Chloranthus serratus - Unknown
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Internal ID UUID644010ef30d1f688192866
Scientific name Chloranthus serratus
Authority Roem. & Schult.
First published in Syst. Veg., ed. 15 bis 3: 461 (1818)

Description Top

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Synonyms Top

Scientific name Authority First published in
Chloranthus blumeanus Cordem. Adansonia 3: 296 (1863)
Chloranthus japonicus Siebold Nova Acta Phys.-Med. Acad. Caes. Leop.-Carol. Nat. Cur. 14(2): 681 (1828)
Chloranthus macranthera Schult.f. ex Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 130. 1867
Nigrina serrata Thunb. Nova Acta Regiae Soc. Sci. Upsal. 7: 142 (1815)
Tricercandra japonica Nakai Fl. Sylv. Kor. 18: 14 (1930)

Common names Top

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Language Common/alternative name
Japanese フタリシズカ
Japanese ふたりしずか
Korean 꽃대
lzh 及己
Russian Хлорант пильчатый
Russian Зеленоцвет пильчатый
Chinese 四大王
Chinese 獐耳细辛
Chinese 四大金刚
Chinese 四叶细辛
Chinese 四叶箭
Chinese 四叶对
Chinese 及已
Chinese 及己
Chinese 四叶金
Chinese 对叶四块瓦
Chinese 四大天王
Chinese 四块瓦

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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 South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Kuril Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000603128
Tropicos 7300004
KEW urn:lsid:ipni.org:names:167822-1
The Plant List kew-2719171
Open Tree Of Life 569909
Observations.org 144289
NCBI Taxonomy 146543
IPNI 167822-1
iNaturalist 447697
GBIF 7339068
Freebase /m/0nbg2k9
EPPO CQNSE
Elurikkus 590474
USDA GRIN 10233
CMAUP NPO6915

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
Why Are There So Few Basidiomycota and Basal Fungi as Endophytes? A Review Rungjindamai N, Jones EB J Fungi (Basel) 15-Jan-2024
PMCID:PMC10820240
doi:10.3390/jof10010067
PMID:38248976
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
A comprehensive review on the chemical constituents, sesquiterpenoid biosynthesis and biological activities of Sarcandra glabra Chu JN, Krishnan P, Lim KH Nat Prod Bioprospect 27-Nov-2023
PMCID:PMC10682397
doi:10.1007/s13659-023-00418-8
PMID:38010490
Bioactive compounds and biomedical applications of endophytic fungi: a recent review Hashem AH, Attia MS, Kandil EK, Fawzi MM, Abdelrahman AS, Khader MS, Khodaira MA, Emam AE, Goma MA, Abdelaziz AM Microb Cell Fact 06-Jun-2023
PMCID:PMC10243280
doi:10.1186/s12934-023-02118-x
PMID:37280587
Antifungal activity of volatile and non-volatile metabolites of endophytes of Chloranthus elatior Sw. Santra HK, Banerjee D Front Plant Sci 17-May-2023
