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Murraya koenigii

Murraya koenigii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64404d7da053b932603274
Scientific name Murraya koenigii
Authority (L.) Spreng.
First published in Syst. Veg. 2: 315 (1825)

Description Top

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The curry tree, also known as Murraya koenigii or Bergera koenigii, is a tropical and sub-tropical tree native to Asia. Its leaves, known as curry leaves, are commonly used in Indian cuisine and traditional medicine. The tree grows up to 6 meters tall and produces small white flowers and edible black berries. It is best grown in well-drained soil with temperatures above 18°C. The name "curry" in its name comes from the widespread use of the leaves in Indian curries. The leaves are also used in other dishes and spice blends in South and Southeast Asian cuisines. In addition, they are believed to have medicinal properties in Ayurvedic and Siddha medicine. The tree can be propagated through seeds or stem cuttings, and its leaves contain various beneficial compounds such as carotenoids and alkaloids.

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)
Bergera koenigii L. Mant. Pl. : 565 (1767)
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)

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 teumuruy
ace teumurui
Afrikaans kerrieboom
Arabic مورايا كونيجية
Assamese নৰসিংহ
Assamese curry leaf
Assamese curry leaves
Assamese curry patta
Assamese curry tree
Assamese curry-leaf tree
Bulgarian къри
Bengali বারসুঙ্গা
br delioù-kari
br kaloupile
Catalan fulla de curri
Catalan arbre de fulla de curri
Czech bergera koenigii
German curryblatt
German curryblätter
German currybaum
dv ހިކަނދިފަތް
Greek Μουρραιΐα του Κένιγκ
Persian درخت کاری
Finnish intianjasmikki
French feuille de curry
French kaloupilé
French karipoulé
French kaloupile
French caloupilé
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 オオバゲッキツ
Japanese 大葉月橘
Japanese ナンヨウザンショウ
Japanese ナンヨウサンショウ
Japanese カレーノキ
Japanese カレーリーフ
Japanese 南洋山椒
Kannada ಕರಿಬೇವಿನ ಮರ
Korean 커리나무
mad enggu'
Malayalam curry tree
Malayalam കരിയേപ്പ്
Malayalam കറിവേപ്പില
Malayalam കറിവേപ്പ്
Marathi कडी पत्ता
Marathi कडीपत्ता
Marathi गोडलिंब
Marathi कढीलिंब
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 fòje de cari
vec àlboro de cari
vec fòja de cari
vec fògia de cari
vec fòge de cari
Chinese 哥埋养榴
Chinese 调料九里香
Chinese 麻绞叶
Chinese 可因氏月橘
Chinese 咖哩樹
Chinese 咖哩葉
Chinese 咖喱叶
Chinese 咖喱树
Chinese 調料九里香
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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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

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
World Flora Online wfo-0001132683
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

