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Allium ampeloprasum

Allium ampeloprasum - Unknown
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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 UUID6440247a434da000231590
Scientific name Allium ampeloprasum
Authority L.
First published in Sp. Pl. : 294 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Porrum sativum Mill. Gard. Dict. ed. 8 : n.º 1 (1768)
Porrum amethystinum Rchb. Fl. Germ. Excurs. : 140(16) (1831)
Porrum ampeloprasum (L.) Mill. Gard. Dict. ed. 8 : n.º 2 (1768)
Porrum commune Rchb. Fl. Germ. Excurs. : 111 (1830)
Allium adscendens Kunth Enum. Pl. 4: 385 (1843)
Allium albescens Guss. Enum. Pl. Inarim. : 338 (1855)
Allium ampeloprasum var. babingtonii (Borrer) Syme Engl. Bot. ed. 3, 9: 204. 1869
Allium ampeloprasum var. bulbiferum Syme Engl. Bot. ed. 3, 9: 204. 1869
Allium ampeloprasum var. holmense Asch. & Graebn. Syn. Mitteleur. Fl. 3: 105. 1905
Allium ampeloprasum f. holmense (Asch. & Graebn.) Holmboe Veg. Cyp. 45 1914
Allium ampeloprasum subsp. leucanthum (K.Koch) K.Richt. Pl. Eur. 1: 201. 1890 (1890)
Allium ampeloprasum var. leucanthum (K.Koch) Ledeb. Fl. Ross. (Ledeb.) 4: 164. 1852
Allium ampeloprasum subsp. polyanthum (Schult. & Schult.f.) O.Bolòs, Vigo, Masalles & Ninot Fl. Man. Paísos Catalans : 1213 (1990)
Allium ampeloprasum subsp. porrum (L.) Hayek Repert. Spec. Nov. Regni Veg. Beih. 30(3): 39. 1932 (1932)
Allium ampeloprasum var. porrum (L.) J.Gay Ann. Sci. Nat., Bot. sér. 3, 8: 218. 1847
Allium ampeloprasum var. wiedemannii Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 3(2): 55. 1875
Allium ascendens Ten. Syll. Pl. Fl. Neapol. 164. 1831 [Jul-Aug 1831]
Allium babingtonii Borrer Engl. Bot. : t. 2906 (1849)
Allium bertoloni De Not. Repert. Fl. Ligust. : 414 (1844)
Allium byzantinum K.Koch Linnaea 22: 240 (1849)
Allium durieuanum Walp. Ann. Bot. Syst. 1: 860 (1849)
Allium gasparrinii Guss. Enum. Pl. Inarim. : 337 (1855)
Allium holmense Mill. ex Kunth Enum. Pl. 4: 384 (1843)
Allium kurrat Schweinf. ex K.Krause Notizbl. Bot. Gart. Berlin-Dahlem 9: 524 (1926)
Allium laetum Salisb. Prodr. Stirp. Chap. Allerton : 235 (1796)
Allium leucanthum K.Koch Linnaea 22: 240 (1849)
Allium leucanthum var. tridentatum Ogan. Fl. Rastitel'nost' Rast. Res. Arm. 12: 12 (1999)
Allium polyanthum Schult. & Schult.f. Syst. Veg., ed. 15 bis 7: 1016 (1830)
Allium porraceum Gray Nat. Arr. Brit. Pl. 2: 181 (1821 publ. 1822)
Allium porrum var. ampeloprasum (L.) Mirb. Dict. Sci. Nat. 1: 384. 1804
Allium pylium De Not. Index Seminum (GE, Genuensis) 1843: 30 (1843)
Allium scopulicola Font Quer Butl. Inst. Catalana Hist. Nat. 24: 144 (1924)
Allium scorodoprasum subsp. babingtonii (Borrer) Nyman Consp. Fl. Eur. 736. 1882 (1882)
Allium spectabile De Not. Repert. Fl. Ligust. : 414 (1844)
Allium syriacum Boiss. Fl. Orient. 5: 232 (1882)
Allium thessalum Boiss. Fl. Orient. 5: 232 (1882)
Allium rotundum var. polyanthum (Schult. & Schult.f.) Asch. & Graebn. Syn. Mitteleur. Fl. 3: 102. 1905
Allium ampeloprasum var. gracile Cavara Bull. Orto Bot. Regia Univ. Napoli 9(1): 46. 1927
Allium ampeloprasum var. caudatum Pamp. Arch. Bot. (Forlì) 12: 21. 1936
Allium porrum subsp. euampeloprasum Breistr. Bull. Soc. Sci. Isère 61: 610 1947
Allium ampeloprasum subsp. euampeloprasum Hayek Repert. Spec. Nov. Regni Veg. Beih. 30(3): 39. 1932 (1932)
Allium ampeloprasum subsp. thessalum (Boiss.) Nyman Consp. Fl. Eur. 735. 1882 (1882)
Allium ampeloprasum subsp. halleri Nyman Consp. Fl. Eur. 735. 1882 (1882)
Allium lineare Mill. Gard. Dict. ed. 8 n.° 4. 1768 (1768)
Allium porrum var. kurrat (Schweinf. ex K.Krause) Seregin Novosti Sist. Vyssh. Rast. 36: 102 (2004)
Allium ampeloprasum var. bertolonii (De Not.) Nyman Consp. Fl. Eur. 735. 1882
Allium ampeloprasum var. gasparrinii (Guss.) Nyman Consp. Fl. Eur. 735. 1882
Allium rotundum var. multiflorum Nyman Consp. Fl. Eur. 735. 1882
Allium ampeloprasum var. pylium (De Not.) Asch. & Graebn. Syn. Mitteleur. Fl. 3: 107. 1905
Allium ampeloprasum var. bulgaricum Podp. Verh. K. K. Zool.-Bot. Ges. Wien 52: 676. 1902
Allium porrum subsp. polyanthum (Schult. & Schult.f.) Jauzein & J.-M.Tison Lejeunia , n.s., 178: 12 (2005)
Allium firmotunicatum var. album Grossh. Fl. Kavkaza 1: 204. 1928

Common names Top

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Language Common/alternative name
English garden leek
English broadleaf wild leek
Spanish ajoporro
Spanish puerro de vinas
Spanish puerro agreste
Spanish allium scorodoprasum subsp. babingtonii
Spanish allium babingtonii
Spanish allium ampeloprasum var. bulbilliferum
Spanish allium ampeloprasum var. bulbiferum
