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Neolamarckia cadamba

Neolamarckia cadamba - 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 UUID643fe429cc7bd358641384
Scientific name Neolamarckia cadamba
Authority (Roxb.) Bosser
First published in Bull. Mus. Natl. Hist. Nat., B, Adansonia 6: 247 (1984)

Description Top

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Synonyms Top

Scientific name Authority First published in
Anthocephalus cadamba Miq. Fl. Ned. Ind. 2: 135 (1856)
Anthocephalus morindifolius Korth.Verh. Verh. Nat. Gesch. Ned. Bezitt., Bot. : t. 48 (1842)
Nauclea cadamba Roxb. Fl. Ind. 2: 121 (1824)
Nauclea megaphylla S.Moore J. Bot. 62(Suppl.): 47 (1924)
Neonauclea megaphylla S.Moore J. Bot. 64(Suppl.): 146 (1926)
Samama cadamba Kuntze Revis. Gen. Pl. 1: 296 (1891)
Sarcocephalus cadamba Kurz Prelim. Rep. Forest Pegu , App. A: lxxviii (1875)
Anthocephalus indicus var. macrophyllus Pierre ex Pit. Fl. Indo-Chine 3: 33. 1922
Anthocephalus indicus var. glabrescens H.L.Li J. Arnold Arbor. 25: 318. 1944

Common names Top

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Language Common/alternative name
English laran
English leichhardt pine
English cadamba
English burflower tree
English kadam
Assamese কদম
ban jabon
bjn kalampayan
bjn kelampayan
bjn kalampaian
Bengali সিন্ধুপুষ্প
Bengali বুল কদম
Bengali নীপ
Bengali কদম
Gujarati કદંબ
Hindi हरिद्र
Hindi नीप
Hindi कदंब वृक्ष
Indonesian kayu jabon
Indonesian pohon jabon
Indonesian jabon
Japanese クビナガタマバナノキ
Japanese カランパヤン
Japanese カダム
Japanese ラブラ
jv jabon
Kannada ಕದಂಬ ಮರ
Malayalam കടമ്പ്
Malayalam ആറ്റുതേക്ക്
Marathi कदंब
Marathi कदंब वृक्ष
Marathi कळंब वृक्ष
Malay pokok kelempayan
Malay kelempayan
Burmese မအူပင်
Polish kadamba
Russian Кадамба
Russian Неоламаркиа кадамба
sa कदम्बः
sa अश्वत्थः
sat ᱠᱟᱫᱟᱢ
Tamil கடப்பம்பூ
Tamil கடம்பு மரம்
Telugu కదంబం
Telugu కదంబము
Telugu కదంబ
Vietnamese gáo tàu
Vietnamese anthocephalus chinensis
Vietnamese gáo trắng
Chinese 圑花
Chinese 黄梁木
Chinese 团花

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000250146
UNII W6R22U76JN
USDA Plants NECA7
Tropicos 50126691
INPN 630216
KEW urn:lsid:ipni.org:names:914296-1
The Plant List kew-133819
PFAF Neolamarckia cadamba
Open Tree Of Life 919146
Observations.org 360304
NCBI Taxonomy 153762
IPNI 914296-1
iNaturalist 334914
GBIF 2896888
Freebase /m/02vlsdt
EOL 1106567
Elurikkus 327268
USDA GRIN 410705
Wikipedia Neolamarckia_cadamba

