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Aristolochia debilis

Aristolochia debilis - 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 UUID64400a8e9b54b253165289
Scientific name Aristolochia debilis
Authority Siebold & Zucc.
First published in Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 197 (1846)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aristolochia recurvilabra Hance J. Bot. 11: 75 (1873)
Aristolochia sinarum Lindl. Gard. Chron. 1859: 708 (1859)

Common names Top

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Language Common/alternative name
Japanese ウマノスズクサ
lzh 馬兜鈴
Chinese 定海根
Chinese 馬兜鈴
Chinese 百骑大栗树
Chinese 野木香根
Chinese 蛇参果
Chinese 独铃根
Chinese 独行根
Chinese 朱砂莲
Chinese 兜铃根
Chinese 三百银药
Chinese 一点气
Chinese 大青木香
Chinese 马兜铃
Chinese 天仙藤
Chinese 青木香

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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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
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000547728
UNII 79D8J3Q25K
Tropicos 2500339
KEW urn:lsid:ipni.org:names:92883-1
The Plant List kew-2651341
Open Tree Of Life 82050
NCBI Taxonomy 158541
IPNI 92883-1
iNaturalist 371228
GBIF 3588727
EPPO ARPDE
EOL 2872732
USDA GRIN 4089
CMAUP NPO24916

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
Effective degradation of anthraquinones in Folium Sennae with Monascus fermentation for toxicity reduce and efficacy enhancement Long M, Pei X, Lu Z, Xu D, Zheng N, Li Y, Ge H, Cao W, Osire T, Xia X Heliyon 26-Jul-2023
PMCID:PMC10407211
doi:10.1016/j.heliyon.2023.e18735
PMID:37560635
Extremely high relative growth rate makes the cabbage white, Pieris rapae, a global pest with highly abundant and migratory nature Konno K Sci Rep 15-Jun-2023
PMCID:PMC10272114
doi:10.1038/s41598-023-36735-8
PMID:37322167
In silico identification of natural compounds against SARS-CoV-2 main protease from Chinese herbal medicines Kuang Y, Shen W, Ma X, Wang Z, Xu R, Rao Q, Yang S Future Sci OA 14-Jun-2023
PMCID:PMC10357396
doi:10.2144/fsoa-2023-0055
PMID:37485448
Asymmetric interactions between two butterfly species mediated by food demand Hashimoto K, Ohgushi T Ecol Evol 08-Jun-2023
PMCID:PMC10249040
doi:10.1002/ece3.10164
PMID:37304371
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Analysis of the chloroplast genome and phylogenetic evolution of Bidens pilosa Zhang D, Tu J, Ding X, Guan W, Gong L, Qiu X, Huang Z, Su H BMC Genomics 14-Mar-2023
PMCID:PMC10015693
doi:10.1186/s12864-023-09195-7
PMID:36918765
Insights into taxonomy and phylogenetic relationships of eleven Aristolochia species based on chloroplast genome Bai X, Wang G, Ren Y, Su Y, Han J Front Plant Sci 13-Feb-2023
PMCID:PMC9969298
doi:10.3389/fpls.2023.1119041
PMID:36860895
The chloroplast genome of black pepper (Piper nigrum L.) and its comparative analysis with related Piper species Gaikwad AB, Kaila T, Maurya A, Kumari R, Rangan P, Wankhede DP, Bhat KV Front Plant Sci 12-Jan-2023
PMCID:PMC9878596
doi:10.3389/fpls.2022.1095781
PMID:36714762
Physiological and biochemical differences in diapause and non-diapause pupae of Sericinus montelus (Lepidoptera: Papilionidae) Xiao QH, He Z, Wu RW, Zhu DH Front Physiol 02-Nov-2022
PMCID:PMC9666684
doi:10.3389/fphys.2022.1031654
PMID:36406979
Carrier-free nanoplatforms from natural plants for enhanced bioactivity Li Z, Xu X, Wang Y, Kong L, Han C J Adv Res 05-Oct-2022
PMCID:PMC10403678
doi:10.1016/j.jare.2022.09.013
PMID:36208834
Antitumor effects of Chinese herbal medicine compounds and their nano-formulations on regulating the immune system microenvironment Sun K, Wu L, Wang S, Deng W Front Oncol 23-Sep-2022
PMCID:PMC9540406
doi:10.3389/fonc.2022.949332
PMID:36212483
Streptococcosis a Re-Emerging Disease in Aquaculture: Significance and Phytotherapy Van Doan H, Soltani M, Leitão A, Shafiei S, Asadi S, Lymbery AJ, Ringø E Animals (Basel) 16-Sep-2022
PMCID:PMC9495100
doi:10.3390/ani12182443
PMID:36139303
Elucidating the mechanism behind and investigating the efficacy of Traditional Chinese Medicine and Traditional Tibetan Medicine in combination with standard therapeutics in hepatocellular carcinoma and cholangiocarcinoma in vitro Suo H, Hochnadel I, Petriv N, Franke R, Schmidt J, Limanska N, Tugai A, Jedicke N, Broenstrup M, Manns MP, Yevsa T Front Pharmacol 12-Sep-2022
PMCID:PMC9511410
doi:10.3389/fphar.2022.906468
PMID:36172191
Rapid and Simultaneous Quantification of Six Aristolochic Acids and Two Lignans in Asari Radix et Rhizoma Using Ultra-Performance Liquid Chromatography-Triple Quadrupole Tandem Mass Spectrometry Liu H, Cheng X, Guan H, Wang C J Anal Methods Chem 10-Sep-2022
PMCID:PMC9482547
doi:10.1155/2022/5269545
PMID:36124165
Electrophysiological and Morphological Characterization of Contact Chemosensilla in Adults and Larvae of the Butterfly, Atrophaneura alcinous Tsuchihara K, Takanashi T, Asaoka K Insects 02-Sep-2022
PMCID:PMC9506408
doi:10.3390/insects13090802
PMID:36135503

