PlantaeDB Logo
Login Sign-up

Magnolia compressa

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fe2323ec44750766539
Scientific name Magnolia compressa
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 17: 417 (1872)

Ethnobotanical Use Top

Suggest a correction!
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.

Magnolia compressa (Magnoliaceae) has a long reputation in East Asia as a calming and digestive herb. The bark of mature branches and the root bark were most commonly employed. In classical Chinese medicine, the drug known as “Houpo” includes Magnolia officinalis and can be substituted by related Magnolia species, and texts describe decoctions of the bark used for abdominal distension and as a tranquilizing aid (according to Tang and Eisenbrand, 1992). In Japanese kampo, the bark of the Japanese magnolia has long been used in decoctions to relieve GI discomfort and to ease agitation, a practice noted in traditional materia medica and modern pharmacopoeial sources (Pharmacopoeia of Japan, 1992). In Korea, the bark of local Magnolias—including M. compressa—has been used in similar decoctions to calm “Qi stagnation,” support digestion, and promote relaxation, as recorded in Korean herbal pharmacopoeias (Korean Pharmacopoeia, 1972). Across these regions, the bitter, aromatic bark is typically simmered in water and the liquid drunk warm.

A simple and widely reported preparation is a decoction of magnolia bark. For a mild tea, use 3–5 g of coarsely cut bark (or root bark) and simmer in 300 ml of water for 15–20 minutes; strain and sip half to two cups over the day. For a more concentrated decoction, use 6–9 g of bark and simmer in 500 ml of water for 25–30 minutes, then strain. These ratios and durations are consistent with traditional East Asian use and appear in traditional pharmacological texts (Korean Pharmacopoeia, 1972; Tang and Eisenbrand, 1992). As a precaution, magnolia bark is bitter and can be sedating; avoid driving or using heavy machinery if you feel drowsy. Traditional texts advise moderation in dosage and note contraindication in pregnancy; avoid if you are pregnant, nursing, or taking sedatives unless supervised by a qualified practitioner.

The bark’s activity is supported by well-established constituents. Extracts are rich in biphenyl lignans magnolol and honokiol, together with related biphenyl ethers; these are consistently reported as the major bioactive markers of Magnolia bark and are used in contemporary quality-control standards for magnolia extracts (according to Shao et al., 1999). These lignans show anxiolytic, spasmolytic, and anti-inflammatory properties, which align with the traditional roles for gastrointestinal comfort and relaxation.

Today, magnolia extracts enriched in magnolol and honokiol appear in dietary supplements, functional foods, and some OTC products for stress support and GI comfort, while decoctions continue to be used in kampo and traditional clinics across the region.

General Uses Top

Suggest a correction!

Common products:
Wood from mature trees is sawn into lumber for furniture-making and general construction.

Wood and fiber:
The wood is utilized for furniture components and structural uses in construction. It is valued for moderate hardness and workability, enabling machining, finishing, and joinery. The species is recognized in national timber standards for identification and grading in the timber trade. Reliable sources: Flora of China (commerce entry); national timber identification resources for Chinese commercial timbers.

Scientific/model use:
M. compressa is a voucher specimen in the Flora of China database and is a stored reference in the Chinese National Specimen Resource Network, supporting plant taxonomy and biodiversity research.

Synonyms Top

Scientific name Authority First published in
Michelia compressa (Maxim.) Sarg. Forest Fl. Japan : 11 (1894)
Michelia compressa var. formosana Kaneh. Trans. Nat. Hist. Soc. Formosa 20: 384 (1930)
Michelia cumingii Merr. & Rolfe Philipp. J. Sci. 3: 100 (1908)
Michelia formosana (Kaneh.) Masam. & Suzuki Rep. (Annual) Taihoku Bot. Gard. 3: 57 (1933)
Michelia compressa var. lanyuensis S.Y.Lu Taiwan J. Forest Sci. 15: 523 (2000)
Michelia compressa var. angustifolia Makino J. Jap. Bot. 3: 39. 1926
Michelia compressa var. latifolia Makino J. Jap. Bot. 3: 39. 1926
Michelia compressa f. latifolia (Makino) Okuyama J. Jap. Bot. 30: 41 1955
Michelia compressa f. angustifolia (Makino) Okuyama J. Jap. Bot. 30: 41 1955
Magnolia formosana (Kaneh.) Yonek. J. Jap. Bot. 86: 231 (2011)
Magnolia compressa var. formosana (Kaneh.) C.F.Chen Magnolia, J. Magnolia Soc. 49(96): 4 (2014)
Magnolia compressa var. lanyuensis (S.Y.Lu) C.F.Chen Magnolia, J. Magnolia Soc. 49: 5 (2014)
Michelia parviflora Merr. Publ. Bur. Sci. Gov. Lab. 35: 70 (1906)
Michelia compressa var. macrantha Hatus. Fl. Ryukyus : 285 (1971)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Japanese オガタマ
Japanese トキワコブシ
Japanese 黄心樹
Japanese オガタマノキ
Korean 초령목
pwn sekazu
tay sikaru
Chinese 烏心石

