Details Top

Internal ID UUID68f91e3036af1545827088
Scientific name Bergera koenigii
Authority L.
First published in Mant. Pl. : 565 (1767)

Ethnobotanical Use Top

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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.

Murraya koenigii, commonly known as the curry‑leaf tree, has a long history of use as an herbal infusion in several South Asian and African traditions. In Ayurvedic practice in India, dried leaves are steeped in hot water to produce a mild tea that is taken to relieve stomach pain, diarrhea, and flatulence; this use is documented in the Indian Pharmacopoeia, 2018. In Sri Lanka, the same leaves are brewed as a tea to soothe coughs and colds, a practice described in the Sri Lankan Traditional Medicine Journal, 2015. In parts of East Africa, particularly Kenya, a decoction of fresh leaves is consumed to reduce fever and to support the treatment of malaria, as reported in the African Journal of Traditional, Complementary and Alternative Medicines, 2014. In all three cultures the primary plant part used is the fresh or dried leaf, and the preparation is an infusion or decoction rather than a maceration or poultice.

A simple, safe recipe for a mild curry‑leaf tea is as follows: take 5 g of dried Murraya koenigii leaves and add them to 250 ml of freshly boiled water. Allow the mixture to steep for 5 minutes, then strain and drink two cups per day. This dosage is well within the limits used in traditional practice and is unlikely to cause adverse effects. However, because the leaves contain essential oils that can be irritating in large amounts, it is advisable to keep the daily intake below 10 g of dried leaves, and pregnant women should consult a healthcare provider before regular consumption.

The therapeutic effects of the tea are largely attributed to the essential‑oil constituents that have been isolated from the leaves. Limonene, linalool, eucalyptol, and beta‑pinene are the most abundant compounds, and each has documented anti‑inflammatory, antimicrobial, and antispasmodic activity. Limonene, for example, has been shown to reduce intestinal inflammation in animal models, while linalool exhibits antidiarrheal properties. The combination of these terpenes likely underlies the traditional use of the infusion for gastrointestinal upset and respiratory irritation.

Modern research continues to validate these ethnobotanical claims. Recent studies in the Journal of Ethnopharmacology, 2022, have demonstrated that Murraya koenigii leaf extract can lower blood glucose levels in diabetic rats, and other investigations have confirmed its antioxidant capacity. The plant remains commercially available as a spice in grocery stores worldwide, and its essential oil is also sold as a natural flavoring and aromatherapy product, ensuring that the traditional uses of this humble leaf are still accessible today.

General Uses Top

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Common products:
Fresh or dried leaf (culinary flavoring); leaf essential oil (flavor/fragrance); seed oil (edible and industrial uses); occasionally fruit pulp (regional food ingredient).

Industrial and craft applications:
Leaf essential oil is used as a flavoring agent in processed foods and as a fragrance component in soaps and detergents; solvent extraction yields an oleoresin used as a natural flavor concentrate in savory foods and feedstocks. The oil contains carbazole alkaloids; eugenol, β-caryophyllene, and α-pinene are prominent components reported in regional spice literature. Seed oil’s fatty acid profile (high in linoleic acid) is suitable for cosmetic emollient applications and industrial uses such as soapstock or as a frying medium under validated food-processing conditions.

Food and beverages (non-medicinal):
Curry leaves (Bergera koenigii) are a staple seasoning in South Asian cuisine, added whole or fried to tempering and spicing mixtures for their distinctive aroma; dried leaves are also used for the same purpose. The seed oil is employed as an edible oil for cooking and frying, and the fruit pulp is used in some regional food products. Non-leaf materials are only mentioned where they are explicitly documented for this species.

Colorants and tanning:
This taxon is not documented as a source of natural dyes, tannins, or colorants for textile or leather processing in the referenced sources.

Wood and fiber:
Wood is used locally for fuel and small crafts; no industrial-grade timber use or fiber applications are documented for this species.

Fragrance and cosmetics:
Leaf essential oil is used in fragrance and flavor blends for soaps, detergents, and processed foods; its carbazole alkaloid content underpins characteristic aromatic notes. The seed oil is used in cosmetic emulsions, where its fatty acid composition provides emollient properties.

Properties relevant to use:
Leaf volatile oil includes eugenol, β-caryophyllene, α-pinene, and γ-terpinene; the oil is described as strongly aromatic. Seed oil is characterized by high linoleic acid content, a favorable iodine value for food and cosmetic uses, and a saponification value typical of non-drying triglyceride oils. The seed oil’s yellow color is noted in spice utilization literature.

Standards and regulation:
Food uses are governed by national food additive and labeling rules where marketed; leaf essential oil and seed oil follow regional practices for flavor/fragrance and cosmetic raw materials. No species-specific ISO/ASTM/EN standards are documented.

Sustainability and sourcing:
Leaves are harvested from smallholder trees in India and neighboring regions; due to high local demand and seasonal supply variability, yields and quality can fluctuate. Sustainable harvesting focuses on leaving sufficient leaf area for tree health and avoiding bark damage during plucking.

Synonyms Top

Scientific name Authority First published in
Nimbo melioides Dennst. Schlüssel Hortus Malab. : 30 (1818)
Murraya siamensis Craib Bull. Misc. Inform. Kew 1926: 340 (1926)
Murraya foetidissima Teijsm. & Binn. Natuurk. Tijdschr. Ned.-Indië 27: 41 (1864)
Camunium koenigii (Spreng.) Kuntze Revis. Gen. Pl. 1: 99. 1891 [5 Nov 1891]
Chalcas koenigii Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 44: 132 (1875)
Chalcas siamensis Tanaka Bull. Soc. Bot. France 75: 710 (1928)
Murraya koenigii (L.) Spreng. Syst. Veg. 2: 315 (1825)
Bergera siamensis (Craib) F.J.Mou Eur. J. Taxon. 860: 168 2023

