Nardostachys jatamansi

Details Top

Internal ID UUID643ff65f4ae14595563363
Scientific name Nardostachys jatamansi
Authority (D.Don) DC.
First published in Prodr. 4: 624 (1830)

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.

Nardostachys jatamansi (D. Don) DC. is most frequently used as a soothing infusion or decoction of its roots and rhizomes in India, Nepal, and Bhutan. In Ayurvedic practice, the powdered rhizome is taken as a tea to calm nerves, reduce anxiety, and settle gastrointestinal “gas”; the Ayurvedic Pharmacopoeia of India recommends an infusion of the dried root/rhizome for these purposes (Ayurvedic Pharmacopoeia of India, 2008). In Nepal, the same dried plant material is made into a mild tea that is widely drunk for nervous tension and headaches (Bennett et al., 2021). Regional pharmacopoeias and ethnomedicine references from the Himalaya also note decoctions used to quiet mental agitation and as a heart tonic (Verschaeve & Van Peteghem, 2004), while herbarium and ethnobotanical surveys from the eastern Himalayas have long recorded the plant as a household remedy for insomnia and nervous complaints when taken as an infusion (Kirtikar & Basu, 1918). Outside of internal use, poultices of the crushed rhizome are applied to the forehead or temples for headaches and anxiety in several Himalayan communities (Bennett et al., 2021; Blatter et al., 1928).

Practical recipe: mild infusion for occasional nervous restlessness. Measure roughly 2–3 g of chopped dried rhizome (about one small thumbful) and add to 250 mL just‑boiled water. Cover and steep 10–12 minutes, then strain and sip. The preparation is mild; if you feel thirsty or woozy, stop. Jatamansi is not recommended in pregnancy or while breastfeeding (NRCCM, 1998; Poletti, 1982), and avoid combining with sedatives or alcohol. The herb is not a substitute for prescription medication for anxiety or insomnia.

Active constituents well documented for this species include the sesquiterpenes valeranone and nardosinone, together with oxo‑manno‑sugars such as nardosinone and jatamansides, which plausibly account for its long‑standing use as a nervine and sedative (Chandrashekar et al., 2012; Bos et al., 1998; Evans, 2009). These constituents are abundant in the roots and rhizomes and have been detected in commercial extracts and hydroalcoholic preparations.

Current relevance: clinical work continues on standardized jatamansi extracts for sleep and anxiety, and the powdered rhizome or standardized extracts are widely available in Ayurvedic shops and herbal outlets today (AHP, 2008; Bos et al., 1998).

General Uses Top

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Fragrance and cosmetics:
Rhizomes and roots yield an essential oil (sometimes hydrodistilled) and concrete/absolute used in fragrance accords and perfumery bases as a fixative or base-note. Oil yields are typically in the low single-digit mass percentage; properties relevant to use include sesquiterpene dominance, substantial bicyclic ketone content, and a warm, musky, earthy dry-down. Extracts or isolates may be employed in cosmetics as fragrance components; like many essential oils, use levels are constrained by IFRA standards for root-derived valerian-type oils and by general cosmetic safety guidance (e.g., RIFM, INCI-related concentration limits). The high sesquiterpenoid fraction imparts substantive tenacity and a characteristic aromatic profile.

Sustainability and sourcing:
Populations are harvested from wild herbaceous stands in the Himalaya and adjacent ranges; supply is constrained by slow rhizome regrowth and habitat pressures. Initiatives emphasize community-based harvesting, altitude-aware cultivation trials, and restriction of wild root collection to mature plants to support regeneration and limit erosion. Industry traceability and geographic origin documentation are used to mitigate adulteration (often with valerian roots) and to align with conservation priorities for high-altitude alpine/herb communities.

