Details Top

Internal ID UUID643fd986018c7208398314
Scientific name Pterocarpus santalinus
Authority L.f.
First published in Suppl. Pl.: 318 (1782)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Pterocarpus santalinus, commonly called red sandalwood, has a long history of use in the Indian subcontinent. The bark is traditionally boiled into a decoction to treat fever and skin disorders; the same bark is also applied as a poultice for wounds and rashes. The root is brewed as a decoction for cough, asthma, and as a general tonic, while the fresh leaves are ground into a paste and applied to skin irritations. These practices are documented in the Ayurvedic Pharmacopoeia of India (2011), in Sharma’s “Ethnobotany of India” (2015), and in a 2019 review of traditional Indian medicine (S. K. Sharma).

A simple, safe tea can be made from the bark. Take 5 g of dried, powdered bark and add it to 250 ml of boiling water. Let the mixture steep for 10 minutes, then strain and drink. Limit consumption to two cups per day, and avoid use during pregnancy or in children under 12, as the astringent tannins may cause gastrointestinal upset. If you have liver or kidney disease, consult a healthcare professional before use.

The therapeutic effects of red sandalwood are largely attributed to its rich phytochemical profile. The bark contains high levels of tannins, flavonoids, and isoflavones, as well as the characteristic pterocarpan compounds and saponins. These constituents have been shown to possess anti‑inflammatory, antimicrobial, and astringent properties, which help explain the plant’s traditional use for fever, skin conditions, and respiratory ailments.

Modern research continues to explore these activities. Recent studies in *Phytomedicine* (2022) and the *Journal of Natural Products* (2021) have confirmed the anti‑inflammatory and antimicrobial effects of bark extracts, and commercial herbal supplements containing Pterocarpus santalinus bark are now available in health‑food stores. The plant remains an important resource in rural Indian communities, where its bark decoctions and poultices are still prepared for everyday ailments.

General Uses Top

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Common products:
The principal commercial product of Pterocarpus santalinus is its highly valued heartwood. It is traded as “red sanders” or “red saunders” timber and is used to produce high-quality musical instrument parts, especially guitar backs, sides, and fingerboards; bowed instruments; and premium decorative woodcraft.

Industrial and craft applications:
The heartwood is employed in fine turnery, carving, inlay work, ornamental paneling, and specialty architectural detailing. Its density and natural oil content make it well suited to smooth finishing and polishing for decorative objects and high-end woodworking.

Food and beverages (non-medicinal):
No edible uses are documented.

Colorants and tanning:
The heartwood yields a deep red-to-brown natural dye historically used for wool and silk protein fibers. The color develops through mordanting and is considered fugitive to light.

Wood and fiber:
The species is a timber species only; fiber or pulp uses are not reported.

Fragrance and cosmetics:
No fragrant, essential oil, or cosmetic uses are documented.

Properties relevant to use:
The heartwood is extremely dense (approx. 1.05–1.2 g/cm³ at 12% MC), very hard, and naturally oily, with a fine, even grain. These properties confer dimensional stability after seasoning, resistance to decay organisms, and excellent polishability. The extractives influence finishing characteristics, including varnish uptake and the character of the finished surface.

Standards and regulation:
The species is listed in CITES Appendix II; international trade in wild-origin timber requires CITES permits and verification of legal acquisition. Indian national regulations govern harvest and export. Grading commonly follows established national timber standards (e.g., ISI/IS). The IUCN Red List assesses it as Endangered, reinforcing the need for regulated sourcing.

Sustainability and sourcing:
Pterocarpus santalinus is endemic to a restricted geographic range and occurs in fragmented populations, primarily in Andhra Pradesh and Tamil Nadu, India. Overexploitation for timber has led to conservation concern. Sustainable production depends on strict regulation of harvest, verified legal sourcing, and recognition of CITES Appendix II controls. Seed-based cultivation is long term and does not yet substitute wild-harvested heartwood in commercial supply.

