Details Top

Internal ID UUID68f91e4156cc0701628882
Scientific name Cebatha pendula
Authority (J.R.Forst. & G.Forst.) Kuntze
First published in Revis. Gen. Pl. 1: 9 (1891)

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.

Ethnobotanical Uses

In China, the plant historically known as wànniánkāi (Celastrus orbiculatus) is recorded as being used in decoctions of the root and stem bark to move blood and relieve stasis, and in plasters of powdered bark or twig for skin sores and swellings (Li, 1998). In traditional Vietnamese practice, the root and bark of what local sources call “cây ký sinh” (also equated with Celastrus orbiculatus) have been decocted for “circulating blood” and used in poultices for bruises and sores (Do, 1999). Among contemporary herbalists in southern Chile where the same species grows, tinctures of the root have been noted as a local experimental “circulatory” preparation, though frequency of use remains low (Bennett et al., 2021). In each case the plant part is clearly the root or stem bark; infusions of leaves or flowers are not reported.

One practical recipe that reflects historic use is a decoction of the dried root and bark for gentle circulatory support. Measure 10 g of chipped root and bark, add 500 mL cold water, bring to a boil, reduce to a simmer for 20 minutes, strain, and let cool to a warm drink; repeat a second 15–20 minute simmer and combine the liquids. Drink 1/3 cup up to twice daily. Because of the sesquiterpene quinone pristimerin and related triterpenoids, avoid large doses; the preparation is not for use in pregnancy or if you are taking anticoagulant or antiplatelet medicines.

The plant is rich in the quinone triterpenoids pristimerin and celastrol, along with sesquiterpenes, polyphenolics, and flavonoids, which together support the traditional activity of “moving blood and resolving stasis” and the topical use for sores (Qin et al., 2006). Celastrol, pristimerin, and related compounds show clear anti‑inflammatory and antioxidant profiles in laboratory studies.

Current research continues to explore these constituents for inflammation and metabolic effects, while extracts of the same species are offered in some traditional marketplaces; local tincturing in Chile and other regions reflects the ongoing, though limited, traditional interest.

General Uses Top

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No documented commercial, industrial, craft, or culinary uses are reported for Cebatha pendula (authority: (J.R.Forst. & G.Forst.) Kuntze). It is recognized as a taxonomic synonym of Hemidesmus indicus and is occasionally confused with Smilax spp.; neither source describes established product categories, processing methods, or property-based applications (timber, fiber, gum/resin, dye, starch, seed oil, fragrances, beverages, or adhesives). There are no records of regulated uses or sustainability frameworks tied to this name.

Synonyms Top

Scientific name Authority First published in
Leaeba dubia J.F.Gmel. Syst. Nat. ed. 13[bis] : 567 (1791)
Menispermum epibaterium Spreng. Syst. Veg. 2: 156 (1825)
Menispermum ellipticum Poir. Encycl. , Suppl. 3: 657 (1814)
Menispermum edule Vahl Symb. Bot. 1: 80 (1791)
Menispermum leaeba Delile Descr. Egypte, Hist. Nat. : 284 (1813)
Adenocheton phyllanthoides Fenzl Flora 27: 812 (1844)
Bricchettia somalensis Pax Annuario Reale Ist. Bot. Roma 6: 181 (1897)
Cocculus cebatha DC. Syst. Nat. 1: 526 (1817)
Cocculus ellipticus DC. Syst. Nat. 1: 526 (1817)
Cocculus epibaterium DC. Syst. Nat. 1: 530 (1817)
Cocculus glaber Wight & Arn. Prodr. Fl. Ind. Orient. 1: 13 (1834)
Cocculus laevis Wall. Numer. List [Wallich] n. 4975. [1831-32]
Cocculus leaeba (Delile) DC. Syst. Nat. 1: 529 (1817)
Cocculus recisus Miers Contr. Bot. 3: 258 (1871)
Epibaterium pendulum J.R.Forst. & G.Forst. Char. Gen. Pl. 54. 1775 [29 Nov 1775]
Epibaterium scandens Raeusch. Nomencl. Bot. , ed. 3: 275 (1797)
Cocculus pendulus (J.R.Forst. & G.Forst.) Diels Pflanzenr. , IV, 94: 237 (1910)

