Senna tora - Unknown
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Internal ID UUID643fd5c5d2458729760756
Scientific name Senna tora
Authority (L.) Roxb.
First published in Fl. Ind. ed. 1832, 2: 340 (1832)

Description Top

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Senna tora, also known as sickle senna or sickle wild sensitive-plant, is a plant species in the Fabaceae family. It is native to Central America but can be found growing wild in most tropical regions. It is considered a weed in many places and is often confused with Chinese senna. The plant has a distinct smell when young and produces pale yellow flowers with unequal stamens. Its pods are flattened and sickle-shaped, giving it its common name. Senna tora is a stress-tolerant annual weed that is easily grown and can remain viable for up to twenty years. It has many traditional medicinal uses and its seeds and leaves are edible. The plant is also used as a natural pesticide and in various industrial applications. Senna tora is cultivated in many countries, with India being the largest producer. Its taxonomic history is confusing, with many synonyms being used for this species. It is found in many parts of the world, including Afghanistan, India, Nigeria, China, and Nepal. However, it is considered invasive in New-Caledonia.

Synonyms Top

Scientific name Authority First published in
Cassia tora L. Sp. Pl.: 376 (1753)
Cassia humilis Collad. Hist. Nat. Méd. Casses: 96 (1816)
Cassia borneensis Miq. Nieuwe Verh. Eerste Kl. Kon. Ned. Inst. Wetensch. Amsterdam, ser. 3, 3: 9 (1850)
Cassia tora var. borneensis (Miq.) Miq.
Cassia gallinaria Collad. Hist. Nat. Méd. Casses: 96 (1816)
Cassia numilis Collad.
Cassia sagera Lam. Encycl.1: 643 (1785)
Cassia tula Desv. ex Steud. Nomencl. Bot., ed. 2, 1: 308 (1840)
Diallobus tora (L.) Raf. Sylva Tellur. 128 1838
Cassia tagera L. Sp. Pl.: 376 (1753)
Cassia tora f. hirsuta Chodat & Hassl. Bull. Herb. Boissier, sér. 2, 4: 693 (1904)
Emelista tora (L.) Britton & Rose N.L.Britton & P.Wilson, Sci. Surv. Porto Rico & Virgin Islands5: 371 (1924)
Diallobus tora (L.) B.D.Jacks. Index Kew. 1(2): 741 1893
Diallobus thora (L.) Raf. Sylva Tellur.: 128 (1838)
Cassia contorta Vogel Gen. Cass. Syn.: 17 (1837)
Cassia sunsub Forssk. Fl. Aegypt.-Arab.: 86 (1775)
Cassia tala Desv. J. Bot. Agric.3: 23 (1814)
Chamaefistula contorta (Vogel) G.Don Gen. Hist.2: 452 (1832)
Chamaecrista tagera (L.) Standl. Contr. U.S. Natl. Herb.18: 104 (1916)
Tagera filiformis Raf. Sylva Tellur.: 129 (1838)
Cassia obtusifolia var. humilis (Collad.) Torr. & A.Gray Fl. N. Amer.1: 394 (1840)
Cassia foetida Salisb. Prodr. Stirp. Chap. Allerton: 325 (1796)

Common names Top

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Language Common/alternative name
English sickle senna
Bengali বন চাকুন্দা
Finnish sirppisenna
Indonesian ketepeng kecil
Kannada thagathe soppu
Korean 결명차
Malayalam വട്ടത്തകര
Nepali सानो ताप्रे
Sinhala තෝර (ශාකය)
Tamil தகரை
Thai ชุมเห็ดไทย
Chinese 草决明
Chinese 決明
Chinese 茳芒决明
Chinese 决明子
Chinese 决明
Chinese 野花生

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Tanzania
    • Northeast Tropical Africa
      • Chad
      • Socotra
      • Sudan
    • West Tropical Africa
      • Benin
      • Gambia
      • Ghana
      • Guinea
      • Liberia
      • Mali
      • Mauritania
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Gulf Of Guinea Islands
      • Zaïre
    • Western Indian Ocean
      • Madagascar
      • Mauritius
