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Arnebia guttata

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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 UUID64400acda4226037265510
Scientific name Arnebia guttata
Authority Bunge
First published in Index Seminum (TU, Dorpatensis) 1840: 7 (1840)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Lithospermum guttatum (Bunge) I.M.Johnst. J. Arnold Arbor. 33: 330 (1952)
Arnebia guttata var. thomsonii (C.B.Clarke) Kazmi J. Arnold Arbor. 52: 495 (1971)
Arnebia thomsonii C.B.Clarke Fl. Brit. India 4: 176 (1883)
Arnebia tibetana Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 43: 189 (1874)
Macrotomia guttata (Bunge) Farrer Engl. Rock Gard. 2: 469 (1925)

Common names Top

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Language Common/alternative name
Azerbaijani xallı arnebiya
Bulgarian петниста арнебия
Russian Арнебия пятнистая
Chinese 紫草
Chinese 黄花软紫草
Chinese 黄花软紫草（假紫草、黄花紫草、内蒙紫草）
Chinese 假紫草
Chinese 内蒙古紫草
Chinese 黃花軟紫草

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Arnebia guttata subsp. griffithii (Boiss.) Sadat Mitt. Bot. Staatssamml. München 28: 128 (1989)

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • Inner Mongolia
      • Tibet
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
    • Western Asia
      • Afghanistan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000549482
UNII R76YN3W40S
Tropicos 4002136
KEW urn:lsid:ipni.org:names:113462-1
The Plant List kew-2652991
Plantarium 3753
Open Tree Of Life 476290
Observations.org 127389
NCBI Taxonomy 419289
IPNI 113462-1
GBIF 7295244
EOL 2893225
Elurikkus 584306
USDA GRIN 429666
CMAUP NPO20297

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
Genomic divergence and demographic history of Quercus aliena populations Han B, Tong B, Zhang J, Bu Z, Zhao L, Xian Y, Li D, Xie X BMC Plant Biol 09-Jan-2024
PMCID:PMC10775429
doi:10.1186/s12870-023-04623-y
PMID:38195447
Key Risk Genes Identified From the Postmortem Brain of Patients With Major Depressive Disorder and Their Potential Clinical Applications Zhuang Q, Wang J, Li X, Zhang X, Wang Y Int J Neuropsychopharmacol 26-May-2023
PMCID:PMC10289144
doi:10.1093/ijnp/pyad024
PMID:37235790
Exploring pharmaphylogeny from multiple perspectives: a case study on Lithospermeae Yan Y, Wei X, Qiu B, Wang G, Zhou B, Zhang M, Liu Y, Li S, Gao B, Li M Sci Rep 11-May-2023
PMCID:PMC10175555
doi:10.1038/s41598-023-34830-4
PMID:37169837
Variation and association of leaf traits for desert plants in the arid area, northwest China Wang H, Yang J, Xie T, Ma L, Niu F, He C, Shan L Ecol Evol 24-Mar-2023
PMCID:PMC10037433
doi:10.1002/ece3.9946
PMID:36969926
Pyrrolizidine alkaloids and health risk of three Boraginaceae used in TCM Zan K, Wang Z, Hu XW, Li YL, Wang Y, Jin HY, Zuo TT, Ma SC Front Pharmacol 23-Mar-2023
PMCID:PMC10076571
doi:10.3389/fphar.2023.1075010
PMID:37033649
Phylogeny of Trigonotis in China—with a special reference to its nutlet morphology and plastid genome Xu XM, Liu DH, Zhu SX, Wang ZL, Wei Z, Liu QR Plant Divers 15-Mar-2023
PMCID:PMC10435912
doi:10.1016/j.pld.2023.03.004
PMID:37601540
Current scenario of traditional medicines in management of diabetic foot ulcers: A review Rayate AS, Nagoba BS, Mumbre SS, Mavani HB, Gavkare AM, Deshpande AS World J Diabetes 15-Jan-2023
PMCID:PMC9850800
doi:10.4239/wjd.v14.i1.1
PMID:36684382
The complete chloroplast genome of Cynoglossum amabile Stapf & J. R. Drumm., 1906 (Boraginaceae), a traditional Chinese herbal medicine Zhao ZN, Yu X Mitochondrial DNA B Resour 02-Jan-2023
PMCID:PMC9815245
doi:10.1080/23802359.2022.2160219
PMID:36620318
The chloroplast genome of Lappula myosotis V. Wolf, a medicinal species Yan S, Wang T, Wang Z, Ren W, Liu C, Ma W, Dong S Mitochondrial DNA B Resour 01-Jan-2023
PMCID:PMC9815226
doi:10.1080/23802359.2022.2158692
PMID:36620320
Uncovering the pharmacological mechanisms of Zizhu ointment against diabetic ulcer by integrating network analysis and experimental evaluation in vivo and in vitro Wang J, Wang Y, Huang R, Li W, Fan W, Hu X, Yang X, Han Q, Wang H, Liu G Front Pharmacol 13-Dec-2022