PMCID:PMC10229785
doi:10.3389/fpls.2023.1156323
PMID:37265637
Antibacterial and Antifungal Terpenes from the Medicinal Angiosperms of Asia and the Pacific: Haystacks and Gold Needles Wiart C, Kathirvalu G, Raju CS, Nissapatorn V, Rahmatullah M, Paul AK, Rajagopal M, Sathiya Seelan JS, Rusdi NA, Lanting S, Sulaiman M Molecules 04-May-2023
PMCID:PMC10180233
doi:10.3390/molecules28093873
PMID:37175283
Ecological and Geographical Structure of the Plant Cover of the East Asian Boreal–Nemoral Ecotone (the Lower Amur Region, Far East Russia) Kryukova MV Plants (Basel) 30-Jan-2023
PMCID:PMC9919551
doi:10.3390/plants12030615
PMID:36771699
The complete plastid genome sequence of Chloranthus fortunei (A. Gray) Solms-Laub. in Chloranthaceae Kang JS, Kim BY, Yoo KO Mitochondrial DNA B Resour 25-Oct-2022
PMCID:PMC9621198
doi:10.1080/23802359.2022.2132840
PMID:36325282
Antibacterial and Antifungal Sesquiterpenoids: Chemistry, Resource, and Activity Li HY, Yang WQ, Zhou XZ, Shao F, Shen T, Guan HY, Zheng J, Zhang LM Biomolecules 09-Sep-2022
PMCID:PMC9496053
doi:10.3390/biom12091271
PMID:36139108
Crystal structure and Hirshfeld analysis of (1aS,3aR,4aS,5aR)-15-acet­oxy­linden-7(11),8-trieno-12,8-lactone Lu QQ, Shi XW, Zhou YF, Cui XA, Wang H Acta Crystallogr E Crystallogr Commun 20-May-2022
PMCID:PMC9431784
doi:10.1107/S2056989022004625
PMID:36072141
Identification of Causal Agent Inciting Powdery Mildew on Common Bean and Screening of Resistance Cultivars Deng D, Sun S, Wu W, Duan C, Wang Z, Zhang S, Zhu Z Plants (Basel) 25-Mar-2022
PMCID:PMC9003302
doi:10.3390/plants11070874
PMID:35406856
Activities and Molecular Mechanisms of Diterpenes, Diterpenoids, and Their Derivatives in Rheumatoid Arthritis Torequl Islam M, Quispe C, Herrera-Bravo J, Rahaman MM, Hossain R, Sarkar C, Raihan MA, Chowdhury MM, Uddin SJ, Shilpi JA, Marcelo de Castro e Sousa J, Melo-Cavalcante AA, Mubarak MS, Sharifi-Rad J, Calina D Evid Based Complement Alternat Med 25-Mar-2022
PMCID:PMC8975657
doi:10.1155/2022/4787643
PMID:35368757
Chloranthus genome provides insights into the early diversification of angiosperms Guo X, Fang D, Sahu SK, Yang S, Guang X, Folk R, Smith SA, Chanderbali AS, Chen S, Liu M, Yang T, Zhang S, Liu X, Xu X, Soltis PS, Soltis DE, Liu H Nat Commun 26-Nov-2021
PMCID:PMC8626473
doi:10.1038/s41467-021-26922-4
PMID:34836973
Diterpenoid Compounds Isolated from Chloranthus oldhamii Solms Exert Anti-Inflammatory Effects by Inhibiting the IKK/NF-κB Pathway Chiu LC, Wang JY, Lin CH, Hsu CH, Lin LC, Fu SL Molecules 29-Oct-2021