      • Rodrigues
      • Réunion
      • Seychelles
  • Asia-temperate
    • Arabian Peninsula
      • Oman
      • Saudi Arabia
      • Yemen
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
      • Inner Mongolia
      • Manchuria
      • Qinghai
    • Eastern Asia
      • Korea
      • Nansei-shoto
      • Taiwan
    • Russian Far East
      • Primorye
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Laccadive Islands
      • Maldives
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • South China Sea
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands
  • Australasia
    • Australia
      • Northern Territory
      • Queensland
      • Western Australia
  • Pacific
    • Northwestern Pacific
      • Marianas
    • South-central Pacific
      • Cook Islands
      • Marquesas
      • Society Islands
    • Southwestern Pacific
      • Fiji
      • New Caledonia
      • Samoa
      • Tonga
      • Vanuatu
      • Wallis-Futuna Islands
  • Southern America
    • Caribbean
      • Trinidad-Tobago
    • Central America
      • Belize
      • El Salvador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000165011
UNII PV11964Q61
USDA Plants SETO4
Tropicos 13032871
INPN 670755
KEW urn:lsid:ipni.org:names:518369-1
The Plant List ild-1143
Open Tree Of Life 1084528
NCBI Taxonomy 362788
Nature Serve 2.145000
IPNI 518369-1
iNaturalist 168855
GBIF 2957728
Freebase /m/03gq5lz
EPPO CASTO
EOL 418194
USDA GRIN 313456
Wikipedia Senna_tora
CMAUP NPO31136
CMAUP NPO7672

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_014851425.1 ASM1485142v1 Chromosome National Institute of Agricultural Sciences 2020-10-07 146.0x 501.97 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
Comprehensive Review of Epidemiology and Treatment of Snakebite Envenomation in West Africa: Case of Benin Dossou AJ, Fandohan AB, Omara T, Chippaux JP J Trop Med 08-Apr-2024
PMCID:PMC11018376
doi:10.1155/2024/8357312
PMID:38623180
Targeted remodeling of the human gut microbiome using Juemingzi (Senna seed extracts) Narrowe AB, Lemons JM, Mahalak KK, Firrman J, den Abbeele PV, Baudot A, Deyaert S, Li Y, Yu L(, Liu L Front Cell Infect Microbiol 04-Apr-2024
PMCID:PMC11024242
doi:10.3389/fcimb.2024.1296619
Leaf functional traits and resource use strategies facilitate the spread of invasive plant Parthenium hysterophorus across an elevational gradient in western Himalayas Sharma P, Rathee S, Ahmad M, Siddiqui MH, Alamri S, Kaur S, Kohli RK, Singh HP, Batish DR BMC Plant Biol 02-Apr-2024
PMCID:PMC10985864
doi:10.1186/s12870-024-04904-0
PMID:38561674
Chromosome-level genome assembly provides insights into the genome evolution and functional importance of the phenylpropanoid–flavonoid pathway in Thymus mongolicus Dang Z, Xu Y, Zhang X, Mi W, Chi Y, Tian Y, Liu Y, Ren W BMC Genomics 19-Mar-2024
PMCID:PMC10949689
doi:10.1186/s12864-024-10202-8
PMID:38504151
The Complete Mitochondrial Genome of Paeonia lactiflora Pall. (Saxifragales: Paeoniaceae): Evidence of Gene Transfer from Chloroplast to Mitochondrial Genome Tang P, Ni Y, Li J, Lu Q, Liu C, Guo J Genes (Basel) 14-Feb-2024
PMCID:PMC10888214
doi:10.3390/genes15020239
PMID:38397228
Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review Islam Shawon S, Nargis Reyda R, Qais N Heliyon 01-Feb-2024
PMCID:PMC10864916
doi:10.1016/j.heliyon.2024.e25340
PMID:38356556
Ayurvedic clinical decision-making methods to predict, prevent and manage childhood allergic disorders Karthik KP, Dileep A, Rajagopala S, Arun Kumar M, Dharmarajan P, Vellela J J Ayurveda Integr Med 18-Jan-2024