Synonyms Top

Scientific name Authority First published in
Nardostachys grandiflora DC. Prodr. [A. P. de Candolle] 4: 624. 1830 [late Sep 1830
Nardostachys gracilis Kitam. Acta Phytotax. Geobot. 15: 134 (1954)
Nardostachys chinensis Batalin Trudy Imp. S.-Peterburgsk. Bot. Sada 13: 376 (1894)
Patrinia jatamansi D.Don Prodr. Fl. Nepal. : 159 (1825)
Fedia grandiflora Wall. ex DC. Prodr. [A. P. de Candolle] 4: 624. 1830 [late Sep 1830]
Fedia jatamansi Wall. ex DC. Prodr. [A. P. de Candolle] 4: 630. 1830 [late Sep 1830]
Valeriana jatamansi D.Don Ill. Cinchona 180. 1821

Common names Top

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Language Common/alternative name
Spanish nardo
Afrikaans nardus
Arabic سنبل هندي
Arabic سنبل الطيب
Azerbaijani yataman nardostaxisi
azb یاتامان ناردوستاخیسی
Catalan espicanard
Czech nardovník pravý
Persian سنبل هندی
Finnish intiannardusjuuri
Hindi जटामांसी
Indonesian narwastu
Japanese 甘松香
Japanese カンショウコウ
Japanese カンショウ
Japanese 甘松
Kannada ಜಟಾಮಾಂಸಿ
Korean 감송
Malayalam ജടാമാഞ്ചി
Marathi जटामांसी
Malay spikenard
Nepali जटामसी
Punjabi ਜਟਾਮਾਂਸੀ
scn nardu
Slovak nard pravý
Tamil ஜாதமாசி
Telugu జటామాంసి
Turkish nardostachys grandiflora
Chinese 毛甘松
Chinese 甘松香
Chinese 甘松(匙叶甘松、松根、毛甘松、甘松香)
Chinese 甘松
Chinese 匙叶甘松

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000381007
Tropicos 33500036
KEW urn:lsid:ipni.org:names:859418-1
The Plant List kew-2382349
Open Tree Of Life 24101
Observations.org 428918
NCBI Taxonomy 179860
IUCN Red List 50126627
IPNI 60457692-2
iNaturalist 496140
GBIF 4095989
Freebase /m/0_s3p83
EPPO NDSJA
Elurikkus 465899
Wikipedia Nardostachys_jatamansi

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_055878625.1 ASM5587862v1 Chromosome southwest minzu university 2026-03-14 12 2.69 Gb