PMCID:PMC8588554
doi:10.3390/molecules26216540
PMID:34770952
Plant-Based Natural Products and Extracts: Potential Source to Develop New Antiviral Drug Candidates Thomas E, Stewart LE, Darley BA, Pham AM, Esteban I, Panda SS Molecules 14-Oct-2021
PMCID:PMC8537559
doi:10.3390/molecules26206197
PMID:34684782

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 / Diterpenoids
(E)-4-[(1S,4aR,6S,8aR)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-2-methylbut-2-enal 57409862 Click to see CC(=CCC1C(=C)CCC2C1(CCC(C2(C)C)O)C)C=O 290.40 unknown https://doi.org/10.1021/NP200968P
(E)-4-[(1S,4R,4aR,6S,8aR)-4,6-dihydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-2-methylbut-2-enal 57409863 Click to see CC(=CCC1C(=C)CC(C2C1(CCC(C2(C)C)O)C)O)C=O 306.40 unknown https://doi.org/10.1021/NP200968P
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
(3E,7S,8E,10S,13R)-7-hydroxy-10-(2-hydroxypropan-2-yl)-10-methoxy-3,7,13-trimethylcyclotetradeca-3,8-dien-1-one 162883340 Click to see CC1CCC(C=CC(CCC=C(CC(=O)C1)C)(C)O)(C(C)(C)O)OC 352.50 unknown https://doi.org/10.1016/0031-9422(92)80281-I
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
[(1S,3S,4R,8S,9S,10S,12R,14S,15R)-3-hydroxy-5,5,9,15-tetramethyl-16-oxo-11-oxapentacyclo[12.2.1.01,10.04,9.010,12]heptadecan-8-yl] acetate 101689866 Click to see CC1C2CC3C4(O3)C5(C(CCC(C5C(CC4(C2)C1=O)O)(C)C)OC(=O)C)C 376.50 unknown https://doi.org/10.1016/0031-9422(92)80281-I
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(6R)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-5,7-dihydro-1-benzofuran-4-one 137705001 Click to see CC1=COC2=C1C(=O)C(C(C2)(C)C=C)C(=C)C 230.30 unknown https://doi.org/10.1021/NP800543F
(6S)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-5,7-dihydro-1-benzofuran-4-one 5316218 Click to see CC1=COC2=C1C(=O)C(C(C2)(C)C=C)C(=C)C 230.30 unknown https://doi.org/10.1021/NP800543F
chlorantene F 25147592 Click to see CC1=COC2=C1C(=O)C(C(C2=O)(C)C=C)C(=C)C 244.28 unknown https://doi.org/10.1021/NP800543F
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Oplodiol 12313756 Click to see CC(C)C1=CCC2(C(CCC(C2C1)(C)O)O)C 238.37 unknown via CMAUP database
Selina-4(15),7(11)-dien-8-one 13986100 Click to see CC(=C1CC2C(=C)CCCC2(CC1=O)C)C 218.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(4aR,5S,8aR)-5-hydroxy-3,5,8a-trimethyl-4a,6,7,9-tetrahydrobenzo[f][1]benzofuran-4,8-dione 102279301 Click to see CC1=COC2=C1C(=O)C3C(CCC(=O)C3(C2)C)(C)O 262.30 unknown https://doi.org/10.1021/NP800543F
Chlorantene B 25180316 Click to see CC1=COC2=C1C(=O)C3C(CCC(C3(C2)C)[N+](=O)[O-])(C)O 293.31 unknown https://doi.org/10.1021/NP800543F
