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Cocculus laurifolius

Cocculus laurifolius - 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 UUID644012624a277779963808
Scientific name Cocculus laurifolius
Authority DC.
First published in Syst. Nat. 1: 520 (1817)

Description Top

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Synonyms Top

Scientific name Authority First published in
Menispermum laurifolium Roxb. Fl. Ind. ed. 1832 , 3: 815 (1832)
Cebatha laurifolia (DC.) Kuntze Revis. Gen. Pl. 1: 9 (1891)
Cinnamomum esquirolii H.Lév. Fl. Kouy-Tchéou : 218 (1915)
Cocculus angustifolius Hassk. Cat. Hort. Bot. Bogor. Alt. : 172 (1844)
Cocculus bariensis Pierre ex Gagnep. Fl. Indo-Chine 1: 141 (1908)
Galloa trinervis Hassk. Cat. Hort. Bot. Bogor. Alt. : 172 (1844)
Holopeira laurifolia (DC.) Miers Ann. Mag. Nat. Hist. , ser. 3, 19: 29 (1867)

Common names Top

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Language Common/alternative name
English laurel-leaf snailseed
Arabic عنيبية غارية الأوراق
Catalan còcul
Catalan còccul
Hebrew סהרון קשה עלים
Malayalam ആടുകൊല്ലി
Russian Коккулус лавролистный
Chinese 衡州乌药
Chinese 樟叶木防己
Chinese 樟葉木防己
Chinese 牛十八
Chinese 铁面虎

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • West Himalaya
    • Indo-China
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Philippines
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000613563
USDA Plants COLA20
Tropicos 20600005
INPN 629387
KEW urn:lsid:ipni.org:names:580575-1
The Plant List kew-2729674
Open Tree Of Life 918349
NCBI Taxonomy 152359
IUCN Red List 208114450
IPNI 580575-1
iNaturalist 135341
GBIF 3829341
Freebase /m/03cj47l
EPPO COULA
EOL 2886371
USDA GRIN 312658
Wikipedia Cocculus_laurifolius

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
A cornucopia of diversity—Ranunculales as a model lineage Becker A, Bachelier JB, Carrive L, Conde e Silva N, Damerval C, Del Rio C, Deveaux Y, Di Stilio VS, Gong Y, Jabbour F, Kramer EM, Nadot S, Pabón-Mora N, Wang W J Exp Bot 18-Dec-2023
PMCID:PMC10967251
doi:10.1093/jxb/erad492
PMID:38109712
Ethnobotanical study on herbal tea drinks in Guangxi, China Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064729
doi:10.1186/s13002-023-00579-3
PMID:37004116
Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 12-May-2022
PMCID:PMC9096882
doi:10.2903/j.efsa.2022.7298
PMID:35592020
What does ‘toughness’ look like? An examination of the breakdown of young and mature leaves under cyclical loading Traff J, Daegling DJ Interface Focus 13-Aug-2021
PMCID:PMC8361580
doi:10.1098/rsfs.2020.0087
PMID:34938435
Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM Plants (Basel) 04-Jul-2021
PMCID:PMC8309379
doi:10.3390/plants10071367
PMID:34371570
Erythrina velutina Willd. alkaloids: Piecing biosynthesis together from transcriptome analysis and metabolite profiling of seeds and leaves Chacon DS, Torres TM, da Silva IB, de Araújo TF, Roque AD, Pinheiro FA, Selegato D, Pilon A, Reginaldo FP, da Costa CT, Vilasboa J, Freire RT, Voigt EL, Zuanazzi JA, Libonati R, Rodrigues JA, Santos FL, Scortecci KC, Lopes NP, Ferreira LD, dos Santos LV, Cavalheiro AJ, Fett-Neto AG, Giordani RB J Adv Res 10-Feb-2021
PMCID:PMC8655131
doi:10.1016/j.jare.2021.01.017
PMID:35024185
Natural Products and Their Bioactive Compounds: Neuroprotective Potentials against Neurodegenerative Diseases Mohd Sairazi NS, Sirajudeen KN Evid Based Complement Alternat Med 14-Feb-2020
PMCID:PMC7042511
doi:10.1155/2020/6565396
PMID:32148547
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
Alkaloids of the Leaves of Cocculus laurifolius DC. (3) Structures of Erythlaurine and Erythramide MOTOHARU JUICHI, YUKARI FUJITANI, HIROSHI FURUKAWA Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.104.9_946
VI Mitteilung ueber die Alkaloide von Sinomenium-und Cocculusarten : Ueber das Alkaloid von Cocculus laurifolius D. C. T. Kondo, H. Kondo Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1881.1925.524_876
Novel Approach to Classify Plants Based on Metabolite-Content Similarity Liu K, Abdullah AA, Huang M, Nishioka T, Altaf-Ul-Amin M, Kanaya S Biomed Res Int 09-Jan-2017
PMCID:PMC5253511
doi:10.1155/2017/5296729
PMID:28164123
Isolation and Characterization of Reticuline N-Methyltransferase Involved in Biosynthesis of the Aporphine Alkaloid Magnoflorine in Opium Poppy Morris JS, Facchini PJ J Biol Chem 15-Sep-2016
PMCID:PMC5095398
doi:10.1074/jbc.M116.750893
PMID:27634038
Endocarps of menispermaceous plants in Taiwan Yang SZ, Chen PH Bot Stud 15-Jul-2016
PMCID:PMC5432898
doi:10.1186/s40529-016-0129-7
PMID:28597424
Coclauril, a nonglucosidic 2-cyclohexen-1-ylideneacetonitrile, from Cocculus lauriforius DC. Motoi YOGO, Satoko ISHIGURO, Hiroyuki MURATA, Hiroshi FURUKAWA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.38.225
Studies on the Alkaloids of Menispermaceous Plants. CI. : Alkaloids of Cocculus laurifolius DC. (Suppl. III) Masao Tomita, Fuyuki Kusuda Pharmaceutical Society of Japan 25-Oct-2011
doi:10.1248/CPB1953.1.1