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000233065
Tropicos 19300454
KEW urn:lsid:ipni.org:names:554664-1
The Plant List kew-117514
Missouri Botanical Garden 282545
Open Tree Of Life 831108
NCBI Taxonomy 85872
IUCN Red List 193918
IPNI 554664-1
iNaturalist 439984
GBIF 3153607
EPPO MIACO
EOL 1155018
USDA GRIN 23097
Wikipedia Magnolia_compressa

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
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
Pharmacological potential of micheliolide: A focus on anti-inflammatory and anticancer activities Uddin J, Fatima M, Riaz A, Kamal GM, Muhsinah AB, Ahmed AR, Iftikhar R Heliyon 05-Mar-2024
PMCID:PMC10944196
doi:10.1016/j.heliyon.2024.e27299
PMID:38496875
Synthesis and Anti-Inflammatory Activity of Ferulic Acid-Sesquiterpene Lactone Hybrids Duan X, Liu N, Lv K, Wang J, Li M, Zhang Y, Huo X, Bao S, Shen Z, Zhang X Molecules 21-Feb-2024
PMCID:PMC10933920
doi:10.3390/molecules29050936
PMID:38474447
Michelia compressa-Derived Santamarine Inhibits Oral Cancer Cell Proliferation via Oxidative Stress-Mediated Apoptosis and DNA Damage Lu HI, Chen KL, Yen CY, Chen CY, Chien TM, Shu CW, Chen YH, Jeng JH, Chen BH, Chang HW Pharmaceuticals (Basel) 09-Feb-2024
PMCID:PMC10892349
doi:10.3390/ph17020230
PMID:38399445
A taxonomic revision of the genus Angelica (Apiaceae) in Taiwan with a new species A. aliensis Wang JC, Chen HH, Hsu TW, Hung KH, Huang CC Bot Stud 22-Jan-2024
PMCID:PMC10803708
doi:10.1186/s40529-023-00407-7
PMID:38252347
Micheliolide prevents estrogen deficiency-induced bone loss via inhibiting osteoclast bone resorption Gan Z, Huang J, Xu M, Yuan X, Shang X, Chen X, Chen K Aging (Albany NY) 11-Oct-2023
PMCID:PMC10599737
doi:10.18632/aging.205111
PMID:37827691
Comparison of Composition, Free-Radical-Scavenging Capacity, and Antibiosis of Fresh and Dry Leave Aqueous Extract from Michelia shiluensis Wu W, Li G, Zhou W, Wang E, Zhao X, Song X, Zhao Y Molecules 08-Aug-2023
PMCID:PMC10457956
doi:10.3390/molecules28165935
PMID:37630187
Micheliolide exerts effects in myeloproliferative neoplasms through inhibiting STAT3/5 phosphorylation via covalent binding to STAT3/5 proteins Huang H, Liu J, Yang L, Yan Y, Chen M, Li B, Xu Z, Qin T, Qu S, Wang L, Huang G, Chen Y, Xiao Z Blood Sci 12-Jul-2023
PMCID:PMC10629731
doi:10.1097/BS9.0000000000000168
PMID:37941916
Micheliolide attenuates neuroinflammation to improve cognitive impairment of Alzheimer's disease by inhibiting NF-κB and PI3K/Akt signaling pathways Yang G, Hu Y, Qin X, Sun J, Miao Z, Wang L, Ke Z, Zheng Y Heliyon 04-Jul-2023
PMCID:PMC10344752
doi:10.1016/j.heliyon.2023.e17848
PMID:37456020
Emerging drugs targeting cellular redox homeostasis to eliminate acute myeloid leukemia stem cells Costa RG, Silva SL, Dias IR, Oliveira MD, Rodrigues AC, Dias RB, Bezerra DP Redox Biol 02-Apr-2023
PMCID:PMC10119960
doi:10.1016/j.redox.2023.102692
PMID:37031536
Effect of geographic isolation on genetic variation and population structure of Euphrasia nankotaizanensis, a threatened endemic alpine herb in Taiwan Chen SY, Huang CC, Cheng YT, Wang CC, Li CY, Lai IL, Hung KH Heliyon 04-Mar-2023
PMCID:PMC10018478
doi:10.1016/j.heliyon.2023.e14228
PMID:36938387
Sesquiterpene Lactones and Cancer: New Insight into Antitumor and Anti-inflammatory Effects of Parthenolide-Derived Dimethylaminomicheliolide and Micheliolide Dong Y, Qian X, Li J Comput Math Methods Med 18-Jul-2022
PMCID:PMC9313921
doi:10.1155/2022/3744837
PMID:35898475
Discovery of TCMs and derivatives against the main protease of SARS-CoV-2 via high throughput screening, ADMET analysis, and inhibition assay in vitro Qi X, Li B, Omarini AB, Gand M, Zhang X, Wang J J Mol Struct 12-Jul-2022
PMCID:PMC9273959
doi:10.1016/j.molstruc.2022.133709
PMID:35846732
Scaling relationships of leaf vein and areole traits versus leaf size for nine Magnoliaceae species differing in venation density Shi P, Miao Q, Niinemets Ü, Liu M, Li Y, Yu K, Niklas KJ Am J Bot 01-Jun-2022
PMCID:PMC9327518
doi:10.1002/ajb2.1856
PMID:35471633
Mecheliolide elicits ROS-mediated ERS driven immunogenic cell death in hepatocellular carcinoma Xu Z, Xu J, Sun S, Lin W, Li Y, Lu Q, Li F, Yang Z, Lu Y, Liu W Redox Biol 28-May-2022
PMCID:PMC9168183
doi:10.1016/j.redox.2022.102351
PMID:35671636

