Salacia reticulata - Unknown
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Internal ID UUID643ffcae9b17b514431430
Scientific name Salacia reticulata
Authority Wight
First published in Ill. Ind. Bot. 1: 134 (1839)

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Synonyms Top

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Language Common/alternative name
English kothala himbutu
Catalan kothala himbutu
Japanese コタラヒムブツ
Korean 코타라힘부투
Malayalam salaretin
Malayalam ഏകനായകം
Dutch kothala himbutu
Sinhala කොතලහිඹුටු
Chinese 五层龙
Chinese 五层龍

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Sri Lanka
    • Indo-China
      • Andaman Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000435705
Tropicos 100412780
KEW urn:lsid:ipni.org:names:162694-1
Open Tree Of Life 5750051
NCBI Taxonomy 1565083
IPNI 162694-1
GBIF 5579938
Freebase /m/0jw_077
USDA GRIN 470519
Wikipedia Salacia_reticulata

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
Role of the thiosugar ring in the inhibitory activity of salacinol, a potent natural α-glucosidase inhibitor Takashima K, Nakamura S, Nagayama M, Marumoto S, Ishikawa F, Xie W, Nakanishi I, Muraoka O, Morikawa T, Tanabe G RSC Adv 02-Feb-2024
PMCID:PMC10835759
doi:10.1039/d3ra08485j
PMID:38312722
Anti-protein glycation and free-radical scavenging properties of Sri Lankan antidiabetic medicinal plant Salacia reticulata l. (Kothala Himbutu) Premakumara GA, Abeysekera WK BMC Complement Med Ther 03-Nov-2023
PMCID:PMC10623713
doi:10.1186/s12906-023-04169-4
PMID:37924066
Promising role of Vitamin D and plant metabolites against COVID-19: Clinical trials review Srivastava R, Singh N, Kanda T, Yadav S, Yadav S, Choudhary P, Atri N Heliyon 21-Oct-2023
PMCID:PMC10618788
doi:10.1016/j.heliyon.2023.e21205
PMID:37920525
The Effect of Salacia Reticulata Extract Biscuits on Blood Sugar Control of Type 2 Diabetes Mellitus Patients: A Two-Period, Two-Sequence, Crossover, Randomized, Triple-Blind, Placebo-Controlled, Clinical Trial Siribaddana S, Medagama A, Wickramasinghe N, Siribaddana NM, Agampodi S, Fernando D Cureus 25-Sep-2023
PMCID:PMC10599346
doi:10.7759/cureus.45921
PMID:37885536
The Effect of Fenugreek in Type 2 Diabetes and Prediabetes: A Systematic Review and Meta-Analysis of Randomized Controlled Trials Kim J, Noh W, Kim A, Choi Y, Kim YS Int J Mol Sci 12-Sep-2023
PMCID:PMC10531284
doi:10.3390/ijms241813999
PMID:37762302
Synergistic Combination of NAPROC-13 and NMR 13C DFT Calculations: A Powerful Approach for Revising the Structure of Natural Products Sánchez-Martínez HA, Morán-Pinzón JA, del Olmo Fernández E, Eguiluz DL, Adserias Vistué JF, López-Pérez JL, De León EG J Nat Prod 07-Sep-2023
PMCID:PMC10616860
doi:10.1021/acs.jnatprod.3c00437
PMID:37675572
Salacia reticulata Extract Suppresses Fat Accumulation by Regulating Lipid Metabolism Jung J, Park J, Lee M, Kim J, Oh D, Jun W, Kim OK, Lee J Foods 22-Aug-2023
PMCID:PMC10487061
doi:10.3390/foods12173149
PMID:37685080
Revisiting the Green Synthesis of Nanoparticles: Uncovering Influences of Plant Extracts as Reducing Agents for Enhanced Synthesis Efficiency and Its Biomedical Applications Singh H, Desimone MF, Pandya S, Jasani S, George N, Adnan M, Aldarhami A, Bazaid AS, Alderhami SA Int J Nanomedicine 18-Aug-2023
PMCID:PMC10444627
doi:10.2147/IJN.S419369
PMID:37621852
Biogenic Synthesis of Copper Nanoparticles: A Systematic Review of Their Features and Main Applications Luque-Jacobo CM, Cespedes-Loayza AL, Echegaray-Ugarte TS, Cruz-Loayza JL, Cruz I, de Carvalho JC, Goyzueta-Mamani LD Molecules 18-Jun-2023
PMCID:PMC10301071
doi:10.3390/molecules28124838
PMID:37375393
