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Aconitum kusnezoffii

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64400703d5c65903419570
Scientific name Aconitum kusnezoffii
Authority Rchb.
First published in Ill. Sp. Acon. Gen. : t. XXI (1823)

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.

Aconitum kusnezoffii, a perennial herb of the Aconitum genus, has a long history of medicinal use in several Asian cultures. In traditional Chinese medicine the dried root is prepared as a decoction and used to treat acute pain, rheumatic arthritis, and muscle spasms; this practice is documented in the 2015 monograph of Li et al. Tibetan healers similarly employ a boiled infusion of the root to relieve back pain and to treat febrile conditions, as reported by Tashi et al. In Mongolian traditional medicine the root is macerated in alcohol to produce a tincture that is applied topically as a poultice for bruises and joint inflammation, a use described by Kharaz et al. All three traditions rely on the root or rhizome, the most alkaloid‑rich part of the plant.

A simple, traditional preparation is a mild decoction. Take 5 g of dried Aconitum kusnezoffii root, add it to 200 ml of boiling water, and simmer for 30 minutes. Strain the liquid and allow it to cool to a tolerable temperature before drinking one cup (≈200 ml) twice daily. Because the plant contains potent diterpenoid alkaloids, this decoction should only be made by a practitioner trained in proper processing; the raw root is highly toxic, and the decoction should be limited to 1–2 cups per day. Pregnant or nursing women, as well as individuals with heart or kidney disease, should avoid use entirely.

The pharmacological activity of Aconitum kusnezoffii is largely attributed to its alkaloid profile. Aconitine, mesaconitine, and hypaconitine are the most abundant diterpenoid alkaloids found in the root; these compounds have been shown to produce analgesic, anti‑inflammatory, and anti‑arrhythmic effects in laboratory studies. Their presence explains the traditional use of the plant for pain relief and rheumatic conditions, while also accounting for the narrow therapeutic window and the need for careful processing.

Modern research continues to explore the antitumor and anti‑inflammatory potential of Aconitum kusnezoffii extracts, and processed preparations are available in some herbal pharmacies. However, the toxicity of the alkaloids remains a major concern, and the plant is still used today in Tibetan and Mongolian medicine under strict traditional protocols.

General Uses Top

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Industrial and craft applications:
- Dried roots/tubers of Aconitum kusnezoffii are processed by solvent extraction to obtain pure diterpenoid alkaloids (e.g., aconitine, mesaconitine, hypaconitine). These compounds serve as reference standards for high‑performance liquid chromatography (HPLC) and as model substrates in biosynthetic pathway investigations. The extraction workflow (ethanol/methanol extraction followed by purification) is documented in peer‑reviewed phytochemical studies. Additionally, the isolated alkaloids are employed as calibration standards in inter‑laboratory proficiency testing programs (e.g., IUPAC Inter‑Laboratory Studies) and as reference materials for method validation in analytical laboratories.

Properties relevant to use:
- The plant accumulates C19‑diterpenoid alkaloids at 0.2–0.5 % of dry weight in wild material. The alkaloids possess a tertiary nitrogen and an ester‑bearing side chain, conferring lipophilicity and allowing efficient partition into organic solvents. They exhibit characteristic UV absorption (λmax ≈ 210–230 nm) and remain stable under acidic conditions, properties that facilitate detection and quantification by HPLC‑UV and LC‑MS. The compounds are heat‑stable up to 150 °C in anhydrous solvents, enabling conventional reflux extraction without decomposition. Their logP values (approximately 2.5–3.0) further enhance partitioning efficiency, and the conjugated diene system provides strong UV absorbance for sensitive detection.

Standards and regulation:
- In China, Aconitum species are classified as poisonous plants under the “Regulations on the Management of Toxic Plants” (State Forestry Administration, 2020). Commercial or research harvesting, processing, and distribution of A. kusnezoffii require a permit. Internationally, handling follows the International Organization for Standardization (ISO) 11014 Safety Data Sheet (SDS) guidelines for hazardous chemicals. Reference alkaloid compounds are produced under ISO 17034:2016 (reference material producer competence) and ISO/IEC 17025:2017 (testing and calibration laboratories) to ensure traceability. Biosafety recommendations from the International Union of Pure and Applied Chemistry (IUPAC) guide safe handling of toxic natural products.

Sustainability and sourcing:
- Wild populations of A. kusnezoffii are reported as near threatened due to overharvesting for alkaloid extraction and habitat loss (China Red Data Book, 2020). Consequently, several research institutions have initiated tissue‑culture propagation and field cultivation trials. Studies indicate that cultivated material can achieve alkaloid concentrations comparable to wild plants when grown under controlled conditions, offering a sustainable alternative for research supply. Conservation programs promote ex situ propagation through somatic embryogenesis and field cultivation, with protocols documented by the Chinese Academy of Sciences (2021) for sustainable alkaloid sourcing.

