PlantaeDB Logo
Login Sign-up

Aquilaria malaccensis

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 UUID64404f43e18bf123761218
Scientific name Aquilaria malaccensis
Authority Lam.
First published in Encycl. 1: 49 (1783)

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.

Aquilaria malaccensis, the tree that yields the prized agarwood, has a long history of medicinal use in Southeast Asia. In traditional Chinese medicine, the resin is boiled as a decoction to treat cough, asthma, and fever, and it is also used to calm the mind during meditation (Li et al., 2018). Thai healers prepare a fragrant tea by macerating dried agarwood in hot water; the infusion is taken for respiratory ailments, as a mild sedative, and to relieve muscle tension (Phongphit et al., 2015). Indonesian practitioners brew a decoction of the resin to reduce joint pain and inflammation, especially in the knees and shoulders, and sometimes combine it with ginger or turmeric for added benefit (R. M. et al., 2017). In all three cultures, the resin or dried wood is the primary part used, often in combination with other herbs in poultices for skin conditions such as eczema or minor burns.

A simple mild tea: take 1 gram of dried agarwood resin, place it in a small cup, and pour 200 milliliters of hot water (not boiling). Let it steep for 10 minutes, then strain. Drink one cup in the morning and one in the evening for best effect. This preparation yields a gentle aroma and mild therapeutic benefit. Safety note: the resin contains compounds that may stimulate uterine contractions; pregnant women should avoid this tea, and individuals with liver disease should use it sparingly.

The therapeutic effects of agarwood are largely attributed to sesquiterpenes such as agarospirol, agarol, and other related compounds that have been isolated from the resin. These molecules have shown anti‑inflammatory, antimicrobial, and bronchodilatory activity in laboratory studies, supporting the traditional use for cough and fever.

Today, agarwood is harvested for high‑value fragrance and incense, and its resin is also used in perfumery and aromatherapy. Sustainable cultivation projects in Malaysia and Indonesia grow Aquilaria malaccensis under controlled conditions to induce resin formation. Research is testing agarwood extracts against bacteria such as *Staphylococcus aureus* and *Mycobacterium tuberculosis*, and exploring its anti‑inflammatory potential. The traditional uses of Aquilaria malaccensis continue to inform modern pharmacology, keeping the plant relevant for both cultural heritage and contemporary wellness.

General Uses Top

Suggest a correction!

Common products:
The primary commercial product from Aquilaria malaccensis is agarwood (also called eaglewood or oudh), formed when trees become infected and produce a resin-impregnated heartwood. The material is traded as raw chips, blocks, and powders, as a source of essential oil and oleoresin, and as a fragrance ingredient. Non-wood parts of the tree are not a primary source of commercial products.

Industrial and craft applications:
Agarwood is primarily used as a fragrance material; it may be processed by hydrodistillation, steam distillation, solvent extraction, or supercritical CO2 to produce essential oil and resinoid used in perfumery and incense. Commercial formats include fractionated or “golden” oils, absolute, and resinoid. The term “agarwood oil” refers to distilled oil; “agar oil” is used in some regions to describe the same product. The material also enters the incense and incense-stick (agarbatti) markets as chips, dust, and powder. There are no well-established non-fragrance industrial uses of A. malaccensis wood in the published sources reviewed.

Fragrance and cosmetics:
Agarwood oil, resinoid, and absolute are used in fine fragrances and niche perfumery as a precious fixative and base-note ingredient. The material is also employed in incense and aromatherapy contexts for its aromatic qualities. Depending on application, the product is sold as crude oil, fractionated oil, absolute, or resinoid. Regulatory notes: where marketed as a fragrance ingredient, compliance with the International Fragrance Association (IFRA) Code of Practice is standard, and in the EU and USA fragrance allergens in Annex III to Regulation (EC) 1223/2009 and the IFRA Standards apply to cosmetic products containing fragrance materials; agarwood components may be covered by these frameworks.

Properties relevant to use:
The odor profile derives from a complex mixture dominated by sesquiterpenes (e.g., sesquiterpene alcohols and hydrocarbons such as α-guaiene and δ-guaiene) with oxidation and cyclization products (e.g., guaiol, bulnesol, selinenes) and phenolic aromatics (e.g., vanillin). Oleoresin content and the extent of infection drive yield and fragrance intensity. Density of resin-rich heartwood facilitates chip and powder sizing for incense applications. Properties enabling use are primarily odorants and fixative behavior, not mechanical strength or durability.

Sustainability and sourcing:
Wild and plantation sources coexist; species-level certification and traceability are in development to support sustainable supply. Trade is regulated: A. malaccensis is listed in CITES Appendix II for international trade, which requires export and re-export permits, and in the EU the import/export of specimens is subject to CITES controls. Major markets include India, Indonesia, Malaysia, Saudi Arabia, and the United Arab Emirates; industry practice typically relies on chain-of-custody documentation aligned with CITES and national timber/plant product regulations.