Synergistic Influence of Yeast Extract and Calcium Oxide Nanoparticles on the Synthesis of Bioactive Antioxidants and Metabolites in Swertia chirata In Vitro Callus Cultures Sardar T, Maqbool M, Ishtiaq M, Mazhar MW, El-Sheikh MA, Casini R, Mahmoud EA, Elansary HO Molecules 07-Jun-2023
PMCID:PMC10301036
doi:10.3390/molecules28124607
PMID:37375162
Xanthones: Biosynthesis and Trafficking in Plants, Fungi and Lichens Badiali C, Petruccelli V, Brasili E, Pasqua G Plants (Basel) 04-Feb-2023
PMCID:PMC9967055
doi:10.3390/plants12040694
PMID:36840041
Comparative synthesis and characterization of nanocomposites using chemical and green approaches including a comparison study on in vivo and in vitro biological properties G S, S VP, E P, G A Nanoscale Adv 13-Dec-2022
PMCID:PMC9890937
doi:10.1039/d2na00677d
PMID:36756509
Metabolites extracted from microorganisms as potential inhibitors of glycosidases (α-glucosidase and α-amylase): A review Wang X, Li J, Shang J, Bai J, Wu K, Liu J, Yang Z, Ou H, Shao L Front Microbiol 17-Nov-2022
PMCID:PMC9712454
doi:10.3389/fmicb.2022.1050869
PMID:36466660
Targeting matrix metalloproteases: A promising strategy for herbal medicines to treat rheumatoid arthritis Li RL, Duan HX, Liang Q, Huang YL, Wang LY, Zhang Q, Wu CJ, Liu SQ, Peng W Front Immunol 09-Nov-2022
PMCID:PMC9682071
doi:10.3389/fimmu.2022.1046810
PMID:36439173
Efficacy and safety of traditional chinese medicine treatment for overweight and obese individuals: A systematic review and meta-analysis Wen ZG, Zhang QQ, Zhang LL, Shen MF, Huang YS, Zhao LH Front Pharmacol 05-Oct-2022
PMCID:PMC9581128
doi:10.3389/fphar.2022.964495
PMID:36278196

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
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
Macquarimicin C 10339132 Click to see CC1CC2C(C1=O)C=CC3C2C(C45C(C3)CC(CC4=O)OC5=O)CC(=O)C 370.40 unknown https://doi.org/10.1016/S0040-4020(01)80566-4
https://doi.org/10.1016/S0031-9422(00)83123-4
https://doi.org/10.1016/0031-9422(96)00886-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4bS,8S,8aR)-8-(hydroxymethyl)-4b,8-dimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol 21632843 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)CO)C)O 302.50 unknown https://doi.org/10.1093/JN/132.7.1819
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(4aR,6aS,6aS,6bR,8aR,12aR,14aR,14bS)-3-hydroxy-4,6a,6b,8a,14a-pentamethyl-11-methylidene-2-oxo-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-1H-picene-4a-carbaldehyde 101995822 Click to see CC1=C(C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(=C)CC5)C)C)C)C)C=O)O 438.60 unknown https://doi.org/10.1080/10575639308043876
https://doi.org/10.1016/0031-9422(96)00886-2
[1-Acetyloxy-5-hydroxy-7,8-dimethyl-7-(3-methylpenta-2,4-dienyl)-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-3-yl] acetate 72817010 Click to see CC1CCC23C(C1(C)CC=C(C)C=C)CC(C=C2C(OC3OC(=O)C)OC(=O)C)O 418.50 unknown https://doi.org/10.1016/0031-9422(90)89066-I
3-hydroxy-4,6a,6b,8a,14a-pentamethyl-11-methylidene-2-oxo-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-1H-picene-4a-carbaldehyde 162911009 Click to see CC1=C(C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(=C)CC5)C)C)C)C)C=O)O 438.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,4aS,6aS,6aR,6bS,8aS,9R,12aS,14aS,14bR)-2,4a,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-2-carbaldehyde 14108939 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C=O)C)C)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
(2S,4aS,6aS,6aR,6bS,8aS,9R,12aS,14aS,14bR)-2,4a,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-2-carboxylic acid 14108946 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)C 456.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