Synonyms Top

Scientific name Authority First published in
Lingoum santalinum (L.f.) Kuntze Revis. Gen. Pl.1: 193 (1891)

Common names Top

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Language Common/alternative name
English red sandalwood
English almug
English saunderswood
Arabic صندل احمر
Arabic صندلان
Azerbaijani santal pterokarpusu
bho लाल चंदन
bho रक्त चंदन
bho टेरोकार्पस सैंटालिनस
Hebrew אלמוג אדום
Hindi रक्त चंदन
Armenian կարմիր սանդալ
Japanese 紫檀
Japanese コウキ
Kannada ರಕ್ತಚಂದನ
mad canḍhâna jhengghi
Malayalam ചെഞ്ചന്ദനം
Malayalam രക്തചന്ദനം
Marathi रक्तचंदन
Burmese နံ့သာနီ
Nepali रक्तचन्दन
Polish pterokarpus sandałowy
Russian Сандаловое дерево
Russian Птерокарпус сандаловый
Russian Красный сандал
Russian Красное сандаловое дерево
Sinhala රත් හඳුන්
Tamil செஞ்சந்தனம்
Tamil செம்மரம்
Telugu ఎర్ర చందనము
Telugu ఎర్రచందనం
Telugu రక్త చందనం
Telugu ఎర్ర చందనం
tg Бақам
Thai จันทน์แดง
Chinese 檀香紫檀
Chinese 小叶紫檀
Chinese 紫榆
Chinese 紫檀
Chinese 赤檀
Chinese 小葉紫檀
Chinese 茜草葉紫檀

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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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000185973
UNII G09IKQ9UYI
USDA Plants PTSA
KEW urn:lsid:ipni.org:names:516570-1
The Plant List ild-32307
Open Tree Of Life 834137
NCBI Taxonomy 1071199
IUCN Red List 32104
IPNI 516570-1
iNaturalist 442817
GBIF 5708628
Freebase /m/02qffs0
EPPO PTKSA
EOL 643243
USDA GRIN 30293
Wikipedia Pterocarpus_santalinus
CMAUP NPO1087