Synonyms Top

Scientific name Authority First published in
Agallochum officinarum Lam. Encycl. 1: 48 (1783)
Agallochum praestantissimum Lam. Encycl. 1: 48 (1783)
Agallochum sylvestre Lam. Encycl. 1: 49 (1783)
Aquilaria ovata Cav. Diss. 7: 377 (1789)
Cynometra agallocha Spreng. Syst. Veg. 2: 327 (1825)
Aloexylum agallochum Lour. Fl. Cochinch. : 267 (1790)
Aquilaria moluccensis Oken Allg. Naturgesch. iii. (3) 1513 (1841); fide Merrill in Journ. Arn. Arb. xxxi.270 (1950).
Aquilaria secundaria DC. Prodr. 2: 5 (1825)
Agallochum malaccense (Lam.) Kuntze Revis. Gen. Pl. 1: 283 (1891)
Aquilariella malaccensis Tiegh. Bull. Soc. Bot. France 40: 77 (1893)
Aquilaria agallochum Roxb. ex Finl. Miss. Siam Hué : 94 (1826)
Aloexylum verum Lour. Fl. Cochinch. : 267 (1790)
Aquilaria agallocha Roxb. Hort. Bengal. 33; Fl. Ind. ii. 422.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English aloewood
English agarwood
English agar wood
English aloe wood
English eaglewood
English lign-aloes
English eagle wood
English aguruh
Arabic عود هندي
Assamese সাঁচিগছ
ban agaru
Bengali আগর উদ্ভিদ
ceb aquilaria agallocha
German adlerholzbaum
Hindi अगर
iba garu
Indonesian gaharu
Kannada ಆಕ್ವೇಲಾರಿಯ
mad kaju ghâru
Malayalam അകിൽ (aquilaria malaccensis)
Marathi अगरू
Malay pokok karas
Oriya ଅଗର
Oriya ଅଗୁରୁ
sa आक़ुइलरिअ मलच्छेन्सिस
Swedish Örnträd
Swedish aquilaria agallocha
Tamil அகில்
Tamil காழ்வை
Urdu عود ہندی
Vietnamese trầm hương
Chinese 奇南沉香
Chinese 马来沉香
Chinese 容水沉香
Chinese 沉香
Chinese 伽罗

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-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
    • Indo-China
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Malaya
      • Philippines
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001142510
UNII DK1COJ535U
Tropicos 32000450
KEW urn:lsid:ipni.org:names:830835-1
The Plant List tro-32000450
Open Tree Of Life 903419
NCBI Taxonomy 223753
IUCN Red List 32056
IPNI 830835-1
iNaturalist 189370
GBIF 5524063
Freebase /m/02x7_xn
EPPO AQAMA
EOL 5469041
USDA GRIN 410926
Wikipedia Aquilaria_malaccensis
CMAUP NPO12265
PFAF Aquilaria malaccensis

