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Chrysopogon zizanioides

Chrysopogon zizanioides - 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 UUID64402f5b55421171853824
Scientific name Chrysopogon zizanioides
Authority (L.) Roberty
First published in Bull. Inst. Fondam. Afrique Noire, Sér. A, Sci. Nat. 22: 106 (1960)

Description Top

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Synonyms Top

Scientific name Authority First published in
Agrostis verticillata Lam. Encycl. 1: 59 (1783)
Anatherum muricatum P.Beauv. Ess. Agrostogr. : 150 (1812)
Anatherum zizanioides Hitchc. & Chase Contr. U.S. Natl. Herb. 18: 285 (1917)
Andropogon aromaticus Roxb. ex Schult. Mant. 2: 442, 481. 1824 [Jan-Apr 1824]
Andropogon muricatum Retz. Observ. Bot. 3: 43 (1783)
Andropogon muricatus Retz. Observ. Bot. 3: 43 (1783)
Andropogon nardus Trin. Neue Entdeck. Pflanzenk. 2: 90. 1821
Andropogon odoratus Auct. ex Steud. Nomencl. Bot. , ed. 2, 1: 92 (1840)
Andropogon zizanioides (L.) Urb. Symb. Antill. 4: 79 (1903)
Chamaeraphis muricata Merr. Enum. Philipp. Fl. Pl. 1: 75 (1923)
Holcus zizanioides (L.) Stuck. Anales Mus. Nac. Buenos Aires 11: 48. 1904 (1904)
Oplismenus abortivus Auct. ex Roem. & Schult. Syst. Veg., ed. 15 bis 2: 808 (1817)
Phalaris zizanioides L. Mant. Pl. 2: 183 (1771)
Rhaphis muricata Nees Ill. Bot. Himal. Mts. [Royle] 416; et ex Steud. Syn. Pl. Gram. 394. 1840 [Mar-Apr 1840]
Rhaphis zizanioides (L.) Roberty Fl. Ouest-Afr. : 404 (1954)
Sorghum zizanodes Kuntze Revis. Gen. Pl. 2: 791. 1891 [5 Nov 1891]
Vetiveria arundinacea Griseb. Fl. Brit. W. I. : 559 (1864)
Vetiveria muricata Griseb. Fl. Brit. W. I. : 560 (1864)
Vetiveria odorata Virey J. Pharm. Sci. Accessoires 13: 499 (1827)
Vetiveria odoratissima Lem.-Lis. Bull. Sci. Soc. Philom. Paris 1922: 42 1822
Vetiveria zizanioides (L.) Nash Fl. S.E. U.S. : 67 (1903)
Vetiveria zizanioides var. tonkinensis A.Camus Bull. Mus. Natl. Hist. Nat. 25: 674. 1919
Vetiveria odoratissima Bory ex Cloquet Bull. Sci. Soc. Philom. Paris 1822: 44 (1822)

Common names Top

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Language Common/alternative name
English khas, khuskhus, sandalwood fan, sevendra
English vetiver
Spanish pachuli
Spanish vetiver
Spanish andropogon festucoides
Spanish andropogon squarrosus
ace ganti
Arabic نجيل الهند
Assamese বিৰিণা
Azerbaijani zizaniyəbənzər vetivera
azb وتیور اوتو
ban padang sanur
Catalan vetiver
Czech vetiverie ovsuchovitá
Czech zlatovous draslavý
Czech vousatka draslavá
German vetiver-Öl
German vetiveröl
German vetyver
German vetiver
Estonian lõhnav puuritshein
Estonian andropogon muricatus
Estonian lõhnav vetiveeria
Persian علف وتیور
Finnish vetiveriaheinä
Hebrew וטיבר
Hindi खसखस
hif gadraa
ht vetivè
Hungarian vetiver
Indonesian akar wangi
Indonesian narwastu
Indonesian rumput akar wangi
Indonesian serai wangi
io vetivero
Italian vetiver
Japanese ベチバー
Georgian ვეტივერია
Kannada ಲಾವಂಚ
la vetiver
Lithuanian kvapusis auksabarzdis
mad karabisto
Malayalam vetiver
Malayalam രാമച്ചം
Marathi वाळा
Malay akar wangi
Malay narwastu
Malay kusu-kusu
Malay naga setu
Malay rumput wangi
Malay vetiveria zizanioides
Burmese ဗာတီဗာမြက်
Dutch vetiver
Oriya ବେଣା
Oriya ବେଣା ଚେର
Oriya ଖସ୍ଖସ୍
Oriya ଉଶୀର
Polish wetiwer
Polish wetiweria pachnąca
Portuguese grama das índias
Portuguese grama cheirosa
Portuguese grama-cheirosa
Portuguese grama-das-índias
Portuguese khas khas
Portuguese khus khus
Portuguese Óleo da tranqüilidade
Portuguese raiz-de-cheiro
Portuguese vetivert
Portuguese vetiver
Portuguese falso-pachuli
Portuguese capim-vetiver
Portuguese raiz de cheiro
Portuguese capim vetiver
Russian Ветивер
sa उशीरसस्यम्
Sinhala සැවැන්දරා
su usar
Swahili mzumai
Tamil வெட்டிவேர்
tcy ಲಾವಂಚ
Telugu వట్టివేరు
Thai หญ้าแฝก
Tonga ahi siaina
Tonga ahisiaina
Turkish vetiver
Ukrainian Золотобородник
Vietnamese cỏ hương lau
Vietnamese cỏ vetiver
Vietnamese cỏ hương bài
Chinese 香根草
Chinese 岩蘭草
Chinese 培地茅