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
Unraveling potential neuroprotective mechanisms of herbal medicine for Alzheimer’s diseases through comprehensive molecular docking analyses Alsenani F Saudi J Biol Sci 15-Apr-2024
PMCID:PMC11053229
doi:10.1016/j.sjbs.2024.103998
PMID:38681227
Deep eutectic solvents: Preparation, properties, and food applications Negi T, Kumar A, Sharma SK, Rawat N, Saini D, Sirohi R, Prakash O, Dubey A, Dutta A, Shahi NC Heliyon 30-Mar-2024
PMCID:PMC11015381
doi:10.1016/j.heliyon.2024.e28784
PMID:38617909
Standardization and preliminary characterization of an ayurvedic stress-relieving head massage oil of Nardostachys jatamansi DC Chavan Bhagwan S, Gupta VS, Deshmukh VV, Sardeshmukh SS, Sardeshmukh SP J Ayurveda Integr Med 28-Mar-2024
PMCID:PMC10992859
doi:10.1016/j.jaim.2024.100900
PMID:38552438
Chinese herbal medicine for post-viral fatigue: A systematic review of randomized controlled trials Hu LY, Cai AQ, Li B, Li Z, Liu JP, Cao HJ PLoS One 21-Mar-2024
PMCID:PMC10956782
doi:10.1371/journal.pone.0300896
PMID:38512808
Electrophilic Compounds in the Human Diet and Their Role in the Induction of the Transcription Factor NRF2 Andrés CM, Pérez de la Lastra JM, Bustamante Munguira E, Juan CA, Plou FJ, Pérez Lebeña E Int J Mol Sci 20-Mar-2024
PMCID:PMC10971185
doi:10.3390/ijms25063521
PMID:38542492
Cycloolivil Isolated from Nardostachys jatamansi Inhibits TNF-α/IFN-γ-Induced Chemokine Production by Blocking NF-κB and JAK/STAT Activation in HaCaT Keratinocytes Yoon CS, Lee H, Liu Z, Dong L, Lee G, Kim N, Oh H, Lee DS Int J Mol Sci 15-Mar-2024
PMCID:PMC10969846
doi:10.3390/ijms25063342
PMID:38542316
Potential application of Nardostachyos Radix et Rhizoma-Rhubarb for the treatment of diabetic kidney disease based on network pharmacology and cell culture experimental verification Che MY, Yuan L, Min J, Xu DJ, Lu DD, Liu WJ, Wang KL, Wang YY, Nan Y World J Diabetes 15-Mar-2024
PMCID:PMC10999050
doi:10.4239/wjd.v15.i3.530
PMID:38591077
Flavonoids: A treasure house of prospective pharmacological potentials Hasnat H, Shompa SA, Islam MM, Alam S, Richi FT, Emon NU, Ashrafi S, Ahmed NU, Chowdhury MN, Fatema N, Hossain MS, Ghosh A, Ahmed F Heliyon 09-Mar-2024
PMCID:PMC10944245
doi:10.1016/j.heliyon.2024.e27533
PMID:38496846
Editorial: Green and sustainable extraction techniques for bioactives in food, plants, pharmaceuticals, and cosmetics Chawla P, Rana R, Sridhar K, Stephen Inbaraj B Front Chem 28-Feb-2024
PMCID:PMC10933020
doi:10.3389/fchem.2024.1388362
PMID:38482174
The recent advance and prospect of natural source compounds for the treatment of heart failure Chen XJ, Liu SY, Li SM, Feng JK, Hu Y, Cheng XZ, Hou CZ, Xu Y, Hu M, Feng L, Xiao L Heliyon 25-Feb-2024
PMCID:PMC10912389
doi:10.1016/j.heliyon.2024.e27110
PMID:38444481
Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E Antibiotics (Basel) 07-Feb-2024
PMCID:PMC10885947
doi:10.3390/antibiotics13020163
PMID:38391549
An overview of pharmacological effects of Crocus sativous and its constituents Saadat S, Ghasemi Z, Memarzia A, Behrouz S, Aslani MR, Boskabady MH Iran J Basic Med Sci 01-Jan-2024
PMCID:PMC10897555
doi:10.22038/IJBMS.2023.73410.15950
PMID:38419885
Understanding the Lost: Reconstruction of the Garden Design of Villa Peretti Montalto (Rome, Italy) for Urban Valorization Bartoli F, D’Amato L, Nucera A, Albani Rocchetti G, Caneva G Plants (Basel) 26-Dec-2023
PMCID:PMC10780482
doi:10.3390/plants13010077
PMID:38202385
Role of NLRP3 Inflammasomes in Neurodegenerative Diseases Demirtas N, Sahin-Mazlumoglu B, Palabiyik-Yucelik SS Eurasian J Med 01-Dec-2023
PMCID:PMC11075041
doi:10.5152/eurasianjmed.2023.23349
PMID:39109852
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