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
A modified CTAB method for the extraction of high-quality RNA from mono-and dicotyledonous plants rich in secondary metabolites Kiss T, Karácsony Z, Gomba-Tóth A, Szabadi KL, Spitzmüller Z, Hegyi-Kaló J, Cels T, Otto M, Golen R, Hegyi ÁI, Geml J, Váczy KZ Plant Methods 04-May-2024
PMCID:PMC11069240
doi:10.1186/s13007-024-01198-z
PMID:38704591
Chemical Profiling and Biological Activities on Nepalese Medicinal Plant Extracts and Isolation of Active Fraction of Nyctanthes arbor-tristis Khadka A, Budha Magar A, Sharma KR ScientificWorldJournal 14-Mar-2024
PMCID:PMC10957254
doi:10.1155/2024/5080176
PMID:38515931
Advances in the Effects of Dietary Macronutrients on the Gut Microbiota of Tilapia (Oreochromis spp.) Ou W, Guo Z, Pan Y, Huang K, Ma Y, Qin Z Microorganisms 08-Mar-2024
PMCID:PMC10972434
doi:10.3390/microorganisms12030543
PMID:38543594
Genetic Diversity and Structure of Terminalia bellerica (Gaertn. Roxb.) Population in India as Revealed by Genetic Analysis Umesh Kanna S, Parthiban KT, Senthilraja K, Venkatesan S, Udhaya Nandhini D, Mohan Kumar S, Dhasarathan M, Kumaresan P, Sai MJ, Raveendran M, Geethalakshmi V Plants (Basel) 06-Feb-2024
PMCID:PMC10892032
doi:10.3390/plants13040470
PMID:38498452
A Community-Based Framework Integrates Interspecific Interactions into Forest Genetic Conservation Wang X, Xiao Y, Lv YW, He ZH, Yeh FC, Hu XS Plants (Basel) 01-Feb-2024
PMCID:PMC10856838
doi:10.3390/plants13030435
PMID:38337968
Effects of Neolamarckia cadamba leaves extract on microbial community and antibiotic resistance genes in cecal contents and feces of broilers challenged with lipopolysaccharides Wang C, Wu S, Zhou W, Hu L, Hu Q, Cao Y, Wang L, Chen X, Zhang Q Appl Environ Microbiol 17-Jan-2024
PMCID:PMC10880616
doi:10.1128/aem.01107-23
PMID:38231769
Assessment of Carbon Sequestration in Private Forests across Two Different Physiographic Regions of Nepal: Implications for Conservation and Climate Change Mitigation Joshi R, Shrestha TK, Mishra B, Gautam J, Maharjan B, Gosai KR, Maraseni T, Neupane B Scientifica (Cairo) 04-Dec-2023
PMCID:PMC10713251
doi:10.1155/2023/6599067
PMID:38089447
Cationic Surfactant-Modified Tetraselmis sp. for the Removal of Organic Dyes from Aqueous Solution Buhani, Istikomah, Suharso, Sumadi, Sutarto, Alghamdi HM, Elwakeel KZ Molecules 29-Nov-2023
PMCID:PMC10708098
doi:10.3390/molecules28237839
PMID:38067566
The Rauvolfia tetraphylla genome suggests multiple distinct biosynthetic routes for yohimbane monoterpene indole alkaloids Stander EA, Lehka B, Carqueijeiro I, Cuello C, Hansson FG, Jansen HJ, Dugé De Bernonville T, Birer Williams C, Vergès V, Lezin E, Lorensen MD, Dang TT, Oudin A, Lanoue A, Durand M, Giglioli-Guivarc’h N, Janfelt C, Papon N, Dirks RP, O’connor SE, Jensen MK, Besseau S, Courdavault V Commun Biol 24-Nov-2023
PMCID:PMC10673892
doi:10.1038/s42003-023-05574-8
PMID:38001233
Genome mining of metabolic gene clusters in the Rubiaceae family Correia de Lemos SM, Paschoal AR, Guyot R, Medema M, Domingues DS Comput Struct Biotechnol J 20-Nov-2023
PMCID:PMC10698576
doi:10.1016/j.csbj.2023.11.034
PMID:38075396
A target enrichment probe set for resolving phylogenetic relationships in the coffee family, Rubiaceae Ball LD, Bedoya AM, Taylor CM, Lagomarsino LP Appl Plant Sci 17-Nov-2023
PMCID:PMC10719880
doi:10.1002/aps3.11554
PMID:38106541
In vitro induction of tetraploidy and its effects on phenotypic variations in Populus hopeiensis Wu J, Zhou Q, Sang Y, Zhao Y, Kong B, Li L, Du J, Ma L, Lu M, Zhang P BMC Plant Biol 13-Nov-2023
PMCID:PMC10641996
doi:10.1186/s12870-023-04578-0
PMID:37957587
Transcriptome Analysis Reveals the Stress Tolerance Mechanisms of Cadmium in Zoysia japonica Xu Y, Li Y, Li Y, Zhai C, Zhang K Plants (Basel) 12-Nov-2023
PMCID:PMC10674853
doi:10.3390/plants12223833
PMID:38005730
Integrated Transcriptomic and Metabolomic Analysis Reveals the Mechanism of Gibberellic Acid Regulates the Growth and Flavonoid Synthesis in Phellodendron chinense Schneid Seedlings Yang L, Luo S, Jiao J, Yan W, Zeng B, He H, He G Int J Mol Sci 07-Nov-2023
PMCID:PMC10671667
doi:10.3390/ijms242216045
PMID:38003235
Evaluation of Antioxidant and Anti-Inflammatory Activities, and Metabolite Profiling of Selected Medicinal Plants of Nepal Shrivastava AK, Keshari M, Neupane M, Chaudhary S, Dhakal PK, Shrestha L, Palikhey A, Yadav CK, Lamichhane G, Shekh MU, Yadav RK J Trop Med 03-Nov-2023
PMCID:PMC10637841
doi:10.1155/2023/6641018
PMID:37954133