chlorantene D 25147590 Click to see CC1=COC2=C1C(=O)C3=C(C(=O)CC(C3(C2)C)O)C 260.28 unknown https://doi.org/10.1021/NP800543F
Shizukafuranol 14239916 Click to see CC1=COC2=C1CC3C(C2)(CCCC3(C)O)C 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(-)-(7S,10S)-7-hydroxyeudesm-4-en-6-one 91750135 Click to see CC1=C2C(=O)C(CCC2(CCC1)C)(C(C)C)O 236.35 unknown https://doi.org/10.1080/00021369.1985.10866891
(2S,4aR)-4a,8-dimethyl-2-propan-2-yl-2,3,4,5,6,7-hexahydronaphthalen-1-one 14733783 Click to see CC1=C2C(=O)C(CCC2(CCC1)C)C(C)C 220.35 unknown https://doi.org/10.1080/00021369.1985.10866891
2-hydroxy-4a,8-dimethyl-2-propan-2-yl-4,5,6,7-tetrahydro-3H-naphthalen-1-one 162842267 Click to see CC1=C2C(=O)C(CCC2(CCC1)C)(C(C)C)O 236.35 unknown https://doi.org/10.1080/00021369.1985.10866891
4-Eudesmen-6-one 5320047 Click to see CC1=C2C(=O)C(CCC2(CCC1)C)C(C)C 220.35 unknown https://doi.org/10.1080/00021369.1985.10866891
4a-methyl-8-methylidene-2-propan-2-yl-3,4,5,6,7,8a-hexahydro-2H-naphthalen-1-one 12444761 Click to see CC(C)C1CCC2(CCCC(=C)C2C1=O)C 220.35 unknown https://doi.org/10.1080/00021369.1985.10866891
Acolamone 71587142 Click to see CC(C)C1CCC2(CCCC(=C)C2C1=O)C 220.35 unknown https://doi.org/10.1080/00021369.1985.10866891
chlorantene G 25147593 Click to see CC(C)C1(CCC2(CCCC(=C)C2C1=O)C)O 236.35 unknown https://doi.org/10.1021/NP800543F
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1aS,10aR,E)-1a,5,9-Trimethyl-2,3,6,10a-tetrahydrooxireno[2',3':4,5]cyclodeca[1,2-b]furan-10(1aH)-one 72982958 Click to see CC1=CCCC2(C(O2)C(=O)C3=C(C1)OC=C3C)C 246.30 unknown https://doi.org/10.1080/00021369.1985.10866891
(2Z,6Z)-3,7-dimethyl-10-(propan-2-yl)cyclodeca-2,6-dien-1-one 24976912 Click to see CC1=CCCC(=CC(=O)C(CC1)C(C)C)C 220.35 unknown https://doi.org/10.1080/00021369.1985.10866891
(5E,9E)-3,6,10-trimethyl-8,11-dihydro-7H-cyclodeca[b]furan-4-one 6506548 Click to see CC1=CC(=O)C2=C(CC(=CCC1)C)OC=C2C 230.30 unknown https://doi.org/10.1080/00021369.1985.10866891
(5E,9Z)-3,6,10-Trimethyl-8,11-dihydro-7H-cyclodeca[b]furan-4-one 13559418 Click to see CC1=CC(=O)C2=C(CC(=CCC1)C)OC=C2C 230.30 unknown https://doi.org/10.1021/NP800543F
https://doi.org/10.1080/00021369.1985.10866891
(5R,8E)-5,9,14-trimethyl-4,12-dioxatricyclo[9.3.0.03,5]tetradeca-1(11),8,13-trien-2-one 5315431 Click to see CC1=CCCC2(C(O2)C(=O)C3=C(C1)OC=C3C)C 246.30 unknown https://doi.org/10.1080/00021369.1985.10866891
https://doi.org/10.1021/NP800543F