Spanish allium ampeloprasum var babingtonii
Spanish ajos de cigueña
Spanish ajos de ciguena
Spanish ajoporro de monte
Spanish ajoborde
Spanish ajo chilote
Spanish ajo de las vinas
Spanish ajo de las viñas
Spanish ajo puerro silvestre
Spanish allium ampeloprasum var bulbiferum
Arabic كراث نبطي
azb کاوار
Bulgarian гроздов лук
Czech pór zahradní
Czech pór letní
Welsh cenhinen wyllt
Welsh cennin gwyllt
Danish porre-løg
German ackerlauch
German sommerknoblauch
German riesenknoblauch
German elefantenknoblauch
German Ägyptischer lauch
German ackerknoblauch
diq sirek
Greek Πράσο
Greek Άγριο πράσο
Greek Άλλιον το αμπελόπρασο
Estonian viinamäelauk
Estonian porrulauk
Estonian porru
Estonian porro
Persian تره کوهی
Persian تره
Persian گندنه
Finnish kesäpurjo
French poireau d'été
French poireau d'ete
frr gäärslook
Galician allo porro
Galician porro
Hebrew שום גבוה
Croatian poriluk
Upper Sorbian tołsty kobołk
Upper Sorbian porej
Hungarian francia v. nyári hagyma
Armenian ձիասխտոր
Armenian Այգեպրաս
Japanese リーキ
Japanese リーキ (種)
Kabyle tarnast
Korean 코끼리마늘
Macedonian широколистен див праз
Macedonian Праз
Macedonian див праз
mzn انگیسن
Norwegian Bokmål perleløk
Dutch prei
Norwegian Nynorsk villpurre
Portuguese alho-porro
Portuguese alho porro bravo
Portuguese porro
Portuguese alho-porro-bravo
Portuguese alho-poró
Quechua k'ita pulla
Quechua kita pulla
Quechua allium scorodoprasum
Russian лук виноградный
Turkish pırasa
Chinese 象大蒜
Chinese 韭葱
Chinese 南欧蒜

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Azores
      • Canary Islands
      • Madeira
    • Northeast Tropical Africa
      • Ethiopia
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Middle Asia
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey
  • Australasia
    • Australia
      • New South Wales
      • South Australia
      • Tasmania
      • Victoria
      • Western Australia
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Czechoslovakia
    • Northern Europe
      • Great Britain
      • Ireland
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • North-central U.S.A.
      • Illinois
    • Northeastern U.S.A.
      • New York
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Kentucky
      • Tennessee
    • Southwestern U.S.A.
      • California
  • Southern America
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Puerto Rico
    • Southern South America
      • Argentina Northeast
    • Western South America
      • Galápagos

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000755607
UNII P99JA4S769
Flora of Alabama 4398
USDA Plants ALAM
Tropicos 18400005
INPN 81313
Flora of Italy 6917
KEW urn:lsid:ipni.org:names:332079-2
The Plant List kew-294972
Plantarium 1876
Missouri Botanical Garden 281717
PFAF Allium ampeloprasum
Open Tree Of Life 748378
Observations.org 114216
NCBI Taxonomy 4681
NBN Atlas NBNSYS0000034220
Nature Serve 2.135847
IUCN Red List 172192
IPNI 332079-2
iNaturalist 122912
GBIF 2856037
Freebase /m/06cg_x
EPPO ALLAM
EOL 8790855
Elurikkus 208878
USDA GRIN 2217
Wikipedia Allium_ampeloprasum
CMAUP NPO22210

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
Potential Interest of Oxalis pes-caprae L., a Wild Edible Plant, for the Food and Pharmaceutical Industries Clemente-Villalba J, Burló F, Hernández F, Carbonell-Barrachina ÁA Foods 12-Mar-2024
PMCID:PMC10969124
doi:10.3390/foods13060858
PMID:38540848
Scopoletin: a review of its pharmacology, pharmacokinetics, and toxicity Gao XY, Li XY, Zhang CY, Bai CY Front Pharmacol 23-Feb-2024
PMCID:PMC10923241
doi:10.3389/fphar.2024.1268464
PMID:38464713
A Novel Plant-Based Nutraceutical Combined with Exercise Can Revert Oxidative Status in Plasma and Liver in a Diet-Induced-Obesity Animal Model Guzmán-Carrasco A, Kapravelou G, López-Jurado M, Bermúdez F, Andrés-León E, Terrón-Camero LC, Prados J, Melguizo C, Porres JM, Martínez R Antioxidants (Basel) 23-Feb-2024
PMCID:PMC10967303
doi:10.3390/antiox13030274
PMID:38539808
Anti-Cancer and Anti-Inflammatory Properties of Black Garlic Stępień AE, Trojniak J, Tabarkiewicz J Int J Mol Sci 01-Feb-2024
PMCID:PMC10855366
doi:10.3390/ijms25031801
PMID:38339077
Origins of the central Macaronesian psyllid lineages (Hemiptera; Psylloidea) with characterization of a new island radiation on endemic Convolvulus floridus (Convolvulaceae) in the Canary Islands Bastin S, Reyes-Betancort JA, Siverio de la Rosa F, Percy DM PLoS One 26-Jan-2024
PMCID:PMC10817144
doi:10.1371/journal.pone.0297062
PMID:38277393
The Impact Ground Phonolite Rock’s Potassium Solubilization in Tropical Soil Depends on the Cultivated Forage Species da Rocha Neto AR, de Mello Prado R, da Cruz MC Plants (Basel) 11-Jan-2024