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Zambia
      • Zimbabwe
    • West Tropical Africa
      • Ghana
      • Liberia
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Congo
      • Gabon
      • Zaïre
    • Western Indian Ocean
      • Comoros
      • Madagascar
      • Mauritius
      • Rodrigues
      • Réunion
      • Seychelles
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Kazan-retto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sumatera
    • Papuasia
      • New Guinea
  • Northern America
    • Mexico
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
      • Louisiana
  • Pacific
    • Northwestern Pacific
      • Caroline Islands
    • South-central Pacific
      • Cook Islands
      • Society Islands
      • Tubuai Islands
    • Southwestern Pacific
      • Fiji
      • New Caledonia
      • Niue
      • Samoa
      • Tonga
      • Wallis-Futuna Islands
  • Southern America
    • Brazil
      • Brazil Northeast
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Honduras
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
    • Western South America
      • Colombia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000859932
UNII J2F8377BJJ
Tropicos 25551115
INPN 632480
KEW urn:lsid:ipni.org:names:396213-1
The Plant List kew-405169
Open Tree Of Life 281780
NCBI Taxonomy 167337
IPNI 396213-1
iNaturalist 142763
GBIF 5677150
Freebase /m/04jmqh
EOL 1115280
USDA GRIN 424704
Wikipedia Chrysopogon_zizanioides
PFAF Chrysopogon zizanioides