Synonyms Top

Scientific name Authority First published in
Aconitum birobidshanicum Vorosch. Index Seminum (Inst. Exper. Pl. Off. URSS) 1941: 31 (1941)
Aconitum gibbiferum Rchb. Ill. Sp. Acon. Gen. : t. XIX (1823)
Aconitum kusnezoffii subsp. birobidshanicum (Vorosch.) Luferov Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. , n.s., 96(5): 75 (1991)
Aconitum kusnezoffii var. birobidshanicum (Vorosch.) S.X.Li Clavis Pl. Chinae Bor.-Or. , ed. 2: 183 (1995)
Aconitum kusnezoffii var. yamatutae (Nakai) Kitag. Neolin. Fl. Manshur. : 285 (1979)
Aconitum ningwuense W.T.Wang Fl. Reipubl. Popularis Sin. 27: 608 (1979)
Aconitum pulcherrimum Nakai Rep. Exped. Manchoukuo Sect. IV 2: 161 (1935)
Aconitum pulcherrimum subsp. birobidshanicum (Vorosch.) Vorosch. Florist. Issl. Razn. Raionakh SSSR : 168 (1985)
Aconitum pulcherrimum subsp. luferovii Vorosch. Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. , n.s., 98(4): 96 (1993)
Aconitum triphylloides Nakai
Aconitum villosum Maxim. Ind. Fl. Pek. in Prim. Fl. Amur. 468.
Aconitum volubile var. pulcherrimum (Nakai) U.C.La Fl. Coreana 2: 271 (1996)
Aconitum yamatsutae Nakai Rep. Exped. Manchoukuo Sect. IV 2: 153 (1933 publ. 1935)
Aconitum kusnezoffii var. crispulum W.T.Wang Acta Phytotax. Sin., Addit. 1: 92 1965
Aconitum kusnezoffii var. nutans Finet & Gagnep. Bull. Soc. Bot. France 51: 508 1904
Aconitum kusnezoffii var. tenuisectum Regel Bull. Soc. Imp. Naturalistes Moscou 34: 94 1861
Aconitum pulcherrimum var. tenuisectum (Regel) Nakai Rep. Exped. Manchoukou Sect. IV 2: 162 1935
Aconitum pulcherrimum var. dissectum (Regel) Nakai

Common names Top

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Language Common/alternative name
Spanish aconitum yamatsutae
Spanish aconitum villosum
Spanish aconitum triphylloides
Spanish aconitum pulcherrimum var. tenuisectum
Spanish aconitum pulcherrimum var. dissectum
Spanish aconitum pulcherrimum subsp. luferovii
Spanish aconitum pulcherrimum
Spanish aconitum kusnezoffii var. tenuisectum
Spanish aconitum gibbiferum
Spanish aconitum volubile var. pulcherrimum
Spanish acónito de kusnezov
Spanish aconito de kusnezov
Azerbaijani kuznetsov kəpənəkçiçəyi
Russian Борец Кузнецова
Chinese 北烏頭
Chinese 草烏
Chinese 草乌
Chinese 鸦头
Chinese 蓝附子
Chinese 穴种
Chinese 小叶鸦儿芦
Chinese 勒革拉花
Chinese 五毒根
Chinese 草乌芽
Chinese 北乌头
Chinese 东北草乌
Chinese 草乌叶
Chinese 小叶芦
Chinese 鸡头草
Chinese 蓝靰鞡花
Chinese 草乌头
Chinese 射罔

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Aconitum kusnezoffii var. gibbiferum (Rchb.) Regel Index Seminum (LE) 1861: 44 1861

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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Germination Improved by GA3: Gibberellic Acid(GA3) is a plant growth hormone that can break dormancy and improve germination rates for seeds that are otherwise difficult to sprout.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
seed very poisonous, wash hands after handling, 20°C x 4 weeks, then -7°C x 6 weeks, then 10°C; germinates well from seed stored dry 5 months and with GA3 if stored longer than 5 months

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Buryatiya
      • Chita
      • Irkutsk
      • Yakutskiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000517499
UNII QU71159N2W
Tropicos 27101190
KEW urn:lsid:ipni.org:names:707505-1
The Plant List kew-2618937
Open Tree Of Life 141633
Observations.org 130959
NCBI Taxonomy 239685
IPNI 707505-1
GBIF 7277127
EOL 2873316
Elurikkus 581711
USDA GRIN 1343
CMAUP NPO8847
PFAF Aconitum kusnezoffii

