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Neorautanenia mitis

Neorautanenia mitis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fd8fc07e1b747123273
Scientific name Neorautanenia mitis
Authority (A.Rich.) Verdc.
First published in B.Verdcourt & E.C.Trump, Camm. Poison. Pl. E. Afr.: 89 (1969)

Description Top

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Synonyms Top

Scientific name Authority First published in
Neorautanenia amboensis Schinz Bull. Herb. Boissier7: 35 (1899)
Neorautanenia brachypus (Harms) C.A.Sm. J.Burtt Davy, Man. Pl. Transvaal2: 418 (1932)
Neorautanenia seineri (Harms) C.A.Sm. J.Burtt Davy, Man. Pl. Transvaal2: 418 (1932)
Neorautanenia coriacea C.A.Sm. J.Burtt Davy, Man. Pl. Transvaal2: 417 (1932)
Neorautanenia edulis C.A.Sm. J.Burtt Davy, Man. Pl. Transvaal2: 418 (1932)
Neorautanenia lugardii (N.E.Br.) C.A.Sm. J.Burtt Davy, Man. Pl. Transvaal2: 417 (1932)
Neorautanenia rogersii (L.Bolus) C.A.Sm. J.Burtt Davy, Man. Pl. Transvaal2: 417 (1932)
Neorautanenia orbicularis (Welw. ex Baker) Torre Bol. Soc. Brot., sér. 2, 39: 216 (1965)
Neorautanenia pseudopachyrrhiza (Harms) Milne-Redh. Kew Bull.5: 355 (1950 publ. 1951)
Dolichos orbicularis (Welw. ex Baker) Baker f. Legum. Trop. Africa: 451 (1929)
Pueraria hochstetteri Chiov. Annuario Reale Ist. Bot. Roma8: 434 (1908 publ. 1907)
Cacara orbicularis (Welw. ex Baker) Hiern Cat. Afr. Pl.1: 261 (1896)
Dolichos ellenbeckii Harms Bot. Jahrb. Syst.33: 177 (1902)
Dolichos mitis A.Rich. Tent. Fl. Abyss.1: 224 (1847)
Pachyrhizus orbicularis Welw. ex Baker D.Oliver & auct. suc. (eds.), Fl. Trop. Afr.2: 208 (1871)
Dolichos brachypus Harms Bot. Jahrb. Syst.26: 323 (1899)
Dolichos pseudopachyrhizus Harms Bot. Jahrb. Syst.26: 320 (1899)
Dolichos seineri Harms Notizbl. Königl. Bot. Gart. Berlin5: 206 (1911)
Galactia lugardii N.E.Br. Bull. Misc. Inform. Kew1909: 104 (1909)
Pueraria rogersii L.Bolus Ann. Bolus Herb.1: 189 (1915)
Dolichos pseudopachyrhizus var. kilimandschari Harms Bot. Jahrb. Syst.26: 320 (1899)
Dolichos pseudopachyrhizus var. subintegrifolius Harms Bot. Jahrb. Syst.26: 320 (1899)
Neorautanenia pseudopachyrrhiza var. ellenbeckii (Harms) Cufod. Bull. Jard. Bot. Natl. Belg.39(Suppl.): XXV (1969)

Common names Top

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Language Common/alternative name
Chinese 柔茎豆

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Caprivi Strip
      • Namibia
      • Northern Provinces
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Ivory Coast
      • Nigeria
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Rwanda
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000182738
Tropicos 13062666
KEW urn:lsid:ipni.org:names:509555-1
The Plant List ild-2881
Open Tree Of Life 324035
NCBI Taxonomy 167620
IPNI 509555-1
iNaturalist 590560
GBIF 2971170
EPPO NRNMI
EOL 645102
USDA GRIN 436703
CMAUP NPO24293