Common names Top

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Language Common/alternative name
English curryleaftree
Spanish arbol de curry
Spanish Árbol de curry
Spanish arbol del curry
Spanish Árbol del curry
ace teumurui
ace teumuruy
Afrikaans kerrieboom
Arabic مورايا كونيجية
Assamese curry tree
Assamese curry patta
Assamese curry leaves
Assamese নৰসিংহ
Assamese curry-leaf tree
Assamese curry leaf
Bulgarian къри
Bengali বারসুঙ্গা
br delioù-kari
br kaloupile
Catalan arbre de fulla de curri
Catalan fulla de curri
German curryblatt
German curryblätter
German currybaum
dv ހިކަނދިފަތް
Greek Μουρραιΐα του Κένιγκ
Persian درخت کاری
Finnish intianjasmikki
French caloupilé
French feuille de curry
French kaloupile
French karipoulé
French kaloupilé
Gujarati મીઠો લીમડો
Hebrew קארי
Hindi करी पत्ता
Hindi मीठी नीम
Hindi कढ़ी पत्ते का पेड़
Indonesian daun kari
Indonesian temurui
Indonesian salam koja
Japanese カレーノキ
Japanese カレーリーフ
Japanese ナンヨウサンショウ
Japanese ナンヨウザンショウ
Japanese 南洋山椒
Japanese 大葉月橘
Japanese オオバゲッキツ
Kannada ಕರಿಬೇವಿನ ಮರ
Korean 커리나무
mad enggu'
Malayalam കറിവേപ്പ്
Malayalam curry tree
Malayalam കരിയേപ്പ്
Malayalam കറിവേപ്പില
Marathi गोडलिंब
Marathi कढीलिंब
Marathi कडी पत्ता
Marathi कडीपत्ता
Malay pokok kari
Dutch kerrieblad
Dutch kerrieboom
Oriya ଭୃସଙ୍ଗ ଗଛ
Punjabi ਕੜ੍ਹੀ ਪੱਤੇ ਦਾ ਰੁੱਖ
pam curry tree
Polish murraja koeniga
Polish liście curry
Portuguese caril
Russian Муррайя Кёнига
Russian Дерево карри
sa कृष्णनिम्बपत्रम्
sa कालशाकम्
Sinhala කරපිංචා
Tamil கறிவேம்பு
Tamil கறிவேப்பிலை
tcy ಬೇಸೊಪ್ಪು
Telugu కరివేపాకు
Ukrainian дерево каррі
vec àlboro de cari
vec fòje de cari
vec fòja de cari
vec fògia de cari
vec fòge de cari
Chinese 調料九里香
Chinese 咖喱树
Chinese 咖喱叶
Chinese 咖哩葉
Chinese 咖哩樹
Chinese 可因氏月橘
Chinese 麻绞叶
Chinese 哥埋养榴
Chinese 调料九里香
Chinese 九里香

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
UNII 67UQM80W9W
USDA Plants MUKO
Tropicos 28100029
INPN 706554
KEW urn:lsid:ipni.org:names:774433-1
The Plant List tro-28100029
Missouri Botanical Garden 286747
NCBI Taxonomy 159030
IPNI 774433-1
iNaturalist 123745
GBIF 5421333
Freebase /m/03h5wg
EPPO MUYKO
EOL 483522
Elurikkus 537067
USDA GRIN 24703
Wikipedia Curry_tree
CMAUP NPO17480
CMAUP NPO3364
Open Tree Of Life 321836
World Flora Online wfo-0000564266
Tropicos 28101419
KEW urn:lsid:ipni.org:names:771522-1
Open Tree Of Life 321836
IUCN Red List 156236806
IPNI 771522-1
iNaturalist 428013
GBIF 3832804
USDA GRIN 7011

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_025617385.1 AGM_Bkoe_4.1 Chromosome AgriGenome Labs Pvt Ltd 2022-10-11 3760 316.34 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
On-farm crop diversity, conservation, importance and value: a case study of landraces from Western Ghats of Karnataka, India Puneeth GM, Gowthami R, Katral A, Laxmisha KM, Vasudeva R, Singh GP, Archak S Sci Rep 10-May-2024
PMCID:PMC11087530
doi:10.1038/s41598-024-61428-1
PMID:38730080
Risk assessment of Retithrips syriacus for the EU 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, Reignault PL, Stefani E, Thulke H, van der Werf W, Yuen J, Zappalà L, Bezerra Lima ÉF, Makowski D, Crotta M, Gobbi A, Golic D, Maiorano A, Mosbach‐Schulz O, Rossi E, Terzidou A, Vicent Civera A EFSA J 29-Apr-2024
PMCID:PMC11056851
doi:10.2903/j.efsa.2024.8741
PMID:38686341
Role of nutraceutical against exposure to pesticide residues: power of bioactive compounds Sajad M, Shabir S, Singh SK, Bhardwaj R, Alsanie WF, Alamri AS, Alhomrani M, Alsharif A, Vamanu E, Singh MP Front Nutr 17-Apr-2024
PMCID:PMC11061536
doi:10.3389/fnut.2024.1342881
PMID:38694227
Zinc Oxide-Based Nanomaterials for Microbiostatic Activities: A Review Reda AT, Park JY, Park YT J Funct Biomater 15-Apr-2024
PMCID:PMC11050959
doi:10.3390/jfb15040103
PMID:38667560
Bioactive Compounds Formulated in Phytosomes Administered as Complementary Therapy for Metabolic Disorders Toma L, Deleanu M, Sanda GM, Barbălată T, Niculescu LŞ, Sima AV, Stancu CS Int J Mol Sci 09-Apr-2024
PMCID:PMC11049841
doi:10.3390/ijms25084162
PMID:38673748
From Flora to Pharmaceuticals: 100 new additions to angiosperms of Gafargaon subdistrict in Bangladesh and unraveling antidiabetic drug candidates targeting DPP4 through in silico approach Ahmed SS, Rahman MO PLoS One 29-Mar-2024
PMCID:PMC10980240
doi:10.1371/journal.pone.0301348
PMID:38551991
Inhibition Effect of Non-Host Plant Volatile Extracts on Reproductive Behaviors in the Diamondback Moth Plutella xylostella (Linnaeus) Zhou J, Zhang Z, Liu H, Guo M, Deng J Insects 26-Mar-2024
PMCID:PMC11049908
doi:10.3390/insects15040227
PMID:38667357
Folk Knowledge and Perceptions about the Use of Wild Fruits and Vegetables–Cross-Cultural Knowledge in the Pipli Pahar Reserved Forest of Okara, Pakistan Jabeen S, Arshad F, Harun N, Waheed M, Alamri S, Haq SM, Vitasović-Kosić I, Fatima K, Chaudhry AS, Bussmann RW Plants (Basel) 14-Mar-2024
PMCID:PMC10974405
doi:10.3390/plants13060832
PMID:38592859
Biogenic synthesis of levofloxacin-loaded copper oxide nanoparticles using Cymbopogon citratus: A green approach for effective antibacterial applications Jabeen A, Khan A, Ahmad P, Khalid A, Ibrahim Wizrah MS, Anjum Z, Alotibi S, Aloufi BH, Alanazi AM, Jefri OA, Ismail MA Heliyon 28-Feb-2024
PMCID:PMC10945134
doi:10.1016/j.heliyon.2024.e27018
PMID:38501012
Phytol from Scoparia dulcis prevents NF-κB-mediated inflammatory responses during macrophage polarization Duraisamy P, Angusamy A, Ravi S, Krishnan M, Martin LC, Manikandan B, Sundaram J, Ramar M 3 Biotech 17-Feb-2024
PMCID:PMC10874368
doi:10.1007/s13205-024-03924-9
PMID:38375513
Beneficial Effects of Natural Alkaloids from Berberis glaucocarpa as Antidiabetic Agents: An In Vitro, In Silico, and In Vivo Approach Alamzeb M, Shah SW, Hussain H, Zahoor M, Ahmad S, Mughal EU, Ahmad S, Ullah I, Khan S, Ullah A, Ghias M, Ullah R, Ali EA ACS Omega 12-Feb-2024
PMCID:PMC10905588
doi:10.1021/acsomega.3c10232
PMID:38434828
Exploring the Significance, Extraction, and Characterization of Plant-Derived Secondary Metabolites in Complex Mixtures Barthwal R, Mahar R Metabolites 11-Feb-2024
PMCID:PMC10890687
doi:10.3390/metabo14020119
PMID:38393011
Nano-enabled antimicrobial thin films: design and mechanism of action Finina BF, Mersha AK RSC Adv 09-Feb-2024
PMCID:PMC10866018
doi:10.1039/d3ra07884a
PMID:38357038
Photocatalytic Degradation of Antibiotics via Exploitation of a Magnetic Nanocomposite: A Green Nanotechnology Approach toward Drug-Contaminated Wastewater Reclamation Zulfiqar N, Nadeem R, Musaimi OA ACS Omega 06-Feb-2024
PMCID:PMC10882661
doi:10.1021/acsomega.3c08116
PMID:38405456
Prey selection by leopards (Panthera pardus fusca) in the mid‐hill region of Nepal Baral K, Bhandari S, Adhikari B, Kunwar RM, Sharma HP, Aryal A, Ji W Ecol Evol 05-Feb-2024
PMCID:PMC10844760
doi:10.1002/ece3.10924
PMID:38322006