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
> Alkaloids and derivatives / Cinchona alkaloids
(1S)-((2R,4S,5R)-5-Ethylquinuclidin-2-yl)(quinolin-4-yl)methanol 11630759 Click to see CCC1CN2CCC1CC2C(C3=CC=NC4=CC=CC=C34)O 296.40 unknown https://doi.org/10.1055/S-2007-969733
[(2R,4S)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-quinolin-4-ylmethanol 92131260 Click to see C=CC1CN2CCC1CC2C(C3=CC=NC4=CC=CC=C34)O 294.40 unknown https://doi.org/10.1055/S-2007-969733
Cinchonan-9-ol, (9S)- 90454 Click to see C=CC1CN2CCC1CC2C(C3=CC=NC4=CC=CC=C34)O 294.40 unknown https://doi.org/10.1055/S-2007-969733
> Alkaloids and derivatives / Yohimbine alkaloids
3beta-Isodihydrocadambine 188431 Click to see COC(=O)C1=COC(C2C1CC3C4=C(CCN3C2CO)C5=CC=CC=C5N4)OC6C(C(C(C(O6)CO)O)O)O 546.60 unknown https://doi.org/10.1248/CPB.51.232
Isodihydrocadambine 53463365 Click to see COC(=O)C1=COC(C2C1CC3C4=C(CCN3C2CO)C5=CC=CC=C5N4)OC6C(C(C(C(O6)CO)O)O)O 546.60 unknown https://doi.org/10.1016/S0040-4039(01)91901-X
https://doi.org/10.1016/S0040-4039(00)77808-7
https://doi.org/10.1248/CPB.51.232
methyl (1R,14R,15S,16S,20S)-14-(hydroxymethyl)-16-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate 163187709 Click to see COC(=O)C1=COC(C2C1CC3C4=C(CCN3C2CO)C5=CC=CC=C5N4)OC6C(C(C(C(O6)CO)O)O)O 546.60 unknown https://doi.org/10.1016/S0040-4039(00)77808-7
methyl (1S,14R,15S,16S,20S)-14-(hydroxymethyl)-16-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate 163185278 Click to see COC(=O)C1=COC(C2C1CC3C4=C(CCN3C2CO)C5=CC=CC=C5N4)OC6C(C(C(C(O6)CO)O)O)O 546.60 unknown https://doi.org/10.1016/S0040-4039(00)77808-7
methyl (1S,14R,15S,16S,20S)-14-(hydroxymethyl)-16-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate 154804625 Click to see COC(=O)C1=COC(C2C1CC3C4=C(CCN3C2CO)C5=CC=CC=C5N4)OC6C(C(C(C(O6)CO)O)O)O 546.60 unknown https://doi.org/10.1016/S0040-4039(01)91901-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-1,2,6b,9,9,12a-hexamethyl-4a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-10-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 10010531 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)O)O)C)C)C2C1C)C(=O)O)C(=O)OC7C(C(C(C(O7)CO)O)O)O 795.00 unknown https://doi.org/10.3184/030823400103165536
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 101681776 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 811.00 unknown https://doi.org/10.1002/(SICI)1097-458X(199911)37:11<837::AID-MRC567>3.0.CO;2-Y
(1S,2R,4aS,6aR,6bR,8aR,10S,12aR,12bR,14bS)-1,2,6b,9,9,12a-hexamethyl-10-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-4a-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)carbonyl)-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-6a-carboxylic acid 14194010 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)C2C1C)C(=O)O)C(=O)OC7C(C(C(C(O7)CO)O)O)O 811.00 unknown https://doi.org/10.3184/030823400103165536
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14aR)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6b,9,9,12a-hexamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a-tetradecahydropicene-4a,6a-dicarboxylic acid 100998576 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C(=O)O)C(=O)O)C 811.00 unknown https://doi.org/10.1002/(SICI)1097-458X(199911)37:11<837::AID-MRC567>3.0.CO;2-Y
1,2,6b,9,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 14194008 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)C2C1C)C(=O)O)C(=O)OC7C(C(C(C(O7)CO)O)O)O 811.00 unknown https://doi.org/10.3184/030823400103165536
10-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 162915755 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 811.00 unknown https://doi.org/10.1002/(SICI)1097-458X(199911)37:11<837::AID-MRC567>3.0.CO;2-Y