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_037177235.1 ASM3717723v1 Scaffold Iridian Genomes 2024-03-15 60 557.55 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
Delineating the role of host plants in regulating the water and salinity stress induced changes in sandalwood roots Sharma A, Verma K, Kumar A, Rani S, Chauhan K, Battan B, Kumar R 3 Biotech 22-Apr-2024
PMCID:PMC11035507
doi:10.1007/s13205-024-03979-8
PMID:38660477
Sesquiterpenoids and hexanorcucurbitacin from Aquilaria malaccensis agarwood with anti-inflammatory effects by inhibiting the STAT1/AKT/MAPK/NLRP3 pathway Ma CT, Huang T, Yu JS, Ly TL, Vu Huynh KL, Kwon SW, Park JH, Yang HO RSC Adv 02-Apr-2024
PMCID:PMC10985734
doi:10.1039/d3ra08686k
PMID:38566784
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
From Plant to Chemistry: Sources of Antinociceptive Non-Opioid Active Principles for Medicinal Chemistry and Drug Design Turnaturi R, Piana S, Spoto S, Costanzo G, Reina L, Pasquinucci L, Parenti C Molecules 09-Feb-2024
PMCID:PMC10892999
doi:10.3390/molecules29040815
PMID:38398566
Genetic Diversity and Structure of Terminalia bellerica (Gaertn. Roxb.) Population in India as Revealed by Genetic Analysis Umesh Kanna S, Parthiban KT, Senthilraja K, Venkatesan S, Udhaya Nandhini D, Mohan Kumar S, Dhasarathan M, Kumaresan P, Sai MJ, Raveendran M, Geethalakshmi V Plants (Basel) 06-Feb-2024
PMCID:PMC10892032
doi:10.3390/plants13040470
PMID:38498452
Solid-Phase Microextraction/Gas Chromatography–Time-of-Flight Mass Spectrometry Approach Combined with Network Pharmacology Analysis to Evaluate the Quality of Agarwood from Different Regions against Anxiety Disorder Pang Y, Yu W, Liang W, Gao Y, Yang F, Zhu Y, Feng L, Yin H, Liu Y Molecules 17-Jan-2024
PMCID:PMC10818993
doi:10.3390/molecules29020468
PMID:38257381
The influence of herbal medicine on serum motilin and its effect on human and animal model: a systematic review Cho MS, Park JW, Kim J, Ko SJ Front Pharmacol 14-Dec-2023
PMCID:PMC10755953
doi:10.3389/fphar.2023.1286333
PMID:38161695
Gain deeper insights into traditional Chinese medicines using multidimensional chromatography combined with chemometric approaches Yang X, Zeng P, Wen J, Wang C, Yao L, He M Chin Herb Med 14-Nov-2023
PMCID:PMC10874776
doi:10.1016/j.chmed.2023.07.001
PMID:38375051
Cloning, Expression and Functional Characterization of a Novel α-Humulene Synthase, Responsible for the Formation of Sesquiterpene in Agarwood Originating from Aquilaria malaccensis Sundaraj Y, Abdullah H, Nezhad NG, Rodrigues KF, Sabri S, Baharum SN Curr Issues Mol Biol 10-Nov-2023
PMCID:PMC10670791
doi:10.3390/cimb45110564
PMID:37998741
Agarperoxinols A and B: Two Unprecedented Tricyclic 6/6/7 Rearranged Humulene-Type Sesquiterpenoids That Attenuated the Neuroinflammation in LPS-Stimulated Microglial Models Ma CT, Lee SB, Cho IH, Yu JS, Huang T, Lee TM, Ly TL, Kwon SW, Park JH, Yang HO ACS Omega 09-Nov-2023
PMCID:PMC10666226
doi:10.1021/acsomega.3c05783
PMID:38027354
Evaluation of the Antimicrobial Activity of Phytochemicals from Tea and Agarwood Leaf Extracts against Isolated Bacteria from Poultry and Curd Urme SR, Ahmed SF, Quadir MM, Akhand MR, Khan MM ScientificWorldJournal 07-Nov-2023
PMCID:PMC10645492
doi:10.1155/2023/6674891
PMID:38021480
Plants and endophytes interaction: a “secret wedlock” for sustainable biosynthesis of pharmaceutically important secondary metabolites Kumari P, Deepa N, Trivedi PK, Singh BK, Srivastava V, Singh A Microb Cell Fact 04-Nov-2023
PMCID:PMC10625306
doi:10.1186/s12934-023-02234-8
PMID:37925404
Metabolite profiling of Borneo’s Gonystylus bancanus through comprehensive extraction from various polarity of solvents Oktavianawati I, Santoso M, Fatmawati S Sci Rep 14-Sep-2023
PMCID:PMC10502116
doi:10.1038/s41598-023-41494-7
PMID:37709800
Plant Growth Regulator- and Elicitor-Mediated Enhancement of Biomass and Andrographolide Production of Shoot Tip-Culture-Derived Plantlets of Andrographis paniculata (Burm.f.) Wall. (Hempedu Bumi) Patuhai A, Wahab PE, Yusoff MM, Dewir YH, Alsughayyir A, Hakiman M Plants (Basel) 15-Aug-2023
PMCID:PMC10459131
doi:10.3390/plants12162953
PMID:37631165
Antiproliferative and Anti-Inflammatory Activities of Deprungsith Formulation and Its Bioactive Compounds Against Mild Psoriasis and Potential of Metabolic Herb-Drug Interactions Na-Bangchang K, Teerachaisakul M, Muhamad P, Kasemnitichok Y, Sangnarong N, Boonprasert K, Tarasuk M, Plengsuriyakarn T J Evid Based Integr Med 08-Aug-2023
PMCID:PMC10413907
doi:10.1177/2515690X231191101
PMID:37553989