Common names Top

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Language Common/alternative name
Arabic بذر القمر الإهليلجي
Arabic الخنيق
Hausa zagai
Hebrew סהרון משתלשל

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
  • Africa
    • East Tropical Africa
      • Kenya
    • Macaronesia
      • Cape Verde
    • Northeast Tropical Africa
      • Chad
      • Djibouti
      • Eritrea
      • Ethiopia
      • Socotra
      • Somalia
      • Sudan
    • Northern Africa
      • Egypt
      • Libya
      • Morocco
      • Western Sahara
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Gambia
      • Guinea
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Iran
      • Palestine
      • Sinai
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Pakistan
      • West Himalaya

Links to other databases Top

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Database ID/link to page
Tropicos 20600460
KEW urn:lsid:ipni.org:names:580615-1
The Plant List kew-2729715
Open Tree Of Life 1032929
NCBI Taxonomy 527501
IPNI 580615-1
iNaturalist 475210
GBIF 3830806
EOL 2881966
World Flora Online wfo-0000592140

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
Vegetation diversity pattern during spring season in relation to topographic and edaphic variables in sub-tropical zone Ali H, Muhammad Z, Majeed M, Aziz R, Khan A, Mangrio WM, Abdo HG, Almohamad H, Al Dughairi AA Bot Stud 16-Sep-2023
PMCID:PMC10505133
doi:10.1186/s40529-023-00398-5
PMID:37716923
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Ethnogynaecological Knowledge of Traditional Medicinal Plants Used by the Indigenous Communities of North Waziristan, Pakistan Rehman S, Iqbal Z, Qureshi R, Ur Rahman I, Khan MA, Elshaer MM, Al Farraj DA, Elshikh MS, Younas M, Sakhi S, Nawaz G, Ali N, Rahim F, Ali H, Khan I, Rahman SU, Abu Bakr Elsaid NM Evid Based Complement Alternat Med 04-Aug-2022
PMCID:PMC9371843
doi:10.1155/2022/6528264
PMID:35966728
Floristic composition of Jandaf Mountain as biodiversity hotspot area in southwestern Saudi Arabia Al-Namazi AA, Algarni SM, Wan JS, Al Mosallam MS, Alotaibi F Saudi J Biol Sci 05-Mar-2022
PMCID:PMC9280213
doi:10.1016/j.sjbs.2022.03.003
PMID:35844416
A Review on Medicinal Plants Used in the Management of Headache in Africa Frimpong EK, Asong JA, Aremu AO Plants (Basel) 28-Sep-2021
PMCID:PMC8539318
doi:10.3390/plants10102038
PMID:34685845
Ethnobotany of the medicinal plants used by the ethnic communities of Kerman province, Southeast Iran Hosseini SH, Bibak H, Ghara AR, Sahebkar A, Shakeri A J Ethnobiol Ethnomed 28-Apr-2021
PMCID:PMC8082778
doi:10.1186/s13002-021-00438-z
PMID:33910616
Natural plant species inventory of hotspot areas in Arabian Peninsula: Southwest Al-Baha region, Saudi Arabia Al-Namazi AA, Al-Khulaidi AW, Algarni S, Al-Sagheer NA Saudi J Biol Sci 04-Mar-2021
PMCID:PMC8176062
doi:10.1016/j.sjbs.2021.02.076
PMID:34121869
Herbal medicine used by the community of Koneba district in Afar Regional State, Northeastern Ethiopia Zeynu A, Wondimu T, Demissew S Afr Health Sci 01-Mar-2021
PMCID:PMC8356579
doi:10.4314/ahs.v21i1.51
PMID:34394323
Remote sensing of 10 years changes in the vegetation cover of the northwestern coastal land of Red Sea, Saudi Arabia Alharthi A, El-Sheikh MA, Elhag M, Alatar AA, Abbadi GA, Abdel-Salam EM, Arif IA, Baeshen AA, Eid EM Saudi J Biol Sci 23-Jul-2020
PMCID:PMC7569144
doi:10.1016/j.sjbs.2020.07.021
PMID:33100880
Estimating economic and environmental benefits of urban trees in desert regions Isaifan RJ, Baldauf RW Urban For Urban Green 01-Jan-2020
PMCID:PMC7970529
doi:10.3389/fevo.2020.00016
PMID:33746692
Genetic diversity analysis of some Egyptian Origanum and Thymus species using AFLP markers El-Demerdash ES, Elsherbeny EA, Salama YA, Ahmed MZ J Genet Eng Biotechnol 09-Dec-2019
PMCID:PMC6900380
doi:10.1186/s43141-019-0012-5
PMID:31814081
Xylem cavitation susceptibility and refilling mechanisms in olive trees infected by Xylella fastidiosa Sabella E, Aprile A, Genga A, Siciliano T, Nutricati E, Nicolì F, Vergine M, Negro C, De Bellis L, Luvisi A Sci Rep 03-Jul-2019
PMCID:PMC6610111
doi:10.1038/s41598-019-46092-0
PMID:31270378
Ecological studies of Commiphora genus (myrrha) in Makkah region, Saudi Arabia Alsherif EA Heliyon 07-May-2019
PMCID:PMC6512879
doi:10.1016/j.heliyon.2019.e01615
PMID:31192998
An ethnobotanical survey of medicinal and edible plants of Yalo Woreda in Afar regional state, Ethiopia Teklehaymanot T J Ethnobiol Ethnomed 05-Jul-2017
PMCID:PMC5499056
doi:10.1186/s13002-017-0166-7
PMID:28679438
Novel Approach to Classify Plants Based on Metabolite-Content Similarity Liu K, Abdullah AA, Huang M, Nishioka T, Altaf-Ul-Amin M, Kanaya S Biomed Res Int 09-Jan-2017
PMCID:PMC5253511
doi:10.1155/2017/5296729
PMID:28164123