PMCID:PMC10819162
doi:10.3390/plants13020199
PMID:38256753
Quinces (Cydonia oblonga, Chaenomeles sp., and Pseudocydonia sinensis) as Medicinal Fruits of the Rosaceae Family: Current State of Knowledge on Properties and Use Kostecka-Gugała A Antioxidants (Basel) 03-Jan-2024
PMCID:PMC10812678
doi:10.3390/antiox13010071
PMID:38247495
Pharmaceutical Terminology in Ancient and Medieval Time – andrachne, chrysocolla and Others Zipser B, Scott AC, Allkin R, Gan P, Lardos A, Lazarou R, Lev E, Nesbitt M, Patmore K Stud Ceranea 30-Dec-2023
PMCID:PMC7615763
doi:10.18778/2084-140X.13.49
PMID:38524312
Understanding the Lost: Reconstruction of the Garden Design of Villa Peretti Montalto (Rome, Italy) for Urban Valorization Bartoli F, D’Amato L, Nucera A, Albani Rocchetti G, Caneva G Plants (Basel) 26-Dec-2023
PMCID:PMC10780482
doi:10.3390/plants13010077
PMID:38202385
Bactericera tremblayi (Wagner, 1961) (Hemiptera: Triozidae): The Prevalent Psyllid Species in Leek Fields of Northwestern Spain Santiago-Calvo Y, Baños-Picón L, Flores-Pérez D, Asensio-S.-Manzanera MC Insects 21-Dec-2023
PMCID:PMC10816366
doi:10.3390/insects15010004
PMID:38276818
Exploring the potential of Crotalaria juncea flower extracts as a source of antioxidants, antimicrobials, and cytoprotective agents for biomedical applications Mahasawat P, Boukaew S, Prasertsan P BioTechnologia (Pozn) 21-Dec-2023
PMCID:PMC10777724
doi:10.5114/bta.2023.132772
PMID:38213478
Green Onion (Allium fistulosum): An Aromatic Vegetable Crop Esteemed for Food, Nutritional and Therapeutic Significance Kim SH, Yoon JB, Han J, Seo YA, Kang BH, Lee J, Ochar K Foods 16-Dec-2023
PMCID:PMC10742967
doi:10.3390/foods12244503
PMID:38137307
Biological Control of Fusarium oxysporum, the Causal Agent of Fusarium Basal Rot in Onion by Bacillus spp. Shin JH, Lee HK, Lee SC, Han YK Plant Pathol J 01-Dec-2023
PMCID:PMC10721391
doi:10.5423/PPJ.OA.08.2023.0118
PMID:38081320
Rhizoglomus variabile and Nanoglomus plukenetiae, Native to Peru, Promote Coffee Growth in Western Amazonia Corazon-Guivin MA, Romero-Cachique G, Del Aguila KM, Padilla-Domínguez A, Hernández-Amasifuen AD, Cerna-Mendoza A, Coyne D, Oehl F Microorganisms 29-Nov-2023
PMCID:PMC10745942
doi:10.3390/microorganisms11122883
PMID:38138027
The efficacy of Allium ampeloprasum L. in reducing neutrophil recovery time in childhood cancer with febrile neutropenia: a randomized, double-blind, placebo-controlled trial Bordbar M, Vahidifar M, Zarshenas MM, Haghpanah S, Zareifar S, Shahriari M, Zekavat OR, Karimi M, Fathpour G, Zargaran A, Shakibazad N Am J Blood Res 15-Oct-2023
PMCID:PMC10658031
PMID:38023416

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
Trimethylbenzene 10686 Click to see CC1=C(C(=CC=C1)C)C 120.19 unknown https://doi.org/10.1080/10412905.1991.9697935
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives
Antimycin A19 56600064 Click to see CCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)C(C)C(C)C 548.60 unknown via CMAUP database
Antimycin A20 54764156 Click to see CCCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)C 506.50 unknown via CMAUP database
Antimycin A2a 447434 Click to see CCCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)C(C)C 534.60 unknown via CMAUP database
Antimycin A3 245869 Click to see CCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)CC(C)C 520.60 unknown via CMAUP database
Antimycin A3a 2'R-epimer 86278330 Click to see CCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)C(C)CC 520.60 unknown via CMAUP database
Benzoic acid, 3-(formylamino)-2-hydroxy- 15409159 Click to see C1=CC(=C(C(=C1)NC=O)O)C(=O)O 181.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Dibutyl Phthalate 3026 Click to see CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC 278.34 unknown https://doi.org/10.1080/10412905.1991.9697935
Diethyl Phthalate 6781 Click to see CCOC(=O)C1=CC=CC=C1C(=O)OCC 222.24 unknown https://doi.org/10.1080/10412905.1991.9697935
Dimethyl Phthalate 8554 Click to see COC(=O)C1=CC=CC=C1C(=O)OC 194.18 unknown https://doi.org/10.1080/10412905.1991.9697935
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Phthalic acid 1017 Click to see C1=CC=C(C(=C1)C(=O)O)C(=O)O 166.13 unknown https://doi.org/10.1080/10412905.1991.9697935
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Methyl-3-hydroxyanthranilic acid 95222 Click to see CC1=C(C(=C(C=C1)C(=O)O)N)O 167.16 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2-Methoxy-4-vinylphenol 332 Click to see COC1=C(C=CC(=C1)C=C)O 150.17 unknown https://doi.org/10.1080/10412905.1991.9697935