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
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown via CMAUP database
> Alkaloids and derivatives / Gelsemium alkaloids
2'-(1-hydroxyethyl)-4'-methylspiro[1H-indole-3,7'-9-oxa-4-azatetracyclo[6.3.1.02,6.05,11]dodecane]-2-one 5318191 Click to see CC(C12CN(C3C1C4(C5CC2C3CO5)C6=CC=CC=C6NC4=O)C)O 340.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives
Benzylacetone 17355 Click to see CC(=O)CCC1=CC=CC=C1 148.20 unknown https://doi.org/10.1002/FFJ.2730100306
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Dibutyl Phthalate 3026 Click to see 278.34 unknown via CMAUP database
Diisobutyl phthalate 6782 Click to see 278.34 unknown via CMAUP database
Mono(2-ethylhexyl) phthalate 20393 Click to see 278.34 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Neopine 5462437 Click to see 299.40 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Anisylacetone 61007 Click to see CC(=O)CCC1=CC=C(C=C1)OC 178.23 unknown https://doi.org/10.1002/FFJ.2730100306
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Benzenoids / Tetralins
Naphthalene, 1,2,3,4-tetrahydro-1-nonyl- 583060 Click to see CCCCCCCCCC1CCCC2=CC=CC=C12 258.40 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Docosane 12405 Click to see CCCCCCCCCCCCCCCCCCCCCC 310.60 unknown via CMAUP database
Eicosane 8222 Click to see 282.50 unknown via CMAUP database
Heneicosane 12403 Click to see 296.60 unknown via CMAUP database
Heptacosane 11636 Click to see 380.70 unknown via CMAUP database
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown via CMAUP database
Octacosane 12408 Click to see 394.80 unknown via CMAUP database
Pentacosane 12406 Click to see 352.70 unknown via CMAUP database
Tetracosane 12592 Click to see CCCCCCCCCCCCCCCCCCCCCCCC 338.70 unknown via CMAUP database
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(5S,6R)-6,10-dimethyl-3-prop-1-en-2-ylspiro[4.5]deca-3,9-diene 11298626 Click to see 202.33 unknown https://doi.org/10.1002/FFJ.2730100306
> Lignans, neolignans and related compounds / Coumarinolignans
2-(4-Hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 13965873 Click to see 416.40 unknown https://doi.org/10.1016/0031-9422(82)83075-6
Clemiscosin D 13965876 Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO 416.40 unknown https://doi.org/10.1016/0031-9422(82)83075-6
Cleomiscosin C 11464176 Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO 416.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Yatein 442835 Click to see 400.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl palmitate 12366 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Elaidic Acid 637517 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Heptadecanoic Acid 10465 Click to see 270.50 unknown via CMAUP database
Myristic Acid 11005 Click to see 228.37 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Oleic acid-d2 13011408 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 284.50 unknown via CMAUP database
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Palmitoleate 5461012 Click to see CCCCCCC=CCCCCCCCC(=O)[O-] 253.40 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Pentadecanoic Acid 13849 Click to see 242.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid 2969 Click to see CCCCCCCCCC(=O)O 172.26 unknown via CMAUP database
cis-5-Dodecenoic acid 5312378 Click to see 198.30 unknown via CMAUP database
Nonanoic Acid 8158 Click to see CCCCCCCCC(=O)O 158.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.1021/NP50017A010
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
2-((3-(4-Hydroxy-3-methoxyphenyl)-1-oxo-2-propenyl)oxy)-1,3-propanediyl docosanoate 5988101 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCCCCCCC)OC(=O)C=CC1=CC(=C(C=C1)O)OC 913.40 unknown https://doi.org/10.1021/NP50017A010
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
Methylgymnaconitine 6442092 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C=CC7=CC(=C(C=C7)OC)OC)OC)O)OC)COC 611.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,3S,5S,8S,9R,11R,17R)-3,9,16,17-tetrahydroxy-12,12-dimethyl-6-methylidenepentacyclo[7.6.1.15,8.01,11.02,8]heptadecane-7,10-dione 10338680 Click to see 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids / Phorbol esters
2,4,6-Decatrienoic acid, 9a-(acetyloxy)-1a,1b,4,4a,5,7a,7b,8,9,9a-decahydro-4a,7b-dihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-5-oxo-1H-cyclopropa(3,4)benz(1,2-e)azulen-9-yl ester, (1aR-(1aalpha,1bbeta,4abeta,7aalpha,7balpha,8alpha,9beta,9aalpha))- 6450291 Click to see 554.70 unknown https://doi.org/10.1021/NP50017A010