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
Anti-rheumatoid arthritis effects of traditional Chinese medicine Fufang Xiaohuoluo pill on collagen-induced arthritis rats and MH7A cells Yin Q, Huang Q, Zhang H, Zhang X, Fan C, Wang H Front Pharmacol 29-Apr-2024
PMCID:PMC11089244
doi:10.3389/fphar.2024.1374485
PMID:38741593
Exploring the Biomedical Potential of Terpenoid Alkaloids: Sources, Structures, and Activities Wang X, Xin J, Sun L, Sun Y, Xu Y, Zhao F, Niu C, Liu S Molecules 25-Apr-2024
PMCID:PMC11085545
doi:10.3390/molecules29091968
PMID:38731459
Comparative study on registration application of proprietary Chinese medicine in the Guangdong-Hong Kong-Macau Greater Bay Area of China Liu Z, Zhao J, Wang Y, Luo H J Pharm Policy Pract 27-Mar-2024
PMCID:PMC11020596
doi:10.1080/20523211.2024.2325516
PMID:38628567
Comparative analysis of the organelle genomes of Aconitum carmichaelii revealed structural and sequence differences and phylogenetic relationships Zhang R, Xiang N, Qian C, Liu S, Zhao Y, Zhang G, Wei P, Li J, Yuan T BMC Genomics 08-Mar-2024
PMCID:PMC10921738
doi:10.1186/s12864-024-10136-1
PMID:38454328
Genomic insights into the clonal reproductive Opuntia cochenillifera: mitochondrial and chloroplast genomes of the cochineal cactus for enhanced understanding of structural dynamics and evolutionary implications Liu J, Feng Y, Chen C, Yan J, Bai X, Li H, Lin C, Xiang Y, Tian W, Qi Z, Yu J, Yan X Front Plant Sci 07-Mar-2024
PMCID:PMC10954886
doi:10.3389/fpls.2024.1347945
PMID:38516667
Characterization of the Complete Mitochondrial Genome of Wintersweet (Chimonanthus praecox) and Comparative Analysis within Magnoliids Yu X, Feng Y, Zhang J Life (Basel) 25-Jan-2024
PMCID:PMC10890521
doi:10.3390/life14020182
PMID:38398691
Preliminary discussion on the mechanism of active components of Radix Aconiti kusnezoffii in the treatment of migraine based on network pharmacology Wu S, Baolechaolu, Hongmei, Huhemuren, Bai C, Gao J Medicine (Baltimore) 29-Dec-2023
PMCID:PMC10754605
doi:10.1097/MD.0000000000030640
PMID:38206698
The traditional use, structure, and immunostimulatory activity of bioactive polysaccharides from traditional Chinese root medicines: A review Bo S, Zhang M, Dan M Heliyon 13-Dec-2023
PMCID:PMC10770551
doi:10.1016/j.heliyon.2023.e23593
PMID:38187324
Insight into chloroplast genome structural variation of the Mongolian endemic species Adonis mongolica (Ranunculaceae) in the Adonideae tribe Nyamgerel N, Baasanmunkh S, Oyuntsetseg B, Bayarmaa GA, Erst A, Park I, Choi HJ Sci Rep 12-Dec-2023
PMCID:PMC10716127
doi:10.1038/s41598-023-49381-x
PMID:38086985
TCM and related active compounds in the treatment of gout: the regulation of signaling pathway and urate transporter Sun X, Yang L, Sun H, Sun Y, Wei S, Han Y, Wang W, Kong L, Wang X Front Pharmacol 29-Nov-2023
PMCID:PMC10716793
doi:10.3389/fphar.2023.1275974
PMID:38094893
A Comprehensive Review of the Pharmacology, Chemistry, Traditional Uses and Quality Control of Star Anise (Illicium verum Hook. F.): An Aromatic Medicinal Plant Zou Q, Huang Y, Zhang W, Lu C, Yuan J Molecules 01-Nov-2023
PMCID:PMC10648513
doi:10.3390/molecules28217378
PMID:37959797
Assembly and comparative analysis of the complete mitochondrial genome of Isopyrum anemonoides (Ranunculaceae) Yisilam G, Liu Z, Turdi R, Chu Z, Luo W, Tian X PLoS One 05-Oct-2023
PMCID:PMC10553351
doi:10.1371/journal.pone.0286628
PMID:37796878
Crocus sativus L. Extract (Saffron) Effectively Reduces Arthritic and Inflammatory Parameters in Monotherapy and in Combination with Methotrexate in Adjuvant Arthritis Chrastina M, Dráfi F, Pružinská K, Poništ S, Kamga KS, Khademnematolahi S, Bilka F, Novák P, Pašková Ľ, Bauerová K Nutrients 22-Sep-2023
PMCID:PMC10574733
doi:10.3390/nu15194108
PMID:37836391
Advances in research and utilization of botanical pesticides for agricultural pest management in Inner Mongolia, China Guo C, Wang L, Chen N, Zhang M, Jia J, Lv L, Li M Chin Herb Med 28-Aug-2023
PMCID:PMC11064588
doi:10.1016/j.chmed.2023.04.002
PMID:38706822
Functional immune boosters; the herb or its dead microbiome? Antigenic TLR4 agonist MAMPs found in 65 medicinal roots and algae’s Mazzio E, Barnes A, Badisa R, Fierros-Romero G, Williams H, Council S, Soliman KF J Funct Foods 29-Jul-2023
PMCID:PMC10469438
doi:10.1016/j.jff.2023.105687
PMID:37654434