PMCID:PMC10828817
doi:10.1016/j.jaim.2023.100857
PMID:38237455
Recent advances in the extraction, purification, structural-property correlations, and antiobesity mechanism of traditional Chinese medicine-derived polysaccharides: a review Zhi N, Chang X, Wang X, Guo J, Chen J, Gui S Front Nutr 17-Jan-2024
PMCID:PMC10828026
doi:10.3389/fnut.2023.1341583
PMID:38299183
Ethnobotanical study of medicinal plants used by the indigenous community of the western region of Mizoram, India Ralte L, Sailo H, Singh YT J Ethnobiol Ethnomed 03-Jan-2024
PMCID:PMC10765666
doi:10.1186/s13002-023-00642-z
PMID:38172927
Silvicultural Practices for Diversity Conservation and Invasive Species Suppression in Forest Ecosystems of the Bundala National Park, Sri Lanka Suraweera C, Gallo J, Vacek Z, Cukor J, Vacek S, Baláš M Plants (Basel) 31-Dec-2023
PMCID:PMC10780521
doi:10.3390/plants13010121
PMID:38202429
The Global Impact of COVID-19: Historical Development, Molecular Characterization, Drug Discovery and Future Directions Dofuor AK, Quartey NK, Osabutey AF, Boateng BO, Lutuf H, Osei JH, Ayivi-Tosuh SM, Aiduenu AF, Ekloh W, Loh SK, Opoku MJ, Aidoo OF Clin Pathol 23-Dec-2023
PMCID:PMC10748929
doi:10.1177/2632010X231218075
PMID:38144436
Chromosomal dynamics in Senna: comparative PLOP–FISH analysis of tandem repeats and flow cytometric nuclear genome size estimations Nguyen TH, Kang BY, Kim HH Front Plant Sci 14-Dec-2023
PMCID:PMC10762312
doi:10.3389/fpls.2023.1288220
PMID:38173930
Assembly and comparative analysis of the complete mitochondrial genome of Trigonella foenum-graecum L. He Y, Liu W, Wang J BMC Genomics 08-Dec-2023
PMCID:PMC10704837
doi:10.1186/s12864-023-09865-6
PMID:38066419
Recent updates on nano-phyto-formulations based therapeutic intervention for cancer treatment WAHI A, BISHNOI M, RAINA N, SINGH MA, VERMA P, GUPTA PK, KAUR G, TULI HS, GUPTA M Oncol Res 15-Nov-2023
PMCID:PMC10767243
doi:10.32604/or.2023.042228
PMID:38188681
Efficacy of Khaya grandifoliola Stem Bark Ethanol Extract in the Treatment of Cerebral Malaria in Swiss albino Mice Using Plasmodium berghei NK65 Strain Guy-Armand GN, Cedric Y, Nadia NA, Kevin TD, Sandra TN, Sidiki NN, Azizi MA, Payne VK J Parasitol Res 09-Nov-2023
PMCID:PMC10653973
doi:10.1155/2023/5700782
PMID:38028126

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
(12S)-7,17-dimethoxy-3,5-dioxa-11-azapentacyclo[10.7.1.0^{2,6.0^{8,20.0^{14,19]icosa-1,6,8(20),14,16,18-hexaen-16-ol 3467447 Click to see COC1=C(C=C2CC3C4=C(CCN3)C(=C5C(=C4C2=C1)OCO5)OC)O 341.40 unknown via CMAUP database
> Alkaloids and derivatives / Harmala alkaloids
(2S,3R,12bS)-3-ethyl-2-[[(1R)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl]methyl]-1,2,3,4,6,7,7a,12,12a,12b-decahydroindolo[2,3-a]quinolizine 44559929 Click to see CCC1CN2CCC3C(C2CC1CC4C5=C(CCN4)C6=CC=CC=C6N5)NC7=CC=CC=C37 440.60 unknown via CMAUP database
> Benzenoids / Anthracenes
(3S)-3,8,9-trihydroxy-6-methoxy-3-methyl-5-[(6S)-1,6,9-trihydroxy-3-methoxy-6-methyl-8-oxo-5,7-dihydroanthracen-2-yl]-2,4-dihydroanthracen-1-one 10460737 Click to see CC1(CC2=CC3=C(C(=CC(=C3C4=C(C5=C(C6=C(CC(CC6=O)(C)O)C=C5C=C4OC)O)O)OC)O)C(=C2C(=O)C1)O)O 574.60 unknown https://doi.org/10.1248/CPB.42.2588
1(2H)-Anthracenone, 3,4-dihydro-3,8,9-trihydroxy-6-methoxy-3-methyl- 10446798 Click to see CC1(CC2=CC3=CC(=CC(=C3C(=C2C(=O)C1)O)O)OC)O 288.29 unknown via CMAUP database
