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Nardostachys jatamansi

Nardostachys jatamansi - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

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

Description Top

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The spikenard of the Bible is also thought to be derived from Nardostachys jatamansi.

Nardostachys jatamansi is a flowering plant of the valerian family that grows in the Himalayas. It is a source of an intensely aromatic amber-colored essential oil, spikenard, which has been used since ancient times as a perfume, traditional medicine, and in religious ceremonies. The oil is made from the plant's rhizomes, and contains acaciin, ursolic acid, octacosanol, kanshone A, nardosinonediol, nardosinone, aristolen-9beta-ol, oleanolic acid, and beta-sitosterol. It is thought to be the source of the spikenard of the Bible, and is currently considered endangered due to overharvesting, overgrazing, loss of habitats, and forest degradation.

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
Kannada ಜಟಾಮಾಂಸಿ
Korean 감송
Malayalam ജടാമാഞ്ചി
Marathi जटामांसी
Malay spikenard
Nepali जटामसी
Punjabi ਜਟਾਮਾਂਸੀ
scn nardu
Slovak nard pravý
Tamil ஜாதமாசி
Telugu జటామాంసి
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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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

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

Links to other databases Top

Suggest others/fix!
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

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
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
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
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
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
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1007/S12272-014-0328-2
> Benzenoids / Phenols / Methoxyphenols
3-(3-Methoxy-4-hydroxyphenyl)oxirane-2-methanol 57403796 Click to see COC1=C(C=CC(=C1)C2C(O2)CO)O 196.20 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
4-[(2S,3R)-3-(hydroxymethyl)oxiran-2-yl]-2-methoxyphenol 162973236 Click to see COC1=C(C=CC(=C1)C2C(O2)CO)O 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
> 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 CC1CCC2=C1CC3CCC2(C3(C)C)C 204.35 unknown https://doi.org/10.1055/S-0028-1099517
beta-Patchoulene 101731 Click to see CC1CCC2=C1CC3CCC2(C3(C)C)C 204.35 unknown https://doi.org/10.1055/S-0028-1099517
> Lignans, neolignans and related compounds / Furanoid lignans
(+/-)-Pinoresinol 234817 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 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 CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 396.70 unknown https://doi.org/10.1007/BF02972980
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-Isopropyl-5-methylanisole 14104 Click to see CC1=CC(=C(C=C1)C(C)C)OC 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 CC(C)C1CCC(=C)C2(C1)CCCC2(C)O 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 CC1C(CC2C1C(OC=C2COC(=O)CC(C)C)OC(=O)CC(C)C)O 368.50 unknown https://doi.org/10.1055/S-2006-962351
Nardostachin 196699 Click to see CC1C(CC2C1C(OC=C2COC(=O)CC(C)C)OC(=O)CC(C)C)O 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 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
(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 CC1CC(=O)C2=C1C(C3(C(CC2(OO3)C)O)C(C)C)O 282.33 unknown https://doi.org/10.1016/S0040-4020(00)00682-7
(1R,5R,7R,8R)-7-hydroxy-1,5-dimethyl-8-propan-2-yl-11-oxatricyclo[6.2.1.02,6]undec-2(6)-en-3-one 10848304 Click to see CC1CC(=O)C2=C1C(C3(CCC2(O3)C)C(C)C)O 250.33 unknown https://doi.org/10.1016/S0040-4020(00)00682-7
https://doi.org/10.1016/S0040-4039(97)10844-9
(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 CC1CC(=O)C2=C1C(C3(C(CC2(OO3)C)O)C(C)C)O 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 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,8S)-8-hydroxy-5-(2-hydroxypropan-2-yl)-3,8-dimethyl-2,3,6,7-tetrahydroazulen-1-one 15884949 Click to see CC1CC(=O)C2=C1C=C(CCC2(C)O)C(C)(C)O 250.33 unknown https://doi.org/10.1016/S0040-4020(00)00681-5
1,1,9,9a-tetramethyl-3aH,4H,7H,8H,9H,9bH-naphtho[2,1-c][1,2]dioxol-5-one 281075 Click to see CC1CCC=C2C1(C3C(CC2=O)OOC3(C)C)C 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 CC1CC(CC2=C(CCC12)C)C=C(C)C(=O)O 234.33 unknown https://doi.org/10.1002/CHIN.200525180