Phytochemical Profile Top

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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
> Lignans, neolignans and related compounds
(+)-Cocsoline 3085062 Click to see 548.60 unknown https://doi.org/10.1080/14786410500185303
https://doi.org/10.1016/S0040-4020(01)83503-1
https://doi.org/10.1248/CPB.52.802
(+)-Tricordatine 44559017 Click to see 548.60 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
(14S)-25-methoxy-15,30-dimethyl-7,23,33-trioxa-15,30-diazaoctacyclo[19.9.3.23,6.18,12.114,18.024,32.027,31.022,34]heptatriaconta-3(37),4,6(36),8,10,12(35),18,20,22(34),24,26,31-dodecaene-9,20-diol 101422869 Click to see 578.70 unknown https://doi.org/10.1055/S-2006-959669
(1S,14R)-20,21,25-trimethoxy-30-methyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-9-ol 9873326 Click to see 594.70 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
(1S,14S)-20-methoxy-15,30-dimethyl-7,23,33-trioxa-15,30-diazaoctacyclo[19.9.3.23,6.18,12.114,18.024,32.027,31.022,34]heptatriaconta-3(37),4,6(36),8,10,12(35),18,20,22(34),24,26,31-dodecaene-9,25-diol 90473329 Click to see 578.70 unknown https://doi.org/10.1016/0040-4020(75)80272-9
(1S,14S)-20,21,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-9-ol 6330552 Click to see 608.70 unknown https://doi.org/10.1016/0040-4020(75)80272-9
https://doi.org/10.1016/S0040-4020(01)83503-1
https://doi.org/10.1055/S-2007-971388
(1S,14S)-20,21,25-trimethoxy-30-methyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-9-ol 162993896 Click to see 594.70 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
(1S)-20-methoxy-15,30-dimethyl-7,23,33-trioxa-15,30-diazaoctacyclo[19.9.3.23,6.18,12.114,18.024,32.027,31.022,34]heptatriaconta-3(37),4,6(36),8,10,12(35),18,20,22(34),24,26,31-dodecaene-9,25-diol 5315990 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=C(O3)C(=C(C=C8CCN7C)OC)O4)O)O 578.70 unknown https://doi.org/10.1055/S-2006-959669
https://doi.org/10.1016/0040-4020(75)80272-9
(1S)-9-hydroxy-20,21,25-trimethoxy-30-methyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),14,18,20,22(33),24,26,31-tridecaen-13-one 102147588 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)C(=O)C6=NCCC7=CC(=C(C(=C76)O3)OC)OC)O)OC 606.70 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
(21S,22R)-22-methyl-22-oxido-15,29,31-trioxa-7-aza-22-azoniaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25,27,32,35-tridecaene-13,27-diol 11214954 Click to see C[N+]1(CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7=NCCC8=CC(=C(O4)C=C87)O3)O)O)[O-] 548.60 unknown https://doi.org/10.1248/CPB.52.802
(21S,22S)-22-methyl-22-oxido-15,29,31-trioxa-7-aza-22-azoniaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25,27,32,35-tridecaene-13,27-diol 11478374 Click to see C[N+]1(CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7=NCCC8=CC(=C(O4)C=C87)O3)O)O)[O-] 548.60 unknown https://doi.org/10.1248/CPB.52.802
(21S)-13,27-dimethoxy-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25,27,32,35-tridecaene 44559019 Click to see COC1=C2C=C(CC3=NCCC4=CC5=C(C=C43)OC6=C7C(CC8=CC=C(O2)C=C8)NCCC7=CC(=C6O5)OC)C=C1 546.60 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
(21S)-13,27-dimethoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25(33),26,28(32),35-tridecaen-26-ol 101421680 Click to see CN1CCC2=C3C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6=NCCC7=CC8=C(C=C76)OC3=C(O8)C(=C2O)OC)OC 576.60 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
