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Sandoricum koetjape

Sandoricum koetjape - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Sandoricum koetjape - 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 UUID64400511c26ca149889454
Scientific name Sandoricum koetjape
Authority Merr.
First published in Philipp. J. Sci., C 7: 237 (1912)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Melia koetjape Burm.f. Fl. Indica : 101 (1768)
Trichilia venosa Spreng. Syst. Veg. 3: 68 (1826)
Trichilia nervosa Vahl Symb. Bot. 1: 31 (1790)
Sandoricum indicum Cav. Diss. 7: 359 (1788)
Sandoricum harmsianum Perkins Fragm. Pl. Filip. : 31 (1851)
Sandoricum harmandii Pierre Fl. Forest. Cochinch. : t. 353B (1897)
Sandoricum glaberrimum Hassk. Retzia 1: 145 (1855)
Sandoricum maingayi Hiern Fl. Brit. India 1: 554 (1875)
Sandoricum vidalii Merr. Publ. Bur. Sci. Gov. Lab. 6: 8 (1904)
Sandoricum venosum M.Roem. Fam. Nat. Syn. Monogr. 1: 109 (1846)
Sandoricum ternatum Blanco Fl. Filip. : 346 (1837)
Sandoricum serratum G.Don Gen. Hist. 1: 680 (1831)
Sandoricum radiatum King J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 64: 21 (1895)
Sandoricum nervosum Blume Bijdr. Fl. Ned. Ind. : 163 (1825)
Azedarach edule Noronha Verh. Batav. Genootsch. Kunst. 5(Art. 4): 5. 1790

Common names Top

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Language Common/alternative name
English santol
ace seutui (boh kayèe)
ban sentul
bcl santol
Bulgarian сантол
bjn katapi
Catalan santol
German santol
French santol
Indonesian kecapi
ilo santol
Japanese サントウ
Japanese センダン科の植物
jv kecapi
Khmer បំពេញរាជ្យ
koi Сантол
kv Сантол
lbe Сантол
mad sentol
Malayalam സാന്റോൾ
Malayalam santol
mrj Сантол
Malay pokok sentul
Burmese သစ်တို
Dutch santol
Dutch ketjapi
pam santul
Polish santol
Portuguese santol
Russian Сантол
su sentul
Thai กระท้อน
Thai กระท้อนพันธุ์อีล่า
udm Сантол
war santol
Chinese 仙都果
Chinese 山陀兒
Chinese 山陀儿
Chinese 山道楝

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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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-tropical
    • Indian Subcontinent
      • 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
      • New Guinea
  • Southern America
    • Caribbean
      • Puerto Rico
      • Windward Islands
    • Central America
      • El Salvador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000504875
UNII 6N9QW56357
USDA Plants SAKO4
Tropicos 20400410
INPN 706771
KEW urn:lsid:ipni.org:names:579210-1
The Plant List kew-2601089
Open Tree Of Life 594342
NCBI Taxonomy 356285
IUCN Red List 61803664
IPNI 579210-1
iNaturalist 181340
GBIF 3850843
Freebase /m/0fj1j7
EPPO SNOKO
EOL 6955155
USDA GRIN 33013
Wikipedia Sandoricum_koetjape
CMAUP NPO15299

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 Metagenomic Survey of Wood Decay Fungi in the Urban Trees of Singapore Hong Y, Tan JY, Xue H, Chow ML, Ali M, Ng A, Leong A, Yeo J, Koh SM, Tang MS, Lee YY, Choong AM, Lee SM, Delli Ponti R, Chan PM, Lee D, Wong JY, Mutwil M, Fong YK J Fungi (Basel) 10-Apr-2023
PMCID:PMC10145048
doi:10.3390/jof9040460
PMID:37108914
Dual determination of nitrite and iron by a single greener sequential injection spectrophotometric system employing a simple single aqueous extract from Areca catechu Linn. serving as a natural reagent Ponhong K, Siriangkhawut W, Lee CY, Teshima N, Grudpan K, Supharoek SA RSC Adv 11-Jul-2022
PMCID:PMC9272472
doi:10.1039/d2ra03870f
PMID:35919603