(4aS,6aR,6aS,6bR,8aS,11R,12aR,14aS,14bS)-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 137705381 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(96)00886-2
(4R,4aR,6aS,6aS,6bS,8aS,10R,12aR,14aS,14bR)-10-hydroxy-6b-(hydroxymethyl)-4,4a,6a,8a,11,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 162986902 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(C5)O)(C)C)C)CO)C)C)C 458.70 unknown https://doi.org/10.1016/S0040-4020(01)80566-4
(4R,4aS,6aR,6aR,6bR,8aR,12aS,14aS,14bR)-6a-(hydroxymethyl)-4,4a,6b,8a,11,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 162993436 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)CO)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
(4R,4aS,6aR,6aS,6bR,8aR,12aS,14aS,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 11870447 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
(4R,4aS,6aR,6aS,6bR,8aS,10R,12aR,14aS,14bS)-10-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 163190499 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(C5)O)(C)C)C)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
(4R,4aS,6aR,6aS,6bR,8aS,12aR,14aS,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,4,5,6,6a,7,8,9,12,12a,13,14,14b-tetradecahydropicene-3,10-dione 162952237 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(=O)C5)(C)C)C)C)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
(4R,4aS,6aR,6aS,6bS,8aS,10R,12aR,14aS,14bS)-10-hydroxy-6b-(hydroxymethyl)-4,4a,6a,8a,11,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 162986903 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(C5)O)(C)C)C)CO)C)C)C 458.70 unknown https://doi.org/10.1016/S0040-4020(01)80566-4
(4R,4aS,6aS,6aS,6bR,8aS,10R,11S,12aR,14aS,14bS)-10-hydroxy-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 14466315 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(C5)O)(C)CO)C)C)C)C)C 458.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
(4R,4aS,6aS,6aS,6bR,8aS,11S,12aR,14aS,14bS)-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 14108942 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
(4R,4aS,6aS,6aS,6bS,8aS,10R,12aR,14aS,14bS)-10-hydroxy-6b-(hydroxymethyl)-4,4a,6a,8a,11,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 21723750 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(C5)O)(C)C)C)CO)C)C)C 458.70 unknown https://doi.org/10.1016/0031-9422(96)00886-2
https://doi.org/10.1016/S0031-9422(00)83123-4
10-hydroxy-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 14466314 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(C5)O)(C)CO)C)C)C)C)C 458.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
10-Hydroxy-2,4a,6a,6a,9,14a-hexamethyl-11-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylic acid 4274774 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)O 450.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
10-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 14466313 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(C5)O)(C)C)C)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
2,4a,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-2-carbaldehyde 14108937 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C=O)C)C)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
24-Nor-D:A-friedooleana-1(10),5,7-tetraen-29-oic acid, 3-hydroxy-2-oxo-, methyl ester 264268 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
29-Hydroxyfriedelan-3-one 14108943 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(96)00886-2
6a-(hydroxymethyl)-4,4a,6b,8a,11,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 73817657 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)CO)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1021/NP50104A012