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 acid esters
[(1R,2R,3S,4R,5R,6S,7R,10S,12R,15S,18S,19R)-13-ethyl-5,7-dihydroxy-6,18-dimethoxy-15-(methoxymethyl)-11-oxa-13-azahexacyclo[8.8.1.12,5.01,12.03,8.015,19]icos-8-en-4-yl] benzoate 100927670 Click to see CCN1CC2(CCC(C34C2C(C=C5C6C3CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC41)OC)COC 555.70 unknown https://doi.org/10.1021/NP960481T
[(1R,2S,3R,4S,5S,6R,7R,10S,12R,15S,18S,19R)-13-ethyl-5,7-dihydroxy-6,18-dimethoxy-15-(methoxymethyl)-11-oxa-13-azahexacyclo[8.8.1.12,5.01,12.03,8.015,19]icos-8-en-4-yl] benzoate 162825657 Click to see CCN1CC2(CCC(C34C2C(C=C5C6C3CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC41)OC)COC 555.70 unknown https://doi.org/10.1021/NP960481T
[5,9-Dihydroxy-6,20,22-trimethoxy-17-(methoxymethyl)-10,14-dimethyl-14-azahexacyclo[9.9.2.12,5.01,12.03,10.017,21]tricosan-4-yl] benzoate 53399238 Click to see CC12C(CCC(C3(CC(C1C3OC(=O)C4=CC=CC=C4)C56C(CCC7(C5C(C2C6CN(CC7)C)OC)COC)OC)O)OC)O 627.80 unknown via CMAUP database
[5,9,16-trihydroxy-6,18,20-trimethoxy-15-(methoxymethyl)-10,13-dimethyl-13-azahexacyclo[9.7.2.12,5.01,12.03,10.015,19]henicosan-4-yl] benzoate 53399190 Click to see CC12C(CCC(C3(CC(C1C3OC(=O)C4=CC=CC=C4)C56C(CC(C7(C5C(C2C6N(C7)C)OC)COC)O)OC)O)OC)O 615.80 unknown via CMAUP database
6-Benzoylheteratisine 5487064 Click to see 495.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
((1S,2R,3R,4S,5R,6S,8R,9R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo(7.7.2.12,5.01,10.03,8.013,17)nonadecan-4-yl) 4-methoxybenzoate 20055981 Click to see 627.80 unknown via CMAUP database
(1a,3a,6a,14a,15a,16b)-1,6,16-Trimethoxy-4-(methoxymethyl)-20-methyl-aconitane-3,8,13,14,15-pentol 8-acetate 14-benzoate 145994469 Click to see 631.70 unknown https://doi.org/10.1007/BF01373796
(1R,2S,3S,4S,5S,6R,7S,8R,9S,10R,13S,16S,17R)-11-ethyl-6-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-3,4,7,8,16-pentol 101465272 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(C(C(C6CC4C5(C6O)O)OC)O)O)O)COC 439.50 unknown via CMAUP database
(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 97960151 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC 481.60 unknown via CMAUP database
(1S,2R,3R,4S,5S,6R,7S,8R,9R,10R,13S,16S,17R,18R)-11-ethyl-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,7,8,16-tetrol 102316689 Click to see 453.60 unknown via CMAUP database
(1S,2R,3R,4S,5S,6S,8R,10R,13S,16S,17R,18R)-11-ethyl-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol 102004921 Click to see 437.60 unknown via CMAUP database
(1S,2R,3R,4S,5S,6S,8R,9R,10R,13S,16S,17R,18R)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 57412952 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)OC)COC 451.60 unknown via CMAUP database
(1S,2R,3R,4S,5S,6S,8S,10R,13S,16S,17R)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 102004486 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown via CMAUP database
(1S,2R,3R,4S,5S,6S,8S,9S,13R,16S,17R)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 71307576 Click to see 421.60 unknown via CMAUP database
(1S,4S,5R,7S,8S,9R,10R, 11S,13S,14S,16S,17R)-N-methyl-8,14-dihydroxy-1,16-trimethoxy-4-(methoxymethylene)aconitane 57506227 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown via CMAUP database
(2R,3R,6S,8R,13S,17R)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 5315807 Click to see 451.60 unknown https://doi.org/10.1055/S-2007-971658
(2S,3R,5S,8S,13S,17R)-11-ethyl-6,18-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-2,4,8,16-tetrol 138114026 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4(C5C6O)O)OC)O)OC)O)COC 453.60 unknown https://doi.org/10.1007/BF01373796
[(1R,2S,3S,4R,5R,6S,7S,8S,13R,14R,16S,17R,18R)-8-acetyloxy-2,5,7,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 118701715 Click to see 647.70 unknown https://doi.org/10.1007/BF01373796
[(1R,2S,3S,4R,5R,6S,7S,8S,9R,10R,13R,14R,16S,17R,18R)-8-acetyloxy-2,5,7,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 101289637 Click to see 647.70 unknown https://doi.org/10.1021/NP960481T
[(1R,2S,3S,4R,5R,6S,7S,8S,9R,13R,14R,16S,17R,18R)-4,8-diacetyloxy-11-ethyl-2,5,7-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-14-yl] acetate 24832651 Click to see 641.70 unknown via CMAUP database
[(1R,2S,3S,4R,5R,6S,7S,8S,9R,13R,14R,16S,17R,18R)-8-acetyloxy-2,5,7,14,18-pentahydroxy-6,16-dimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 441712 Click to see 633.70 unknown https://doi.org/10.1007/BF01373796
[(1R,2S,3S,4R,5R,6S,7S,8S,9S,13R,14R,16S,18R)-8-acetyloxy-2,5,7,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 102601273 Click to see CC(=O)OC12C3C(C4C5(CN(C3C4(C(CC5O)OC)C6(C1C(C(C6)(C(C2O)OC)O)OC(=O)C7=CC=CC=C7)O)C)COC)OC 647.70 unknown via CMAUP database
[(1R,2S,4S,5S,6S,7S,8S,9R,13R,14S,16S,18R)-8-acetyloxy-2,5,7,14,18-pentahydroxy-6,16-dimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 50989178 Click to see CC(=O)OC12C3C(C4C5(CN(C3C4(C(CC5O)OC)C6(C1C(C(C6)(C(C2O)OC)O)OC(=O)C7=CC=CC=C7)O)C)COC)O 633.70 unknown via CMAUP database
[(1S,2R,3R,4R,5R,6R,7S,8S,9R,10R,13S,16S,17R,18R)-8-acetyloxy-5,7-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 71749430 Click to see CC(=O)OC12C3C(CC(C3OC(=O)C4=CC=CC=C4)(C(C1O)OC)O)C56C(CCC7(C5C(C2C6N(C7)C)OC)COC)OC 615.70 unknown via CMAUP database
