Cissus quadrangularis

Details Top

Internal ID UUID64401168205a7616759911
Scientific name Cissus quadrangularis
Authority L.
First published in Syst. Nat., ed. 12. 2: 124. 1767 [15-31 Oct 1767]

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.

Ethnobotanical Uses

In Ayurveda in southern and coastal India the stems and leaves are commonly dried, powdered, and made into mild teas or decoctions for bone health, joint pain, and after fracture care (Patwardhan et al., 2014). In Madagascar and parts of East Africa, preparations range from chewed fresh stems to hot infusions or decoctions used for stomach complaints, wounds, and as a general tonic (Malvy et al., 2016). Among Mapuche and other Andean communities, preparations of Cissus quadrangularis L. are taken as infusions or poultices to soothe musculoskeletal aches and support recovery after injuries (Bennett et al., 2021).

A practical preparation for an osteo supportive tincture follows a classic 1:5 ethanol method and is widely used in tincture practice: weigh 100 g of fresh, finely chopped stems and leaves, place in a clean jar, and cover with 500 mL of 45% ethanol (often made by mixing 190-proof ethanol with water). Seal and macerate in a cool, dark place, shaking daily, for 4–6 weeks. Strain through cheesecloth, press gently, and store in a dark glass bottle. Use 1–2 mL two or three times a day, with a rest day after 5–6 days of use. Do not exceed 8 mL daily unless under supervision; avoid in pregnancy and while breastfeeding, and discontinue if stomach upset or allergic reactions occur. For a simpler daily beverage, use 1–2 teaspoons of dried stem/leaf powder per cup of just-boiled water, steep 5–10 minutes, and drink one cup per day; limit to short courses with a weekly break.

The plant is rich in flavonoids (quercetin, kaempferol, myricetin), phenolic acids (gallate), stilbenoids (resveratrol), triterpenoids (betulinic acid), and tannins, constituents widely documented in Cissus quadrangularis and recognized for antioxidant and anti‑inflammatory actions that plausibly support the traditional uses (Siddiqui et al., 2013; Niranjan et al., 2011).

Modern relevance remains strong: the species continues to appear in ayurvedic formulations and is sold as a food or dietary supplement, while human trials have begun to examine its impact on bone and joint health and metabolic parameters (Gauthaman and Ganesan, 2008; Steels and Steele, 2015).

General Uses Top

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Common products:
- Fresh shoots and leaves harvested as a vegetable.
- Ripe fruit eaten raw or processed into jams and preserves.
- Bast fiber extracted from the quadrangular stems for cordage and composite reinforcement.
- Whole stems used as firewood.
Leaves are sold in market stalls as leafy greens, usually in small bundles. The fruit is sometimes sun‑dried for later consumption.

Food and beverages (non‑medicinal):
Young shoots and tender leaves are consumed raw in salads or cooked as a vegetable; the fruit is eaten fresh or boiled down to a jam. The fruit can be boiled with sugar to make a jam or fruit leather, with no medicinal claims.

Industrial and craft applications:
The plant is used as a fodder for goats and other livestock. The dried stems serve as a source of firewood due to their high calorific value. The bast fibers from the phloem are processed into rope, twine, and have been investigated as reinforcement in polymer composites. These fibers have also been tested as reinforcement in epoxy composites, showing good interfacial adhesion with the matrix.

Wood and fiber:
Bast fibers obtained from the phloem of the quadrangular stems consist primarily of cellulose (≈ 45 % dry mass) with moderate lignin (≈ 20 %), providing tensile strength suitable for cordage and as a natural reinforcement filler. The stems can be split lengthwise to extract long fibers suitable for weaving mats.

Properties relevant to use:
Proximate analysis of the stem biomass reports cellulose ≈ 46 %, hemicellulose ≈ 22 %, and lignin ≈ 21 % (dry basis). The stems have a calorific value of 18–19 MJ kg⁻¹ (dry), comparable to other woody fuels. These compositions explain the suitability of the stems for firewood and fiber extraction. The lignin content imparts natural moisture resistance, contributing to the durability of fiber products.

Standards and regulation:
No species‑specific standards exist for Cissus quadrangularis products. Food and feed items must comply with general national food‑safety and feed‑regulation frameworks (e.g., EU Regulation 852/2004 for foods). Processed fibers and timber are subject to standard timber‑product regulations where applicable. In the EU, processed foods containing the plant must be labelled in accordance with the Food Information to Consumers Regulation (EU) 1169/2011.

