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Eremurus chinensis

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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 UUID6440260b26574560934836
Scientific name Eremurus chinensis
Authority O.Fedtsch.
First published in Gard. Chron. , ser. 3, 41: 199 (1907)

Description Top

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Synonyms Top

Scientific name Authority First published in
Asphodelus bonatii H.Lév. & Vaniot Repert. Spec. Nov. Regni Veg. 6: 113 (1908)
Henningia chinensis (O.Fedtsch.) Khokhr. Erem. Cult. : 78 (1965)

Common names Top

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Language Common/alternative name
Chinese 蜥蜴
Chinese 独尾草
Chinese 獨尾草

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Tibet

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000766594
Tropicos 18406410
KEW urn:lsid:ipni.org:names:534689-1
The Plant List kew-305452
PaleoBotany 117048
Open Tree Of Life 893089
NCBI Taxonomy 928054
IPNI 534689-1
iNaturalist 881780
GBIF 2778797
EOL 1087926
USDA GRIN 15386
CMAUP NPO24659

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
The complete chloroplast genome of Eremurus zoae Vved. (Asphodelaceae), an endemic species of Kyrgyz Republic Jang JE, Jeong HJ, Kim AL, Choi YR, Lazkov GA, Jang CG, Choi HJ, Gil HY Mitochondrial DNA B Resour 03-Apr-2024
PMCID:PMC10993749
doi:10.1080/23802359.2024.2336003
PMID:38586509
Molecular characterization of endangered endemic plant Aloe pseudorubroviolacea using chloroplast matK and plastid rbcL gene Alaklabi A, Ahamed A, Al Qthanin RN, Arif IA, Panneerselvam A, Al-Khulaidi AW Saudi J Biol Sci 17-Nov-2020
PMCID:PMC7783787
doi:10.1016/j.sjbs.2020.11.042
PMID:33424406
Aquaporins as Targets of Dietary Bioactive Phytocompounds Tesse A, Grossini E, Tamma G, Brenner C, Portincasa P, Marinelli RA, Calamita G Front Mol Biosci 18-Apr-2018
PMCID:PMC5915544
doi:10.3389/fmolb.2018.00030
PMID:29721498
Regulation of Aquaporin Functional Properties Mediated by the Antioxidant Effects of Natural Compounds Pellavio G, Rui M, Caliogna L, Martino E, Gastaldi G, Collina S, Laforenza U Int J Mol Sci 08-Dec-2017
PMCID:PMC5751267
doi:10.3390/ijms18122665
PMID:29292793
(R)-(−)-Aloesaponol III 8-Methyl Ether from Eremurus persicus: A Novel Compound against Leishmaniosis Rossi D, Ahmed KM, Gaggeri R, Della Volpe S, Maggi L, Mazzeo G, Longhi G, Abbate S, Corana F, Martino E, Machado M, Varandas R, Sousa MD, Collina S Molecules 24-Mar-2017
PMCID:PMC6154379
doi:10.3390/molecules22040519
PMID:28338625
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes Chen S, Kim DK, Chase MW, Kim JH PLoS One 18-Mar-2013
PMCID:PMC3605904
doi:10.1371/journal.pone.0059472
PMID:23544071
Chemical constituents from Sambucus chinensis TAO Jiayi China Journal of Chinese Materia Medica 21-Jun-2012
doi:10.4268/CJCMM20121011
Polar constituents of Mosla Chinensis SHEN Juanjuan China Journal of Chinese Materia Medica 13-Jul-2011
doi:10.4268/CJCMM20111319
Molecular phylogenetics of Ruscaceae sensu lato and related families (Asparagales) based on plastid and nuclear DNA sequences Kim JH, Kim DK, Forest F, Fay MF, Chase MW Ann Bot 07-Oct-2010
PMCID:PMC2958784
doi:10.1093/aob/mcq167
PMID:20929900
Constituents of Eremurus chinensis. Li C, Shi JG, Zhang YP, Zhang CZ J Nat Prod 01-May-2000
doi:10.1021/NP9904915
PMID:10843579

