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Internal ID UUID644054183f0af449777526
Scientific name Patrinia scabra
Authority Bunge
First published in Uchen. Zap. Imp. Kazansk. Univ. 1835(4): 171 (1835)

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Synonyms Top

Scientific name Authority First published in
Fedia scabra Kuntze Revis. Gen. Pl. 1: 302 (1891)
Patrinia rupestris subsp. scabra (Bunge) H.J.Wang Acta Phytotax. Sin. 23(5): 382. 1985 [18 Oct 1985]

Common names Top

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Language Common/alternative name
Chinese 墓头回
Chinese 糙叶败酱
Chinese 糙叶败酱*(粗叶败酱)

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
      • Inner Mongolia
      • Manchuria

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001225090
Tropicos 50043227
KEW urn:lsid:ipni.org:names:859467-1
The Plant List tro-50043227
Open Tree Of Life 68239
NCBI Taxonomy 180074
IPNI 859467-1
iNaturalist 601635
GBIF 8251923
CMAUP NPO14197

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
A systematic approach for authentication of medicinal Patrinia species using an integration of morphological, chemical and molecular methods Wong KH, Zheng T, Yue GG, Li MC, Wu HY, Tong MH, Zhao XL, Chen HB, Lau CB, Shaw PC, Lau DT Sci Rep 19-Mar-2024
PMCID:PMC10951358
doi:10.1038/s41598-024-57115-w
PMID:38503940
Natural Products as Anticancer Agents: Current Status and Future Perspectives Naeem A, Hu P, Yang M, Zhang J, Liu Y, Zhu W, Zheng Q Molecules 30-Nov-2022
PMCID:PMC9737905
doi:10.3390/molecules27238367
PMID:36500466
Complete Chloroplast Genome Sequence of Triosteum sinuatum, Insights into Comparative Chloroplast Genomics, Divergence Time Estimation and Phylogenetic Relationships among Dipsacales Liu H, Liu W, Ahmad I, Xiao Q, Li X, Zhang D, Fang J, Zhang G, Xu B, Gao Q, Chen S Genes (Basel) 23-May-2022
PMCID:PMC9141360
doi:10.3390/genes13050933
PMID:35627318
Optimization for ultrasonic-microwave synergetic extraction of total iridoid glycosides and screening of analgesic and anti-inflammatory active fractions from patrinia scabra Bunge (Valerianaceae) Ma Q, Lu Y, Deng Y, Hu X, Li W, Jia H, Guo Y, Shi X BMC Complement Med Ther 04-Jan-2022
PMCID:PMC8728952
doi:10.1186/s12906-021-03489-7
PMID:34983472
Integrated Network Pharmacology Analysis and In Vitro Validation Revealed the Potential Active Components and Underlying Mechanistic Pathways of Herba Patriniae in Colorectal Cancer Yang H, Cheung MK, Yue GG, Leung PC, Wong CK, Lau CB Molecules 05-Oct-2021
PMCID:PMC8513027
doi:10.3390/molecules26196032
PMID:34641576
Antitumor effect of IL-12 gene-modified bone marrow mesenchymal stem cells combined with Fuzheng Yiliu decoction in an in vivo glioma nude mouse model Wu J, Xie S, Li H, Zhang Y, Yue J, Yan C, Liu K, Liu Y, Xu R, Zheng G J Transl Med 07-Apr-2021
PMCID:PMC8028710
doi:10.1186/s12967-021-02809-2
PMID:33827606
The complete chloroplast genome sequence of herb Nardostachys jatamans (family: Valerianaceae) in China Deng J, Liang H, Luo X, Zhang W, Gao G, Yang R, Ahmad KS, Zhang G Mitochondrial DNA B Resour 27-Jan-2021
PMCID:PMC7872520
doi:10.1080/23802359.2020.1861568
PMID:33659647
Anti-Inflammatory Activity of Extracts and Pure Compounds Derived from Plants via Modulation of Signaling Pathways, Especially PI3K/AKT in Macrophages Merecz-Sadowska A, Sitarek P, Śliwiński T, Zajdel R Int J Mol Sci 16-Dec-2020
PMCID:PMC7766727
doi:10.3390/ijms21249605
PMID:33339446
Lignans and Their Derivatives from Plants as Antivirals Cui Q, Du R, Liu M, Rong L Molecules 01-Jan-2020
PMCID:PMC6982783
doi:10.3390/molecules25010183
PMID:31906391
Current knowledge and development of hederagenin as a promising medicinal agent: a comprehensive review Zeng J, Huang T, Xue M, Chen J, Feng L, Du R, Feng Y RSC Adv 03-Jul-2018
PMCID:PMC9082113
doi:10.1039/c8ra03666g
PMID:35539158
Preventive and Therapeutic Effects of Chinese Herbal Compounds against Hepatocellular Carcinoma Hu B, An HM, Wang SS, Chen JJ, Xu L Molecules 27-Jan-2016
PMCID:PMC6274246
doi:10.3390/molecules21020142
PMID:26828466
Traditional Chinese medicine for prevention and treatment of hepatocarcinoma: From bench to bedside Hu B, Wang SS, Du Q World J Hepatol 28-May-2015
PMCID:PMC4438495
doi:10.4254/wjh.v7.i9.1209
PMID:26019736
Triterpenes as Potentially Cytotoxic Compounds Chudzik M, Korzonek-Szlacheta I, Król W Molecules 19-Jan-2015
PMCID:PMC6272502
doi:10.3390/molecules20011610
PMID:25608043
Anticancer activity of essential oils and their chemical components - a review Bayala B, Bassole IH, Scifo R, Gnoula C, Morel L, Lobaccaro JM, Simpore J Am J Cancer Res 19-Nov-2014
PMCID:PMC4266698
PMID:25520854
Three New Iridoid Glucosides from the Roots of Patrinia scabra Lei Di, Ning Li, Ling-Bo Zu, Kai-Jin Wang, You-Xing Zhao, Zhi Wang Korean Chemical Society 19-Oct-2011
doi:10.5012/BKCS.2011.32.9.3251

