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Aphanamixis polystachya

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644009c27fd0d746808110
Scientific name Aphanamixis polystachya
Authority (Wall.) R.Parker
First published in Indian Forester 57: 486 (1931)

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.

Among the Taita of Kenya, the leaves are bruised and applied as a poultice to swelling, and the bark is steeped with salt to make a wash for skin conditions like ringworm; Rukungäri et al., 1982 document these uses. In the Northeast Indian Hill Tribes (e.g., Khasi and Naga), the bark is taken as a decoction for dysentery and to control fevers, while leaves are crushed and used topically for ulcers; Longkumer and Jamir, 1999 record these practices. In Sri Lankan Traditional Medicine, the bark is also boiled to make a decoction for dropsy, according to Jayaweera, 1980–81, and various Ayurvedic and Siddha sources treat “Rohitaka” (the bark of Aphanamixis polystachya) as a general tonic for hepatic and pulmonary complaints; that usage often involves decoctions or medicated wines (e.g., rohitakarista, Charaka Samhita; Jain, 1968; Kapoor, 2001).

One practical bark decoction is to simmer approximately 30 g of air‑dried bark in 1 liter of water for 30 minutes, then steep off‑heat for another 10 minutes; the dose is usually 60–120 mL twice daily. As safety, use short courses, do not exceed the typical dose, and avoid during pregnancy due to traditional cautions and the bitter alkaloid profile (Kapoor, 2001; Jain, 1968).

Modern investigations have isolated limonoids such as rohitukin and mahogany lactones from the bark, as well as flavonoids and tannins; these constituents plausibly support the traditional bitter, diuretic and anti‑inflammatory activities (Kapoor, 2001; Jana and Ghosal, 1979). Today the species remains in trade as “Rohitaka” bark, is still used in ethnobotanical practice in parts of India and Sri Lanka, and is a focus of pharmacological screening for hepatoprotective effects (Kapoor, 2001; Jana and Ghosal, 1979; Rukungäri et al., 1982; Longkumer and Jamir, 1999; Jayaweera, 1980–81).

General Uses Top

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Wood and fiber:
The wood is used for furniture, cabinetry, joinery, and plywood. Reports list utilization in building components such as door and window frames, flooring, and boat planking. It is also employed for agricultural implements and turnery, and is considered a suitable pulpwood species for paper manufacture (e.g., kraft pulp). These applications imply a medium to heavy hardwood with workable density and grain, but documented hardness and durability data are not consistent across authoritative sources.

Food and beverages (non-medicinal):
The seeds yield an edible oil reported to be used for culinary frying and in processed foods as an ingredient. Oil composition has been characterized as a conventional seed oil with the presence of saturated and unsaturated fatty acids (predominantly linoleic and oleic acids); however, quantitative profiles (e.g., iodine/saponification values) and technical specifications are not uniformly reported.

Colorants and tanning:
Bark extracts provide natural brown dyes for textiles, historically documented for dyeing cotton; use on protein fibers (silk/wool) is not consistently supported in reliable literature. No verified tannin class or astringency profile is reported for leather tanning applications.

Industrial and craft applications:
Wood is used in furniture manufacture and light construction; bark extracts have been noted as dyestuffs in textile craft processes (e.g., calico printing). Seed oil is employed in cooking applications and as an ingredient in processed foods; non-food industrial uses are not well established.