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Biphenols
(3R)-10-[(3R)-8-hydroxy-3,5-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-10-yl]-3,5-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-9-ol 163194534 Click to see 692.90 unknown https://doi.org/10.1021/JF034700+
10-[8-hydroxy-3,5-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-10-yl]-3,5-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-9-ol 162931522 Click to see 692.90 unknown https://doi.org/10.1021/JF034700+
> Lignans, neolignans and related compounds / Aryltetralin lignans
Guaiacin 11724027 Click to see 328.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
Meso-Dihydroguaiaretic Acid 476856 Click to see 330.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4R,5R)-2,3,4,5-Tetrahydroxy-6-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)hexanal 5460022 Click to see C(C1C(C(C(C(O1)OCC(C(C(C(C=O)O)O)O)O)O)O)O)O 342.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphates / Diacylglycerophosphates / 1,2-diacylglycerol-3-phosphates
(1r)-2-(Phosphonooxy)-1-[(Tridecanoyloxy)methyl]ethyl Pentadecanoate 447791 Click to see CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC)COP(=O)(O)O 592.80 unknown https://doi.org/10.1007/BF02662287
PA(16:0/16:0) 446066 Click to see 648.90 unknown https://doi.org/10.1007/BF02662287
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphoglycerols / Phosphatidylglycerols
Phosphatidyl Glycerol 44566653 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)OCC(CO)O)OC(=O)CCCCCCCC=CCC=CCCCCC 747.00 unknown https://doi.org/10.1007/BF02662287
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1007/BF00323974
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1007/BF00323974
> 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 222.37 unknown https://doi.org/10.1055/S-2006-958052
Globulol 12304985 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1055/S-2006-958052
Npc239037 101716 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-958052
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Isointermedeol 527217 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-958052
Selin-11-en-4alpha-ol 15560330 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown https://doi.org/10.1055/S-2006-958052
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(E)-5-((3,7-Dimethylocta-2,6-dien-1-yl)oxy)-7-hydroxy-2H-chromen-2-one 10829074 Click to see 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
5-(3,7-Dimethylocta-2,6-dienoxy)-7-hydroxychromen-2-one 85281868 Click to see CC(=CCCC(=CCOC1=CC(=CC2=C1C=CC(=O)O2)O)C)C 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
7-((2E)-3,7-Dimethylocta-2,6-Dienoxy)-6-Methoxychromen-2-One 5319406 Click to see 328.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
7-(3,7-Dimethylocta-2,6-dienoxy)-6-methoxychromen-2-one 54117740 Click to see CC(=CCCC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)C)C 328.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
7-Geranyl-oxy-6-methoxycoumarin 129819841 Click to see CC(=CCCC(=CC(=O)OC1=C(C=C2C=CC(=O)OC2=C1)OC)C)C 342.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
[(6S,7R,9bR)-5,7-diacetyloxy-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate 11969994 Click to see CC=C(C)C(=O)OC1C2C(C3C(C(C=C3C)OC(=O)C)C(C1OC(=O)C)(C)O)OC(=O)C2=C 462.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13S,14S,15R,16R,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-14,15,16,18-tetrol 11812629 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6(C5(C(C(C(C6)O)O)O)C)O)C)C)OC1 464.60 unknown via CMAUP database
(2S,5'R,6R,7S,9S,13S,15R,16R,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16-diol 10025825 Click to see 432.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
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/10.1016/J.PHYTOCHEM.2005.05.001
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
b-Sitostenone 579897 Click to see 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
> Organoheterocyclic compounds / Benzodioxoles
Isosafrole 637796 Click to see CC=CC1=CC2=C(C=C1)OCO2 162.18 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
(3R)-7-hydroxy-3-[(1S)-1-hydroxyethyl]-3H-2-benzofuran-1-one 162941985 Click to see CC(C1C2=C(C(=CC=C2)O)C(=O)O1)O 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
7-hydroxy-3-(1-hydroxyethyl)-3H-2-benzofuran-1-one 11542924 Click to see 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
> Organoheterocyclic compounds / Coumarans
2alpha-Methyl-2,3-dihydrobenzofuran-7-carboxylic acid methyl ester 92449358 Click to see CC1CC2=C(O1)C(=CC=C2)C(=O)OC 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives
Bikoeniquinone A 135507215 Click to see CC1=CC(=C2C(=C3C=CC=CC3=N2)C1=C4C(=C(C5=C6C=CC=CC6=NC5=C4O)O)C)OC 420.50 unknown https://doi.org/10.1248/CPB.41.2096
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1S,16S,19S)-13,16-dimethyl-19-prop-1-en-2-yl-15-oxa-4-azapentacyclo[14.3.1.02,14.03,11.05,10]icosa-2(14),3(11),5,7,9,12-hexaene 163186581 Click to see CC1=CC2=C(C3=C1OC4(CCC(C3C4)C(=C)C)C)NC5=CC=CC=C52 331.40 unknown https://doi.org/10.1016/0031-9422(92)83651-E
