PlantaeDB Logo
Login Sign-up

Strychnos potatorum

Strychnos potatorum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644004ea4e426067199298
Scientific name Strychnos potatorum
Authority L.f.
First published in Suppl. Pl. : 148 (1782)

Description Top

Suggest a correction or write a new one!
Strychnos potatorum, also known as the clearing-nut tree, is a deciduous tree that can reach up to 40 feet in height. It is known by different names in various languages, such as chillaginj in Telugu, kataka in Kannada, and thethankottai in Tamil. The tree's seeds are widely used in traditional medicine and for water purification in India and Myanmar.

Synonyms Top

Scientific name Authority First published in
Strychnos monosperma Stokes Bot. Mat. Med. 1: 415 (1812)
Strychnos tetankotta Retz. Observ. Bot. 2: 12 (1781)
Strychnos stuhlmannii Gilg Bot. Jahrb. Syst. 17: 570 (1893)
Strychnos heterodoxa Gilg Bot. Jahrb. Syst. 28: 118 (1899)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English black bitterberry
Afrikaans swartbitterbessie
Arabic نقد
Malayalam തേറ്റാമ്പരൽ
Burmese ခပေါင်းရေကြည်
Burmese ခပေါင်းရေကြည်၊ အပင်
Burmese ခပေါင်းရေကြည်ပင်
Tamil தேற்றாங்கொட்டை
Tamil தேற்றா
Telugu ఇండుపు

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Tanzania
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Caprivi Strip
      • Northern Provinces
    • West-central Tropical Africa
      • Burundi
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Madagascar
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Sri Lanka
    • Indo-China
      • Myanmar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000502951
UNII 05Z64T1GSG
Tropicos 19000162
KEW urn:lsid:ipni.org:names:547420-1
The Plant List kew-2598232
Open Tree Of Life 729041
NCBI Taxonomy 85835
IPNI 547420-1
iNaturalist 340100
GBIF 5645740
Freebase /m/0h95jc2
USDA GRIN 35852
Wikipedia Strychnos_potatorum
CMAUP NPO26262

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
A comprehensive review of antimalarial medicinal plants used by Tanzanians Kacholi DS Pharm Biol 25-Jan-2024
PMCID:PMC10812860
doi:10.1080/13880209.2024.2305453
PMID:38270178
Microplastic Removal in Wastewater Treatment Plants (WWTPs) by Natural Coagulation: A Literature Review Reza T, Mohamad Riza ZH, Sheikh Abdullah SR, Abu Hasan H, Ismail N‘, Othman AR Toxics 22-Dec-2023
PMCID:PMC10819662
doi:10.3390/toxics12010012
PMID:38250968
A Poly-D-Mannose Synthesized by a One-Pot Method Exhibits Anti-Biofilm, Antioxidant, and Anti-Inflammatory Properties In Vitro Tian D, Qiao Y, Peng Q, Zhang Y, Gong Y, Shi L, Xiong X, He M, Xu X, Shi B Antioxidants (Basel) 08-Aug-2023
PMCID:PMC10451989
doi:10.3390/antiox12081579
PMID:37627574
A lexical review on Vishaghna Dravyas of Kaideva Nighantu Yadav S, Sharma A, Vishnoi R, Rani J Ayu 02-Aug-2023
PMCID:PMC10468017
doi:10.4103/ayu.ayu_199_22
PMID:37655171