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 3760.0x 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
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
In Silico Molecular Docking of Phytochemicals of Murraya koenigii Against Streptococcus mutans Uma Maheswari K, Sankar S Cureus 05-Feb-2024
PMCID:PMC10918300
doi:10.7759/cureus.53679
PMID:38455815
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 CC1=CC2=C(C3=C1OC(C=C3)(C)CCC=C(C)C)NC4=C2C=CC(=C4C5=CC(=CC6=C5NC7=C6C=C(C8=C7C=CC(O8)(C)CCC=C(C)C)C)O)O 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 CC1=CC2=C(C3=C1OC(C=C3)(C)CCC=C(C)C)NC4=C2C=CC(=C4C5=CC(=CC6=C5NC7=C6C=C(C8=C7C=CC(O8)(C)CCC=C(C)C)C)O)O 692.90 unknown https://doi.org/10.1021/JF034700+
> Lignans, neolignans and related compounds / Aryltetralin lignans
Guaiacin 11724027 Click to see CC1CC2=CC(=C(C=C2C(C1C)C3=CC(=C(C=C3)O)OC)O)OC 328.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
Dihydroguaiaretic acid, meso- 476856 Click to see CC(CC1=CC(=C(C=C1)O)OC)C(C)CC2=CC(=C(C=C2)O)OC 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
2-(Hexadecanoyloxy)-1-[(phosphonooxy)methyl]ethyl hexadecanoate 446066 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)O)OC(=O)CCCCCCCCCCCCCCC 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
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1007/BF00323974
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 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 CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1055/S-2006-958052
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Isointermedeol 527217 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 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 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
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-(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
7-Geranyloxy-6-methoxycoumarin 5319406 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
> 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 CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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/J.PHYTOCHEM.2005.05.001
https://doi.org/10.1016/S0367-326X(99)00163-X
24-Ethylcholest-5-en-3beta-ol 22012 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
Beta-Sitosterol 222284 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/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-4-en-3-one, (24S)- 579897 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
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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
3-(1-Hydroxyethyl)-7-hydroxyisobenzofuran-1(3H)-one 11542924 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
> 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
(+)-Mahanimbicine 4072580 Click to see CC1=CC2=C(C=C1)NC3=C2C=CC4=C3C=CC(O4)(C)CCC=C(C)C 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
(1-methoxy-9H-carbazol-3-yl)methanol 375152 Click to see COC1=CC(=CC2=C1NC3=CC=CC=C32)CO 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
(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 CC1=CC2=C(C3=C1OC(C=C3)(C)CCC=C(C)C)NC4=C2C=CC(=C4C5=C(C=C6C(=C5)C7=C(N6)C8=C(C(=C7)C)OC(C=C8)(C)CCC=C(C)C)O)O 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 CC1=CC2=C(C(=C1O)C3=C(C=C4C(=C3)C5=C(N4)C6=C(C(=C5)C)OC(C=C6)(C)CCC=C(C)C)O)NC7=C2C=CC8=C7C=CC(O8)(C)CCC=C(C)C 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 CC1=CC2=C(C=C1O)NC3=C2C=CC4=C3C=CC(O4)(C)CCC=C(C)C 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 CC1=CC2=C(C=C1)NC3=C2C=CC4=C3C=CC(O4)(C)CCC=C(C)C 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 CC1=CC2=C(C3=C1OC(C=C3)(C)CCC=C(C)C)NC4=C2C=CC(=C4)OC 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 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
(3S,4aS,11bR)-3,5-dimethyl-3,4a,11,11b-tetrahydropyrano[3,2-a]carbazole 163190428 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
(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 CC1=CC2=C(C3=C1OC(C=C3)(C)CCC=C(C)C)NC4=C2C=CC(=C4)O 347.40 unknown https://doi.org/10.1021/JF010621R
https://doi.org/10.1021/JF9805808
https://doi.org/10.1016/0031-9422(92)83651-E
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264343/
https://doi.org/10.1248/CPB.41.2096
[(2S)-1-methoxypropan-2-yl] 2-(3-formylcarbazol-9-yl)acetate 163103665 Click to see CC(COC)OC(=O)CN1C2=C(C=C(C=C2)C=O)C3=CC=CC=C31 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 CC1=CC2=C(C(=C1O)C3=C(C(=CC4=C3NC5=CC=CC=C54)C)O)NC6=CC=CC=C62 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 CC(=CCC1=C(C(=CC2=C1NC3=C2C=CC=C3OC)C=O)O)C 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 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-(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 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-[(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-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 CC1=CC2=C(C(=C1O)C3=C(C=C4C(=C3)C5=C(N4)C6=C(C(=C5)C)OC(C=C6)(C)CCC=C(C)C)O)NC7=C2C=CC8=C7C=CC(O8)(C)CCC=C(C)C 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 CC1=CC(=C2C(=C1C3=C(C(=O)C4=C(C3=O)NC5=CC=CC=C54)C)C6=CC=CC=C6N2)OC 420.50 unknown https://doi.org/10.1248/CPB.41.2096