(9E)-3,10-dimethyl-6-methylidene-7,8-dihydrocyclodeca[b]furan-4,11-dione 102279302 Click to see CC1=CCCC(=C)CC(=O)C2=C(C1=O)OC=C2C 244.28 unknown https://doi.org/10.1021/NP800543F
3,6,10-Trimethyl-4,7,8,11-tetrahydro-cyclodeca[b]furan 99117375 Click to see CC1=CCC2=C(CC(=CCC1)C)OC=C2C 216.32 unknown https://doi.org/10.1080/00021369.1985.10866891
3,6,10-Trimethyl-4H,7H,8H,11H-cyclodeca[B]furan 171597 Click to see CC1=CCC2=C(CC(=CCC1)C)OC=C2C 216.32 unknown https://doi.org/10.1080/00021369.1985.10866891
3,7-Dimethyl-10-propan-2-ylcyclodeca-2,6-dien-1-one 71437970 Click to see CC1=CCCC(=CC(=O)C(CC1)C(C)C)C 220.35 unknown https://doi.org/10.1080/00021369.1985.10866891
5,9,14-Trimethyl-4,12-dioxa-tricyclo[9.3.0.0^3,5^]tetradeca-1(11),8,13-trien-2-one 139069309 Click to see CC1=CCCC2(C(O2)C(=O)C3=C(C1)OC=C3C)C 246.30 unknown https://doi.org/10.1080/00021369.1985.10866891
https://doi.org/10.1021/NP800543F
Acoragermacrone 14262632 Click to see CC1=CCCC(=CC(=O)C(CC1)C(C)C)C 220.35 unknown https://doi.org/10.1080/00021369.1985.10866891
CID 179413 179413 Click to see CC1=CC(=O)C2=C(CC(=CCC1)C)OC=C2C 230.30 unknown https://doi.org/10.1080/00021369.1985.10866891
Furanodiene 636458 Click to see CC1=CCC2=C(CC(=CCC1)C)OC=C2C 216.32 unknown https://doi.org/10.1080/00021369.1985.10866891
Furanodienone 5317425 Click to see CC1=CC(=O)C2=C(CC(=CCC1)C)OC=C2C 230.30 unknown https://doi.org/10.1080/00021369.1985.10866891
https://doi.org/10.1021/NP800543F
Isofuranodiene 5317424 Click to see CC1=CCC2=C(CC(=CCC1)C)OC=C2C 216.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3aR,5R,5aR,9aR)-3a,5,9a-trihydroxy-1,5-dimethyl-8-methylidene-5a,6,7,9-tetrahydro-4H-benzo[e][1]benzofuran-2-one 57409961 Click to see CC1=C2C3(CC(=C)CCC3C(CC2(OC1=O)O)(C)O)O 280.32 unknown https://doi.org/10.1021/NP200968P
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(4aR,5S,6S,8aS,9aS)-4a,5,6-trihydroxy-3,5,8a-trimethyl-4,6,9,9a-tetrahydrobenzo[f][1]benzofuran-2-one 101482732 Click to see CC1=C2CC3(C(CC2OC1=O)(C=CC(C3(C)O)O)C)O 280.32 unknown https://doi.org/10.1002/HLCA.200800450
(4aR,5S,8aR,9aS)-5-hydroxy-3,5,8a-trimethyl-4a,6,7,8,9,9a-hexahydro-4H-benzo[f][1]benzofuran-2-one 57409864 Click to see CC1=C2CC3C(CCCC3(C)O)(CC2OC1=O)C 250.33 unknown https://doi.org/10.1021/NP200968P
(4aR,5S,8aR,9aS)-5,9a-dihydroxy-3,5,8a-trimethyl-4,4a,6,7,8,9-hexahydrobenzo[f][1]benzofuran-2-one 57409865 Click to see CC1=C2CC3C(CCCC3(C)O)(CC2(OC1=O)O)C 266.33 unknown https://doi.org/10.1021/NP200968P
(4aS,5R,8S,8aS,9aR)-5,8-dihydroxy-8a-(hydroxymethyl)-3,5-dimethyl-4a,6,7,8,9,9a-hexahydro-4H-benzo[f][1]benzofuran-2-one 162976275 Click to see CC1=C2CC3C(CCC(C3(CC2OC1=O)CO)O)(C)O 282.33 unknown https://doi.org/10.1002/HLCA.200800450