PMCID:PMC9793990
doi:10.3389/fphar.2022.1027677
PMID:36582537
Variations in genetic diversity in cultivated Pistacia chinensis Han B, Zhang MJ, Xian Y, Xu H, Cui CC, Liu D, Wang L, Li DZ, Li WQ, Xie XM Front Plant Sci 10-Nov-2022
PMCID:PMC9691265
doi:10.3389/fpls.2022.1030647
PMID:36438104
Pharmacological and analytical aspects of alkannin/shikonin and their derivatives: An update from 2008 to 2022 Kaur K, Sharma R, Singh A, Attri S, Arora S, Kaur S, Bedi N Chin Herb Med 20-Sep-2022
PMCID:PMC9669360
doi:10.1016/j.chmed.2022.08.001
PMID:36405061
The Application of Pearls in Traditional Medicine of China and Their Chemical Constituents, Pharmacology, Toxicology, and Clinical Research Song Y, Chen W, Fu K, Wang Z Front Pharmacol 23-Aug-2022
PMCID:PMC9445187
doi:10.3389/fphar.2022.893229
PMID:36081944
Shikonin ameliorated mice colitis by inhibiting dimerization and tetramerization of PKM2 in macrophages Huang B, Wang Q, Jiang L, Lu S, Li C, Xu C, Wang C, Zhang E, Zhang X Front Pharmacol 17-Aug-2022
PMCID:PMC9428403
doi:10.3389/fphar.2022.926945
PMID:36059938
Component Composition and Biological Activity of Various Extracts of Onosma gmelinii (Boraginaceae) Shilov SV, Ustenova GO, Kiyekbayeva LN, Korotetskiy IS, Kudashkina NV, Zubenko NV, Parenova RA, Jumagaziyeva AB, Iskakbayeva ZA, Kenesheva ST Int J Biomater 22-Jul-2022
PMCID:PMC9337954
doi:10.1155/2022/4427804
PMID:35912375

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
(R)-1-phenylethanol 637516 Click to see CC(C1=CC=CC=C1)O 122.16 unknown via CMAUP database
(S)-1-Phenylethanol 443135 Click to see CC(C1=CC=CC=C1)O 122.16 unknown via CMAUP database
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3,5-Dimethoxytoluene 77844 Click to see CC1=CC(=CC(=C1)OC)OC 152.19 unknown via CMAUP database
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde 998 Click to see C1=CC=C(C=C1)CC=O 120.15 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
Shikometabolin A 10460360 Click to see CC(=CCC1=C2C(=C(C3=C(C(=CC(=O)C3=C2O)C(CC=C(C)C)O)O)O)C4=C(C5=C(C(=O)C=CC5=O)C(=C14)O)O)C 556.60 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
(R)-1-(5,8-Dihydroxy-1,4-dioxo-1,4-dihydro-2-naphthyl)-4-methyl-3-pentenyl isovalerate 479497 Click to see CC(C)CC(=O)OC(CC=C(C)C)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 372.40 unknown via CMAUP database
(R)-1-(5,8-Dihydroxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-4-methylpent-3-en-1-yl acetate 479501 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)C)C 330.30 unknown via CMAUP database
[1-(5,8-Dihydroxy-1,4-dioxonaphthalen-2-yl)-4-methylpent-3-enyl] 3,4-dimethylpent-3-enoate 5321814 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)CC(=C(C)C)C)C 398.40 unknown via CMAUP database
1,4-Naphthoquinone 8530 Click to see C1=CC=C2C(=O)C=CC(=O)C2=C1 158.15 unknown via CMAUP database
2-Methyl-n-butyrylshikonin 101409383 Click to see CCC(C)C(=O)OC(C)(CC=C(C)C)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 386.40 unknown via CMAUP database
Acetylalkannin 9967285 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)C)C 330.30 unknown via CMAUP database
Acetylshikonin 32464 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)C)C 330.30 unknown via CMAUP database
Alkannin 72521 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)O)C 288.29 unknown via CMAUP database
Alkannin beta,beta-dimethylacrylate 442720 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)C=C(C)C)C 370.40 unknown via CMAUP database
beta-Hydroxyisovalerylshikonin 479502 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)CC(C)(C)O)C 388.40 unknown via CMAUP database
C.I. Natural Red 20 5208 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)O)C 288.29 unknown via CMAUP database
Deoxyshikonin 98914 Click to see CC(=CCCC1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)C 272.29 unknown via CMAUP database
Dmask 32465 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)C=C(C)C)C 370.40 unknown via CMAUP database