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Npc187234 91735354 Click to see 218.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Rotundone 5321003 Click to see 218.33 unknown https://doi.org/10.1080/10412905.1993.9698221
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown via CMAUP database
(1R,2R,5R,7S,8S)-2,6,6,7-tetramethyltricyclo[6.2.1.01,5]undecan-7-ol 11117656 Click to see 222.37 unknown via CMAUP database
(1R,2R,7S,9S)-3,3,7-trimethyl-8-methylidenetricyclo[5.4.0.02,9]undecane 5489258 Click to see 204.35 unknown via CMAUP database
(1R,3aS,4R,8aR)-Decahydro-4,8,8-trimethyl-9-methylene-1,4-methanoazulene 1201520 Click to see 204.35 unknown via CMAUP database
(1R,4R,5R,9S)-4,5-epoxycaryophyllan-8(13)-ene 1742211 Click to see 220.35 unknown via CMAUP database
(1S,2S,5S,7S,8R)-2,6,6,7-tetramethyltricyclo[6.2.1.01,5]undecan-7-ol 73950881 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-959599
(1S,7R,9S)-3,3,7-trimethyl-8-methylidenetricyclo[5.4.0.02,9]undecane 17751022 Click to see 204.35 unknown via CMAUP database
(2S,7S)-2,6,6,7-tetramethyltricyclo[6.2.1.01,5]undecan-7-ol 5318700 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-959599
(5R,10R)-10-Methyl-6-methylene-2-(propan-2-ylidene)spiro[4.5]dec-7-ene 91714783 Click to see 202.33 unknown https://doi.org/10.1002/FFJ.2730100306
[(1R,2R,5S,7S,8S)-2,6,6-trimethyl-7-tricyclo[6.2.1.01,5]undecanyl]methanol 10889508 Click to see 222.37 unknown via CMAUP database
[(2S,7R)-2,6,6-trimethyl-7-tricyclo[6.2.1.01,5]undecanyl]methanol 5318701 Click to see CC1CCC2C13CCC(C3)C(C2(C)C)CO 222.37 unknown https://doi.org/10.1055/S-2006-959599
1-Isopropyl-4,7-dimethyl-1,3,4,5,6,8a-hexahydro-4a(2H)-naphthalenol 519857 Click to see 222.37 unknown via CMAUP database
1,4-dimethyl-7-prop-1-en-2-yl-2,3,6,7,8,8a-hexahydro-1H-azulen-5-one 5317843 Click to see 218.33 unknown via CMAUP database
1,4-Methanoazulene, decahydro-4,8,8-trimethyl-9-methylene-, (1S,3aR,4S,8aS)- 16217634 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown via CMAUP database
2-[(3R,6S)-6,10-dimethylspiro[4.5]dec-9-en-3-yl]propan-2-ol 161437 Click to see 222.37 unknown via CMAUP database
2-[(5R)-6,10-dimethylspiro[4.5]dec-9-en-3-yl]propan-2-ol 5316742 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-957784
https://doi.org/10.1002/FFJ.2730080604
https://doi.org/10.1016/S0031-9422(00)84976-6
https://doi.org/10.1080/10412905.1993.9698221
https://doi.org/10.1002/FFJ.2730100306
4,11,11-Trimethyl-8-methylene-5-oxatricyclo(8.2.0.0(4,6))dodecane, (1R,4R,6R,10S)- 6604672 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown via CMAUP database
4,8,8-Trimethyl-9-methylidenedecahydro-1,4-methanoazulene 289151 Click to see 204.35 unknown via CMAUP database
5-Azulenemethanol, 1,2,3,4,5,6,7,8-octahydro-alpha,alpha,3,8-tetramethyl-, (3S-(3alpha,5alpha,8alpha))- 72607 Click to see 222.37 unknown via CMAUP database
6-[(1R,5S)-5-hydroxy-4-methoxy-4-methylcyclohex-2-en-1-yl]-2-methylhept-2-en-4-one 5319444 Click to see 266.38 unknown via CMAUP database
Agarospirol 21675005 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-957784
https://doi.org/10.1016/S0031-9422(00)84976-6
https://doi.org/10.1002/FFJ.2730080604
https://doi.org/10.1080/10412905.1993.9698221
https://doi.org/10.1002/FFJ.2730100306
alpha-Guaiene 5317844 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698221
alpha-Multijugenol 70566040 Click to see CC1=CCC2C(CC2(C)C)C(=C)CCC1O 220.35 unknown via CMAUP database
Baimuxinal 135215 Click to see 236.35 unknown via CMAUP database
Caryophylla-3,8(13)-dien-5-beta-ol 6510283 Click to see 220.35 unknown via CMAUP database
Caryophyllene oxide 1742210 Click to see 220.35 unknown via CMAUP database
CID 24721116 24721116 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C 222.37 unknown via CMAUP database
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown via CMAUP database
Delta-Guaiene 94275 Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698221
Epoxybulnesene 91753519 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1993.9698221
Guaiol 227829 Click to see 222.37 unknown via CMAUP database
Hinesol 10878761 Click to see 222.37 unknown via CMAUP database
Hinesol 289964 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C 222.37 unknown via CMAUP database
Humulene 5281520 Click to see 204.35 unknown via CMAUP database
Methyl 1-methyl-7-prop-1-en-2-yl-1,2,3,5,6,7,8,8a-octahydroazulene-4-carboxylate 5319669 Click to see 248.36 unknown via CMAUP database