Mapping Risk of Nipah Virus Transmission from Bats to Humans in Thailand Chaiyes A, Duengkae P, Suksavate W, Pongpattananurak N, Wacharapluesadee S, Olival KJ, Srikulnath K, Pattanakiat S, Hemachudha T Ecohealth 03-Jun-2022
PMCID:PMC10116436
doi:10.1007/s10393-022-01588-6
PMID:35657574
Ethnomedicinal Plants in Herbal Remedies Used for Treatment of Skin Diseases by Traditional Healers in Songkhla Province, Thailand Saising J, Maneenoon K, Sakulkeo O, Limsuwan S, Götz F, Voravuthikunchai SP Plants (Basel) 25-Mar-2022
PMCID:PMC9003147
doi:10.3390/plants11070880
PMID:35406860
Cervical anticancer activities of Annona squamosa Linn. leaf isolate Swantara MD, Rita WS, Dira MA, Karang Agustina K Vet World 24-Jan-2022
PMCID:PMC8924393
doi:10.14202/vetworld.2022.124-131
PMID:35369588
A Review of Franklinothrips vespiformis (Thysanoptera: Aeolothripidae): Life History, Distribution, and Prospects as a Biological Control Agent Hussain M, Wang Z, Arthurs SP, Gao J, Ye F, Chen L, Mao R Insects 18-Jan-2022
PMCID:PMC8879288
doi:10.3390/insects13020108
PMID:35206682
Ethnobotanical Documentation of Medicinal Plants Used by the Indigenous Panay Bukidnon in Lambunao, Iloilo, Philippines Cordero CS, Meve U, Alejandro GJ Front Pharmacol 10-Jan-2022
PMCID:PMC8784692
doi:10.3389/fphar.2021.790567
PMID:35082673
Putative Anticancer Compounds from Plant-Derived Endophytic Fungi: A Review Hridoy M, Gorapi MZ, Noor S, Chowdhury NS, Rahman MM, Muscari I, Masia F, Adorisio S, Delfino DV, Mazid MA Molecules 04-Jan-2022
PMCID:PMC8746379
doi:10.3390/molecules27010296
PMID:35011527
Gut Microbiota as Potential Biomarker and/or Therapeutic Target to Improve the Management of Cancer: Focus on Colibactin-Producing Escherichia coli in Colorectal Cancer Veziant J, Villéger R, Barnich N, Bonnet M Cancers (Basel) 05-May-2021
PMCID:PMC8124679
doi:10.3390/cancers13092215
PMID:34063108
Seedling diversity in actively and passively restored tropical forest understories Wills J, Herbohn J, Wells J, Maranguit Moreno MO, Ferraren A, Firn J Ecol Appl 01-Mar-2021
PMCID:PMC8047924
doi:10.1002/eap.2286
PMID:33421244
Oligosaccharides increase the genotoxic effect of colibactin produced by pks+ Escherichia coli strains Oliero M, Calvé A, Fragoso G, Cuisiniere T, Hajjar R, Dobrindt U, Santos MM BMC Cancer 17-Feb-2021
PMCID:PMC7890614
doi:10.1186/s12885-021-07876-8
PMID:33596864
Wild food plants and fungi sold in the markets of Luang Prabang, Lao PDR Łuczaj Ł, Lamxay V, Tongchan K, Xayphakatsa K, Phimmakong K, Radavanh S, Kanyasone V, Pietras M, Karbarz M J Ethnobiol Ethnomed 26-Jan-2021
PMCID:PMC7835671
doi:10.1186/s13002-020-00423-y
PMID:33499871
Natural Compounds in Sex Hormone-Dependent Cancers: The Role of Triterpenes as Therapeutic Agents Şoica C, Voicu M, Ghiulai R, Dehelean C, Racoviceanu R, Trandafirescu C, Roșca OJ, Nistor G, Mioc M, Mioc A Front Endocrinol (Lausanne) 21-Jan-2021
PMCID:PMC7859451
doi:10.3389/fendo.2020.612396
PMID:33552000
Total Vitamin C, Ascorbic Acid, Dehydroascorbic Acid, Antioxidant Properties, and Iron Content of Underutilized and Commonly Consumed Fruits in Sri Lanka Abeysuriya HI, Bulugahapitiya VP, Loku Pulukkuttige J Int J Food Sci 20-Aug-2020
PMCID:PMC7474787
doi:10.1155/2020/4783029
PMID:32908860
Quantitative ethnopharmacological documentation and molecular confirmation of medicinal plants used by the Manobo tribe of Agusan del Sur, Philippines Dapar ML, Alejandro GJ, Meve U, Liede-Schumann S J Ethnobiol Ethnomed 05-Mar-2020
PMCID:PMC7227330
doi:10.1186/s13002-020-00363-7
PMID:32138749

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
> Alkaloids and derivatives / Aporphines