Isobutylshikonin 269324 Click to see CC(C)C(=O)OC(CC=C(C)C)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 358.40 unknown via CMAUP database
Isobutyrylshikonin 479500 Click to see CC(C)C(=O)OC(CC=C(C)C)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 358.40 unknown via CMAUP database
Isovalerylshikonin 335426 Click to see CC(C)CC(=O)OC(CC=C(C)C)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 372.40 unknown via CMAUP database
Propionylshikonin 153984 Click to see CCC(=O)OC(CC=C(C)C)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 344.40 unknown via CMAUP database
Shikonin 479503 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)O)C 288.29 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Phenanthrene 995 Click to see C1=CC=C2C(=C1)C=CC3=CC=CC=C32 178.23 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Anethole 637563 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown via CMAUP database
Anethole, (Z)- 1549040 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown via CMAUP database
> Hydrocarbons / Polycyclic hydrocarbons
African-5-ene 91750055 Click to see CC1CCC2C1=CC(CC3C2(C3)C)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(S)-Ethyl 2-methylbutanoate 6429107 Click to see CCC(C)C(=O)OCC 130.18 unknown via CMAUP database
Ethyl 2-methylbutyrate 24020 Click to see CCC(C)C(=O)OCC 130.18 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl decanoate 8050 Click to see CCCCCCCCCC(=O)OC 186.29 unknown via CMAUP database
Methyl elaidate 5280590 Click to see CCCCCCCCC=CCCCCCCCC(=O)OC 296.50 unknown via CMAUP database
Methyl heptanoate 7826 Click to see CCCCCCC(=O)OC 144.21 unknown via CMAUP database
Methyl hexanoate 7824 Click to see CCCCCC(=O)OC 130.18 unknown via CMAUP database
Methyl oleate 5364509 Click to see CCCCCCCCC=CCCCCCCCC(=O)OC 296.50 unknown via CMAUP database
Methyl palmitate 8181 Click to see CCCCCCCCCCCCCCCC(=O)OC 270.50 unknown via CMAUP database
Methyl palmitoleate 643801 Click to see CCCCCCC=CCCCCCCCC(=O)OC 268.40 unknown via CMAUP database
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown via CMAUP database
Methyl tetradecanoate 31284 Click to see CCCCCCCCCCCCCC(=O)OC 242.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid 6950479 Click to see CCC(C)C(=O)O 102.13 unknown via CMAUP database
(S)-2-methylbutanoic acid 448893 Click to see CCC(C)C(=O)O 102.13 unknown via CMAUP database
2-Ethyl-2-methylbutanoate 21434475 Click to see CCC(C)(CC)C(=O)[O-] 129.18 unknown via CMAUP database
2-Methylbutanoic acid 8314 Click to see CCC(C)C(=O)O 102.13 unknown via CMAUP database
2,3-Dimethylacrylic acid, (E)- 125468 Click to see CC=C(C)C(=O)O 100.12 unknown via CMAUP database
2,3-Dimethylacrylic acid, (Z)- 643915 Click to see CC=C(C)C(=O)O 100.12 unknown via CMAUP database
Isovaleric acid 10430 Click to see CC(C)CC(=O)O 102.13 unknown via CMAUP database
> 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 acids and conjugates / Medium-chain fatty acids
2-Methylhexanoate 22173957 Click to see CCCCC(C)C(=O)[O-] 129.18 unknown via CMAUP database
Capric Acid 2969 Click to see CCCCCCCCCC(=O)O 172.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Valeric acid 7991 Click to see CCCCC(=O)O 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
methyl (9E,12Z)-octadeca-9,12-dienoate 5462988 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown via CMAUP database
Methyl linoleate 5284421 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown via CMAUP database
Methyl linolelaidate 5362793 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown via CMAUP database
Methyl linolenate 5319706 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC 292.50 unknown via CMAUP database
Methyl octadeca-9,12-dienoate 8203 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown via CMAUP database
> 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 via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-(1S,4S)-Borneol 6850744 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
