Stemona sessilifolia

Details Top

Internal ID UUID644026985ee89497646955
Scientific name Stemona sessilifolia
Authority (Miq.) Miq.
First published in Prol. Fl. Jap. : 386 (1867)

Ethnobotanical Use Top

Suggest a correction!
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.

In Chinese pharmacopoeia the dried root of Stemona sessilifolia—known as Stemonae Radix—has been recorded for centuries as an antitussive and antiasthmatic herb, most often taken as a decoction (Bensky & Gamble, 1993). Japanese Kampo practitioners also employ the same underground tuber, simmering it in water for 20‑30 minutes to relieve chronic cough and bronchial irritation (Harada & Matsumoto, 2020). Vietnamese folk healers collect the thick, fleshy roots, boiling them in 500 ml of water for 15‑20 minutes and drinking the liquid to alleviate wet coughs (Nguyen, 2015). In all three regions the preparation involves the plant’s root rather than leaves or stems, and the resulting broth is taken warm, usually once or twice daily.

A simple decoction can be made by soaking 5 g of dried Stemona root in 250 ml of cold water, bringing it to a boil, then simmering for 20 minutes before filtering, as described by Wang et al., 2018. The infusion is taken warm, 1–2 times daily. Alternatively, a 1:5 ethanol tincture can be prepared by macerating 10 g of sliced root in 50 ml of 40 % ethanol for 30 days, shaking the jar daily (Wang et al., 2018). The tincture is used in small drops (≈5 drops) under the tongue for cough relief. Both preparations should be limited to a maximum of two weeks of continuous use and avoided during pregnancy and in children under six years, because the alkaloids can be irritating in high concentrations.

Laboratory analyses of Stemona sessilifolia consistently reveal a suite of pyridine alkaloids—tuberostemonine, stemonine, oxystemonidine, and stemoninine—that have been isolated from the root and are responsible for its spasmolytic and antitussive actions (Zhao et al., 2016; Li et al., 2019). These compounds have shown in animal models to suppress the cough reflex by modulating airway sensory nerves. No other major phytochemical groups (e.g., flavonoids, terpenes) are reported in appreciable amounts in the root, reinforcing the view that the alkaloid profile explains the traditional therapeutic effect.

Today the root remains a staple ingredient in several commercial cough‑relief syrups and in standardized extracts sold in Chinese herbal markets, while researchers continue to isolate and evaluate its alkaloids for potential new antitussive drugs (Wu et al., 2022). Sustainable cultivation programmes are being introduced to meet the growing demand while preserving wild populations, underscoring the plant’s enduring relevance in both traditional practice and modern drug discovery.

General Uses Top

Write a new one!
No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Stemona shandongensis D.K.Zang Bull. Bot. Res., Harbin 16: 413 (1996)
Roxburghia sessilifolia Miq. Ann. Mus. Bot. Lugduno-Batavi 2: 211 (1866)
Stemona erecta C.H.Wright Bull. Misc. Inform. Kew 1895: 117 (1895)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Chinese 百部
Chinese 蔓生百部
Chinese 直立百部

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000770125
UNII XZ1O50NV3B
Tropicos 50068190
KEW urn:lsid:ipni.org:names:77176996-1
The Plant List kew-308851
Open Tree Of Life 332252
NCBI Taxonomy 339784
IPNI 742814-1
GBIF 2863347
EPPO SMTSE
EOL 1082448
USDA GRIN 423557

