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Cissus quadrangularis

Cissus quadrangularis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

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]

Description Top

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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)

Common names Top

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Language Common/alternative name
English veldt-grape
Spanish asthisamharaka
Arabic حلوق مرباع
Assamese হাড় জোৰা লতা
Bambara wuluncɔlɔkɔ
Bengali হাড়জোড়া
Czech Žumen čtyřhranný
Fulah gaadal ceembal
Hindi हड़जोड़
Kannada ಮಂಗರವಳ್ಳಿ
Malayalam ചങ്ങലംപരണ്ട
Oriya ହାଡ଼ଭଙ୍ଗା
Kinyarwanda umubogora
Tamil பிரண்டை
tcy ಸಂದ್ ಬೂರು
Telugu నల్లేరు
Thai เพชรสังฆาต
Chinese 四稜粉藤
Chinese 方茎青紫葛
Chinese 四棱翡翠阁
Chinese 四稜翡翠閣
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)

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

Suggest others/fix!
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!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_002878655.1 ASM287865v1 Scaffold Centre for Cellular and Molecular Platforms 2018-01-12 47.1x 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
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
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
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
Determinants of plant community along environmental gradients in Geramo forest, the western escarpment of the rift valley of Ethiopia Getaneh ZA, Demissew S, Woldu Z, Aynekulu E PLoS One 27-Nov-2023
PMCID:PMC10681247
doi:10.1371/journal.pone.0294324
PMID:38011089
Anticancer Property of Digera muricata Leaf Extract: An In Vitro Study Varadarajan PS, Roy A, Jagadeswaran D Cureus 23-Nov-2023
PMCID:PMC10746918
doi:10.7759/cureus.49276
PMID:38143601
Green Synthesis of Metal and Metal Oxide Nanoparticles: A Review of the Principles and Biomedical Applications Radulescu DM, Surdu VA, Ficai A, Ficai D, Grumezescu AM, Andronescu E Int J Mol Sci 20-Oct-2023
PMCID:PMC10607471
doi:10.3390/ijms242015397
PMID:37895077
Dietary supplementation of Polygonum chinense improves the immunity of Asian seabass, Lates calcarifer (Bloch, 1790) against Vibrio harveyi infection Rashidah AR, Shariff M, Yusoff FM, Ismail IS Fish Shellfish Immunol Rep 01-Oct-2023
PMCID:PMC10563064
doi:10.1016/j.fsirep.2023.100118
PMID:37822351
Potential Curative Effects of Aqueous Extracts of Cissus quadrangularis (Vitaceae) and Jatropha gossypiifolia (Euphorbiaceae) on Acetaminophen-Induced Liver Injury in Mice Guemmogne Temdie RJ, Ymele Chiogo Vouffo E, Tietcheu Galani BR, Dabole Ladane B, Bianzoumbe J, Kuum Minoue MG, Ntchapda F, Dimo T Curr Ther Res Clin Exp 30-Sep-2023
PMCID:PMC10587700
doi:10.1016/j.curtheres.2023.100716
PMID:37869400