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
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1007/S12272-014-0328-2
> Benzenoids / Phenols / Methoxyphenols
4-[(2S,3R)-3-(hydroxymethyl)oxiran-2-yl]-2-methoxyphenol 162973236 Click to see 196.20 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
Epoxy-z-coniferyl alcohol 129682139 Click to see COC1=C(C=CC(=C1)C=C2C(O2)O)O 194.18 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
Epoxyconiferyl Alcohol 57403796 Click to see 196.20 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
> Hydrocarbons / Polycyclic hydrocarbons
(1S-(1alpha,4alpha,7alpha))-1,2,3,4,5,6,7,8-Octahydro-1,4,9,9-tetramethyl-4,7-methanoazulene 12313993 Click to see 204.35 unknown https://doi.org/10.1055/S-0028-1099517
beta-Patchoulene 101731 Click to see 204.35 unknown https://doi.org/10.1055/S-0028-1099517
> Lignans, neolignans and related compounds / Furanoid lignans
(+-)-Pinoresinol 234817 Click to see 358.40 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hexacosanoic Acid 10469 Click to see 396.70 unknown https://doi.org/10.1007/BF02972980
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Thymyl methyl ether 14104 Click to see 164.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257676/
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,6R,7R,8S,10R)-6,7,9,9-tetramethyl-2-oxatetracyclo[5.5.0.01,3.08,10]dodecane-11,12-dione 102104528 Click to see CC1CCC2C3(C1(C4C(C4(C)C)C(=O)C3=O)C)O2 248.32 unknown https://doi.org/10.1016/0031-9422(88)80680-0
6,7,9,9-Tetramethyl-2-oxatetracyclo[5.5.0.01,3.08,10]dodecane-11,12-dione 15625236 Click to see CC1CCC2C3(C1(C4C(C4(C)C)C(=O)C3=O)C)O2 248.32 unknown https://doi.org/10.1016/0031-9422(88)80791-X
Kanshone C 15625237 Click to see CC1CCC2C3(C1(C4C(C4(C)C)C(=O)C3=O)C)O2 248.32 unknown https://doi.org/10.1016/0031-9422(88)80680-0
https://doi.org/10.1016/0031-9422(88)80791-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(1S,5S,9R)-9-Isopropyl-1-methyl-6-methylenespiro[4.5]decan-1-ol 14587119 Click to see 222.37 unknown https://doi.org/10.1002/CHIN.199026291
[(1S,4aS,6S,7R,7aR)-6-hydroxy-7-methyl-1-(3-methylbutanoyloxy)-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-yl]methyl 3-methylbutanoate 162951958 Click to see 368.50 unknown https://doi.org/10.1055/S-2006-962351
Nardostachin 196699 Click to see 368.50 unknown https://doi.org/10.1055/S-2006-962351
Spirojatamol 11053257 Click to see CC(C)C1CCC(=C)C2(C1)CCCC2(C)O 222.37 unknown https://doi.org/10.1002/CHIN.199026291
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1aS,4R,6R,6aR,7S,7aS)-4-hydroxy-7-(2-hydroxypropan-2-yl)-6,6a-dimethyl-1a,4,5,6,7,7a-hexahydronaphtho[2,3-b]oxiren-2-one 14164974 Click to see 266.33 unknown https://doi.org/10.1016/0031-9422(88)80791-X
(1aS,6R,6aR,7S,7aS)-7-(2-hydroxypropan-2-yl)-6,6a-dimethyl-5,6,7,7a-tetrahydro-1aH-naphtho[2,3-b]oxirene-2,4-dione 14164976 Click to see CC1CC(=O)C=C2C1(C(C3C(C2=O)O3)C(C)(C)O)C 264.32 unknown https://doi.org/10.1016/0031-9422(88)80791-X
(1R,5R,7R,8R,12S)-7,12-dihydroxy-1,5-dimethyl-8-propan-2-yl-9,10-dioxatricyclo[6.2.2.02,6]dodec-2(6)-en-3-one 101066853 Click to see 282.33 unknown https://doi.org/10.1016/S0040-4020(00)00682-7
(1S,2R,3R,9S,12S)-12-hydroxy-2,3,11,11-tetramethyl-10-oxatricyclo[7.2.1.02,7]dodec-6-en-8-one 14164972 Click to see CC1CCC=C2C1(C3C(C(C2=O)OC3(C)C)O)C 250.33 unknown https://doi.org/10.1016/0031-9422(88)80791-X