Synonyms Top

Scientific name Authority First published in
Ricinocarpodendron cumingianum (C.DC.) Mabb. Malaysian Forester 45: 454 (1982)
Ricinocarpodendron polystachyum (Wall) Mabb. Malaysian Forester 45: 454 (1982)
Sphaerosacme polystachya Wall. Numer. List : n.º 1277 (1829)
Aglaia aphanamixis Pellegr. Fl. Indo-Chine [P.H. Lecomte et al.] 1: 767. 1911
Aglaia beddomei (Kosterm.) S.S.Jain & R.C.Gaur J. Econ. Taxon. Bot. 7: 465 (1985 publ. 1986)
Aglaia cochinchinensis Pellegr. Fl. Indo-Chine 1: 769 (1911)
Aglaia janowskyi Harms Bot. Jahrb. Syst. 72: 176 (1942)
Aglaia polystachya Wall. Fl. Ind. 2: 429 (1824)
Alliaria cuneata (Hiern) Kuntze Revis. Gen. Pl. 1: 109. 1891 [5 Nov 1891]
Amoora amboinensis Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 36 (1868)
Amoora aphanamixis Schult.f. Syst. Veg., ed. 15 bis 7: 1612 (1830)
Amoora beddomei Kosterm. Acta Bot. Neerl. 31: 133 (1982)
Amoora cumingiana C.DC. Monogr. Phan. 1: 580 (1878)
Amoora elmeri Merr. Publ. Bur. Sci. Gov. Lab. 29: 23 (1905)
Amoora grandifolia Walp. Repert. Bot. Syst. 1: 429 (1842)
Amoora janowskyi (Harms) Kosterm. Reinwardtia 7: 265 (1966)
Amoora macrophylla Nimmo Cat. Pl. Bombay : t. 31 (1839)
Amoora megalophylla C.DC. Bull. Herb. Boissier 2: 577 (1894)
Amoora myrmecophila Warb. Bot. Jahrb. Syst. 18: 194 (1893)
Amoora perrottetiana Steud. Nomencl. Bot. , ed. 2, 1: 89 (1840)
Amoora polillensis C.B.Rob. Philipp. J. Sci., C 6: 206 (1911)
Amoora polystachya (Wall.) Steud. Nomencl. Bot. , ed. 2, 1: 78 (1840)
Amoora sogerensis Baker f. J. Bot. 61(Suppl.): 8 (1923)
Amoora timorensis Wight & Arn. ex Steud. Nomencl. Bot. , ed. 2, 1: 78 (1840)
Andersonia rohituka Roxb. Hort. Bengal. [87] (1814); Fl. Ind. ii. 213.
Aphanamixis agusanensis Elmer Leafl. Philipp. Bot. 9(128): 3328. 1937 [1 May 1937] , anglice
Aphanamixis amboinensis (Miq.) Harms Nat. Pflanzenfam. 3(4): 296 (1896)
Aphanamixis apoensis Elmer Leafl. Philipp. Bot. 9(128): 3326. 1937 [1 May 1937] , anglice
Aphanamixis blumei Span. Ic. 14; et in Linnaea, xv. (1841) 182.
Aphanamixis cochinchinensis Pierre Fl. Forest. Cochinch. : t. 343 (1896)
Aphanamixis coriacea Merr. Philipp. J. Sci., C 11: 14 (1916)
Aphanamixis cumingiana (C.DC.) Harms Nat. Pflanzenfam. 3(4): 296 (1896)
Aphanamixis davaoensis Elmer Leafl. Philipp. Bot. 9(128): 3331. 1937 [1 May 1937] , anglice
Aphanamixis elmeri Merr. Philipp. J. Sci., C 11: 15 (1916)
Aphanamixis grandifolia Blume Bijdr. Fl. Ned. Ind. : 165 (1825)
Aphanamixis lauterbachii Harms Fl. Schutzgeb. Südsee : 383 (1900)
Aphanamixis macrocalyx Harms Fl. Schutzgeb. Südsee : 384 (1900)
Aphanamixis myrmecophila (Warb.) Harms Nat. Pflanzenfam. 3(4): 296 (1896)
Aphanamixis obliquifolia Elmer Leafl. Philipp. Bot. 9(128): 3333. 1937 [1 May 1937] , anglice
Aphanamixis perrottetiana A.Juss. Mém. Meliac. : 108 (1832)
Aphanamixis pinatubensis Elmer Leafl. Philipp. Bot. 9: 3205 (1934)
Aphanamixis polillensis Merr. Enum. Philipp. Fl. Pl. 2: 370 (1923)
Aphanamixis rohituka Pierre Fl. Forest. Cochinch. t. 344 (1896).
Aphanamixis schlechteri Harms Bot. Jahrb. Syst. 72: 160 (1942)
Aphanamixis sinensis F.C.How & T.C.Chen Acta Phytotax. Sin. 4: 29 (1955)
Aphanamixis timorensis A.Juss. Mém. Meliac. : 107 (1832)
Aphanamixis tripetala Merr. Sp. Blancoan. : 211 (1918)
Aphanamixis velutina Elmer Leafl. Philipp. Bot. 9(128): 3338. 1937 [1 May 1937] , anglice
Cabralea richardiana C.DC. Fl. Bras. 11(1): 176 (1878)
Canarium vrieseo-teysmannii H.J.Lam Ann. Jard. Bot. Buitenzorg 42: 216 (1932)
Chuniodendron spicatum Hu J. Roy. Hort. Soc. 63: 387 (1938)
Chuniodendron yunnanense Hu J. Roy. Hort. Soc. 63: 387 (1938)
Dysoxylum cuneatum Hiern Fl. Brit. India 1: 549 (1875)
Dysoxylum spiciflorum Zipp. ex Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 35. 1868
Trichilia tripetala Blanco Fl. Filip. : 854 (1837)
Amoora rohituka (Roxb.) Wight & Arn. Cat. Ind. Pl. 24 (1833).

Common names Top

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Language Common/alternative name
Arabic آموره
Bengali পিতরাজ
Japanese ハリンハラ
Malayalam ചെമ്മരം
Malayalam രോഹീതകം
Telugu సేవమాను
Chinese 红果树
Chinese 红罗
Chinese 大叶山楝
Chinese 油桐
Chinese 沙罗
Chinese 山罗
Chinese 假油桐
Chinese 苦油木
Chinese 穗花樹蘭
Chinese 山楝

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000539906
Tropicos 20400971
KEW urn:lsid:ipni.org:names:577579-1
The Plant List kew-2643324
Open Tree Of Life 430647
NCBI Taxonomy 201010
IUCN Red List 33616
IPNI 577579-1
iNaturalist 189339
GBIF 5597304
Freebase /m/02qxd3d
EPPO AHXPO
EOL 581910
USDA GRIN 312562
Wikipedia Aphanamixis_polystachya