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
CID 12305611 12305611 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC)C 342.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
Glaucine 16754 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
https://doi.org/10.1007/BF00629835
Norisoboldine 14539911 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)O 313.30 unknown https://doi.org/10.1007/BF00629835
S-(+)-N-methylcorydine 52949574 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC)C 356.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
Talikmidine 12151115 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=CC(=C2)OC)OC)OC 325.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
> Alkaloids and derivatives / Erythrina alkaloids / Erythrinanes
(13bS)-2,12-dimethoxy-5,6,8,9-tetrahydroindolo[7a,1-a]isoquinolin-3-one 162869118 Click to see COC1=CC2=C(CCN3C24C=C(C(=O)C=C4CC3)OC)C=C1 297.30 unknown https://doi.org/10.1016/0040-4020(80)88040-9
(2R,13bS)-12-hydroxy-2-methoxy-1,2,8,9-tetrahydroindolo[7a,1-a]isoquinolin-6-one 154496358 Click to see COC1CC23C(=CC(=O)N2CCC4=C3C=C(C=C4)O)C=C1 283.32 unknown https://doi.org/10.1016/0040-4020(80)88040-9
(2R,13bS)-2,12-dimethoxy-1,2,5,6,8,9-hexahydroindolo[7a,1-a]isoquinolin-3-one 162885972 Click to see COC1CC23C(=CC1=O)CCN2CCC4=C3C=C(C=C4)OC 299.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
(2R,13bS)-2,12-dimethoxy-1,2,8,9-tetrahydroindolo[7a,1-a]isoquinolin-6-one 163016314 Click to see COC1CC23C(=CC(=O)N2CCC4=C3C=C(C=C4)OC)C=C1 297.30 unknown https://doi.org/10.1016/0040-4020(80)88040-9
(2R,13bS)-2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline 162864647 Click to see COC1CC23C(=CCN2CCC4=C3C=C(C=C4)OC)C=C1 283.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
(2R,3R,13bS)-2-methoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinoline-3,12-diol 162949024 Click to see COC1CC23C(=CC1O)CCN2CCC4=C3C=C(C=C4)O 287.35 unknown https://doi.org/10.1016/0040-4020(80)88040-9
(2R,3R,13bS)-2,12-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-3-ol 162992005 Click to see COC1CC23C(=CC1O)CCN2CCC4=C3C=C(C=C4)OC 301.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
(2R,4aR,13bS)-2-methoxy-2,4a,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-12-ol 163041801 Click to see COC1CC23C(CCN2CCC4=C3C=C(C=C4)O)C=C1 271.35 unknown https://doi.org/10.1016/0040-4020(80)88040-9
(2R,4aR,9R,13bS)-2,9-dimethoxy-2,4a,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-12-ol 162904271 Click to see COC1CC23C(CCN2CC(C4=C3C=C(C=C4)O)OC)C=C1 301.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
(2R,4aS,13bS)-2-methoxy-2,4a,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-12-ol 163041802 Click to see COC1CC23C(CCN2CCC4=C3C=C(C=C4)O)C=C1 271.35 unknown https://doi.org/10.1016/0040-4020(80)88040-9
(2R,4aS,13bS)-2,12-dimethoxy-2,4a,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinoline 163029889 Click to see COC1CC23C(CCN2CCC4=C3C=C(C=C4)OC)C=C1 285.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
(2R,4aS,9S,13bS)-2,9-dimethoxy-2,4a,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-12-ol 162904270 Click to see COC1CC23C(CCN2CC(C4=C3C=C(C=C4)O)OC)C=C1 301.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
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/10.1016/0040-4020(80)88040-9
12-Hydroxy-2-methoxy-1,2,8,9-tetrahydroindolo[7a,1-a]isoquinolin-6-one 162852127 Click to see COC1CC23C(=CC(=O)N2CCC4=C3C=C(C=C4)O)C=C1 283.32 unknown https://doi.org/10.1016/0040-4020(80)88040-9