Effect of Ayurveda water purification method on total dissolved solutes in water Pruthi Z, Kotekar AS, Saranya K Ayu 24-Jun-2023
PMCID:PMC10405888
doi:10.4103/ayu.ayu_366_20
PMID:37554414
A comparative study on polyaluminum chloride (PACl) and Moringa oleifera (MO) chemically enhanced primary treatment (CEPT) in enhanced biogas production: anaerobic digestion performance and the Gompertz model Amoohadi V, Pasalari H, Esrafili A, Gholami M, Farzadkia M RSC Adv 09-Jun-2023
PMCID:PMC10251396
doi:10.1039/d3ra02112b
PMID:37304783
HPTLC and GC–MS finger-printing of two potential multifunctional siddha tailams: Mathan and maha megarajanga tailam Senthilnathan S, Jayaraman S, Priya Veeraraghavan V, Masood Khan J, Ahmed MZ, Ahmad A, Gnanamani A Saudi J Biol Sci 01-Jun-2023
PMCID:PMC10276281
doi:10.1016/j.sjbs.2023.103700
PMID:37333677
Composite Hydrogels with Included Solid-State Nanoparticles Bearing Anticancer Chemotherapeutics Zhivkov AM, Popov TT, Hristova SH Gels 17-May-2023
PMCID:PMC10217488
doi:10.3390/gels9050421
PMID:37233012
Potential plant leaves as sustainable green coagulant for turbidity removal Khalid Salem A, Fadhile Almansoory A, Al-Baldawi IA Heliyon 15-May-2023
PMCID:PMC10213182
doi:10.1016/j.heliyon.2023.e16278
PMID:37251892
Herbal Treatment of COPD and Asthma According to Persian Medicine: a Review of Current Evidence Baniamerian R, Tahermohammadi H, Daneshfard B, Agin K, Sadr S, Kaveh S, Shakeri N, Ilkhani R Tanaffos 01-Feb-2023
PMCID:PMC11016916
PMID:38628881
Medicinal plants used for the management of respiratory diseases in Zimbabwe: Review and perspectives potential management of COVID-19 Nyagumbo E, Pote W, Shopo B, Nyirenda T, Chagonda I, Mapaya RJ, Maunganidze F, Mavengere WN, Mawere C, Mutasa I, Kademeteme E, Maroyi A, Taderera T, Bhebhe M Phys Chem Earth (2002) 21-Sep-2022
PMCID:PMC9489988
doi:10.1016/j.pce.2022.103232
PMID:36161239
Review of unique ophthalmic formulations in Vaidya Manorama: A traditional Kerala Ayurveda literature Balakrishnan P, Ajayan S, Mukkudakkattu S, Nechiyil K, Nambi N J Ayurveda Integr Med 02-Jun-2022
PMCID:PMC9168494
doi:10.1016/j.jaim.2022.100576
PMID:35661934
Seeds as Potential Sources of Phenolic Compounds and Minerals for the Indian Population Sahu PK, Cervera-Mata A, Chakradhari S, Singh Patel K, Towett EK, Quesada-Granados JJ, Martín-Ramos P, Rufián-Henares JA Molecules 17-May-2022
PMCID:PMC9144825
doi:10.3390/molecules27103184
PMID:35630662
Comparative study of six antidiabetic polyherbal formulation for its multimodal approaches in diabetes management Paul S, Majumdar M 3 Biotech 17-Apr-2022
PMCID:PMC9013732
doi:10.1007/s13205-022-03166-7
PMID:35547015
Strychnos PotatorumL. Seed Polysaccharide-Based Stimuli-Responsive Hydrogels and Their Silver Nanocomposites for the Controlled Release of Chemotherapeutics and Antimicrobial Applications Nagaraja K, Rao KM, Hemalatha D, Zo S, Han SS, Rao KS ACS Omega 06-Apr-2022
PMCID:PMC9026062
doi:10.1021/acsomega.2c00131
PMID:35474817