10-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6b,9,9,12a-hexamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a-tetradecahydropicene-4a,6a-dicarboxylic acid 162963246 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C(=O)O)C(=O)O)C 811.00 unknown https://doi.org/10.1002/(SICI)1097-458X(199911)37:11<837::AID-MRC567>3.0.CO;2-Y
Quinovic acid 3-O-(6-deoxyglucoside) 28-O-glucosyl ester 3829741 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)O)O)C)C)C2C1C)C(=O)O)C(=O)OC7C(C(C(C(O7)CO)O)O)O 795.00 unknown https://doi.org/10.3184/030823400103165536
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
1,10-Dihydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 73657100 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)CO)O)C)C)C2C1(C)O)C)C(=O)O 504.70 unknown https://doi.org/10.1080/10286020.2019.1670646
https://doi.org/10.1080/10286020.2011.606812
alpha-Hederagenin 258538 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1080/10286020.2011.606812
https://doi.org/10.1080/10286020.2019.1670646
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1080/10286020.2011.606812
https://doi.org/10.1080/10286020.2019.1670646
Clethric acid 20055826 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)CO)O)C)C)C2C1(C)O)C)C(=O)O 504.70 unknown https://doi.org/10.1080/10286020.2019.1670646
https://doi.org/10.1080/10286020.2011.606812
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1080/10286020.2019.1670646
https://doi.org/10.1080/10286020.2011.606812
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1080/10286020.2019.1670646
https://doi.org/10.1080/10286020.2011.606812
> 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/10.1080/10286020.2019.1670646
https://doi.org/10.1080/10286020.2011.606812
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/10.1080/10286020.2011.606812
https://doi.org/10.1080/10286020.2019.1670646
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,3S,5R,8Z,10R,11S,12R)-3,8,12-trimethyl-12-[(Z)-2-methylbut-2-enoyl]oxy-13-oxo-4,14-dioxatricyclo[9.3.0.03,5]tetradec-8-en-10-yl] (Z)-2-methylbut-2-enoate 101260393 Click to see CC=C(C)C(=O)OC1C=C(CCC2C(O2)(CC3C1C(C(=O)O3)(C)OC(=O)C(=CC)C)C)C 446.50 unknown https://doi.org/10.1021/NP50027A005
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1002/PTR.2650090307
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[3,4-Dihydroxy-5-[[3,4,5-trihydroxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methoxy]oxolan-3-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 85286250 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC3C(C(CO3)(COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O)O 640.60 unknown https://doi.org/10.1248/CPB.44.1162
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(3,4,5-trimethoxyphenoxy)oxane-3,4,5-triol 13922633 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 478.40 unknown https://doi.org/10.1248/CPB.44.1162
Kelampayoside A 10552637 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 478.40 unknown https://doi.org/10.1248/CPB.44.1162
Kelampayoside B 10841818 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC3C(C(CO3)(COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O)O 640.60 unknown https://doi.org/10.1248/CPB.44.1162
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
3-Dihydrocadambine 162138 Click to see COC(=O)C1=COC(C2C1CC3C4=C(CCN3CC2O)C5=CC=CC=C5N4)OC6C(C(C(C(O6)CO)O)O)O 546.60 unknown https://doi.org/10.1016/S0040-4039(01)82603-4
https://doi.org/10.1248/CPB.51.232
Cadambine 398038 Click to see COC(=O)C1=COC(C2C1CC34C5=C(CCN3CC2O4)C6=CC=CC=C6N5)OC7C(C(C(C(O7)CO)O)O)O 544.50 unknown https://doi.org/10.1016/S0040-4039(01)82603-4
https://doi.org/10.1080/10286020.2011.606812
https://doi.org/10.1002/CHIN.200330225