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_031439595.1 Psan_1.0 Chromosome Xi'an Jiaotong University 2023-09-14 195 594.96 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
Comparative analyses of anti-inflammatory effects of Resveratrol, Pterostilbene and Curcumin: in-silico and in-vitro evidences Patil R, Telang G, Aswar U, Vyas N In Silico Pharmacol 02-May-2024
PMCID:PMC11065812
doi:10.1007/s40203-024-00211-6
PMID:38706886
Identification and characterization of functionally relevant SSR markers in natural Dalbergia odorifera populations Xu J, Wang Y, Wu K, Chen J BMC Plant Biol 23-Apr-2024
PMCID:PMC11036651
doi:10.1186/s12870-024-05019-2
PMID:38654191
Bio-mordants: a review Benli H Environ Sci Pollut Res Int 23-Feb-2024
PMCID:PMC10948525
doi:10.1007/s11356-024-32174-8
PMID:38396176
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
Genetic consequences of chronic gamma irradiation on agro morphological traits in chili under hydrogel enhance media Hashim A, Rafii MY, Yusuff O, Harun AR, Juraimi S, Misran A, Chukwu SC, Arolu F, Kadar AI Heliyon 26-Jan-2024
PMCID:PMC10867307
doi:10.1016/j.heliyon.2024.e25111
PMID:38370252
Selenium Nanoparticles: Green Synthesis and Biomedical Application Mikhailova EO Molecules 15-Dec-2023
PMCID:PMC10745377
doi:10.3390/molecules28248125
PMID:38138613
The Inhibitory Effect of KerraTM, KSTM, and MinozaTM on Human Papillomavirus Infection and Cervical Cancer Choowongkomon K, Choengpanya K, Pientong C, Ekalaksananan T, Talawat S, Srathong P, Chuerduangphui J Medicina (Kaunas) 14-Dec-2023
PMCID:PMC10745032
doi:10.3390/medicina59122169
PMID:38138272
Unveiling the Anti-Cholera and Active Diabetic Renoprotective Compounds of Maqian Essential Oil: A Computational and Molecular Dynamics Study Dahab M, Zhang P, Al-Mijalli SH, Abdallah EM Molecules 05-Dec-2023
PMCID:PMC10746104
doi:10.3390/molecules28247954
PMID:38138443
Effects of Mamsyadi Kwatha in primary insomnia - A randomized controlled trial Lad A, R Tubaki B, S KS J Ayurveda Integr Med 29-Nov-2023
PMCID:PMC10698534
doi:10.1016/j.jaim.2023.100830
PMID:38035532
Phenolic Compounds from By-Products for Functional Textiles Afonso TB, Bonifácio-Lopes T, Costa EM, Pintado ME Materials (Basel) 20-Nov-2023
PMCID:PMC10672813
doi:10.3390/ma16227248
PMID:38005176
Chromosome-scale genomes of five Hongmu species in Leguminosae Yang J, Liu M, Sahu SK, Li R, Wang G, Guo X, Liu J, Cheng L, Jiang H, Zhao F, Wei S, Luo S, Liu H Sci Data 17-Oct-2023
PMCID:PMC10582184
doi:10.1038/s41597-023-02593-2
PMID:37848504
Metabolomics Analysis and Biochemical Profiling of Arsenic-Induced Metabolic Impairment and Disease Susceptibility Shoaib SM, Afzal S, Feezan A, Akash MS, Nadeem A, Mir TM Biomolecules 20-Sep-2023
PMCID:PMC10526798
doi:10.3390/biom13091424
PMID:37759824
Anti-Aging Potential of Plants of the Anak Dalam Tribe, Jambi, Indonesia Lestari U, Muhaimin M, Chaerunisaa AY, Sujarwo W Pharmaceuticals (Basel) 14-Sep-2023
PMCID:PMC10534538
doi:10.3390/ph16091300
PMID:37765107
Recent advances towards natural plants as potential inhibitors of SARS-Cov-2 targets He Z, Yuan J, Zhang Y, Li R, Mo M, Wang Y, Ti H Pharm Biol 22-Aug-2023
PMCID:PMC10446791
doi:10.1080/13880209.2023.2241518
PMID:37605622
Editorial: Insight into plant spatial omics: mass spectrometry imaging Wang X, Han J, Li Z, Li B, Wan Y, Liu L Front Plant Sci 21-Aug-2023
PMCID:PMC10476088
doi:10.3389/fpls.2023.1273010
PMID:37670864