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Decane 15600 Click to see CCCCCCCCCC 142.28 unknown https://doi.org/10.1080/10412905.1991.9697935
Dodecane 8182 Click to see CCCCCCCCCCCC 170.33 unknown https://doi.org/10.1080/10412905.1991.9697935
Heneicosane 12403 Click to see CCCCCCCCCCCCCCCCCCCCC 296.60 unknown https://doi.org/10.1080/10412905.1991.9697935
Heptacosane 11636 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC 380.70 unknown https://doi.org/10.1080/10412905.1991.9697935
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown https://doi.org/10.1080/10412905.1991.9697935
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1080/10412905.1991.9697935
Nonadecane 12401 Click to see CCCCCCCCCCCCCCCCCCC 268.50 unknown https://doi.org/10.1080/10412905.1991.9697935
Pentacosane 12406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC 352.70 unknown https://doi.org/10.1080/10412905.1991.9697935
Tetradecane 12389 Click to see CCCCCCCCCCCCCC 198.39 unknown https://doi.org/10.1080/10412905.1991.9697935
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown https://doi.org/10.1080/10412905.1991.9697935
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://doi.org/10.1080/10412905.1991.9697935
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
2,6,7-Trimethyl-10-methylidenetricyclo[5.3.1.02,6]undec-8-ene 101414595 Click to see CC12CCCC1(C3(CC2C(=C)C=C3)C)C 202.33 unknown https://doi.org/10.1080/10412905.1991.9697935
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
(E)-1,11-Tridecadiene-3,5,7,9-tetrayne 5352703 Click to see CC=CC#CC#CC#CC#CC=C 164.20 unknown via CMAUP database
1,11-Tridecadiene-3,5,7,9-tetrayne 5322026 Click to see CC=CC#CC#CC#CC#CC=C 164.20 unknown via CMAUP database
trans,trans-1,3,11-Tridecatriene-5,7,9-triyne 5322028 Click to see CC=CC#CC#CC#CC=CC=C 166.22 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Heptadecene 23217 Click to see CCCCCCCCCCCCCCCC=C 238.50 unknown https://doi.org/10.1080/10412905.1991.9697935
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Methyl 2-methylhexadecanoate 94236 Click to see CCCCCCCCCCCCCCC(C)C(=O)OC 284.50 unknown https://doi.org/10.1080/10412905.1991.9697935
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown https://doi.org/10.1016/S0031-9422(00)85486-2
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://doi.org/10.1080/10412905.1991.9697935
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1016/S0031-9422(00)85486-2
https://doi.org/10.1080/10412905.1991.9697935
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1016/S0031-9422(00)85486-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.1080/10412905.1991.9697935
https://doi.org/10.1016/S0031-9422(00)85486-2
Tetracosanoic acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown https://doi.org/10.1016/S0031-9422(00)85486-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(4R)-3-(hydroxymethyl)-5,5-dimethyl-4-[(3R)-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-2-en-1-one 162960579 Click to see CC(CCC1C(=CC(=O)CC1(C)C)CO)OC2C(C(C(C(O2)CO)O)O)O 388.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
(4R)-3,5,5-trimethyl-4-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxybutyl]cyclohex-2-en-1-one 163101720 Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O)(C)C 504.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
(4R)-4-[(3R)-3-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one 162890969 Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)O)(C)C 534.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
(2E,10E)-2,10,12-Tridecatriene-4,6,8-triyn-1-ol acetate 14729087 Click to see CC(=O)OCC=CC#CC#CC#CC=CC=C 224.25 unknown via CMAUP database
2,12-Tridecadiene-4,6,8,10-tetrayne-1-ol acetate 14729084 Click to see CC(=O)OCC=CC#CC#CC#CC#CC=C 222.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown https://doi.org/10.1080/10412905.1991.9697935
1-Octen-3-OL 18827 Click to see CCCCCC(C=C)O 128.21 unknown https://doi.org/10.1080/10412905.1991.9697935
2-Ethylhexan-1-ol 7720 Click to see CCCCC(CC)CO 130.23 unknown https://doi.org/10.1080/10412905.1991.9697935
Virginiae butanolide A 10036830 Click to see CC(C)CCCC(C1C(COC1=O)CO)O 230.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
2,10,12-Tridecatriene-4,6,8-triyne-1-ol 14729088 Click to see C=CC=CC#CC#CC#CC=CCO 182.22 unknown via CMAUP database
2,12-Tridecadiene-4,6,8,10-tetrayne-1-ol 14729085 Click to see C=CC#CC#CC#CC#CC=CCO 180.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
(2E,10E)-2,10,12-Tridecatriene-4,6,8-triynal 14729086 Click to see C=CC=CC#CC#CC#CC=CC=O 180.20 unknown via CMAUP database