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
> Alkaloids and derivatives / Aporphines
1-((7aR)-5,6,7a,8-Tetrahydro-7H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-7-yl)ethanone 6453733 Click to see 307.30 unknown https://doi.org/10.1007/S10600-010-9606-5
https://doi.org/10.1007/S10600-010-9463-2
https://doi.org/10.1080/14786410802497356
1,2-Methylenedioxynoraporphine 3462225 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown https://doi.org/10.1007/S10600-010-9463-2
https://doi.org/10.1080/14786410802497356
https://doi.org/10.1007/S10600-010-9606-5
3,5-Dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaene-11-carbaldehyde 23251787 Click to see C1CN(C2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5)C=O 293.30 unknown https://doi.org/10.1007/S10600-010-9463-2
7-Hydroxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,12,14,16,18-heptaene-9,10-dione 163008074 Click to see 307.26 unknown https://doi.org/10.1080/14786410802497356
7H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline-7-carboxaldehyde,5,6,7a,8-tetrahydro-, (7aR)- 158516 Click to see C1CN(C2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5)C=O 293.30 unknown https://doi.org/10.1007/S10600-010-9463-2
Anonaine 160597 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown https://doi.org/10.1007/S10600-010-9606-5
https://doi.org/10.1080/14786410802497356
https://doi.org/10.1007/S10600-010-9463-2
Lanuginosine 97622 Click to see 305.30 unknown https://doi.org/10.1007/S10600-010-9463-2
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown https://doi.org/10.1007/S10600-010-9606-5
https://doi.org/10.1080/14786410802497356
https://doi.org/10.1007/S10600-010-9463-2
https://doi.org/10.1248/YAKUSHI1947.82.6_925
https://doi.org/10.1016/S0031-9422(00)88656-2
N-Acetylbongaridine 78411088 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 307.30 unknown https://doi.org/10.1007/S10600-010-9463-2
https://doi.org/10.1080/14786410802497356
https://doi.org/10.1007/S10600-010-9606-5
N-Acetylnornuciferine 101630664 Click to see 323.40 unknown https://doi.org/10.1007/S10600-010-9463-2
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
(12R,13S)-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaen-13-ol 162976267 Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=CC=CC=C54)O)OCO3 295.30 unknown https://doi.org/10.1248/YAKUSHI1947.82.6_925
7-Methyl-6,7,7a,8-tetrahydro-5H-benzo[g][1,3]dioxolo[4',5':4,5]benzo[1,2,3-de]quinolin-8-ol 431013 Click to see 295.30 unknown https://doi.org/10.1248/YAKUSHI1947.82.6_925
> Alkaloids and derivatives / Aristolactams
7-Hydroxy-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(19),2(6),7,11,13,15,17-heptaen-9-one 163030136 Click to see 279.25 unknown https://doi.org/10.1080/14786410802497356
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(R)-Canadine 443422 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown https://doi.org/10.1248/YAKUSHI1947.80.5_705
Canadine 34458 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown https://doi.org/10.1248/YAKUSHI1947.80.5_705
Corypalmine 11186895 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)OC 341.40 unknown https://doi.org/10.1248/YAKUSHI1947.80.5_705
Tetrahydrojateorrhizine 185605 Click to see 341.40 unknown https://doi.org/10.1248/YAKUSHI1947.80.5_705
> 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/10.1007/S10600-010-9463-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.1007/S10600-010-9463-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown https://doi.org/10.1007/S10600-010-9463-2
> Benzenoids / Perylenequinones
1,8,15-Trihydroxy-4,19-dioxaheptacyclo[10.8.1.12,7.03,5.016,21.018,20.011,22]docosa-7,9,11(22),12(21),13,15-hexaene-6,17-dione 102335565 Click to see 364.30 unknown https://doi.org/10.1007/S10600-010-9463-2
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1007/S10600-010-9463-2
Feruloyltyramine 5280537 Click to see 313.30 unknown https://doi.org/10.1007/S10600-010-9463-2
https://doi.org/10.1007/S10600-010-9606-5