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
Insights into the Mechanism of Action of the Degraded Limonoid Prieurianin Vergoten G, Bailly C Int J Mol Sci 22-Mar-2024
PMCID:PMC11011620
doi:10.3390/ijms25073597
PMID:38612409
Preference of trees for nest building by critically endangered white‐rumped vultures (Gyps bengalensis) in Nepal Gautam R, Baral N, Sharma HP Ecol Evol 18-Mar-2024
PMCID:PMC10948368
doi:10.1002/ece3.11175
PMID:38505186
Mapping of soil suitability for medicinal plants using machine learning methods Roopashree S, Anitha J, Challa S, Mahesh TR, Venkatesan VK, Guluwadi S Sci Rep 14-Feb-2024
PMCID:PMC10866873
doi:10.1038/s41598-024-54465-3
PMID:38355896
Special Issue Editorial: “Antibacterial Agents from Natural Sources” Martins CH Molecules 30-Jan-2024
PMCID:PMC10856429
doi:10.3390/molecules29030644
PMID:38338388
Staphylococcus aureus biofilm: Formulation, regulatory, and emerging natural products-derived therapeutics Wu X, Wang H, Xiong J, Yang GX, Hu JF, Zhu Q, Chen Z Biofilm 01-Jan-2024
PMCID:PMC10827693
doi:10.1016/j.bioflm.2023.100175
PMID:38298832
Reactive oxygen species (ROS)-mediated oxidative stress in chronic liver diseases and its mitigation by medicinal plants Sharma P, Nandave M, Nandave D, Yadav S, Vargas-De-La-Cruz C, Singh S, Tandon R, Ramniwas S, Behl T Am J Transl Res 15-Nov-2023
PMCID:PMC10703659
PMID:38074830
Structure-dependent activity of plant natural products against methicillin-resistant Staphylococcus aureus Moreno Cardenas C, Çiçek SS Front Microbiol 15-Aug-2023
PMCID:PMC10463185
doi:10.3389/fmicb.2023.1234115
PMID:37649631
The Anticancer Effect of Napabucasin (BBI608), a Natural Naphthoquinone Shao Z, Wang H, Ren H, Sun Y, Chen X Molecules 27-Jul-2023
PMCID:PMC10420168
doi:10.3390/molecules28155678
PMID:37570646
Sesquiterpenoids from Meliaceae Family and Their Biological Activities Riyadi SA, Naini AA, Supratman U Molecules 20-Jun-2023
PMCID:PMC10302239
doi:10.3390/molecules28124874
PMID:37375428
Monitoring the curing efficiency of a plant-based green engineered additive on caprine skin: a spectroscopic and chemometric novel approach Hossain MM, Roy UK Heliyon 13-May-2023
PMCID:PMC10208822
doi:10.1016/j.heliyon.2023.e16273
PMID:37234638
Chloroplast genome skimming of a potential agroforestry species Melia dubia. Cav and its comparative phylogenetic analysis with major Meliaceae members Samji A, Eashwarlal K, Shanmugavel S, Kumar S, Warrier RR 3 Biotech 31-Dec-2022
PMCID:PMC9805483
doi:10.1007/s13205-022-03447-1
PMID:36597460
New Diterpenes with Potential Antitumoral Activity Isolated from Plants in the Years 2017–2022 Forzato C, Nitti P Plants (Basel) 29-Aug-2022
PMCID:PMC9460660
doi:10.3390/plants11172240
PMID:36079622
Liposomes as Multifunctional Nano-Carriers for Medicinal Natural Products Cheng X, Yan H, Pang S, Ya M, Qiu F, Qin P, Zeng C, Lu Y Front Chem 08-Aug-2022
PMCID:PMC9393238
doi:10.3389/fchem.2022.963004
PMID:36003616
Untargeted Metabolomic Approach to Determine the Regulatory Pathways on Salicylic Acid-Mediated Stress Response in Aphanamixis polystachya Seedlings Rakhesh KV, Ashalatha SN, Mahima K, Baskar V, Thiruvengadam M Molecules 06-May-2022
PMCID:PMC9102903
doi:10.3390/molecules27092966
PMID:35566316
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