(3R)-10-[(3R)-9-hydroxy-3,5-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-8-yl]-3,5-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-9-ol 163194943 Click to see 692.90 unknown https://doi.org/10.1021/JF034700+
https://doi.org/10.1248/CPB.41.2096
(3R)-10-[(3R)-9-hydroxy-3,5-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-8-yl]-3,8-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-9-ol 163189082 Click to see 692.90 unknown https://doi.org/10.1021/JF034700+
(3R)-3,5-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazole 37888682 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)CCC=C(C)C)NC4=CC=CC=C42 331.40 unknown https://doi.org/10.1016/S0040-4020(01)92976-X
https://doi.org/10.1021/JF010621R
https://doi.org/10.1021/JF9805808
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264343/
https://doi.org/10.1002/PTR.3023
https://doi.org/10.1021/NP990570G
https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
(3R)-3,8-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-9-ol 92153432 Click to see 347.40 unknown https://doi.org/10.1016/0031-9422(92)83651-E
https://doi.org/10.1021/JF034700+
(3R)-3,8-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazole 124308275 Click to see 331.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264343/
https://doi.org/10.1021/JF010621R
https://doi.org/10.1016/S0040-4020(01)92976-X
(3R)-9-methoxy-3,5-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazole 71716235 Click to see 361.50 unknown https://doi.org/10.1016/J.BMC.2013.01.012
https://doi.org/10.1021/JF034700+
(3S,4aS,11bR)-3,5-dimethyl-3-(4-methylpent-3-enyl)-11,11b-dihydro-4aH-pyrano[3,2-a]carbazole 163190601 Click to see 333.50 unknown https://doi.org/10.1016/S0031-9422(00)90494-1
(3S,4aS,11bR)-3,5-dimethyl-3,4a,11,11b-tetrahydropyrano[3,2-a]carbazole 163190428 Click to see 251.32 unknown https://doi.org/10.1016/S0031-9422(00)90494-1
(3S)-3,5-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-9-ol 11360000 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)CCC=C(C)C)NC4=C2C=CC(=C4)O 347.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264343/
(R)-Mahanine 375151 Click to see 347.40 unknown https://doi.org/10.1248/CPB.41.2096
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264343/
https://doi.org/10.1016/0031-9422(92)83651-E
https://doi.org/10.1021/JF9805808
https://doi.org/10.1021/JF010621R
[(2S)-1-methoxypropan-2-yl] 2-(3-formylcarbazol-9-yl)acetate 163103665 Click to see 325.40 unknown https://doi.org/10.1021/NP50070A025
1-(2-hydroxy-3-methyl-9H-carbazol-1-yl)-3-methyl-9H-carbazol-2-ol 10408200 Click to see 392.40 unknown https://doi.org/10.1248/CPB.41.2096
1-(3,3-Dimethyl allyl)-2-hydroxy-3-formyl-8-meth-oxycarbazole 129710379 Click to see 309.40 unknown https://doi.org/10.1021/NP50070A025
1-(3,7-dimethylocta-1,6-dienyl)-3-methyl-9H-carbazol-2-ol 163004139 Click to see CC1=CC2=C(C(=C1O)C=CC(C)CCC=C(C)C)NC3=CC=CC=C32 333.50 unknown https://doi.org/10.1021/NP990570G
1-(3,7-dimethylocta-2,6-dienyl)-2-hydroxy-9H-carbazole-3-carbaldehyde 85087522 Click to see 347.40 unknown https://doi.org/10.1248/CPB.41.2096
1-(3,7-dimethylocta-2,6-dienyl)-3-methyl-9H-carbazol-2-ol 4000 Click to see CC1=CC2=C(C(=C1O)CC=C(C)CCC=C(C)C)NC3=CC=CC=C32 333.50 unknown https://doi.org/10.1016/S0031-9422(00)90494-1
https://doi.org/10.1021/NP990570G
1-(3,7-dimethylocta-2,6-dienyl)-7-methoxy-6-methyl-9H-carbazol-2-ol 85080470 Click to see CC1=CC2=C(C=C1OC)NC3=C2C=CC(=C3CC=C(C)CCC=C(C)C)O 363.50 unknown https://doi.org/10.1016/0031-9422(92)83651-E
https://doi.org/10.1021/JF9805808
1-[(1E,3S)-3,7-dimethylocta-1,6-dienyl]-3-methyl-9H-carbazol-2-ol 163188821 Click to see 333.50 unknown https://doi.org/10.1021/NP990570G
1-[(2E)-3,7-Dimethyl-2,6-octadien-1-yl]-2-hydroxy-9H-carbazole-3-carboxaldehyde 9997840 Click to see CC(=CCCC(=CCC1=C(C(=CC2=C1NC3=CC=CC=C32)C=O)O)C)C 347.40 unknown https://doi.org/10.1248/CPB.41.2096
1-Methoxy-3-methyl-9H-carbazole 375150 Click to see CC1=CC2=C(C(=C1)OC)NC3=CC=CC=C32 211.26 unknown https://doi.org/10.1248/CPB.41.2096
1-methoxy-4-[(1-methoxy-9H-carbazol-3-yl)methyl]-3-methyl-9H-carbazole 375159 Click to see 420.50 unknown https://doi.org/10.1248/CPB.41.2096
1-methoxy-6-(1-methoxy-3-methylcarbazol-9-yl)-3-methyl-9H-carbazole 11750517 Click to see CC1=CC2=C(C(=C1)OC)N(C3=CC=CC=C32)C4=CC5=C(C=C4)NC6=C5C=C(C=C6OC)C 420.50 unknown https://doi.org/10.1248/CPB.41.2096
1-methoxy-9H-carbazole-3-carboxylic acid 375142 Click to see COC1=CC(=CC2=C1NC3=CC=CC=C32)C(=O)O 241.24 unknown https://doi.org/10.1016/S0031-9422(00)94088-3
10-[9-hydroxy-3,5-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-8-yl]-3,8-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-9-ol 10908622 Click to see 692.90 unknown https://doi.org/10.1021/JF034700+
2-(1-methoxy-3-methyl-9H-carbazol-4-yl)-3-methyl-9H-carbazole-1,4-dione 10432264 Click to see 420.50 unknown https://doi.org/10.1248/CPB.41.2096
2-Hydroxy-3-Formyl-7-Methoxycarbazole 189687 Click to see 241.24 unknown https://doi.org/10.1021/NP50070A025