2-methoxy-2,4a,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-12-ol 163041800 Click to see COC1CC23C(CCN2CCC4=C3C=C(C=C4)O)C=C1 271.35 unknown https://doi.org/10.1016/0040-4020(80)88040-9
2-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-12-ol 78302584 Click to see COC1CC23C(=CCN2CCC4=C3C=C(C=C4)O)C=C1 269.34 unknown https://doi.org/10.1007/BF01937378
https://doi.org/10.1016/0040-4020(80)88040-9
2,11-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinoline-12-carboxamide 162889932 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C=C4CC3)OC)C(=O)N 328.40 unknown https://doi.org/10.1248/YAKUSHI1947.104.9_946
2,12-Dimethoxy-1,2,5,6,8,9-hexahydroindolo[7a,1-a]isoquinolin-3-one 162885971 Click to see COC1CC23C(=CC1=O)CCN2CCC4=C3C=C(C=C4)OC 299.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
2,12-Dimethoxy-1,2,8,9-tetrahydroindolo[7a,1-a]isoquinolin-6-one 132539037 Click to see COC1CC23C(=CC(=O)N2CCC4=C3C=C(C=C4)OC)C=C1 297.30 unknown https://doi.org/10.1016/0040-4020(80)88040-9
2,12-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-3-ol 162992004 Click to see COC1CC23C(=CC1O)CCN2CCC4=C3C=C(C=C4)OC 301.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
2,12-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinoline 15834863 Click to see COC1CC=C2CCN3C2(C1)C4=C(CC3)C=CC(=C4)OC 285.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
2,12-dimethoxy-2,4a,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinoline 3488097 Click to see COC1CC23C(CCN2CCC4=C3C=C(C=C4)OC)C=C1 285.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline 162864646 Click to see COC1CC23C(=CCN2CCC4=C3C=C(C=C4)OC)C=C1 283.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
2,12-Dimethoxy-5,6,8,9-tetrahydroindolo[7a,1-a]isoquinolin-3-one 162869117 Click to see COC1=CC2=C(CCN3C24C=C(C(=O)C=C4CC3)OC)C=C1 297.30 unknown https://doi.org/10.1016/0040-4020(80)88040-9
2,9-dimethoxy-2,4a,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-12-ol 162904269 Click to see COC1CC23C(CCN2CC(C4=C3C=C(C=C4)O)OC)C=C1 301.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
Cocculine 21769966 Click to see COC1CC=C2CCN3C2(C1)C4=C(CC3)C=CC(=C4)O 271.35 unknown https://doi.org/10.1016/0040-4020(80)88040-9
https://doi.org/10.1007/BF00629835
Cocculitine 72945082 Click to see COC1CC=C2CCN3C2(C1)C4=C(CC3)C=CC(=C4)OC 285.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
Coccuvine 3085221 Click to see COC1CC23C(=CCN2CCC4=C3C=C(C=C4)O)C=C1 269.34 unknown https://doi.org/10.1007/BF01937378
https://doi.org/10.1016/0040-4020(80)88040-9
Dihydroerysodine 22295116 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C=C4CC3)O)OC 301.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
https://doi.org/10.1248/CPB1953.4.225
Dihydroerysodine 618044 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C=C4CC3)O)OC 301.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
https://doi.org/10.1248/CPB1953.4.225
methyl (2S,13bS)-2,11-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinoline-12-carboxylate 12308908 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C=C4CC3)OC)C(=O)OC 343.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
methyl 10-hydroxy-2,11-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinoline-12-carboxylate 163041803 Click to see COC1CC=C2CCN3C2(C1)C4=C(CC3)C(=C(C(=C4)C(=O)OC)OC)O 359.40 unknown https://doi.org/10.1248/YAKUSHI1947.104.9_946