https://doi.org/10.1080/10286020.2019.1670646
https://doi.org/10.1248/CPB.51.232
https://doi.org/10.1021/NP50027A005
https://doi.org/10.3184/030823400103165536
https://doi.org/10.1055/S-2007-969733
https://doi.org/10.1016/S0040-4039(00)77808-7
CID 21723831 21723831 Click to see COC(=O)C1=COC(C2C1CC34C5=C(CCN3CC2O4)C6=CC=CC=C6N5)OC7C(C(C(C(O7)CO)O)O)O 544.50 unknown https://doi.org/10.1016/S0040-4039(01)82603-4
https://doi.org/10.1080/10286020.2019.1670646
https://doi.org/10.1080/10286020.2011.606812
https://doi.org/10.1248/CPB.51.232
methyl (1R,14R,15R,16S,20S)-14-(hydroxymethyl)-16-methoxy-3,13,17-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate 51042543 Click to see COC1C2C(CC3C4=C(CCN3C2CO)C5=CC=CC=C5N4)C(=CN1)C(=O)OC 397.50 unknown https://doi.org/10.1248/CPB.59.291
methyl (1R,15S,16S,17S,21S)-15-hydroxy-17-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-18-oxa-3,13-diazapentacyclo[11.9.0.02,10.04,9.016,21]docosa-2(10),4,6,8,19-pentaene-20-carboxylate 163185281 Click to see COC(=O)C1=COC(C2C1CC3C4=C(CCN3CC2O)C5=CC=CC=C5N4)OC6C(C(C(C(O6)CO)O)O)O 546.60 unknown https://doi.org/10.1016/S0040-4039(00)77808-7
methyl (1S,15S,16S,17S,21S)-15-hydroxy-17-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-18-oxa-3,13-diazapentacyclo[11.9.0.02,10.04,9.016,21]docosa-2(10),4,6,8,19-pentaene-20-carboxylate 163186677 Click to see COC(=O)C1=COC(C2C1CC3C4=C(CCN3CC2O)C5=CC=CC=C5N4)OC6C(C(C(C(O6)CO)O)O)O 546.60 unknown https://doi.org/10.1016/S0040-4039(00)77808-7
methyl (1S,15S,16S,17S,21S)-17-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-18,23-dioxa-3,13-diazahexacyclo[13.7.1.01,13.02,10.04,9.016,21]tricosa-2(10),4,6,8,19-pentaene-20-carboxylate 163191222 Click to see COC(=O)C1=COC(C2C1CC34C5=C(CCN3CC2O4)C6=CC=CC=C6N5)OC7C(C(C(C(O7)CO)O)O)O 544.50 unknown https://doi.org/10.1016/S0040-4039(00)77808-7
methyl (1S,15S,16S,17S,21S)-17-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-18,23-dioxa-3,13-diazahexacyclo[13.7.1.01,13.02,10.04,9.016,21]tricosa-2(10),4,6,8,19-pentaene-20-carboxylate 134716644 Click to see COC(=O)C1=COC(C2C1CC34C5=C(CCN3CC2O4)C6=CC=CC=C6N5)OC7C(C(C(C(O7)CO)O)O)O 544.50 unknown https://doi.org/10.3184/030823400103165536
https://doi.org/10.1055/S-2007-969733
https://doi.org/10.1002/CHIN.200330225
https://doi.org/10.1021/NP50027A005
https://doi.org/10.1002/HLCA.201100038
Methyl 14-(hydroxymethyl)-16-methoxy-3,13,17-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate 75605179 Click to see COC1C2C(CC3C4=C(CCN3C2CO)C5=CC=CC=C5N4)C(=CN1)C(=O)OC 397.50 unknown https://doi.org/10.1248/CPB.59.291
Methyl 14-(hydroxymethyl)-3,13,17-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15,17,19-heptaene-19-carboxylate 73657079 Click to see COC(=O)C1=C2CC3C4=C(CCN3C(C2=CN=C1)CO)C5=CC=CC=C5N4 363.40 unknown https://doi.org/10.1021/NP50027A005
Pyrano[4'',3'':4',5']azepino[1',2':1,2]pyrido[3,4-b]indole-1-carboxylic acid, 4-(beta-D-glucopyranosyloxy)-4,4a,5,6,8,9,14,14b,15,15a-decahydro-5-hydroxy-, methyl ester, (4S,4aS,5S,14bS,15aS)- 73981561 Click to see COC(=O)C1=COC(C2C1CC3C4=C(CCN3CC2O)C5=CC=CC=C5N4)OC6C(C(C(C(O6)CO)O)O)O 546.60 unknown https://doi.org/10.1016/S0040-4039(01)82603-4
https://doi.org/10.3184/030823400103165536
https://doi.org/10.1016/S0040-4039(00)77808-7
https://doi.org/10.1248/CPB.51.232
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[2-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 85183017 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O 520.50 unknown https://doi.org/10.1248/CPB.44.1162
3'-O-Caffeoylsweroside 10553980 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O 520.50 unknown https://doi.org/10.1248/CPB.44.1162

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