6-Methylanthracene-1,2,8-triol 221502 Click to see CC1=CC2=C(C=C3C(=C2)C=CC(=C3O)O)C(=C1)O 240.25 unknown via CMAUP database
Emodin anthrone 122635 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2)C=C(C=C3O)O 256.25 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
4,5-Dihydroxy-7-methyl-9,10-dioxoanthracene-2-carboxylic acid 3009664 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)C(=O)O 298.25 unknown via CMAUP database
9,10-dioxo-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-2-carboxylic acid 5320960 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4OC5C(C(C(C(O5)CO)O)O)O)C(=O)O 608.50 unknown via CMAUP database
Rhein 10168 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)C(=O)O 284.22 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
(2S,3R)-8-hydroxy-1-methoxy-3-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydroanthracene-9,10-dione 162876260 Click to see CC1C=C2C(=C(C1OC3C(C(C(C(O3)CO)O)O)O)OC)C(=O)C4=C(C2=O)C=CC=C4O 448.40 unknown https://doi.org/10.1016/0031-9422(89)85040-X
1,8-Dihydroxy-3-methyl-4a,9a-dihydroanthracene-9,10-dione 24867638 Click to see CC1=CC2C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 256.25 unknown via CMAUP database
2-(4,5-dihydroxy-2-methoxy-7-methyl-10-oxo-9H-anthracen-1-yl)-1,8-dihydroxy-3-methoxy-6-methylanthracene-9,10-dione 9985077 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2)C(=C(C=C3O)OC)C4=C(C=C5C(=C4O)C(=O)C6=C(C5=O)C=C(C=C6O)C)OC 552.50 unknown https://doi.org/10.1248/CPB.42.2588
8-hydroxy-1-methoxy-3-methyl-2-[(2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione 158957192 Click to see CC1=CC2=C(C(=C1OC3C(C(C(C(O3)CO)O)O)O)OC)C(=O)C4=C(C2=O)C=CC=C4O 446.40 unknown https://doi.org/10.1248/CPB.6.397
8-Hydroxy-1-methoxy-3-methyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydroanthracene-9,10-dione 162876259 Click to see CC1C=C2C(=C(C1OC3C(C(C(C(O3)CO)O)O)O)OC)C(=O)C4=C(C2=O)C=CC=C4O 448.40 unknown https://doi.org/10.1016/0031-9422(89)85040-X
Aloe emodin 10207 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)CO 270.24 unknown via CMAUP database
Anthraquinone 6780 Click to see C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3C2=O 208.21 unknown via CMAUP database
Chryso-obtusin glucoside 442730 Click to see CC1=CC2=C(C(=C1OC3C(C(C(C(O3)CO)O)O)O)OC)C(=O)C4=C(C(=C(C=C4C2=O)OC)OC)OC 520.50 unknown https://doi.org/10.1016/J.BMCL.2015.10.014
Chrysophanein 6324923 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=CC=C4O 416.40 unknown via CMAUP database
Chrysophanic acid 10208 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 254.24 unknown via CMAUP database
Chrysophanol 8-(6-O-galloyl-beta-D-glucopyranoside) 5315852 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O 568.50 unknown via CMAUP database
Danthron 2950 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 240.21 unknown via CMAUP database
Floribundone 1 11757663 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)C4=C(C=C(C5=C4C(=O)C6=C(C5=O)C(=CC(=C6)C)O)O)OC)O 566.50 unknown https://doi.org/10.1248/CPB.42.2588
Obtusifolin 2-glucoside 442761 Click to see CC1=CC2=C(C(=C1OC3C(C(C(C(O3)CO)O)O)O)OC)C(=O)C4=C(C2=O)C=CC=C4O 446.40 unknown https://doi.org/10.1248/CPB.6.397
https://doi.org/10.1016/J.BMCL.2015.10.014
Physcion 8-gentiobioside 442762 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)OC 608.50 unknown https://doi.org/10.1016/J.BMCL.2015.10.014
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown https://doi.org/10.1016/J.BMCL.2015.10.014