methyl 2,11-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinoline-12-carboxylate 5317208 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C=C4CC3)OC)C(=O)OC 343.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
https://doi.org/10.1248/YAKUSHI1947.104.9_946
> Alkaloids and derivatives / Phthalide isoquinolines
(+)-Corlumine 5316069 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown https://doi.org/10.1016/S0040-4020(01)87469-X
Corlumine 72615 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown https://doi.org/10.1016/S0040-4020(01)87469-X
> Alkaloids and derivatives / Proaporphines
(+)-Stepharine 193686 Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC 297.30 unknown https://doi.org/10.1016/0040-4020(80)88040-9
Pronuciferine 200480 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC 311.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
Stepharine 98455 Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC 297.30 unknown https://doi.org/10.1016/0040-4020(80)88040-9
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
3,9-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,10-diol 5290 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)O 327.40 unknown https://doi.org/10.1248/YAKUSHI1947.104.9_946
Cavidine 193148 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC5=C4OCO5)OC)OC 353.40 unknown https://doi.org/10.1016/S0040-4020(01)87469-X
D-Tetrahydropalmatine 969488 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown https://doi.org/10.1016/S0040-4020(01)91809-5
l-Stepholidine 6917970 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)O 327.40 unknown https://doi.org/10.1248/YAKUSHI1947.104.9_946
Sinactine 5321317 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)OC 339.40 unknown https://doi.org/10.1016/S0040-4020(01)88546-X
Tetrahydropalmatine 72301 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown https://doi.org/10.1016/S0040-4020(01)91809-5
Tetrahyeroepiberberine 12442795 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)OC 339.40 unknown https://doi.org/10.1016/0040-4020(75)80272-9
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1248/CPB.38.225
> Benzenoids / Benzene and substituted derivatives / Styrenes
4-[(Z)-2-[[(1S,5S)-5-hydroxy-2-methylcyclohex-2-en-1-yl]-methylamino]ethenyl]phenol 163191122 Click to see CC1=CCC(CC1N(C)C=CC2=CC=C(C=C2)O)O 259.34 unknown https://doi.org/10.1007/BF00629835
4-[(Z)-2-[[(1S,5S)-5-methoxy-2-methylcyclohex-2-en-1-yl]-methylamino]ethenyl]phenol 163011136 Click to see CC1=CCC(CC1N(C)C=CC2=CC=C(C=C2)O)OC 273.37 unknown https://doi.org/10.1007/BF00629835
4-[2-[(5-Hydroxy-2-methylcyclohex-2-en-1-yl)-methylamino]ethenyl]phenol 162940686 Click to see CC1=CCC(CC1N(C)C=CC2=CC=C(C=C2)O)O 259.34 unknown https://doi.org/10.1007/BF00629835
4-[2-[(5-Methoxy-2-methylcyclohex-2-en-1-yl)-methylamino]ethenyl]phenol 163011134 Click to see CC1=CCC(CC1N(C)C=CC2=CC=C(C=C2)O)OC 273.37 unknown https://doi.org/10.1007/BF00629835
> Benzenoids / Phenanthrenes and derivatives
4,5,13-Trimethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6,10,13-pentaen-12-one 5255766 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=CC(=C(C=C34)OC)OC)OC 341.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
O-Methylflavinantine 11724883 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=CC(=C(C=C34)OC)OC)OC 341.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
https://doi.org/10.1248/YAKUSHI1947.104.9_946
> Benzenoids / Phenol ethers / Anisoles