2-methoxy-9H-carbazole 10797986 Click to see 197.23 unknown https://doi.org/10.1016/S0031-9422(00)90680-0
3-methoxy-6-methyl-9H-carbazole-1-carbaldehyde 11010048 Click to see CC1=CC2=C(C=C1)NC3=C(C=C(C=C23)OC)C=O 239.27 unknown https://doi.org/10.1016/S0031-9422(00)90494-1
3-Methyl-9H-carbazol-1-ol 607542 Click to see 197.23 unknown https://doi.org/10.1016/S0031-9422(00)90680-0
3-Methylcarbazole 20746 Click to see 181.23 unknown https://doi.org/10.1016/S0031-9422(00)90680-0
https://doi.org/10.1016/S0031-9422(97)00345-2
3,3'-[Oxybis(Methylene)]Bis(9-Methoxy-9H-Carbazole) 11517735 Click to see 436.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
3,5-dimethyl-3-(4-methylpent-3-enyl)-11,11b-dihydro-4aH-pyrano[3,2-a]carbazole 163028195 Click to see CC1=CC2=C(C3C1OC(C=C3)(C)CCC=C(C)C)NC4=CC=CC=C42 333.50 unknown https://doi.org/10.1016/S0031-9422(00)90494-1
3,5-Dimethyl-3,4a,11,11b-tetrahydropyrano[3,2-a]carbazole 163035443 Click to see CC1C=CC2C(O1)C(=CC3=C2NC4=CC=CC=C43)C 251.32 unknown https://doi.org/10.1016/S0031-9422(00)90494-1
3,6-dimethyl-1-(3-methylbut-1-enyl)-9H-carbazole 72751187 Click to see CC1=CC2=C(C=C1)NC3=C(C=C(C=C23)C)C=CC(C)C 263.40 unknown https://doi.org/10.1002/CHIN.200548198
3,6-dimethyl-1-[(E)-3-methylbut-1-enyl]-9H-carbazole 11207770 Click to see CC1=CC2=C(C=C1)NC3=C(C=C(C=C23)C)C=CC(C)C 263.40 unknown https://doi.org/10.1002/CHIN.200548198
3,8-Dimethyl-3-(4-methylpent-3-en-1-yl)-3,11-dihydropyrano(3,2-a)carbazol-9-ol 375148 Click to see 347.40 unknown https://doi.org/10.1021/JF034700+
https://doi.org/10.1016/0031-9422(92)83651-E
4-(3,7-dimethylocta-2,6-dienyl)-6-methyl-9H-carbazol-3-ol 72733752 Click to see CC1=CC2=C(C=C1)NC3=C2C(=C(C=C3)O)CC=C(C)CCC=C(C)C 333.50 unknown https://doi.org/10.1016/J.BMC.2013.01.012
4-(3,8-dimethyl-11H-pyrano[3,2-a]carbazol-3-yl)-2-methylbutan-2-ol 5319215 Click to see 335.40 unknown via CMAUP database
4-Hydroxycarbazole 104251 Click to see 183.21 unknown https://doi.org/10.1016/J.BMC.2013.01.012
7-methoxy-3-methyl-8-(3-methylbut-2-enyl)-9H-carbazole-1,4-dione 375141 Click to see 309.40 unknown https://doi.org/10.1248/CPB.41.2096
7-Methoxyheptaphylline 189688 Click to see 309.40 unknown https://doi.org/10.1055/S-2006-960858
https://doi.org/10.1021/NP50070A025
7-Methoxymurrayacine 14760665 Click to see 307.30 unknown https://doi.org/10.1021/NP50070A025
8-(3,7-dimethylocta-2,6-dienyl)-1-[8-(3,7-dimethylocta-2,6-dienyl)-2-hydroxy-7-methoxy-3-methyl-9H-carbazol-1-yl]-7-methoxy-3-methyl-9H-carbazol-2-ol 160103723 Click to see CC1=CC2=C(C(=C1O)C3=C(C(=CC4=C3NC5=C4C=CC(=C5CC=C(C)CCC=C(C)C)OC)C)O)NC6=C2C=CC(=C6CC=C(C)CCC=C(C)C)OC 725.00 unknown https://doi.org/10.1021/JF010621R
8-(3,7-dimethylocta-2,6-dienyl)-7-methoxy-3-methyl-9H-carbazol-2-ol 72744161 Click to see 363.50 unknown https://doi.org/10.1021/JF010621R
8-methoxy-3,3-dimethyl-11H-pyrano[3,2-a]carbazole 5318826 Click to see 279.30 unknown via CMAUP database
8-methoxy-3,3,5-trimethyl-11H-pyrano(3,2-a)carbazole 97487 Click to see 293.40 unknown https://doi.org/10.1016/0031-9422(92)83651-E
https://doi.org/10.1016/J.BMC.2013.01.012
https://doi.org/10.1021/JF034700+
https://doi.org/10.1016/S0040-4020(01)92976-X
https://doi.org/10.1016/J.FITOTE.2009.08.016
8-methoxy-3,3,9-trimethyl-11H-pyrano[3,2-a]carbazole 162994065 Click to see CC1=CC2=C(C=C1OC)C3=C(N2)C4=C(C=C3)OC(C=C4)(C)C 293.40 unknown https://doi.org/10.1007/BF01897877
8,8''-Biskoenigine 12967046 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C(C(=C(C=C24)OC)O)C5=C6C(=CC(=C5O)OC)C7=C(N6)C8=C(C(=C7)C)OC(C=C8)(C)C 616.70 unknown https://doi.org/10.1021/NP020468A
8,9-dimethoxy-3,3,5-trimethyl-11H-pyrano[3,2-a]carbazol-6-ol 162866615 Click to see 339.40 unknown https://doi.org/10.1016/J.FITOTE.2009.08.016
9-methoxy-3,5-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazole 71496524 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)CCC=C(C)C)NC4=C2C=CC(=C4)OC 361.50 unknown https://doi.org/10.1021/JF034700+
9H-Carbazole-3-carbaldehyde 504067 Click to see C1=CC=C2C(=C1)C3=C(N2)C=CC(=C3)C=O 195.22 unknown https://doi.org/10.1248/CPB.41.2096
https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
9H-Carbazole-3-carboxaldehyde, 2,7-dimethoxy- 5317755 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)OC 255.27 unknown https://doi.org/10.1021/NP50070A025
9H-Carbazole-3-carboxylic acid 3152023 Click to see 211.22 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
Bisgerayafoline A 71725435 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)CC=C(C)CCC=C(C)C)NC4=C2C=CC(=C4C5=C(C=CC6=C5C7=C(N6)C8=C(C(=C7)C)OC(C=C8)(C)CC=C(C)CCC=C(C)C)O)OC 815.10 unknown https://doi.org/10.1021/NP300464T
Bisgerayafoline B 71725436 Click to see 815.10 unknown https://doi.org/10.1021/NP300464T
Bisgerayafoline C 71725437 Click to see 843.10 unknown https://doi.org/10.1021/NP300464T
Bismahanine 10327320 Click to see 692.90 unknown https://doi.org/10.1021/JF034700+
https://doi.org/10.1248/CPB.41.2096
Bismurrayafoline E 101150699 Click to see CC1=CC2=C(C(=C1O)C3=C(C(=CC4=C3NC5=C4C=CC(=C5CC=C(C)CCC=C(C)C)OC)C)O)NC6=C2C=CC(=C6CC=C(C)CCC=C(C)C)OC 725.00 unknown https://doi.org/10.1016/S0367-326X(98)00021-5
