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Cinnamomum verum

Cinnamomum verum - 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 UUID6440114473a6a550280073
Scientific name Cinnamomum verum
Authority J.Presl
First published in Prir. Rostlin 2: 36 (1823)

Description Top

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Synonyms Top

Scientific name Authority First published in
Laurus rigida Wall. Numer. List : n.º 2570 (1830)
Laurus cinnamifera Stokes Bot. Mat. Med. 2: 412 (1812)
Laurus cinnamomea Salisb. Prodr. Stirp. Chap. Allerton : 343 (1796)
Laurus montana Link ex Meisn. Prodr. 15(1): 13 1864
Laurus culitlaban Buch.-Ham. ex Nees Pl. Asiat. Rar. 2: 74 (1831)
Laurus cinnamomum L. Sp. Pl. : 369 (1753)
Persea cinnamomum Spreng. Syst. Veg. 2: 267 (1825)
Cinnamomum zeylanicum var. cassia Meisn. Prodr. 15(1): 14 1864
Cinnamomum zeylanicum var. cordifolium Hayne Getreue Darstell. Gew. 12: t. 21 1833
Cinnamomum zeylanicum var. foeniculaceum Meisn. Prodr. 15(1): 14 1864
Cinnamomum zeylanicum var. inodorum Meisn. Prodr. 15(1): 13 1864
Cinnamomum zeylanicum var. microphyllum Meisn. Prodr. 15(1): 14 1864
Camphora mauritiana Lukman. Nomencl. Icon. Cannel. : 22 (1878)
Camphorina cinnamomum (L.) Farw. Druggists' Circ. 62: 535 (1918)
Cinnamomum alexii Kosterm. Reinwardtia 7: 454 (1969)
Cinnamomum antillarum Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum barthii Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum bengalense Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum biafranum Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum bonplandii Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum boutonii Lukman. Nomencl. Icon. Cannel. : 4 (1878)
Cinnamomum capense Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum carolinense var. oblongum Kaneh. Bot. Mag. (Tokyo) 46: 452 1932
Cinnamomum cayennense Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum commersonii Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum cordifolium Blume ex Lukman. Nomencl. Icon. Cannel. : 4 (1878)
Cinnamomum decandollei Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum delessertii Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum ellipticum Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum erectum Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum humboldtii Lukman. Nomencl. Icon. Cannel. : 6 (1878)
Cinnamomum karrouwa Lukman. Nomencl. Icon. Cannel. : 8 (1878)
Cinnamomum leptopus A.C.Sm. J. Arnold Arbor. 32: 31 (1951)
Cinnamomum leschenaultii Lukman. Nomencl. Icon. Cannel. : 6 (1878)
Cinnamomum madrassicum Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum maheanum Lukman. Nomencl. Icon. Cannel. : 8 (1878)
Cinnamomum mauritianum Lukman. Nomencl. Icon. Cannel. : 4 (1878)
Cinnamomum meissneri Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum ovatum Lukman. Nomencl. Icon. Cannel. : 4 (1878)
Cinnamomum pallasii Lukman. Nomencl. Icon. Cannel. : 6 (1878)
Cinnamomum pleei Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum pourretii Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum regelii Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum riedelii Lukman. Nomencl. Icon. Cannel. : 6 (1878)
Cinnamomum roxburghii Lukman. Nomencl. Icon. Cannel. : 6 (1878)
Cinnamomum sieberi Lukman. Nomencl. Icon. Cannel. : 4 (1878)
Cinnamomum sonneratii Lukman. Nomencl. Icon. Cannel. : 5 (1878)
Cinnamomum vaillantii Lukman. Nomencl. Icon. Cannel. : 4 (1878)
Cinnamomum variabile Lukman. Nomencl. Icon. Cannel. : 4 (1878)
Cinnamomum wolkensteinii Lukman. Nomencl. Icon. Cannel. : 6 (1878)
Cinnamomum zeylanicum Blume Bijdr. Fl. Ned. Ind. : 11, 568 (1825)
Cinnamomum zollingeri Lukman. Nomencl. Icon. Cannel. : 4 (1878)
Cinnamomum maheanum var. karrouwa Lukman. Nomencl. Icon. Cannel. 8 1889
Cinnamomum mathewianum Remya Kr., E.S.S.Kumar, Radhamany, Valsalad. & R.Jagad. Int. J. Advanced Res. 2(7): 29 (2014)
Laurus cassia Burm.f. Fl. Indica: 91 (1768)
Cinnamomum zeylanicum subsp. antillanum Lukman. Nomencl. Icon. Cannel.: 5 (1878)