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 / Harmala alkaloids
(2R,3R,12bS)-3-ethyl-2-(9H-pyrido[3,4-b]indol-1-ylmethyl)-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine 163195424 Click to see CCC1CN2CCC3=C(C2CC1CC4=NC=CC5=C4NC6=CC=CC=C56)NC7=CC=CC=C37 434.60 unknown https://doi.org/10.1016/0031-9422(92)83650-N
(2S,3R,12bR)-3-ethyl-2-[[(1S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl]methyl]-1,2,3,4,6,7,7a,12,12a,12b-decahydroindolo[2,3-a]quinolizine 44559859 Click to see CCC1CN2CCC3C(C2CC1CC4C5=C(CCN4)C6=CC=CC=C6N5)NC7=CC=CC=C37 440.60 unknown https://doi.org/10.1021/NP020070E
(2S,3R,12bS)-3-ethyl-2-[[(1R)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl]methyl]-1,2,3,4,6,7,7a,12,12a,12b-decahydroindolo[2,3-a]quinolizine 44559929 Click to see CCC1CN2CCC3C(C2CC1CC4C5=C(CCN4)C6=CC=CC=C6N5)NC7=CC=CC=C37 440.60 unknown https://doi.org/10.1021/NP020070E
3-ethyl-2-(9H-pyrido[3,4-b]indol-1-ylmethyl)-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine 162976671 Click to see CCC1CN2CCC3=C(C2CC1CC4=NC=CC5=C4NC6=CC=CC=C56)NC7=CC=CC=C37 434.60 unknown https://doi.org/10.1016/0031-9422(92)83650-N
9H-Pyrido[3,4-b]indole-1-carboxamide 611121 Click to see C1=CC=C2C(=C1)C3=C(N2)C(=NC=C3)C(=O)N 211.22 unknown https://doi.org/10.1016/0031-9422(92)83650-N
Ochrolifuanine A 215338 Click to see CCC1CN2CCC3=C(C2CC1CC4C5=C(CCN4)C6=CC=CC=C6N5)NC7=CC=CC=C37 438.60 unknown https://doi.org/10.1016/0031-9422(92)83650-N
https://doi.org/10.1021/NP020070E
> Alkaloids and derivatives / Macroline alkaloids
19-(Z)-Akuammidine 138113962 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)(CO)C(=O)OC 352.40 unknown https://doi.org/10.1016/0031-9422(92)83650-N
methyl (12S,14S,15E)-15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 134716693 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)(CO)C(=O)OC 352.40 unknown https://doi.org/10.1016/0031-9422(92)83650-N
Normacusine B 5318845 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)CO 294.40 unknown https://doi.org/10.1016/0031-9422(92)83650-N
> Alkaloids and derivatives / Pleiocarpaman alkaloids
Normavacurine 11969908 Click to see CC=C1CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)CO 294.40 unknown https://doi.org/10.3987/COM-89-4987
https://doi.org/10.1016/0031-9422(92)83650-N
> Alkaloids and derivatives / Strychnos alkaloids
(17R)-1-Acetyl-19,20-didehydro-17,18-epoxycuran-17-ol 321983 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3O)C6=CC=CC=C61 352.40 unknown https://doi.org/10.1016/0031-9422(92)83650-N
(1R,11R,12R,13R,14E,19S,21S)-10-[(2S,3R,12bS)-3-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-14-ethylidene-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,9-tetraen-11-ol 163195322 Click to see CCC1CN2CCC3=C(C2CC1C4=CN5C6C(C4O)C7CC8C6(CCN8CC7=CC)C9=CC=CC=C95)NC1=CC=CC=C31 572.80 unknown https://doi.org/10.1016/0031-9422(92)83650-N
(4aR,5aS,8aR,13aR,15aS,15bR)-15-[(2S,3R,12bS)-3-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-2,4a,5,5a,7,8,13a,15a,15b,16-decahydro4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinoline 163185646 Click to see CCC1CN2CCC3=C(C2CC1C4=CN5C6C7C4OCC=C8C7CC9C6(CCN9C8)C1=CC=CC=C15)NC1=CC=CC=C31 570.80 unknown https://doi.org/10.1016/0031-9422(92)83650-N
[(12S,13R,14S,19R,21S)-11-acetyl-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5,7,9,17-tetraen-14-yl] acetate 101286227 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3OC(=O)C)C6=CC=CC=C61 394.50 unknown https://doi.org/10.1016/0031-9422(92)83650-N
1-(14-Hydroxy-8-methoxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5(10),6,8,17-tetraen-11-yl)ethanone 13994711 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3O)C6=C1C=C(C=C6)OC 382.50 unknown https://doi.org/10.1016/0031-9422(92)83650-N
1-[(12S,13R,14R,19R,21S)-14-hydroxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5,7,9,17-tetraen-11-yl]ethanone 101667973 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3O)C6=CC=CC=C61 352.40 unknown https://doi.org/10.1016/0031-9422(92)83650-N
1-[(4R,12R,13S,14S,19R,21S)-14-hydroxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5,7,9,17-tetraen-11-yl]ethanone 163059967 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3O)C6=CC=CC=C61 352.40 unknown https://doi.org/10.1016/0031-9422(92)83650-N
1-[(4R,12R,13S,14S,19R,21S)-14-hydroxy-8-methoxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5(10),6,8,17-tetraen-11-yl]ethanone 163188144 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3O)C6=C1C=C(C=C6)OC 382.50 unknown https://doi.org/10.1016/0031-9422(92)83650-N
1-[(4R,12R,13S,14S,19R,21S)-9,14-dihydroxy-8-methoxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5(10),6,8,17-tetraen-11-yl]ethanone 163002951 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3O)C6=C1C(=C(C=C6)OC)O 398.50 unknown https://doi.org/10.1016/0031-9422(92)83650-N
11-Methoxydiaboline 13994712 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3O)C6=C1C=C(C=C6)OC 382.50 unknown https://doi.org/10.1016/0031-9422(92)83650-N
15-(3-Ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl)-2,4a,5,5a,7,8,13a,15a,15b,16-decahydro4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinoline 162902327 Click to see CCC1CN2CCC3=C(C2CC1C4=CN5C6C7C4OCC=C8C7CC9C6(CCN9C8)C1=CC=CC=C15)NC1=CC=CC=C31 570.80 unknown https://doi.org/10.1016/0031-9422(92)83650-N
Condensamine 181484 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3OC(=O)C)C6=C1C=C(C=C6)OC 424.50 unknown https://doi.org/10.1016/0031-9422(92)83650-N