[(1S,2R,3R,4R,5R,6S,7S,8R,10R,13R,14R,16S,17S,18R)-11-ethyl-5,7,8,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 102004487 Click to see 603.70 unknown via CMAUP database
[(1S,2R,3R,4R,5R,6S,7S,8R,10R,13R,14R,16S,17S,18R)-5,7,8,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 102004490 Click to see 589.70 unknown via CMAUP database
[(1S,2R,3R,4R,5R,6S,7S,8R,10R,13R,14R,16S,17S,18R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 24014401 Click to see 645.70 unknown via CMAUP database
[(1S,2R,3R,4R,5R,6S,7S,8R,10R,13R,14R,16S,17S,18R)-8-acetyloxy-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 102004423 Click to see 631.70 unknown via CMAUP database
[(1S,2R,3R,4R,5R,6S,7S,8R,10R,13R,14R,16S,17S,18R)-8,14-diacetyloxy-11-ethyl-5,7-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 102004916 Click to see 687.80 unknown via CMAUP database
[(1S,2R,3R,4R,5R,6S,7S,8R,10R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-5,7-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 102004860 Click to see 629.70 unknown https://doi.org/10.1007/BF01373796
[(1S,2R,3R,4R,5R,6S,7S,8R,10R,13S,16S,17R,18R)-8-acetyloxy-5,7-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 102004422 Click to see CC(=O)OC12C3C(CC(C3OC(=O)C4=CC=CC=C4)(C(C1O)OC)O)C56C(CCC7(C5C(C2C6N(C7)C)OC)COC)OC 615.70 unknown via CMAUP database
[(1S,2R,3R,4R,5R,6S,7S,8R,9R,10R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-5,7-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 60155415 Click to see 629.70 unknown via CMAUP database
[(1S,2R,3R,4R,5R,6S,7S,8R,9R,10S,13R,14R,16R,17S,18R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 70697623 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)O)COC 645.70 unknown via CMAUP database
[(1S,2R,3R,4R,5R,6S,7S,8R,9R,13R,14R,16S,17S,18R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 441741 Click to see 675.80 unknown via CMAUP database
[(1S,2R,3R,4R,5R,7S,8R,9R,10R,13S,17R,18R)-8-acetyloxy-11-ethyl-5,7-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 101289529 Click to see 629.70 unknown via CMAUP database
[(1S,2R,3R,4R,5S,6S,7S,8R,9R,13R,16S,17S,18R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 139593379 Click to see 645.70 unknown https://doi.org/10.1007/BF01373796
[(1S,2R,3R,4S,5S,6R,7S,8R,9R,10R,13S,16S,17R,18R)-8-acetyloxy-7-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 102146471 Click to see 599.70 unknown via CMAUP database
[(1S,2R,3R,6S,7S,8R,9R,13S,16S,18R)-5,7,8-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 71571448 Click to see CN1CC2(CCC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC)OC)COC 573.70 unknown via CMAUP database
[(1S,3R,4R,6S,7S,8R,10R,13R,14R,16S,18R)-11-ethyl-5,7,8,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 121312 Click to see 603.70 unknown via CMAUP database
[(1S,3R,4R,6S,7S,8R,10R,13R,14R,16S)-11-ethyl-5,7,8,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 49868330 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC)OC)O)COC 603.70 unknown via CMAUP database
[(1S,4R,5R,6R,7S,8R,9R,10R,13R,14R,16S,18R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 6713948 Click to see 645.70 unknown via CMAUP database
[(1S,4R,5R,7S,8R,9R,10R,13R,16S,18R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 45358103 Click to see 645.70 unknown via CMAUP database
[(1S,4R,5S,6S,8R,13R,14R,16S,18R)-8-acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 11422434 Click to see 659.80 unknown via CMAUP database
[(1S,5R,6R,7S,8R,9R,10R,13R,14R,16S)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 54742366 Click to see 645.70 unknown via CMAUP database
[(1S,5R,6S,7S,8R,9S,10S,13R,14R,16R)-11-ethyl-5,7,8,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 42616714 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC)OC)O)COC 603.70 unknown via CMAUP database
[(1S,5R,8R,13R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 44135351 Click to see 645.70 unknown via CMAUP database
[(1S,6S,7S,8R,9R,13R,14R,16S,18R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 91746192 Click to see 645.70 unknown via CMAUP database
[(2R,3R,4R,5R,6R,7S,8S,10R,13S,16S,17R,18R)-8-acetyloxy-5,7-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 77906396 Click to see CC(=O)OC12C3C(CC(C3OC(=O)C4=CC=CC=C4)(C(C1O)OC)O)C56C(CCC7(C5C(C2C6N(C7)C)OC)COC)OC 615.70 unknown via CMAUP database
[(2R,3R,4R,5R,6R,7S,8S,9R,10S,13R,14R,16S,17S,18R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 71313016 Click to see 645.70 unknown via CMAUP database
[(2R,3R,4R,5R,6S,7S,8R,10S,13R,14R,16R,18R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 118705467 Click to see 645.70 unknown via CMAUP database
[(2R,3R,4R,5R,6S,7S,8R,13R,14R,16S,17S,18R)-5,7,8,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 78358527 Click to see 589.70 unknown via CMAUP database
[(2R,3R,4R,5R,6S,7S,8R,13R,14R,16S,17S,18R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 92044462 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)O)COC 645.70 unknown via CMAUP database
[(2R,3R,5R,6S,8R,10R,17S)-8-acetyloxy-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 17679 Click to see CC(=O)OC12C3C(CC(C3OC(=O)C4=CC=CC=C4)(C(C1O)OC)O)C56C(CC(C7(C5C(C2C6N(C7)C)OC)COC)O)OC 631.70 unknown via CMAUP database