(E)-2,12-Tridecadiene-4,6,8,10-tetraynal 14729083 Click to see C=CC#CC#CC#CC#CC=CC=O 178.19 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Ethyl octadecadienoate 54522427 Click to see CCCCCCCCCCCCCC=CC=CC(=O)OCC 308.50 unknown https://doi.org/10.1080/10412905.1991.9697935
Octadecadienoic acid, methyl ester 176473 Click to see CCCCCCCCCCCCCC=CC=CC(=O)OC 294.50 unknown https://doi.org/10.1080/10412905.1991.9697935
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Isophytol 10453 Click to see CC(C)CCCC(C)CCCC(C)CCCC(C)(C=C)O 296.50 unknown https://doi.org/10.1080/10412905.1991.9697935
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Biflorane and serrulatane diterpenoids
seco-pseudopterosin H 11477080 Click to see CC1CCC(C2=C1C(=C(C(=C2)C)OC3C(C(C(CO3)OC(=O)C)O)O)O)C(C)CCC=C(C)C 476.60 unknown https://doi.org/10.1080/10412905.1991.9697935
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Neophytadiene 10446 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=C)C=C 278.50 unknown https://doi.org/10.1080/10412905.1991.9697935
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
CID 162861143 162861143 Click to see CC(=O)OC1CCC(C(C12COC(=O)C34C2C(CC(C3)C5(C4OC(=O)C)CO5)OC(=O)C)C=O)(C)C 506.50 unknown https://doi.org/10.1039/AI9943100325
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,15S,16R,19R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16,19-triol 9547211 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)O)O)C)O)C)C)OC1 448.60 unknown https://doi.org/10.1021/NP960657R
(25s)-5alpha-Spirostane-2beta,3beta,6beta-triol 102330027 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)O)O)C)O)C)C)OC1 448.60 unknown https://doi.org/10.1021/NP960657R
(5'R,7S,9S,13R,16S,18S,19R)-16,19-dihydroxy-5',7,9,13,18-pentamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 5318799 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CC(C6(C5(CCC(C6)O)C)C)O)C)C)OC1 460.60 unknown https://doi.org/10.1016/S0040-4020(97)00062-8
12-Ketoporrigenin 10575381 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CC(C6C5(CCC(C6)O)C)O)C)C)OC1 446.60 unknown via CMAUP database
12-Ketoporrigenin 73313119 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CC(C6C5(CCC(C6)O)C)O)C)C)OC1 446.60 unknown https://doi.org/10.1016/S0040-4020(97)00062-8
Agigenin 44566818 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)O)O)C)O)C)C)OC1 448.60 unknown https://doi.org/10.1021/NP960657R
Neoagigenin 52931439 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)O)O)C)O)C)C)OC1 448.60 unknown https://doi.org/10.1021/NP960657R
Neoporrigenin B 91871146 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(=O)C(C6)O)C)O)C)C)OC1 446.60 unknown https://doi.org/10.1021/NP960657R
Porrigenin A 44566819 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)O)O)C)O)C)C)OC1 448.60 unknown https://doi.org/10.1021/NP960657R
Porrigenin B 44566820 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(=O)C(C6)O)C)O)C)C)OC1 446.60 unknown https://doi.org/10.1021/NP960657R
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1R,2S,4S,6S,7S,8R,9S,12S,13R,15R,16R,18S,19R)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,19-triol 162872040 Click to see CC1C2C(CC3C2(CCC4C3CC(C5C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)O)O)O)O)O)C)O)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O 953.10 unknown https://doi.org/10.1248/CPB.36.3480
(1R,2S,4S,6S,7S,8R,9S,12S,13R,15R,16R,18S,19R)-16-[(2R,3R,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,19-triol 162847337 Click to see CC1C2C(CC3C2(CCC4C3CC(C5C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O)O)C)O)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1115.20 unknown https://doi.org/10.1248/CPB.36.3480
(2alpha,3beta,5alpha,6beta,25R)-2,6-Dihydroxyspirostan-3-yl O-beta-D-glucopyranosyl-(1-->3)-O-beta-D-glucopyranosyl-(1-->4)-beta-D-galactopyranoside 163092465 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)O)C)O)C)C)OC1 935.10 unknown https://doi.org/10.1248/CPB.36.3480
(2R,3R,4S,5R,6R)-2-[(2R,3S,4R,5R,6R)-6-[(5'R,7S,9S,13R,15R,16R,18S,19R)-15,19-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 6325838 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)O)O)O)C)O)C)C)OC1 772.90 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,15R,16R,18S,19R)-15,19-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 101609012 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)O)C)C)OC1 1067.20 unknown https://doi.org/10.1016/0305-1978(87)90089-5
https://doi.org/10.1271/BBB.62.1904
https://doi.org/10.1248/CPB.47.738
https://doi.org/10.1021/JF000331V