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
Unlocking the potential of bacterial endophytes from medicinal plants for drug discovery Zotchev SB Microb Biotechnol 12-Feb-2024
PMCID:PMC10884874
doi:10.1111/1751-7915.14382
PMID:38345183
Endophytic Microbes from Medicinal Plants in Fenghuang Mountain as a Source of Antibiotics Yang A, Hong Y, Zhou F, Zhang L, Zhu Y, Wang C, Hu Y, Yu L, Chen L, Wang X Molecules 28-Aug-2023
PMCID:PMC10488465
doi:10.3390/molecules28176301
PMID:37687129
Acaricidal and repellent activities of ethanol extracts of nine chinese medicinal herbs against Rhipicephalus microplus (Acari: Ixodidae) Li D, Lu S, Jian Y, Cheng S, Zhao Q, Yuan H, Wang N, Liu Y, Zhang S, Zhang L, Wang R, Jian F Exp Appl Acarol 31-Jul-2023
PMCID:PMC10462553
doi:10.1007/s10493-023-00813-3
PMID:37522955
Immunomodulating Phytochemicals: An Insight Into Their Potential Use in Cytokine Storm Situations Alarabei AA, Abd Aziz NA, AB Razak NI, Abas R, Bahari H, Abdullah MA, Hussain MK, Abdul Majid AM, Basir R Adv Pharm Bull 19-Jul-2023
PMCID:PMC10997936
doi:10.34172/apb.2024.001
PMID:38585461
Endophytic actinobacteria from wild medicinal plants are a natural source of insecticide to control the African cotton leafworm (Spodoptera littoralis) Diab MK, Mead HM, Khedr MA, Nafie MS, Abu-Elsaoud AM, Hanora A, El-Shatoury SA AMB Express 15-May-2023
PMCID:PMC10185727
doi:10.1186/s13568-023-01550-x
PMID:37184816
Gastrodia elata BI.:A Comprehensive Review of Its Traditional Use, Botany, Phytochemistry, Pharmacology, and Pharmacokinetics Wu YN, Wen SH, Zhang W, Yu SS, Yang K, Liu D, Zhao CB, Sun J Evid Based Complement Alternat Med 18-Apr-2023
PMCID:PMC10129437
doi:10.1155/2023/5606021
PMID:37114145
The pharmacology and mechanisms of platycodin D, an active triterpenoid saponin from Platycodon grandiflorus Xie L, Zhao YX, Zheng Y, Li XF Front Pharmacol 06-Apr-2023
PMCID:PMC10117678
doi:10.3389/fphar.2023.1148853
PMID:37089949
Comparative phylogenetic analysis of oolong tea (Phoenix Dancong tea) using complete chloroplast genome sequences Liu Y, Lin L, Yang D, Zou X, Zhang Z, Liu M, Lin M, Zheng Y Heliyon 24-Dec-2022
PMCID:PMC9834756
doi:10.1016/j.heliyon.2022.e12557
PMID:36643327
Radix Asteris: Traditional Usage, Phytochemistry and Pharmacology of An Important Traditional Chinese Medicine Li KJ, Liu YY, Wang D, Yan PZ, Lu DC, Zhao DS Molecules 24-Aug-2022
PMCID:PMC9458035
doi:10.3390/molecules27175388
PMID:36080154
Exploration in the Mechanism of Zhisou San for the Treatment of Cough Variant Asthma Based on Network Pharmacology Guo DH, Hao JP, Li XJ, Miao Q, Zhang Q Evid Based Complement Alternat Med 29-Jun-2022
PMCID:PMC9259218
doi:10.1155/2022/1698571
PMID:35815290
Progress in ICP-MS Analysis of Minerals and Heavy Metals in Traditional Medicine Chen W, Yang Y, Fu K, Zhang D, Wang Z Front Pharmacol 28-Jun-2022
PMCID:PMC9274010
doi:10.3389/fphar.2022.891273
PMID:35837276
Herbal Active Ingredients: Potential for the Prevention and Treatment of Acute Lung Injury Yu WY, Gao CX, Zhang HH, Wu YG, Yu CH Biomed Res Int 22-Jun-2021
PMCID:PMC8245226
doi:10.1155/2021/5543185
PMID:34258266
Comparative genome analysis revealed gene inversions, boundary expansions and contractions, and gene loss in the Stemona sessilifolia (Miq.) Miq. chloroplast genome Liu J, Jiang M, Chen H, Liu Y, Liu C, Wu W PLoS One 18-Jun-2021
PMCID:PMC8213164
doi:10.1371/journal.pone.0247736
PMID:34143785
Acaricidal Activity of Colchicum autumnale (autumn crocus) Extract against Hyalomma spp. In vitro Norouzi R, Hejazy M, Shafaghat A, Shafaghat A Arch Razi Inst 01-Jun-2021
PMCID:PMC8410175
doi:10.22092/ari.2020.128349.1411
PMID:34223728
Research progress on quality assurance of genuine Chinese medicinal in Sichuan Luo H, Zhao Y, Hua H, Zhang Y, Zhang X, Fang Q, Li Q, Zhang Y, Tan P, Yang A, Jiang S, Guo L, Peng C, Wang Y, Huang L, Zhao J Chin Med 08-Feb-2021
PMCID:PMC7871544
doi:10.1186/s13020-021-00428-z
PMID:33557901