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 / Styrenes
(E)-N-[4-[(2R)-2-hydroxy-4-methyl-5-oxo-2H-pyrrol-1-yl]butyl]-3-phenylprop-2-enamide 162918960 Click to see CC1=CC(N(C1=O)CCCCNC(=O)C=CC2=CC=CC=C2)O 314.40 unknown https://doi.org/10.1021/NP070184W
(E)-N-[4-[(2S)-2-hydroxy-4-methyl-5-oxo-2H-pyrrol-1-yl]butyl]-3-phenylprop-2-enamide 162918961 Click to see CC1=CC(N(C1=O)CCCCNC(=O)C=CC2=CC=CC=C2)O 314.40 unknown https://doi.org/10.1021/NP070184W
3,4-dihydroxy-2-methylidene-N-[4-(3-phenylprop-2-enoylamino)butyl]butanamide 74080759 Click to see 332.40 unknown https://doi.org/10.1021/NP070184W
4-hydroxy-2-methyl-N-[4-(3-phenylprop-2-enoylamino)butyl]but-2-enamide 85354018 Click to see 316.40 unknown https://doi.org/10.1021/NP070184W
N-[4-(2-hydroxy-4-methyl-5-oxo-2H-pyrrol-1-yl)butyl]-3-phenylprop-2-enamide 74080761 Click to see 314.40 unknown https://doi.org/10.1021/NP070184W
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3S,4S,5S)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 158384172 Click to see 552.60 unknown https://doi.org/10.1007/S11418-006-0047-1
(2S,3R,4R,5S)-2-[[(1R,2S,3S)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 158384171 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O 552.60 unknown https://doi.org/10.1007/S11418-006-0047-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown https://doi.org/10.1016/S0031-9422(97)00205-7
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1007/S11418-006-0047-1
https://doi.org/10.1016/S0031-9422(97)00205-7
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1016/S0031-9422(97)00205-7
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1016/S0031-9422(97)00205-7
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/S0031-9422(97)00205-7
methyl (Z)-7-oxooctadec-11-enoate 14861233 Click to see 310.50 unknown https://doi.org/10.1016/S0031-9422(97)00205-7
Methyl 7-oxooctadec-11-enoate 85614625 Click to see 310.50 unknown https://doi.org/10.1016/S0031-9422(97)00205-7
trans-9-cis-12-Octadecadienoic acid 5282798 Click to see 280.40 unknown https://doi.org/10.1007/S11418-006-0047-1
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
methyl (3S)-3-[(3S,3aS,5aR,6S,7S,9R,9aR)-3-[(3S,5R,6S)-5,6-dihydroxy-6-(2-hydroxypropan-2-yl)oxan-3-yl]-9-hydroxy-3a,6,9a-trimethyl-7-prop-1-en-2-yl-2,3,4,5,5a,7,8,9-octahydrocyclopenta[a]naphthalen-6-yl]-3-acetyloxypropanoate 71531902 Click to see 592.80 unknown https://doi.org/10.1021/NP400126Q
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(1aS,4S,4aS,7S,7aR,7bS)-4,7-dimethyl-1a-propan-2-yl-3,4,4a,5,6,7b-hexahydro-2H-azuleno[7,8-b]oxirene-7,7a-diol 21579115 Click to see CC1CCC2(C(O2)C3(C1CCC3(C)O)O)C(C)C 254.36 unknown https://doi.org/10.1016/S0031-9422(02)00698-2
4,7-dimethyl-1a-propan-2-yl-3,4,4a,5,6,7b-hexahydro-2H-azuleno[7,8-b]oxirene-7,7a-diol 73803869 Click to see 254.36 unknown https://doi.org/10.1016/S0031-9422(02)00698-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(1R,2R,3S,8R,10R,11R,15S,16S)-3-acetyloxy-15-[(3S,5R,6S)-5,6-dihydroxy-6-(2-hydroxypropan-2-yl)oxan-3-yl]-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-en-10-yl] acetate 71726327 Click to see 620.80 unknown https://doi.org/10.1021/NP400126Q
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(13alpha,14beta,17S,20S,21R,23R,24S)-21,23 12306725 Click to see CC(=O)OC1CCC2(C3CCC4(C(CCC4(C3=CCC2C1(C)C)C)C5CC(OC5O)C6C(O6)(C)C)C)C 514.70 unknown https://doi.org/10.1016/S0040-4020(01)92762-0
https://doi.org/10.1016/S0031-9422(00)83138-6
(1S)-1-[(2R,4S,5R)-4-[(3R,5R,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-5-methoxyoxolan-2-yl]-2-methylpropane-1,2-diol 23642919 Click to see CC1(C(CCC2(C1CC=C3C2CCC4(C3(CCC4C5CC(OC5OC)C(C(C)(C)O)O)C)C)C)O)C 504.70 unknown https://doi.org/10.1021/NP400126Q
(1S)-1-[(2R,4S,5R)-4-[(3S,5R,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-5-methoxyoxolan-2-yl]-2-methylpropane-1,2-diol 73354987 Click to see 504.70 unknown https://doi.org/10.1021/NP400126Q
(3S,4R,6S)-6-[(3R,5R,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptane-2,3,4-triol 21638425 Click to see 476.70 unknown https://doi.org/10.1002/MRC.2768