16-[5-[3-[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-19-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15-one 131751416 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(=O)C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)O)C)C)OC1 1227.30 unknown https://doi.org/10.1271/BBB.62.1904
Ampeloside Bf1 14187144 Click to see CC1C2C(CC3C2(CCC4C3CC(C5C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O)O)C)O)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1115.20 unknown https://doi.org/10.1248/CPB.36.3480
Ampeloside Bf2 14187146 Click to see CC1C2C(CC3C2(CCC4C3CC(C5C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)O)O)O)O)O)C)O)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O 953.10 unknown https://doi.org/10.1248/CPB.36.3480
Ampeloside Bs1 14187142 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)O)C)O)C)C)OC1 935.10 unknown https://doi.org/10.1248/CPB.36.3480
Dioscin 119245 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown https://doi.org/10.1248/CPB.47.738
https://doi.org/10.1271/BBB.62.1904
Yayoisaponin A 5101819 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)O)C)O)C)C)OC1 1229.30 unknown https://doi.org/10.1271/BBB.62.1904
Yayoisaponin C 85125467 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)O)C)C)OC1 1097.20 unknown https://doi.org/10.1248/CPB.47.738
https://doi.org/10.1271/BBB.62.1904
> Mixed metal/non-metal compounds / Other mixed metal/non-metal oxoanionic compounds / Non-metal selenates
Hydroxysulfanyl hydrogen selenate 163192398 Click to see OSO[Se](=O)(=O)O 193.05 unknown https://doi.org/10.1039/AI9943100325
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
3-(Propylsulphinyl)-L-alanine 87309 Click to see CCCS(=O)CC(C(=O)O)N 179.24 unknown https://doi.org/10.1021/JF990938F
https://doi.org/10.1016/0305-1978(95)00072-0
Methiin 9578071 Click to see CS(=O)CC(C(=O)O)N 151.19 unknown https://doi.org/10.1021/JF990938F
S-Methylcysteine sulfoxide 82142 Click to see CS(=O)CC(C(=O)O)N 151.19 unknown https://doi.org/10.1021/JF990938F
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / D-alpha-amino acids
S-Allyl-L-cysteine sulfoxide 15558642 Click to see C=CCS(=O)CC(C(=O)O)N 177.22 unknown https://doi.org/10.1021/JF990938F
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
3-(Allylsulphinyl)-L-alanine 87310 Click to see C=CCS(=O)CC(C(=O)O)N 177.22 unknown https://doi.org/10.1016/0305-1978(95)00072-0
https://doi.org/10.1021/JF990938F
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-acyl-alpha amino acids and derivatives
antimycin A1 14957 Click to see CCCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)CC(C)C 548.60 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Mercaptomethyl acetate 15354425 Click to see CC(=O)OCS 106.15 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organic acids and derivatives / Keto acids and derivatives / Alpha-keto acids and derivatives
Ketomycin 19489 Click to see C1CC(CC=C1)C(=O)C(=O)O 154.16 unknown via CMAUP database
> Organic acids and derivatives / Organic thiosulfuric acids and derivatives / S-alkyl thiosulfates
S-Propyl thiosulfate 3083960 Click to see CCCSS(=O)(=O)O 156.20 unknown https://doi.org/10.1021/NP0503350
> Organic acids and derivatives / Thiosulfinic acid esters
1-Propanesulfinothioic acid, S-methyl ester 20209223 Click to see CCCS(=O)SC 138.30 unknown https://doi.org/10.1021/NP0503350
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
1-Penten-3-OL 12020 Click to see CCC(C=C)O 86.13 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
Oleandomycin 72493 Click to see CC1CC(C(C(O1)OC2C(CC3(CO3)C(=O)C(C(C(C(OC(=O)C(C(C2C)OC4CC(C(C(O4)C)O)OC)C)C)C)O)C)C)O)N(C)C 687.90 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Glycosylamines
9-[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]-3H-purin-6-one 21785357 Click to see C1C(C(C(C(O1)N2C=NC3=C2NC=NC3=O)O)O)O 268.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
Acetoin 179 Click to see CC(C(=O)C)O 88.11 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Isovaleraldehyde 11552 Click to see CC(C)CC=O 86.13 unknown https://doi.org/10.1080/10412905.1991.9697935
Valeraldehyde 8063 Click to see CCCCC=O 86.13 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
2,3-Thiophenedicarboxaldehyde 573752 Click to see C1=CSC(=C1C=O)C=O 140.16 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Hexanal 6184 Click to see CCCCCC=O 100.16 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated aldehydes / Enals
2-Methyl-pent-2-enal 12177 Click to see CCC=C(C)C=O 98.14 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
1-Octen-3-one 61346 Click to see CCCCCC(=O)C=C 126.20 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