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
> Alkaloids and derivatives / Aporphines
Magnoflorine 73337 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C 342.40 unknown via CMAUP database
Magnoflorine iodide, (+)-(RG) 131664584 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)[O-])OC)C.I 469.30 unknown via CMAUP database
> Alkaloids and derivatives / Aristolactams
Aristolactam II 148745 Click to see C1OC2=C(O1)C3=C4C(=C2)C(=O)NC4=CC5=CC=CC=C53 263.25 unknown via CMAUP database
Aristololactam 96710 Click to see COC1=CC=CC2=C3C4=C(C=C21)NC(=O)C4=CC5=C3OCO5 293.27 unknown https://doi.org/10.1016/J.JPBA.2010.01.023
Aristololactam IIIa 5319620 Click to see C1OC2=C(O1)C3=C4C=C(C=CC4=CC5=C3C(=C2)C(=O)N5)O 279.25 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
1,2-Benzenedi(carboxylic-14C)acid, dibutyl ester 171810 Click to see CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC 282.33 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Aristolochic acids and derivatives
9-Hydroxy-8-methoxy-6-nitro-phenanthrol[3,4-D][1,3]dioxole-5-carboxylic acid 1941 Click to see COC1=C(C=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O)O 357.30 unknown via CMAUP database
Ariskanin A 5320068 Click to see COC1=C(C2=C(C(=C1)C(=O)OC)C(=CC3=CC=CC=C32)[N+](=O)[O-])OC 341.30 unknown via CMAUP database
Aristolochic acid 2236 Click to see COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O 341.27 unknown https://doi.org/10.1016/J.JPBA.2010.01.023
Aristolochic acid C 165274 Click to see C1OC2=C(O1)C3=C4C=C(C=CC4=CC(=C3C(=C2)C(=O)O)[N+](=O)[O-])O 327.24 unknown via CMAUP database
Aristolochic acid d 161218 Click to see COC1=CC(=CC2=C3C(=C(C=C12)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O)O 357.30 unknown via CMAUP database
Aristolochic acid Ia 148297 Click to see C1OC2=C(O1)C3=C4C=CC=C(C4=CC(=C3C(=C2)C(=O)O)[N+](=O)[O-])O 327.24 unknown via CMAUP database
Aristolochic acid II 108168 Click to see C1OC2=C(O1)C3=C(C(=C2)C(=O)O)C(=CC4=CC=CC=C43)[N+](=O)[O-] 311.24 unknown via CMAUP database
Aristolochic acid IV 167493 Click to see COC1=CC2=C3C(=C(C=C2C(=C1)OC)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O 371.30 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown via CMAUP database
> Lignans, neolignans and related compounds
Isotetrandrine 5422 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Acyl carnitines
Heptadecanoyl carnitine 53477803 Click to see CCCCCCCCCCCCCCCCC(=O)OC(CC(=O)[O-])C[N+](C)(C)C 413.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Octadecanoic 1-14C acid 164708 Click to see CCCCCCCCCCCCCCCCCC(=O)O 286.50 unknown via CMAUP database
Pentadecanoate 22169126 Click to see CCCCCCCCCCCCCCC(=O)[O-] 241.39 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
12-Deuteriododecanoic acid 11252659 Click to see CCCCCCCCCCCC(=O)O 201.32 unknown via CMAUP database
Dodecanoate 4149208 Click to see CCCCCCCCCCCC(=O)[O-] 199.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
methyl (9E,13E)-octadeca-9,13-dienoate 5319705 Click to see CCCCC=CCCC=CCCCCCCCC(=O)OC 294.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E,7R,11R)-15-methyl-3,7,11-tri((113C)methyl)(1,5,9,13,16-13C5)hexadec-2-en-1-ol 11301173 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 304.47 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1021/NP50052A041
> 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 via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(-)-Myrtenal 1201529 Click to see CC1(C2CC=C(C1C2)C=O)C 150.22 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 23308299 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1021/NP50052A041
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1021/NP50052A041
L-Born-2-yl acetate 44630108 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Tricyclene 79035 Click to see CC1(C2CC3C1(C3C2)C)C 136.23 unknown via CMAUP database
> 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
Carvone, (-)- 439570 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown via CMAUP database
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown via CMAUP database