(+)-1,2-Methylenedioxy-5,6,6aalpha,7-tetrahydro-4H-dibenzo[de,g]quinoline 26202781 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown via CMAUP database
(R)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo(de,g)quinoline 1078819 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown via CMAUP database
1-[(12R)-16-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-11-yl]ethanone 10246449 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5)OC)OCO3 337.40 unknown via CMAUP database
7H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline-7-carboxaldehyde,5,6,7a,8-tetrahydro-, (7aR)- 158516 Click to see C1CN(C2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5)C=O 293.30 unknown via CMAUP database
Anonaine 160597 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown via CMAUP database
Lanuginosine 97622 Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O 305.30 unknown via CMAUP database
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown via CMAUP database
N-acetylanonaine 6453733 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 307.30 unknown via CMAUP database
Roemerine 119204 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown via CMAUP database
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
(12R,13S)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaen-13-ol 15560530 Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O 281.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
[1,1'-Biphenyl]-4-ol, 2'-methoxy-3,5'-di-2-propenyl- 11857938 Click to see COC1=C(C=C(C=C1)CC=C)C2=CC(=C(C=C2)O)CC=C 280.40 unknown via CMAUP database
4-O-Methylhonokiol 155160 Click to see COC1=C(C=C(C=C1)C2=C(C=CC(=C2)CC=C)O)CC=C 280.40 unknown via CMAUP database
Caryolanemagnolol 21726647 Click to see CC1(CC2C1CCC3(CC2(CCC3O)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C)C 486.70 unknown via CMAUP database
Honokiol 72303 Click to see C=CCC1=CC(=C(C=C1)O)C2=CC(=C(C=C2)O)CC=C 266.30 unknown via CMAUP database
Magnaldehyde E 5319190 Click to see C=CCC1=C(C=CC(=C1)C2=C(C=CC(=C2)C=O)O)O 254.28 unknown via CMAUP database
Magnolol 72300 Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC=C)O 266.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
2,3,4-Trihydroxy-5-(4-prop-2-enylphenoxy)benzaldehyde 71812224 Click to see C=CCC1=CC=C(C=C1)OC2=C(C(=C(C(=C2)C=O)O)O)O 286.28 unknown via CMAUP database
3-[3,4-Dihydroxy-5-(4-prop-2-enylphenoxy)phenyl]prop-2-enal 134367 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O 296.30 unknown via CMAUP database
3,4-Dihydroxy-5-(4-prop-2-enylphenoxy)benzaldehyde 23259953 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=O 270.28 unknown via CMAUP database
5-[(E)-3-methoxyprop-1-enyl]-3-(4-prop-2-enylphenoxy)benzene-1,2-diol 71812222 Click to see COCC=CC1=CC(=C(C(=C1)OC2=CC=C(C=C2)CC=C)O)O 312.40 unknown via CMAUP database
Obovatal 6439677 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O 296.30 unknown via CMAUP database
Obovatol 100771 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)CC=C 282.30 unknown via CMAUP database
Phenol, 2-[3-hydroxy-4-(2-propenyl)phenoxy]-5-(2-propenyl)- 10016628 Click to see C=CCC1=CC(=C(C=C1)OC2=CC(=C(C=C2)CC=C)O)O 282.30 unknown via CMAUP database
Phenol, 4-(2-propenyl)-2-(4-(2-propenyl)phenoxy)- 159137 Click to see C=CCC1=CC=C(C=C1)OC2=C(C=CC(=C2)CC=C)O 266.30 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Allylphenol 68148 Click to see C=CCC1=CC=C(C=C1)O 134.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1021/NP50083A016