https://doi.org/10.1248/CPB.55.1476
Pulmatin 442731 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1-Desmethylobtusin 13675113 Click to see CC1=CC2=C(C(=C1O)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)OC)O 330.29 unknown via CMAUP database
1,2,6,8-Tetrahydroxy-3-methylanthraquinone 2-O-b-D-glucoside 131751347 Click to see CC1=CC2=C(C(=C1OC3C(C(C(C(O3)CO)O)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(98)00151-4
1,3-Dihydroxy-8-methoxy-6-methylanthracene-9,10-dione 10469084 Click to see CC1=CC2=C(C(=C1)OC)C(=O)C3=C(C2=O)C=C(C=C3O)O 284.26 unknown via CMAUP database
1,3,5-Trihydroxy-6,7-dimethoxy-2-methylanthraquinone 131751404 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C(=C3C2=O)O)OC)OC)O 330.29 unknown https://doi.org/10.1055/S-0028-1099569
1,6,8-trihydroxy-3-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione 162922112 Click to see CC1=CC2=C(C(=C1OC3C(C(C(C(O3)CO)O)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(98)00151-4
2,6,8-Trihydroxy-1-methoxy-3-methylanthracene-9,10-dione 10086148 Click to see CC1=CC2=C(C(=C1O)OC)C(=O)C3=C(C2=O)C=C(C=C3O)O 300.26 unknown via CMAUP database
7-Hydroxyemodin 12548 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)O)O)O 286.24 unknown via CMAUP database
7-Methoxy obtusifolin 122196300 Click to see CC1=CC2=C(C(=C1O)OC)C(=O)C3=C(C2=O)C=CC(=C3O)OC 314.29 unknown https://doi.org/10.1016/J.BMCL.2015.10.014
Aurantio-obtusin 155011 Click to see CC1=CC2=C(C(=C1O)OC)C(=O)C3=C(C(=C(C=C3C2=O)O)OC)O 330.29 unknown https://doi.org/10.1007/BF02976245
https://doi.org/10.1007/BF02979126
https://doi.org/10.1016/J.BMCL.2015.10.014
Aurantio-obtusin beta-D-glucoside 442725 Click to see CC1=CC2=C(C(=C1O)OC)C(=O)C3=C(C(=C(C=C3C2=O)OC4C(C(C(C(O4)CO)O)O)O)OC)O 492.40 unknown https://doi.org/10.1248/CPB.55.1476
https://doi.org/10.1016/J.BMCL.2015.10.014
Chrysoobtusin 155381 Click to see CC1=CC2=C(C(=C1O)OC)C(=O)C3=C(C(=C(C=C3C2=O)OC)OC)OC 358.30 unknown https://doi.org/10.1016/J.BMCL.2015.10.014
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown https://doi.org/10.1016/J.BMCL.2015.10.014
Emodin(1-) 25201450 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3[O-])O 269.23 unknown via CMAUP database
Glucoaurantio-obtusin 4483731 Click to see CC1=CC2=C(C(=C1O)OC)C(=O)C3=C(C(=C(C=C3C2=O)OC4C(C(C(C(O4)CO)O)O)O)OC)O 492.40 unknown https://doi.org/10.1248/CPB.55.1476
Obtusifolin 3083575 Click to see CC1=CC2=C(C(=C1O)OC)C(=O)C3=C(C2=O)C=CC=C3O 284.26 unknown https://doi.org/10.1016/J.BMCL.2015.10.014
Obtusin 155380 Click to see CC1=CC2=C(C(=C1O)OC)C(=O)C3=C(C(=C(C=C3C2=O)OC)OC)O 344.30 unknown https://doi.org/10.1016/J.BMCL.2015.10.014
Questin 160717 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC)O 284.26 unknown via CMAUP database
Questin-2-olate 25203706 Click to see CC1=CC2=C(C(=C1)[O-])C(=O)C3=C(C2=O)C=C(C=C3OC)O 283.25 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzonitriles
Chlorothalonil 15910 Click to see C(#N)C1=C(C(=C(C(=C1Cl)Cl)Cl)C#N)Cl 265.90 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
N-(4-{4-[(aminocarbonyl)amino]benzyl}phenyl)urea 318591 Click to see C1=CC(=CC=C1CC2=CC=C(C=C2)NC(=O)N)NC(=O)N 284.31 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Sulfanilides
Dichlofluanid 14145 Click to see CN(C)S(=O)(=O)N(C1=CC=CC=C1)SC(F)(Cl)Cl 333.20 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
1,3-Naphthalenediol 8601 Click to see C1=CC=C2C(=C1)C=C(C=C2O)O 160.17 unknown via CMAUP database