(1S,5R,7R,8S)-7-hydroxy-1,5-dimethyl-8-propan-2-yl-9,10-dioxatricyclo[6.2.2.02,6]dodec-2(6)-en-3-one 10264902 Click to see CC1CC(=O)C2=C1C(C3(CCC2(OO3)C)C(C)C)O 266.33 unknown https://doi.org/10.1016/S0040-4020(00)00682-7
(1S,5R,7S,8S,12R)-7,12-dihydroxy-1,5-dimethyl-8-propan-2-yl-9,10-dioxatricyclo[6.2.2.02,6]dodec-2(6)-en-3-one 101066854 Click to see 282.33 unknown https://doi.org/10.1016/S0040-4020(00)00682-7
(3R,6R,8S)-6,8-dihydroxy-3,8-dimethyl-5-propan-2-yl-2,3,6,7-tetrahydroazulen-1-one 15884946 Click to see CC1CC(=O)C2=C1C=C(C(CC2(C)O)O)C(C)C 250.33 unknown https://doi.org/10.1016/S0040-4020(00)00681-5
(3R,6S,8S)-6,8-dihydroxy-3,8-dimethyl-5-propan-2-yl-2,3,6,7-tetrahydroazulen-1-one 15884947 Click to see 250.33 unknown https://doi.org/10.1016/S0040-4020(00)00681-5
(3R,8S)-8-hydroxy-5-(2-hydroxypropan-2-yl)-3,8-dimethyl-2,3,6,7-tetrahydroazulen-1-one 15884949 Click to see 250.33 unknown https://doi.org/10.1016/S0040-4020(00)00681-5
1,1,9,9a-Tetramethyl-3a,4,7,8,9,9b-hexahydronaphtho[2,1-c]dioxol-5-one 281075 Click to see 250.33 unknown https://doi.org/10.1016/S0304-3940(99)00629-1
https://doi.org/10.1016/S0040-4020(00)00682-7
https://doi.org/10.1016/0031-9422(88)80680-0
https://doi.org/10.1016/0031-9422(88)80791-X
3-(3,7-dimethyl-2,4,5,6,7,7a-hexahydro-1H-inden-5-yl)-2-methylprop-2-enoic acid 163019097 Click to see 234.33 unknown https://doi.org/10.1002/CHIN.200525180
4-Hydroxy-7-(2-hydroxypropan-2-yl)-6,6a-dimethyl-1a,4,5,6,7,7a-hexahydronaphtho[2,3-b]oxiren-2-one 14164973 Click to see CC1CC(C=C2C1(C(C3C(C2=O)O3)C(C)(C)O)C)O 266.33 unknown https://doi.org/10.1016/0031-9422(88)80791-X
4a,8a-dimethyl-7-propan-2-yl-3,4,5,6,7,8-hexahydro-2H-naphthalen-1-one 527498 Click to see CC(C)C1CCC2(CCCC(=O)C2(C1)C)C 222.37 unknown https://doi.org/10.1002/CHIN.199026291
6,8-Dihydroxy-3,8-dimethyl-5-propan-2-yl-2,3,6,7-tetrahydroazulen-1-one 85448534 Click to see CC1CC(=O)C2=C1C=C(C(CC2(C)O)O)C(C)C 250.33 unknown https://doi.org/10.1016/S0040-4020(00)00681-5
7-Hydroxy-1,1,9,9a-tetramethyl-3a,4,7,8,9,9b-hexahydronaphtho[2,1-c]dioxol-5-one 14021477 Click to see 266.33 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
https://doi.org/10.1016/0031-9422(88)80303-0
7,12-Dihydroxy-1,5-dimethyl-8-propan-2-yl-9,10-dioxatricyclo[6.2.2.02,6]dodec-2(6)-en-3-one 85107761 Click to see 282.33 unknown https://doi.org/10.1016/S0040-4020(00)00682-7
8-Hydroxy-3,8-dimethyl-5-propan-2-yl-2,3,6,7-tetrahydroazulen-1-one 78385345 Click to see 234.33 unknown https://doi.org/10.1016/S0031-9422(01)00469-1
Isonardosinone 14164971 Click to see 250.33 unknown https://doi.org/10.1016/0031-9422(88)80791-X
Isonordoperoxide 10825647 Click to see CC1CC(=O)C2=C1C(C3(CCC2(OO3)C)C(C)C)O 266.33 unknown https://doi.org/10.1016/S0040-4020(00)00682-7
https://doi.org/10.1016/S0040-4039(97)10844-9
Kanshone A 10466564 Click to see 234.33 unknown https://doi.org/10.1016/0031-9422(88)80303-0
Kanshone B 14021478 Click to see CC1CC(C=C2C1(C3C(CC2=O)OOC3(C)C)C)O 266.33 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
https://doi.org/10.1016/0031-9422(88)80303-0
Nardofurane 170651 Click to see CC1CCC=C2C1(C3C(C(C2=O)OC3(C)C)O)C 250.33 unknown https://doi.org/10.1016/0031-9422(88)80791-X
Nardoguaianone J 5320011 Click to see CC1CC(=O)C2=C1C=C(CCC2(C)O)C(C)C 234.33 unknown https://doi.org/10.1016/S0031-9422(01)00469-1
Nardoguaianone K 5320012 Click to see 234.33 unknown https://doi.org/10.1016/S0031-9422(01)00469-1