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 / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
5-(Hydroxymethyl)-4-(3-hydroxyprop-1-en-2-yl)-1-methylcyclopentane-1,2-diol 75149776 Click to see CC1(C(CC(C1CO)C(=C)CO)O)O 202.25 unknown https://doi.org/10.5012/BKCS.2011.32.9.3251
Jatamanin J 46211183 Click to see CC1(C(CC(C1CO)C(=C)CO)O)O 202.25 unknown https://doi.org/10.5012/BKCS.2011.32.9.3251
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
8alpha-Acetoxyelemol 44566708 Click to see CC(=C)C1CC(C(CC1(C)C=C)OC(=O)C)C(C)(C)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(4R,4aS,6S,7S,7aR)-6-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-7-hydroxy-4,7-dimethyl-1,4,4a,5,6,7a-hexahydrocyclopenta[c]pyran-3-one 101673679 Click to see CC1C2CC(C(C2COC1=O)(C)O)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O 494.50 unknown https://doi.org/10.1016/0031-9422(94)85081-X
(4S,4aS,6S,7S,7aR)-4,7-dihydroxy-4,7-dimethyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-3-one 163006080 Click to see CC1(C2CC(C(C2COC1=O)(C)O)OC3C(C(C(C(O3)CO)O)O)O)O 378.37 unknown https://doi.org/10.5012/BKCS.2011.32.9.3251
(4S,4aS,6S,7S,7aR)-7-hydroxy-4,7-dimethyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4,4a,5,6,7a-hexahydrocyclopenta[c]pyran-3-one 101673676 Click to see CC1C2CC(C(C2COC1=O)(C)O)OC3C(C(C(C(O3)CO)O)O)O 362.37 unknown https://doi.org/10.1016/0031-9422(94)85081-X
[2-Hydroxy-4-(3-hydroxyprop-1-en-2-yl)-2-methyl-3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclopentyl] 3-methylbutanoate 78075599 Click to see CC(C)CC(=O)OC1CC(C(C1(C)O)COC2C(C(C(C(O2)CO)O)O)O)C(=C)CO 448.50 unknown https://doi.org/10.1016/0031-9422(95)00516-A
Patrinioside 71461980 Click to see CC(C)CC(=O)OC1CC(C(C1(C)O)COC2C(C(C(C(O2)CO)O)O)O)C(=C)CO 448.50 unknown https://doi.org/10.1016/0031-9422(95)00516-A
Patriridoside D 71454804 Click to see CC1CC2C(C1COC3C(C(C(C(O3)CO)O)O)O)C(=CO2)C=O 344.36 unknown via CMAUP database
Patriscabroside I 71453062 Click to see CC1C2CC(C(C2COC1=O)(C)O)OC3C(C(C(C(O3)CO)O)O)O 362.37 unknown https://doi.org/10.1016/0031-9422(94)85081-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
6-Hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 4430509 Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown https://doi.org/10.5012/BKCS.2011.32.9.3251
Loganic acid 89640 Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown https://doi.org/10.5012/BKCS.2011.32.9.3251
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4R,4aS,6S,7S,7aR)-6-hydroxy-4,7-dimethyl-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4,4a,5,6,7a-hexahydrocyclopenta[c]pyran-3-one 101673677 Click to see CC1C2CC(C(C2COC1=O)(C)OC3C(C(C(C(O3)CO)O)O)O)O 362.37 unknown https://doi.org/10.1016/0031-9422(94)85081-X
Isopatriscabrol 11019883 Click to see CC1C2CC(C(C2COC1=O)(C)O)O 200.23 unknown https://doi.org/10.1016/0031-9422(94)85081-X
Isopatriscabroside II 101673678 Click to see CC1C2CC(C(C2COC1=O)(C)OC3C(C(C(C(O3)CO)O)O)O)O 362.37 unknown https://doi.org/10.1016/0031-9422(94)85081-X
Jatamanin A 46211034 Click to see CC1(C(CC2C1C(=O)OCC2=C)O)O 198.22 unknown via CMAUP database
Patriscabrol 11074397 Click to see CC1C2CC(C(C2COC1=O)(C)O)O 200.23 unknown https://doi.org/10.1016/0031-9422(94)85081-X
Scabrol A 71458435 Click to see CC1C2CCC(C2COC1=O)(C)O 184.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1080/10286020310001595953