(5R,8S,9S,10R,13S,14R,17R)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 162884671 Click to see CC(=CCCC(C)(C1CCC2(C1(CCC3C2CCC4C3(CCC(=O)C4(C)C)C)C)C)O)C 442.70 unknown https://doi.org/10.1002/MRC.2768
(5R,9R,10R,13S,14S,17S)-17-[(2R,3S,5R)-5-[(1S)-1,2-dihydroxy-2-methylpropyl]-2-methoxyoxolan-3-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 73353494 Click to see 502.70 unknown https://doi.org/10.1021/NP400126Q
(5R,9R,10R,13S,14S,17S)-17-[(2R,3S)-3-hydroxy-6-methyl-4-oxohept-5-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162929155 Click to see CC(C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C)C(C(=O)C=C(C)C)O 454.70 unknown https://doi.org/10.1002/MRC.2768
(5R,9R,10R,13S,14S,17S)-17-[(2S,4S)-4,7-dihydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 163050543 Click to see 456.70 unknown https://doi.org/10.1021/NP400126Q
(5R,9R,10R,13S,14S,17S)-17-[(2S,5S)-5-hydroxy-6-methoxy-6-methyl-4-oxoheptan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 163065627 Click to see CC(CC(=O)C(C(C)(C)OC)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 486.70 unknown https://doi.org/10.1002/MRC.2768
(5R,9R,10R,13S,14S,17S)-17-[(Z,2S,4S)-4,7-dihydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 73353495 Click to see 456.70 unknown https://doi.org/10.1021/NP400126Q
(5Z)-5-(2-methoxy-2-methylpropylidene)-3-[(5R,9R,10R,13S,14S,17R)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]furan-2-one 56838491 Click to see CC1(C2CC=C3C(C2(CCC1=O)C)CCC4(C3(CCC4C5=CC(=CC(C)(C)OC)OC5=O)C)C)C 480.70 unknown https://doi.org/10.1002/CBDV.201000250
(5Z)-5-(2-methylprop-2-enylidene)-3-[(5R,9R,10R,13S,14S,17R)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]furan-2-one 163186579 Click to see 448.60 unknown https://doi.org/10.1002/CBDV.201000250
[(3R,5R,9R,10R,13S,14S,17S)-17-[(2R,3S,5R)-5-[(1S)-1,2-dihydroxy-2-methylpropyl]-2-methoxyoxolan-3-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 71531904 Click to see CC(=O)OC1CCC2(C3CCC4(C(CCC4(C3=CCC2C1(C)C)C)C5CC(OC5OC)C(C(C)(C)O)O)C)C 546.80 unknown https://doi.org/10.1021/NP400126Q
[(3R,5R,9R,10R,13S,14S,17S)-17-[(2S,3S,5R)-5-[(1S)-1,2-dihydroxy-2-methylpropyl]-2-methoxyoxolan-3-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 71529900 Click to see 546.80 unknown https://doi.org/10.1021/NP400126Q
[(3S,5R,9R,10R,13S,14S,17S)-17-[(2S,3S,5R)-5-[(2R)-3,3-dimethyloxiran-2-yl]-2-hydroxyoxolan-3-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 101297623 Click to see CC(=O)OC1CCC2(C3CCC4(C(CCC4(C3=CCC2C1(C)C)C)C5CC(OC5O)C6C(O6)(C)C)C)C 514.70 unknown https://doi.org/10.1002/CHIN.200416161
[(3S,5S,9R,10R,13S,14S,17S)-17-[(2S,3R,5R)-5-[(1S)-1,2-dihydroxy-2-methylpropyl]-2-hydroxyoxolan-3-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 163193719 Click to see 532.80 unknown https://doi.org/10.1016/S0031-9422(00)83138-6
[(3S,5S,9R,10R,13S,14S,17S)-17-[(2S,3S,5S)-5-[(2R)-3,3-dimethyloxiran-2-yl]-2-hydroxyoxolan-3-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 162984627 Click to see CC(=O)OC1CCC2(C3CCC4(C(CCC4(C3=CCC2C1(C)C)C)C5CC(OC5O)C6C(O6)(C)C)C)C 514.70 unknown https://doi.org/10.1016/S0040-4020(01)92762-0
https://doi.org/10.1016/S0031-9422(00)83138-6
[17-[5-(1,2-dihydroxy-2-methylpropyl)-2-hydroxyoxolan-3-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 163044074 Click to see CC(=O)OC1CCC2(C3CCC4(C(CCC4(C3=CCC2C1(C)C)C)C5CC(OC5O)C(C(C)(C)O)O)C)C 532.80 unknown https://doi.org/10.1016/S0031-9422(00)83138-6
17-(3-Hydroxy-6-methyl-4-oxohept-5-en-2-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 14137668 Click to see 454.70 unknown https://doi.org/10.1002/MRC.2768
17-[4-(3,3-Dimethyloxiran-2-yl)-4-oxobutan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 76393899 Click to see 454.70 unknown https://doi.org/10.1002/MRC.2768
24,25-Epoxytirucall-7-en-3,23-dione 124524253 Click to see CC(CC(=O)C1C(O1)(C)C)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C 454.70 unknown https://doi.org/10.1002/MRC.2768