(4aS,5R,8S,8aS,9aR)-5,8,9a-trihydroxy-3,5,8a-trimethyl-4,4a,6,7,8,9-hexahydrobenzo[f][1]benzofuran-2-one 162879567 Click to see CC1=C2CC3C(CCC(C3(CC2(OC1=O)O)C)O)(C)O 282.33 unknown https://doi.org/10.1002/HLCA.200800450
4a,5,6-Trihydroxy-3,5,8a-trimethyl-4,6,9,9a-tetrahydrobenzo[f][1]benzofuran-2-one 162845385 Click to see CC1=C2CC3(C(CC2OC1=O)(C=CC(C3(C)O)O)C)O 280.32 unknown https://doi.org/10.1002/HLCA.200800450
5,8-dihydroxy-8a-(hydroxymethyl)-3,5-dimethyl-4a,6,7,8,9,9a-hexahydro-4H-benzo[f][1]benzofuran-2-one 162976274 Click to see CC1=C2CC3C(CCC(C3(CC2OC1=O)CO)O)(C)O 282.33 unknown https://doi.org/10.1002/HLCA.200800450
5,8,9a-Trihydroxy-3,5,8a-trimethyl-4,4a,6,7,8,9-hexahydrobenzo[f][1]benzofuran-2-one 75597610 Click to see CC1=C2CC3C(CCC(C3(CC2(OC1=O)O)C)O)(C)O 282.33 unknown https://doi.org/10.1002/HLCA.200800450
8-Hydroxy-3,5,8a-trimethyl-4,4a,7,8,9,9a-hexahydrobenzo[f][1]benzofuran-2-one 75058505 Click to see CC1=CCC(C2(C1CC3=C(C(=O)OC3C2)C)C)O 248.32 unknown https://doi.org/10.1002/HLCA.200800450
Chloraeudolide, (rel)- 50993975 Click to see CC1=C2CC3C(CCC(C3(CC2(OC1=O)O)C)O)(C)O 282.33 unknown via CMAUP database
Chlorajapolide A, (rel)- 50993826 Click to see CC1=C2C(CC3(C4CC4C(=C3C2O)C=O)C)OC1=O 260.28 unknown via CMAUP database
Chlorajapolide B, (rel)- 50993898 Click to see CC1=C2C(CC3(C4CC4C5=C3C2OC5O)C)OC1=O 260.28 unknown via CMAUP database
Chlorajapolide C, (rel)- 50993899 Click to see CC1=C2CC3=C(C4CC4C3(CC2OC1=O)C)CO 246.30 unknown via CMAUP database
Chlorajapolide D, (rel)- 50993900 Click to see CC1=C2CC3C(CC2OC1=O)(C4CC4C3(CO)O)C 264.32 unknown via CMAUP database
Chlorajapolide E, (rel)- 50993901 Click to see CC(=O)OCC1C2CC2C3(C1CC4=C(C(=O)OC4(C3O)OC)CO)C 352.40 unknown via CMAUP database
Chlorajaposide, (rel)- 53316475 Click to see CC1=C2CC3C(=C)C4CC4C3(CC2(OC1=O)OC5C(C(C(C(O5)CO)O)O)O)C 408.40 unknown via CMAUP database
Sarcandralactone B 44627499 Click to see CC1=CCC(C2(C1CC3=C(C(=O)OC3C2)C)C)O 248.32 unknown https://doi.org/10.1002/HLCA.200800450
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2S,4S,5S,7R,8S,10S,16R,28E,33S,34S,36R,37R)-10-ethoxy-4,33-dihydroxy-1,8,13,29-tetramethyl-11,17,21,26,31-pentaoxadecacyclo[17.17.3.14,8.02,16.05,7.010,14.016,39.033,37.034,36.015,40]tetraconta-13,15(40),19(39),28-tetraene-9,12,18,22,25,30-hexone 57409860 Click to see CCOC12C(=C(C(=O)O1)C)C3=C4C(C2=O)(C5CC5C4(CC6C37C8=C(COC(=O)CCC(=O)OCC=C(C(=O)OCC9(C1CC1C6(C9C8)C)O)C)C(=O)O7)O)C 760.80 unknown https://doi.org/10.1021/NP200968P