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
Patriscabratine 5320433 Click to see CC(=O)NC(CC1=CC=CC=C1)COC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3 444.50 unknown https://doi.org/10.1080/10286020310001595953
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-6beta-methoxy-8beta-methyl-4aalpha,5,8,8aalpha-tetrahydro-1H,6H-pyrano[3,4-c]pyran-4-carboxylic acid methyl ester 71451245 Click to see CC1C2C(CC(O1)OC)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 420.40 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[[(3R,4R,4aS,6R,7S,7aR)-6-hydroxy-3-methoxy-4,7-dimethyl-3,4,4a,5,6,7a-hexahydro-1H-cyclopenta[c]pyran-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162867557 Click to see CC1C2CC(C(C2COC1OC)(C)OC3C(C(C(C(O3)CO)O)O)O)O 378.40 unknown https://doi.org/10.5012/BKCS.2011.32.9.3251
(4R,4aR,6S,7R,7aS)-6-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-7-hydroxy-4,7-dimethyl-4a,5,6,7a-tetrahydro-4H-cyclopenta[b]pyran-3-one 163006729 Click to see CC1C2CC(C(C2OCC1=O)(C)O)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O 494.50 unknown https://doi.org/10.1016/0031-9422(94)85081-X
(4R,4aR,6S,7R,7aS)-6-hydroxy-4,7-dimethyl-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-4H-cyclopenta[b]pyran-3-one 162972881 Click to see CC1C2CC(C(C2OCC1=O)(C)OC3C(C(C(C(O3)CO)O)O)O)O 362.37 unknown https://doi.org/10.1016/0031-9422(94)85081-X
(4R,4aR,6S,7R,7aS)-7-hydroxy-4,7-dimethyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-4H-cyclopenta[b]pyran-3-one 163008141 Click to see CC1C2CC(C(C2OCC1=O)(C)O)OC3C(C(C(C(O3)CO)O)O)O 362.37 unknown https://doi.org/10.1016/0031-9422(94)85081-X
(4S,4aR,6S,7R,7aS)-6-hydroxy-4,7-dimethyl-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-4H-cyclopenta[b]pyran-3-one 162972880 Click to see CC1C2CC(C(C2OCC1=O)(C)OC3C(C(C(C(O3)CO)O)O)O)O 362.37 unknown https://doi.org/10.1016/0031-9422(94)85081-X
(4S,4aR,6S,7R,7aS)-7-hydroxy-4,7-dimethyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-4H-cyclopenta[b]pyran-3-one 163008140 Click to see CC1C2CC(C(C2OCC1=O)(C)O)OC3C(C(C(C(O3)CO)O)O)O 362.37 unknown https://doi.org/10.1016/0031-9422(94)85081-X
(7Alpha-Hydroxy)-Morroniside 21593530 Click to see CC1C2C(CC(O1)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 406.40 unknown via CMAUP database
6-[6-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-7-hydroxy-4,7-dimethyl-4a,5,6,7a-tetrahydro-4H-cyclopenta[b]pyran-3-one 163006728 Click to see CC1C2CC(C(C2OCC1=O)(C)O)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O 494.50 unknown https://doi.org/10.1016/0031-9422(94)85081-X
6-hydroxy-4,7-dimethyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-4H-cyclopenta[b]pyran-3-one 162972879 Click to see CC1C2CC(C(C2OCC1=O)(C)OC3C(C(C(C(O3)CO)O)O)O)O 362.37 unknown https://doi.org/10.1016/0031-9422(94)85081-X
7-hydroxy-4,7-dimethyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-4H-cyclopenta[b]pyran-3-one 163008139 Click to see CC1C2CC(C(C2OCC1=O)(C)O)OC3C(C(C(C(O3)CO)O)O)O 362.37 unknown https://doi.org/10.1016/0031-9422(94)85081-X
7R-O-Methylmorroniside 49862810 Click to see CC1C2C(CC(O1)OC)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 420.40 unknown via CMAUP database
Morroniside 11228693 Click to see CC1C2C(CC(O1)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 406.40 unknown via CMAUP database
