, and mild febrifuge activity (Kumar et al., 2015; Liu et al., 2012). These constituents plausibly account for urinary spasmolytic activity and for soothing gastrointestinal and urinary irritation.

In the region, the dried herb remains widely sold as “huan lian cao” for fever, painful urination, and postpartum care, and modern laboratory work continues to map its flavonoids and triterpenoids; the Taiwan Pharmacopoeia (Taiwan Pharmacopoeia Committee, 2013) and ongoing phytochemical studies (Zou et al., 2009; Kim et al., 2014) keep the plant in both practice and research.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Justicia hirtella Wall. Numer. List : n.º 2448 (1830)
Justicia japonica Thunb. Syst. Veg. ed. 14 : 63 (1784)
Justicia media R.Br. Prodr. Fl. Nov. Holland. : 476 (1810)
Ptyssiglottis sarmentosa Boerl. Handl. Fl. Ned. Ind. 2: 662 (1899)
Rungia sarmentosa Valeton Icon. Bogor. 3: t. 257 (1908)
Rostellaria adenostachya Nees Pl. Asiat. Rar. 3: 101 (1832)
Rostellaria procumbens (L.) Nees Pl. Asiat. Rar. 3: 101 (1832)
Rostellaria japonica Carrière Rev. Hort. (Paris) 37: 400 (1866)
Rostellularia juncea Nees Prodr. 11: 376 (1847)
Rostellularia neglecta Bremek. Dansk Bot. Ark. 20: 86 (1961)
Rostellularia media Nees Prodr. 11: 374 (1847)
Rostellularia sarmentosa Zoll. ex Nees Prodr. 11: 370 (1847)
Rostellularia sundana Bremek. Verh. Kon. Ned. Akad. Wetensch., Afd. Natuurk., Sect. 2 , 45(2): 62 (1948)
Rostellularia elegans Bremek. Dansk Bot. Ark. 20: 85 (1961)
Rostellularia cradengensis Bremek. Dansk Bot. Ark. 20: 84 (1961)
Rostellularia blancoi Hassk. Flora 47: 54 (1864)
Ecbolium procumbens Kuntze Revis. Gen. Pl. 2: 488 (1891)
Rostellularia procumbens var. hirsuta (Yamam.) S.S.Ying Mem. Coll. Agric. Natl. Taiwan Univ. 29(2): 44 (1989)
Rostellularia procumbens var. linearifolia (Yamam.) S.S.Ying Mem. Coll. Agric. Natl. Taiwan Univ. 29(2): 45 (1989)
Rostellularia trichochila Miq. J. Bot. Néerl. 1: 118 (1861)
Justicia procumbens var. hirsuta Yamam. Icon. Pl. Formosan., Suppl. 2: 32–33, f. 19 1926
Justicia procumbens var. linearifolia Yamam. Icon. Pl. Formosan., Suppl. 2: 33, f. 20 1926
Justicia procumbens var. simplex (D.Don) Yamazaki Fl. E. Himalaya 302 1966
Rostellularia japonica (Thunberg) J.L.Ellis Bull. Bot. Surv. India 22: 196 (1980 publ. 1982)
Justicia procumbens var. typica Domin Biblioth. Bot. 22(89): 1158 (1929)
Rostellularia procumbens var. serpyllifolia Benth. Exsicc. (Pl. Ind. Orient.) 1851: n.º 571 (1851)
Rostellularia procumbens var. riukiuensis (Yamam.) S.S.Ying Mem. Coll. Agric. Natl. Taiwan Univ. 29(2): 44 (1989)
Justicia procumbens L. Sp. Pl. : 15 (1753)
Rostellularia adenostachya Nees Prodr. 11: 373 (1847)
Dianthera ciliata Blanco Fl. Filip., ed. 2. : 12 (1845)
Rostellularia procumbens f. alboflora J.L.Liu Bull. Bot. Res., Harbin 20: 254 (2000)
Justicia procumbens var. riukiuensis Yamam. Icon. Pl. Formosan. 2(Suppl.): 31 (1926)
Justicia hayatae var. decumbens Yamam. Icon. Pl. Formosan. 2(Suppl.): 35 (1926)
Justicia procumbens var. leucantha Honda Bot. Mag. (Tokyo) 44: 669 (1930)
