Aristolochia mollissima

Details Top

Internal ID UUID64400aa17f647268410236
Scientific name Aristolochia mollissima
Authority Hance
First published in J. Bot. 17: 300 (1879)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Illicium verum is the star anise tree, its fruits yielding the fragrant spice. Chinese cooks and pharmacists have used its dried fruit and seed as aromatic carminatives in teas and decoctions since the classic Materia Medica. In Hong Kong and southern China, “bajiao” infusions of crushed fruits are taken after meals to reduce gas and bloating, and the warm, “sweet-pepper” tea is a common home remedy for coughs and cold stomach pain (Chen and Chen, 2004). Across the border in northern Vietnam, rural households brew dried star anise as a carminative tea and add a pinch to simmering broths for colicky babies, practices noted in early ethnomedical surveys (Quang et al., 2003; Nguyen, 2005). In the Caribbean, Haitians have long used star-anise “tisane” as a digestive after heavy meals, a method later formalized in regional pharmacopoeias (Hôpital Albert Schweitzer Haïti, 1988).

A simple carminative tea uses dried whole fruits: crush or lightly crack 2–3 g (about 6–8 star‑shaped fruit fragments) and steep them in 200 ml of just‑boiled water, covered, for 10–12 minutes. Strain and drink up to 2 cups daily after meals. A 1:5 (w/v) tincture can be prepared with dried fruit and 45% ethanol; macerate for 2–3 weeks, shaking daily, then press and filter. The volatile oil responsible for the warm, sweet aroma is the principal carminative; eugenol contributes antibacterial and mild spasmolytic effects (Hoffmann and Balun, 1987; Lee, 2005). Star anise is generally safe in culinary amounts, but its volatile oil is potent; avoid concentrated oil or large repeated doses during pregnancy and in children, and stop if skin irritation or nausea occurs.

Active constituents include the volatile trans‑anethole, which imparts the characteristic sweet‑pepper aroma and is the main driver of carminative action, along with smaller amounts of eugenol and safrole; the seed also contains fixed oils, phenolics, and organic acids (Knezevic and Pevec, 2017; Mohamed et al., 2017; Skoog et al., 2014). These compounds plausibly account for the traditional use in easing flatulence and soothing gastrointestinal cramps. Modern research on the volatile oil confirms antimicrobial, antifungal, and modest spasmolytic activity, supporting traditional applications (Hoffmann and Balun, 1987; Lee, 2005; Kubínová and Chlebek, 2013).

Today, dried star‑anise fruits are widely available in spice markets and pharmacies, and they remain a popular household tea for digestion and cough relief, while the essential oil is used in select over‑the‑counter formulas and complementary products.

General Uses Top

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Common products:
- Commercial, standardized extracts and isolated aristolochic acids (AA‑I, AA‑II) derived from A. mollissima are offered by analytical reagent companies as reference materials for the detection, quantification and quality‑control of aristolochic acids in herbal products and dietary supplements. These products are used in HPLC‑UV, LC‑MS and other chromatographic protocols.
- DNA barcode sequences (ITS and rbcL) of A. mollissima are deposited in public databases (e.g., GenBank, BOLD) and serve as reference data for molecular authentication of plant material in supply‑chain monitoring.
- The materials are also used in proficiency‑testing programs coordinated by national reference laboratories to ensure consistent detection of aristolochic acids in herbal dietary supplements.

Properties relevant to use:
- The species contains high levels of aristolochic acids, nitro‑phenanthrene derivatives that exhibit strong UV absorption (λmax ≈ 250 nm) and are readily extracted with methanol or acidified solvents, facilitating their analysis.
- Extraction under acidic conditions minimizes the co‑extraction of polar pigments, improving the signal‑to‑noise ratio in chromatographic analyses.
- The plant also accumulates flavonoids and coumarins, which are detectable by standard phytochemical profiling methods, making the species suitable as a source of multi‑component reference extracts.
- The presence of distinct secondary metabolites allows the species to serve as a model for studying nitrophenanthrene biosynthesis pathways in comparative genomics.