2-Acetyl-3-methyl-1,6,8-trihydroxynaphthalene 23643241 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)O)O 232.23 unknown https://doi.org/10.1248/CPB.55.1476
Torachrysone 5321977 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)O)OC 246.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Heptanoate 93052 Click to see CCCCCCC(=O)[O-] 129.18 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
2,3-Dihydroxypropyl hexadecanoate 14900 Click to see CCCCCCCCCCCCCCCC(=O)OCC(CO)O 330.50 unknown https://doi.org/10.1271/BBB.58.1343
Glyceryl monooleate 5283468 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(CO)O 356.50 unknown https://doi.org/10.1271/BBB.58.1343
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
[(4S,6R,7S)-7-(2-acetyloxypropan-2-yl)-1,4-dimethyl-2-oxo-3,3a,4,5,6,7,8,8a-octahydro-1H-azulen-6-yl] (Z)-2-methylbut-2-enoate 5321981 Click to see CC=C(C)C(=O)OC1CC(C2CC(=O)C(C2CC1C(C)(C)OC(=O)C)C)C 378.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
(2S,3R,5R,10R,13S,14R)-2,3,14-trihydroxy-10,13-dimethyl-1,2,3,4,5,9,11,12,15,16-decahydrocyclopenta[a]phenanthrene-6,17-dione 10042510 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2=O)O 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Tetrahydroxy bile acids, alcohols and derivatives
17-(3,4-Dihydroxy-6-methylheptan-2-yl)-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 13982109 Click to see CC(C)CC(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 450.70 unknown https://doi.org/10.1271/BBB.58.1343
24-epi-Castasterone 13039027 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 464.70 unknown https://doi.org/10.1271/BBB.58.1343
28-Norcastasterone 13982110 Click to see CC(C)CC(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 450.70 unknown https://doi.org/10.1271/BBB.58.1343
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Trihydroxy bile acids, alcohols and derivatives
17-(3,4-Dihydroxy-5,6-dimethylheptan-2-yl)-3-hydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 13475117 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CCC(C4)O)C)C)O)O 448.70 unknown https://doi.org/10.1271/BBB.58.1343
Teasterone 13475125 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CCC(C4)O)C)C)O)O 448.70 unknown https://doi.org/10.1271/BBB.58.1343
Typhasterol 13475120 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CCC(C4)O)C)C)O)O 448.70 unknown https://doi.org/10.1271/BBB.58.1343
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Brassinolides and derivatives
24-Epibrassinolide 3239 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 480.70 unknown https://doi.org/10.1271/BBB.58.1343
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 6432744 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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 via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
2-Oxonioacetate 3698251 Click to see C(C(=O)[O-])[OH2+] 76.05 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Ononitol 5320294 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1016/J.PHYMED.2009.02.006
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[1-hydroxy-6-methoxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-2-naphthyl]ethanone 503732 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)OC 570.50 unknown https://doi.org/10.1248/CPB.55.1476
1-[1,6-dihydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 100753 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)O 394.40 unknown https://doi.org/10.1248/CPB.55.1476