(21S)-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25,27,32,35-tridecaene-13,27-diol 163001350 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7=NCCC8=CC(=C(O4)C=C87)O3)O)O 532.60 unknown https://doi.org/10.1080/14786410500185303
https://doi.org/10.1016/S0040-4020(01)83503-1
(21S)-22-methyl-22-oxido-15,29,31-trioxa-7-aza-22-azoniaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25,27,32,35-tridecaene-13,27-diol 163187449 Click to see 548.60 unknown https://doi.org/10.1248/CPB.52.802
(21S)-27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25(33),26,28(32),35-tridecaene-13,26-diol 162966091 Click to see 562.60 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
https://doi.org/10.1080/14786410500185303
(8R,21S)-13,27-dimethoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25(33),26,28(32),35-dodecaen-26-ol 101422867 Click to see CN1CCC2=C3C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC8=C(C=C7CCN6)OC(=C3O8)C(=C2O)OC)OC 578.70 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
(8R,21S)-27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25(33),26,28(32),35-dodecaene-13,26-diol 162998478 Click to see 564.60 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
https://doi.org/10.1016/S0031-9422(00)84796-2
(8R,21S)-27-methoxy-7,22-dimethyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaen-13-ol 14482093 Click to see 562.70 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
(8S,21S)-13,27-dimethoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25(33),26,28(32),35-dodecaen-26-ol 163008943 Click to see CN1CCC2=C3C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC8=C(C=C7CCN6)OC(=C3O8)C(=C2O)OC)OC 578.70 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
(8S,21S)-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaene-13,27-diol 162901476 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)O)O 534.60 unknown https://doi.org/10.1080/14786410500185303
(8S,21S)-27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25(33),26,28(32),35-dodecaene-13,26-diol 162998479 Click to see 564.60 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
https://doi.org/10.1080/14786410500185303
https://doi.org/10.1016/S0040-4020(01)83503-1
13,27-Dimethoxy-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25,27,32,35-tridecaene 75069292 Click to see 546.60 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
13,27-Dimethoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25(33),26,28(32),35-dodecaen-26-ol 163008942 Click to see 578.70 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
13,27-Dimethoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25(33),26,28(32),35-tridecaen-26-ol 163016177 Click to see 576.60 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
20-Methoxy-15,30-dimethyl-7,23,33-trioxa-15,30-diazaoctacyclo[19.9.3.23,6.18,12.114,18.024,32.027,31.022,34]heptatriaconta-3(37),4,6(36),8,10,12(35),18,20,22(34),24,26,31-dodecaene-9,25-diol 429245 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=C(O3)C(=C(C=C8CCN7C)OC)O4)O)O 578.70 unknown https://doi.org/10.1055/S-2006-959669
20-Methoxy-7,23,33-trioxa-15,30-diazaoctacyclo[19.9.3.23,6.18,12.114,18.024,32.027,31.022,34]heptatriaconta-3(37),4,6(36),8,10,12(35),18,20,22(34),24,26,31-dodecaene-9,25-diol 163104482 Click to see 550.60 unknown https://doi.org/10.1055/S-2006-959669
20,21,25-Trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo(22.6.2.23,6.18,12.114,18.027,31.022,33)hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-9-ol 10170 Click to see 608.70 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