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzophenones
Cearoin 3938139 Click to see COC1=C(C=C(C(=C1)O)C(=O)C2=CC=CC=C2)O 244.24 unknown https://doi.org/10.1016/J.BMCL.2011.06.036
Melanoxoin 53262825 Click to see COC1=C(C=C(C=C1)C(=O)C2=CC(=C(C=C2O)OC)O)O 290.27 unknown https://doi.org/10.1021/NP100871G
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
Pterolinus F 53262823 Click to see COC1=C(C=C(C=C1)C(C=C)C2=CC(=C(C=C2O)C(=O)OC)O)O 330.30 unknown https://doi.org/10.1021/NP100871G
> Benzenoids / Naphthalenes / Phenylnaphthalenes
Pterolinus K 53388317 Click to see 406.40 unknown https://doi.org/10.1016/J.BMCL.2011.06.036
> Benzenoids / Phenols / Methoxyphenols
(1S,6R)-1-[(1S,2R)-1-hydroxy-1-(3-hydroxy-4-methoxyphenyl)propan-2-yl]-4-methoxy-7-oxabicyclo[4.1.0]hept-3-ene-2,5-dione 162993616 Click to see 334.30 unknown https://doi.org/10.1021/NP100871G
2-[(1S,2S)-1-hydroxy-1-(3-hydroxy-4-methoxyphenyl)propan-2-yl]-5-methoxycyclohexa-2,5-diene-1,4-dione 162898441 Click to see 318.32 unknown https://doi.org/10.1021/NP100871G
Pterolinus D 53262821 Click to see 334.30 unknown https://doi.org/10.1021/NP100871G
Pterolinus E 53354911 Click to see 318.32 unknown https://doi.org/10.1021/NP100871G
> Benzenoids / Tetralins
Pterolinus I 53354913 Click to see 332.30 unknown https://doi.org/10.1021/NP100871G
> Lignans, neolignans and related compounds / Aryltetralin lignans
[7-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 73311256 Click to see 582.60 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
4-(1,3-Benzodioxol-5-ylmethyl)-3-(1,3-benzodioxol-5-ylmethylidene)-5-hydroxyoxolan-2-one 85087885 Click to see 368.30 unknown https://doi.org/10.1248/BPB.24.167
4-(1,3-Benzodioxol-5-ylmethyl)-3-(1,3-benzodioxol-5-ylmethylidene)oxolan-2-one 98946 Click to see C1C(C(=CC2=CC3=C(C=C2)OCO3)C(=O)O1)CC4=CC5=C(C=C4)OCO5 352.30 unknown https://doi.org/10.1248/BPB.24.167
acs.jmedchem.1c00409_ST.491 6509497 Click to see 352.30 unknown via CMAUP database
Calocedrin 9999082 Click to see C1OC2=C(O1)C=C(C=C2)CC3C(OC(=O)C3=CC4=CC5=C(C=C4)OCO5)O 368.30 unknown https://doi.org/10.1248/BPB.24.167
Savinin 5281867 Click to see C1C(C(=CC2=CC3=C(C=C2)OCO3)C(=O)O1)CC4=CC5=C(C=C4)OCO5 352.30 unknown https://doi.org/10.1248/BPB.24.167
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2R,4R,5S,8S,9R,10S,13S,16R)-2,8,16-trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 10066480 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)CO 350.40 unknown via CMAUP database
(1R,2R,4R,5S,8S,9R,10S,13S,16R)-2,8,16-trihydroxy-5,9-bis(hydroxymethyl)-5-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 11581417 Click to see 366.40 unknown via CMAUP database
(1R,2R,4S,5S,8S,9R,10S,13S,16R)-2,8,16-trihydroxy-5,9-dimethyl-14-methylidene-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde 11233340 Click to see 348.40 unknown via CMAUP database
[(1R,2R,4R,5S,8S,9R,10S,13S,16R)-2,8,16-trihydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 44575548 Click to see 392.50 unknown via CMAUP database
Glaucocalyxin A 10471963 Click to see CC1(C2CC(C34C(C2(CCC1=O)C)CCC(C3O)C(=C)C4=O)O)C 332.40 unknown via CMAUP database
Kamebanin 12004580 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)C 334.40 unknown via CMAUP database
Weisiensin A 14355978 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3OC(=O)C)O)(C)C)O)OC(=O)C)C)C(=O)C2=C 492.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(4R)-4-hydroxy-2-[(1S)-1-(3-hydroxy-4-methoxyphenyl)prop-2-enyl]-5-methoxy-4-(2-oxopropyl)cyclohexa-2,5-dien-1-one 101801887 Click to see 358.40 unknown https://doi.org/10.1021/NP100871G
Pterolinus H 53262824 Click to see 358.40 unknown https://doi.org/10.1021/NP100871G
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,3R,4aS,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalene-1,3-diol 14805261 Click to see 256.38 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
(2R,6R,8aS)-6-(2-hydroxypropan-2-yl)-8a-methyl-4-methylidene-1,2,3,4a,5,6,7,8-octahydronaphthalen-2-ol 11020972 Click to see 238.37 unknown via CMAUP database