Cadalene 10225 Click to see CC1=CC2=C(C=CC(=C2C=C1)C)C(C)C 198.30 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Clovanemagnolol 10323149 Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C 486.70 unknown via CMAUP database
Isocaryophyllene oxide 1742211 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1021/NP50083A016
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-Alloaromadendrene 10899740 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1021/NP50083A016
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1021/NP50083A016
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
[2R-cis]-1,2,3,4,4a,5,6,7-Octahydro-alpha,alpha,4a,8-tetramethyl-2-naphthalenemethanol 91730386 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown via CMAUP database
2-[(2R,4aS,8aR)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-ol 118976561 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown via CMAUP database
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown via CMAUP database
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown via CMAUP database
Eudeshonokiol A 14587421 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)C4=C(C=CC(=C4)CC=C)O)CC=C 488.70 unknown via CMAUP database
Eudeshonokiol B 21726646 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)CC=C)C4=CC(=C(C=C4)O)CC=C 488.70 unknown via CMAUP database
Eudesmagnolol 14587417 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)CC=C)C4=C(C=CC(=C4)CC=C)O 488.70 unknown via CMAUP database
Eudesobovatol A 442837 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=CC(=CC(=C3O)OC4=CC=C(C=C4)CC=C)CC=C 504.70 unknown via CMAUP database
Eudesobovatol B 10346031 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3OC4=CC=C(C=C4)CC=C)CC=C)O 504.70 unknown via CMAUP database
gamma-EUDESMOL 6432005 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown via CMAUP database
Proximadiol 165258 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O 240.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
10-Hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid 495454 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 456.70 unknown https://doi.org/10.1078/0944-7113-00339
https://doi.org/10.1021/NP010196W
https://doi.org/10.1021/NP990104R
https://doi.org/10.1248/BPB.26.1351
https://doi.org/10.1039/JR9600004738
https://doi.org/10.1021/NP50083A016
14,14b-Dihydroxy-2,4a,6a,9,9,12a,14a-heptamethyl-10-oxo-1,3,4,5,6,6a,8,8a,11,12,13,14-dodecahydropicene-2-carboxylic acid 85110087 Click to see CC1(C2CC=C3C(C2(CCC1=O)C)CC(C4(C3(CCC5(C4(CC(CC5)(C)C(=O)O)O)C)C)C)O)C 486.70 unknown https://doi.org/10.1021/NP010196W
2,4a,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-2-carboxylic acid 495453 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 454.70 unknown https://doi.org/10.1021/NP50083A016
https://doi.org/10.1078/0944-7113-00339
https://doi.org/10.1248/BPB.26.1351
https://doi.org/10.1021/NP990104R
https://doi.org/10.1021/NP010196W
3-(Hydroxyimino)oleana-12-ene-29-oic acid 44566380 Click to see CC1(C2CCC3(C(C2(CCC1=NO)C)CC=C4C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 469.70 unknown https://doi.org/10.1021/NP990104R
3-Benzyloximo-olean-12-en-29-oic acid 44566378 Click to see CC1(C2CCC3(C(C2(CCC1=NOCC4=CC=CC=C4)C)CC=C5C3(CCC6(C5CC(CC6)(C)C(=O)O)C)C)C)C 559.80 unknown https://doi.org/10.1021/NP990104R
3-Epikatonic acid 10434225 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 456.70 unknown https://doi.org/10.1021/NP010196W
3-Methyloximo-olean-12-en-29-oic acid 44566379 Click to see CC1(C2CCC3(C(C2(CCC1=NOC)C)CC=C4C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 483.70 unknown https://doi.org/10.1021/NP990104R