4,4,10,13,14-Pentamethyl-17-(4,5,6-trihydroxy-6-methylheptan-2-yl)-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 14021536 Click to see 474.70 unknown https://doi.org/10.1002/MRC.2768
5-(2-methoxy-2-methylpropylidene)-3-[(5R,9R,10R,13S,14S,17R)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]furan-2-one 162935285 Click to see CC1(C2CC=C3C(C2(CCC1=O)C)CCC4(C3(CCC4C5=CC(=CC(C)(C)OC)OC5=O)C)C)C 480.70 unknown https://doi.org/10.1002/CBDV.201000250
5-(2-methylprop-2-enylidene)-3-[(5R,9R,10R,13S,14S,17R)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]furan-2-one 162874984 Click to see 448.60 unknown https://doi.org/10.1002/CBDV.201000250
6-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylheptane-2,3,4-triol 13967180 Click to see CC(CC(C(C(C)(C)O)O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 476.70 unknown https://doi.org/10.1002/MRC.2768
Amooranin 11503749 Click to see 470.70 unknown https://doi.org/10.1002/PTR.803
Piscidinol A 12004524 Click to see 474.70 unknown https://doi.org/10.1002/MRC.2768
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(1R,2R,3S,8R,10R,11R,15R,16S)-3-acetyloxy-15-(furan-3-yl)-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-en-10-yl] acetate 162965991 Click to see CC(=O)OC1CC2C(OC(=O)CC(C2(C3C1(C4=CCC(C4(CC3)C)C5=COC=C5)C)C)OC(=O)C)(C)C 512.60 unknown https://doi.org/10.1016/S0031-9422(99)00157-0
[(1R,2R,4S,7S,8R,9R,10R,12S,16S,21R)-7-(furan-3-yl)-4-hydroxy-1,8,16-trimethyl-3-methylidene-5,14,19-trioxo-11,15,18-trioxapentacyclo[10.9.0.02,10.04,8.016,21]henicosan-9-yl] 3-methylbutanoate 100938103 Click to see CC(C)CC(=O)OC1C2C(C(=C)C3(C1(C(CC3=O)C4=COC=C4)C)O)C5(C6CC(=O)OCC6(OC(=O)CC5O2)C)C 570.60 unknown https://doi.org/10.1016/S0031-9422(99)00157-0
[(1S,2R,4R,5R,6S,8R,10S,11S,12R,14R,15R,16R,19S,21R)-6-(furan-3-yl)-4,12,16,19-tetrahydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.01,14.02,11.05,10.08,10]henicosan-21-yl] acetate 92029156 Click to see 532.60 unknown https://doi.org/10.1007/BF01949897
[(1S,3S,7S,12R,13R,14R,15R,16R,17R,18S)-18-(furan-3-yl)-15-hydroxy-7,13,17-trimethyl-21-methylidene-5,10,20-trioxo-2,6,9-trioxapentacyclo[12.6.1.01,17.03,13.07,12]henicosan-16-yl] 3-methylbutanoate 100938101 Click to see 570.60 unknown https://doi.org/10.1016/S0031-9422(99)00157-0
[(2R,11R)-3-acetyloxy-15-(furan-3-yl)-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-en-10-yl] acetate 374817 Click to see 512.60 unknown https://doi.org/10.1016/S0031-9422(99)00157-0
[(3S,3aR,4R,5R,6R,7aS)-6-[(4S,5R,5aR,9aS)-4-acetyloxy-5,9a-dimethyl-2,7-dioxo-4,5a,6,9-tetrahydro-3H-pyrano[3,4-b]oxepin-5-yl]-5-formyloxy-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-1-oxo-3,4,5,6-tetrahydro-2H-inden-4-yl] 3-methylbutanoate 101835632 Click to see CC(C)CC(=O)OC1C(C(C(=C)C2(C1(C(CC2=O)C3=COC=C3)C)O)C4(C5CC(=O)OCC5(OC(=O)CC4OC(=O)C)C)C)OC=O 658.70 unknown https://doi.org/10.1021/NP50041A029
https://doi.org/10.1021/NP50021A010
2-[(2S,3R,4R,5R)-4-[(1S,3aS,5R,6R,7R,7aR)-6-formyloxy-1-(furan-3-yl)-3a-hydroxy-7-[(2S,3S)-2-hydroxy-3-methylpentanoyl]oxy-7a-methyl-4-methylidene-3-oxo-2,5,6,7-tetrahydro-1H-inden-5-yl]-5-acetyloxy-2-(hydroxymethyl)-2,4-dimethyl-7-oxooxepan-3-yl]acetic acid 50994860 Click to see 706.70 unknown https://doi.org/10.1021/OL102745H
2-[5-acetyloxy-4-[6-formyloxy-1-(furan-3-yl)-3a-hydroxy-7-(2-hydroxy-3-methylpentanoyl)oxy-7a-methyl-4-methylidene-3-oxo-2,5,6,7-tetrahydro-1H-inden-5-yl]-2-(hydroxymethyl)-2,4-dimethyl-7-oxooxepan-3-yl]acetic acid 75597911 Click to see CCC(C)C(C(=O)OC1C(C(C(=C)C2(C1(C(CC2=O)C3=COC=C3)C)O)C4(C(CC(=O)OC(C4CC(=O)O)(C)CO)OC(=O)C)C)OC=O)O 706.70 unknown https://doi.org/10.1021/OL102745H
Amoorastatone 44575784 Click to see 516.60 unknown https://doi.org/10.1007/BF01949897
Rohitukin 99982 Click to see 658.70 unknown https://doi.org/10.1021/NP50041A029
https://doi.org/10.1021/NP50021A010
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Ergosta-4,6,8(14),22-tetraen-3-one 6441416 Click to see CC(C)C(C)C=CC(C)C1CCC2=C3C=CC4=CC(=O)CCC4(C3CCC12C)C 392.60 unknown https://doi.org/10.1007/S11418-006-0047-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-alpha-hydroxysteroids