https://doi.org/10.1016/0031-9422(96)00886-2
Celastrol 122724 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)O 450.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
D:A-Friedooleanan-3-one, 29-hydroxy-, (20alpha)- 588284 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(96)00886-2
https://doi.org/10.1016/0031-9422(90)89066-I
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
Kotalagenin 16-acetate 10601920 Click to see CC1C(=O)CC(=O)C2C1(CCC3C2(CCC4(C3(CC(C5(C4CC(CC5)(C)C)C)OC(=O)C)CO)C)C)C 514.70 unknown https://doi.org/10.1093/JN/132.7.1819
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(83)83027-1
methyl (2R,4aS,6aR,6aS,14aS,14bR)-10-hydroxy-2-(hydroxymethyl)-4a,6a,6a,9,14a-pentamethyl-11-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylate 10552750 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(CO)C(=O)OC)C)C)C)C)O 480.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
Methyl 10-hydroxy-2-(hydroxymethyl)-4a,6a,6a,9,14a-pentamethyl-11-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylate 85182479 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(CO)C(=O)OC)C)C)C)C)O 480.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(96)00886-2
Polpunonic acid 343427 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)C 456.70 unknown https://doi.org/10.1016/0031-9422(90)89066-I
Pristimerin 159516 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown https://doi.org/10.1016/0031-9422(90)89066-I
https://doi.org/10.1016/0031-9422(96)00886-2
https://doi.org/10.1016/S0031-9422(00)83123-4
Triptotriterpenic acid A 21594203 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5O)(C)C(=O)O)C)C)C)C 472.70 unknown https://doi.org/10.1093/JN/132.7.1819
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids
Methyl 10-hydroxy-2,4a,6,9,12b,14a-hexamethyl-11-oxo-1,2,3,4,4a,5,11,12b,13,14,14a,14b-dodecahydropicene-2-carboxylate 188842 Click to see CC1=C2C3=CC=C4C(=C(C(=O)C=C4C3(CCC2(C5CC(CCC5(C1)C)(C)C(=O)OC)C)C)O)C 462.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
Netzahualcoyene 21636463 Click to see CC1=C2C3=CC=C4C(=C(C(=O)C=C4C3(CCC2(C5CC(CCC5(C1)C)(C)C(=O)OC)C)C)O)C 462.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/0031-9422(96)00886-2
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/10.1016/0031-9422(96)00886-2
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/10.1016/0031-9422(96)00886-2
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
3,9-Dihydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione 500289 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(C(C1=O)O)C 436.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
Tingenin B 73147 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(C(C1=O)O)C 436.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0968-0896(01)00422-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose 5984 Click to see C(C(C(C(C(=O)CO)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0968-0896(01)00422-9
D-Fructose 2723872 Click to see C1C(C(C(C(O1)(CO)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0968-0896(01)00422-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0968-0896(01)00422-9
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0968-0896(01)00422-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol 11850 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1016/S0968-0896(01)00422-9
Glycerin 753 Click to see C(C(CO)O)O 92.09 unknown https://doi.org/10.1016/S0968-0896(01)00422-9
Hexitol 453 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1016/S0968-0896(01)00422-9
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