[(2R,3R,5R,8R,10R,17R)-8-Acetyloxy-5,7-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 23337 Click to see 615.70 unknown via CMAUP database
[(2R,3R,5S,6S,8R,13R,17S)-8-acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 5315414 Click to see 659.80 unknown https://doi.org/10.1002/PTR.5495
[(2S,3R,4R,5S,6S,7S,8R,13R,14R,17S,18R)-5,7,8,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 45115059 Click to see 589.70 unknown via CMAUP database
[(2S,3S,5R,8R,13S,17S)-8-acetyloxy-5,7-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 138115321 Click to see CC(=O)OC12C3C(CC(C3OC(=O)C4=CC=CC=C4)(C(C1O)OC)O)C56C(CCC7(C5C(C2C6N(C7)C)OC)COC)OC 615.70 unknown https://doi.org/10.1007/BF01373796
https://doi.org/10.1021/NP960481T
[(6R,7S,10R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 27806 Click to see 675.80 unknown via CMAUP database
[8-Acetyloxy-11-ethyl-2,5,7,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 3748601 Click to see 661.70 unknown https://doi.org/10.1021/NP960481T
[8-Acetyloxy-11-ethyl-5,7-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 14108159 Click to see 629.70 unknown https://doi.org/10.1002/JSSC.201500059
[8-Acetyloxy-2,5,7,14-tetrahydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 73813823 Click to see 647.70 unknown https://doi.org/10.1021/NP960481T
[8-Acetyloxy-5,7-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 4526188 Click to see 615.70 unknown via CMAUP database
10-Hydroxy aconitine 16401086 Click to see 661.70 unknown https://doi.org/10.1021/NP960481T
10-Hydroxymesaconitine 6426872 Click to see 647.70 unknown via CMAUP database
10-OH-Mesaconitine 78358536 Click to see 647.70 unknown via CMAUP database
3-Acetylaconitine 53595 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)OC(=O)C)COC 687.80 unknown https://doi.org/10.1002/JMS.510
3-Acetylaconitine 102063144 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)OC(=O)C)COC 687.80 unknown via CMAUP database
3-Deoxyaconitine 78358503 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)COC 629.70 unknown via CMAUP database
8-(Acetyloxy)-20-ethyl-3,13-dihydroxy-1,6,16-trimethoxy-4-(methoxymethyl)aconitan-14-yl 4-methoxybenzoate 155569 Click to see 659.80 unknown via CMAUP database
Acetylaconitine 21599000 Click to see 687.80 unknown via CMAUP database
Aconifine 441705 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4(CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC(=O)C)OC)OC)O)COC 661.70 unknown https://doi.org/10.1021/NP960481T
Aconitane-13,14,15-triol, 20-ethyl-1,6,8,16-tetramethoxy-4-(methoxymethyl)-, 14-benzoate, (1alpha,6alpha,14alpha,15alpha,16beta)- 78358553 Click to see 601.70 unknown via CMAUP database
Aconitane-3,8,13,14,15-pentol,1,6,16-trimethoxy-4-(methoxymethyl)-20-methyl-, 8-acetate14-benzoate, (1a,3a,6a,14a,15a,16b)- 416228 Click to see 631.70 unknown via CMAUP database
Aconitin 24832676 Click to see 645.70 unknown via CMAUP database
Aconitine 245005 Click to see 645.70 unknown https://doi.org/10.1007/BF01373796
Aconitine, analytical standard 6419868 Click to see 645.70 unknown via CMAUP database
Ambap2752-64-9 118701205 Click to see 631.70 unknown via CMAUP database
Benzoylaconine 60155417 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC)OC)O)COC 603.70 unknown https://doi.org/10.1002/JSSC.201300775
Benzoylaconitine 20055771 Click to see 603.70 unknown via CMAUP database
Benzoylhypacoitine 78358526 Click to see CN1CC2(CCC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC)OC)COC 573.70 unknown via CMAUP database
Benzoylmesaconine 24832659 Click to see CN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC)OC)O)COC 589.70 unknown via CMAUP database
Bullatine B 120682 Click to see 437.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4523871/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890449/
https://doi.org/10.1007/BF01373796
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120301/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268769/
Bullatine B 146014456 Click to see 437.60 unknown https://doi.org/10.1007/BF01373796
Chasmanine 20055812 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)OC)COC 451.60 unknown via CMAUP database
CID 11250863 11250863 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)O)COC 659.80 unknown via CMAUP database
CID 11969475 11969475 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)O)COC 645.70 unknown via CMAUP database
CID 15559774 15559774 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC)OC)O)COC 603.70 unknown https://doi.org/10.1007/S13318-016-0356-Z
https://doi.org/10.1055/S-0030-1250362
https://doi.org/10.1080/14786419.2016.1198348
https://doi.org/10.1016/J.JEP.2014.04.039
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787335/
https://doi.org/10.1002/JSSC.201500059
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890449/
https://doi.org/10.1016/J.LFS.2015.02.011
https://doi.org/10.1002/JSSC.201300775
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5051147/
CID 165283 165283 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)OC)COC 451.60 unknown https://doi.org/10.1055/S-2007-971658
https://doi.org/10.1021/JF104879H
CID 197019 197019 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)COC 629.70 unknown via CMAUP database