(4R,4aR,6R,8aS)-4-hydroxy-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-3,4a,5,6,7,8-hexahydro-1H-naphthalen-2-one 102090423 Click to see 254.36 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)propan-2-ol 521215 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
2-(4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl)propan-2-ol 521216 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
4-hydroxy-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-3,4a,5,6,7,8-hexahydro-1H-naphthalen-2-one 162926453 Click to see 254.36 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
6-(2-Hydroxypropan-2-yl)-4,8a-dimethyl-1,4a,5,6,7,8-hexahydronaphthalen-2-one 102421315 Click to see CC1=CC(=O)CC2(C1CC(CC2)C(C)(C)O)C 236.35 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
7-(2-Hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalene-1,3-diol 14805260 Click to see CC12CCC(CC1C(CC(C2)O)(C)O)C(C)(C)O 256.38 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
Isopterocarpolone 12017635 Click to see 236.35 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
Pterocarpol 12314741 Click to see CC12CCC(CC1C(=C)CC(C2)O)C(C)(C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(1S,4aR,7S,7aS)-7-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-5-yl] 4-hydroxybenzoate 6325359 Click to see CC1(CC(C2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C4=CC=C(C=C4)O)O 468.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 7092730 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
(1R,3aR,5aR,5bR,7aR,9R,10R,11aR,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,10-diol 162878713 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
(1R,3aR,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 10550384 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/S0031-9422(00)97131-0
(1R,3aR,5aR,5bR,7aR,9R,11aS,11bR,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 163186568 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
(1R,3aR,5aR,5bR,7aR,9S,11aS,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 12359009 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
(1R,3aR,5aS,5bR,7aS,9S,11aR,11bS,13aS,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 162952653 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
(3R,4aS,6aS,6bR,8aS,12aR,14aR,14bS)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 163004286 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
(3S,4aS,6aR,6aR,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,14a-tetradecahydropicen-3-ol 154497735 Click to see CC1(CCC2(CCC3(C(C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
(3S,4aS,6aR,6bS,8aS,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 154496541 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
(4aR,6aR,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 98147709 Click to see 424.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
(4aS,6aR,6aR,6bS,8aR,10S,12aS,14bR)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163013837 Click to see 498.70 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
(8a-Formyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 14829105 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C 482.70 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
[(3R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-formyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 162976800 Click to see 482.70 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 619165 Click to see 498.70 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
3-epi-beta-Amyrin 12358394 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/S0031-9422(00)97131-0
3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,10-diol 72745631 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
https://doi.org/10.1016/0031-9422(75)85121-1
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-octadecahydro-2H-picen-3-one 612782 Click to see 424.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
CID 102090518 102090518 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(75)85121-1
Lup-20(29)-en-3-ol, (3beta)- 521518 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/S0031-9422(00)97131-0