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 / Anthracenes
(4S)-4,8,9-trihydroxy-6-methyl-3,4-dihydro-2H-anthracen-1-one 90474413 Click to see CC1=CC2=CC3=C(C(=O)CCC3O)C(=C2C(=C1)O)O 258.27 unknown https://doi.org/10.4268/CJCMM20121011
(4S)-4,9-dihydroxy-6-(hydroxymethyl)-8-methoxy-3,4-dihydro-2H-anthracen-1-one 10779698 Click to see COC1=CC(=CC2=CC3=C(C(=O)CCC3O)C(=C21)O)CO 288.29 unknown https://doi.org/10.1021/NP9904915
(4S)-4,9-dihydroxy-8-methoxy-6-methyl-3,4-dihydro-2H-anthracen-1-one 74764104 Click to see CC1=CC2=CC3=C(C(=O)CCC3O)C(=C2C(=C1)OC)O 272.29 unknown https://doi.org/10.1021/NP9904915
4,9-dihydroxy-6-(hydroxymethyl)-8-methoxy-3,4-dihydro-2H-anthracen-1-one 21603497 Click to see COC1=CC(=CC2=CC3=C(C(=O)CCC3O)C(=C21)O)CO 288.29 unknown https://doi.org/10.1021/NP9904915
4,9-dihydroxy-8-methoxy-6-methyl-3,4-dihydro-2H-anthracen-1-one 21603498 Click to see CC1=CC2=CC3=C(C(=O)CCC3O)C(=C2C(=C1)OC)O 272.29 unknown https://doi.org/10.4268/CJCMM20111319
https://doi.org/10.1021/NP9904915
> Benzenoids / Anthracenes / Anthraquinones
1-Hydroxy-8-methoxy-3-methylanthracene-9,10-dione 11300144 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC 268.26 unknown https://doi.org/10.1021/NP9904915
2-(1,8-dihydroxy-6-methyl-9,10-dioxoanthracen-2-yl)-1-hydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione 10770709 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC(=C3O)C4=C(C5=C(C=C4C)C(=O)C6=C(C5=O)C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)O 668.60 unknown https://doi.org/10.1021/NP9904915
2-(1,8-Dihydroxy-6-methyl-9,10-dioxoanthracen-2-yl)-1-hydroxy-3-methyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione 85262451 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC(=C3O)C4=C(C5=C(C=C4C)C(=O)C6=C(C5=O)C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)O 668.60 unknown https://doi.org/10.1021/NP9904915
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Benzenoids / Naphthalenes
2-Acetyl-3-methyl-1,8-dimethoxynaphthalene 10776684 Click to see CC1=CC2=C(C(=CC=C2)OC)C(=C1C(=O)C)OC 244.28 unknown https://doi.org/10.1021/NP9904915
> Benzenoids / Naphthalenes / Naphthols and derivatives
Ethanone, 1-(1-hydroxy-8-methoxy-3-methyl-2-naphthalenyl)- 10585541 Click to see CC1=CC2=C(C(=CC=C2)OC)C(=C1C(=O)C)O 230.26 unknown https://doi.org/10.1021/NP9904915
https://doi.org/10.4268/CJCMM20111319
> Benzenoids / Tetralins
(4S)-10-Nor-calamenen-10-one 73350586 Click to see CC1=CC2=C(C=C1)C(=O)CCC2C(C)C 202.29 unknown via CMAUP database
Oxyphyllenotriol A 51041015 Click to see CC(C)C1=C2C(C(CCC2=C(C=C1)O)(C)O)O 236.31 unknown via CMAUP database
Oxyphyllone G 51041016 Click to see CC1=C(C2=C(C=C1)C(=O)CCC2C(C)C)O 218.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Tetracosanoic acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Labda-8(17),12-diene-15,16-dial 11077520 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1r,2r)-p-Menth-3-en-1,2-diol 71423340 Click to see CC(C)C1=CC(C(CC1)(C)O)O 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,3R,6S,7S)-1-hydroxy-3,7-dimethyl-10-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undec-9-en-8-one 76285513 Click to see CC1CCC2C1C3(C(=CC(=O)C2(O3)C)C(C)C)O 250.33 unknown via CMAUP database