3-Oxooleana-12-ene-29-oic acid methyl ester 14707316 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C 468.70 unknown via CMAUP database
Katonic acid 9804114 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 456.70 unknown https://doi.org/10.1078/0944-7113-00339
https://doi.org/10.1021/NP010196W
https://doi.org/10.1021/NP990104R
https://doi.org/10.1248/BPB.26.1351
https://doi.org/10.1039/JR9600004738
https://doi.org/10.1021/NP50083A016
Katononic acid 9981416 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 454.70 unknown https://doi.org/10.1021/NP50083A016
https://doi.org/10.1248/BPB.26.1351
https://doi.org/10.1078/0944-7113-00339
https://doi.org/10.1021/NP990104R
https://doi.org/10.1021/NP010196W
Sandorinic acid B 10323148 Click to see CC1(C2CC=C3C(C2(CCC1=O)C)CC(C4(C3(CCC5(C4(CC(CC5)(C)C(=O)O)O)C)C)C)O)C 486.70 unknown https://doi.org/10.1021/NP010196W
> Lipids and lipid-like molecules / Steroids and steroid derivatives
methyl (3R,4aR,4bS,6aR,7S,8S,10bS,12aS)-7-(3-methoxy-3-oxopropyl)-3,4b,7,10b,12a-pentamethyl-8-prop-1-en-2-yl-2,4,4a,5,6,6a,8,9,11,12-decahydro-1H-chrysene-3-carboxylate 163029136 Click to see CC(=C)C1CC=C2C(C1(C)CCC(=O)OC)CCC3(C2(CCC4(C3CC(CC4)(C)C(=O)OC)C)C)C 498.70 unknown https://doi.org/10.1016/0031-9422(94)E0242-K
methyl (3R,4aR,4bS,7S,8S,10bS,12aS)-7-(3-methoxy-3-oxopropyl)-3,4b,7,10b,12a-pentamethyl-8-prop-1-en-2-yl-2,4,4a,5,6,8,9,10,11,12-decahydro-1H-chrysene-3-carboxylate 162982949 Click to see CC(=C)C1CCC2=C(C1(C)CCC(=O)OC)CCC3(C2(CCC4(C3CC(CC4)(C)C(=O)OC)C)C)C 498.70 unknown https://doi.org/10.1016/0031-9422(94)E0242-K
methyl 7-(3-methoxy-3-oxopropyl)-3,4b,7,10b,12a-pentamethyl-8-prop-1-en-2-yl-2,4,4a,5,6,6a,8,9,11,12-decahydro-1H-chrysene-3-carboxylate 163029135 Click to see CC(=C)C1CC=C2C(C1(C)CCC(=O)OC)CCC3(C2(CCC4(C3CC(CC4)(C)C(=O)OC)C)C)C 498.70 unknown https://doi.org/10.1016/0031-9422(94)E0242-K
methyl 7-(3-methoxy-3-oxopropyl)-3,4b,7,10b,12a-pentamethyl-8-prop-1-en-2-yl-2,4,4a,5,6,8,9,10,11,12-decahydro-1H-chrysene-3-carboxylate 162982948 Click to see CC(=C)C1CCC2=C(C1(C)CCC(=O)OC)CCC3(C2(CCC4(C3CC(CC4)(C)C(=O)OC)C)C)C 498.70 unknown https://doi.org/10.1016/0031-9422(94)E0242-K
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 19-oxosteroids
Sentulic acid 70683988 Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CC=C3C2(CCC4(C3CC(CC4)(C)C)C)C(=O)O)C 470.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids
(3S,4aR,6aR,7R,8S,10aR,10bS,12aS)-7-(2-carboxyethyl)-3,7,10a,10b,12a-pentamethyl-8-prop-1-en-2-yl-2,4,4a,6,6a,8,9,10,11,12-decahydro-1H-chrysene-3-carboxylic acid 157217432 Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CC=C3C2(CCC4(C3CC(CC4)(C)C(=O)O)C)C)C 470.70 unknown https://doi.org/10.1021/NP010196W
20-Epikoetjapic acid 10790564 Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CC=C3C2(CCC4(C3CC(CC4)(C)C(=O)O)C)C)C 470.70 unknown https://doi.org/10.1021/NP010196W
https://doi.org/10.1021/NP990104R
7-(2-carboxyethyl)-3,7,10a,10b,12a-pentamethyl-8-prop-1-en-2-yl-2,4,4a,6,6a,8,9,10,11,12-decahydro-1H-chrysene-3-carboxylic acid 73197058 Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CC=C3C2(CCC4(C3CC(CC4)(C)C(=O)O)C)C)C 470.70 unknown https://doi.org/10.1248/BPB.26.1351
https://doi.org/10.1021/NP990104R
https://doi.org/10.1021/NP010196W
Koetjapic acid 15513441 Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CC=C3C2(CCC4(C3CC(CC4)(C)C(=O)O)C)C)C 470.70 unknown https://doi.org/10.1021/NP50083A016
https://doi.org/10.1248/BPB.26.1351
https://doi.org/10.1078/0944-7113-00339