Common names Top

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Language Common/alternative name
English cinnamon
English ceylon cinnamon
English sri lanka cinnamon
English true cinnamon
Arabic قرفة حقيقية
ban kulit manis
Belarusian Карычнае дрэва
Bulgarian цейлонска канела
bjn kayu manis
Bengali দারুচিনি
Catalan canyeller
Czech skořicovník cejlonský
Czech skořicovník pravý
German echter zimtbaum
German ceylon-zimtbaum
Greek Κιννάμωμον το γνήσιον
Esperanto vera cinamomo
Estonian tseiloni kaneelipuu
Basque kanelondo
Persian دارچین
Finnish ceyloninkaneli
French cannelier de ceylan
frr ceylon-kaneel
Irish canelita
Galician caneleira
Hindi दालचीनी
Upper Sorbian skoričnik
Hungarian cinnamomum zeylanicum
Hungarian fahéjfa
Hungarian valódi fahéjfa
Hungarian cimetfa
Hungarian ceyloni fahéjfa
Armenian Դարչին
Indonesian kulit kayu manis
Italian cannella
Italian cinnamomum zeylanicum
Italian cinnamomo
Japanese セイロンニッケイ
Korean 계피
Lithuanian ceiloninis cinamonas
min kayu manih
Malayalam കറുവ
nan ceylon jio̍k-kùi
Nepali दालचिनीको बोट
Norwegian Nynorsk kaneltre
Polish cynamonowiec cejloński
Portuguese cinnamomum zeylanicum
Quechua kanila sach'a
Russian Корица
Serbo-Croatian cimet
Sinhala සත්ය කුරුඳු
Sinhala ශ්රී ලාංකා කුරුඳු
Sinhala සිලෝන් කුරුඬු
Sinhala සිනමෝමම් වේරම්
Sinhala සිනමෝමම් සිලනිකම්
Slovak škoricovník cejlónsky
Slovenian cimetovec
Swedish äkta kanel
Swedish Äkta kanel
Tamil கருவா
Tamil கருவா மரம்
Tamil கறுவா (மரம்)
tcy ಇಜಿನ್ದ ಮರ
Telugu శ్రీలంక దాల్చిన చెక్క
Thai อบเชยลังกา
Ukrainian Кориця
Vietnamese quế quan
Chinese 錫蘭肉桂
Chinese 斯里兰卡肉桂
Chinese 铁箍散
Chinese 贴骨散
Chinese 锡兰肉桂
Chinese 锡兰肉桂、(斯里兰卡肉桂）
Chinese 琉璃草

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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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
  • Africa
    • East Tropical Africa
      • Tanzania
    • South Tropical Africa
      • Angola
    • West-central Tropical Africa
      • Gulf Of Guinea Islands
    • Western Indian Ocean
      • Comoros
      • Mauritius
      • Seychelles
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Myanmar
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Philippines
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
    • South-central Pacific
      • Cook Islands
      • Society Islands
    • Southwestern Pacific
      • Fiji
      • Samoa
  • Southern America
    • Brazil
      • Brazil Southeast
    • Caribbean
      • Leeward Islands
      • Windward Islands
    • Southern South America
      • Argentina Northeast

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000605512
UNII SC5767R2RD
USDA Plants CIVE2
Tropicos 17800682
INPN 447272
KEW urn:lsid:ipni.org:names:463752-1
The Plant List kew-2721692
Open Tree Of Life 481247
Observations.org 457525
NCBI Taxonomy 128608
Nature Serve 2.127952
IPNI 463752-1
iNaturalist 122777
IFPNI 6D190EAF-E5E2-FEA0-B085-3EBA6C05417B
GBIF 3033987
Freebase /m/0crd3q1
EPPO CINZE
EOL 490672
Elurikkus 353645
US Library of Congress sh85026033
USDA GRIN 70183
Wikipedia Cinnamomum_verum