(alphaR,2R)-alpha,5alpha-Dimethyl-6alpha-[(1E,3E,5E,7E,9S)-1,9-diethyl-14-oxo-14-(1H-pyrrole-2-yl)-1,3,5,7-tetradecatetraenyl]tetrahydro-2H-pyran-2beta-acetic acid 101789368 Click to see CCC(CCCCC(=O)C1=CC=CN1)C=CC=CC=CC=C(CC)C2C(CCC(O2)C(C)C(=O)O)C 495.70 unknown via CMAUP database
Indanomycin 10345604 Click to see CCC1CCC2C1C=CC(C2C(=O)C3=CC=CN3)C=CC=C(CC)C4C(CCC(O4)C(C)C(=O)O)C 493.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals
Acetal 7765 Click to see CCOC(C)OCC 118.17 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organic oxygen compounds / Organooxygen compounds / Ethers / Hemiacetals
1-(Ethylthio)ethanethiol 12499749 Click to see CCSC(C)S 122.30 unknown https://doi.org/10.1080/10412905.1991.9697935
Ethylthiopropanethiol 21516151 Click to see CCC(S)SCC 136.30 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organoheterocyclic compounds / Azacyclic compounds
Trimethyldihydrodithiazine 129676057 Click to see CC1(C=CSSN1C)C 161.30 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
Porric acid A 478958 Click to see CC1=CC(=C(C2=C1C3=C(O2)C(=CC(=C3)OC)C(=O)O)O)OC 302.28 unknown https://doi.org/10.1002/(SICI)1099-0690(199804)1998:4<661::AID-EJOC661>3.0.CO;2-V
Porric acid B 478957 Click to see CC1=CC(=C(C2=C1C3=C(O2)C(=CC(=C3)O)C(=O)O)O)OC 288.25 unknown https://doi.org/10.1002/(SICI)1099-0690(199804)1998:4<661::AID-EJOC661>3.0.CO;2-V
Porric acid C 478956 Click to see CC1=CC(=CC2=C1C3=C(O2)C(=CC(=C3)O)C(=O)O)O 258.23 unknown https://doi.org/10.1002/(SICI)1099-0690(199804)1998:4<661::AID-EJOC661>3.0.CO;2-V
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
(2R)-6',10-Dihydroxy-7',9'-dimethoxy-4',5',9-trioxo-4,4',5',9-tetrahydrospiro[benzo[1,2-b:5,4-c']dipyran-2(3H),2'(3'H)-naphtho[1,2-b]furan]-7-carboxylic acid methyl ester 97042233 Click to see COC1=CC(=C(C2=C1C3=C(CC4(O3)CCC5=C(O4)C(=C6C(=C5)C=C(OC6=O)C(=O)OC)O)C(=O)C2=O)O)OC 536.40 unknown via CMAUP database
gamma-Rubromycin 5464075 Click to see COC1=CC(=O)C2=C(C1=O)C(=C3C(=C2O)CC4(O3)CCC5=C(O4)C(=C6C(=C5)C=C(OC6=O)C(=O)OC)O)O 522.40 unknown via CMAUP database
> Organoheterocyclic compounds / Bi- and oligothiophenes
2,2':5',2''-Terthiophene 65067 Click to see C1=CSC(=C1)C2=CC=C(S2)C3=CC=CS3 248.40 unknown via CMAUP database
5-(3-Buten-1-ynyl)-2,2'-bithiophene 70813 Click to see C=CC#CC1=CC=C(S1)C2=CC=CS2 216.30 unknown via CMAUP database
5-Ethenyl-5'-(1-propenyl)-2,2'-bithiophene 14704544 Click to see CC=CC1=CC=C(S1)C2=CC=C(S2)C=C 232.40 unknown via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinoxalines / Phenazines and derivatives
6-Acetylphenazine-1-carboxylic acid 443635 Click to see CC(=O)C1=C2C(=CC=C1)N=C3C(=N2)C=CC=C3C(=O)O 266.25 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Ethylfuran 18554 Click to see CCC1=CC=CO1 96.13 unknown https://doi.org/10.1080/10412905.1991.9697935
2-Pentylfuran 19602 Click to see CCCCCC1=CC=CO1 138.21 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organoheterocyclic compounds / Imidazodiazepines
Pentostatin 439693 Click to see C1C(C(OC1N2C=NC3=C2NC=NCC3O)CO)O 268.27 unknown via CMAUP database
Vira A deaminase inhibitor 44283251 Click to see C1C(C(OC1N2C=NC3=C2NC=NCC3O)CO)O 268.27 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3R,4R,5S)-3-hexyl-4-hydroxy-5-methyloxolan-2-one 11030843 Click to see CCCCCCC1C(C(OC1=O)C)O 200.27 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
2,3-Secoporrigenin 10837674 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC6C(C5(C)CC(=O)O)CC(=O)O6)C)C)OC1 460.60 unknown via CMAUP database
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
2-(3-Buten-1-ynyl)-5-[(E)-3-penten-1-ynyl]thiophene 14550074 Click to see CC=CC#CC1=CC=C(S1)C#CC=C 198.29 unknown via CMAUP database
Thiophene B 14262770 Click to see CC#CC#CC1=CC=C(S1)C#CC=C 196.27 unknown via CMAUP database
> Organosulfur compounds
Oxo-prop-1-enyl-propoxy-sulfanylidene-lambda6-sulfane 54203861 Click to see CCCOS(=O)(=S)C=CC 180.30 unknown https://doi.org/10.1080/10412905.1991.9697935
Propyl sulfinothioic acid 19020798 Click to see CCCS(=S)O 124.23 unknown https://doi.org/10.1021/JF00024A018
https://doi.org/10.1021/JF00024A017
> Organosulfur compounds / Allyl sulfur compounds
3-(Prop-2-enyldisulfanyl)pentane 163195820 Click to see CCC(CC)SSCC=C 176.30 unknown https://doi.org/10.1080/10412905.1991.9697935
Allyl methyl disulfide 62434 Click to see CSSCC=C 120.20 unknown https://doi.org/10.1080/10412905.1991.9697935
Allyl propyl disulfide 16591 Click to see CCCSSCC=C 148.30 unknown https://doi.org/10.1080/10412905.1991.9697935
Allyl propyl sulfide 98781 Click to see CCCSCC=C 116.23 unknown https://doi.org/10.1080/10412905.1991.9697935