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1007/S10600-010-9463-2
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol 100067 Click to see 418.40 unknown https://doi.org/10.1007/S10600-010-9463-2
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://doi.org/10.1007/S10600-010-9463-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1007/S10600-010-9606-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3R)-5-[(1R,3R,4aR,5R,8aS)-5-(acetyloxymethyl)-3-hydroxy-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 162865808 Click to see 380.50 unknown https://doi.org/10.1080/14786411003792157
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(4S)-4-acetyl-2-chromen-2-ylidene-4-hydroxy-5,5-dimethylcyclopentane-1,3-dione 162902928 Click to see 312.30 unknown https://doi.org/10.1080/14786410903281774
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1S,2S,4R,7E,11S,12R)-4,8,12-trimethyl-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one 163077852 Click to see CC1C2CCC(=CCCC3(C(C2OC1=O)O3)C)C 250.33 unknown https://doi.org/10.1016/S0031-9422(00)88656-2
CID 4692 4692 Click to see CC1=CCCC2(C(O2)C3C(CC1)C(=C)C(=O)O3)C 248.32 unknown https://doi.org/10.1080/14786410802497356
Parthenolide 6473881 Click to see 248.32 unknown https://doi.org/10.1080/14786410802497356
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Compressanolide 10977878 Click to see CC1C2CCC(=C)C3CCC(C3C2OC1=O)(C)O 250.33 unknown https://doi.org/10.1016/S0031-9422(00)88656-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1007/S10600-010-9463-2
(6beta,24R)-6-Hydroxystigmast-4-en-3-one 14769504 Click to see 428.70 unknown https://doi.org/10.1007/S10600-010-9606-5
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1007/S10600-010-9463-2
17-(5-Ethyl-6-methylhept-3-en-2-yl)-6-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 73838057 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 426.70 unknown https://doi.org/10.1007/S10600-010-9606-5
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/10.1007/S10600-010-9463-2
6-Hydroxystigmasta-4,22-dien-3-one 10071143 Click to see 426.70 unknown https://doi.org/10.1007/S10600-010-9606-5
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see 428.70 unknown https://doi.org/10.1007/S10600-010-9606-5
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1007/S10600-010-9463-2
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown https://doi.org/10.1007/S10600-010-9463-2
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
2,6-Dimethoxy-1-acetonylquinol 241783 Click to see 226.23 unknown https://doi.org/10.1007/S10600-010-9606-5
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(+)-O-Methylarmepavine 11067397 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC)OC)OC 327.40 unknown https://doi.org/10.1007/S10600-010-9606-5
Csh 068 259676 Click to see 327.40 unknown https://doi.org/10.1007/S10600-010-9606-5
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(8E)-4,9,12-trimethyl-3,14-dioxatricyclo[9.3.0.02,4]tetradec-8-en-13-one 5381212 Click to see CC1C2CC(=CCCCC3(C(C2OC1=O)O3)C)C 250.33 unknown https://doi.org/10.1016/S0031-9422(00)88656-2
> Organoheterocyclic compounds / Oxolanes
(3S)-4-methylideneoxolan-3-ol 89323980 Click to see C=C1COCC1O 100.12 unknown https://doi.org/10.1080/14786411003792157
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-cis-Feruloyl tyramine 6440659 Click to see 313.30 unknown https://doi.org/10.1007/S10600-010-9463-2
N-feruloyltyramine; Moupinamide 125213 Click to see 313.30 unknown https://doi.org/10.1007/S10600-010-9463-2
https://doi.org/10.1007/S10600-010-9606-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Biondinin D 71448950 Click to see 300.40 unknown https://doi.org/10.1080/14786410903281774
Bornyl p-coumarate 6442489 Click to see 300.40 unknown https://doi.org/10.1080/14786410903281774
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.1007/S10600-010-9463-2
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1007/S10600-010-9463-2

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.