Agastache rugosa - Unknown
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Details Top

Internal ID UUID64403318d4ce3765712567
Scientific name Agastache rugosa
Authority Kuntze
First published in Revis. Gen. Pl. 2: 511 (1891)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lophanthus formosanus Hayata Icon. Pl. Formosan. 8: 87 (1919)
Lophanthus rugosus Fisch. & C.A.Mey. Index Seminum [St.Petersburg (Petropolitanus)] i. 31.
Agastache rugosa f. alba Y.N.Lee Bull. Korea Pl. Res. 5: 24 (2005)
Cedronella japonica Hassk. Acta Soc. Regiae Sci. Indo-Neêrl. 1: 37 (1856)
Agastache formosana (Hayata) Hayata Fl. Japan ed. 2: 1006. 1931 (1931)
Elsholtzia monostachys H.Lév. & Vaniot Repert. Spec. Nov. Regni Veg. 8: 424 (1910)

Common names Top

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Language Common/alternative name
Spanish blue licorice
Spanish korean mint
Spanish lophanthus argyi
Spanish menta coreana
Spanish patchouli herb
Spanish purple giant hyssop
Spanish wrinkled giant hyssop
Spanish indian mint
Spanish huo xiang
Arabic أغستاش خشن
German koreaminze
German koreanische minze
German ostasiatischer riesenysop
Persian نعنای کرهای
Japanese カワミドリ
Korean 방아잎
Korean 방앗잎
Korean 배초향
lzh 藿香
Malayalam ഇരുവേലി
Russian Агастахис морщинистый
Russian Многоколосник морщинистый
Vietnamese hoắc hương núi
Chinese 猫巴虎
Chinese 鱼子苏
Chinese 香荆芥花
Chinese 青茎薄荷
Chinese 苏藿香
Chinese 苍告
Chinese 红花小茴香
Chinese 白薄荷
Chinese 白荷
Chinese 仁丹草
Chinese 排香草
Chinese 香薷
Chinese 薄荷
Chinese 野薄荷
Chinese 山薄荷
Chinese 山茴香
Chinese 小薄荷
Chinese 野苏子
Chinese 鱼香
Chinese 藿香
Chinese 野藿香
Chinese 鸡苏
Chinese 紫苏草
Chinese 草菇
Chinese 藿香(土藿香)
Chinese 拉拉香
Chinese 兜娄婆香
Chinese 八蒿
Chinese 叶藿香
Chinese 合香
Chinese 土藿香
Chinese 大叶薄荷
Chinese 大薄荷
Chinese 家茴香
Chinese 山灰香
Chinese 山猫巴
Chinese 把蒿
Chinese 杏仁花
Chinese 水蔴叶
Chinese 猫尾巴香
Chinese 猫巴蒿

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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Maintain seeds at a constant 10°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Manchuria
      • Tibet
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan
    • Russian Far East
      • Amur
      • Khabarovsk
      • Kuril Islands
      • Primorye
  • Europe
    • Eastern Europe
      • Central European Russia
    • Middle Europe
      • Austria
      • Germany
    • Northern Europe
      • Great Britain
      • Sweden

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000906745
UNII U4KXI7P9Z1
Tropicos 17602232
INPN 788815
KEW urn:lsid:ipni.org:names:444504-1
The Plant List kew-4494
Open Tree Of Life 485528
Observations.org 141905
NCBI Taxonomy 39271
IPNI 444504-1
iNaturalist 506801
GBIF 7307327
Freebase /m/026jh3n
EPPO AJTRG
EOL 2893655
Elurikkus 586209
USDA GRIN 1675
Wikipedia Agastache_rugosa
CMAUP NPO26351
Plantarium 906

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_031470985.1 ASM3147098v1 Chromosome Chungbuk National University 2023-09-15 447.6x 391.65 Mb