https://doi.org/10.1021/NP990104R
https://doi.org/10.1021/NP010196W
Secobryononic acid 78101312 Click to see CC(=C)C1CCC2=C(C1(C)CCC(=O)O)CCC3(C2(CCC4(C3CC(CC4)(C)C(=O)O)C)C)C 470.70 unknown https://doi.org/10.1016/0031-9422(94)E0242-K
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1078/0944-7113-00339
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1078/0944-7113-00339
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 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 via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Lincomycin B 3081983 Click to see CCC1CC(N(C1)C)C(=O)NC(C2C(C(C(C(O2)SC)O)O)O)C(C)O 392.50 unknown https://doi.org/10.1021/NP010196W
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1S,3R,4R,5R,7S,8R,10R,11S,12S,13S,16S)-5,16-diacetyloxy-13-(furan-3-yl)-11-hydroxy-7-(2-methoxy-2-oxoethyl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.01,12.03,8]heptadecan-4-yl] (2R)-2-methylbutanoate 163194114 Click to see CCC(C)C(=O)OC1C2C(C(C(C1OC(=O)C)(C)C)CC(=O)OC)(C(=O)C3C(C4(C(OC(=O)C(C4(C3=C)O2)OC(=O)C)C5=COC=C5)C)O)C 702.70 unknown https://doi.org/10.1016/S0031-9422(03)00500-4
[5,16-Diacetyloxy-13-(furan-3-yl)-11-hydroxy-7-(2-methoxy-2-oxoethyl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.01,12.03,8]heptadecan-4-yl] 2-methylbutanoate 163074053 Click to see CCC(C)C(=O)OC1C2C(C(C(C1OC(=O)C)(C)C)CC(=O)OC)(C(=O)C3C(C4(C(OC(=O)C(C4(C3=C)O2)OC(=O)C)C5=COC=C5)C)O)C 702.70 unknown https://doi.org/10.1016/S0031-9422(03)00500-4
[5,16-Diacetyloxy-13-(furan-3-yl)-11-hydroxy-7-(2-methoxy-2-oxoethyl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.01,12.03,8]heptadecan-4-yl] 2-methylpropanoate 163027414 Click to see CC(C)C(=O)OC1C2C(C(C(C1OC(=O)C)(C)C)CC(=O)OC)(C(=O)C3C(C4(C(OC(=O)C(C4(C3=C)O2)OC(=O)C)C5=COC=C5)C)O)C 688.70 unknown https://doi.org/10.1016/S0031-9422(03)00500-4
methyl 2-[(1S,3R,4R,5R,7S,8R,10R,11S,12S,13S,16S)-4,5,16-triacetyloxy-13-(furan-3-yl)-11-hydroxy-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.01,12.03,8]heptadecan-7-yl]acetate 101268501 Click to see CC(=O)OC1C2C(C(C(C1OC(=O)C)(C)C)CC(=O)OC)(C(=O)C3C(C4(C(OC(=O)C(C4(C3=C)O2)OC(=O)C)C5=COC=C5)C)O)C 660.70 unknown https://doi.org/10.1016/S0031-9422(03)00500-4
Methyl 2-[4,5,16-triacetyloxy-13-(furan-3-yl)-11-hydroxy-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.01,12.03,8]heptadecan-7-yl]acetate 163098326 Click to see CC(=O)OC1C2C(C(C(C1OC(=O)C)(C)C)CC(=O)OC)(C(=O)C3C(C4(C(OC(=O)C(C4(C3=C)O2)OC(=O)C)C5=COC=C5)C)O)C 660.70 unknown https://doi.org/10.1016/S0031-9422(03)00500-4
Sandrapin B 101268502 Click to see CCC(C)C(=O)OC1C2C(C(C(C1OC(=O)C)(C)C)CC(=O)OC)(C(=O)C3C(C4(C(OC(=O)C(C4(C3=C)O2)OC(=O)C)C5=COC=C5)C)O)C 702.70 unknown https://doi.org/10.1016/S0031-9422(03)00500-4
Sandrapin C 101268503 Click to see CC(C)C(=O)OC1C2C(C(C(C1OC(=O)C)(C)C)CC(=O)OC)(C(=O)C3C(C4(C(OC(=O)C(C4(C3=C)O2)OC(=O)C)C5=COC=C5)C)O)C 688.70 unknown https://doi.org/10.1016/S0031-9422(03)00500-4
Sandrapin D 101273497 Click to see CC=C(C)C(=O)OC1C2C(C(C(C1OC(=O)C)(C)C)CC(=O)OC)(C(=O)C3C(C4(C(OC(=O)C(C4(C3=C)O2)OC(=O)C)C5=COC=C5)C)O)C 700.70 unknown via CMAUP database
Sandrapin E 101273498 Click to see CC(=C)C(=O)OC1C2C(C(C(C1OC(=O)C)(C)C)CC(=O)OC)(C(=O)C3C(C4(C(OC(=O)C(C4(C3=C)O2)OC(=O)C)C5=COC=C5)C)O)C 686.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
6-Hydroxysandoricin 196858 Click to see CC(=O)OC1CC2C(=C)C3(C1(C(OC(=O)C3O)C4=COC=C4)C)OC5C2(C(C(C(C5)OC(=O)C)(C)C)C(C(=O)OC)O)C 604.60 unknown https://doi.org/10.1021/NP50073A025