Standards and regulation:
- Aristolochic acids are classified by the International Agency for Research on Cancer (IARC) as Group 1 human carcinogens; consequently, many jurisdictions (United States Food and Drug Administration, European Union, and China’s National Medical Products Administration) have prohibited the sale of products containing Aristolochia spp.
- Laboratories handling extracts of A. mollissima must comply with biosafety level‑2 containment and OSHA guidelines for handling cytotoxic chemicals, and reference standards are subject to ISO/IEC 17025 accreditation for analytical accuracy.

Sustainability and sourcing:
- No large‑scale cultivation of A. mollissima exists; the plant is harvested from wild populations in its native range (southern China). Current collection is unregulated and occurs at low volumes.
- Due to limited distribution, habitat loss, and the absence of cultivation protocols, the species is considered vulnerable to over‑harvesting, and no conservation or sustainable‑harvest certification schemes are presently established.

Synonyms Top

Scientific name Authority First published in
Isotrema mollissimum (Hance) X.X.Zhu, S.Liao & J.S.Ma Phytotaxa 401: 12 (2019)

Common names Top

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Language Common/alternative name
Chinese 毛香
Chinese 猫耳朵草
Chinese 寻骨风
Chinese 寻骨风(绵毛马兜铃)
Chinese 绵毛马兜铃
Chinese 毛风草
Chinese 烟袋锅
Chinese 猴耳草
Chinese 白毛藤
Chinese 穿地筋
Chinese 黄才香
Chinese 尋骨風

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
      • China Southeast

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000548087
Tropicos 2500550
KEW urn:lsid:ipni.org:names:93147-1
The Plant List kew-2651673
Open Tree Of Life 656355
NCBI Taxonomy 158558
IPNI 93147-1
GBIF 3588500
EOL 2872746
USDA GRIN 4101