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
Medicinal plants for allergic rhinitis: A systematic review and meta-analysis Lim XY, Lau MS, Zolkifli NA, Sastu@Zakaria UR, Mohd Rahim NS, Lai NM, Tan TY PLoS One 11-Apr-2024
PMCID:PMC11008904
doi:10.1371/journal.pone.0297839
PMID:38603736
Immunomodulatory effect of Unani polyherbal formulation - Tiryaq Wabai in mild to moderate COVID-19 patients – A randomized placebo-controlled clinical trial Kumar A, Khan MS, Haque ZU, Rai A, Fazil M, Rabbani G J Ayurveda Integr Med 04-Apr-2024
PMCID:PMC10997826
doi:10.1016/j.jaim.2024.100903
PMID:38574518
Management of Otitis externa with Ayurvedic formulation Gandhak Rasayana- A case report Patil S, Bhat P J Ayurveda Integr Med 01-Apr-2024
PMCID:PMC10999474
doi:10.1016/j.jaim.2024.100893
PMID:38564934
Larvicidal, Ovicidal, and Repellent Activities of Leucas stachydiformis (Hochst. ex Benth.) Briq Essential Oil against Anopheles arabiensis Fikru S, Tolossa K, Lindemann P, Bucar F, Asres K J Trop Med 29-Mar-2024
PMCID:PMC10997417
doi:10.1155/2024/1051086
PMID:38586242
Herbal Theranostics: Controlled, Targeted Delivery and Imaging of Herbal Molecules Setia A, Vallamkonda B, Challa RR, Mehata AK, Badgujar P, Muthu MS Nanotheranostics 25-Mar-2024
PMCID:PMC10988210
doi:10.7150/ntno.94987
PMID:38577318
An in vitro study elucidating the synergistic effects of aqueous cinnamon extract and an anti-TNF-α biotherapeutic: implications for a complementary and alternative therapy for non-responders Khedkar S, Khan MA BMC Complement Med Ther 23-Mar-2024
PMCID:PMC10960381
doi:10.1186/s12906-024-04438-w
PMID:38521924
Activity of isoflavone in managing polycystic ovary syndrome symptoms (Review) Raihanah C, Sukrasno S, Kurniati NF Biomed Rep 21-Mar-2024
PMCID:PMC10999901
doi:10.3892/br.2024.1768
PMID:38590945
Rice false smut pathogen: implications for mycotoxin contamination, current status, and future perspectives Zhou L, Mubeen M, Iftikhar Y, Zheng H, Zhang Z, Wen J, Khan RA, Sajid A, Solanki MK, Sohail MA, Kumar A, Massoud EE, Chen L Front Microbiol 20-Mar-2024
PMCID:PMC10996400
doi:10.3389/fmicb.2024.1344831
PMID:38585697
Evaluation of Thai Silkworm (Bombyx mori L.) Hydrolysate Powder for Blood Pressure Reduction in Hypertensive Rats Anuduang A, Mustapha WA, Lim SJ, Jomduang S, Phongthai S, Ounjaijean S, Boonyapranai K Foods 20-Mar-2024
PMCID:PMC10969865
doi:10.3390/foods13060943
PMID:38540933
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Therapeutic potential of Thai herbal formula for cognitive impairment: A metabolomics approach for Comprehensive Insights Akarasereenont P, Pattanapholkornsakul S, Limsuvan S, Mamaethong D, Booranasubkajorn S, Pakaprot N, Tripatara P, Pilakasiri K Heliyon 16-Mar-2024
PMCID:PMC10981045
doi:10.1016/j.heliyon.2024.e28027
PMID:38560220
Nuclear Magnetic Resonance Fingerprints and Mini DNA Markers for the Authentication of Cinnamon Species Ingredients Used in Food and Natural Health Products Ragupathy S, Thirugnanasambandam A, Vinayagam V, Newmaster SG Plants (Basel) 14-Mar-2024
PMCID:PMC10975438
doi:10.3390/plants13060841
PMID:38592863
Enzyme-Based Antiviral Potential of Cinnamomum verum J. Presl. Essential Oil and Its Major Component (E)-Cinnamaldehyde Karadağ AE, Biltekin SN, Ghani U, Demirci B, Demirci F ACS Omega 13-Mar-2024
PMCID:PMC10975636
doi:10.1021/acsomega.3c09595
PMID:38559956
A multi-center cross-sectional study of Chinese Herbal Medicine-Drug adverse reactions using active surveillance in Singapore’s Traditional Chinese Medicine clinics Ng CY, Zhao Y, Wang N, Chia KL, Teo CH, Peh W, Yeo P, Zhong LL Chin Med 07-Mar-2024
PMCID:PMC10918936
doi:10.1186/s13020-024-00915-z
PMID:38454483
Using Essential Oils to Reduce Yersinia enterocolitica in Minced Meat and in Biofilms Vidaković Knežević S, Knežević S, Vranešević J, Milanov D, Ružić Z, Karabasil N, Kocić-Tanackov S Foods 06-Mar-2024
PMCID:PMC10931311
doi:10.3390/foods13050806
PMID:38472919