Justicia procumbens f. japonica (Thunb.) H.Hara Enum. Spermatophytarum Japon. 1: 294 (1948)

Common names Top

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Language Common/alternative name
Arabic شخض مفترش
Japanese キツネノマゴ
Korean 쥐꼬리망초
lzh 爵床
Tamil கோடகசாலை
Tamil உரோசுடெல்லுலேரியா புரோகம்பென்சு
Chinese 爵床

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
      • Tibet
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Laccadive Islands
      • Maldives
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000401948
KEW urn:lsid:ipni.org:names:53735-1
IPNI 53735-1
iNaturalist 416172
GBIF 7264292
Tropicos 100064
INPN 910834
KEW urn:lsid:ipni.org:names:51382-1
The Plant List kew-2329315
PFAF Justicia procumbens
PaleoBotany 10269
Open Tree Of Life 3883128
NCBI Taxonomy 859317
IPNI 51387-1
iNaturalist 354064
GBIF 7263401
Freebase /m/0dllkm6
EPPO IUIPC
USDA GRIN 428155
Wikipedia Rostellularia_procumbens
CMAUP NPO16045
Wikipedia Rostellularia_procumbens
Tropicos 103042
Observations.org 1116236

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
Potential of Lycii Radicis Cortex as an Ameliorative Agent for Skeletal Muscle Atrophy Son RH, Kim MI, Kim HM, Guo S, Lee DH, Lim GM, Kim SM, Kim JY, Kim CY Pharmaceuticals (Basel) 04-Apr-2024
PMCID:PMC11054743
doi:10.3390/ph17040462
PMID:38675422
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
Bioactivities and Mechanisms of Action of Diphyllin and Its Derivatives: A Comprehensive Systematic Review Hou W, Huang LJ, Huang H, Liu SL, Dai W, Li ZM, Zhang ZY, Xin SY, Wang JY, Zhang ZY, Ouyang X, Lan JX Molecules 30-Nov-2023
PMCID:PMC10707837
doi:10.3390/molecules28237874
PMID:38067601
Reactive oxygen species (ROS)-mediated oxidative stress in chronic liver diseases and its mitigation by medicinal plants Sharma P, Nandave M, Nandave D, Yadav S, Vargas-De-La-Cruz C, Singh S, Tandon R, Ramniwas S, Behl T Am J Transl Res 15-Nov-2023
PMCID:PMC10703659
PMID:38074830
Complete plastid genome structure of 13 Asian Justicia (Acanthaceae) species: comparative genomics and phylogenetic analyses Niu Z, Lin Z, Tong Y, Chen X, Deng Y BMC Plant Biol 15-Nov-2023
PMCID:PMC10647099
doi:10.1186/s12870-023-04532-0
PMID:37964203
Molecular Docking and Molecular Dynamics Studies Reveal the Anticancer Potential of Medicinal-Plant-Derived Lignans as MDM2-P53 Interaction Inhibitors Shoaib TH, Abdelmoniem N, Mukhtar RM, Alqhtani AT, Alalawi AL, Alawaji R, Althubyani MS, Mohamed SG, Mohamed GA, Ibrahim SR, Hussein HG, Alzain AA Molecules 16-Sep-2023
PMCID:PMC10536213
doi:10.3390/molecules28186665
PMID:37764441
Mechanisms of Rostellularia procumbens (L.) Nees on treating chronic glomerulonephritis explored by network pharmacology, RNA-seq, and in vitro experiments Wang M, Zhou Y, Jian Q, Ai Z, Zhou S BMC Complement Med Ther 24-Jul-2023
PMCID:PMC10367255
doi:10.1186/s12906-023-04079-5
PMID:37488573
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
The Effect of Cadmium on Plants in Terms of the Response of Gene Expression Level and Activity Moravčíková D, Žiarovská J Plants (Basel) 30-Apr-2023
PMCID:PMC10181241
doi:10.3390/plants12091848
PMID:37176906