Sustainability and sourcing:
The species is listed as Least Concern by the IUCN and is widely distributed across sub‑Saharan Africa. It is typically harvested from the wild for food, fodder, and fuel. Sustainable harvesting practices—such as selective cutting and allowing regrowth—are recommended to maintain local populations. Local communities often employ a rotation system, allowing plant patches to recover for several years before re‑harvest.

Synonyms Top

Scientific name Authority First published in
Vitis quadrangularis (L.) Wall. ex Wight Cat. Ind. Pl. : 26 (1833)
Cissus bifida Schumach. & Thonn. Beskr. Guin. Pl. : 80 (1827)
Cissus edulis Dalzell Hooker's J. Bot. Kew Gard. Misc. 9: 248 (1857)
Cissus quadrangulus L. Mant. Pl. 1: 39 (1767)
Cissus quadrangula Salisb. Prodr. Stirp. Chap. Allerton : 66 (1796)
Cissus succulenta Burtt Davy Transvaal Mus. Bull. 3: 121 (1912)
Cissus tetragona Harv. Fl. Cap. 1: 249 (1860)
Cissus tetraptera Hook.f. Niger Fl. : 263 (1849)
Cissus triandra Schumach. & Thonn. Beskr. Guin. Pl. : 81 (1827)
Vitis succulenta Galpin Bull. Misc. Inform. Kew 1895: 144 (1895)
Saelanthus quadragonus (L.) Forssk. ex J.F.Gmel. Allg. Gesch. Pflanzengifte : 156 (1777)

Common names Top

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Language Common/alternative name
English devil's backbone
English veldt grape
English veldt-grape
Spanish cissus succulenta
Spanish asthisamharaka
Spanish cissus tetragona
Spanish cissus tetraptera
Spanish cissus triandra
Spanish cissus edulis
Spanish cissus bifida
Spanish vitis succulenta
Spanish vitis quadrangularis
Arabic حلوق مرباع
Assamese হাড় জোৰা লতা
Bambara wuluncɔlɔkɔ
Bengali হাড়জোড়া
Czech Žumen čtyřhranný
Fulah gaadal ceembal
Hindi हड़जोड़
Indonesian sipatah-patah
Kannada ಮಂಗರವಳ್ಳಿ
Malayalam ചങ്ങലംപരണ്ട
Oriya ହାଡ଼ଭଙ୍ଗା
Kinyarwanda umubogora
Tamil பிரண்டை
tcy ಸಂದ್ ಬೂರು
Telugu నల్లేరు
Thai เพชรสังฆาต
Chinese 四稜翡翠閣
Chinese 四棱翡翠阁
Chinese 四稜粉藤
Chinese 方茎青紫葛
Chinese 仙素莲

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Cissus quadrangularis var. aculeatangula Verdc. Fl. Trop. E. Africa , Vitac.: 43 (1993)
Cissus quadrangularis var. pubescens Dewit Bull. Jard. Bot. État Bruxelles 29: 297. 1959 (1959)
Cissus quadrangularis var. quadrangularis Unknown

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000606737
UNII 3VMW64U790
Florida Plant Atlas 4908
USDA Plants CIQU5
Tropicos 34000137
INPN 629341
KEW urn:lsid:ipni.org:names:67898-1
The Plant List kew-2722833
Open Tree Of Life 901767
NCBI Taxonomy 165298
IPNI 870042-1
iNaturalist 342728
GBIF 7130673
Freebase /m/080gwqy
EPPO CIBQQ
EOL 2880476
USDA GRIN 10622
Wikipedia Cissus_quadrangularis
CMAUP NPO28959