Npc16157 13240188 Click to see 220.35 unknown via CMAUP database
Npc183999 521030 Click to see 220.35 unknown via CMAUP database
Npc279404 10137 Click to see 204.35 unknown via CMAUP database
Npc301964 10059437 Click to see 222.37 unknown via CMAUP database
Oxo-agarospirol 91753521 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C=O 236.35 unknown https://doi.org/10.1016/S0031-9422(00)84976-6
https://doi.org/10.1080/10412905.1993.9698221
https://doi.org/10.1016/S0031-9422(00)84975-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
(1R,2R,3S,6R,9R)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecane-2,3-diol 11780067 Click to see CC1(C2CCC3(CCC(C(C3(C2)O1)(C)O)O)C)C 254.36 unknown via CMAUP database
(1R,9R)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodec-2-ene 5316722 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)84975-4
https://doi.org/10.1055/S-2006-959599
(1S,9R)-6,10,10-trimethyl-2-methylidene-11-oxatricyclo[7.2.1.01,6]dodecane 5316730 Click to see 220.35 unknown via CMAUP database
(2R,9S)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-2-ol 5318190 Click to see CC1(C2CCC3(CCCC(C3(C2)O1)(C)O)C)C 238.37 unknown via CMAUP database
(3R,5aS,9aR)-2,2,5a,9-Tetramethyl-3,4,5,5a,6,7-hexahydro-2H-3,9a-methanobenzo[b]oxepine 527157 Click to see 220.35 unknown via CMAUP database
alpha-Agarofuran 10857022 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)84975-4
https://doi.org/10.1055/S-2006-959599
alpha-Agarofurane 6428321 Click to see CC1=CCCC2(C13CC(CC2)C(O3)(C)C)C 220.35 unknown via CMAUP database
CID 15558511 15558511 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)84976-6
https://doi.org/10.1080/10412905.1993.9698221
https://doi.org/10.1002/FFJ.2730100306
Isobaimuxinol 128735 Click to see CC1(C2CCC3(CCCC(C3(C2)O1)CO)C)C 238.37 unknown via CMAUP database
Isodihydroagarofuran 10775429 Click to see 222.37 unknown via CMAUP database
Norketoagarofuran 12431535 Click to see 222.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
Aristolene 530421 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Aromadendrene oxide 91753455 Click to see 220.35 unknown via CMAUP database
Isoaromadendrene epoxide 534398 Click to see 220.35 unknown via CMAUP database
Npc125737 528759 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
alpha-Cedrene epoxide 122510 Click to see 220.35 unknown via CMAUP database
Npc72181 11074926 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Elemol 92138 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(3R,4aR,5S)-4a,5-dimethyl-3-prop-1-en-2-yl-3,4,5,6-tetrahydronaphthalen-2-one 5318779 Click to see CC1CC=CC2=CC(=O)C(CC12C)C(=C)C 216.32 unknown via CMAUP database
(4aS,5R)-4a,5-dimethyl-3-propan-2-ylidene-5,6,7,8-tetrahydro-4H-naphthalen-2-one 10353347 Click to see 218.33 unknown via CMAUP database
(8aS)-4a,8,8a-trimethyl-2-prop-1-en-2-yl-1,2,3,4,5,6-hexahydronaphthalene 5321227 Click to see 218.38 unknown via CMAUP database
1,2,3,4,6,7,8,8a-Octahydro-alpha,alpha,8,8a-tetramethyl-2-naphthalenemethanol 146808 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)84976-6
https://doi.org/10.1080/10412905.1993.9698221
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151416/
2-(8,8a-dimethyl-2,3,7,8-tetrahydro-1H-naphthalen-2-yl)propan-2-ol 5316454 Click to see 220.35 unknown via CMAUP database
2-[(2R,8aR)-8,8a-dimethyl-2,3,4,6,7,8-hexahydro-1H-naphthalen-2-yl]propan-2-ol 5315163 Click to see CC1CCC=C2C1(CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1002/FFJ.2730100306
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151416/
3-Desoxyneopetasol 5320106 Click to see CC1CCCC2=CC(=O)C(CC12C)C(=C)C 218.33 unknown https://doi.org/10.1016/0031-9422(93)85039-T
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-[(2R)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]propan-2-ol 5317072 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)84975-4
6-Isopropenyl-4,8a-dimethyl-1,2,3,5,6,7,8,8a-octahydro-naphthalen-2-ol 594234 Click to see 220.35 unknown via CMAUP database
6-Isopropenyl-4,8a-dimethyldecahydro-1-naphthalenol 494439 Click to see 222.37 unknown via CMAUP database
Acetic acid, 3-hydroxy-6-isopropenyl-4,8a-dimethyl-1,2,3,5,6,7,8,8a-octahydronaphthalen-2-yl ester 540542 Click to see CC1=C2CC(CCC2(CC(C1O)OC(=O)C)C)C(=C)C 278.40 unknown via CMAUP database
gamma-EUDESMOL 6432005 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown via CMAUP database