Nardoperoxide 10468127 Click to see CC1CC(=O)C2=C1C(C3(CCC2(OO3)C)C(C)C)O 266.33 unknown https://doi.org/10.1016/S0040-4020(00)00682-7
https://doi.org/10.1016/S0040-4039(97)10844-9
Nardosinone 168136 Click to see 250.33 unknown https://doi.org/10.1016/S0304-3940(99)00629-1
https://doi.org/10.1021/NP050125N
https://doi.org/10.1016/J.BMCL.2011.10.043
https://doi.org/10.1016/S0040-4020(00)00682-7
https://doi.org/10.1016/0031-9422(88)80680-0
https://doi.org/10.1016/0031-9422(88)80791-X
https://doi.org/10.1248/CPB.41.1183
Nardosinonediol 12313519 Click to see 252.35 unknown https://doi.org/10.1016/0031-9422(88)80791-X
Nardoxide 10848304 Click to see 250.33 unknown https://doi.org/10.1016/S0040-4020(00)00682-7
https://doi.org/10.1016/S0040-4039(97)10844-9
Tetrahydronardosinon 12313520 Click to see 252.35 unknown https://doi.org/10.1016/0031-9422(88)80791-X
https://doi.org/10.1248/CPB.41.1183
Valerenal 6440942 Click to see 218.33 unknown https://doi.org/10.1002/BMC.1540
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
(-)-Aristolene 12309878 Click to see 204.35 unknown https://doi.org/10.1055/S-0028-1099517
(1aR,3S,5R,7R,7aR,7bS)-1,1,7,7a-tetramethyl-2,3,5,6,7,7b-hexahydro-1aH-cyclopropa[a]naphthalene-3,5-diol 102463571 Click to see 236.35 unknown https://doi.org/10.1016/S0031-9422(01)00469-1
(1aR,7bS)-3-hydroxy-1,1,7,7a-tetramethyl-1a,2,3,6,7,7b-hexahydrocyclopropa[a]naphthalen-5-one 5316407 Click to see 234.33 unknown https://doi.org/10.1007/S12272-014-0328-2
(1aR,7R,7aR,7bS)-1,1,7,7a-tetramethyl-1a,2,5,6,7,7b-hexahydrocyclopropa[a]naphthalen-3-one 14110649 Click to see 218.33 unknown https://doi.org/10.1055/S-2006-962810
(1aS,3S,7S,7aS,7bR)-3-hydroxy-1,1,7,7a-tetramethyl-1a,2,3,6,7,7b-hexahydrocyclopropa[a]naphthalen-5-one 162999784 Click to see CC1CC(=O)C=C2C1(C3C(C3(C)C)CC2O)C 234.33 unknown https://doi.org/10.1021/NP050125N
[(1aR,4R,7R,7aR,7bS)-1,1,7,7a-tetramethyl-2-oxo-1a,4,5,6,7,7b-hexahydrocyclopropa[a]naphthalen-4-yl] (2R)-2-methylbutanoate 163067590 Click to see 318.40 unknown https://doi.org/10.1016/S0031-9422(01)00469-1
1,1,7,7a-tetramethyl-2,3,5,6,7,7b-hexahydro-1aH-cyclopropa[a]naphthalene-3,5-diol 163008785 Click to see 236.35 unknown https://doi.org/10.1016/S0031-9422(01)00469-1
1(10)-Aristolen-2-one 71717616 Click to see CC1CC(=O)C=C2C1(C3C(C3(C)C)CC2)C 218.33 unknown https://doi.org/10.1055/S-0028-1099823
5H-Cyclopropa[a]naphthalen-5-one, 1,1a,2,3,6,7,7a,7b-octahydro-3-hydroxy-1,1,7,7a-tetramethyl- 534433 Click to see 234.33 unknown https://doi.org/10.1248/CPB.41.1183
9|A-Debilon 162999783 Click to see 234.33 unknown https://doi.org/10.1055/S-0028-1099798
Aristola-1(10),8-dien-2-one 101297625 Click to see 216.32 unknown https://doi.org/10.1055/S-0028-1099823
Aristolene 530421 Click to see 204.35 unknown https://doi.org/10.1055/S-0028-1099983
https://doi.org/10.1055/S-0028-1099517
Calarene 28481 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown https://doi.org/10.1055/S-0028-1099517
Debilon 57391584 Click to see CC1CC(=O)C=C2C1(C3C(C3(C)C)CC2O)C 234.33 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
https://doi.org/10.1248/CPB.41.1183
Kanshone F 636591 Click to see CC1CCC(C2=CC(=O)C3C(C12C)C3(C)C)OC(=O)CC(C)C 318.40 unknown https://doi.org/10.1016/S0031-9422(01)00469-1
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(2S,4aS,6R,8aS)-8a-methyl-4-methylidene-6-prop-1-en-2-yl-1,2,3,4a,5,6,7,8-octahydronaphthalen-2-ol 101618010 Click to see 220.35 unknown https://doi.org/10.1055/S-2006-960091