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
Therapeutic potential of Thai herbal formula for cognitive impairment: A metabolomics approach for Comprehensive Insights Akarasereenont P, Pattanapholkornsakul S, Limsuvan S, Mamaethong D, Booranasubkajorn S, Pakaprot N, Tripatara P, Pilakasiri K Heliyon 16-Mar-2024
PMCID:PMC10981045
doi:10.1016/j.heliyon.2024.e28027
PMID:38560220
Plant Essential Oils: Dual Action of Toxicity and Egg-Laying Inhibition on Tetranychus urticae (Acari: Tetranychidae), Unveiling Their Potential as Botanical Pesticides Zhu Y, Wu T, Hu Q, He W, Zheng Y, Xie Y, Rao Q, Liu X Plants (Basel) 08-Mar-2024
PMCID:PMC10975855
doi:10.3390/plants13060763
PMID:38592755
Pb uptake, accumulation, and translocation in plants: Plant physiological, biochemical, and molecular response: A review Ur Rahman S, Qin A, Zain M, Mushtaq Z, Mehmood F, Riaz L, Naveed S, Ansari MJ, Saeed M, Ahmad I, Shehzad M Heliyon 07-Mar-2024
PMCID:PMC10945279
doi:10.1016/j.heliyon.2024.e27724
PMID:38500979
Purification Effect of Water Eutrophication Using the Mosaic System of Submerged–Emerged Plants and Growth Response Chang B, Xu Y, Zhang Z, Wang X, Jin Q, Wang Y Plants (Basel) 19-Feb-2024
PMCID:PMC10891872
doi:10.3390/plants13040560
PMID:38498525
Synergistic interactions of assorted ameliorating agents to enhance the potential of heavy metal phytoremediation Sanjana S, Jazeel K, Janeeshma E, Nair SG, Shackira AM Stress Biol 16-Feb-2024
PMCID:PMC10873264
doi:10.1007/s44154-024-00153-1
PMID:38363436
Synergistic Effect of Nilavembu Choornam–Gold Nanoparticles on Antibiotic-Resistant Bacterial Susceptibility and Contact Lens Contamination-Associated Infectious Pathogenicity Almutleb ES, Ramachandran S, Khan AA, El-Hiti GA, Alanazi SA Int J Mol Sci 09-Feb-2024
PMCID:PMC10889799
doi:10.3390/ijms25042115
PMID:38396792
Enhancing growth, vitality, and aromatic richness: unveiling the dual magic of silicon dioxide and titanium dioxide nanoparticles in Ocimum tenuiflorum L. Bhat UH, Uddin M, Chishti AS, Singh S, Singh S, Khan MM, Mukarram M Front Plant Sci 06-Feb-2024
PMCID:PMC10880381
doi:10.3389/fpls.2024.1335965
PMID:38384769
Eleven years of disease free survival in a case of Invasive Ductal Carcinoma (IDC) Rt Breast grade 3, stage 3, treated with add on Ayurveda treatment: A case report Nimbalkar R, Baheti AM, Pawar AT, Tagalpallewar AA, Nimbalkar MR J Ayurveda Integr Med 01-Feb-2024
PMCID:PMC10847158
doi:10.1016/j.jaim.2023.100881
PMID:38306823
Network of Soil Fungi and the Microfauna Community under Diverse Anthropic Disturbances under Chrysopogon zizanioides Planting in the Reservoir Lin X, Han X, Yang J, Liu F, Li Y, Chen Z Plants (Basel) 29-Jan-2024
PMCID:PMC10857095
doi:10.3390/plants13030393
PMID:38337926
Nonessential amino acids in tropical ruminant feed: Investigating grass and legume forages of Indonesia Tresia GE, Anggraeny YN, Winarsih WH, Setiasih S, Rohaeni ES, Mariyono M, Pamungkas D J Adv Vet Anim Res 31-Dec-2023
PMCID:PMC10868679
doi:10.5455/javar.2023.j739
PMID:38370889
Ixodes scapularis Is the Most Susceptible of the Three Canonical Human-Biting Tick Species of North America to Repellent and Acaricidal Effects of the Natural Sesquiterpene, (+)-Nootkatone Siegel EL, Xu G, Li AY, Pearson P, D’hers S, Elman N, Mather TN, Rich SM Insects 22-Dec-2023
PMCID:PMC10816182
doi:10.3390/insects15010008
PMID:38249014
Phytochemical profile and anti-inflammatory activity of the hull of γ-irradiated wheat mutant lines (Triticum aestivum L.) Park J, Kil YS, Ryoo GH, Jin CH, Hong MJ, Kim JB, Jung CH, Nam JW, Han AR Front Nutr 22-Dec-2023
PMCID:PMC10771830
doi:10.3389/fnut.2023.1334344
PMID:38188878
Valorization of Spent Vetiver Roots for Biochar Generation Neve S, Sarkar D, Warke M, Bandosz T, Datta R Molecules 21-Dec-2023
PMCID:PMC10779468
doi:10.3390/molecules29010063
PMID:38202646
The Metabolomics Response of Solanum melongena L. Leaves to Various Forms of Pb Zhang S, Zhao B, Zhang X, Wu F, Zhao Q Nanomaterials (Basel) 08-Nov-2023
PMCID:PMC10675538
doi:10.3390/nano13222911
PMID:37999265
Olfactory Stimulation as Environmental Enrichment for Domestic Horses—A Review Bini de Lima AC, Sebastião da Fé VC, Palermo Hernandes MS, Oliveira dos Santos VM Animals (Basel) 12-Oct-2023
PMCID:PMC10603683
doi:10.3390/ani13203180
PMID:37893904