Phytochemical Profile Top

Add a new one!
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
> Benzenoids / Benzene and substituted derivatives
3-Phenylpropanal 7707 Click to see C1=CC=C(C=C1)CCC=O 134.17 unknown https://doi.org/10.1021/JF60218A031
Phenethyl acetate 7654 Click to see CC(=O)OCCC1=CC=CC=C1 164.20 unknown https://doi.org/10.1021/JF60218A031
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1021/JF60218A031
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown https://doi.org/10.1515/ZNC-2002-11-1206
https://doi.org/10.1021/JF60218A031
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1021/JF052736R
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown https://doi.org/10.1055/S-0028-1099572
https://doi.org/10.1515/ZNC-2002-11-1206
https://doi.org/10.1021/JF60218A031
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown https://doi.org/10.1021/JF60218A031
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1021/JF60218A031
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde 998 Click to see C1=CC=C(C=C1)CC=O 120.15 unknown https://doi.org/10.1021/JF60218A031
> Benzenoids / Benzene and substituted derivatives / Styrenes
2-Ethenylphenol 135442 Click to see C=CC1=CC=CC=C1O 120.15 unknown https://doi.org/10.1021/JF60218A031
3-Phenylprop-2-enyl acetate 7660 Click to see CC(=O)OCC=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.1055/S-0028-1099572
https://doi.org/10.1016/0021-9673(88)90035-0
Cinnamyl acetate 5282110 Click to see CC(=O)OCC=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.1515/ZNC-2002-11-1206
https://doi.org/10.1055/S-0028-1099572
https://doi.org/10.1016/0021-9673(88)90035-0
> Benzenoids / Phenol esters
Eugenol acetate 7136 Click to see CC(=O)OC1=C(C=C(C=C1)CC=C)OC 206.24 unknown https://doi.org/10.1021/JF60218A031
https://doi.org/10.1055/S-0028-1099572
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown https://doi.org/10.1021/JF60218A031
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Phenol 996 Click to see C1=CC=C(C=C1)O 94.11 unknown https://doi.org/10.1021/JF60218A031
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1055/S-0028-1099572
https://doi.org/10.1021/JF60218A031
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1693916/
https://doi.org/10.1016/0021-9673(88)90035-0
Isoeugenol 853433 Click to see CC=CC1=CC(=C(C=C1)O)OC 164.20 unknown https://doi.org/10.1021/JF60218A031
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1021/JF60218A031
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown https://doi.org/10.1515/ZNC-2002-11-1206
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1021/JF60218A031
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1021/JF60218A031
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown https://doi.org/10.1021/JF60218A031
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1021/JF60218A031
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1021/JF60218A031
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1021/JF60218A031
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1021/JF60218A031
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1055/S-0028-1099572
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1055/S-0028-1099572
https://doi.org/10.1021/JF60218A031
Linalyl acetate 8294 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown https://doi.org/10.1021/JF60218A031
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1021/JF60218A031
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1021/JF60218A031
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1055/S-0028-1099572
Cuminaldehyde 326 Click to see CC(C)C1=CC=C(C=C1)C=O 148.20 unknown https://doi.org/10.1021/JF60218A031
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1055/S-0028-1099572
https://doi.org/10.1021/JF60218A031
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1055/S-0028-1099572
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/JF60218A031
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1021/JF60218A031
alpha-Bergamotene, (E)-(-)- 6429302 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1515/ZNC-2002-11-1206
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1055/S-0028-1099572
https://doi.org/10.1021/JF60218A031
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/JF60218A031
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1021/JF60218A031
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1021/JF60218A031
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1021/JF60218A031
https://doi.org/10.1055/S-0028-1099572
Camphor (synthetic) 159055 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1055/S-0028-1099572
Fenchone 14525 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown https://doi.org/10.1021/JF60218A031
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1021/JF60218A031