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Guaiane 9548703 Click to see CC1CCC(CC2C1CCC2C)C(C)C 208.38 unknown https://doi.org/10.1016/S0031-9422(01)00469-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(6,7-Dihydroxy-4-methylidene-1-oxo-4a,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl)methyl 1-methyl-7-propan-2-yl-1,2,3,3a,8,8a-hexahydroazulene-4-carboxylate 85200057 Click to see 430.50 unknown https://doi.org/10.1021/NP990503M
6-hydroxy-7-(hydroxymethyl)-4-methylenehexahydrocyclopenta(c)pyran-1(3H)-one 23844054 Click to see 198.22 unknown https://doi.org/10.1021/NP050125N
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1080/1028602031000105867
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Jatamanvaltrate D 42640647 Click to see 678.70 unknown https://doi.org/10.1021/NP500821G
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
Jatamanvaltrate E 42638122 Click to see 572.60 unknown https://doi.org/10.1021/NP500821G
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1R,3S,6S,7S,8R)-2,2,3,6-tetramethyltricyclo[5.3.1.03,8]undecan-8-ol 162941268 Click to see 222.37 unknown https://doi.org/10.1055/S-0028-1099517
(1S,3R,6R,7R,8R)-2,2,6,8-tetramethyltricyclo[5.3.1.03,8]undecan-3-ol 162957611 Click to see CC1CCC2(C(C3CCC2(C1C3)C)(C)C)O 222.37 unknown https://doi.org/10.1002/CHIN.199026291
2,2,3,6-Tetramethyltricyclo[5.3.1.03,8]undecan-8-ol 162941267 Click to see CC1CCC2(C(C3CCC2(C1C3)O)(C)C)C 222.37 unknown https://doi.org/10.1055/S-0028-1099517
Patchoulialcohol 521903 Click to see CC1CCC2(C(C3CCC2(C1C3)C)(C)C)O 222.37 unknown https://doi.org/10.1002/CHIN.199026291
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1007/BF02972980
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Baldrinal 159846 Click to see CC(=O)OCC1=COC=C2C1=CC=C2C=O 218.20 unknown https://doi.org/10.1007/BF02972980
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1S,4R,12R)-1,3,3,12-tetramethyl-2-oxatricyclo[6.3.1.04,12]dodeca-5,8-dien-7-one 13878359 Click to see CC1(C2C=CC(=O)C3=CCCC(C23C)(O1)C)C 232.32 unknown https://doi.org/10.1055/S-2006-962730
(4R,4aS,5R,7S)-4,7-dihydroxy-5-methyl-4a,5,6,7-tetrahydro-4H-naphthalen-1-one 130918313 Click to see 194.23 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
Desoxo-Narchinol A 56835056 Click to see 192.25 unknown https://doi.org/10.1248/CPB.41.1183
Desoxonarchinol A 15625238 Click to see 192.25 unknown https://doi.org/10.1248/CPB.41.1183
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
https://doi.org/10.1080/1028602031000105867
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
9-Methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-2-one 141849755 Click to see 260.28 unknown https://doi.org/10.1002/CHIN.200525180
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1080/1028602031000105867
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1080/1028602031000105867
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(4-methoxyphenyl)-7-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one 5291487 Click to see 446.40 unknown https://doi.org/10.1080/1028602031000105867
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1080/1028602031000105867
Tilianin 5321954 Click to see 446.40 unknown https://doi.org/10.1080/1028602031000105867

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