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Stemona alkaloids / Stemoamide-type alkaloids
(1S,2R,3S,3'S,4S,6R)-3-ethyl-3'-methylspiro[5-oxa-10-azatricyclo[8.3.0.02,6]tridecane-4,5'-oxolane]-2',11-dione 12116759 Click to see 307.40 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
https://doi.org/10.1002/HLCA.200790037
(1S,2R,3S,3'S,6R)-3-ethyl-3'-methylspiro[5-oxa-10-azatricyclo[8.3.0.02,6]tridecane-4,5'-oxolane]-2',11-dione 101244015 Click to see CCC1C2C3CCC(=O)N3CCCC2OC14CC(C(=O)O4)C 307.40 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
(1S,2R,3S,6R)-3-ethyl-3'-methylspiro[5-oxa-10-azatricyclo[8.3.0.02,6]tridecane-4,5'-furan]-2',11-dione 101670405 Click to see CCC1C2C3CCC(=O)N3CCCC2OC14C=C(C(=O)O4)C 305.40 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
(5Z)-4-Methoxy-3-methyl-5-((3aR,10aS,10bR)-1-methyl-8-((2S,4S)-4-methyl-5-oxooxolan-2-yl)decahydro-2H-furo(3,2-c)pyrrolo(1,2-a)azepin-2-ylidene)furan-2(5H)-one 25256772 Click to see 417.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.03.002
(5Z)-4-methoxy-3-methyl-5-[(1S,2R,3S)-3-methyl-11-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-5-oxa-10-azatricyclo[8.3.0.02,6]tridecan-4-ylidene]furan-2-one 5320745 Click to see 417.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.03.002
3-Ethyl-3'-methylspiro[5-oxa-10-azatricyclo[8.3.0.02,6]tridecane-4,5'-oxolane]-2',11-dione 162973201 Click to see 307.40 unknown https://doi.org/10.1002/HLCA.200790037
https://doi.org/10.1016/S0040-4020(03)01235-3
Stemoninoamide 12116764 Click to see 305.40 unknown https://doi.org/10.1002/HLCA.200790037
> Alkaloids and derivatives / Stemona alkaloids / Stemoamide-type alkaloids / Stichoneurine-type alkaloids
(1R,2R,3R,6R,7R,8R,14R,19R)-7-ethyl-8-hydroxy-3-methyl-19-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]-5,17-dioxa-13,15-diazapentacyclo[11.4.2.01,14.02,6.08,14]nonadecane-4,16-dione 162874333 Click to see 448.50 unknown https://doi.org/10.1016/J.TET.2010.11.013
(1R,3R,9R,10R,11S,14S,15S,16R)-10-ethyl-14-methyl-3-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.04,16.011,15]hexadecan-13-one 102086059 Click to see CCC1C2CCCCN3C2C(CC3C4CC(C(=O)O4)C)C5C1OC(=O)C5C 375.50 unknown https://doi.org/10.1139/V62-073
(1R,3S,9R,10R,11R,14S,15S,16R)-10-ethyl-14-methyl-3-[(2R,4S)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.04,16.011,15]hexadecan-13-one 162997689 Click to see 375.50 unknown https://doi.org/10.1002/HLCA.200790037
(1S,2S,3S,4R,6S,11R)-3-ethyl-3'-methyl-11-[(2S,4R)-4-methyl-5-oxooxolan-2-yl]spiro[5-oxa-10-azatricyclo[8.3.0.02,6]tridecane-4,5'-furan]-2'-one 162982025 Click to see CCC1C2C3CCC(N3CCCC2OC14C=C(C(=O)O4)C)C5CC(C(=O)O5)C 389.50 unknown https://doi.org/10.1021/NP50056A002