Allylthiosulfinsaure 53743786 Click to see C=CCS(=S)O 122.21 unknown https://doi.org/10.1021/JF00024A017
Diallyl disulfide 16590 Click to see C=CCSSCC=C 146.30 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Organic disulfides
Dipropenyldisulfid 171311 Click to see CC=CSSC=CC 146.30 unknown https://doi.org/10.1080/10412905.1991.9697935
Methyl 1-propenyl disulfide 521863 Click to see CC=CSSC 120.20 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Organic disulfides / Dialkyldisulfides
1-Ethylsulfanyl-1-(1-ethylsulfanylethyldisulfanyl)ethane 163192318 Click to see CCSC(C)SSC(C)SCC 242.50 unknown https://doi.org/10.1080/10412905.1991.9697935
1-Ethylsulfanyl-1-(1-ethylsulfanylhexyldisulfanyl)hexane 163195823 Click to see CCCCCC(SCC)SSC(CCCCC)SCC 354.70 unknown https://doi.org/10.1080/10412905.1991.9697935
2-Ethylsulfanyl-1-(2-ethylsulfanylbutyldisulfanyl)butane 163192583 Click to see CCC(CSSCC(CC)SCC)SCC 298.60 unknown https://doi.org/10.1080/10412905.1991.9697935
2-Methylsulfanyl-1-(2-methylsulfanylbutyldisulfanyl)butane 163195731 Click to see CCC(CSSCC(CC)SC)SC 270.60 unknown https://doi.org/10.1080/10412905.1991.9697935
2-Methylsulfanyl-1-(2-methylsulfanylpentyldisulfanyl)pentane 163192316 Click to see CCCC(CSSCC(CCC)SC)SC 298.60 unknown https://doi.org/10.1080/10412905.1991.9697935
3-Methylsulfanyl-1-(3-methylsulfanylbutyldisulfanyl)butane 163192417 Click to see CC(CCSSCCC(C)SC)SC 270.60 unknown https://doi.org/10.1080/10412905.1991.9697935
3-Propylsulfanyl-1-(3-propylsulfanylbutyldisulfanyl)butane 163195821 Click to see CCCSC(C)CCSSCCC(C)SCCC 326.70 unknown https://doi.org/10.1080/10412905.1991.9697935
3-Propylsulfanyl-1-(3-propylsulfanylpentyldisulfanyl)pentane 163192250 Click to see CCCSC(CC)CCSSCCC(CC)SCCC 354.70 unknown https://doi.org/10.1080/10412905.1991.9697935
Dipropyl disulfide 12377 Click to see CCCSSCCC 150.30 unknown https://doi.org/10.1080/10412905.1991.9697935
Ethyl-1-(ethylthio)ethyldisulfid 129890562 Click to see CCCC(SCC)SSC(CCC)SCC 298.60 unknown https://doi.org/10.1080/10412905.1991.9697935
Methyl propyl disulfide 16592 Click to see CCCSSC 122.30 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Organic trisulfides
Allyl propyl trisulfide 525330 Click to see CCCSSSCC=C 180.40 unknown https://doi.org/10.1080/10412905.1991.9697935
Dipropyl trisulfide 22383 Click to see CCCSSSCCC 182.40 unknown https://doi.org/10.1080/10412905.1991.9697935
Methyl propyl trisulfide 5319765 Click to see CCCSSSC 154.30 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Sulfenyl compounds
1-(Methylpentasulfanyl)prop-1-ene 85619639 Click to see CC=CSSSSSC 216.40 unknown https://doi.org/10.1080/10412905.1991.9697935
1-(Prop-1-enyltetrasulfanyl)propane 528717 Click to see CCCSSSSC=CC 212.40 unknown https://doi.org/10.1080/10412905.1991.9697935
Dipropyl tetrasulfide 104285 Click to see CCCSSSSCCC 214.40 unknown https://doi.org/10.1080/10412905.1991.9697935
Methyl propyl pentasulfide 528716 Click to see CCCSSSSSC 218.50 unknown https://doi.org/10.1080/10412905.1991.9697935
Methyl propyl tetrasulphide 528709 Click to see CCCSSSSC 186.40 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Thioacetals / Dithioacetals
1-Methylsulfanyl-1-(1-methylsulfanylethylsulfanyl)ethane 12687136 Click to see CC(SC)SC(C)SC 182.40 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Thioethers / Dialkylthioethers
3-(Ethylsulfanyl)pentane 15709057 Click to see CCC(CC)SCC 132.27 unknown https://doi.org/10.1080/10412905.1991.9697935
Dipropyl sulfide 8118 Click to see CCCSCCC 118.24 unknown https://doi.org/10.1080/10412905.1991.9697935
> Organosulfur compounds / Thiols / Alkylthiols
2-Propanethiol 6364 Click to see CC(C)S 76.16 unknown via CMAUP database
3-Aminopropanethiol 97436 Click to see C(CN)CS 91.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Anthracyclines
Cinerubin B 73593 Click to see CCC1(CC(C2=C(C3=C(C=C2C1C(=O)OC)C(=O)C4=C(C=CC(=C4C3=O)O)O)O)OC5CC(C(C(O5)C)OC6CC7C(C(O6)C)OC8C(O7)CC(=O)C(O8)C)N(C)C)O 825.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-Phenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 22446905 Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=CC=CC=C3O2)OC4C(C(C(C(O4)CO)O)O)O 400.40 unknown https://doi.org/10.1021/NP0503350
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(01)00039-5
Kaempferol 3-neohesperidoside 5318761 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(01)00039-5
> Phenylpropanoids and polyketides / Macrolactams
Desferrioxamine X5 85625752 Click to see C1CCCN(C(=O)CCC(=O)NCCCCCN(C(=O)CCC(=O)NCCCCCNC(=O)CCC(=O)NCC1)O)O 598.70 unknown https://doi.org/10.1016/S0031-9422(00)85486-2

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