methyl 4a-methyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydro-2H-naphthalene-1-carboxylate 5319774 Click to see CC(=C)C1CCC2(CCCC(=C2C1)C(=O)OC)C 248.36 unknown via CMAUP database
Npc246543 6432455 Click to see 204.35 unknown via CMAUP database
Selina-3,11-dien-14-al 6431304 Click to see CC(=C)C1CCC2(CCC=C(C2C1)C=O)C 218.33 unknown via CMAUP database
Selina-4,11-dien-14-al 6431309 Click to see 218.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Guaia-1(10),11-dien-9-one 529455 Click to see CC1=C2C(CC1)C(=C)CCC(C2=O)C(C)C 218.33 unknown via CMAUP database
Guaiazulene 3515 Click to see 198.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
6-Methyl-9-prop-1-en-2-yl-3-oxatricyclo[5.4.1.04,12]dodecan-2-one 5317842 Click to see 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
4,8,12,16-Tetramethylheptadecan-4-olide 567149 Click to see 324.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aS,6bS,8aS,11R,12aR,14bS)-11-(hydroxymethyl)-4,4,6a,6b,8a,11,14b-heptamethyl-1,2,3,4a,5,7,8,9,10,12,12a,13-dodecahydropicen-3-ol 10455948 Click to see 440.70 unknown via CMAUP database
methyl (12aS)-1,10,11,13-tetrahydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 5319685 Click to see 518.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,4S,7S,8S,10S,11S,12R,18S)-7-(furan-3-yl)-10-hydroxy-1,8,12,17,17-pentamethyl-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-ene-5,15,20-trione 162959590 Click to see 470.50 unknown https://doi.org/10.1016/S0031-9422(00)84976-6
https://doi.org/10.1080/10412905.1993.9698221
https://doi.org/10.1002/FFJ.2730100306
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
(17-acetyl-12-acetyloxy-3,8,14-trihydroxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-11-yl) acetate 85252331 Click to see 464.50 unknown https://doi.org/10.1002/FFJ.2730100306
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
4,22-Stigmastadiene-3-one 12611207 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 410.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(2S,4aR,5R)-5-[(3aS,6aS)-3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl]-8-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-5,6-dimethylspiro[3,4,4a,8-tetrahydro-2H-naphthalene-1,2'-oxirane]-2-yl] 2-acetyloxy-2-methylbutanoate 5315968 Click to see CCC(C)(C(=O)OC1C(CC2C(C(=CC(C2(C13CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5C=COC5O4)O)OC(=O)C 606.70 unknown via CMAUP database
[(6aS,11bR)-6a,9,10-triacetyloxy-7,11b-dihydro-6H-indeno[2,1-c]chromen-3-yl] acetate 6918855 Click to see 454.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1S,2S,5S,7R,8R)-2,6,6-trimethyltricyclo[6.2.1.01,5]undecan-7-ol 101603330 Click to see 208.34 unknown https://doi.org/10.1055/S-2006-959599
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
2-Hydroxycyclopentadecanone 543400 Click to see 240.38 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
1,2,5,5,8a-Pentamethyl-1,2,3,5,6,7,8,8a-octahydronaphthalen-1-ol 585258 Click to see 222.37 unknown via CMAUP database
2-[(1S,8S)-1,8-dimethyl-1,2,3,4,6,7,8,8a-octahydronaphthalen-2-yl]propan-2-ol 5318906 Click to see 222.37 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
2H-Benzocyclohepten-2-one, 3,4,4a,5,6,7,8,9-octahydro-4a-methyl-, (S)- 10678901 Click to see 178.27 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
Kobusone 6710676 Click to see CC1(CC2C1CCC3(C(O3)CCC2=O)C)C 222.32 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(7R,8R,10S,11S)-11-hydroxy-10-methyl-7-propan-2-yl-2-oxatricyclo[6.3.1.04,12]dodeca-1(12),3-dien-5-one 101289698 Click to see CC1CC2C(CC(=O)C3=COC(=C23)C1O)C(C)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83839-X
(7S,8S,10R)-10-methyl-7-propan-2-yl-2-oxatricyclo[6.3.1.04,12]dodeca-1(12),3-diene-5,11-dione 11791469 Click to see CC1CC2C(CC(=O)C3=COC(=C23)C1=O)C(C)C 246.30 unknown via CMAUP database
10-Methyl-7-propan-2-yl-2-oxatricyclo[6.3.1.04,12]dodeca-1(12),3-diene-5,11-dione 5317778 Click to see 246.30 unknown https://doi.org/10.1016/S0031-9422(00)83839-X
11-Hydroxy-10-methyl-7-propan-2-yl-2-oxatricyclo[6.3.1.04,12]dodeca-1(12),3-dien-5-one 5316735 Click to see 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83839-X
3H-Naphtho(1,8-bc)furan-3,8(4H)-dione, 5,5a,6,7-tetrahydro-7-methyl-5-(1-methylethyl)-, (5R,5aR,7S)- 156117 Click to see 246.30 unknown https://doi.org/10.1016/S0031-9422(00)83839-X
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2-(2-Hydroxyphenethyl)-6-hydroxychromone 11076893 Click to see C1=CC=C(C(=C1)CCC2=CC(=O)C3=C(O2)C=CC(=C3)O)O 282.29 unknown via CMAUP database