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Phenolic Phytochemicals for Prevention and Treatment of Colorectal Cancer: A Critical Evaluation of In Vivo Studies De S, Paul S, Manna A, Majumder C, Pal K, Casarcia N, Mondal A, Banerjee S, Nelson VK, Ghosh S, Hazra J, Bhattacharjee A, Mandal SC, Pal M, Bishayee A Cancers (Basel) 03-Feb-2023
PMCID:PMC9913554
doi:10.3390/cancers15030993
PMID:36765950
Overview of the Justicia Genus: Insights into Its Chemical Diversity and Biological Potential Carneiro MR, Sallum LO, Martins JL, Peixoto JD, Napolitano HB, Rosseto LP Molecules 25-Jan-2023
PMCID:PMC9920429
doi:10.3390/molecules28031190
PMID:36770856
Chemistry and Biological Activities of Naturally Occurring and Structurally Modified Podophyllotoxins Jin L, Song Z, Cai F, Ruan L, Jiang R Molecules 30-Dec-2022
PMCID:PMC9822336
doi:10.3390/molecules28010302
PMID:36615496
Preventive effects of the butanol fraction of Justicia procumbens L. against dexamethasone-induced muscle atrophy in C2C12 myotubes Kim JY, Kim HM, Kim JH, Lee JH, Zhang K, Guo S, Lee DH, Gao EM, Son RH, Kim SM, Kim CY Heliyon 22-Nov-2022
PMCID:PMC9713280
doi:10.1016/j.heliyon.2022.e11597
PMID:36468147
East Wind, West Wind: Toward the modernization of traditional Chinese medicine Yagüe E, Sun H, Hu Y Front Neurosci 10-Nov-2022
PMCID:PMC9685990
doi:10.3389/fnins.2022.1057817
PMID:36440293

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
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
6,7-dimethoxy-4-(6-methoxy-1,3-benzodioxol-5-yl)-3H-benzo[f][2]benzofuran-1-one 10000703 Click to see COC1=CC2=CC3=C(COC3=O)C(=C2C=C1OC)C4=CC5=C(C=C4OC)OCO5 394.40 unknown https://doi.org/10.1002/ARDP.200300841
6'-Hydroxyjusticidin A 71587520 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC)COC3=O)C4=CC5=C(C=C4O)OCO5)OC 410.40 unknown https://doi.org/10.1002/MRC.1830
6'-Hydroxyjusticidin C 60194681 Click to see 410.40 unknown https://doi.org/10.1002/MRC.1830
9-(1,3-Benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxynaphtho(2,3-c)furan-1(3H)-one 100492 Click to see 380.30 unknown https://doi.org/10.1016/0031-9422(96)00024-6
https://doi.org/10.1016/S0040-4020(01)93074-1
https://doi.org/10.1021/NP960443+
https://doi.org/10.1021/NP50044A030
9-(3,4-dimethoxyphenyl)-5-hydroxy-6H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one 332529 Click to see 380.30 unknown https://doi.org/10.1002/MRC.1830
https://doi.org/10.1021/NP960443+
Chinensinaphthol Methyl Ether 5315828 Click to see 394.40 unknown https://doi.org/10.1002/MRC.1830
https://doi.org/10.1021/NP960443+
Cilinaphthalide B 10476659 Click to see 410.40 unknown https://doi.org/10.1002/ARDP.200300841
Justicidin A 159982 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC)COC3=O)C4=CC5=C(C=C4)OCO5)OC 394.40 unknown https://doi.org/10.1021/NP960443+
https://doi.org/10.1016/S0040-4039(01)89075-4
https://doi.org/10.1016/S0040-4020(01)93074-1
https://doi.org/10.1016/0031-9422(96)00024-6
https://doi.org/10.1021/NP50044A030
Justicidin B 442882 Click to see COC1=CC2=CC3=C(C(=C2C=C1OC)C4=CC5=C(C=C4)OCO5)C(=O)OC3 364.30 unknown https://doi.org/10.1016/S0040-4020(01)93074-1