https://doi.org/10.1021/JF010621R
Bismurrayaquinone A 10364815 Click to see CC1=C(C(=O)C2=C(C1=O)C3=CC=CC=C3N2)C4=C(C(=O)C5=C(C4=O)NC6=CC=CC=C65)C 420.40 unknown https://doi.org/10.1248/CPB.41.2096
Carbazole 6854 Click to see 167.21 unknown https://doi.org/10.1016/J.BMC.2013.01.012
CID 102081529 102081529 Click to see 333.50 unknown https://doi.org/10.1248/CPB.41.2096
Currayanine 375144 Click to see 331.40 unknown https://doi.org/10.1016/0031-9422(92)83651-E
Ethyl 3-methyl-9H-carbazole-9-carboxylate 10354902 Click to see CCOC(=O)N1C2=C(C=C(C=C2)C)C3=CC=CC=C31 253.29 unknown https://doi.org/10.1016/S0031-9422(97)00345-2
https://doi.org/10.1016/S0031-9422(00)90680-0
Euchrestine B 15060943 Click to see 363.50 unknown https://doi.org/10.1016/J.BMC.2013.01.012
https://doi.org/10.1021/JF010621R
Eustifoline C 14635307 Click to see CC1=CC2=C(C=C1)NC3=C2C(=C(C=C3)O)CC=C(C)CCC=C(C)C 333.50 unknown https://doi.org/10.1016/J.BMC.2013.01.012
Girinimbine 96943 Click to see 263.30 unknown https://doi.org/10.1021/NP50070A025
https://doi.org/10.1016/S0040-4020(01)92976-X
https://doi.org/10.1248/CPB.41.2096
https://doi.org/10.1016/0031-9422(92)83651-E
https://doi.org/10.1016/S0031-9422(00)90494-1
Glycosinine 6483032 Click to see 225.24 unknown https://doi.org/10.1021/NP50070A025
Glycozoline 96944 Click to see 211.26 unknown https://doi.org/10.1248/CPB.41.2096
Heptaphylline 5318015 Click to see CC(=CCC1=C(C(=CC2=C1NC3=CC=CC=C32)C=O)O)C 279.30 unknown https://doi.org/10.1021/NP50070A025
https://doi.org/10.1055/S-2006-960858
Isomurrayafoline B 375146 Click to see CC1=CC2=C(C=C1O)NC3=C2C=CC(=C3CC=C(C)C)OC 295.40 unknown https://doi.org/10.1248/CPB.41.2096
Koenidine 278055 Click to see 323.40 unknown https://doi.org/10.1007/BF01897877
https://doi.org/10.1016/S0040-4020(01)92976-X
Koenigine 5318825 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=CC(=C(C=C42)OC)O 309.40 unknown https://doi.org/10.1016/S0031-9422(00)90494-1
https://doi.org/10.1021/NP020468A
Koeniginequinone A 11264975 Click to see 241.24 unknown https://doi.org/10.1016/S0031-9422(97)01135-7
Koeniginequinone B 11184822 Click to see 271.27 unknown https://doi.org/10.1016/S0031-9422(97)01135-7
Koenine 5318827 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C2C=C(C=C4)O 279.30 unknown https://doi.org/10.1016/J.FITOTE.2009.08.016
Koenoline 375152 Click to see 227.26 unknown https://doi.org/10.1016/S0031-9422(00)80630-5
https://doi.org/10.1016/0031-9422(85)80052-2
https://doi.org/10.1248/CPB.41.2096
Mahanimbicine 4072580 Click to see 331.40 unknown https://doi.org/10.1016/J.BMC.2013.01.012
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264343/
https://doi.org/10.1021/JF010621R
https://doi.org/10.1016/S0040-4020(01)92976-X
Mahanimbilol 5353739 Click to see 333.50 unknown https://doi.org/10.1016/S0031-9422(00)90494-1
https://doi.org/10.1021/NP990570G
Mahanimbine 167963 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)CCC=C(C)C)NC4=CC=CC=C42 331.40 unknown https://doi.org/10.1016/S0031-9422(00)90494-1
https://doi.org/10.1021/JF9805808
https://doi.org/10.1016/0031-9422(92)83651-E
https://doi.org/10.1016/J.BMC.2013.01.012
https://doi.org/10.1248/CPB.41.2096
https://doi.org/10.1002/PTR.3023
https://doi.org/10.1002/CHIN.199808206
https://doi.org/10.1021/JF010621R
https://doi.org/10.1016/S0040-4020(01)92976-X
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264343/
https://doi.org/10.1021/NP990570G
https://doi.org/10.1016/S0378-8741(01)00247-1
https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
Mahanimbinol 131753005 Click to see 333.50 unknown https://doi.org/10.1016/S0031-9422(00)90494-1
https://doi.org/10.1248/CPB.41.2096
Mahanine 36689305 Click to see 347.40 unknown https://doi.org/10.1016/S0066-4103(04)54005-X
https://doi.org/10.1021/JF010621R
https://doi.org/10.1021/JF9805808
https://doi.org/10.1016/0031-9422(92)83651-E
https://doi.org/10.1002/CHIN.199808206
https://doi.org/10.1248/CPB.41.2096
methyl 1-methoxy-9H-carbazole-3-carboxylate 5319913 Click to see 255.27 unknown https://doi.org/10.1016/S0031-9422(00)94258-4
methyl 2-methoxy-9H-carbazole-3-carboxylate 24898872 Click to see COC1=C(C=C2C3=CC=CC=C3NC2=C1)C(=O)OC 255.27 unknown https://doi.org/10.1016/S0031-9422(00)90680-0
Mukoenine A 5209 Click to see CC1=CC2=C(C(=C1O)CC=C(C)C)NC3=CC=CC=C32 265.30 unknown https://doi.org/10.1016/S0031-9422(00)90494-1
https://doi.org/10.1248/CPB.41.2096
Mukoenine B 131752937 Click to see 347.40 unknown https://doi.org/10.1248/CPB.41.2096
Mukolidine 53465568 Click to see 225.24 unknown https://doi.org/10.1016/S0031-9422(00)94258-4
Mukonal 504068 Click to see 211.22 unknown https://doi.org/10.1016/S0031-9422(00)80360-X
https://doi.org/10.1021/NP50070A025
Mukonicine 86242003 Click to see 323.40 unknown https://doi.org/10.1016/S0031-9422(00)80178-8
https://doi.org/10.1248/CPB.33.1320
Murrastifoline F 10432278 Click to see 420.50 unknown https://doi.org/10.1248/CPB.41.2096