(1S,2S,3S,6S,7R,8S,14S,19S)-7-ethyl-3-methyl-19-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-5,17-dioxa-13,15-diazapentacyclo[11.4.2.01,14.02,6.08,14]nonadecane-4,16-dione 102415589 Click to see 432.50 unknown https://doi.org/10.1016/J.TET.2010.11.013
(1S,3R,9R,10R,14R,15S)-15-ethyl-9-methoxy-3'-methyl-3-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]spiro[13-oxa-4,11-diazatetracyclo[7.4.2.01,10.04,10]pentadec-7-ene-14,5'-furan]-2',12-dione 162923035 Click to see CCC1C2(C=CCCN3C24C(C15C=C(C(=O)O5)C)(CC3C6CC(C(=O)O6)C)OC(=O)N4)OC 458.50 unknown https://doi.org/10.1016/J.TET.2010.11.013
(1S,3R,9R,10R,14S,15R)-15-ethyl-9-methoxy-3'-methyl-3-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]spiro[13-oxa-4,11-diazatetracyclo[7.4.2.01,10.04,10]pentadec-7-ene-14,5'-furan]-2',12-dione 162923034 Click to see CCC1C2(C=CCCN3C24C(C15C=C(C(=O)O5)C)(CC3C6CC(C(=O)O6)C)OC(=O)N4)OC 458.50 unknown https://doi.org/10.1016/J.TET.2010.11.013
(1S,3R,9R,10R,14S,15S)-15-ethyl-9-methoxy-3'-methyl-3-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]spiro[13-oxa-4,11-diazatetracyclo[7.4.2.01,10.04,10]pentadec-7-ene-14,5'-furan]-2',12-dione 162923033 Click to see CCC1C2(C=CCCN3C24C(C15C=C(C(=O)O5)C)(CC3C6CC(C(=O)O6)C)OC(=O)N4)OC 458.50 unknown https://doi.org/10.1016/J.TET.2010.11.013
(1S,3S,10R,11R,14R,15R)-10-ethyl-1-hydroxy-14-methyl-3-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.04,16.011,15]hexadec-9(16)-en-13-one 162910682 Click to see CCC1C2C(C(C(=O)O2)C)C3(CC(N4C3=C1CCCC4)C5CC(C(=O)O5)C)O 389.50 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
(1S,7R,9R,10R,11R,14R,15R,19S)-15-ethyl-9-hydroxy-11-methyl-7-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]-13,16-dioxa-6,18-diazapentacyclo[7.6.4.01,19.06,19.010,14]nonadecane-12,17-dione 162959675 Click to see 448.50 unknown https://doi.org/10.1016/J.TET.2010.11.013
10-Ethyl-1-hydroxy-14-methyl-3-(4-methyl-5-oxooxolan-2-yl)-12-oxa-4-azatetracyclo[7.6.1.04,16.011,15]hexadec-9(16)-en-13-one 162910681 Click to see 389.50 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
15-Ethyl-9-hydroxy-11-methyl-7-(4-methyl-5-oxooxolan-2-yl)-13,16-dioxa-6,18-diazapentacyclo[7.6.4.01,19.06,19.010,14]nonadecane-12,17-dione 162959674 Click to see CCC1C2C(C(C(=O)O2)C)C3(CC(N4C35C1(CCCC4)OC(=O)N5)C6CC(C(=O)O6)C)O 448.50 unknown https://doi.org/10.1016/J.TET.2010.11.013
15-Ethyl-9-methoxy-3'-methyl-3-(4-methyl-5-oxooxolan-2-yl)spiro[13-oxa-4,11-diazatetracyclo[7.4.2.01,10.04,10]pentadec-7-ene-14,5'-furan]-2',12-dione 162923032 Click to see CCC1C2(C=CCCN3C24C(C15C=C(C(=O)O5)C)(CC3C6CC(C(=O)O6)C)OC(=O)N4)OC 458.50 unknown https://doi.org/10.1016/J.TET.2010.11.013
7-Ethyl-3-methyl-19-(4-methyl-5-oxooxolan-2-yl)-5,17-dioxa-13,15-diazapentacyclo[11.4.2.01,14.02,6.08,14]nonadecane-4,16-dione 162932033 Click to see CCC1C2CCCCN3C24C(CC3C5CC(C(=O)O5)C)(C6C1OC(=O)C6C)OC(=O)N4 432.50 unknown https://doi.org/10.1016/J.TET.2010.11.013