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/JF60218A031
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Phellandrene 443160 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1055/S-0028-1099572
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1055/S-0028-1099572
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1021/JF60218A031
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1021/JF60218A031
https://doi.org/10.1055/S-0028-1099572
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1021/JF60218A031
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1055/S-0028-1099572
https://doi.org/10.1021/JF60218A031
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1055/S-0028-1099572
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1055/S-0028-1099572
https://doi.org/10.1021/JF60218A031
Piperitone 6987 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown https://doi.org/10.1021/JF60218A031
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1021/JF60218A031
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-beta-Caryophyllene 20831623 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-0028-1099572
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1515/ZNC-2002-11-1206
(+)-gamma-Cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/JF60218A031
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1515/ZNC-2002-11-1206
(1S,2S,6S,7R,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 101607926 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/JF60218A031
https://doi.org/10.1021/JF60218A031
(E,Z)-farnesol 1549109 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1021/JF60218A031
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1515/ZNC-2002-11-1206
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1021/JF60218A031
https://doi.org/10.1515/ZNC-2002-11-1206
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1S,4E,9R)- 26318 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-0028-1099572
Cadalene 10225 Click to see CC1=CC2=C(C=CC(=C2C=C1)C)C(C)C 198.30 unknown https://doi.org/10.1515/ZNC-2002-11-1206
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/JF60218A031
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1021/JF60218A031
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/JF60218A031
Farnesol 3327 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1021/JF60218A031
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/JF60218A031
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1021/JF60218A031
https://doi.org/10.1515/ZNC-2002-11-1206
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1515/ZNC-2002-11-1206
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-Selinene 442393 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1021/JF60218A031
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1515/ZNC-2002-11-1206
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S)-2,3,5-trihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxypentanal 644161 Click to see C1C(C(C(C(O1)OC(CO)C(C(C=O)O)O)O)O)O 282.24 unknown https://doi.org/10.1016/0008-6215(87)80062-9
(2R,3S,4S)-2,4,5-trihydroxy-3-[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxypentanal 162947816 Click to see C1C(C(C(C(O1)OC(C(CO)O)C(C=O)O)O)O)O 282.24 unknown https://doi.org/10.1016/0008-6215(87)80062-9
2,4,5-Trihydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxypentanal 86244302 Click to see C1C(C(C(C(O1)OC(C(CO)O)C(C=O)O)O)O)O 282.24 unknown https://doi.org/10.1016/0008-6215(87)80062-9
Xylobiose, >=90% (HPLC) 5107731 Click to see C1C(C(C(C(O1)OC(CO)C(C(C=O)O)O)O)O)O 282.24 unknown https://doi.org/10.1016/0008-6215(87)80062-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
4-[3,4-Dihydroxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-2,3,5-trihydroxypentanal 162999274 Click to see C1C(C(C(C(O1)OC2COC(C(C2O)O)OC(CO)C(C(C=O)O)O)O)O)O 414.36 unknown https://doi.org/10.1016/0008-6215(87)80062-9
Pen(?1-4)Pen(?1-4)Pen(?1-4)aldehydo-Pen 146160895 Click to see C1C(C(C(C(O1)OC2COC(C(C2O)O)OC3COC(C(C3O)O)OC(CO)C(C(C=O)O)O)O)O)O 546.50 unknown https://doi.org/10.1016/0008-6215(87)80062-9
Xyl(b1-4)Xyl(b1-4)aldehydo-Ara 162999275 Click to see C1C(C(C(C(O1)OC2COC(C(C2O)O)OC(CO)C(C(C=O)O)O)O)O)O 414.36 unknown https://doi.org/10.1016/0008-6215(87)80062-9
Xyl(b1-4)Xyl(b1-4)Xyl(b1-4)aldehydo-Ara 162848741 Click to see C1C(C(C(C(O1)OC2COC(C(C2O)O)OC3COC(C(C3O)O)OC(CO)C(C(C=O)O)O)O)O)O 546.50 unknown https://doi.org/10.1016/0008-6215(87)80062-9
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Furfural 7362 Click to see C1=COC(=C1)C=O 96.08 unknown https://doi.org/10.1021/JF60218A031
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1021/JF60218A031
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2-Hydroxy-3-methoxy-5-prop-2-enylphenyl)ethanone 121013785 Click to see CC(=O)C1=C(C(=CC(=C1)CC=C)OC)O 206.24 unknown https://doi.org/10.1021/JF60218A031