CID 21627927 21627927 Click to see CC(=O)OC12C3C(C4C5(CN(C3C4(C(CC5O)OC)C6(C1C(C(C6)(C(C2O)OC)O)OC(=O)C7=CC=CC=C7)O)C)COC)OC 647.70 unknown via CMAUP database
CID 6426869 6426869 Click to see 615.70 unknown via CMAUP database
CID 6426870 6426870 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)COC 629.70 unknown via CMAUP database
CID 6426871 6426871 Click to see 631.70 unknown via CMAUP database
CID 78358486 78358486 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC)OC)O)COC 603.70 unknown via CMAUP database
Deoxyaconitine 44445634 Click to see 629.70 unknown via CMAUP database
Deoxyaconitine 21598997 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(C6C4CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)OC(=O)C)OC)OC)COC 629.70 unknown via CMAUP database
Fuziline 102004854 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(C6C4CC(C6O)C(C5O)OC)O)OC)O)COC 453.60 unknown via CMAUP database
Hypaconitine 91973803 Click to see 615.70 unknown via CMAUP database
Hypaconitine 441737 Click to see CC(=O)OC12C3C(CC(C3OC(=O)C4=CC=CC=C4)(C(C1O)OC)O)C56C(CCC7(C5C(C2C6N(C7)C)OC)COC)OC 615.70 unknown https://doi.org/10.1007/BF01373796
https://doi.org/10.1021/NP960481T
Hypaconitine (Standard) 92044463 Click to see 615.70 unknown via CMAUP database
Isotalatisidine 12304578 Click to see 407.50 unknown https://doi.org/10.1007/BF01373796
Jesaconitine 76963334 Click to see 675.80 unknown via CMAUP database
Mesaconine 101671037 Click to see CN1CC2(C(CC(C34C2C(C(C31)C5(C6C4CC(C6O)(C(C5O)OC)O)O)OC)OC)O)COC 485.60 unknown via CMAUP database
Mesaconitine 16401314 Click to see CC(=O)OC12C3C(CC(C3OC(=O)C4=CC=CC=C4)(C(C1O)OC)O)C56C(CC(C7(C5C(C2C6N(C7)C)OC)COC)O)OC 631.70 unknown via CMAUP database
Mesaconitine (Standard) 23641113 Click to see 631.70 unknown via CMAUP database
N-desethyl-N-methylaconitine 441747 Click to see 631.70 unknown https://doi.org/10.1007/BF01373796
Neoline 10003218 Click to see 437.60 unknown via CMAUP database
Npc287766 24832657 Click to see 589.70 unknown via CMAUP database
Npc312658 14163819 Click to see 453.60 unknown via CMAUP database
Npc87288 2012 Click to see 645.70 unknown via CMAUP database
Pharmakon1600-01500655 6708463 Click to see 645.70 unknown via CMAUP database
Sdccgsbi-0633679.P001 16210989 Click to see 645.70 unknown via CMAUP database
SureCN2848738 10008952 Click to see 615.70 unknown via CMAUP database
SureCN4184478 118701203 Click to see 675.80 unknown via CMAUP database
Talatisamine 159891 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown via CMAUP database
Talatisidine 139066658 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)COC 407.50 unknown https://doi.org/10.1007/BF01373796
Talatizamine 441761 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown via CMAUP database
Yunaconitine 6918110 Click to see 659.80 unknown via CMAUP database
Yunaconitine (Vilmorrianine B and other names) 45033610 Click to see 659.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2R,4S,5R,8S,12R,13S,14R,17R,19R)-11-ethyl-19-hydroxy-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.01,14.02,12.04,13.05,10.08,13]icosan-16-one 100930478 Click to see 355.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids / Napelline-type diterpenoid alkaloids
(1R,2R,4S,5R,7R,8R,9R,13R,16S,17R)-11-Ethyl-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecane-4,7,16-triol 6325720 Click to see 359.50 unknown via CMAUP database
(1R,2R,4S,5S,7R,8R,9R,13R,16S,17R)-11-ethyl-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecane-4,7,16-triol 441749 Click to see 359.50 unknown via CMAUP database
(1R,2R,5R,7R,8R,9R,13R,16S,17R)-11-ethyl-7,16-dihydroxy-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-4-one 441755 Click to see 357.50 unknown https://doi.org/10.1007/BF01373796
(1R,4S,7R,8R,9R,13R,16S)-11-ethyl-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecane-4,7,16-triol 118701206 Click to see 359.50 unknown via CMAUP database
(1R,5S,7R,8R,9R,13R)-11-ethyl-7,16-dihydroxy-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-4-one 139291804 Click to see 357.50 unknown https://doi.org/10.1007/BF01373796
(2R,4S,5R,7R,10R,13R,16S,17R)-11-ethyl-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecane-4,7,16-triol 90473812 Click to see 359.50 unknown via CMAUP database
(2R,4S,5R,7R,13R,16S,17R)-11-ethyl-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecane-4,7,16-triol 165280 Click to see 359.50 unknown via CMAUP database
(3R,6S,6aR,6bR,8S,9S,11R,11aR,12R,14R)-1-ethyl-3-methyl-10-methylenetetradecahydro-3,6a,12-(epiethane[1,1,2]triyl)-9,11a-methanoazuleno[2,1-b]azocine-6,8,11-triol 16394550 Click to see 359.50 unknown via CMAUP database
Bullatine G;Songorin; Songorine;Napellonine 20055028 Click to see 357.50 unknown via CMAUP database
CID 16394536 16394536 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4CC(=O)C(C5)C(=C)C6O)O)C 357.50 unknown via CMAUP database
CID 6713970 6713970 Click to see 359.50 unknown via CMAUP database
Napelline 17749282 Click to see 359.50 unknown via CMAUP database
Napellonine 120706 Click to see 357.50 unknown via CMAUP database
Songorine 71456946 Click to see 357.50 unknown via CMAUP database
Zongorine 6915738 Click to see CCN1CC2(CCC(C34C2CC(C31)C56C4CC(=O)C(C5)C(=C)C6O)O)C 357.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Lappaconitine-type diterpenoid alkaloids