(1S,2S,4S,5S,7R,8S,9R,10S,16R,28E,33S,34S,36R,37R)-4,9,33-trihydroxy-10-methoxy-1,8,13,29-tetramethyl-11,17,21,26,31-pentaoxadecacyclo[17.17.3.14,8.02,16.05,7.010,14.016,39.033,37.034,36.015,40]tetraconta-13,15(40),19(39),28-tetraene-12,18,22,25,30-pentone 70698149 Click to see CC1=CCOC(=O)CCC(=O)OCC2=C3CC4C(C5CC5C4(COC1=O)O)(C6C3(C7=C8C(C9CC9C8(C6)O)(C(C1(C7=C(C(=O)O1)C)OC)O)C)OC2=O)C 748.80 unknown via CMAUP database
(1S,2S,5S,7R,8S,9R,10S,16R,28E,33S,34S,36R,37R)-9,10,33-trihydroxy-1,8,13,29-tetramethyl-11,17,21,26,31-pentaoxadecacyclo[17.17.3.14,8.02,16.05,7.010,14.016,39.033,37.034,36.015,40]tetraconta-3,13,15(40),19(39),28-pentaene-12,18,22,25,30-pentone 57409861 Click to see CC1=CCOC(=O)CCC(=O)OCC2=C3CC4C(C5CC5C4(COC1=O)O)(C6C3(C7=C8C(=C6)C9CC9C8(C(C1(C7=C(C(=O)O1)C)O)O)C)OC2=O)C 716.70 unknown https://doi.org/10.1021/NP200968P
[(1R,2S,8R,9S,10S,12R,13S,14S,17S,19R,20S,21R)-9,21-dihydroxy-5-(hydroxymethyl)-23-(1-methoxy-1-oxopropan-2-ylidene)-13,20-dimethyl-4,22-dioxo-3-oxaoctacyclo[14.7.1.02,6.02,14.08,13.010,12.017,19.020,24]tetracosa-5,16(24)-dien-9-yl]methyl (E)-2-methylbut-2-enoate 145712282 Click to see CC=C(C)C(=O)OCC1(C2CC2C3(C1CC4=C(C(=O)OC45C3CC6=C7C5C(=C(C)C(=O)OC)C(=O)C(C7(C8C6C8)C)O)CO)C)O 634.70 unknown https://doi.org/10.1016/0031-9422(92)80281-I
[9,21-Dihydroxy-5-(hydroxymethyl)-23-(1-methoxy-1-oxopropan-2-ylidene)-13,20-dimethyl-4,22-dioxo-3-oxaoctacyclo[14.7.1.02,6.02,14.08,13.010,12.017,19.020,24]tetracosa-5,16(24)-dien-9-yl]methyl 2-methylbut-2-enoate 78089497 Click to see CC=C(C)C(=O)OCC1(C2CC2C3(C1CC4=C(C(=O)OC45C3CC6=C7C5C(=C(C)C(=O)OC)C(=O)C(C7(C8C6C8)C)O)CO)C)O 634.70 unknown https://doi.org/10.1016/0031-9422(92)80281-I
CID 127045559 127045559 Click to see CC1=C2CC3C(=C)C4CC4C3(C5C2(C6C7=C(C5)C8CC8C7(C(C(=O)C6=C(C)C(=O)OC)O)C)OC1=O)C 502.60 unknown https://doi.org/10.1016/0031-9422(92)80281-I
CID 74400395 74400395 Click to see CC1=CCOC(=O)CCC(=O)OCC2=C3CC4C(C5CC5C4(COC1=O)O)(C6C3(C7C8=C(C6)C9CC9C8(C(C(=O)C7=C(C)C(=O)OC)O)C)OC2=O)C 732.80 unknown https://doi.org/10.1016/0031-9422(92)80281-I
Methyl 2-[9-(acetyloxymethyl)-21-hydroxy-5-(hydroxymethyl)-13,20-dimethyl-4,22-dioxo-3-oxaoctacyclo[14.7.1.02,6.02,14.08,13.010,12.017,19.020,24]tetracosa-5,16(24)-dien-23-ylidene]propanoate 72670386 Click to see CC(=C1C2C3=C(CC4C25C(=C(C(=O)O5)CO)CC6C4(C7CC7C6COC(=O)C)C)C8CC8C3(C(C1=O)O)C)C(=O)OC 578.60 unknown https://doi.org/10.1016/0031-9422(92)80281-I
shizukaol B 56661508 Click to see CC1=CCOC(=O)CCC(=O)OCC2=C3CC4C(C5CC5C4(COC1=O)O)(C6C3(C7C8=C(C6)C9CC9C8(C(C(=O)C7=C(C)C(=O)OC)O)C)OC2=O)C 732.80 unknown https://doi.org/10.1016/0031-9422(92)80281-I