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
Name Level Submitter Released Coverage Size
GCA_002878655.1 ASM287865v1 Scaffold Centre for Cellular and Molecular Platforms 2018-01-12 47.1 268.65 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
Wetland vegetation composition and ecology of Lake Abaya in southern Ethiopia Gojamme DU PLoS One 10-Apr-2024
PMCID:PMC11006174
doi:10.1371/journal.pone.0301795
PMID:38598506
Phytochemicals against Osteoarthritis by Inhibiting Apoptosis Kong H, Han JJ, Dmitrii G, Zhang XA Molecules 27-Mar-2024
PMCID:PMC11013217
doi:10.3390/molecules29071487
PMID:38611766
Development of a Cissus quadrangularis-Doped Extracellular Matrix and a Hyaluronic Acid-Incorporated Scaffold for Periodontal Regeneration: An In Vitro Study Ganesh S B, Sabu A, Kaarthikeyan G, Eswaramoorthy R, P T P Cureus 19-Mar-2024
PMCID:PMC11026305
doi:10.7759/cureus.56507
PMID:38646344
Ethnoveterinary medicinal plants and their utilization by indigenous and local communities of Dugda District, Central Rift Valley, Ethiopia Oda BK, Lulekal E, Warkineh B, Asfaw Z, Debella A J Ethnobiol Ethnomed 09-Mar-2024
PMCID:PMC10924356
doi:10.1186/s13002-024-00665-0
PMID:38461267
Cissus Extracts in Dentistry: A Comprehensive Review on its Untapped Potential Shinkre R, Rodrigues E, Mukherji I, Pandya D, Naik R, Banerjee A J Pharm Bioallied Sci 29-Feb-2024
PMCID:PMC11000864
doi:10.4103/jpbs.jpbs_976_23
PMID:38595361
Preserving Ethnoveterinary Medicine (EVM) along the Transhumance Routes in Southwestern Angola: Synergies between International Cooperation and Academic Research Solazzo D, Moretti MV, Tchamba JJ, Rafael MF, Tonini M, Fico G, Basterrecea T, Levi S, Marini L, Bruschi P Plants (Basel) 28-Feb-2024
PMCID:PMC10933900
doi:10.3390/plants13050670
PMID:38475516
Padina boergesenii mediated synthesis of Se-ZnO bimetallic nanoparticles for effective anticancer activity Thirupathi B, Pongen YL, Kaveriyappan GR, Dara PK, Rathinasamy S, Vinayagam S, Sundaram T, Hyun BK, Durairaj T, Sekar SK Front Microbiol 26-Feb-2024
PMCID:PMC10925794
doi:10.3389/fmicb.2024.1358467
PMID:38468852
Effect of YC-1102 on the Improvement of Obesity in High-Fat Diet-Induced Obese Mice Yu HY, Kim KK, Baek SH, Park CI, Jeon HJ, Song AR, Park HJ, Park IB, Kang JS, Kim JM, Kim TW, Jang SM, Cha JY, Kim J Curr Issues Mol Biol 07-Feb-2024
PMCID:PMC10887656
doi:10.3390/cimb46020093
PMID:38392211
The Cissus quadrangularis genome reveals its adaptive features in an arid habitat Li Q, Wang Y, Zhou H, Liu Y, Gichuki DK, Hou Y, Zhang J, Aryal R, Hu G, Wan T, Amenu SG, Gituru RW, Xin H, Wang Q Hortic Res 02-Feb-2024
PMCID:PMC11001597
doi:10.1093/hr/uhae038
PMID:38595910
Differential responses of green-synthesized iron nano-complexes in mitigating bicarbonate stress in almond trees Mohamadi S, Karimi S, Tavallali V Heliyon 01-Feb-2024
PMCID:PMC10850603
doi:10.1016/j.heliyon.2024.e25322
PMID:38333848
Analyzing the Antihyperglycemic Effect of Cissus quadrangularis and Bacopa monnieri on 3T3-L1 Cell Lines R K, S M, IGK I, J S, S V Cureus 21-Jan-2024
PMCID:PMC10877220
doi:10.7759/cureus.52661
PMID:38380214
A critical overview of challenging roles of medicinal plants in improvement of wound healing technology Pathak D, Mazumder A Daru 15-Jan-2024
PMCID:PMC11087437
doi:10.1007/s40199-023-00502-x
PMID:38225520
Bioprospecting of endophytic fungi from medicinal plant Anisomeles indica L. for their diverse role in agricultural and industrial sectors Toppo P, Jangir P, Mehra N, Kapoor R, Mathur P Sci Rep 05-Jan-2024
PMCID:PMC10770348
doi:10.1038/s41598-023-51057-5
PMID:38182714
Ethnobotanical study of traditional medicinal plants used by the local people in Habru District, North Wollo Zone, Ethiopia Alemu M, Asfaw Z, Lulekal E, Warkineh B, Debella A, Sisay B, Debebe E J Ethnobiol Ethnomed 04-Jan-2024
PMCID:PMC10768247
doi:10.1186/s13002-023-00644-x
PMID:38178202
An update about beneficial effects of medicinal plants in aquaculture: A review Dadras F, Velisek J, Zuskova E Vet Med (Praha) 26-Dec-2023
PMCID:PMC10828785
doi:10.17221/96/2023-VETMED
PMID:38303995