1-[3-[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-1,6-dimethoxy-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 122196301 Click to see CC(=O)C1=C(C2=C(C=C(C=C2C=C1OC3C(C(CO3)(CO)O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC 556.50 unknown https://doi.org/10.1016/J.BMCL.2015.10.014
Musizin glucoside, 6-hydroxy 338716 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)O 394.40 unknown https://doi.org/10.1248/CPB.55.1476
Torachrysone 8-beta-gentiobioside 78195599 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)OC 570.50 unknown https://doi.org/10.1248/CPB.55.1476
Torachrysone 8-O-Glucoside 11972479 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)OC 408.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
1-[8-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1-hydroxy-6-methoxy-3-methylnaphthalen-2-yl]ethanone 23658649 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)OC 732.70 unknown https://doi.org/10.1248/CPB.55.1476
1-[8-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1-hydroxy-6-methoxy-3-methylnaphthalen-2-yl]ethanone 10700904 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O)O)O)OC 894.80 unknown https://doi.org/10.1248/CPB.55.1476
1-[8-[6-[[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1-hydroxy-6-methoxy-3-methylnaphthalen-2-yl]ethanone 74081776 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)OC 732.70 unknown https://doi.org/10.1248/CPB.55.1476
6-Methoxymusizin 8-O-[b-D-glucopyranosyl-(1->6)-b-D-glucopyranosyl-(1->3)-b-D-glucopyranosyl-(1->6)-b-D-glucopyranoside] 85238177 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O)O)O)OC 894.80 unknown https://doi.org/10.1248/CPB.55.1476
8-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1-hydroxy-3-methylanthracene-9,10-dione 162874029 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1248/CPB.55.1476
8-[6-[[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1-hydroxy-3-methylanthracene-9,10-dione 162874028 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1248/CPB.55.1476
9-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-10-hydroxy-7-methoxy-3-methylbenzo[g]isochromen-1-one 10533146 Click to see CC1=CC2=CC3=CC(=CC(=C3C(=C2C(=O)O1)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)OC 758.70 unknown https://doi.org/10.1248/CPB.55.1476
9-[6-[[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-10-hydroxy-7-methoxy-3-methylbenzo[g]isochromen-1-one 85175328 Click to see CC1=CC2=CC3=CC(=CC(=C3C(=C2C(=O)O1)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)OC 758.70 unknown https://doi.org/10.1248/CPB.55.1476
Chrysophanol 1-tetraglucoside 14213508 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O)O)O)C(=O)C7=C(C2=O)C=CC=C7O 902.80 unknown https://doi.org/10.1016/0031-9422(89)85040-X
Chrysophanol 1-triglucoside 14213506 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)C(=O)C6=C(C2=O)C=CC=C6O 740.70 unknown https://doi.org/10.1016/0031-9422(89)85040-X
Chrysophanol tetraglucoside 11972361 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O)O)O)C(=O)C7=C(C2=O)C=CC=C7O 902.80 unknown https://doi.org/10.1016/0031-9422(89)85040-X
Chrysophanol triglucoside 5317697 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)C(=O)C6=C(C2=O)C=CC=C6O 740.70 unknown https://doi.org/10.1016/0031-9422(89)85040-X
Rubrofusarin 6-[glucosyl-(1->3)-glucosyl-(1->6)-glucoside] 85229275 Click to see CC1=CC(=O)C2=C(C3=C(C=C(C=C3C=C2O1)OC)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O 758.70 unknown https://doi.org/10.1248/CPB.55.1476