https://doi.org/10.1016/0031-9422(96)00024-6
https://doi.org/10.1016/S0040-4039(01)89075-4
https://doi.org/10.1021/NP960443+
https://doi.org/10.1021/NP030142H
Justicidin C 493173 Click to see 394.40 unknown https://doi.org/10.1021/NP50044A030
https://doi.org/10.1016/S0040-4020(01)93074-1
https://doi.org/10.1002/MRC.1830
https://doi.org/10.1016/0031-9422(96)00024-6
https://doi.org/10.1021/NP960443+
Justicidin D 5318737 Click to see 378.30 unknown https://doi.org/10.1021/NP50044A030
https://doi.org/10.1021/NP960443+
https://doi.org/10.1016/0031-9422(96)00024-6
Justicidin E 363128 Click to see C1C2=C(C=C3C=C4C(=CC3=C2C5=CC6=C(C=C5)OCO6)OCO4)C(=O)O1 348.30 unknown https://doi.org/10.1021/NP50044A030
Justicidin F 11740369 Click to see COC1=C2COC(=O)C2=C(C3=CC4=C(C=C31)OCO4)C5=CC6=C(C=C5)OCO6 378.30 unknown https://doi.org/10.1021/NP960443+
https://doi.org/10.1002/MRC.1830
Justicidin H 60194680 Click to see COC1=CC2=CC3=C(C(=C2C=C1OC)C4=CC5=C(C=C4O)OCO5)C(=O)OC3 380.30 unknown https://doi.org/10.1002/MRC.1830
Retrochinensin 122805 Click to see COC1=C(C=C(C=C1)C2=C3C=C4C(=CC3=CC5=C2COC5=O)OCO4)OC 364.30 unknown https://doi.org/10.1016/0031-9422(96)00024-6
https://doi.org/10.1016/S0040-4039(01)89075-4
https://doi.org/10.1021/NP960443+
Taiwanin E 493164 Click to see 364.30 unknown https://doi.org/10.1021/NP960443+
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
[(2R,3R)-3-(acetyloxymethyl)-2-(1,3-benzodioxol-5-ylmethyl)-4-(3,4,5-trimethoxyphenyl)butyl] acetate 21600064 Click to see CC(=O)OCC(CC1=CC2=C(C=C1)OCO2)C(CC3=CC(=C(C(=C3)OC)OC)OC)COC(=O)C 488.50 unknown https://doi.org/10.1021/NP9703860
[(2R,3R)-3-(acetyloxymethyl)-2-(1,3-benzodioxol-5-ylmethyl)-4-(4-hydroxy-3-methoxyphenyl)butyl] acetate 10551264 Click to see CC(=O)OCC(CC1=CC2=C(C=C1)OCO2)C(CC3=CC(=C(C=C3)O)OC)COC(=O)C 444.50 unknown https://doi.org/10.1021/NP9703860
[(2R,3R)-3-(acetyloxymethyl)-2-(1,3-benzodioxol-5-ylmethyl)-4-(4-hydroxy-3,5-dimethoxyphenyl)butyl] acetate 10672178 Click to see 474.50 unknown https://doi.org/10.1021/NP9703860
[(2R,3R)-3-(acetyloxymethyl)-2-[(3,4-dimethoxyphenyl)methyl]-4-(3,4,5-trimethoxyphenyl)butyl] acetate 10529518 Click to see 504.60 unknown https://doi.org/10.1021/NP9703860
[(2R,3R)-3-(acetyloxymethyl)-4-(3,4-dimethoxyphenyl)-2-[(3,4-dimethoxyphenyl)methyl]butyl] acetate 14213270 Click to see CC(=O)OCC(CC1=CC(=C(C=C1)OC)OC)C(CC2=CC(=C(C=C2)OC)OC)COC(=O)C 474.50 unknown https://doi.org/10.1021/NP9703860
[3-(Acetyloxymethyl)-2-(1,3-benzodioxol-5-ylmethyl)-4-(3,4,5-trimethoxyphenyl)butyl] acetate 73797361 Click to see CC(=O)OCC(CC1=CC2=C(C=C1)OCO2)C(CC3=CC(=C(C(=C3)OC)OC)OC)COC(=O)C 488.50 unknown https://doi.org/10.1021/NP9703860
[3-(Acetyloxymethyl)-2-(1,3-benzodioxol-5-ylmethyl)-4-(4-hydroxy-3-methoxyphenyl)butyl] acetate 10575282 Click to see 444.50 unknown https://doi.org/10.1021/NP9703860
[3-(Acetyloxymethyl)-2-(1,3-benzodioxol-5-ylmethyl)-4-(4-hydroxy-3,5-dimethoxyphenyl)butyl] acetate 85227215 Click to see 474.50 unknown https://doi.org/10.1021/NP9703860