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
Advances in the application of traditional Chinese medicine during the COVID-19 recovery period: A review Zhang W, Ma L, Xie W, Li X, Zhang J, Sun J Medicine (Baltimore) 05-Apr-2024
PMCID:PMC10994423
doi:10.1097/MD.0000000000037683
PMID:38579075
The complete chloroplast genome of Lagochilus ilicifolius Bunge ex Bentham, Labiat. Gen. 1834 (Lamiaceae) and its phylogenetic analysis Hou WJ, Men WX, Xing YP, Yang YY, Xu L, Kang TG, Song YY Mitochondrial DNA B Resour 02-Apr-2024
PMCID:PMC10993758
doi:10.1080/23802359.2024.2334013
PMID:38586511
Flower opening dynamics, pollen-ovule ratio, stigma receptivity and stigmatic pollen germination (in-vivo) in Chaenomeles speciosa (Sweet) Nakai Wan X, Sun D, Gao C Sci Rep 26-Mar-2024
PMCID:PMC10965984
doi:10.1038/s41598-024-57655-1
PMID:38531911
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
Traditional and contemporary herbal medicines in management of cancer: A scoping review Imtiaz I, Schloss J, Bugarcic A J Ayurveda Integr Med 23-Feb-2024
PMCID:PMC10901831
doi:10.1016/j.jaim.2024.100904
PMID:38395014
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
D-Limonene Affects the Feeding Behavior and the Acquisition and Transmission of Tomato Yellow Leaf Curl Virus by Bemisia tabaci Wei Y, Gao L, Zhang Z, Li K, Zhang Z, Zhang D, Chen J, Peng J, Gao Y, Du J, Yan S, Shi X, Liu Y Viruses 15-Feb-2024
PMCID:PMC10891612
doi:10.3390/v16020300
PMID:38400075
Effects of Traditional Chinese Medicine “Fuzheng Qingdu Decoction” on Autonomic Function and Cancer-Related Symptoms in Patients with Advanced Gastric Cancer undergoing Chemotherapy: A Controlled Trial Yuan C, Wu S, Wu Y, Tian C, Wang Z, Zhang X Integr Cancer Ther 07-Feb-2024
PMCID:PMC10851715
doi:10.1177/15347354241229414
PMID:38323452
Increased Accumulation of Ginsenosides in Panax ginseng Sprouts Cultivated with Kelp Fermentates Park KW, Kim JH, Jeong BG, Park JK, Jang HY, Oh YS, Kang KY Plants (Basel) 05-Feb-2024
PMCID:PMC10856821
doi:10.3390/plants13030463
PMID:38337995
Traditional Uses, Chemical Constituents and Pharmacological Activities of the Toona sinensis Plant Zhao M, Li H, Wang R, Lan S, Wang Y, Zhang Y, Sui H, Li W Molecules 04-Feb-2024
PMCID:PMC10856474
doi:10.3390/molecules29030718
PMID:38338461
Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C J Ethnobiol Ethnomed 15-Jan-2024
PMCID:PMC10790445
doi:10.1186/s13002-023-00638-9
PMID:38225656
Eco-friendly approaches to phytochemical production: elicitation and beyond Jalota K, Sharma V, Agarwal C, Jindal S Nat Prod Bioprospect 10-Jan-2024
PMCID:PMC10776560
doi:10.1007/s13659-023-00419-7
PMID:38195902
Medicine for chronic atrophic gastritis: a systematic review, meta- and network pharmacology analysis Weng J, Wu XF, Shao P, Liu XP, Wang CX Ann Med 03-Jan-2024
PMCID:PMC10769149
doi:10.1080/07853890.2023.2299352
PMID:38170849
The influence of herbal medicine on serum motilin and its effect on human and animal model: a systematic review Cho MS, Park JW, Kim J, Ko SJ Front Pharmacol 14-Dec-2023
PMCID:PMC10755953
doi:10.3389/fphar.2023.1286333
PMID:38161695
Effects of Exogenous Ethanol Treatment in Nutrient Solution on Growth and Secondary Metabolite Contents of Three Herb Species in an Indoor Vertical Farming System Shin J, Lee Y, Hahm S, Lee K, Park J Plants (Basel) 14-Nov-2023
PMCID:PMC10675256
doi:10.3390/plants12223842
PMID:38005739