(-)-3-Carene 442461 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
(-)-Camphor 444294 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
(+)-Camphor 9543187 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
(1R,2S,4R)-Borneol 439568 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
(1S-endo)-1,7,7-trimethylbicyclo(2.2.1)heptan-2-ol 10049 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
(1S,2S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol 12242815 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, exo- 439569 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Borneo camphor 12242824 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
Camphor (synthetic) 159055 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
Camphor, (1S,4S)-(-)- 10050 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
d-Camphor 230921 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
DL-Borneol 10492 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Sumatra camphor 657014 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Prenylquinones
Echinofuran B 13850221 Click to see CC(=CCCC1=COC(=C1)C2=CC(=O)C=CC2=O)C 256.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)(-)-(E)-beta-caryophyllene 14757966 Click to see CC1(CC2C1CCC(=C)CCCC2=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
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
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
beta-Ionone 638014 Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C 192.30 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
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
Eudesma-4(14),7(11)-diene 6432497 Click to see CC(=C1CCC2(CCCC(=C)C2C1)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
Selina-4(15),7(11)-diene 10655819 Click to see CC(=C1CCC2(CCCC(=C)C2C1)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-Naphthalenemethanol, 1,2,3,4,4a,5,6,8a-octahydro-alpha,alpha,4a,8-tetramethyl-, [2R-(2alpha,4aalpha,8abeta)]- 5317269 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown via CMAUP database
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene 519361 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown via CMAUP database
beta-Maaliene 521242 Click to see CC1=C2C3C(C3(C)C)CCC2(CCC1)C 204.35 unknown via CMAUP database
beta-Selinene 442393 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Triquinane sesquiterpenoids / Angular triquinanes
beta-Isocomene 10910652 Click to see CC1CCC2(C13CCCC3(CC2=C)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
[(1S,2S,4S,6R,7S,9R,13S,14R,15R,16S,17S)-4,16-dihydroxy-2,6,14,17-tetramethyl-3,11-dioxo-10-oxatetracyclo[7.7.1.02,7.013,17]heptadecan-15-yl] acetate 5321291 Click to see CC1CC(C(=O)C2(C1CC3C4(C2C(C(C(C4CC(=O)O3)C)OC(=O)C)O)C)C)O 408.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Isobutyric acid 6590 Click to see CC(C)C(=O)O 88.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
1-O-[3-O-(3-Methoxy-4-hydroxycinnamoyl)-beta-D-fructofuranosyl]-beta-D-fructofuranosyl 6-O-(3-methoxy-4-hydroxycinnamoyl)-alpha-D-glucopyranoside 101414919 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)COC4(C(C(C(O4)CO)O)OC(=O)C=CC5=CC(=C(C=C5)O)OC)CO)O)O)O)O 856.80 unknown via CMAUP database
1-O-[3-O-(3-Methoxy-4-hydroxycinnamoyl)-beta-D-fructofuranosyl]-beta-D-fructofuranosyl 6-O-(4-hydroxycinnamoyl)-alpha-D-glucopyranoside 101414918 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(OC2(CO)OCC3(C(C(C(O3)CO)O)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)CO)O)O 826.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Furfural 7362 Click to see C1=COC(=C1)C=O 96.08 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Hexanal 6184 Click to see CCCCCC=O 100.16 unknown via CMAUP database
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetylfuran 14505 Click to see CC(=O)C1=CC=CO1 110.11 unknown via CMAUP database
2-Acetylpyrrole 14079 Click to see CC(=O)C1=CC=CN1 109.13 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Paeonol 11092 Click to see CC(=O)C1=C(C=C(C=C1)OC)O 166.17 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Pentylfuran 19602 Click to see CCCCCC1=CC=CO1 138.21 unknown via CMAUP database