2-Hydroxy-7-methoxy-9H-carbazole-3-carbaldehyde 189687 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)O 241.24 unknown https://doi.org/10.1021/NP50070A025
2-methoxy-9H-carbazole 10797986 Click to see COC1=CC2=C(C=C1)C3=CC=CC=C3N2 197.23 unknown https://doi.org/10.1016/S0031-9422(00)90680-0
2-methoxy-9H-carbazole-3-carbaldehyde 6483032 Click to see COC1=CC2=C(C=C1C=O)C3=CC=CC=C3N2 225.24 unknown https://doi.org/10.1021/NP50070A025
3-[(2E)-3,7-dimethylocta-2,6-dienyl]-8-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-9-methoxy-3,5-dimethyl-11H-pyrano[3,2-a]carbazol-10-yl]-3,5-dimethyl-11H-pyrano[3,2-a]carbazol-7-ol 71725436 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)CC=C(C)CCC=C(C)C)NC4=C2C=CC(=C4C5=C(C6=C(C=C5)NC7=C6C=C(C8=C7C=CC(O8)(C)CC=C(C)CCC=C(C)C)C)O)OC 815.10 unknown https://doi.org/10.1021/NP300464T
3-[(2E)-3,7-dimethylocta-2,6-dienyl]-8-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-9-methoxy-3,5-dimethyl-11H-pyrano[3,2-a]carbazol-10-yl]-9-methoxy-3,5,11-trimethylpyrano[3,2-a]carbazole 71725437 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)CC=C(C)CCC=C(C)C)NC4=C2C=CC(=C4C5=C(C=C6C(=C5)C7=C(N6C)C8=C(C(=C7)C)OC(C=C8)(C)CC=C(C)CCC=C(C)C)OC)OC 843.10 unknown https://doi.org/10.1021/NP300464T
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 CC1=CC2=C(C(=C1)O)NC3=CC=CC=C32 197.23 unknown https://doi.org/10.1016/S0031-9422(00)90680-0
3-Methylcarbazole 20746 Click to see CC1=CC2=C(C=C1)NC3=CC=CC=C32 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 CON1C2=C(C=C(C=C2)COCC3=CC4=C(C=C3)N(C5=CC=CC=C54)OC)C6=CC=CC=C61 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 CC1=CC2=C(C=C1O)NC3=C2C=CC4=C3C=CC(O4)(C)CCC=C(C)C 347.40 unknown https://doi.org/10.1016/0031-9422(92)83651-E
https://doi.org/10.1021/JF034700+
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 CC1=CC2=C(C=C1)NC3=C2C=CC4=C3C=CC(O4)(C)CCC(C)(C)O 335.40 unknown via CMAUP database
4-Hydroxycarbazole 104251 Click to see C1=CC=C2C(=C1)C3=C(N2)C=CC=C3O 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 CC1=CC(=O)C2=C(C1=O)C3=C(N2)C(=C(C=C3)OC)CC=C(C)C 309.40 unknown https://doi.org/10.1248/CPB.41.2096
7-Methoxyheptaphylline 189688 Click to see CC(=CCC1=C(C(=CC2=C1NC3=C2C=CC(=C3)OC)C=O)O)C 309.40 unknown https://doi.org/10.1055/S-2006-960858
https://doi.org/10.1021/NP50070A025
7-Methoxymurrayacine 14760665 Click to see CC1(C=CC2=C(O1)C(=CC3=C2NC4=C3C=CC(=C4)OC)C=O)C 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 CC1=CC2=C(C=C1O)NC3=C2C=CC(=C3CC=C(C)CCC=C(C)C)OC 363.50 unknown https://doi.org/10.1021/JF010621R
8-methoxy-3,3-dimethyl-11H-pyrano[3,2-a]carbazole 5318826 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C=C(C=C4)OC)C 279.30 unknown via CMAUP database
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 CC1=C(C2=C(C3=C1OC(C=C3)(C)C)NC4=CC(=C(C=C42)OC)OC)O 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 C1=CC=C2C(=C1)C3=C(N2)C=CC(=C3)C(=O)O 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
Bismahanine 10327320 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)CCC=C(C)C)NC4=C2C=CC(=C4C5=C(C=C6C(=C5)C7=C(N6)C8=C(C(=C7)C)OC(C=C8)(C)CCC=C(C)C)O)O 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 C1=CC=C2C(=C1)C3=CC=CC=C3N2 167.21 unknown https://doi.org/10.1016/J.BMC.2013.01.012
Chrestifoline A 375159 Click to see CC1=CC(=C2C(=C1CC3=CC4=C(C(=C3)OC)NC5=CC=CC=C54)C6=CC=CC=C6N2)OC 420.50 unknown https://doi.org/10.1248/CPB.41.2096
CID 102081529 102081529 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/10.1248/CPB.41.2096
Currayanine 375144 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
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(00)90680-0
https://doi.org/10.1016/S0031-9422(97)00345-2
Euchrestine B 15060943 Click to see CC1=CC2=C(C=C1O)NC3=C2C=CC(=C3CC=C(C)CCC=C(C)C)OC 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 CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=CC=CC=C42 263.30 unknown https://doi.org/10.1016/S0031-9422(00)90494-1
https://doi.org/10.1016/0031-9422(92)83651-E
https://doi.org/10.1248/CPB.41.2096
https://doi.org/10.1016/S0040-4020(01)92976-X
https://doi.org/10.1021/NP50070A025
Glycozoline 96944 Click to see CC1=CC2=C(C=C1)NC3=C2C=C(C=C3)OC 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
Koenigicine 278055 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=CC(=C(C=C42)OC)OC 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 CC1=CC(=O)C2=C(C1=O)C3=C(N2)C=C(C=C3)OC 241.24 unknown https://doi.org/10.1016/S0031-9422(97)01135-7
Koeniginequinone B 11184822 Click to see CC1=CC(=O)C2=C(C1=O)C3=CC(=C(C=C3N2)OC)OC 271.27 unknown https://doi.org/10.1016/S0031-9422(97)01135-7
Koenimbine 97487 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C2C=C(C=C4)OC 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
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
Mahanimbilol 5353739 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
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 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/10.1248/CPB.41.2096
Mahanine 36689305 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)CCC=C(C)C)NC4=C2C=CC(=C4)O 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 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 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