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
[2-(4-Hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-3-yl]methyl 4-hydroxybenzoate 73817269 Click to see COC1=C(C=CC(=C1)C=C2COC(C2COC(=O)C3=CC=C(C=C3)O)C4=CC(=C(C=C4)O)OC)O 478.50 unknown https://doi.org/10.1021/NP010425E
Agastenol 10073783 Click to see COC1=C(C=CC(=C1)C=C2COC(C2COC(=O)C3=CC=C(C=C3)O)C4=CC(=C(C=C4)O)OC)O 478.50 unknown https://doi.org/10.1021/NP010425E
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
p-Anisaldehyde 31244 Click to see COC1=CC=C(C=C1)C=O 136.15 unknown https://doi.org/10.1080/10412905.1992.9698139
https://doi.org/10.1080/10412905.2001.9699669
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1080/10412905.1992.9698139
> Benzenoids / Phenol ethers / Anisoles
Anethole 637563 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown via CMAUP database
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown https://doi.org/10.1248/YAKUSHI1947.90.12_1514
https://doi.org/10.1080/10412905.2001.9699669
https://doi.org/10.1080/10412905.1992.9698139
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Allylphenol 68148 Click to see C=CCC1=CC=C(C=C1)O 134.17 unknown https://doi.org/10.1080/10412905.1992.9698139
> Benzenoids / Phenols / Methoxyphenols
Chavibetol 596375 Click to see COC1=C(C=C(C=C1)CC=C)O 164.20 unknown https://doi.org/10.1080/10412905.1992.9698139
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1080/10412905.1992.9698139
> Hydrocarbons / Polycyclic hydrocarbons
(-)-Isoledene 91873614 Click to see CC1CCC2C(C2(C)C)C3=C1CCC3C 204.35 unknown via CMAUP database
(1aR,4R,7R,7bS)-1,1,4,7-Tetramethyl-1a,2,3,4,5,6,7,7b-octahydro-1H-cyclopropa[e]azulene 15431199 Click to see CC1CCC2C(C2(C)C)C3=C1CCC3C 204.35 unknown via CMAUP database
Isoledene 530426 Click to see CC1CCC2C(C2(C)C)C3=C1CCC3C 204.35 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[2-(4-Hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methyl 4-hydroxybenzoate 22297730 Click to see COC1=C(C=CC(=C1)CC2COC(C2COC(=O)C3=CC=C(C=C3)O)C4=CC(=C(C=C4)O)OC)O 480.50 unknown https://doi.org/10.1021/NP010425E
Agastinol 637406 Click to see COC1=C(C=CC(=C1)CC2COC(C2COC(=O)C3=CC=C(C=C3)O)C4=CC(=C(C=C4)O)OC)O 480.50 unknown https://doi.org/10.1021/NP010425E
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(R)-3-Octanol 445789 Click to see CCCCCC(CC)O 130.23 unknown https://doi.org/10.1248/YAKUSHI1947.90.12_1514
1-Octen-3-OL 18827 Click to see CCCCCC(C=C)O 128.21 unknown https://doi.org/10.1248/YAKUSHI1947.90.12_1514
3-Octanol 11527 Click to see CCCCCC(CC)O 130.23 unknown https://doi.org/10.1248/YAKUSHI1947.90.12_1514
cis-3-Hexen-1-ol 5281167 Click to see CCC=CCCO 100.16 unknown via CMAUP database
trans-3-Hexen-1-ol 5284503 Click to see CCC=CCCO 100.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Agastaquinone 177257 Click to see CC(C)C1=C(C(=O)C2=C3C=CC(=O)C(C3=CC(=C2C1=O)O)(C)C)OC 340.40 unknown https://doi.org/10.1007/BF02976440
https://doi.org/10.1021/NP50125A011
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1248/YAKUSHI1947.90.12_1514
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1248/YAKUSHI1947.90.12_1514
https://doi.org/10.1080/10412905.1992.9698139
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown via CMAUP database
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1248/YAKUSHI1947.90.12_1514
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 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 https://doi.org/10.1248/YAKUSHI1947.90.12_1514
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.90.12_1514
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene 12223113 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.90.12_1514
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.90.12_1514
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol 443162 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
(-)-cis-Carveol 330573 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1992.9698139
(-)-Pulegone 638012 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown via CMAUP database
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1992.9698139
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
Carveol 7438 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1992.9698139
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.90.12_1514
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.90.12_1514
https://doi.org/10.1080/10412905.2001.9699669
p-Menth-4(8)-en-3-one 6988 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown via CMAUP database
Pulegone 442495 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Cubebene 86609 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown via CMAUP database