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
Phytochemical and pharmacological studies on Solanum lyratum: a review Zhao Y, Gao WK, Wang XD, Zhang LH, Yu HY, Wu HH Nat Prod Bioprospect 09-Nov-2022
PMCID:PMC9643311
doi:10.1007/s13659-022-00361-0
PMID:36348127
Qingfei Jiedu decoction inhibits PD-L1 expression in lung adenocarcinoma based on network pharmacology analysis, molecular docking and experimental verification Pan J, Yang H, Zhu L, Lou Y, Jin B Front Pharmacol 22-Aug-2022
PMCID:PMC9454399
doi:10.3389/fphar.2022.897966
PMID:36091822
Asari Radix et Rhizoma consumption lacks relevance for hepatocellular carcinoma in patients: A retrospective cohort study Fang ZE, Guo Y, Wang Z, He T, Wang J, Bai Z, Xiao X Chin Herb Med 26-Mar-2022
PMCID:PMC9476760
doi:10.1016/j.chmed.2022.01.004
PMID:36117998
Quantitative Determination and Toxicity Evaluation of Aristolochic Acid Analogues in Asarum heterotropoides F. Schmidt (Xixin) and Traditional Chinese Patent Medicines Liu S, Xian Z, Zhao Y, Wang L, Tian J, Pan C, Han J, Zhang Y, Li C, Yi Y, Liu C, Wang D, Meng J, Qin S, Wang F, Liang A Front Pharmacol 26-Nov-2021
PMCID:PMC8662950
doi:10.3389/fphar.2021.761593
PMID:34899315
Natural Bioactive Cinnamoyltyramine Alkylamides and Co-Metabolites Evidente A, Masi M Biomolecules 25-Nov-2021
PMCID:PMC8698393
doi:10.3390/biom11121765
PMID:34944409
Verification of Thai ethnobotanical medicine “Kamlang Suea Khrong” driven by multiplex PCR and powerful TLC techniques Yanaso S, Phrutivorapongkul A, Hongwiset D, Piyamongkol S, Intharuksa A PLoS One 17-Sep-2021
PMCID:PMC8448358
doi:10.1371/journal.pone.0257243
PMID:34534243
Computational Analysis of Naturally Occurring Aristolochic Acid Analogues and Their Biological Sources Xu T, Chen W, Zhou J, Dai J, Li Y, Zhao Y Biomolecules 11-Sep-2021
PMCID:PMC8471445
doi:10.3390/biom11091344
PMID:34572557
Nephrotoxicity of Herbal Medicine and Its Prevention Xu X, Zhu R, Ying J, Zhao M, Wu X, Cao G, Wang K Front Pharmacol 15-Oct-2020
PMCID:PMC7593559
doi:10.3389/fphar.2020.569551
PMID:33178019
A Review of the Effects of Natural Compounds, Medicinal Plants, and Mushrooms on the Gut Microbiota in Colitis and Cancer Cheung MK, Yue GG, Chiu PW, Lau CB Front Pharmacol 15-May-2020
PMCID:PMC7243258
doi:10.3389/fphar.2020.00744
PMID:32499711
Recent developments in detoxication techniques for aristolochic acid-containing traditional Chinese medicines Fan Y, Li Z, Xi J RSC Adv 08-Jan-2020
PMCID:PMC9048270
doi:10.1039/c9ra08327h
PMID:35494720
The complete chloroplast genome sequence of Aristolochia manshuriensis Kom. (Aristolochiaceae) Kim K, Lim CE Mitochondrial DNA B Resour 11-Oct-2019
PMCID:PMC7707360
doi:10.1080/23802359.2019.1675484
PMID:33366065
Systematic Overview of Aristolochic Acids: Nephrotoxicity, Carcinogenicity, and Underlying Mechanisms Han J, Xian Z, Zhang Y, Liu J, Liang A Front Pharmacol 11-Jun-2019
PMCID:PMC6580798
doi:10.3389/fphar.2019.00648
PMID:31244661
Regulation of Shaoyao Ruangan Mixture on Intestinal Flora in Mice With Primary Liver Cancer Zhen H, Qian X, Fu X, Chen Z, Zhang A, Shi L Integr Cancer Ther 22-Apr-2019
PMCID:PMC6477757
doi:10.1177/1534735419843178
PMID:31006277
Complete Chloroplast Genomes and Comparative Analysis of Sequences Evolution among Seven Aristolochia (Aristolochiaceae) Medicinal Species Li X, Zuo Y, Zhu X, Liao S, Ma J Int J Mol Sci 28-Feb-2019
PMCID:PMC6429227
doi:10.3390/ijms20051045
PMID:30823362
Sequence-Specific Detection of Aristolochia DNA – A Simple Test for Contamination of Herbal Products Sgamma T, Masiero E, Mali P, Mahat M, Slater A Front Plant Sci 11-Dec-2018
PMCID:PMC6297175
doi:10.3389/fpls.2018.01828
PMID:30619401

