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Pelargonium endlicherianum

Pelargonium endlicherianum - 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 UUID64400043d1f9e977084577
Scientific name Pelargonium endlicherianum
Authority Fenzl
First published in Pug. Pl. Nov. Syr. : 6 (1842)

Description Top

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Synonyms Top

Scientific name Authority First published in
Geraniospermum endlicherianum Kuntze Revis. Gen. Pl. 1: 94 (1891)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Start at 20°C; if no germination occurs within 3 months, cool seeds to 4°C for 1-2 months, then return to 20°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000466190
Tropicos 13900807
KEW urn:lsid:ipni.org:names:376089-1
Open Tree Of Life 551608
Observations.org 124373
NCBI Taxonomy 158596
IPNI 376089-1
GBIF 3828799
Elurikkus 420170
USDA GRIN 27120

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
Leaf variegation caused by plastome structural variation: an example from Dianella tasmanica Zhou S, Ma K, Mower JP, Liu Y, Zhou R Hortic Res 10-Jan-2024
PMCID:PMC10923649
doi:10.1093/hr/uhae009
PMID:38464478
Review green synthesis of silver nanoparticles by using plant extracts and their antimicrobial activity Abada E, Mashraqi A, Modafer Y, Al Abboud MA, El-Shabasy A Saudi J Biol Sci 26-Nov-2023
PMCID:PMC10749906
doi:10.1016/j.sjbs.2023.103877
PMID:38148949
Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK Int J Mol Sci 01-Jan-2023
PMCID:PMC9821772
doi:10.3390/ijms24010739
PMID:36614181
Synergistic Action of AMX Associated with 1,8-Cineole and Its Effect on the ESBL Enzymatic Resistance Mechanism Akhmouch AA, Hriouech S, Mzabi A, Tanghort M, Chefchaou H, Remmal A, Chami N Antibiotics (Basel) 26-Jul-2022
PMCID:PMC9331605
doi:10.3390/antibiotics11081002
PMID:35892393
Activity of Silver Nanoparticles against Staphylococcus spp. Swolana D, Wojtyczka RD Int J Mol Sci 13-Apr-2022
PMCID:PMC9028791
doi:10.3390/ijms23084298
PMID:35457115
Marine Macroalgae Display Bioreductant Efficacy for Fabricating Metallic Nanoparticles: Intra/Extracellular Mechanism and Potential Biomedical Applications Mahmood Ansari S, Saquib Q, De Matteis V, Awad Alwathnani H, Ali Alharbi S, Ali Al-Khedhairy A Bioinorg Chem Appl 27-Nov-2021
PMCID:PMC8643268
doi:10.1155/2021/5985377
PMID:34873399
A review of the phytochemical mediated synthesis of AgNP (silver nanoparticle): the wonder particle of the past decade Shaikh WA, Chakraborty S, Owens G, Islam RU Appl Nanosci 30-Oct-2021
PMCID:PMC8556825
doi:10.1007/s13204-021-02135-5
PMID:34745812
Study on potential applications and toxicity analysis of green synthesized nanoparticles GARG R, RANI P, GARG R, EDDY NO Turk J Chem 27-Sep-2021
PMCID:PMC10734732
doi:10.3906/kim-2106-59
PMID:38144602
Prospective Application of Nanoparticles Green Synthesized Using Medicinal Plant Extracts as Novel Nanomedicines Selvakesavan RK, Franklin G Nanotechnol Sci Appl 23-Sep-2021
PMCID:PMC8476107
doi:10.2147/NSA.S333467
PMID:34588770
Extreme Enlargement of the Inverted Repeat Region in the Plastid Genomes of Diatoms from the Genus Climaconeis Gastineau R, Davidovich NA, Davidovich OI, Lemieux C, Turmel M, Wróbel RJ, Witkowski A Int J Mol Sci 02-Jul-2021
PMCID:PMC8268801
doi:10.3390/ijms22137155
PMID:34281209
Green synthesis of silver nanoparticles using plant extracts and their antimicrobial activities: a review of recent literature Vanlalveni C, Lallianrawna S, Biswas A, Selvaraj M, Changmai B, Rokhum SL RSC Adv 13-Jan-2021
PMCID:PMC8694026
doi:10.1039/d0ra09941d
PMID:35424248
Anti-inflammatory Effects of Pelargonium endlicherianum Fenzl. Extracts in Lipopolysaccharide-stimulated Macrophages CUMAOĞLU A, KARATOPRAK GŞ, YERER MB, KOŞAR M Turk J Pharm Sci 02-Apr-2018
PMCID:PMC7227898
doi:10.4274/tjps.86580
PMID:32454648
A review on biosynthesis of silver nanoparticles and their biocidal properties Siddiqi KS, Husen A, Rao RA J Nanobiotechnology 16-Feb-2018
PMCID:PMC5815253
doi:10.1186/s12951-018-0334-5
PMID:29452593
Nanosilver: new ageless and versatile biomedical therapeutic scaffold Ullah Khan S, Saleh TA, Wahab A, Khan MH, Khan D, Ullah Khan W, Rahim A, Kamal S, Ullah Khan F, Fahad S Int J Nanomedicine 02-Feb-2018
PMCID:PMC5799856
doi:10.2147/IJN.S153167
PMID:29440898
Report on Second International Conference on Natural Products for Cancer Prevention and Therapy Held in Kayseri, Turkey, 8–11 November 2017 Yerer MB, Bishayee A Nutrients 23-Dec-2017
PMCID:PMC5793236
doi:10.3390/nu10010008
PMID:29295493