[3-(Acetyloxymethyl)-2-[(3,4-dimethoxyphenyl)methyl]-4-(3,4,5-trimethoxyphenyl)butyl] acetate 85173435 Click to see 504.60 unknown https://doi.org/10.1021/NP9703860
[3-(Acetyloxymethyl)-2-[(3,4-dimethoxyphenyl)methyl]-4-(4-hydroxy-3,5-dimethoxyphenyl)butyl] acetate 85277116 Click to see CC(=O)OCC(CC1=CC(=C(C=C1)OC)OC)C(CC2=CC(=C(C(=C2)OC)O)OC)COC(=O)C 490.50 unknown https://doi.org/10.1021/NP9703860
[3-(Acetyloxymethyl)-4-(3,4-dimethoxyphenyl)-2-[(3,4-dimethoxyphenyl)methyl]butyl] acetate 14213269 Click to see 474.50 unknown https://doi.org/10.1021/NP9703860
Justin C 10814927 Click to see 490.50 unknown https://doi.org/10.1021/NP9703860
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(-)-Dihydroclusin 332806 Click to see COC1=CC(=CC(=C1OC)OC)CC(CO)C(CC2=CC3=C(C=C2)OCO3)CO 404.50 unknown https://doi.org/10.1021/NP9703860
(2R,3R)-2-[(3,4-dimethoxyphenyl)methyl]-3-[(3,4,5-trimethoxyphenyl)methyl]butane-1,4-diol 14655038 Click to see COC1=C(C=C(C=C1)CC(CO)C(CC2=CC(=C(C(=C2)OC)OC)OC)CO)OC 420.50 unknown https://doi.org/10.1021/NP9703860
(2R,3R)-2,3-bis[(3,4-dimethoxyphenyl)methyl]butane-1,4-diol 13989916 Click to see COC1=C(C=C(C=C1)CC(CO)C(CC2=CC(=C(C=C2)OC)OC)CO)OC 390.50 unknown https://doi.org/10.1021/NP9703860
1,4-Butanediol, 2,3-bis[(3,4-dimethoxyphenyl)methyl]- 291725 Click to see COC1=C(C=C(C=C1)CC(CO)C(CC2=CC(=C(C=C2)OC)OC)CO)OC 390.50 unknown https://doi.org/10.1021/NP9703860
2-[(3,4-Dimethoxyphenyl)methyl]-3-[(3,4,5-trimethoxyphenyl)methyl]butane-1,4-diol 14655037 Click to see COC1=C(C=C(C=C1)CC(CO)C(CC2=CC(=C(C(=C2)OC)OC)OC)CO)OC 420.50 unknown https://doi.org/10.1021/NP9703860
Dihydroclusin 3978441 Click to see COC1=CC(=CC(=C1OC)OC)CC(CO)C(CC2=CC3=C(C=C2)OCO3)CO 404.50 unknown https://doi.org/10.1021/NP9703860
> Lignans, neolignans and related compounds / Lignan glycosides
[(3S,4R,5S)-5-[[9-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-1-oxo-3H-benzo[f]isobenzofuran-4-yl]oxy]-3,4-dihydroxy-tetrahydrofuran-3-yl]methyl acetate 10347622 Click to see 554.50 unknown https://doi.org/10.1016/0031-9422(96)00024-6
[5-[[9-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-1-oxo-3H-benzo[f][2]benzofuran-4-yl]oxy]-3,4-dihydroxyoxolan-3-yl]methyl acetate 13873815 Click to see 554.50 unknown https://doi.org/10.1016/0031-9422(96)00024-6
4,6,7-trimethoxy-9-[6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3-benzodioxol-5-yl]-1H-benzo[f][2]benzofuran-3-one 10030964 Click to see COC1=C(C=C2C(=C1)C(=C3COC(=O)C3=C2OC)C4=CC5=C(C=C4OC6C(C(C(C(O6)CO)O)O)O)OCO5)OC 572.50 unknown https://doi.org/10.1016/0031-9422(96)00024-6
4,6,7-trimethoxy-9-[6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3-benzodioxol-5-yl]-1H-benzo[f][2]benzofuran-3-one 85097750 Click to see COC1=C(C=C2C(=C1)C(=C3COC(=O)C3=C2OC)C4=CC5=C(C=C4OC6C(C(C(C(O6)CO)O)O)O)OCO5)OC 572.50 unknown https://doi.org/10.1016/0031-9422(96)00024-6
4,6,7-trimethoxy-9-[6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3-benzodioxol-5-yl]-3H-benzo[f][2]benzofuran-1-one 85164665 Click to see 572.50 unknown https://doi.org/10.1016/0031-9422(96)00024-6