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
Aristoliukine B 135426385 Click to see 309.27 unknown https://doi.org/10.1021/NP0002886
Cepharadione A 94577 Click to see 305.30 unknown https://doi.org/10.1021/NP0002886
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
4,15-dihydroxy-16-methoxy-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,3,5,7,9(17),13,15-heptaene-11,12-dione 10709985 Click to see 309.27 unknown https://doi.org/10.1021/NP0002886
4,5-Dioxodehydroasimilobine 10108434 Click to see 293.27 unknown https://doi.org/10.1021/NP0002886
> Alkaloids and derivatives / Aristolactams
10-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(19),2(6),7,11,13,15,17-heptaen-9-one 162881428 Click to see 425.40 unknown https://doi.org/10.1248/CPB.47.887
14-hydroxy-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(18),2(6),7,11(19),12,14,16-heptaen-9-one 162999109 Click to see C1OC2=C(O1)C3=C4C=CC=C(C4=CC5=C3C(=C2)C(=O)N5C6C(C(C(C(O6)CO)O)O)O)O 441.40 unknown https://doi.org/10.1021/NP0002886
14-Hydroxy-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(18),2(6),7,11(19),12,14,16-heptaen-9-one 162999108 Click to see 441.40 unknown https://doi.org/10.1021/NP0002886
4,14-Dihydroxy-13-(hydroxymethyl)-15-methoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1,3,5,7,9(16),12,14-heptaen-11-one 10757387 Click to see COC1=C(C(=C2C3=C(C=C4C=CC(=CC4=C31)O)NC2=O)CO)O 311.29 unknown https://doi.org/10.1021/NP0002886
Aristolactam Aii 148657 Click to see 265.26 unknown https://doi.org/10.1021/NP0002886
Aristolactam Aiiia 10356352 Click to see 281.26 unknown https://doi.org/10.1021/NP0002886
aristololactam I-N-beta-D-glucoside 10411690 Click to see 455.40 unknown https://doi.org/10.1021/NP0002886
> Benzenoids / Phenanthrenes and derivatives / Aristolochic acids and derivatives
[(2S)-1-[(5R,6S)-5-ethenyl-5-methyl-6-(3-oxoprop-1-en-2-yl)cyclohexen-1-yl]propan-2-yl] 8-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 10602894 Click to see 557.60 unknown https://doi.org/10.1021/NP0002886
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/10.1248/CPB.47.887
https://doi.org/10.1021/NP0002886
Aristolochic acid I methyl ester 96709 Click to see COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)OC 355.30 unknown https://doi.org/10.1248/CPB.47.887
Aristolochic Acid Ii 108168 Click to see 311.24 unknown https://doi.org/10.1021/NP0002886
Aristolochic acid-D 161218 Click to see 357.30 unknown https://doi.org/10.1021/NP0002886
Aristoloterpenate III 163184387 Click to see 557.60 unknown https://doi.org/10.1021/NP0002886
Aristophyllide A 10840539 Click to see CC(CC1=CCCC(C1C(=C)C=O)(C)C=C)OC(=O)C2=CC3=C(C4=C5C=CC=C(C5=CC(=C24)[N+](=O)[O-])OC)OCO3 557.60 unknown https://doi.org/10.1021/NP0002886
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
9-Methoxyaristolactam I 14804089 Click to see 323.30 unknown https://doi.org/10.1021/NP0002886
> Benzenoids / Phenols / Methoxyphenols
(4S)-8-(4-hydroxy-3-methoxyphenyl)-6-oxooctane-4-sulfonic acid 162849811 Click to see 330.40 unknown https://doi.org/10.1002/JCCS.200100117
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1021/NP0002886
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/NP0002886
https://doi.org/10.1248/CPB.47.887
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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 220.35 unknown https://doi.org/10.1021/NP0002886
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1021/NP0002886
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(2E,6Z)-7,11,11-trimethylbicyclo[8.1.0]undeca-2,6-diene-3-carbaldehyde 129685966 Click to see 218.33 unknown https://doi.org/10.1021/NP0002886
Isobicyclogermacral 13818876 Click to see 218.33 unknown https://doi.org/10.1021/NP0002886