> Organoheterocyclic compounds / Benzodioxoles
Safrole 5144 Click to see C=CCC1=CC2=C(C=C1)OCO2 162.18 unknown https://doi.org/10.1021/JF60218A031
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dihydrodehydroconiferyl alcohol 4-O-glucoside 14681438 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO 522.50 unknown https://doi.org/10.1021/JF052736R
Urolignoside 10602086 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO 522.50 unknown https://doi.org/10.1021/JF052736R
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-(2-Methoxyphenyl)acrylaldehyde 15173 Click to see COC1=CC=CC=C1C=CC=O 162.18 unknown https://doi.org/10.1016/0021-9673(88)90035-0
3-Phenyl-propenal 307 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown https://doi.org/10.1002/PTR.3419
https://doi.org/10.1016/0021-9673(88)90035-0
https://doi.org/10.1055/S-0028-1099572
https://doi.org/10.1021/JF60218A031
https://doi.org/10.2116/BUNSEKIKAGAKU.35.3_202
Cinnamaldehyde 637511 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1693916/
https://doi.org/10.1002/PTR.3419
https://doi.org/10.1016/0021-9673(88)90035-0
https://doi.org/10.1055/S-0028-1099572
https://doi.org/10.1021/JF60218A031
https://doi.org/10.2116/BUNSEKIKAGAKU.35.3_202
https://doi.org/10.1007/BF02974062
https://doi.org/10.1021/NP50033A025
O-Methoxycinnamaldehyde, (E)- 641298 Click to see COC1=CC=CC=C1C=CC=O 162.18 unknown https://doi.org/10.1016/0021-9673(88)90035-0
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
3-Phenyl-2-propenoic acid methyl ester 7644 Click to see COC(=O)C=CC1=CC=CC=C1 162.18 unknown https://doi.org/10.1021/JF60218A031
Ethyl 3-phenylprop-2-enoate 7649 Click to see CCOC(=O)C=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.1021/JF60218A031
Ethyl cinnamate 637758 Click to see CCOC(=O)C=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.1021/JF60218A031
Methyl cinnamate 637520 Click to see COC(=O)C=CC1=CC=CC=C1 162.18 unknown https://doi.org/10.1021/JF60218A031
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1021/JF60218A031
https://doi.org/10.1016/0021-9673(88)90035-0
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1016/0021-9673(88)90035-0
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Cinnamyl alcohol 5315892 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown https://doi.org/10.1016/0021-9673(88)90035-0
https://doi.org/10.1055/S-0028-1099572
https://doi.org/10.1021/JF60218A031
Phenylallyl alcohol 308 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown https://doi.org/10.1016/0021-9673(88)90035-0
https://doi.org/10.1055/S-0028-1099572
https://doi.org/10.1021/JF60218A031
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown https://doi.org/10.1021/JF60218A031
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1R,5R,6R,7S,13S,15R,20S,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,16,18-pentaene-6,9,17,19,21-pentol 162935107 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C7C(C=C(C=C7O)O)OC(C6O)(O5)C8=CC(=C(C=C8)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 866.80 unknown https://doi.org/10.1021/JF052736R
(2R,2'R,3R,3'R)-2,2'-Bis(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-2H,2'H-4,8'-bichromene-3,3',5,5',7,7'-hexol 5320711 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1039/P19830002139
5,13-bis(3,4-dihydroxyphenyl)-7-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,16,18-pentaene-6,9,17,19,21-pentol 162935106 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C7C(C=C(C=C7O)O)OC(C6O)(O5)C8=CC(=C(C=C8)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 866.80 unknown https://doi.org/10.1021/JF052736R
Cinnamtannin B1 475277 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1021/NP1007944
Cinnamtannin B2 16130973 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=C(C(=CC(=C67)O)O)C8C(C(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.1021/NP1007944
Pavetannin B6 13990885 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1021/NP1007944
Proanthocyanidin 108065 Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(O2)C(=C(C=C3O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)O 592.50 unknown https://doi.org/10.1039/P19830002139
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1039/P19830002139
Procyanidin C1 169853 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1039/P19830002139
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1039/P19830002139
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF052736R
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF052736R
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1021/JF052736R
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1021/JF052736R

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