Oxyphyllanene D 57396910 Click to see CC(=C)C1(CCC2(CCC(=O)C3(C2(C1)O3)C)C)O 250.33 unknown via CMAUP database
Oxyphyllol E 51041018 Click to see CC(=C)C1(CCC2(CCC(=O)C3(C2(C1)O3)C)C)O 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(11S)-Nootkatone-11,12-diol 15601439 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(C)(CO)O)C 252.35 unknown via CMAUP database
(1S)-1,2,3,4,4a,5,6,7-Octahydro-4beta,4abeta-dimethyl-6alpha-(1-methylethenyl)naphthalene-1beta-ol 44576208 Click to see CC1CCC(C2=CCC(CC12C)C(=C)C)O 220.35 unknown via CMAUP database
(3S,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-3,4,5,6-tetrahydro-2H-naphthalene-1,7-dione 72715093 Click to see CC1CC(=O)C=C2C1(CC(CC2=O)C(=C)C)C 232.32 unknown via CMAUP database
(4R,4aR)-6-acetyl-4,4a-dimethyl-3,4,7,8-tetrahydronaphthalen-2-one 117654813 Click to see CC1CC(=O)C=C2C1(C=C(CC2)C(=O)C)C 218.29 unknown via CMAUP database
(4R,4aS,6R)-6-(2-hydroxypropan-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 89960876 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(C)(C)O)C 236.35 unknown via CMAUP database
(4R,4aS,6R)-6-(3-hydroxyprop-1-en-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 53249021 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)CO)C 234.33 unknown via CMAUP database
(4R)-4beta,4abeta-Dimethyl-6alpha-isopropenyl-8alpha-hydroxy-2,3,4,4a,5,6,7,8-octahydronaphthalene-2-one 11651584 Click to see CC1CC(=O)C=C2C1(CC(CC2O)C(=C)C)C 234.33 unknown via CMAUP database
Nootkatene 25200342 Click to see CC1CC=CC2=CCC(CC12C)C(=C)C 202.33 unknown via CMAUP database
Nootkatol 182645 Click to see CC1CC(C=C2C1(CC(CC2)C(=C)C)C)O 220.35 unknown via CMAUP database
Nootkatone 1268142 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C 218.33 unknown via CMAUP database
oxyphyllol C 10857540 Click to see CC1CCC(C2(C1(CC(CC2)C(=C)C)C)O)O 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4aR,7R,8aS)-1,4a-dimethyl-7-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol 15560338 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown via CMAUP database
(2R,4aS,7R,8aR)-4a-Methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalen-2-ol 14076604 Click to see CC(=C)C1CCC2(CCC(C(=C)C2C1)O)C 220.35 unknown via CMAUP database
(4aS,7S,8R)-8-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one 57393410 Click to see CC1=C2C(C(CCC2(CCC1=O)C)C(=C)C)O 234.33 unknown via CMAUP database
(4aS,7S)-7-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-4,5,6,8-tetrahydro-3H-naphthalen-2-one 57335617 Click to see CC1=C2CC(CCC2(CCC1=O)C)(C(=C)C)O 234.33 unknown via CMAUP database
7-Epi-Teucrenone B 57393409 Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C 234.33 unknown via CMAUP database
Ligucyperonol 14681770 Click to see CC1=C2CC(CCC2(C(CC1=O)O)C)C(=C)C 234.33 unknown via CMAUP database
Oxyphyllol A 637451 Click to see CC(=C)C1CCC2(CCCC(C2=C1)(C)O)C 220.35 unknown via CMAUP database
Rel-Oxyphyllanene E 57400339 Click to see CC(=C)C1(CCC2(CCC(C(=C)C2C1)O)C)O 236.35 unknown via CMAUP database