(-)-beta-Bourbonene 324224 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698139
(+)-alpha-Muurolene 12306049 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown via CMAUP database
(+)-beta-Caryophyllene 20831623 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
(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/10.1080/10412905.1992.9698139
(4Z)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene 5322111 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
(Z,E)-alpha-Farnesene 5362889 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown via CMAUP database
(Z)-caryophyllene 6429301 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
1-[(1S,3aR,7S,7aS)-4-methylidene-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl]ethanone 14038847 Click to see CC(C)C1CCC(=C)C2C1C(CC2)C(=O)C 220.35 unknown https://doi.org/10.1080/10412905.1992.9698139
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 via CMAUP database
4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenol 519662 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
4,11,11-Trimethyl-8-methylene-5-oxatricyclo(8.2.0.0(4,6))dodecane, (1R,4R,6R,10S)- 6604672 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
7-Acetyl-2-hydroxy-2-methyl-5-isopropylbicyclo[4.3.0]nonane 539857 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown https://doi.org/10.1080/10412905.1992.9698139
alpha-Cadinene 12306052 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown via CMAUP database
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1992.9698139
alpha-Cadinol #1 6431302 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
Alpha-Farnesene 5281516 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown via CMAUP database
alpha-Multijugenol 70566040 Click to see CC1=CCC2C(CC2(C)C)C(=C)CCC1O 220.35 unknown https://doi.org/10.1080/10412905.1992.9698139
beta-Bourbonene 62566 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698139
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1992.9698139
Cadina-4,9-diene 91748288 Click to see CC1CCC2C(=CCC(C2=C1)C(C)C)C 204.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698139
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1992.9698139
Caryophyllene oxide 2 13240188 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
delta-Cadinene 12306054 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown via CMAUP database
gamma-Elemene 94254 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown via CMAUP database
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698139
Isocaryophyllene 5281522 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Isocaryophyllene oxide 1742211 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Naphthalene, 1,2,3,4,4a,5,6,8a-octahydro-7-methyl-4-methylene-1-(1-methylethyl)-, (1alpha,4aalpha,8aalpha)- 6432308 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown via CMAUP database
Naphthalene, 1,2,3,5,6,8a-hexahydro-4,7-dimethyl-1-(1-methylethyl)-, (1S-cis)- 12306059 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown via CMAUP database
Oplopanone 10466745 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown https://doi.org/10.1080/10412905.1992.9698139
tau-Muurolol 6432221 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(+)-Aromadendrene 11095734 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown via CMAUP database
(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 via CMAUP database
(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/10.1080/10412905.1992.9698139
(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/10.1080/10412905.1992.9698139
1H-Cycloprop[e]azulen-4-ol, decahydro-1,1,4,7-tetramethyl-, [1ar-(1aalpha,4beta,4abeta,7alpha,7abeta,7balpha)]- 6432543 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown via CMAUP database
beta-Diploalbicene 177445 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown via CMAUP database
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(+)-Bicyclogermacrene 11820258 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown via CMAUP database
(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 via CMAUP database
(1S,2E,6E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 13894537 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown via CMAUP database
(1S,2Z,6Z,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 13894533 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown via CMAUP database
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown via CMAUP database
> 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 via CMAUP database