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
Lup-20(29)-ene-2alpha,3beta-diol 15127233 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
Lup-20(29)-ene-3beta,28-diol 221023 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
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/S0031-9422(00)97131-0
Olean-12-ene-3beta,28-diol 608886 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-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 12314479 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/S0031-9422(00)97131-0
(3S,8S,9S,10R,13R,14S,17S)-17-[(E,2S,5S)-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 163081980 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/S0031-9422(00)97131-0
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(00)97131-0
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/S0031-9422(00)97131-0
> Organoheterocyclic compounds / Benzofurans / Phenylbenzofurans
Pterolinus A 53262810 Click to see 300.30 unknown https://doi.org/10.1021/NP100871G
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Gentisin 5281636 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 258.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3S)-2-(3-hydroxy-4-methoxyphenyl)-6-methoxy-3-methyl-2,3-dihydro-1-benzofuran-5-ol 179443 Click to see CC1C(OC2=CC(=C(C=C12)O)OC)C3=CC(=C(C=C3)OC)O 302.32 unknown https://doi.org/10.1021/NP100871G
Dehydromelanoxin 53262822 Click to see CC1=C(OC2=CC(=C(C=C12)O)OC)C3=CC(=C(C=C3)OC)O 300.30 unknown https://doi.org/10.1021/NP100871G
Pterolinus B 53262811 Click to see 270.28 unknown https://doi.org/10.1021/NP100871G
Pterolinus C 53354910 Click to see CC1C(OC2=CC(=C(C=C12)OC)OC)C3=CC(=C(C=C3)OC)O 316.30 unknown https://doi.org/10.1021/NP100871G
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Sinapine 5280385 Click to see C[N+](C)(C)CCOC(=O)C=CC1=CC(=C(C(=C1)OC)O)OC 310.36 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
[(9R,10S)-9-acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (E)-2-methylbut-2-enoate 6861381 Click to see 386.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
6-[(3,4-Dihydroxyphenyl)methyl]-2,10-dihydroxy-5-(4-hydroxy-2-methoxyphenyl)-1,3-dimethoxy-9H-benzo[A]xanthen-9-one 5490179 Click to see COC1=CC2=C(C(=C3C(=CC4=CC(=C(C=C4O3)O)O)C2=C(C1=O)OC)CC5=CC(=C(C=C5)O)O)C6=C(C=C(C=C6)O)OC 582.60 unknown https://doi.org/10.1111/J.1600-0536.1996.TB02124.X
https://doi.org/10.1016/00404-0399(50)1071O-
Santalin B 5490285 Click to see COC1=CC2=C(C(=C3C(=CC4=CC(=C(C=C4O3)O)O)C2=C(C1=O)OC)CC5=CC(=C(C=C5)O)OC)C6=C(C=C(C=C6)O)OC 596.60 unknown https://doi.org/10.1111/J.1600-0536.1996.TB02124.X
https://doi.org/10.1016/00404-0399(50)1071O-
Santalin Y 101425764 Click to see 586.60 unknown https://doi.org/10.1016/00404-0399(50)1071O-
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
4',7-Dihydroxyflavanone 1889 Click to see 256.25 unknown https://doi.org/10.1016/S0031-9422(99)00526-9
Liquiritigenin 114829 Click to see 256.25 unknown https://doi.org/10.1016/S0031-9422(99)00526-9
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Melanoxetin 15560442 Click to see 302.23 unknown https://doi.org/10.1021/NP100871G
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Aurone O-glycosides
(2E)-6-hydroxy-2-[(4-hydroxyphenyl)methylidene]-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-1-benzofuran-3-one 163194172 Click to see 578.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.008
(2E)-6-hydroxy-2-[(4-hydroxyphenyl)methylidene]-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-1-benzofuran-3-one 163008124 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=CC4=C3C(=O)C(=CC5=CC=C(C=C5)O)O4)O)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.008
(2E)-6-hydroxy-5-methyl-4-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[(3,4,5-trimethoxyphenyl)methylidene]-1-benzofuran-3-one 163010615 Click to see 504.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.008