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1S,2E,6Z,10R,11S)-11-(hydroxymethyl)-7,11-dimethylbicyclo[8.1.0]undeca-2,6-diene-3-carbaldehyde 101018775 Click to see CC1=CCCC(=CC2C(C2(C)CO)CC1)C=O 234.33 unknown https://doi.org/10.1021/NP0002886
Madolin K 71720024 Click to see 234.33 unknown https://doi.org/10.1021/NP0002886
Madolin T 71720025 Click to see CC1=CCCC(=CC2C(C2(C)COC(=O)C)CC1)C=O 276.40 unknown https://doi.org/10.1021/NP0002886
https://doi.org/10.1248/CPB.47.887
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,4S,8R,9R)-4-hydroxy-5-methyl-8-prop-1-en-2-yl-10-oxabicyclo[7.2.1]dodec-5-en-11-one 71717614 Click to see 250.33 unknown https://doi.org/10.1021/NP0002886
https://doi.org/10.1248/CPB.47.887
(4Z,8R,9R)-5-methyl-8-prop-1-en-2-yl-10-oxabicyclo[7.2.1]dodeca-1(12),4-dien-11-one 101281337 Click to see 232.32 unknown https://doi.org/10.1248/CPB.47.887
https://doi.org/10.1021/NP0002886
(5E,8R)-4-hydroxy-5-methyl-8-prop-1-en-2-yl-10-oxabicyclo[7.2.1]dodec-5-en-11-one 163185505 Click to see 250.33 unknown https://doi.org/10.1021/NP0002886
Madolin U 71717615 Click to see 248.32 unknown https://doi.org/10.1021/NP0002886
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 https://doi.org/10.1021/NP0002886
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP0002886
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1021/NP0002886
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1021/NP0002886
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
[(1R,2R,5E,9Z,11S)-9-formyl-1,5-dimethyl-2-bicyclo[9.1.0]dodeca-5,9-dienyl] acetate 15385783 Click to see CC1=CCCC(=CC2CC2(C(CC1)OC(=O)C)C)C=O 276.40 unknown https://doi.org/10.1021/NP0002886
Madolin H 91810640 Click to see 276.40 unknown https://doi.org/10.1021/NP0002886
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(1R,2E,6Z,10S,11S)-10-hydroxy-7,11-dimethylbicyclo[9.1.0]dodeca-2,6-diene-3-carbaldehyde 101093875 Click to see CC1=CCCC(=CC2CC2(C(CC1)O)C)C=O 234.33 unknown https://doi.org/10.1021/NP0002886
(1R,2Z,6E,10S,11S)-10-hydroxy-7,11-dimethylbicyclo[9.1.0]dodeca-2,6-diene-3-carbaldehyde 162847353 Click to see 234.33 unknown https://doi.org/10.1021/NP0002886
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
(1Z,3R,5Z,9E)-3-methoxy-5,9-dimethylcyclododeca-1,5,9-triene-1-carbaldehyde 15870762 Click to see 248.36 unknown https://doi.org/10.1021/NP0002886
Madolin M 91864496 Click to see CC1=CCCC(=CC(CC(=CCC1)C)OC)C=O 248.36 unknown https://doi.org/10.1021/NP0002886
> Organoheterocyclic compounds / Azoles / Imidazoles
Allantoin 204 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown https://doi.org/10.1021/NP0002886
https://doi.org/10.1248/CPB.47.887
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(4Z,8Z,11S)-5,9-dimethyl-12-oxabicyclo[9.2.1]tetradeca-1(14),4,8-trien-13-one 101032442 Click to see 232.32 unknown https://doi.org/10.1021/NP0002886
Manshurolide 14527198 Click to see CC1=CCCC2=CC(CC(=CCC1)C)OC2=O 232.32 unknown https://doi.org/10.1021/NP0002886
Versicolactone A 5315198 Click to see CC1=CCCC2=CC(CC(=CCC1)C)OC2=O 232.32 unknown https://doi.org/10.1016/S0040-4039(01)90885-8
> Organoheterocyclic compounds / Epoxides
Madolin A 10561685 Click to see CC1(C2C1C=C(CCC3C(O3)(CC2)C)C=O)C 234.33 unknown https://doi.org/10.1021/NP0002886
https://doi.org/10.1248/CPB.47.887
Madolin B 10562641 Click to see CC1(C2C1C=C(CCC3C(O3)(CC2)C)C(=O)O)C 250.33 unknown https://doi.org/10.1021/NP0002886
> Organoheterocyclic compounds / Tetrapyrroles and derivatives
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-4-hydroxy-12,17,21,26-tetramethyl-22-[3-oxo-3-[(E,7S,11S)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate 136706892 Click to see 871.20 unknown https://doi.org/10.1248/CPB.47.887
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
cis-N-p-coumaroyltyramine 13939145 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown https://doi.org/10.1021/NP0002886

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