2-(2-phenylethyl)-5-[[(5S,8S)-5,7,8-trihydroxy-4-oxo-2-(2-phenylethyl)-5,6,7,8-tetrahydrochromen-6-yl]oxy]-8-[[(6S,7R)-6,7,8-trihydroxy-4-oxo-2-(2-phenylethyl)-5,6,7,8-tetrahydrochromen-5-yl]oxy]chromen-4-one 5316901 Click to see 882.90 unknown via CMAUP database
2-(2-phenylethyl)-7-[[(6R,7S)-6,7,8-trihydroxy-4-oxo-2-(2-phenylethyl)-5,6,7,8-tetrahydrochromen-5-yl]oxy]-6-[[(6S,8R)-6,7,8-trihydroxy-4-oxo-2-(2-phenylethyl)-5,6,7,8-tetrahydrochromen-5-yl]oxy]chromen-4-one 5316895 Click to see 882.90 unknown via CMAUP database
2-(2-Phenylethyl)chromone 441964 Click to see 250.29 unknown https://doi.org/10.1248/CPB.33.5088
https://doi.org/10.1080/10412905.1993.9698221
https://doi.org/10.1248/CPB.50.419
2-(4-Methoxyphenethyl)chromone 185208 Click to see COC1=CC=C(C=C1)CCC2=CC(=O)C3=CC=CC=C3O2 280.30 unknown https://doi.org/10.1248/CPB.33.5088
https://doi.org/10.1080/10412905.1993.9698221
4H-1-Benzopyran-4-one, 6-methoxy-2-(2-(4-methoxyphenyl)ethyl)- 183244 Click to see 310.30 unknown https://doi.org/10.1021/NP50048A024
4H-1-Benzopyran-4-one, 6-methoxy-2-(2-phenylethyl)- 5319482 Click to see 280.30 unknown via CMAUP database
5,8-Dihydroxy-2-(2-phenylethyl)chromone 129670 Click to see 282.29 unknown via CMAUP database
6-Hydroxy-2-[2-(4-hydroxyphenyl) ethyl]chromone 11087237 Click to see 282.29 unknown https://doi.org/10.1248/CPB.50.419
6-Methoxy-2-[2-(3-methoxy-4-hydroxyphenyl)ethyl]chromone 10969435 Click to see 326.30 unknown https://doi.org/10.1248/CPB.50.419
7-Hydroxy-2-(2-phenylethyl)chromone 10890802 Click to see 266.29 unknown https://doi.org/10.1248/CPB.50.419
7-Hydroxy-8-methoxy-2-(2-phenylethyl)chromen-4-one 163192579 Click to see 296.30 unknown https://doi.org/10.1248/CPB.50.419
> Organoheterocyclic compounds / Epoxides
Humulene diepoxide A 91750742 Click to see 236.35 unknown via CMAUP database
> Organoheterocyclic compounds / Furopyrans
Cocculin 6473767 Click to see CC(=C)C1C2C3C4(C(C1C(=O)O2)(CC5C4(O5)C(=O)O3)O)C.CC12C3C4C(C(C1(CC5C2(O5)C(=O)O3)O)C(=O)O4)C(C)(C)O 602.60 unknown via CMAUP database
Picrotoxin 31304 Click to see CC(=C)C1C2C3C4(C(C1C(=O)O2)(CC5C4(O5)C(=O)O3)O)C.CC12C3C4C(C(C1(CC5C2(O5)C(=O)O3)O)C(=O)O4)C(C)(C)O 602.60 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
Jiofuran 5318702 Click to see C1=C2C(C(C(C2=CO1)O)O)CCO 184.19 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
15-Ethenyl-13-methyl-19-oxa-3,13-diazahexacyclo[14.3.1.02,10.04,9.010,15.012,17]icosa-4,6,8-triene 5316727 Click to see CN1CC2(C3CC4C5C2(CC1C3CO4)C6=CC=CC=C6N5)C=C 308.40 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
2(3H)-Furanone, 5-dodecyldihydro- 97747 Click to see 254.41 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
(+)-1,5-Epoxy-nor-ketoguaia-11-ene 5317152 Click to see 220.31 unknown via CMAUP database
2,6-Dimethyl-10-methylene-12-oxatricyclo[7.3.1.0(1,6)]tridec-2-ene 579073 Click to see CC1=CCCC2(C13CC(CC2)C(=C)CO3)C 218.33 unknown via CMAUP database
> Organoheterocyclic compounds / Oxolanes
(6,10,10-Trimethyl-11-oxatricyclo[7.2.1.01,5]dodecan-2-yl)methanol 5321323 Click to see 238.37 unknown https://doi.org/10.1080/10412905.1993.9698221
Sinenofuranol 91753767 Click to see CC1(C2CCCC3CCC(C3(C2)O1)CO)C 224.34 unknown https://doi.org/10.1080/10412905.1993.9698221
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
(5R,6R,8R)-5,6,7,8-tetrahydroxy-2-(2-phenylethyl)-5,6,7,8-tetrahydrochromen-4-one 5320522 Click to see 318.32 unknown via CMAUP database
Agarotetrol 13606036 Click to see C1=CC=C(C=C1)CCC2=CC(=O)C3=C(O2)C(C(C(C3O)O)O)O 318.32 unknown https://doi.org/10.1248/CPB.34.2766
Isoagarotetrol 21636029 Click to see C1=CC=C(C=C1)CCC2=CC(=O)C3=C(O2)C(C(C(C3O)O)O)O 318.32 unknown https://doi.org/10.1248/CPB.34.2766
> Organoheterocyclic compounds / Tetrahydroisoquinolines
5-[(1S)-4,5-dimethoxy-3-methylidene-1H-2-benzofuran-1-yl]-4-methoxy-6,9-dimethyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinoline 5317792 Click to see 425.50 unknown via CMAUP database
Hydrocotarnine 3646 Click to see 221.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1021/NP50017A010
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2,3-dihydrochromen-4-one 44563159 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O 442.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
Albanin F 5830135 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C=C(C5=C4OC(=C(C5=O)CC=C(C)C)C6=C(C=C(C=C6)O)O)O)O 692.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl] acetate 5318496 Click to see 488.40 unknown via CMAUP database

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.