3-Hydroxy-4-(2-hydroxypropan-2-yl)-4a,5-dimethyl-2,3,4,5,6,7-hexahydronaphthalen-1-one 12313519 Click to see CC1CCC=C2C1(C(C(CC2=O)O)C(C)(C)O)C 252.35 unknown https://doi.org/10.1016/0031-9422(88)80791-X
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 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
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 CC1CC(=O)C2=C1C(C3(C(CC2(OO3)C)O)C(C)C)O 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 CC1CC(=O)C2=C1C=C(CCC2(C)O)C(C)C 234.33 unknown https://doi.org/10.1016/S0031-9422(01)00469-1
Isonardosinone 14164971 Click to see CC1CCC=C2C1(C(C3C(C2=O)O3)C(C)(C)O)C 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 CC1CCC=C2C1(C(C=CC2=O)C(C)(C)O)C 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 CC1CC(=O)C2=C1C=C(CCC2(C)O)C(C)C 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 CC1CCC=C2C1(C3C(CC2=O)OOC3(C)C)C 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 12313520 Click to see CC1CCC=C2C1(C(C(CC2=O)O)C(C)(C)O)C 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 CC1CCC(C2=C(CCC12)C)C=C(C)C=O 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 CC1CCCC2=CCC3C(C12C)C3(C)C 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 CC1CC(C=C2C1(C3C(C3(C)C)CC2O)C)O 236.35 unknown https://doi.org/10.1016/S0031-9422(01)00469-1
(1aR,3S,7R,7aR,7bS)-3-hydroxy-1,1,7,7a-tetramethyl-1a,2,3,6,7,7b-hexahydrocyclopropa[a]naphthalen-5-one 162999783 Click to see CC1CC(=O)C=C2C1(C3C(C3(C)C)CC2O)C 234.33 unknown https://doi.org/10.1055/S-0028-1099798
(1aR,7bS)-3-hydroxy-1,1,7,7a-tetramethyl-1a,2,3,6,7,7b-hexahydrocyclopropa[a]naphthalen-5-one 5316407 Click to see CC1CC(=O)C=C2C1(C3C(C3(C)C)CC2O)C 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 CC1CCC=C2C1(C3C(C3(C)C)CC2=O)C 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 CCC(C)C(=O)OC1CCC(C2(C1=CC(=O)C3C2C3(C)C)C)C 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 CC1CC(C=C2C1(C3C(C3(C)C)CC2O)C)O 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 CC1CC(=O)C=C2C1(C3C(C3(C)C)CC2O)C 234.33 unknown https://doi.org/10.1248/CPB.41.1183
Aristola-1(10),8-dien-2-one 101297625 Click to see CC1CC(=O)C=C2C1(C3C(C3(C)C)C=C2)C 216.32 unknown https://doi.org/10.1055/S-0028-1099823
Aristolene 530421 Click to see CC1CCCC2=CCC3C(C12C)C3(C)C 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 CC(=C)C1CCC2(CC(CC(=C)C2C1)O)C 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 CC1CCC2C1CC(=CC=C2C(=O)OCC3(C(CC4C3C(=O)OCC4=C)O)O)C(C)C 430.50 unknown https://doi.org/10.1021/NP990503M
6-Hydroxy-7-(hydroxymethyl)-4-methylenehexahydrocyclopenta[c]pyran-1(3h)-one 23844054 Click to see C=C1COC(=O)C2C1CC(C2CO)O 198.22 unknown https://doi.org/10.1021/NP050125N
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/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 CC(C)CC(=O)OC1C2C(CC(C2(COC(=O)C3=CC=CC=C3O)O)OC(=O)C)(C(=CO1)COC(=O)C(C(C)C)OC(=O)CC(C)C)O 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 CC(C)CC(=O)OC1C2C(CC(C2(COC)O)OC(=O)C)(C(=CO1)COC(=O)C(C(C)C)OC(=O)CC(C)C)O 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 CC1CCC2(C(C3CCC2(C1C3)O)(C)C)C 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 CC1CC(C=C2C1C(C=CC2=O)O)O 194.23 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
4-Hydroxy-4a,5-dimethyl-4,5,6,7-tetrahydronaphthalen-1-one 15625238 Click to see CC1CCC=C2C1(C(C=CC2=O)O)C 192.25 unknown https://doi.org/10.1248/CPB.41.1183
Desoxo-Narchinol A 56835056 Click to see CC1CCC=C2C1(C(C=CC2=O)O)C 192.25 unknown https://doi.org/10.1248/CPB.41.1183
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3,4-Dihydroxy cinnamic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/J.BMCL.2011.10.043
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 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 C1=CC(=CC=C1C=CC(=O)O)O 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 CC1(C(CC2=C(O1)C=CC3=C2OC(=O)C=C3)OC)C 260.28 unknown https://doi.org/10.1002/CHIN.200525180
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 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 CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1080/1028602031000105867
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-(beta-D-Galactopyranosyloxy)-5-hydroxy-2-(4-Methoxyphenyl)- 5291487 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1080/1028602031000105867
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1080/1028602031000105867
Tilianin 5321954 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1080/1028602031000105867

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