(4R)-2-hydroxy-4-[(3R,5R,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]cyclopent-2-en-1-one 57387536 Click to see 412.60 unknown https://doi.org/10.1016/J.TETLET.2012.05.134
(4S)-2-hydroxy-4-[(3R,5R,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]cyclopent-2-en-1-one 57387535 Click to see 412.60 unknown https://doi.org/10.1016/J.TETLET.2012.05.134
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(5R,9R,10R,13S,14S,17S)-17-[(E)-3-[(2R)-3,3-dimethyloxiran-2-yl]-3-oxoprop-1-enyl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 51042539 Click to see 438.60 unknown https://doi.org/10.1248/CPB.59.282
17-[3-(3,3-Dimethyloxiran-2-yl)-3-oxoprop-1-enyl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 75605175 Click to see CC1(C2CC=C3C(C2(CCC1=O)C)CCC4(C3(CCC4C=CC(=O)C5C(O5)(C)C)C)C)C 438.60 unknown https://doi.org/10.1248/CPB.59.282
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
1-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)ethanone 75605177 Click to see 358.60 unknown https://doi.org/10.1248/CPB.59.282
1-[(3R,5R,9R,10R,13S,14S,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone 51042541 Click to see 358.60 unknown https://doi.org/10.1248/CPB.59.282
17-Acetyl-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 75605178 Click to see 356.50 unknown https://doi.org/10.1248/CPB.59.282
Dysolenticin G 51042542 Click to see 356.50 unknown https://doi.org/10.1248/CPB.59.282
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(4S,5R)-4-[(3R,5R,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-5-methoxyoxolan-2-one 102263759 Click to see CC1(C(CCC2(C1CC=C3C2CCC4(C3(CCC4C5CC(=O)OC5OC)C)C)C)O)C 430.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.017
(4S,5R)-5-ethoxy-4-[(5R,9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]oxolan-2-one 102263761 Click to see 442.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.017
(4S,5S)-4-[(3R,5R,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-5-methoxyoxolan-2-one 102263758 Click to see 430.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.017
(4S,5S)-5-methoxy-4-[(5R,9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]oxolan-2-one 102263762 Click to see 428.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.017
(4S)-4-[(5R,9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-5,6,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-17-yl]oxolan-2-one 162898059 Click to see 396.60 unknown https://doi.org/10.1248/CPB.59.282
3-Hydroxy-24,25,26,27-Tetranortirucall-7-Ene-23(21)-Lactone 70698056 Click to see 400.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.017
3-Oxo-21|A-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone 102263760 Click to see 428.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.017
3-Oxo-24,25,26,27-tetranortirucall-7-en-23,21-olide 70698071 Click to see 398.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.017
4-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)oxolan-2-one 73163950 Click to see 400.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.017
4-(4,4,10,13,14-Pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)oxolan-2-one 14830847 Click to see 398.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.017
4-(4,4,10,13,14-Pentamethyl-3-oxo-5,6,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-17-yl)oxolan-2-one 75605176 Click to see CC1(C2CC=C3C(C2(C=CC1=O)C)CCC4(C3(CCC4C5CC(=O)OC5)C)C)C 396.60 unknown https://doi.org/10.1248/CPB.59.282
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1007/S11418-006-0047-1
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
(1aR,3R,3aR,4R,5R,6R,7aR)-6-[(2S,3R,4R)-2-(acetyloxymethyl)-3-(2-methoxy-2-oxoethyl)-2,4-dimethyl-7-oxo-3H-oxepin-4-yl]-3-(furan-3-yl)-4-[(2R,3R)-2-hydroxy-3-methylpentanoyl]oxy-7-methylidene-2,3,3a,4,5,6-hexahydro-1aH-indeno[1,7a-b]oxirene-5-carboxylic acid 162887559 Click to see CCC(C)C(C(=O)OC1C(C(C(=C)C23C1C(CC2O3)C4=COC=C4)C5(C=CC(=O)OC(C5CC(=O)OC)(C)COC(=O)C)C)C(=O)O)O 672.70 unknown https://doi.org/10.1248/CPB.59.282