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 / Benzyloxycarbonyls
1-Phenylethyl acetate 62341 Click to see CC(C1=CC=CC=C1)OC(=O)C 164.20 unknown https://doi.org/10.1515/ENERGYO.0090.00002
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Octane 356 Click to see CCCCCCCC 114.23 unknown https://doi.org/10.1515/ENERGYO.0090.00002
https://doi.org/10.1515/ZNB-1992-0324
> 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/10.1515/ENERGYO.0090.00002
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1515/ZNB-1992-0324
https://doi.org/10.1515/ENERGYO.0090.00002
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1515/ZNB-1992-0324
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1515/ENERGYO.0090.00002
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1515/ZNB-1992-0324
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1515/ENERGYO.0090.00002
https://doi.org/10.1515/ZNB-1992-0324
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1515/ZNB-1992-0324
https://doi.org/10.1515/ENERGYO.0090.00002
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1515/ENERGYO.0090.00002
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1515/ZNB-1992-0324
https://doi.org/10.1515/ENERGYO.0090.00002
Carane 79043 Click to see CC1CCC2C(C1)C2(C)C 138.25 unknown https://doi.org/10.1515/ZNB-1992-0324
https://doi.org/10.1515/ENERGYO.0090.00002
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(10,10-Dimethyl-6-methylidene-2-tricyclo[7.1.1.01,5]undecanyl)methanol 162905951 Click to see CC1(C2CCC(=C)C3C1(C2)C(CC3)CO)C 220.35 unknown https://doi.org/10.1246/NIKKASHI1948.88.7_795
(1R,2S,5R,9S)-2,10,10-trimethyl-6-methylidenetricyclo[7.1.1.01,5]undecane 162889296 Click to see CC1CCC2C13CC(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1246/NIKKASHI1948.88.7_795
[(1S,2S,5R,9S)-10,10-dimethyl-6-methylidene-2-tricyclo[7.1.1.01,5]undecanyl]methanol 162905952 Click to see CC1(C2CCC(=C)C3C1(C2)C(CC3)CO)C 220.35 unknown https://doi.org/10.1246/NIKKASHI1948.88.7_795
13-nor-Opposit-4(15)-en-11-one 91747153 Click to see CC(=O)CC1CCC2(C1C(=C)CCC2)C 206.32 unknown https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<61::AID-FFJ865>3.0.CO;2-S
2,10,10-Trimethyl-6-methylidenetricyclo[7.1.1.01,5]undecane 91753599 Click to see CC1CCC2C13CC(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1246/NIKKASHI1948.88.7_795
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1515/ENERGYO.0090.00002
https://doi.org/10.1515/ZNB-1992-0324
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
-Duprezizaenene 73950880 Click to see CC1CCC2C13CCC(C3)C(=C)C2(C)C 204.35 unknown https://doi.org/10.1515/ZNB-1992-0324
(-)-gamma-Cadinene 92313 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1515/ZNB-1992-0324
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0040-4020(01)96690-6
(1S,5S)-3-methyl-8-methylidene-5-propan-2-yl-2,4a,5,6,7,8a-hexahydro-1H-naphthalen-1-ol 91746535 Click to see CC1=CC2C(CCC(=C)C2C(C1)O)C(C)C 220.35 unknown https://doi.org/10.1016/S0040-4020(01)86837-X
https://doi.org/10.1016/S0040-4020(01)96690-6
1a-Methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,7,7a,7b-octahydronaphtho[1,2-b]oxiren-3-ol 13874492 Click to see CC(C)C1CCC(=C)C2C1C3C(O3)(CC2O)C 236.35 unknown https://doi.org/10.1016/S0040-4020(01)96690-6
https://doi.org/10.1016/S0040-4020(01)86837-X
3,4-Dihydrocadalene 528708 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1515/ENERGYO.0090.00002
7,7-Dimethyl-8-methylideneoctahydro-1h-3a,6-methanoazulene-3-carboxylic acid 85973 Click to see CC1(C2CCC3(C2)C(C1=C)CCC3C(=O)O)C 234.33 unknown https://doi.org/10.1021/JF049182X
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0040-4020(01)96690-6
alpha-Calacorene 12302243 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1515/ZNB-1992-0324
beta-Vetivone 442406 Click to see CC1CC(=O)C=C(C12CCC(=C(C)C)C2)C 218.33 unknown https://doi.org/10.1515/ENERGYO.0090.00002
https://doi.org/10.1002/JLAC.199619960720
https://doi.org/10.1515/ZNB-1992-0324