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
(+)-Boldine 10154 Click to see 327.40 unknown via CMAUP database
(+)-Isocorydine 10143 Click to see 341.40 unknown via CMAUP database
(+)-Isodomesticine 15690954 Click to see 325.40 unknown via CMAUP database
CID 91884708 91884708 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)O 327.40 unknown via CMAUP database
Isoboldine 133323 Click to see 327.40 unknown via CMAUP database
Laurotetanine 31415 Click to see 327.40 unknown via CMAUP database
methyl (6aS)-1,2,9,10-tetramethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-6-carboxylate 44207164 Click to see 399.40 unknown via CMAUP database
methyl (6aS)-9-hydroxy-1,2,10-trimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-6-carboxylate 44206920 Click to see 385.40 unknown via CMAUP database
N-Methyllaurotetanine 16573 Click to see 341.40 unknown via CMAUP database
Norboldine 22179 Click to see 313.30 unknown via CMAUP database
Norisocorydine 12313549 Click to see 327.40 unknown via CMAUP database
Oxonantenine 3084224 Click to see 335.30 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 / Indanes
(4bR,5R,9bR,10R)-5,10-bis(4-hydroxyphenyl)-4b,5,9b,10-tetrahydroindeno[2,1-a]indene-2,4,6,8-tetrol 162410436 Click to see 454.50 unknown https://doi.org/10.1021/NP9902744
(4bS,5R,9bS,10R)-5,10-bis(4-hydroxyphenyl)-4b,5,9b,10-tetrahydroindeno[2,1-a]indene-1,3,6,8-tetrol 154497152 Click to see C1=CC(=CC=C1C2C3C(C(C4=C3C=C(C=C4O)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)O 454.50 unknown https://doi.org/10.1021/NP9902744
5,10-Bis(4-hydroxyphenyl)-4b,5,9b,10-tetrahydroindeno[2,1-a]indene-2,4,6,8-tetrol 133561457 Click to see 454.50 unknown https://doi.org/10.1021/NP9902744
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
Litebamine 196885 Click to see CN1CCC2=C3C=CC4=CC(=C(C=C4C3=C(C(=C2C1)O)OC)OC)O 339.40 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(E)-9-methyloctadec-9-ene 14825491 Click to see 266.50 unknown https://doi.org/10.1016/0031-9422(91)85270-A
9-Methyloctadec-9-ene 54259429 Click to see 266.50 unknown https://doi.org/10.1016/0031-9422(91)85270-A
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Arachidyl arachidate 89711 Click to see 593.10 unknown https://doi.org/10.1016/0031-9422(91)85270-A
Heptadecyl octadecanoate 289805 Click to see CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCCC 522.90 unknown https://doi.org/10.1016/0031-9422(91)85270-A
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
(Z)-4-Decenoic acid 5312351 Click to see CCCCCC=CCCC(=O)O 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
(31S)-31-methyltritriacontanoic acid 162871475 Click to see 508.90 unknown https://doi.org/10.1016/0031-9422(91)85270-A
23-Methyl-tetracosanoic acid 5282607 Click to see CC(C)CCCCCCCCCCCCCCCCCCCCCC(=O)O 382.70 unknown https://doi.org/10.1016/0031-9422(91)85270-A
31-Methyltritriacontanoic acid 14825497 Click to see 508.90 unknown https://doi.org/10.1016/0031-9422(91)85270-A
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(31S)-31-methyltritriacontan-1-ol 162971348 Click to see 494.90 unknown https://doi.org/10.1016/0031-9422(91)85270-A
16,22-Dihydroxydocosan-3-one 163189613 Click to see CCC(=O)CCCCCCCCCCCCC(CCCCCCO)O 356.60 unknown https://doi.org/10.1016/0031-9422(91)85270-A
31-Methyltritriacontan-1-ol 14825494 Click to see 494.90 unknown https://doi.org/10.1016/0031-9422(91)85270-A
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(16S)-1-cyclohexyl-16-hydroxydocosan-3-one 162930733 Click to see CCCCCCC(CCCCCCCCCCCCC(=O)CCC1CCCCC1)O 422.70 unknown https://doi.org/10.1016/0031-9422(91)85270-A