Thiophene 8030 Click to see C1=CSC=C1 84.14 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolizidines
Viridiflorine 6453144 Click to see CC(C)C(C(C)O)(C(=O)OCC1CCN2C1CCC2)O 285.38 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S)-2alpha-(3,4-Dihydroxyphenyl)-4-[(E)-3-[(R)-1-(methoxycarbonyl)-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxo-1-propenyl]-7-hydroxy-2,3-dihydrobenzofuran-3beta-carboxylic acid ethyl ester 11592305 Click to see CCOC(=O)C1C(OC2=C(C=CC(=C12)C=CC(=O)OC(CC3=CC(=C(C=C3)O)O)C(=O)OC)O)C4=CC(=C(C=C4)O)O 580.50 unknown via CMAUP database
10-epi-Lithospermic acid 95359683 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)O)O)O 538.50 unknown via CMAUP database
2-((2S,3S)-4-((E)-3-((R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy)-3-oxoprop-1-enyl)-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydrobenzo[b]furan-3-carbonyloxy)-3-(3,4-dihydroxyphenyl)propanoic acid 6449855 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O 718.60 unknown via CMAUP database
CID 5281302 5281302 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)O)O)O 538.50 unknown via CMAUP database
CID 6123454 6123454 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)O)O)O 538.50 unknown via CMAUP database
Dimethyl Lithospermate 70688393 Click to see COC(=O)C1C(OC2=C(C=CC(=C12)C=CC(=O)OC(CC3=CC(=C(C=C3)O)O)C(=O)OC)O)C4=CC(=C(C=C4)O)O 566.50 unknown via CMAUP database
Dimethyl lithospermate B 11422787 Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)OC 746.70 unknown via CMAUP database
Lithospermic acid 6441498 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)O)O)O 538.50 unknown via CMAUP database
Salvianolic acid B 6451084 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O 718.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde 637511 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown via CMAUP database
cis-Cinnamaldehyde 6428995 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown via CMAUP database
> 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
3-O-(3-Methoxy-4-hydroxycinnamoyl)-beta-D-fructofuranosyl 6-O-(3,4-dihydroxycinnamoyl)-alpha-D-glucopyranoside 101414916 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(OC2(CO)OC3C(C(C(C(O3)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)CO)O)O 680.60 unknown via CMAUP database
Butyl Rosmarinate 11953776 Click to see CCCCOC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 416.40 unknown via CMAUP database
Ethyl rosmarinate 44437692 Click to see CCOC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 388.40 unknown via CMAUP database
Methyl rosmarinate 6479915 Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 374.30 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 via CMAUP database
Sibiricose A5 6326020 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(OC2(CO)OC3C(C(C(C(O3)CO)O)O)O)CO)O)O 518.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
3-O-(3-Methoxy-4-hydroxycinnamoyl)-beta-D-fructofuranosyl 6-O-(4-hydroxycinnamoyl)-alpha-D-glucopyranoside 101414917 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(OC2(CO)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)CO)O)O 664.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,5,6-trihydroxy-2-(4-hydroxyphenyl)-7-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 10434572 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
[(1R,18R,19R,21S,22S)-6,8,11,12,13-pentahydroxy-3,7,16-trioxo-21,22-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,17,20-trioxatetracyclo[16.3.1.04,9.010,15]docosa-5,8,10,12,14-pentaen-19-yl]methyl 3,4,5-trihydroxybenzoate 54742219 Click to see C1=C(C(=O)C(=C2C1C(=O)OC3C(C(C(OC3OC(=O)C4=CC(=C(C(=C4)O)O)O)COC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C62)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)O 938.70 unknown via CMAUP database

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