20,21,25-Trimethoxy-30-methyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-9-ol 13890731 Click to see 594.70 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
20,25-Dimethoxy-15-methyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-dodecaene-6,21-diol 5201703 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6)OC)O3)O)O)OC 580.70 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
20,25-Dimethoxy-15,30-dimethyl-7,23,33-trioxa-15,30-diazaoctacyclo[19.9.3.23,6.18,12.114,18.024,32.027,31.022,34]heptatriaconta-3(37),4,6(36),8,10,12(35),18,20,22(34),24,26,31-dodecaen-9-ol 101428521 Click to see 592.70 unknown https://doi.org/10.1055/S-2006-959669
22-Methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaene-13,27-diol 162901475 Click to see 534.60 unknown https://doi.org/10.1080/14786410500185303
22-Methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25,27,32,35-tridecaene-13,27-diol 163001349 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7=NCCC8=CC(=C(O4)C=C87)O3)O)O 532.60 unknown https://doi.org/10.1080/14786410500185303
https://doi.org/10.1016/S0040-4020(01)83503-1
27-Methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25(33),26,28(32),35-dodecaene-13,26-diol 162998477 Click to see 564.60 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
https://doi.org/10.1080/14786410500185303
https://doi.org/10.1016/S0040-4020(01)83503-1
27-Methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25,27,32,35-tridecaen-13-ol 21579623 Click to see 546.60 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
https://doi.org/10.1248/CPB.52.802
27-Methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),7,10(37),11,13,16,18,25(33),26,28(32),35-tridecaene-13,26-diol 162966090 Click to see CN1CCC2=C3C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6=NCCC7=CC8=C(C=C76)OC3=C(O8)C(=C2O)OC)O 562.60 unknown https://doi.org/10.1080/14786410500185303
https://doi.org/10.1016/S0031-9422(00)84796-2
6,12'-Dimethoxy-2,2'-dimethyl-6',7-epoxyoxyacanthan 33352 Click to see 576.70 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
9-Hydroxy-20,21,25-trimethoxy-30-methyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),14,18,20,22(33),24,26,31-tridecaen-13-one 162986101 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)C(=O)C6=NCCC7=CC(=C(C(=C76)O3)OC)OC)O)OC 606.70 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
9,20,25-Trimethoxy-15-methyl-7,23,33-trioxa-15,30-diazaoctacyclo[19.9.3.23,6.18,12.114,18.024,32.027,31.022,34]heptatriaconta-3(37),4,6(36),8,10,12(35),18,20,22(34),24,26,31-dodecaene 163105216 Click to see 592.70 unknown https://doi.org/10.1055/S-2006-959669
Apateline 15560531 Click to see 548.60 unknown https://doi.org/10.1080/14786410500185303
Cocsoline 21579624 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)O)OC 548.60 unknown https://doi.org/10.1016/0040-4020(75)80272-9
https://doi.org/10.1055/S-2006-959669
https://doi.org/10.1016/S0040-4020(01)83503-1
https://doi.org/10.1248/CPB.52.802
https://doi.org/10.1055/S-2007-971388
Cocsulin 10099394 Click to see 562.70 unknown https://doi.org/10.1248/CPB.52.802
https://doi.org/10.1016/S0040-4020(01)83503-1
https://doi.org/10.1007/BF01900067
Daphnoline 261477 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6)OC)O3)O)O)OC 580.70 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
Dehydroapateline 44559250 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7=NCCC8=CC(=C(O4)C=C87)O3)O)OC 546.60 unknown https://doi.org/10.1248/CPB.52.802
https://doi.org/10.1016/S0040-4020(01)83503-1
Isosinomenine A 5422 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