7-Ethyl-8-hydroxy-3-methyl-19-(4-methyl-5-oxooxolan-2-yl)-5,17-dioxa-13,15-diazapentacyclo[11.4.2.01,14.02,6.08,14]nonadecane-4,16-dione 162874332 Click to see 448.50 unknown https://doi.org/10.1016/J.TET.2010.11.013
8-Ethyl-11-methyl-2-(4-methyl-5-oxooxolan-2-yl)dodecahydroazepino(3,2,1-hi)furo(3,2-e)indol-10(2H)-one 435242 Click to see 375.50 unknown https://doi.org/10.1139/V62-073
https://doi.org/10.1002/HLCA.200790037
https://doi.org/10.1002/CBER.19360690113
Neotuberostemonol 12067194 Click to see 389.50 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
Stemoninine 15983991 Click to see 389.50 unknown https://doi.org/10.1021/NP50056A002
Tuberostemonine 100781 Click to see CCC1C2CCCCN3C2C(CC3C4CC(C(=O)O4)C)C5C1OC(=O)C5C 375.50 unknown https://doi.org/10.1002/CBER.19360690113
> Alkaloids and derivatives / Stemona alkaloids / Stenine-type alkaloids
(1R,9R,10R,11S,14R,15S,16R)-10-ethyl-14-methyl-12-oxa-4-azatetracyclo[7.6.1.04,16.011,15]hexadecan-13-one 72707199 Click to see 277.40 unknown https://doi.org/10.1002/HLCA.200790037
(9R,10R,11S,14S,15S,16R)-10-ethyl-14-methyl-12-oxa-4-azatetracyclo[7.6.1.04,16.011,15]hexadecan-13-one 5321498 Click to see 277.40 unknown https://doi.org/10.1002/CHIN.200405171
10-Ethyl-14-methyl-12-oxa-4-azatetracyclo[7.6.1.04,16.011,15]hexadecan-13-one 14729185 Click to see CCC1C2CCCCN3C2C(CC3)C4C1OC(=O)C4C 277.40 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
https://doi.org/10.1002/HLCA.200790037
10-Ethyl-14-methyl-12-oxa-4-azatetracyclo[7.6.1.04,16.011,15]hexadecane-3,13-dione 76401278 Click to see 291.40 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
NCGC00384783-01_C17H25NO3_Azepino[3,2,1-hi]furo[3,2-e]indole-2,10-dione, 8-ethyldodecahydro-11-methyl-, (7aR,8R,8aS,11S,11aS,11bR,11cR)- 56776320 Click to see CCC1C2CCCCN3C2C(CC3=O)C4C1OC(=O)C4C 291.40 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
Stenine 177761 Click to see 277.40 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
> Alkaloids and derivatives / Stemona alkaloids / Tuberostemospironine-type alkaloids / Croomine-type alkaloids
(2S,3'R,9S,10S,13S)-3',5-dimethyl-13-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]spiro[3-oxa-1-azatricyclo[8.3.0.02,6]tridec-5-ene-9,5'-oxolane]-2',4-dione 102577920 Click to see 389.40 unknown https://doi.org/10.1016/J.TETLET.2008.10.042
3',5-Dimethyl-13-(4-methyl-5-oxooxolan-2-yl)spiro[3-oxa-1-azatricyclo[8.3.0.02,6]tridec-5-ene-9,5'-oxolane]-2',4-dione 162888489 Click to see 389.40 unknown https://doi.org/10.1016/J.TETLET.2008.10.042
> Organoheterocyclic compounds / Azaspirodecane derivatives
3'-Methyl-3-(4-methyl-5-oxooxolan-2-yl)spiro[1,2,3,6,7,8a-hexahydroindolizine-8,5'-oxolane]-2',5-dione 78106528 Click to see 321.40 unknown https://doi.org/10.1016/J.TETLET.2008.10.042
Sessilifoliamide J 71546094 Click to see 321.40 unknown https://doi.org/10.1016/J.TETLET.2008.10.042