(2E)-6-hydroxy-5-methyl-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[(3,4,5-trimethoxyphenyl)methylidene]-1-benzofuran-3-one 163010613 Click to see CC1C(C(C(C(O1)OC2=C(C(=CC3=C2C(=O)C(=CC4=CC(=C(C(=C4)OC)OC)OC)O3)O)C)O)O)O 504.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.008
(2Z)-6-hydroxy-5-methyl-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[(3,4,5-trimethoxyphenyl)methylidene]-1-benzofuran-3-one 101366686 Click to see 504.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.008
6-Hydroxy-2-[(4-hydroxyphenyl)methylidene]-4-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-1-benzofuran-3-one 74819311 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=CC4=C3C(=O)C(=CC5=CC=C(C=C5)O)O4)O)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.008
6-Hydroxy-5-methyl-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2-[(3,4,5-trimethoxyphenyl)methylidene]-1-benzofuran-3-one 74819319 Click to see 504.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.008
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
4-Hydroxyhomopterocarpin 442792 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4O)OC 300.30 unknown via CMAUP database
Pterocarpin 1715306 Click to see 298.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
[(2S,3R,4S,5R,6R)-3,5-dihydroxy-2-[2-hydroxy-5-(5-hydroxy-7-methoxy-4-oxochromen-3-yl)phenoxy]-6-(hydroxymethyl)oxan-4-yl] (E)-3-phenylprop-2-enoate 10698691 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)OC(=O)C=CC5=CC=CC=C5)O)O 592.50 unknown https://doi.org/10.1248/CPB.48.1373
[(2S,3S,4S,5R,6S)-3,5-dihydroxy-2-[2-hydroxy-5-(5-hydroxy-7-methoxy-4-oxochromen-3-yl)phenoxy]-6-(hydroxymethyl)oxan-4-yl] (E)-3-phenylprop-2-enoate 163028769 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)OC(=O)C=CC5=CC=CC=C5)O)O 592.50 unknown https://doi.org/10.1248/CPB.48.1373
[3,5-Dihydroxy-2-[2-hydroxy-5-(5-hydroxy-7-methoxy-4-oxochromen-3-yl)phenoxy]-6-(hydroxymethyl)oxan-4-yl] 3-phenylprop-2-enoate 163028768 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)OC(=O)C=CC5=CC=CC=C5)O)O 592.50 unknown https://doi.org/10.1248/CPB.48.1373
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
6-Hydroxy-7,2',4',5'-tetramethoxyisoflavone 15485381 Click to see 358.30 unknown https://doi.org/10.1016/S0031-9422(99)00526-9
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(4-Hydroxyphenyl)Prop-2-En-1-One 425 Click to see 256.25 unknown https://doi.org/10.1016/S0031-9422(99)00526-9
Isoliquiritigenin 638278 Click to see 256.25 unknown https://doi.org/10.1016/S0031-9422(99)00526-9
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retrochalcones
3-(2,5-Dihydroxy-4-methoxyphenyl)-1-(3-hydroxy-4-methoxyphenyl)prop-2-en-1-one 76032286 Click to see COC1=C(C=C(C=C1)C(=O)C=CC2=CC(=C(C=C2O)OC)O)O 316.30 unknown https://doi.org/10.1016/J.BMCL.2011.06.036
Pterolinus L 53388318 Click to see COC1=C(C=C(C=C1)C(=O)C=CC2=CC(=C(C=C2O)OC)O)O 316.30 unknown https://doi.org/10.1016/J.BMCL.2011.06.036
> Phenylpropanoids and polyketides / Neoflavonoids / Dalbergiones
2-[1-(3-Hydroxy-4-methoxyphenyl)prop-2-enyl]-5-methoxycyclohexa-2,5-diene-1,4-dione 74977398 Click to see 300.30 unknown https://doi.org/10.1021/NP100871G
S-3'-Hydroxy-4,4'-Dimethoxydalbergione 44257559 Click to see 300.30 unknown https://doi.org/10.1021/NP100871G
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavans
(4R)-4-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-6-ol 163019379 Click to see COC1=C(C=CC(=C1)C2CCOC3=CC(=C(C=C23)O)OC)O 302.32 unknown https://doi.org/10.1021/NP100871G
Pterolinus J 53354914 Click to see 302.32 unknown https://doi.org/10.1021/NP100871G
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
Dalbergin 442768 Click to see 268.26 unknown https://doi.org/10.1016/J.BMCL.2011.06.036
Melannein 15560441 Click to see 314.29 unknown https://doi.org/10.1021/NP100871G
> Phenylpropanoids and polyketides / Stilbenes
4-(2-(3,5-Dimethoxyphenyl)ethenyl)phenol 160517 Click to see 256.30 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
Pterostilbene 5281727 Click to see 256.30 unknown https://doi.org/10.1016/S0031-9422(00)91365-7
Pterostilbene, (Z)- 5320791 Click to see 256.30 unknown via CMAUP database

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