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
(+)-Isodomesticine 15690954 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC5=C(C=C43)OCO5)OC)O 325.40 unknown via CMAUP database
(6aS)-1,2,9,10-Tetramethoxy-4,5,6,6aalpha-tetrahydro-7H-dibenzo[de,g]quinoline-6-carboxylic acid methyl ester 44207164 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)OC)N(CCC3=C1)C(=O)OC)OC 399.40 unknown via CMAUP database
(6aS)-9-Hydroxy-1,2,10-trimethoxy-4,5,6,6aalpha-tetrahydro-7H-dibenzo[de,g]quinoline-6-carboxylic acid methyl ester 44206920 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)N(CCC3=C1)C(=O)OC)OC 385.40 unknown via CMAUP database
Boldine 10154 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown via CMAUP database
Boldine 2-methyl ether 16573 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC 341.40 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 CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown via CMAUP database
Isocorydine 10143 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown via CMAUP database
Laurolitsine 22179 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O 313.30 unknown via CMAUP database
Laurotetanine 31415 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC 327.40 unknown via CMAUP database
Norisocorydine 12313549 Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O 327.40 unknown via CMAUP database
Oxonantenine 3084224 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC5=C(C=C42)OCO5)OC 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 C1=CC(=CC=C1C2C3C(C(C4=C3C=C(C=C4O)O)C5=CC=C(C=C5)O)C6=C2C=C(C=C6O)O)O 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 C1=CC(=CC=C1C2C3C(C(C4=C3C=C(C=C4O)O)C5=CC=C(C=C5)O)C6=C2C=C(C=C6O)O)O 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 CCCCCCCCC=C(C)CCCCCCCC 266.50 unknown https://doi.org/10.1016/0031-9422(91)85270-A
9-Methyloctadec-9-ene 54259429 Click to see CCCCCCCCC=C(C)CCCCCCCC 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 CCCCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCCCC 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 CCC(C)CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 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 CCC(C)CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 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 CCC(C)CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 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 CCC(C)CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 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 CC(=CC(CCCCCCCCCCCCCCCCCC(=O)C)O)C 366.60 unknown https://doi.org/10.1016/0031-9422(91)85270-A
1-Cyclohexyl-16-hydroxydocosan-3-one 101599898 Click to see CCCCCCC(CCCCCCCCCCCCC(=O)CCC1CCCCC1)O 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 CC(=CC(CCCCCCCCCCCCCCCCCC(=O)C)O)C 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-Dimethyl-2,6-octadien-1-al 8843 Click to see CC(=CCCC(=CC=O)C)C 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
(-)-alpha-Terpineol 443162 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
(-)-Isopulegol 170833 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 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
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Menthoglycol 19100 Click to see CC1CCC(C(C1)O)C(C)(C)O 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 CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(91)85270-A
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(91)85270-A
Taraxerol acetate 94225 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 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 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
(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 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
(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 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
(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
13(18)-Oleanen-3-one 14079468 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/10.1002/PCA.569
https://doi.org/10.1016/S0031-9422(00)80341-6
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 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
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 CC1(CCC2(CCC3(C(=C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1002/PCA.569
https://doi.org/10.1016/S0031-9422(00)80341-6
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/0031-9422(91)85270-A
Friedelan-3-one 244297 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
Friedelin 91472 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
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
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
24-Ethylcholest-5-en-3beta-ol 22012 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/S0031-9422(00)80341-6
https://doi.org/10.1016/0031-9422(91)85270-A
Beta-Sitosterol 222284 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
Clionasterol 457801 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/S0031-9422(00)80341-6
> 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 CC1=CC(=O)OC(CC1)C(C)(C)O 184.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
DL-Tartaric acid 875 Click to see C(C(C(=O)O)O)(C(=O)O)O 150.09 unknown https://doi.org/10.1007/BF03045688
L-Tartaric acid 444305 Click to see C(C(C(=O)O)O)(C(=O)O)O 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 C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 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 C1=CC(=CC=C1C=C2C(C(C3=C2C=C(C=C3O)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 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 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
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]- 5056 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 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 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
2-(3,5-Dihydroxyphenyl)-3-(4-hydroxyphenyl)-1-[(4-hydroxyphenyl)methylidene]-2,3-dihydroindene-4,6-diol 73194217 Click to see C1=CC(=CC=C1C=C2C(C(C3=C2C=C(C=C3O)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1021/NP9902744
parthenocissin A 15411553 Click to see C1=CC(=CC=C1C=C2C(C(C3=C2C=C(C=C3O)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1021/NP9902744
Piceatannol 667639 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://doi.org/10.1021/NP9902744
quadrangularin A 5318096 Click to see C1=CC(=CC=C1C=C2C(C(C3=C2C=C(C=C3O)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1021/NP9902744
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1021/NP9902744

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