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
2-Phenylethyl propionate 31225 Click to see CCC(=O)OCCC1=CC=CC=C1 178.23 unknown https://doi.org/10.1055/S-2006-960872
Phenethyl isobutyrate 7655 Click to see CC(C)C(=O)OCCC1=CC=CC=C1 192.25 unknown https://doi.org/10.1055/S-2006-960872
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Docosane 12405 Click to see CCCCCCCCCCCCCCCCCCCCCC 310.60 unknown https://doi.org/10.1055/S-2006-960872
Dodecane 8182 Click to see CCCCCCCCCCCC 170.33 unknown https://doi.org/10.1055/S-2006-960872
Heneicosane 12403 Click to see CCCCCCCCCCCCCCCCCCCCC 296.60 unknown https://doi.org/10.1055/S-2006-960872
Heptacosane 11636 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC 380.70 unknown https://doi.org/10.1055/S-2006-960872
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown https://doi.org/10.1055/S-2006-960872
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1055/S-2006-960872
Pentacosane 12406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC 352.70 unknown https://doi.org/10.1055/S-2006-960872
Pentadecane 12391 Click to see CCCCCCCCCCCCCCC 212.41 unknown https://doi.org/10.1055/S-2006-960872
Tetracosane 12592 Click to see CCCCCCCCCCCCCCCCCCCCCCCC 338.70 unknown https://doi.org/10.1055/S-2006-960872
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown https://doi.org/10.1055/S-2006-960872
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkatetraenes
1,8,11,14-Heptadecatetraene 5319559 Click to see CCC=CCC=CCC=CCCCCCC=C 232.40 unknown https://doi.org/10.1055/S-2006-960872
1,8,11,14-Heptadecatetraene, (Z,Z,Z)- 5352710 Click to see CCC=CCC=CCC=CCCCCCC=C 232.40 unknown https://doi.org/10.1055/S-2006-960872
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Heptadecene 23217 Click to see CCCCCCCCCCCCCCCC=C 238.50 unknown https://doi.org/10.1055/S-2006-960872
14-Tricosene 62826 Click to see CCCCCCCCCCCCCC=CCCCCCCCC 322.60 unknown https://doi.org/10.1055/S-2006-960872
9-Hexacosene 5363630 Click to see CCCCCCCCCCCCCCCCC=CCCCCCCCC 364.70 unknown https://doi.org/10.1055/S-2006-960872
9-Tricosene 6385060 Click to see CCCCCCCCCCCCCC=CCCCCCCCC 322.60 unknown https://doi.org/10.1055/S-2006-960872
Hexacos-9-ene 522412 Click to see CCCCCCCCCCCCCCCCC=CCCCCCCCC 364.70 unknown https://doi.org/10.1055/S-2006-960872
Pentacos-9-ene 25201650 Click to see CCCCCCCCCCCCCCCC=CCCCCCCCC 350.70 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://doi.org/10.1055/S-2006-960872
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1055/S-2006-960872
Tridecanoic acid 12530 Click to see CCCCCCCCCCCCC(=O)O 214.34 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see CCCCCCCCCCCC(=O)O 200.32 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Dodecanol 8193 Click to see CCCCCCCCCCCCO 186.33 unknown https://doi.org/10.1055/S-2006-960872
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown https://doi.org/10.1055/S-2006-960872
1-Undecanol 8184 Click to see CCCCCCCCCCCO 172.31 unknown https://doi.org/10.1055/S-2006-960872
2-Nonanol 12367 Click to see CCCCCCCC(C)O 144.25 unknown https://doi.org/10.1055/S-2006-960872
Nonan-1-ol 8914 Click to see CCCCCCCCCO 144.25 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
1-Pentadecanol 12397 Click to see CCCCCCCCCCCCCCCO 228.41 unknown https://doi.org/10.1055/S-2006-960872
Cetyl Alcohol 2682 Click to see CCCCCCCCCCCCCCCCO 242.44 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
2-Tetradecenal 5283366 Click to see CCCCCCCCCCCC=CC=O 210.36 unknown https://doi.org/10.1055/S-2006-960872
Hexadecanal 984 Click to see CCCCCCCCCCCCCCCC=O 240.42 unknown https://doi.org/10.1055/S-2006-960872
Icosanal 75458 Click to see CCCCCCCCCCCCCCCCCCCC=O 296.50 unknown https://doi.org/10.1055/S-2006-960872
Octadecanal 12533 Click to see CCCCCCCCCCCCCCCCCC=O 268.50 unknown https://doi.org/10.1055/S-2006-960872
Pentadecanal 17697 Click to see CCCCCCCCCCCCCCC=O 226.40 unknown https://doi.org/10.1055/S-2006-960872
Tetradecanal 31291 Click to see CCCCCCCCCCCCCC=O 212.37 unknown https://doi.org/10.1055/S-2006-960872
Tridecanal 25311 Click to see CCCCCCCCCCCCC=O 198.34 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1055/S-2006-960872
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1055/S-2006-960872
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-Bergamotene 86608 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
alpha-CIS-BERGAMOTENE 6429303 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1055/S-2006-960872
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1055/S-2006-960872
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