p-Menth-3-en-1-ol 11468 Click to see CC(C)C1=CCC(CC1)(C)O 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP50052A041
(+)-gamma-Cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/NP50052A041
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP50052A041
(1S,5S,6S,8S,9S,10R)-5,6,9-trimethyltetracyclo[7.2.1.01,6.08,10]dodecan-4-one 162908765 Click to see CC1C(=O)CCC23C1(CC4C(C2)C4(C3)C)C 218.33 unknown https://doi.org/10.1271/BBB1961.37.341
(1S,5S,6S,9S)-5,6,9-trimethyltetracyclo[7.2.1.01,6.08,10]dodecan-4-one 163195109 Click to see CC1C(=O)CCC23C1(CC4C(C2)C4(C3)C)C 218.33 unknown https://doi.org/10.1271/BBB1961.37.341
(1Z,4E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene 45115091 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown via CMAUP database
(3R,6E)-nerolidol 11241545 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1021/NP50052A041
4-(2,2,6-Trimethylcyclohexyl)-3-buten-2-one 6431122 Click to see CC1CCCC(C1C=CC(=O)C)(C)C 194.31 unknown via CMAUP database
alpha-Cubebene 442359 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP50052A041
alpha-Guaiene 5317844 Click to see CC1CCC(CC2=C1CCC2C)C(=C)C 204.35 unknown https://doi.org/10.1021/NP50052A041
alpha-Santalene 94164 Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)C 204.35 unknown https://doi.org/10.1021/NP50052A041
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP50052A041
Calamenene 6429077 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1021/NP50052A041
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
delta-Guaiene 94275 Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C 204.35 unknown https://doi.org/10.1021/NP50052A041
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/NP50052A041
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1021/NP50052A041
Oxoishwarane 101603270 Click to see CC1CCCC23C1(C(=O)C4C(C2)C4(C3)C)C 218.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
(1S)-1,7beta,7abeta-Trimethyl-1abeta,2,3,5,6,7,7a,7bbeta-octahydro-1H-cyclopropa[a]naphthalene-1beta-carbaldehyde 102188453 Click to see CC1CCC=C2C1(C3C(C3(C)C=O)CC2)C 218.33 unknown https://doi.org/10.1016/S0031-9422(00)83460-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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/10.1021/NP50052A041
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1021/NP50052A041
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Chamigranes
(-)-beta-Chamigrene 442353 Click to see CC1=CCC2(CC1)C(=C)CCCC2(C)C 204.35 unknown https://doi.org/10.1021/NP50052A041
> 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/10.1021/NP50052A041
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
Tetraneurin A 174868 Click to see CC(=O)OCC1CCC2C(C3(C1(CCC3=O)O)C)OC(=O)C2=C 322.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Magnograndiolide 5319198 Click to see CC1(CCC2C(C3C1CCC3(C)O)OC(=O)C2=C)O 266.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 6432744 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 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 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carbothioic S-acids
Pentadecanethioic acid 18413781 Click to see CCCCCCCCCCCCCCC(=O)S 258.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
1-(2,5-Dioxo-2,5-dihydro-1H-imidazol-4-YL)urea 6852197 Click to see C1(=O)C(=NC(=O)N1)NC(=O)N 156.10 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol 7576924 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Hexenal 5281168 Click to see CCCC=CC=O 98.14 unknown https://doi.org/10.1021/NP50052A041
Hexenal 10460 Click to see CCCC=CC=O 98.14 unknown https://doi.org/10.1021/NP50052A041
> Organoheterocyclic compounds / Azoles / Imidazoles
Allantoin 204 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Isoquinoline, 1,2,3,4-tetrahydro-6,7-dimethoxy-1-((4-methoxyphenyl)methyl)-2-methyl- 259676 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC)OC)OC 327.40 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
Eucalyptol 2758 Click to see CC1(C2CCC(O1)(CC2)C)C 154.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
cis-p-Coumaric acid 1549106 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database

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