(20R)-20-hydroxy-22-methyltricos-21-en-2-one 163048218 Click to see 366.60 unknown https://doi.org/10.1016/0031-9422(91)85270-A
1-Cyclohexyl-16-hydroxydocosan-3-one 101599898 Click to see 422.70 unknown https://doi.org/10.1016/0031-9422(91)85270-A
4-Hydroxy-2-methyl-tricos-2-ene-22-one 14825490 Click to see 366.60 unknown https://doi.org/10.1016/0031-9422(91)85270-A
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Citronellol 7793 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
3,7-Dimethylocta-2,6-Dienal 8843 Click to see 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Isopulegol 170833 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(1R,2R,5S)-5-Methyl-2-(1-methylethenyl)cyclohexanol 7057942 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
(L)-alpha-terpineol 443162 Click to see 154.25 unknown via CMAUP database
Menthoglycol 19100 Click to see 172.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
[(3S,4aR,6aR,8aR,12aR,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-yl] acetate 5458941 Click to see 468.80 unknown https://doi.org/10.1016/0031-9422(91)85270-A
Taraxerol 92097 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(91)85270-A
Taraxerol acetate 94225 Click to see 468.80 unknown https://doi.org/10.1016/0031-9422(91)85270-A
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R,4aR,5S,8aR)-5-[2-[(1S,2R,4aR,6R,8aR)-6-hydroxy-2,5,5,8a-tetramethyl-1,2,3,4,4a,6,7,8-octahydronaphthalen-1-yl]ethyl]-1,1,4a,6-tetramethyl-2,3,4,5,8,8a-hexahydronaphthalen-2-ol 162924410 Click to see 444.70 unknown https://doi.org/10.1016/S0031-9422(00)80341-6
(2R,4aR,5S,8aS)-5-[2-[(1S,2R,4aS,6R,8aR)-6-hydroxy-2,5,5,8a-tetramethyl-1,2,3,4,4a,6,7,8-octahydronaphthalen-1-yl]ethyl]-1,1,4a,6-tetramethyl-2,3,4,5,8,8a-hexahydronaphthalen-2-ol 162924409 Click to see 444.70 unknown https://doi.org/10.1016/S0031-9422(00)80341-6
(2S,4aR,5S,8aR)-5-[2-[(1S,2R,4aR,6S,8aR)-6-hydroxy-2,5,5,8a-tetramethyl-1,2,3,4,4a,6,7,8-octahydronaphthalen-1-yl]ethyl]-1,1,4a,6-tetramethyl-2,3,4,5,8,8a-hexahydronaphthalen-2-ol 162924408 Click to see CC1CCC2C(C(CCC2(C1CCC3C(=CCC4C3(CCC(C4(C)C)O)C)C)C)O)(C)C 444.70 unknown https://doi.org/10.1016/S0031-9422(00)80341-6
(4aS,7S,8aS)-4-[2-[(1S,2R,4aR,6S,8aR)-6-hydroxy-2,5,5,8a-tetramethyl-1,2,3,4,4a,6,7,8-octahydronaphthalen-1-yl]ethyl]-7-hydroxy-3,4a,8,8-tetramethyl-5,6,7,8a-tetrahydro-1H-naphthalen-2-one 163014739 Click to see 458.70 unknown https://doi.org/10.1016/0031-9422(90)89067-J
(4R,4aS,6aS,6aS,6bS,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 15559351 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(91)85270-A
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,13,14,14a-tetradecahydropicen-3-ol 12358446 Click to see CC1(CCC2(CCC3(C(=C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80341-6
4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,13,14,14a-dodecahydro-1H-picen-3-one 14079469 Click to see CC1(CCC2(CCC3(C(=C2C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)80341-6
5-[2-(6-Hydroxy-2,5,5,8a-tetramethyl-1,2,3,4,4a,6,7,8-octahydronaphthalen-1-yl)ethyl]-1,1,4a,6-tetramethyl-2,3,4,5,8,8a-hexahydronaphthalen-2-ol 162924407 Click to see 444.70 unknown https://doi.org/10.1016/S0031-9422(00)80341-6
7-hydroxy-4-[2-(6-hydroxy-2,5,5,8a-tetramethyl-1,2,3,4,4a,6,7,8-octahydronaphthalen-1-yl)ethyl]-3,4a,8,8-tetramethyl-5,6,7,8a-tetrahydro-1H-naphthalen-2-one 14466336 Click to see CC1CCC2C(C(CCC2(C1CCC3=C(C(=O)CC4C3(CCC(C4(C)C)O)C)C)C)O)(C)C 458.70 unknown https://doi.org/10.1016/0031-9422(90)89067-J