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)- 9859094 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(+)-germacrene D 24771782 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
(1E)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene 74764030 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
(1Z)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene 92003564 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
(6E,8S)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene 49796490 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
(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/10.1080/10412905.1992.9698139
1-Methyl-5-methylene-8-(1-methylethyl)-1,6-cyclodecadiene 6436582 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)-, [s-(E,E)]- 5373727 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown via CMAUP database
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698139
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Oleanolic aldehyde 10321055 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C=O)C 440.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
1-Hexen-3-yl acetate 118262 Click to see CCCC(C=C)OC(=O)C 142.20 unknown https://doi.org/10.1080/10412905.1992.9698139
1-Octen-3-yl acetate 17121 Click to see CCCCCC(C=C)OC(=O)C 170.25 unknown https://doi.org/10.1080/10412905.1992.9698139
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(E)-jasmone 1549019 Click to see CCC=CCC1=C(CCC1=O)C 164.24 unknown https://doi.org/10.1080/10412905.1992.9698139
Jasmone 1549018 Click to see CCC=CCC1=C(CCC1=O)C 164.24 unknown https://doi.org/10.1080/10412905.1992.9698139
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
3-Octanone 246728 Click to see CCCCCC(=O)CC 128.21 unknown https://doi.org/10.1248/YAKUSHI1947.90.12_1514
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetophenone 7410 Click to see CC(=O)C1=CC=CC=C1 120.15 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Dihydroactinidiolide 6432173 Click to see CC1(CCCC2(C1=CC(=O)O2)C)C 180.24 unknown https://doi.org/10.1080/10412905.1992.9698139
> Phenylpropanoids and polyketides / Cinnamaldehydes
2-Propenal, 3-(4-methoxyphenyl)- 230995 Click to see COC1=CC=C(C=C1)C=CC=O 162.18 unknown https://doi.org/10.1080/10412905.1992.9698139
4-Methoxycinnamaldehyde 641294 Click to see COC1=CC=C(C=C1)C=CC=O 162.18 unknown https://doi.org/10.1080/10412905.1992.9698139
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid 639655 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown via CMAUP database
Rosmarinic acid 5281792 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1007/BF02979163
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Morin 5281670 Click to see C1=CC(=C(C=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 302.23 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown via CMAUP database
Quercetin 3-O-beta-D-xylopyranoside 5320861 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl acetate 5316761 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)OC)O)O)O)O 488.40 unknown https://doi.org/10.1248/CPB.29.1777
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl] acetate 5318496 Click to see CC(=O)OC1C(C(C(OC1OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)OC)O)CO)O)O 488.40 unknown https://doi.org/10.1248/CPB.29.1777
[4,5-Dihydroxy-2-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl] acetate 73981625 Click to see CC(=O)OC1C(C(C(OC1OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)OC)O)CO)O)O 488.40 unknown https://doi.org/10.1248/CPB.29.1777
7-(beta-D-Galactopyranosyloxy)-5-hydroxy-2-(4-Methoxyphenyl)- 5291487 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1016/S0014-5793(01)02379-1
bis[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl] propanedioate 11968428 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC(=O)CC(=O)OCC5C(C(C(C(O5)OC6=CC(=C7C(=C6)OC(=CC7=O)C8=CC=C(C=C8)OC)O)O)O)O)O)O)O)O 960.80 unknown https://doi.org/10.1248/CPB.29.1777
Bis[[3,4,5-trihydroxy-6-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl] propanedioate 73157035 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC(=O)CC(=O)OCC5C(C(C(C(O5)OC6=CC(=C7C(=C6)OC(=CC7=O)C8=CC=C(C=C8)OC)O)O)O)O)O)O)O)O 960.80 unknown https://doi.org/10.1248/CPB.29.1777
Tilianin 5321954 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1248/CPB.29.1777
https://doi.org/10.1016/S0014-5793(01)02379-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown https://doi.org/10.1248/CPB.29.1777
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Pachypodol 5281677 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O 344.30 unknown via CMAUP database

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