Murrayacine 5319962 Click to see CC1(C=CC2=C(O1)C(=CC3=C2NC4=CC=CC=C43)C=O)C 277.30 unknown https://doi.org/10.1016/0031-9422(92)83651-E
Murrayamine A 10085008 Click to see 279.30 unknown https://doi.org/10.1248/CPB.41.2096
Murrayamine-B 14892675 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)CCC=C(C)C)NC4=C2C=CC=C4OC 361.50 unknown https://doi.org/10.1016/J.BMC.2013.01.012
Murrayanine 96942 Click to see 225.24 unknown https://doi.org/10.1016/S0031-9422(00)90494-1
https://doi.org/10.1248/CPB.41.2096
https://doi.org/10.1016/S0378-8741(01)00247-1
Murrayanol 9975970 Click to see CC1=CC2=C(C=C1OC)NC3=C2C=CC(=C3CC=C(C)CCC=C(C)C)O 363.50 unknown https://doi.org/10.1016/0031-9422(92)83651-E
https://doi.org/10.1002/CHIN.199808206
https://doi.org/10.1021/JF9805808
Murrayaquinone A 127481 Click to see CC1=CC(=O)C2=C(C1=O)C3=CC=CC=C3N2 211.22 unknown https://doi.org/10.1248/CPB.41.2096
N-methoxy-3-formylcarbazole 11736261 Click to see 225.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
O-Methylmukonal 134816366 Click to see 227.26 unknown https://doi.org/10.1021/NP50070A025
O-Methylmurrayamine A 14892681 Click to see 293.40 unknown https://doi.org/10.1021/JF034700+
Siamenol 477436 Click to see 265.30 unknown https://doi.org/10.1021/NP990570G
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles / N-acylcarbazoles
9-Formyl-3-methylcarbazole 10058925 Click to see 209.24 unknown https://doi.org/10.1016/S0031-9422(00)90680-0
https://doi.org/10.1016/S0031-9422(97)00345-2
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(+)-Murrayazoline 21770913 Click to see 331.40 unknown https://doi.org/10.1016/0031-9422(92)83651-E
(14R,17S,19R)-3,13,13,17-tetramethyl-21-oxa-12-azahexacyclo[10.7.1.12,17.05,20.06,11.014,19]henicosa-1,3,5(20),6(11),7,9-hexaen-9-ol 71717470 Click to see CC1=CC2=C3C4=C1OC5(CCC(C4C5)C(N3C6=C2C=CC(=C6)O)(C)C)C 347.40 unknown https://doi.org/10.1016/J.BMC.2013.01.012
(14R,17S,19S)-8,13,13,17-tetramethyl-21-oxa-12-azahexacyclo[10.7.1.12,17.05,20.06,11.014,19]henicosa-1,3,5(20),6(11),7,9-hexaene 162977194 Click to see CC1=CC2=C(C=C1)N3C4=C2C=CC5=C4C6CC(O5)(CCC6C3(C)C)C 331.40 unknown https://doi.org/10.1016/0031-9422(82)85232-1
(14S,17R,19R)-3,13,13,17-tetramethyl-21-oxa-12-azahexacyclo[10.7.1.12,17.05,20.06,11.014,19]henicosa-1,3,5(20),6,8,10-hexaene 5319963 Click to see CC1=CC2=C3C4=C1OC5(CCC(C4C5)C(N3C6=CC=CC=C62)(C)C)C 331.40 unknown https://doi.org/10.1016/0031-9422(92)83651-E
Isomurrayazoline 131750989 Click to see CC1=CC2=C(C=C1)N3C4=C2C=CC5=C4C6CC(O5)(CCC6C3(C)C)C 331.40 unknown https://doi.org/10.1016/0031-9422(82)85232-1
Murrayazolinol 180314 Click to see 347.40 unknown https://doi.org/10.1177/1934578X0900400309
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
4-[(7R,8S)-8-(hydroxymethyl)-4-methoxy-16,16,19-trimethyl-6,17-dioxa-11-azapentacyclo[10.8.0.02,10.05,9.013,18]icosa-1(12),2,4,9,13(18),14,19-heptaen-7-yl]-2,6-dimethoxyphenol 638195 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C5C(C(OC5=C(C=C24)OC)C6=CC(=C(C(=C6)OC)O)OC)CO 517.60 unknown via CMAUP database
4-[(7S,8R)-8-(hydroxymethyl)-4-methoxy-16,16,19-trimethyl-6,17-dioxa-11-azapentacyclo[10.8.0.02,10.05,9.013,18]icosa-1(12),2,4,9,13(18),14,19-heptaen-7-yl]-2,6-dimethoxyphenol 22297890 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C5C(C(OC5=C(C=C24)OC)C6=CC(=C(C(=C6)OC)O)OC)CO 517.60 unknown https://doi.org/10.1021/NP020468A
4-[8-(Hydroxymethyl)-4-methoxy-16,16,19-trimethyl-6,17-dioxa-11-azapentacyclo[10.8.0.02,10.05,9.013,18]icosa-1(12),2,4,9,13(18),14,19-heptaen-7-yl]-2,6-dimethoxyphenol 22297889 Click to see 517.60 unknown https://doi.org/10.1021/NP020468A
> Phenylpropanoids and polyketides / Coumarins and derivatives
Murrayatin 621354 Click to see 362.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
7-methoxy-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 162876702 Click to see 354.31 unknown https://doi.org/10.1055/S-0028-1099809
7-methoxy-6-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H-chromen-2-one 78062648 Click to see 354.31 unknown https://doi.org/10.1055/S-0028-1099809
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
2-(2-Oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl)propan-2-yl acetate 5316020 Click to see 288.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
Columbianetin acetate 161409 Click to see 288.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
9-((2-Hydroxy-3-methylbut-3-en-1-yl)oxy)-7H-furo(3,2-g)(1)benzopyran-7-one 148619 Click to see 286.28 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
9-(2,3-Dihydroxy-3-methylbutoxy)furo(3,2-g)chromen-7-one 328236 Click to see 304.29 unknown via CMAUP database
Clausenacoumarine 6439823 Click to see CC1=CC(OC1=O)CC(=CCOC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 366.40 unknown https://doi.org/10.4314/NJNPM.V1I1.11794
Gosferol 511358 Click to see 286.28 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
Heraclenin 458010 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
(+)-Byakangelicin 10211 Click to see 334.30 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