(+)-Lappaconitine >90% 115161 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5(C6OC)O)OC)O)OC)OC(=O)C7=CC=CC=C7NC(=O)C 584.70 unknown via CMAUP database
(11-Ethyl-3,8-dihydroxy-4,6,16-trimethoxy-11-azahexacyclo(7.7.2.12,5.01,10.03,8.013,17)nonadecan-13-yl) 2-acetamidobenzoate 3886 Click to see 584.70 unknown via CMAUP database
[(1S,3S,4S,5R,6S,8S,9S,13S,16S)-11-Ethyl-3,8-dihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-acetamidobenzoate 16464737 Click to see 584.70 unknown via CMAUP database
[(1S,4S,5R,8S,9S,13S)-11-Ethyl-3,8-dihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-acetamidobenzoate 16667701 Click to see 584.70 unknown via CMAUP database
Allapininum 6917827 Click to see 584.70 unknown via CMAUP database
Lannaconitine 5281279 Click to see 584.70 unknown via CMAUP database
Lappaconitine 90479327 Click to see 584.70 unknown via CMAUP database
Npc101515 441743 Click to see 584.70 unknown via CMAUP database
SureCN408157 9896038 Click to see 584.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1R,2S,5R,9R,10S,11R,13R,14S,15R,16R)-7-Ethyl-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.210,13.01,8.05,16.010,15]nonadecane-2,11,14-triol 15226908 Click to see 359.50 unknown https://doi.org/10.1055/S-2006-960125
https://doi.org/10.3987/COM-98-S40
(1S,2S,4R,7R,10R,11R,18S)-18-hydroxy-13-(2-hydroxyethyl)-11-methyl-19-methylidene-13-azapentacyclo[9.3.3.24,7.01,10.02,7]nonadecan-6-one 101104087 Click to see CC12CCCC3(C1CCC45C3CC(CC4=O)C(=C)C5O)CN(C2)CCO 359.50 unknown https://doi.org/10.1080/10286029808039848
(1S,5R,9S,10S,11S,13R,14R,15S,16S)-7-ethyl-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.210,13.01,8.05,16.010,15]nonadecane-11,14-diol 138108665 Click to see 343.50 unknown https://doi.org/10.1055/S-2006-960125
https://doi.org/10.3987/COM-98-S40
(2S,8R,9S,11R,13S,14S,15R,16S)-7-Ethyl-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.210,13.01,8.05,16.010,15]nonadecane-2,11,14-triol 24883709 Click to see 359.50 unknown via CMAUP database
[(3S,5R,17R,18S,19S)-10-acetyloxy-9,19-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-yl] acetate 24838640 Click to see 429.50 unknown via CMAUP database
15,18-Dihydroxy-13-(2-hydroxyethyl)-11-methyl-19-methylidene-13-azapentacyclo[9.3.3.24,7.01,10.02,7]nonadecan-6-one 163106648 Click to see CC12CCC(C3(C1CCC45C3CC(CC4=O)C(=C)C5O)CN(C2)CCO)O 375.50 unknown https://doi.org/10.1080/10286029808039848
Anthorine 441709 Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)C6N(C2)CCO6 343.50 unknown via CMAUP database
Atisine 6426913 Click to see 343.50 unknown via CMAUP database
CID 441729 441729 Click to see 343.50 unknown https://doi.org/10.1055/S-2006-960125
https://doi.org/10.3987/COM-98-S40
CID 6917802 6917802 Click to see 429.50 unknown via CMAUP database
Guanfu base A 101603171 Click to see 429.50 unknown via CMAUP database
Kwan-Fu Base A 78358495 Click to see CC(=O)OC1CC2(CN3C4C2C5(C1)C3C6(C(C7C(C5C6(C4)CC7=C)O)OC(=O)C)O)C 429.50 unknown via CMAUP database
SureCN4187159 118701194 Click to see 343.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4S,6E,10Z,11aR)-4-acetyloxy-6-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl]methyl acetate 10406449 Click to see 364.40 unknown via CMAUP database
[(3aR,4S,6E,10Z,11aR)-4-acetyloxy-6-formyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl]methyl acetate 10428712 Click to see CC(=O)OCC1=CC2C(C(CC(=CCC1)C=O)OC(=O)C)C(=C)C(=O)O2 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 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
Npc29 6432744 Click to see 414.70 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see 112.09 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(-)-Higenamine 440927 Click to see 271.31 unknown via CMAUP database
(R)-(+)-Higenamine 440988 Click to see 271.31 unknown via CMAUP database
Higenamine 114840 Click to see C1CNC(C2=CC(=C(C=C21)O)O)CC3=CC=C(C=C3)O 271.31 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolidines
(1S,2R,3S,6S,9R,10R,11R,14R,17S,18R,19S)-12-ethyl-9,19-dihydroxy-17-methoxy-14-methyl-5-oxa-12-azahexacyclo[8.7.2.12,6.01,11.03,9.014,18]icosan-4-one 101286237 Click to see 391.50 unknown via CMAUP database
(3R,6S,6aS,7R,7aS,10S,12aS,13R,13aR,14S,15R)-1-Ethyltetradecahydro-12a,14-dihydroxy-6-methoxy-3-methyl-8H-13,3,6a-ethanylylidene-7,10-methanooxepino(3,4-i)-1-benzazocin-8-one 78265170 Click to see 391.50 unknown via CMAUP database
4:1A,6B.Heteratisane 441735 Click to see 391.50 unknown via CMAUP database
CID 25084349 25084349 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CCC6CC4C5C(=O)O6)O)O)OC)C 391.50 unknown via CMAUP database
Npc115186 73527 Click to see 391.50 unknown via CMAUP database
Npc212106 431671 Click to see 391.50 unknown via CMAUP database
SureCN3132559 118701059 Click to see 391.50 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
1-Methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol 54456 Click to see CC1C2=CC(=C(C=C2CCN1)O)O 179.22 unknown via CMAUP database
6,7-Isoquinolinediol, 1,2,3,4-tetrahydro-1-methyl-, (R)- 7157331 Click to see 179.22 unknown via CMAUP database
Salsolinol 91588 Click to see 179.22 unknown via CMAUP database

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