4,16-Dimethoxy-10-methyl-10-azatricyclo[11.4.0.02,7]heptadeca-1(13),2,4,6,14,16-hexaen-5-ol 85846863 Click to see CN1CCC2=C(C=C(C=C2)OC)C3=CC(=C(C=C3CC1)O)OC 313.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
4,5,16-Trimethoxy-10-methyl-10-azatricyclo[11.4.0.02,7]heptadeca-1(13),2,4,6,14,16-hexaene 85846862 Click to see CN1CCC2=C(C=C(C=C2)OC)C3=CC(=C(C=C3CC1)OC)OC 327.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
https://doi.org/10.1039/P19760002197
5,16-Dimethoxy-10-methyl-10-azatricyclo[11.4.0.02,7]heptadeca-1(13),2,4,6,14,16-hexaen-4-ol 21768993 Click to see CN1CCC2=C(C=C(C=C2)OC)C3=CC(=C(C=C3CC1)OC)O 313.40 unknown https://doi.org/10.1039/P19760002197
Laurifine 442309 Click to see COC1=CC2=C(CCNCCC3=CC(=C(C=C32)OC)OC)C=C1 313.40 unknown https://doi.org/10.1039/P19760002197
> Lignans, neolignans and related compounds
13,27-Dimethoxy-7-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 3423649 Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)OC)OC6=CC=C(CC7C8=C(O4)C(=C(C=C8CCN7)OC)O3)C=C6 562.70 unknown https://doi.org/10.1248/CPB1953.1.1
Trilobine 169007 Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)OC)OC6=CC=C(CC7C8=C(O4)C(=C(C=C8CCN7)OC)O3)C=C6 562.70 unknown https://doi.org/10.1248/CPB1953.1.1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids / Veatchine-type diterpenoid alkaloids
(1S,2R,5R,7R,8R,11R,12R,18S)-12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.15,8.01,11.02,8.014,18]docosan-7-ol 131879926 Click to see CC12CCCC3(C1CCC45C3CCC(C4)C(=C)C5O)C6N(C2)CCO6 343.50 unknown https://doi.org/10.1016/0040-4020(80)88040-9
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
Coclauril 15927877 Click to see C1C(C=CC(=CC#N)C1O)O 151.16 unknown https://doi.org/10.1248/CPB.38.225
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
(1S,15R)-10,21,22,26-tetramethoxy-16,31-dimethyl-8,24-dioxa-16,31-diazaheptacyclo[23.6.2.13,7.19,13.115,19.028,32.023,34]hexatriaconta-3(36),4,6,9,11,13(35),19,21,23(34),25,27,32-dodecaene 161604992 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=CC=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1016/0040-4020(80)88040-9
> Organoheterocyclic compounds / Benzazepines
(3Beta)-1,6-didehydro-3,15-dimethoxy-erythrinan 5315983 Click to see COC1CC2C3C(=C1)CCN3CCC4=C2C=C(C=C4)OC 285.40 unknown https://doi.org/10.1016/0040-4020(80)88040-9
15-Methoxy-10-azatetracyclo[8.6.1.02,7.013,17]heptadeca-2(7),3,5,13-tetraen-4-ol 5315984 Click to see COC1CC2C3C(=C1)CCN3CCC4=C2C=C(C=C4)O 271.35 unknown https://doi.org/10.1007/BF00629835
https://doi.org/10.1016/0040-4020(80)88040-9
> Organoheterocyclic compounds / Benzofurans
2(6H)-Benzofuranone, 7,7a-dihydro-6-hydroxy-, (6S,7aR)- 155054 Click to see C1C(C=CC2=CC(=O)OC21)O 152.15 unknown https://doi.org/10.1248/CPB.38.225
Aquilegiolide 185347 Click to see C1C(C=CC2=CC(=O)OC21)O 152.15 unknown https://doi.org/10.1248/CPB.38.225
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(S)-N-Methylcoclaurine 440584 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://doi.org/10.1248/CPB1953.1.189
Coclaurine 160487 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1248/YAKUSHI1881.1925.524_876
https://doi.org/10.1016/0040-4020(80)88040-9
Machiline 281691 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1248/YAKUSHI1881.1925.524_876
https://doi.org/10.1016/0040-4020(80)88040-9
N-Methylcoclaurine 2752274 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://doi.org/10.1248/CPB1953.1.189

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