Cyclocopacamphan-12-al 6428370 Click to see CC(C=O)C1CCC2(C3C1C4C2(C4C3)C)C 218.33 unknown https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<61::AID-FFJ865>3.0.CO;2-S
Khusene 12304853 Click to see CC1CCC2C13CCC(C3)C(C2=C)(C)C 204.35 unknown https://doi.org/10.1515/ZNB-1992-0324
Khusimol 167519 Click to see CC1(C2CCC3(C2)C(CCC3C1=C)CO)C 220.35 unknown https://doi.org/10.1021/NP50112A001
https://doi.org/10.1515/ZNB-1992-0324
https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<61::AID-FFJ865>3.0.CO;2-S
https://doi.org/10.1002/1099-1026(200005/06)15:3<153::AID-FFJ885>3.0.CO;2-5
https://doi.org/10.1002/JLAC.199619960720
Khusinodiol 101254194 Click to see CC1=CC2C(CCC(C2C(C1)O)(C)O)C(C)C 238.37 unknown https://doi.org/10.1016/S0040-4020(01)96690-6
Khusol 12304864 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)CO 220.35 unknown https://doi.org/10.1016/S0040-4020(01)86837-X
https://doi.org/10.1016/S0040-4020(01)96690-6
Prezizaan-15-al 6428399 Click to see CC1CCC2C13CCC(C3)C(C2(C)C)C=O 220.35 unknown https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<61::AID-FFJ865>3.0.CO;2-S
Zizanene 12306046 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1515/ZNB-1992-0324
Zizanoic acid 21764437 Click to see CC1(C2CCC3(C2)C(C1=C)CCC3C(=O)O)C 234.33 unknown https://doi.org/10.1021/JF049182X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Alloaromadendren 91746537 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1515/ZNB-1992-0324
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1S,2R,5S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene 442348 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1515/ENERGYO.0090.00002
1,7-di-epi-alpha-Cedrene 10878276 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1515/ZNB-1992-0324
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
2-[(8R,8aR)-8,8a-dimethyl-4,6,7,8-tetrahydro-3H-naphthalen-2-yl]propan-1-ol 91748873 Click to see CC1CCC=C2C1(C=C(CC2)C(C)CO)C 220.35 unknown https://doi.org/10.1002/1099-1026(200005/06)15:3<153::AID-FFJ885>3.0.CO;2-5
https://doi.org/10.1002/JLAC.199619960720
alpha-Vetivone 442405 Click to see CC1CC(=O)C=C2C1(CC(=C(C)C)CC2)C 218.33 unknown https://doi.org/10.1515/ENERGYO.0090.00002
https://doi.org/10.1515/ZNB-1992-0324
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Furfural 7362 Click to see C1=COC(=C1)C=O 96.08 unknown https://doi.org/10.1515/ZNB-1992-0324
https://doi.org/10.1515/ENERGYO.0090.00002
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetyl-5-methylfuran 14514 Click to see CC1=CC=C(O1)C(=O)C 124.14 unknown https://doi.org/10.1515/ENERGYO.0090.00002
https://doi.org/10.1515/ZNB-1992-0324
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
10-epi-Acor-3-en-5-one 11972552 Click to see CC1CCC(C12CCC(=CC2=O)C)C(=C)C 218.33 unknown https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<61::AID-FFJ865>3.0.CO;2-S
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
12-nor-Preziza-7(15)-en-2-one 6428341 Click to see CC1(C2CCC(=O)C23CCC(C3)C1=C)C 204.31 unknown https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<61::AID-FFJ865>3.0.CO;2-S
13-nor-Eudesm-5-en-11-one 6428322 Click to see CC1CCCC2(C1=CC(CC2)C(=O)C)C 206.32 unknown https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<61::AID-FFJ865>3.0.CO;2-S
15-nor-Funebran-3-one 6428352 Click to see CC1CCC2C13CCC(=O)C(C3)C2(C)C 206.32 unknown https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<61::AID-FFJ865>3.0.CO;2-S
15-nor-Prezizaan-7-one 6428353 Click to see CC1CCC2C13CCC(C3)C(=C)C2=O 190.28 unknown https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<61::AID-FFJ865>3.0.CO;2-S
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Butylfuran 20534 Click to see CCCCC1=CC=CO1 124.18 unknown https://doi.org/10.1515/ZNB-1992-0324
https://doi.org/10.1515/ENERGYO.0090.00002
2-Pentylfuran 19602 Click to see CCCCCC1=CC=CO1 138.21 unknown https://doi.org/10.1515/ZNB-1992-0324
https://doi.org/10.1515/ENERGYO.0090.00002

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