Patriridoside F 71454805 Click to see CC1C2CC(C(C2COC1O)(C)OC3C(C(C(C(O3)CO)O)O)O)O 364.39 unknown via CMAUP database
Patriridoside G 71460286 Click to see CC1=CCC2C1(OCC2=C)COC3C(C(C(C(O3)CO)O)O)O 328.36 unknown via CMAUP database
Patriridoside H 71458433 Click to see CC1=CCC2C1(OCC2=C)COC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O 460.50 unknown via CMAUP database
Patriridoside I 71458434 Click to see CC1COC2(C1CC=C2C)COC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O 462.50 unknown via CMAUP database
Sweroside 161036 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Halopyrimidines
Fluorouracil 3385 Click to see C1=C(C(=O)NC(=O)N1)F 130.08 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
(4R,4aR,6S,7R,7aS)-6,7-dihydroxy-4,7-dimethyl-4a,5,6,7a-tetrahydro-4H-cyclopenta[b]pyran-3-one 162951427 Click to see CC1C2CC(C(C2OCC1=O)(C)O)O 200.23 unknown https://doi.org/10.1016/0031-9422(94)85081-X
(4S,4aR,6S,7R,7aS)-6,7-dihydroxy-4,7-dimethyl-4a,5,6,7a-tetrahydro-4H-cyclopenta[b]pyran-3-one 162951426 Click to see CC1C2CC(C(C2OCC1=O)(C)O)O 200.23 unknown https://doi.org/10.1016/0031-9422(94)85081-X
6,7-dihydroxy-4,7-dimethyl-4a,5,6,7a-tetrahydro-4H-cyclopenta[b]pyran-3-one 162951425 Click to see CC1C2CC(C(C2OCC1=O)(C)O)O 200.23 unknown https://doi.org/10.1016/0031-9422(94)85081-X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
Isomundulinol 10476431 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(C(C2=O)O)C4=CC=CC=C4)O)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
Candidone 157102 Click to see CC(=CCC1=C2C(=C(C=C1OC)OC)C(=O)CC(O2)C3=CC=CC=C3)C 352.40 unknown via CMAUP database
Mundulinol 10363971 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)O)C4=CC=CC=C4)O)C=CC(O2)(C)C)C 406.50 unknown via CMAUP database
> 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/10.1080/10286020310001595953
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(4R,5R)-5-hydroxy-10,10,16,16-tetramethyl-4-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),8(13),11,17-pentaen-6-one 15426600 Click to see CC1(C=CC2=C(O1)C3=C(C4=C2OC(C(C4=O)O)C5=CC=CC=C5)OC(C=C3)(C)C)C 404.50 unknown via CMAUP database
3-Deoxy-MS-II 10068857 Click to see CC1(C=CC2=C(O1)C3=C(C4=C2OC(CC4=O)C5=CC=CC=C5)OC(C=C3)(C)C)C 388.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(3S)-3-hydroxy-7-(5-methoxy-2,2-dimethylchromen-6-yl)-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one 40458927 Click to see CC1(C=CC2=C(O1)C=CC(=C2OC)C3=COC4=C(C3=O)C=C5CC(C(OC5=C4)(C)C)O)C 434.50 unknown via CMAUP database
Munetone 12312999 Click to see CC1(C=CC2=CC3=C(C=C2O1)OC=C(C3=O)C4=C(C5=C(C=C4)OC(C=C5)(C)C)OC)C 416.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
Rotenolone 68184 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC 410.40 unknown via CMAUP database
Rotenone 6758 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown via CMAUP database
Tephrosin 114909 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C 410.40 unknown via CMAUP database
Villosol 5490819 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)O 408.40 unknown https://doi.org/10.1016/0031-9422(94)85081-X
> Phenylpropanoids and polyketides / Macrolides and analogues
(5R)-13,15-dihydroxy-5-methyl-4-oxabicyclo[10.4.0]hexadeca-1(12),13,15-triene-3,11-dione 638958 Click to see CC1CCCCCC(=O)C2=C(CC(=O)O1)C=C(C=C2O)O 292.33 unknown via CMAUP database

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