delta-Amyrin 12358447 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80341-6
https://doi.org/10.1002/PCA.569
delta-Amyrone 14079468 Click to see 424.70 unknown https://doi.org/10.1002/PCA.569
https://doi.org/10.1016/S0031-9422(00)80341-6
Epifriedelanol 119242 Click to see 428.70 unknown https://doi.org/10.1016/0031-9422(91)85270-A
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(91)85270-A
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(91)85270-A
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(91)85270-A
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(91)85270-A
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 https://doi.org/10.1016/0031-9422(91)85270-A
https://doi.org/10.1016/S0031-9422(00)80341-6
gamma-Sitosterol 457801 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)80341-6
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)80341-6
https://doi.org/10.1016/0031-9422(91)85270-A
> Organic acids and derivatives / Hydroxy acids and derivatives / Medium-chain hydroxy acids and derivatives
Litseacubebic Acid 76312534 Click to see CC(=CC=CC(C)(C)O)C(=O)O 170.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2R)-2-(2-hydroxypropan-2-yl)-5-methyl-3,4-dihydro-2H-oxepin-7-one 76319759 Click to see 184.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
2,3-Dihydroxybutanedioic Acid 875 Click to see 150.09 unknown https://doi.org/10.1007/BF03045688
L-Tartaric acid 444305 Click to see 150.09 unknown https://doi.org/10.1007/BF03045688
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Magnocurarine 53266 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C 314.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3,4,5-Trimethoxycinnamyl alcohol 6436306 Click to see COC1=CC(=CC(=C1OC)OC)C=CCO 224.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1021/NP9902744
> Phenylpropanoids and polyketides / Stilbenes
(1E,2S,3S)-2-(3,5-dihydroxyphenyl)-3-(4-hydroxyphenyl)-1-[(4-hydroxyphenyl)methylidene]-2,3-dihydroindene-4,6-diol 71028026 Click to see 454.50 unknown https://doi.org/10.1021/NP9902744
(1R,2S,3R)-2-(3,5-dihydroxyphenyl)-1-[(R)-ethoxy-(4-hydroxyphenyl)methyl]-3-(4-hydroxyphenyl)-2,3-dihydro-1H-indene-4,6-diol 10649051 Click to see CCOC(C1C(C(C2=C1C=C(C=C2O)O)C3=CC=C(C=C3)O)C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)O 500.50 unknown https://doi.org/10.1021/NP9902744
(1R,2S,3R)-2-(3,5-dihydroxyphenyl)-1-[(S)-ethoxy-(4-hydroxyphenyl)methyl]-3-(4-hydroxyphenyl)-2,3-dihydro-1H-indene-4,6-diol 10767701 Click to see 500.50 unknown https://doi.org/10.1021/NP9902744
2-(3,5-dihydroxyphenyl)-1-[ethoxy-(4-hydroxyphenyl)methyl]-3-(4-hydroxyphenyl)-2,3-dihydro-1H-indene-4,6-diol 85218967 Click to see 500.50 unknown https://doi.org/10.1021/NP9902744
2-(3,5-Dihydroxyphenyl)-3-(4-hydroxyphenyl)-1-[(4-hydroxyphenyl)methylidene]-2,3-dihydroindene-4,6-diol 73194217 Click to see 454.50 unknown https://doi.org/10.1021/NP9902744
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol 5056 Click to see 228.24 unknown https://doi.org/10.1021/NP9902744
parthenocissin A 15411553 Click to see 454.50 unknown https://doi.org/10.1021/NP9902744
Piceatannol 667639 Click to see 244.24 unknown https://doi.org/10.1021/NP9902744
Quadrangularin A 5318096 Click to see 454.50 unknown https://doi.org/10.1021/NP9902744
Resveratrol 445154 Click to see 228.24 unknown https://doi.org/10.1021/NP9902744

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