Teucrenone 10105443 Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(4aS,8aR,9aR)-3,5,8a-trimethyl-4a,8,9,9a-tetrahydro-4H-benzo[f][1]benzofuran-2,7-dione 71681246 Click to see CC1=CC(=O)CC2(C1CC3=C(C(=O)OC3C2)C)C 246.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Sitosteryl palmitate 9852570 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.4268/CJCMM20121011
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.4268/CJCMM20121011
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.4268/CJCMM20121011
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Pubescone 102054514 Click to see CC(C)C1C2C(C2CCC(=O)C)CCC1=O 222.32 unknown via CMAUP database
Spiro[4.4]nonan-2-one 549163 Click to see C1CCC2(C1)CCC(=O)C2 138.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4aR,6S,8aS)-6-acetyl-4a-hydroxy-4,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-2-one 71681103 Click to see CC1=CC(=O)CC2(C1(CC(CC2)C(=O)C)O)C 236.31 unknown via CMAUP database
(4aR)-7-acetyl-1,4a-dimethyl-3,4,5,6-tetrahydronaphthalen-2-one 71681245 Click to see CC1=C2C=C(CCC2(CCC1=O)C)C(=O)C 218.29 unknown via CMAUP database
4-Hydroxy-11,12,13-trinor-5-eudesmen-7-one 15153217 Click to see CC12CCCC(C1=CC(=O)CC2)(C)O 194.27 unknown via CMAUP database
OxyphyllaneneA 122402647 Click to see CC1=CC(=O)CC2(C1CC(=O)CC2)C 192.25 unknown via CMAUP database
Oxyphyllenodiol A 10082923 Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O 238.32 unknown via CMAUP database
Oxyphyllenodiol B 5279294 Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O 238.32 unknown via CMAUP database
Oxyphyllenone A 10262534 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Oxyphyllenone B 44310512 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Oxyphyllone C 44255203 Click to see CC(C)C1CCC(=O)C2=C1C3C(O3)(CC2)C 220.31 unknown via CMAUP database
Teuhetenone A 15153216 Click to see CC12CCCC(C1=CC(=O)CC2)(C)O 194.27 unknown via CMAUP database
> Organoheterocyclic compounds / Epoxides
(1S,4S,6S,8E,12S)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.04,6]tridec-8-ene 12014673 Click to see CC1(CC2C(O2)(CCC3C(O3)(CC=C1)C)C)C 236.35 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
Oxyphyllanene C 57335616 Click to see CC1=C2C3C(O3)(CCC2(CCC1=O)C)C(=O)C 234.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E)-1-(4-Hydroxy-3-methoxyphenyl)-7-phenyl-1-hepten-3-one 6440365 Click to see COC1=C(C=CC(=C1)C=CC(=O)CCCCC2=CC=CC=C2)O 310.40 unknown via CMAUP database
1-(2,4-Dihydroxy-3-methoxyphenyl)-7-(4-methoxyphenyl)heptan-3-one 72708396 Click to see COC1=CC=C(C=C1)CCCCC(=O)CCC2=C(C(=C(C=C2)O)OC)O 358.40 unknown via CMAUP database
1-(3,5-Dihydroxy-4-methoxyphenyl)-7-phenylheptan-3-one 72708395 Click to see COC1=C(C=C(C=C1O)CCC(=O)CCCCC2=CC=CC=C2)O 328.40 unknown via CMAUP database
Yakuchinone-A 133145 Click to see COC1=C(C=CC(=C1)CCC(=O)CCCCC2=CC=CC=C2)O 312.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5-Dihydroxy-7-methoxy-2-(4-methoxyphenyl)-4H-chromen-4-one 5378823 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)O 314.29 unknown via CMAUP database
Izalpinin 5318691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
Kaempferide 5281666 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.1021/NP9904915

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