Pentadeca-5,7,13-trien-9,11-diyn-4-one 86132489 Click to see CCCC(=O)C=CC=CC#CC#CC=CC 212.29 unknown https://doi.org/10.1093/JN/132.7.1819
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(6aR,6bR,8aS,11R,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione 441687 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
(6aS,6bS,8aS,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-8,9,12,12a,13,14-hexahydro-7H-picen-2-one 46881919 Click to see CC1=CCC2(CCC3(C4=CC=C5C(=C(C(=O)C=C5C4(CCC3(C2C1)C)C)O)C)C)C 404.60 unknown https://doi.org/10.1016/S0031-9422(00)83123-4
24,25,26,30-Tetranoroleana-1(10),3,5,7,20(29)-pentaen-2-one,3-hydroxy-9,13-dimethyl-, (9beta,13alpha,14beta)- 328559 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(=C)CC5)C)C)C)C)O 404.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
3-hydroxy-11-(hydroxymethyl)-4,6a,6b,8a,14a-pentamethyl-8,9,10,11,12,12a,13,14-octahydro-7H-picen-2-one 72962773 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)CO)C)C)C)C)O 422.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
3-Hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione 3527193 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
3-Hydroxy-4,6a,6b,8a,14a-pentamethyl-11-methylidene-7,8,9,10,12,12a,13,14-octahydropicen-2-one 157614 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(=C)CC5)C)C)C)C)O 404.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
3-Hydroxy-4,6b,8a,11,12b,14a-hexamethyl-7,8,8a,9,12,12a,12b,13,14,14a-decahydropicen-2(6bh)-one 162727 Click to see CC1=CCC2(CCC3(C4=CC=C5C(=C(C(=O)C=C5C4(CCC3(C2C1)C)C)O)C)C)C 404.60 unknown https://doi.org/10.1016/S0031-9422(00)83123-4
Isoiguesterin 11373102 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(=C)CC5)C)C)C)C)O 404.60 unknown https://doi.org/10.1021/NP50104A012
https://doi.org/10.1016/0031-9422(96)00886-2
https://doi.org/10.1080/10575639308043876
Isoiguesterol 10477355 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)CO)C)C)C)C)O 422.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
Tingenone 101520 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(6aR,6aS,6bR,8aR,12aR,14aR)-3-hydroxy-4,6a,6b,8a,14a-pentamethyl-11-methylidene-7,8,9,10,12,12a,13,14-octahydro-6aH-picene-2,6-dione 162877038 Click to see CC1=C(C(=O)C=C2C1=CC(=O)C3C2(CCC4(C3(CCC5(C4CC(=C)CC5)C)C)C)C)O 420.60 unknown https://doi.org/10.1016/0031-9422(96)00886-2
3-hydroxy-4,6a,6b,8a,14a-pentamethyl-11-methylidene-7,8,9,10,12,12a,13,14-octahydro-6aH-picene-2,6-dione 162877037 Click to see CC1=C(C(=O)C=C2C1=CC(=O)C3C2(CCC4(C3(CCC5(C4CC(=C)CC5)C)C)C)C)O 420.60 unknown https://doi.org/10.1021/NP50104A012
https://doi.org/10.1016/0031-9422(96)00886-2
https://doi.org/10.1080/10575639308043876
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown https://doi.org/10.1093/JN/132.7.1819
https://doi.org/10.1016/0378-8741(85)90010-8
https://doi.org/10.1248/YAKUSHI.121.371
https://doi.org/10.1248/BPB.25.72
> Organosulfur compounds / Sulfoxides
(1S,3R,4S,5R,6S,8R,10S,11R,12R)-1-oxo-1lambda4-thiacyclotridecane-3,4,5,6,8,10,11,12-octol 162891377 Click to see C1C(CC(C(C(C(CS(=O)CC(C(C1O)O)O)O)O)O)O)O 344.38 unknown https://doi.org/10.1021/NP070604H
1-Oxo-1lambda4-thiacyclotridecane-3,4,5,6,8,10,11,12-octol 24808560 Click to see C1C(CC(C(C(C(CS(=O)CC(C(C1O)O)O)O)O)O)O)O 344.38 unknown https://doi.org/10.1021/NP070604H
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1248/YAKUSHI.121.371
https://doi.org/10.1248/BPB.25.72
https://doi.org/10.1093/JN/132.7.1819
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1093/JN/132.7.1819
https://doi.org/10.1248/BPB.25.72
https://doi.org/10.1248/YAKUSHI.121.371

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