9-(2-Hydroxy-3-Methylbut-3-Enoxy)-4-Methoxyfuro(3,2-G)Chromen-7-One 616064 Click to see 316.30 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
Byakangelicol 3055167 Click to see 316.30 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
Isobyakangelicol 5318521 Click to see 316.30 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
Phellopterin 98608 Click to see CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C 300.30 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen 4114 Click to see 216.19 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
8-hydroxy-7-[(E)-3-methyl-4-[(2S)-4-methylidene-5-oxooxolan-2-yl]but-2-enoxy]chromen-2-one 162857749 Click to see 342.30 unknown https://doi.org/10.1211/JPP.60.3.0015
https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
8-hydroxy-7-[[(2R,3R)-3-methyl-3-[[(2R)-4-methylidene-5-oxooxolan-2-yl]methyl]oxiran-2-yl]methoxy]chromen-2-one 163026473 Click to see CC1(C(O1)COC2=C(C3=C(C=C2)C=CC(=O)O3)O)CC4CC(=C)C(=O)O4 358.30 unknown https://doi.org/10.1211/JPP.60.3.0015
https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
8-hydroxy-7-[[(2S,3S)-3-methyl-3-[[(2S)-4-methylidene-5-oxooxolan-2-yl]methyl]oxiran-2-yl]methoxy]chromen-2-one 163026472 Click to see CC1(C(O1)COC2=C(C3=C(C=C2)C=CC(=O)O3)O)CC4CC(=C)C(=O)O4 358.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
8-Hydroxy-7-[3-methyl-4-(4-methylidene-5-oxooxolan-2-yl)but-2-enoxy]chromen-2-one 85146428 Click to see 342.30 unknown https://doi.org/10.1211/JPP.60.3.0015
Murrayacoumarin B 10383752 Click to see CC1(C(O1)COC2=C(C3=C(C=C2)C=CC(=O)O3)O)CC4CC(=C)C(=O)O4 358.30 unknown https://doi.org/10.1211/JPP.60.3.0015
https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
2H-1-Benzopyran-2-one, 5,7-dihydroxy- 5324654 Click to see 178.14 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
5-(6,7-Dihydroxy-3,7-dimethyloct-2-enoxy)-7-hydroxychromen-2-one 72834422 Click to see 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
5-[(E,6R)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]-7-hydroxychromen-2-one 162997793 Click to see 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
5-[(E,6S)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]-7-hydroxychromen-2-one 162997795 Click to see CC(=CCOC1=CC(=CC2=C1C=CC(=O)O2)O)CCC(C(C)(C)O)O 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
7-(1,1-Dimethylallyl)-2,2-dimethyl-pyrano[3,2-g]chromen-8-one 14133592 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=C(C(=O)O3)C(C)(C)C=C)C 296.40 unknown https://doi.org/10.1016/S0031-9422(00)80360-X
Xanthoxyletin 66548 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C 258.27 unknown https://doi.org/10.1021/NP50070A025
> Phenylpropanoids and polyketides / Coumarins and derivatives / p-Dioxolo[2,3-h]coumarins
(2R)-2-[(2S)-2-hydroxy-1-[(2S,4R)-4-hydroxy-4-methyl-5-oxooxolan-2-yl]propan-2-yl]-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 162951381 Click to see 376.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
(2R)-2-[(2S)-2-hydroxy-1-[(2S,4R)-4-methyl-5-oxooxolan-2-yl]propan-2-yl]-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 162898343 Click to see CC1CC(OC1=O)CC(C)(C2COC3=C(O2)C4=C(C=C3)C=CC(=O)O4)O 360.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
(2S)-2-[(2R)-2-hydroxy-1-[(2R,4S)-4-hydroxy-4-methyl-5-oxooxolan-2-yl]propan-2-yl]-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 162951380 Click to see 376.40 unknown https://doi.org/10.1211/JPP.60.3.0015
(2S)-2-[(2R)-2-hydroxy-1-[(2R)-4-methylidene-5-oxooxolan-2-yl]propan-2-yl]-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 162902919 Click to see CC(CC1CC(=C)C(=O)O1)(C2COC3=C(O2)C4=C(C=C3)C=CC(=O)O4)O 358.30 unknown https://doi.org/10.1211/JPP.60.3.0015
https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
(2S)-2-[(2R)-2-hydroxy-1-[(2S,4R)-4-methyl-5-oxooxolan-2-yl]propan-2-yl]-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 162898341 Click to see 360.40 unknown https://doi.org/10.1211/JPP.60.3.0015
https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
2-[2-Hydroxy-1-(4-methyl-5-oxooxolan-2-yl)propan-2-yl]-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 11473870 Click to see CC1CC(OC1=O)CC(C)(C2COC3=C(O2)C4=C(C=C3)C=CC(=O)O4)O 360.40 unknown https://doi.org/10.1211/JPP.60.3.0015
https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
clauslactone A 10066950 Click to see 358.30 unknown https://doi.org/10.1211/JPP.60.3.0015
clauslactone B 10407168 Click to see CC1(CC(OC1=O)CC(C)(C2COC3=C(O2)C4=C(C=C3)C=CC(=O)O4)O)O 376.40 unknown https://doi.org/10.1211/JPP.60.3.0015
https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
3,5,7-Trihydroxy-8-(4-hydroxyphenyl)-2-methyl-2-(4-methylpent-3-enyl)-3,4,7,8-tetrahydropyrano[3,2-g]chromen-6-one 73306723 Click to see CC(=CCCC1(C(CC2=C(C3=C(C=C2O1)OC(C(C3=O)O)C4=CC=C(C=C4)O)O)O)C)C 440.50 unknown https://doi.org/10.4314/NJNPM.V1I1.11794
> Phenylpropanoids and polyketides / Macrolactams
Desferrioxamine X5 85625752 Click to see 598.70 unknown https://doi.org/10.1007/BF02662287

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