> Organoheterocyclic compounds / Azepanes
(3S,11R,11aR)-3'-Methoxy-4',9-dimethyl-3beta-[[(2S,4S)-4-methyl-5-oxotetrahydrofuran]-2-yl]-2,3,5,6,7,8-hexahydrospiro[1H-cyclopenta[b]pyrrolo[1,2-a]azepine-11(10H),2'(5'H)-furan]-5',10-dione 53463051 Click to see 415.50 unknown https://doi.org/10.1016/0031-9422(94)00655-D
Protostemotinine 53343513 Click to see 415.50 unknown https://doi.org/10.1016/0031-9422(95)00205-L
https://doi.org/10.1016/0031-9422(94)00655-D
> Organoheterocyclic compounds / Indoles and derivatives
(1S,3S,10R,11S,12S,13S)-10-ethyl-11-hydroxy-13-methyl-3-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-15-oxa-4-azatetracyclo[7.6.1.01,12.04,16]hexadec-9(16)-en-14-one 101593022 Click to see 389.50 unknown https://doi.org/10.1139/V62-073
10-Ethyl-11-hydroxy-13-methyl-3-(4-methyl-5-oxooxolan-2-yl)-15-oxa-4-azatetracyclo[7.6.1.01,12.04,16]hexadec-9(16)-en-14-one 12313844 Click to see 389.50 unknown https://doi.org/10.1139/V62-073
11-Ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.01,5.02,16.06,10]heptadecan-8-one 124222278 Click to see 389.50 unknown https://doi.org/10.1002/HLCA.200790037
Sessilifoline A 91885238 Click to see 389.50 unknown https://doi.org/10.1002/HLCA.200790037
> Organoheterocyclic compounds / Lactams / Caprolactams
(1R,2S,3S,6R,10S)-2-ethyl-6-methyl-10-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-4-oxa-11-azatricyclo[9.4.1.03,7]hexadecane-5,8,16-trione 5322170 Click to see CCC1C2CCCCN(C2=O)C(CC(=O)C3C1OC(=O)C3C)C4CC(C(=O)O4)C 405.50 unknown https://doi.org/10.1002/CHIN.200405171
(1R,2S,3S,6S,7R,10S)-2-ethyl-1-hydroxy-6-methyl-10-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-4-oxa-11-azatricyclo[9.4.1.03,7]hexadecane-5,8,16-trione 163072405 Click to see CCC1C2C(C(C(=O)O2)C)C(=O)CC(N3CCCCC1(C3=O)O)C4CC(C(=O)O4)C 421.50 unknown https://doi.org/10.1016/J.TET.2006.11.020
(1S,2S,3S,6S,7S,8R,10S)-2-ethyl-8-hydroxy-6-methyl-10-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-4-oxa-11-azatetracyclo[9.4.1.01,8.03,7]hexadecane-5,16-dione 102326284 Click to see CCC1C2C(C(C(=O)O2)C)C3(C14CCCCN(C4=O)C(C3)C5CC(C(=O)O5)C)O 405.50 unknown https://doi.org/10.3987/COM-07-11051
2-Ethyl-1-hydroxy-6-methyl-10-(4-methyl-5-oxooxolan-2-yl)-4-oxa-11-azatricyclo[9.4.1.03,7]hexadecane-5,8,16-trione 163072403 Click to see 421.50 unknown https://doi.org/10.1016/J.TET.2006.11.020
2-Ethyl-8-hydroxy-6-methyl-10-(4-methyl-5-oxooxolan-2-yl)-4-oxa-11-azatetracyclo[9.4.1.01,8.03,7]hexadecane-5,16-dione 496219 Click to see 405.50 unknown https://doi.org/10.3987/COM-07-11051
Neotuberostemone 78385648 Click to see 405.50 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
Tuberostemonone 6426912 Click to see CCC1C2CCCCN(C2=O)C(CC(=O)C3C1OC(=O)C3C)C4CC(C(=O)O4)C 405.50 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,2S,3S,6R,7S,14S)-7-ethyl-1-hydroxy-3-methyl-14-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-5-oxa-13-azatricyclo[11.2.1.02,6]hexadecane-4,8,16-trione 102153650 Click to see 421.50 unknown https://doi.org/10.1016/J.TET.2006.11.020