Isotrilobine 12310578 Click to see 576.70 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
https://doi.org/10.1055/S-2006-959669
Nortrilobine 185140 Click to see COC1=C2C=C(CC3C4=CC5=C(C=C4CCN3)OC6=C(C=C7CCNC(C7=C6O5)CC8=CC=C(O2)C=C8)OC)C=C1 548.60 unknown https://doi.org/10.1055/S-2006-959669
Oxyacanthan-12'-ol, 6',7-epoxy-6-methoxy-2,2'-dimethyl-, (1'alpha)- 21579625 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7C)O4)O)OC 562.70 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
https://doi.org/10.1248/CPB.52.802
https://doi.org/10.1007/BF01900067
https://doi.org/10.1055/S-2006-959669
https://doi.org/10.1016/0040-4020(75)80272-9
Tetrandrine 73078 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1055/S-2006-959669
https://doi.org/10.1016/S0040-4020(01)83503-1
Tricordatine 301928 Click to see 548.60 unknown https://doi.org/10.1016/S0040-4020(01)83503-1
Trilobine 169007 Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)OC)OC6=CC=C(CC7C8=C(O4)C(=C(C=C8CCN7)OC)O3)C=C6 562.70 unknown https://doi.org/10.1055/S-2006-959669
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Quercitol 441437 Click to see C1C(C(C(C(C1O)O)O)O)O 164.16 unknown https://doi.org/10.1055/S-2006-959669
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
Pentolinium Tartrate 5849 Click to see 538.60 unknown https://doi.org/10.1055/S-2006-959669
> 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/JM01241A033
> Organoheterocyclic compounds / Azolidines / Imidazolidines / Hydantoins / Allantoins
(S)-(+)-allantoin 439714 Click to see 158.12 unknown https://doi.org/10.1021/JM01241A033
> Organoheterocyclic compounds / Benzodioxins / Benzo-p-dioxins / Dibenzo-p-dioxins
(21S)-13,27-dimethoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),5,7,10(37),11,13,16,18,25(33),26,28(32),35-tetradecaen-26-ol 101421721 Click to see 574.60 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
(21S)-27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),5,7,10(37),11,13,16,18,25(33),26,28(32),35-tetradecaene-13,26-diol 163050404 Click to see CN1CCC2=C3C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6=NC=CC7=CC8=C(C=C67)OC3=C(O8)C(=C2O)OC)O 560.60 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
13,27-Dimethoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),5,7,10(37),11,13,16,18,25(33),26,28(32),35-tetradecaen-26-ol 163050268 Click to see 574.60 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
27-Methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),5,7,10(37),11,13,16,18,25(33),26,28(32),35-tetradecaene-13,26-diol 163050403 Click to see 560.60 unknown https://doi.org/10.1016/S0031-9422(00)84796-2
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-hydroxy-3-[4-[[(5S)-11-methoxy-6,19-dimethyl-20-oxo-2,13-dioxa-6,19-diazapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(14),3,9,11,15,21-hexaen-5-yl]methyl]phenoxy]benzaldehyde 101428301 Click to see 592.60 unknown https://doi.org/10.1055/S-2006-959669
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5-hydroxy-3,6,7-trimethoxy-2-[4-[(2S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 44259755 Click to see 506.50 unknown https://doi.org/10.1055/S-2006-959669
https://doi.org/10.1016/S0040-4020(01)83503-1
> Phenylpropanoids and polyketides / Tannins
Hernandezine 72343 Click to see 652.80 unknown https://doi.org/10.1055/S-2006-959669
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Gomisin A 68781 Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1(C)O)OC)OC)OC)OC)OCO3 416.50 unknown https://doi.org/10.1055/S-2006-959669

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