3,6-Dimethyl-9-propan-2-ylspiro[4.5]dec-3-en-10-ol 14286039 Click to see CC1CCC(C(C12CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1055/S-2006-960872
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1055/S-2006-960872
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1055/S-2006-960872
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1055/S-2006-960872
beta-Terpinene 66841 Click to see CC(C)C1=CCC(=C)CC1 136.23 unknown https://doi.org/10.1055/S-2006-960872
Gleenol 6429080 Click to see CC1CCC(C(C12CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1055/S-2006-960872
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1055/S-2006-960872
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-beta-Bourbonene 324224 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
(-)-beta-Sesquiphellandrene 12315492 Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1 204.35 unknown https://doi.org/10.1055/S-2006-960872
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
(+)-gamma-Cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1055/S-2006-960872
(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/10.1055/S-2006-960872
(2R)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol 6506009 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1055/S-2006-960872
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane 5317024 Click to see CC(=C1CCC(C(C1)(C)C(=C)C)(C)C=C)C 218.38 unknown https://doi.org/10.1055/S-2006-960872
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene 101708 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
3-[(2S)-6-methylhept-5-en-2-yl]-6-methylidenecyclohexene 5321277 Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1 204.35 unknown https://doi.org/10.1055/S-2006-960872
6,10,14-Trimethylpentadecan-2-one 10408 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C 268.50 unknown https://doi.org/10.1055/S-2006-960872
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1055/S-2006-960872
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1055/S-2006-960872
alpha-Curcumene 92139 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1055/S-2006-960872
Alpha-Farnesene 5281516 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
beta-Bourbonene 62566 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1055/S-2006-960872
beta-Cubebene 93081 Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1055/S-2006-960872
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
Cedrelanol 160799 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1055/S-2006-960872
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1055/S-2006-960872
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)- 89316 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1055/S-2006-960872
delta-Curcumene 57386731 Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
delta-Elemene 12309449 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
T-Muurolol 3084331 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1055/S-2006-960872
trans-Nerolidol 5284507 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1055/S-2006-960872
Zingiberene 92776 Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1055/S-2006-960872
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1055/S-2006-960872
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1055/S-2006-960872
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1055/S-2006-960872
Alloaromadendren 91746537 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1055/S-2006-960872
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1055/S-2006-960872
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1055/S-2006-960872
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1055/S-2006-960872
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
> 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/10.1055/S-2006-960872
1,7-di-epi-alpha-Cedrene 10878276 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1055/S-2006-960872
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960872
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
beta-Caryophyllene alcohol 61125 Click to see CC1(CC2C1CCC3(CCCC2(C3)O)C)C 222.37 unknown https://doi.org/10.1055/S-2006-960872
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol 53436347 Click to see C12C3C4C1C5(C2C3=C45)O 118.13 unknown https://doi.org/10.1055/S-2006-960872
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Decanal 8175 Click to see CCCCCCCCCC=O 156.26 unknown https://doi.org/10.1055/S-2006-960872
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1055/S-2006-960872

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