Sandoricin 3825286 Click to see CC(=O)OC1CC2C(=C)C3(C1(C(OC(=O)C3O)C4=COC=C4)C)OC5C2(C(C(C(C5)OC(=O)C)(C)C)CC(=O)OC)C 588.60 unknown https://doi.org/10.1021/NP50073A025
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
10-Hydroxy-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,13,14,14b-tetradecahydropicene-2-carboxylic acid 500182 Click to see CC1(C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)86404-3
Bryonolic acid 472768 Click to see CC1(C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)86404-3
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
14-hydroxy-2,4a,6a,9,9,12a,14a-heptamethyl-10-oxo-3,4,5,6,7,8,8a,11,12,13,14,14b-dodecahydro-1H-picene-2-carboxylic acid 85380087 Click to see CC1(C2CCC3=C(C2(CCC1=O)C)CC(C4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)O)C 470.70 unknown https://doi.org/10.1021/NP010196W
Sandorinic acid C 11048975 Click to see CC1(C2CCC3=C(C2(CCC1=O)C)CC(C4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)O)C 470.70 unknown https://doi.org/10.1021/NP010196W
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Inositol 892 Click to see C1(C(C(C(C(C1O)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)86404-3
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2R,4aR,6aR,8aR,12aS,14R,14aS,14bS)-14,14b-dihydroxy-2,4a,6a,9,9,12a,14a-heptamethyl-10-oxo-1,3,4,5,6,7,8,8a,11,12,13,14-dodecahydropicene-2-carboxylic acid 163025339 Click to see CC1(C2CCC3=C(C2(CCC1=O)C)CC(C4(C3(CCC5(C4(CC(CC5)(C)C(=O)O)O)C)C)C)O)C 486.70 unknown https://doi.org/10.1021/NP010196W
14,14b-Dihydroxy-2,4a,6a,9,9,12a,14a-heptamethyl-10-oxo-1,3,4,5,6,7,8,8a,11,12,13,14-dodecahydropicene-2-carboxylic acid 85110086 Click to see CC1(C2CCC3=C(C2(CCC1=O)C)CC(C4(C3(CCC5(C4(CC(CC5)(C)C(=O)O)O)C)C)C)O)C 486.70 unknown https://doi.org/10.1021/NP010196W
Sandorinic acid A 10323147 Click to see CC1(C2CCC3=C(C2(CCC1=O)C)CC(C4(C3(CCC5(C4(CC(CC5)(C)C(=O)O)O)C)C)C)O)C 486.70 unknown https://doi.org/10.1021/NP010196W
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(2R,4aS,6aS,8aR,12aS,14aS,14bR)-2,4a,6a,9,9,12a,14a-heptamethyl-10-oxo-3,4,5,6,7,8,8a,11,12,13,14,14b-dodecahydro-1H-picene-2-carboxylic acid 15756414 Click to see CC1(C2CCC3=C(C2(CCC1=O)C)CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 454.70 unknown https://doi.org/10.1016/S0031-9422(00)86404-3
https://doi.org/10.1016/0031-9422(94)E0242-K
3-Oxo-8-multifloren-29-oic acid 131751810 Click to see CC1(C2CCC3=C(C2(CCC1=O)C)CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 454.70 unknown https://doi.org/10.1016/S0031-9422(00)86404-3
https://doi.org/10.1016/0031-9422(94)E0242-K
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
Magnolianin 9918938 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC3=C2OC(C(O3)C4=CC(=C(C(=C4)OC5=CC=C(C=C5)CC=C)O)O)COC6=C(C=C(C=C6)CC=C)C7=C(C=CC(=C7)CC=C)O)CC=C 827.00 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-7-ol 6093330 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C 314.40 unknown via CMAUP database
Magnocurarine 53266 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C 314.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 21629882 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 624.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumanolignan 24796112 Click to see C=CCC1=CC(=C(C=C1)O)C2=C3C(=CC(=C2)CC=C)C=CC(=O)O3 318.40 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
3-(3,4-dimethoxyphenyl)-7,8-dimethoxy-4H-chromen-4-one 638205 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC)OC)OC 342.30 unknown https://doi.org/10.1016/S0031-9422(00)86404-3

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