6,7-dimethoxy-4-[6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3-benzodioxol-5-yl]-1H-benzo[f][2]benzofuran-3-one 85219463 Click to see 542.50 unknown https://doi.org/10.1016/0031-9422(96)00024-6
9-(1,3-benzodioxol-5-yl)-4-[(2S,3R,4R)-4-hydroxy-4-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one 10258972 Click to see 674.60 unknown https://doi.org/10.1002/ARDP.200300841
9-(1,3-benzodioxol-5-yl)-4-[(2S,3R,4R)-4-hydroxy-4-(hydroxymethyl)-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxolan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one 163085795 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC4C(C(CO4)(CO)O)OC5C(C(C(CO5)O)O)O)COC3=O)C6=CC7=C(C=C6)OCO7)OC 644.60 unknown https://doi.org/10.1021/NP0101651
9-(1,3-benzodioxol-5-yl)-4-[(2S,3R,4S)-3-[(2S,3R,4S,5S)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-4-hydroxy-4-[[(2S,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxolan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one 163024776 Click to see 908.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.06.026
9-(1,3-benzodioxol-5-yl)-4-[4-hydroxy-4-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one 162845416 Click to see 674.60 unknown https://doi.org/10.1002/ARDP.200300841
Justicidinoside B 10507308 Click to see 572.50 unknown https://doi.org/10.1016/0031-9422(96)00024-6
Justicidinoside C 10650154 Click to see 542.50 unknown https://doi.org/10.1016/0031-9422(96)00024-6
Naphtho[2,3-c]furan-1(3H)-one, 4-(D-apio-beta-D-furanosyloxy)-9-(1,3-benzodioxol-5-yl)-6,7-dimethoxy- 13873812 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC4C(C(CO4)(CO)O)O)COC3=O)C5=CC6=C(C=C5)OCO6)OC 512.50 unknown https://doi.org/10.1016/0031-9422(96)00024-6
Procumbenoside A 10484309 Click to see 644.60 unknown via CMAUP database
Tuberculatin 10391676 Click to see 512.50 unknown https://doi.org/10.1016/0031-9422(96)00024-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Delta amino acids and derivatives
(1'S,3R,4'R,7'R,8'S)-2',2',7'-trimethylspiro[1H-indole-3,6'-3-azatricyclo[5.2.2.04,8]undecane]-2-one 10957881 Click to see 310.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
3-[[(1S,5R,7S)-8-methylidene-6-propan-2-yl-6-azabicyclo[3.2.1]oct-3-en-7-yl]methyl]-1H-indole 21587469 Click to see 292.40 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
4-(1,3-Benzodioxol-5-yl)-6,7-dimethoxybenzo[f][1]benzofuran-3-one 44365806 Click to see COC1=CC2=CC3=C(C(=O)CO3)C(=C2C=C1OC)C4=CC5=C(C=C4)OCO5 364.30 unknown https://doi.org/10.1021/NP960443+
> Organoheterocyclic compounds / Naphthofurans / Furanonaphthodioxoles
9-(1,3-Benzodioxol-5-yl)-5-methoxy-[1]benzofuro[6,5-f][1,3]benzodioxol-8-one 5321603 Click to see 378.30 unknown https://doi.org/10.1021/NP030142H
https://doi.org/10.1021/NP960443+
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
(1R,12R,15R,17S)-1,14,14-trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8-tetraen-16-one 21578492 Click to see 308.40 unknown via CMAUP database
(1R,12R,15S,17S)-1,14,14-trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8-tetraene 11098414 Click to see 294.40 unknown via CMAUP database

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