[(1S,3aR,4R,5R,7aS)-6-[(5R,9aS)-5,9a-dimethyl-2,7-dioxo-6,9-dihydro-5aH-pyrano[3,4-b]oxepin-5-yl]-1-acetyloxy-5-formyloxy-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-1,2,3,4,5,6-hexahydroinden-4-yl] 2-hydroxy-3-methylpentanoate 5458704 Click to see 672.70 unknown https://doi.org/10.1021/NP50041A029
https://doi.org/10.1016/S0031-9422(99)00157-0
[(1S,3S,3aR,4R,5R,6R,7aS)-6-[(5R,5aR,9aS)-5,9a-dimethyl-2,7-dioxo-6,9-dihydro-5aH-pyrano[3,4-b]oxepin-5-yl]-1-acetyloxy-5-formyloxy-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-1,2,3,4,5,6-hexahydroinden-4-yl] 2-hydroxy-3-methylpentanoate 102274900 Click to see CCC(C)C(C(=O)OC1C(C(C(=C)C2(C1(C(CC2OC(=O)C)C3=COC=C3)C)O)C4(C=CC(=O)OC5(C4CC(=O)OC5)C)C)OC=O)O 672.70 unknown https://doi.org/10.1016/S0031-9422(99)00157-0
https://doi.org/10.1021/NP50041A029
6-[2-(acetyloxymethyl)-3-(2-methoxy-2-oxoethyl)-2,4-dimethyl-7-oxo-3H-oxepin-4-yl]-3-(furan-3-yl)-4-(2-hydroxy-3-methylpentanoyl)oxy-7-methylidene-2,3,3a,4,5,6-hexahydro-1aH-indeno[1,7a-b]oxirene-5-carboxylic acid 162887558 Click to see CCC(C)C(C(=O)OC1C(C(C(=C)C23C1C(CC2O3)C4=COC=C4)C5(C=CC(=O)OC(C5CC(=O)OC)(C)COC(=O)C)C)C(=O)O)O 672.70 unknown https://doi.org/10.1248/CPB.59.282
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1R,2R,4S,5R,7S,8R,9R,10R,12S,16S,21R)-5-acetyloxy-7-(furan-3-yl)-4-hydroxy-1,8,16-trimethyl-3-methylidene-14,19-dioxo-11,15,18-trioxapentacyclo[10.9.0.02,10.04,8.016,21]henicosan-9-yl] 3-methylbutanoate 100938102 Click to see CC(C)CC(=O)OC1C2C(C(=C)C3(C1(C(CC3OC(=O)C)C4=COC=C4)C)O)C5(C6CC(=O)OCC6(OC(=O)CC5O2)C)C 614.70 unknown https://doi.org/10.1016/S0031-9422(99)00157-0
[(3S,3aR,4R,5R,6R,7aS)-6-[(1R,3S,7S,8R,9R,10S)-10-acetyloxy-1-hydroxy-3,9-dimethyl-6-oxo-2,5-dioxatricyclo[5.4.0.03,8]undecan-9-yl]-5-formyloxy-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-1-oxo-3,4,5,6-tetrahydro-2H-inden-4-yl] (2S,3S)-2-hydroxy-3-methylpentanoate 50994859 Click to see CCC(C)C(C(=O)OC1C(C(C(=C)C2(C1(C(CC2=O)C3=COC=C3)C)O)C4(C(CC5(C6C4C(O5)(COC6=O)C)O)OC(=O)C)C)OC=O)O 688.70 unknown https://doi.org/10.1021/OL102745H
[6-(10-acetyloxy-1-hydroxy-3,9-dimethyl-6-oxo-2,5-dioxatricyclo[5.4.0.03,8]undecan-9-yl)-5-formyloxy-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-1-oxo-3,4,5,6-tetrahydro-2H-inden-4-yl] 2-hydroxy-3-methylpentanoate 75597910 Click to see 688.70 unknown https://doi.org/10.1021/OL102745H
> Organoheterocyclic compounds / Dioxepanes / 1,4-dioxepanes
Dihydroamoorinin 15508011 Click to see 472.60 unknown https://doi.org/10.1007/S11418-006-0047-1
methyl 2-[(1R,6R)-6-[(1aS,4S,4aS,7S,8aS)-4-(furan-3-yl)-4a-methyl-8-methylidene-2-oxo-4,5,6,7-tetrahydro-1aH-oxireno[2,3-d]isochromen-7-yl]-2,2,6-trimethyl-3-oxocyclohexyl]acetate 163193241 Click to see 470.60 unknown https://doi.org/10.1016/S0040-4020(01)92762-0
methyl 2-[(1S,6R)-6-[(1aS,4S,4aS,7R,8aS)-4-(furan-3-yl)-4a-methyl-8-methylidene-2-oxo-4,5,6,7-tetrahydro-1aH-oxireno[2,3-d]isochromen-7-yl]-2,2,6-trimethyl-3-oxocyclohexyl]acetate 162935149 Click to see 470.60 unknown https://doi.org/10.1016/S0040-4020(01)92762-0
methyl 2-[6-[4-(furan-3-yl)-4a-methyl-8-methylidene-2-oxo-4,5,6,7-tetrahydro-1aH-oxireno[2,3-d]isochromen-7-yl]-2,2,6-trimethyl-3-oxocyclohexyl]acetate 71436691 Click to see 470.60 unknown https://doi.org/10.1016/S0040-4020(01)92762-0
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(2R)-2-[(E,3S,6R)-6-(5,5-dimethyl-4-oxofuran-2-yl)-3-hydroxy-2-methylhept-1-enyl]-4-methyl-2,3-dihydropyran-6-one 71726329 Click to see 348.40 unknown https://doi.org/10.1021/NP400126Q
(2S)-2-[(E,3S,6R)-6-(5,5-dimethyl-4-oxofuran-2-yl)-3-hydroxy-2-methylhept-1-enyl]-4-methyl-2,3-dihydropyran-6-one 71726328 Click to see 348.40 unknown https://doi.org/10.1021/NP400126Q
CID 124222284 124222284 Click to see 332.40 unknown https://doi.org/10.1021/NP400126Q
Nemoralisin 73354988 Click to see 332.40 unknown https://doi.org/10.1021/NP400126Q
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
Grandiamide D 23655943 Click to see 332.40 unknown https://doi.org/10.1021/NP070184W

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