Henningsoline 321985 Click to see CC(=O)N1C2C3C4CC5C2(CCN5CC4=CCOC3O)C6=C1C(=C(C=C6)OC)O 398.50 unknown https://doi.org/10.1016/0031-9422(92)83650-N
Nor-C-fluorocurarine 139292102 Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C=O 292.40 unknown https://doi.org/10.1016/0031-9422(92)83650-N
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3aR,5aS,5bR,7aS,9S,11aR,11bS,13aS,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 162931122 Click to see CC(C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 444.70 unknown https://doi.org/10.1055/S-0028-1097877
(3R,3aR,5aS,7aS,9S,11aS,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,12,13,13b-tetradecahydrocyclopenta[a]chrysen-9-ol 162881680 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4=C3CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)89704-6
(3S,4aS,6aR,6aR,6bR,8aR,11R,12S,12aR,14aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,10,11,12,12a,14a-tetradecahydro-1H-picen-3-ol 163023159 Click to see CC1CCC2(CCC3(C(C2C1C)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)89704-6
(3S,4aS,6aR,6aR,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,14a-tetradecahydropicen-3-ol 154497735 Click to see CC1(CCC2(CCC3(C(C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)89704-6
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 51892422 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)89704-6
10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 619165 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1055/S-0028-1097613
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-0028-1097613
3-O-Acetyloleanolic acid 151202 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1055/S-0028-1097613
3a-(Hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 14105774 Click to see CC(C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 444.70 unknown https://doi.org/10.1055/S-0028-1097877
3a,5a,8,8,11a,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,12,13,13b-tetradecahydrocyclopenta[a]chrysen-9-ol 14167343 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4=C3CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)89704-6
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)89704-6
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-0028-1097613
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Azasteroids and derivatives
Hookerianamide K 25016412 Click to see CC(C1CC=C2C1(CCC3C2CCC4=CC(CCC34C)N(C)C)C)N(C)C 370.60 unknown https://doi.org/10.1016/0031-9422(92)83650-N
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 21-hydroxysteroids
Desoxycortone 6166 Click to see CC12CCC3C(C1CCC2C(=O)CO)CCC4=CC(=O)CCC34C 330.50 unknown https://doi.org/10.1016/0031-9422(92)83650-N
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(1S,2S,4S,5R,10R,11S,13R,14R,15R,18S)-15-[(1S)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-5,13-dihydroxy-10,14-dimethyl-3-oxapentacyclo[9.7.0.02,4.05,10.014,18]octadec-7-en-9-one 101316930 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(C(CC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)O)C)C 470.60 unknown https://doi.org/10.1016/0031-9422(92)83650-N
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1097877
(3S,8R,9R,10R,13R,14R,17R)-17-[(E,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 124762119 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1055/S-0028-1097877
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)89704-6
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1055/S-0028-1097877
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1097877
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)89704-6
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
4(1H)-Quinazolinone, 1-methyl- 18992 Click to see CN1C=NC(=O)C2=CC=CC=C21 160.17 unknown via CMAUP database
Arborine 63123 Click to see CN1C2=CC=CC=C2C(=O)N=C1CC3=CC=CC=C3 250.29 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(2R)-2-[(2S,12bS)-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]butan-1-ol 10732852 Click to see CCC(CO)C1CCN2CCC3=C(C2C1)NC4=CC=CC=C34 298.40 unknown https://doi.org/10.1016/0031-9422(92)83650-N
(2S)-2-[(2S,12bS)-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]butan-1-ol 10924514 Click to see CCC(CO)C1CCN2CCC3=C(C2C1)NC4=CC=CC=C34 298.40 unknown https://doi.org/10.1016/0031-9422(92)83650-N
18,20-Seco-E-noryohimban-16-methanol 598566 Click to see CCC(CO)C1CCN2CCC3=C(C2C1)NC4=CC=CC=C34 298.40 unknown https://doi.org/10.1016/0031-9422(92)83650-N
9H-Pyrido[3,4-B]indole 64961 Click to see C1=CC=C2C(=C1)C3=C(N2)C=NC=C3 168.19 unknown https://doi.org/10.1016/0031-9422(92)83650-N
Antirhine 5462421 Click to see C=CC(CO)C1CCN2CCC3=C(C2C1)NC4=CC=CC=C34 296.40 unknown https://doi.org/10.1016/0031-9422(92)83650-N
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Cantleyine 442515 Click to see CC1C(CC2=C(C=NC=C12)C(=O)OC)O 207.23 unknown https://doi.org/10.1016/0031-9422(92)83650-N
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
1,5-Dihydroxy-2,3-dimethoxy-10-methyl-9-acridone 14463129 Click to see CN1C2=CC(=C(C(=C2C(=O)C3=C1C(=CC=C3)O)O)OC)OC 301.29 unknown via CMAUP database
Arborinine 5281832 Click to see CN1C2=CC=CC=C2C(=O)C3=C(C(=C(C=C31)OC)OC)O 285.29 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown via CMAUP database
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database

Biological Material Top ebay Auctions

Please wait .. loading items ..

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.