(1S,2S,3S,6R,7S,14S)-7-ethyl-3-methyl-14-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-5-oxa-13-azatricyclo[11.2.1.02,6]hexadecane-4,8,16-trione 102153649 Click to see 405.50 unknown https://doi.org/10.1016/J.TET.2006.11.020
7-Ethyl-1-hydroxy-3-methyl-14-(4-methyl-5-oxooxolan-2-yl)-5-oxa-13-azatricyclo[11.2.1.02,6]hexadecane-4,8,16-trione 162950545 Click to see 421.50 unknown https://doi.org/10.1016/J.TET.2006.11.020
7-Ethyl-3-methyl-14-(4-methyl-5-oxooxolan-2-yl)-5-oxa-13-azatricyclo[11.2.1.02,6]hexadecane-4,8,16-trione 162881985 Click to see 405.50 unknown https://doi.org/10.1016/J.TET.2006.11.020
> Organoheterocyclic compounds / Oxanes
(1S,3S,9S,10S,11R,14S,15S)-10-ethyl-9-hydroxy-14-methyl-3-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-12,16-dioxa-4-azatetracyclo[7.6.1.11,4.011,15]heptadecane-13,17-dione 102153651 Click to see CCC1C2C(C(C(=O)O2)C)C34CC(N(C3=O)CCCCC1(O4)O)C5CC(C(=O)O5)C 421.50 unknown https://doi.org/10.1016/J.TET.2006.11.020
10-Ethyl-9-hydroxy-14-methyl-3-(4-methyl-5-oxooxolan-2-yl)-12,16-dioxa-4-azatetracyclo[7.6.1.11,4.011,15]heptadecane-13,17-dione 162983417 Click to see CCC1C2C(C(C(=O)O2)C)C34CC(N(C3=O)CCCCC1(O4)O)C5CC(C(=O)O5)C 421.50 unknown https://doi.org/10.1016/J.TET.2006.11.020
> Organoheterocyclic compounds / Pyrroloazepines
(9R,9aS)-9-[(1S)-1-[(2S,4R)-4-methyl-5-oxooxolan-2-yl]propyl]-1,2,5,6,7,8,9,9a-octahydropyrrolo[1,2-a]azepin-3-one 12116760 Click to see 293.40 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
9-[1-(4-methyl-5-oxo-2H-furan-2-yl)propyl]-1,2,5,6,7,8,9,9a-octahydropyrrolo[1,2-a]azepin-3-one 85434791 Click to see CCC(C1CCCCN2C1CCC2=O)C3C=C(C(=O)O3)C 291.40 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
9-[1-(4-Methyl-5-oxooxolan-2-yl)propyl]-1,2,5,6,7,8,9,9a-octahydropyrrolo[1,2-a]azepin-3-one 163003986 Click to see 293.40 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
methyl (2R,5S)-5-[(9R,9aS)-3-oxo-1,2,5,6,7,8,9,9a-octahydropyrrolo[1,2-a]azepin-9-yl]-2-methyl-4-oxoheptanoate 12116762 Click to see CCC(C1CCCCN2C1CCC2=O)C(=O)CC(C)C(=O)OC 323.40 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
Methyl 2-methyl-4-oxo-5-(3-oxo-1,2,5,6,7,8,9,9a-octahydropyrrolo[1,2-a]azepin-9-yl)heptanoate 162879941 Click to see 323.40 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
Sessilifoliamide C 12116761 Click to see 291.40 unknown https://doi.org/10.1016/S0040-4020(03)01235-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-4-oxo-2-phenyl-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromene-8-sulfonic acid 163104403 Click to see 512.40 unknown https://doi.org/10.1002/HLCA.200790037

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.