Rubrofusarin triglucoside 10676583 Click to see CC1=CC(=O)C2=C(C3=C(C=C(C=C3C=C2O1)OC)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O 758.70 unknown https://doi.org/10.1248/CPB.55.1476
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
L-Tartaric acid 444305 Click to see C(C(C(=O)O)O)(C(=O)O)O 150.09 unknown via CMAUP database
> Organoheterocyclic compounds / Benzoxepines
Cassialactone 627638 Click to see CC1(CC2=CC3=CC(=CC(=C3C(=C2C(=O)OC1)O)O)OC)O 304.29 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Norrubrofusarin 135453893 Click to see CC1=CC(=C2C(=CC3=CC(=O)C=C(C3=C2O)O)O1)O 258.23 unknown https://doi.org/10.1007/BF03046320
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
5,6,8-trihydroxy-2-methylbenzo[g]chromen-4-one 5320218 Click to see CC1=CC(=O)C2=C(C3=C(C=C(C=C3C=C2O1)O)O)O 258.23 unknown https://doi.org/10.1248/CPB.55.1476
Toralactone 5321980 Click to see CC1=CC2=CC3=CC(=CC(=C3C(=C2C(=O)O1)O)O)OC 272.25 unknown https://doi.org/10.1248/CPB.55.1476
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones / Naphthopyranone glycosides
10-hydroxy-3-methyl-9-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxybenzo[g]isochromen-1-one 101617058 Click to see CC1=CC2=C(C(=C3C(=C2)C=CC=C3OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)C(=O)O1 566.50 unknown via CMAUP database
10-Hydroxy-3-methyl-9-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxybenzo[g]isochromen-1-one 137796324 Click to see CC1=CC2=C(C(=C3C(=C2)C=CC=C3OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)C(=O)O1 566.50 unknown https://doi.org/10.1248/CPB.47.1121
10-Hydroxy-7-methoxy-3-methyl-9-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxybenzo[g]isochromen-1-one 14189968 Click to see CC1=CC2=CC3=CC(=CC(=C3C(=C2C(=O)O1)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)OC 596.50 unknown https://doi.org/10.1248/CPB.55.1476
Cassiaside 164146 Click to see CC1=CC(=O)C2=C(O1)C=C3C=CC=C(C3=C2O)OC4C(C(C(C(O4)CO)O)O)O 404.40 unknown https://doi.org/10.1055/S-2006-957593
https://doi.org/10.1055/S-2006-962003
https://doi.org/10.1248/CPB.47.1121
https://doi.org/10.1007/BF02979126
Cassiaside C 5317701 Click to see CC1=CC2=CC3=CC(=CC(=C3C(=C2C(=O)O1)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)OC 596.50 unknown https://doi.org/10.1248/CPB.55.1476
https://doi.org/10.1016/J.BMCL.2015.10.014
Rubrofusarin 6-gentiobioside 14189963 Click to see CC1=CC(=O)C2=C(C3=C(C=C(C=C3C=C2O1)OC)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1055/S-2006-962003
Rubrofusarin gentiobioside 503733 Click to see CC1=CC(=O)C2=C(C3=C(C=C(C=C3C=C2O1)OC)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1016/J.BMCL.2015.10.014
Rubrofusarin-6-glucoside 3035617 Click to see CC1=CC(=O)C2=C(C3=C(C=C(C=C3C=C2O1)OC)OC4C(C(C(C(O4)CO)O)O)O)O 434.40 unknown https://doi.org/10.1016/J.BMCL.2015.10.014
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Norsanguinarine 97679 Click to see C1OC2=C(O1)C3=CN=C4C(=C3C=C2)C=CC5=CC6=C(C=C54)OCO6 317.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
Tocris-1610 6603986 Click to see CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)C=CC4=CC=CC=C4)O)O 516.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1248/CPB.42.2588
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.1016/J.BMCL.2015.10.014
https://doi.org/10.1248/CPB.55.1476

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