Mukolidine 53465568 Click to see COC1=CC=CC2=C1NC3=C2C=C(C=C3)C=O 225.24 unknown https://doi.org/10.1016/S0031-9422(00)94258-4
Mukonal 504068 Click to see C1=CC=C2C(=C1)C3=C(N2)C=C(C(=C3)C=O)O 211.22 unknown https://doi.org/10.1016/S0031-9422(00)80360-X
https://doi.org/10.1021/NP50070A025
Mukonicine 86242003 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C2C=C(C=C4OC)OC 323.40 unknown https://doi.org/10.1016/S0031-9422(00)80178-8
https://doi.org/10.1248/CPB.33.1320
Mukonine 5319913 Click to see COC1=CC(=CC2=C1NC3=CC=CC=C32)C(=O)OC 255.27 unknown https://doi.org/10.1016/S0031-9422(00)94258-4
Murrastifoline F 10432278 Click to see CC1=CC2=C(C(=C1)OC)N(C3=CC=CC=C32)C4=C5C6=CC=CC=C6NC5=C(C=C4C)OC 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 CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C2C=CC(=C4)O 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 COC1=CC(=CC2=C1NC3=CC=CC=C32)C=O 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 CON1C2=C(C=C(C=C2)C=O)C3=CC=CC=C31 225.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.05.001
O-Methylmukonal 134816366 Click to see COC1=CC2=C(C=C1CO)C3=CC=CC=C3N2 227.26 unknown https://doi.org/10.1021/NP50070A025
O-Methylmurrayamine A 14892681 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C2C=CC(=C4)OC 293.40 unknown https://doi.org/10.1021/JF034700+
Siamenol 477436 Click to see CC1=CC2=C(C=C1)NC3=C2C=C(C(=C3)O)CC=C(C)C 265.30 unknown https://doi.org/10.1021/NP990570G
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles / N-acylcarbazoles
3-Methyl-9H-carbazole-9-carbaldehyde 10058925 Click to see CC1=CC2=C(C=C1)N(C3=CC=CC=C32)C=O 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
(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
Murrayazoline 21770913 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
Murrayazolinol 180314 Click to see CC1=CC2=C3C4=C1OC5(CC4C(CC5O)C(N3C6=CC=CC=C62)(C)C)C 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 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
> Phenylpropanoids and polyketides / Coumarins and derivatives
Murrayatin 621354 Click to see CC(C)CC(=O)OC(CC1=C(C=CC2=C1OC(=O)C=C2)OC)C(C)(C)O 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 COC1=C(C=C2C=CC(=O)OC2=C1)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1055/S-0028-1099809
7-Methoxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 78062648 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)OC3C(C(C(C(O3)CO)O)O)O 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 CC(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3 288.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
Columbianetin acetate 161409 Click to see CC(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3 288.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.030
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(R)-Pabulenol 511358 Click to see CC(=C)C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O 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 CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)O 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
Heraclenin 458010 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown via CMAUP database
Isogosferol 148619 Click to see CC(=C)C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O 286.28 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Byakangelicin 10211 Click to see CC(C)(C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O)O 334.30 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
Byakangelicol 3055167 Click to see CC1(C(O1)COC2=C3C(=C(C4=C2OC(=O)C=C4)OC)C=CO3)C 316.30 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
Isobyakangelicol 5318521 Click to see CC(C)C(=O)COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2 316.30 unknown https://doi.org/10.1016/S0367-326X(99)00163-X
Neobyakangelicol 616064 Click to see CC(=C)C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O 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
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 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 CC(=CCOC1=C(C2=C(C=C1)C=CC(=O)O2)O)CC3CC(=C)C(=O)O3 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 CC(=CCOC1=C(C2=C(C=C1)C=CC(=O)O2)O)CC3CC(=C)C(=O)O3 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
5-(6,7-Dihydroxy-3,7-dimethyloct-2-enoxy)-7-hydroxychromen-2-one 72834422 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
5-[(E,6R)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]-7-hydroxychromen-2-one 162997793 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
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
5,7-Dihydroxycoumarin 5324654 Click to see C1=CC(=O)OC2=CC(=CC(=C21)O)O 178.14 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 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/10.1016/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 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
(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 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
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 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
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 C1CCCN(C(=O)CCC(=O)NCCCCCN(C(=O)CCC(=O)NCCCCCNC(=O)CCC(=O)NCC1)O)O 598.70 unknown https://doi.org/10.1007/BF02662287

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