Shizukaol D 70698151 Click to see CC(=C1C2C3=C(CC4C25C(=C(C(=O)O5)CO)CC6C4(C7CC7C6COC(=O)C)C)C8CC8C3(C(C1=O)O)C)C(=O)OC 578.60 unknown https://doi.org/10.1016/0031-9422(92)80281-I
shizukaol F 56681897 Click to see CC1=CC(=O)OCC2(C3CC3C4(C2CC5=C(COC(=O)CCC(=O)OC1)C(=O)OC56C4CC7=C8C6C(=C(C)C(=O)OC)C(=O)C(C8(C9C7C9)C)O)C)O 732.80 unknown via CMAUP database
shizukaol H 56659161 Click to see CC1=CC(=O)OCC2(C3CC3C4(C2CC5=C(COC(=O)CC(C(=O)OC1)O)C(=O)OC56C4CC7=C8C6C(=C(C)C(=O)OC)C(=O)C(C8(C9C7C9)C)O)C)O 748.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
((1R,4S,5R)-1-Methyl-4-(prop-1-en-2-yl)spiro[4.5]dec-7-en-8-yl)methanol 91714964 Click to see CC1CCC(C12CCC(=CC2)CO)C(=C)C 220.35 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
dimethyl (2S,5R,7S,8R,12S,15R,17S,18R,19S,24S)-19,24-dihydroxy-2,8,12,18-tetramethyl-20,23-dioxoheptacyclo[12.6.2.28,11.04,9.05,7.015,17.018,22]tetracosa-1(21),4(9),10,14(22)-tetraene-2,12-dicarboxylate 133561951 Click to see CC1(CC2=C3C=C(C(=O)C(C3(C4C2C4)C)O)C(CC5=C6C=C1C(=O)C(C6(C7C5C7)C)O)(C)C(=O)OC)C(=O)OC 548.60 unknown https://doi.org/10.1016/S0031-9422(00)95119-7
> Organoheterocyclic compounds / Cycloheptafurans
Chlorantene A 25180128 Click to see CC1=COC2=C1C(=O)CC3(CCCC3(C2=O)C)C 246.30 unknown https://doi.org/10.1021/NP800543F
> Organoheterocyclic compounds / Naphthofurans
(1R,9R,10R,12S,13R)-13-hydroxy-13-(hydroxymethyl)-4,9-dimethyl-6-oxatetracyclo[7.4.0.03,7.010,12]trideca-3,7-dien-5-one 102441214 Click to see CC1=C2CC3C(C=C2OC1=O)(C4CC4C3(CO)O)C 262.30 unknown https://doi.org/10.1080/00021369.1989.10869234
13-(Hydroxymethyl)-4,9-dimethyl-6-oxatetracyclo[7.4.0.03,7.010,12]trideca-3,7-dien-5-one 138376536 Click to see CC1=C2CC3C(C4CC4C3(C=C2OC1=O)C)CO 246.30 unknown https://doi.org/10.1080/00021369.1985.10866891
13-Hydroxy-13-(hydroxymethyl)-4,9-dimethyl-6-oxatetracyclo[7.4.0.03,7.010,12]trideca-3,7-dien-5-one 14287457 Click to see CC1=C2CC3C(C=C2OC1=O)(C4CC4C3(CO)O)C 262.30 unknown https://doi.org/10.1080/00021369.1989.10869234
Chloranthalactone C 14239912 Click to see CC1=C2CC3C(C4CC4C3(C=C2OC1=O)C)COC(=O)C 288.34 unknown https://doi.org/10.1080/00021369.1985.10866891
Shizukanolide C 124708052 Click to see CC1=C2CC3C(C4CC4C3(C=C2OC1=O)C)CO 246.30 unknown https://doi.org/10.1080/00021369.1985.10866891
Shizukanolide F 14287462 Click to see CC12C=C3C(=C(C(=O)O3)CO)CC1C(C4C2C4)CO 262.30 unknown https://doi.org/10.1080/00021369.1989.10869234
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown via CMAUP database

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