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
Medicinal plants of the upper Aswa River catchment of northern Uganda - a cultural crossroads Masters ET J Ethnobiol Ethnomed 27-Oct-2023
PMCID:PMC10605377
doi:10.1186/s13002-023-00620-5
PMID:37884931
Role of traditional Chinese medicine monomers in cerebral ischemia/reperfusion injury:a review of the mechanism Zheng T, Jiang T, Huang Z, Ma H, Wang M Front Pharmacol 16-Aug-2023
PMCID:PMC10467294
doi:10.3389/fphar.2023.1220862
PMID:37654609
Plant Extracts as a Source of Natural Products with Potential Antimalarial Effects: An Update from 2018 to 2022 Ribeiro GD, Rei Yan SL, Palmisano G, Wrenger C Pharmaceutics 01-Jun-2023
PMCID:PMC10300920
doi:10.3390/pharmaceutics15061638
PMID:37376086
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
The Roots of Neorautanenia mitis (A. Rich) Verdcourt: Further Evidence of Its Antidiarrhoeal Activity Dawurung CJ, Usman JG, Gotep JG, Pyne SG Molecules 09-Jan-2023
PMCID:PMC9863173
doi:10.3390/molecules28020673
PMID:36677731
Integrative Alternative Tactics for Ixodid Control Showler AT, Saelao P Insects 18-Mar-2022
PMCID:PMC8948879
doi:10.3390/insects13030302
PMID:35323601
Isolation of bioactive compounds from medicinal plants used in traditional medicine: Rautandiol B, a potential lead compound against Plasmodium falciparum Dawurung CJ, Nguyen MT, Pengon J, Dokladda K, Bunyong R, Rattanajak R, Kamchonwongpaisan S, Nguyen PT, Pyne SG BMC Complement Med Ther 13-Sep-2021
PMCID:PMC8438977
doi:10.1186/s12906-021-03406-y
PMID:34517853
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465
A Review of Resistance Mechanisms of Synthetic Insecticides and Botanicals, Phytochemicals, and Essential Oils as Alternative Larvicidal Agents Against Mosquitoes Senthil-Nathan S Front Physiol 25-Feb-2020
PMCID:PMC7052130
doi:10.3389/fphys.2019.01591
PMID:32158396
Conservation and sustainable use of the medicinal Leguminosae plants from Angola Catarino S, Duarte MC, Costa E, Carrero PG, Romeiras MM PeerJ 23-May-2019
PMCID:PMC6535223
doi:10.7717/peerj.6736
PMID:31198619
Ethnobotanical knowledge of the lay people of Blouberg area (Pedi tribe), Limpopo Province, South Africa Mongalo NI, Makhafola TJ J Ethnobiol Ethnomed 13-Jul-2018
PMCID:PMC6044033
doi:10.1186/s13002-018-0245-4
PMID:30001728
Antioxidant and Larvicidal Activity of Areal Parts of Scrophularia striata against Malaria Vector Anopheles stephensi Yousefbeyk F, Vatandoost H, Golfakhrabadi F, Mirzaee Z, Abai MR, Amin G, Khanavi M J Arthropod Borne Dis 13-Jun-2018
PMCID:PMC6091803
PMID:30123805
Potential of Traditional Knowledge of Plants in the Management of Arthropods in Livestock Industry with Focus on (Acari) Ticks Wanzala W Evid Based Complement Alternat Med 17-Jul-2017
PMCID:PMC5536150
doi:10.1155/2017/8647919
PMID:28798806
Evaluation of Halogenated Coumarins for Antimosquito Properties Narayanaswamy VK, Gleiser RM, Kasumbwe K, Aldhubiab BE, Attimarad MV, Odhav B ScientificWorldJournal 25-Dec-2014
PMCID:PMC4290031
doi:10.1155/2014/189824
PMID:25610898
Use of Traditional Veterinary Medicine in Nhema Communal Area of the Midlands Province, Zimbabwe Maroyi A Afr J Tradit Complement Altern Med 02-Apr-2012
PMCID:PMC3746665
doi:10.4314/ajtcam.v9i3.3
PMID:23983361

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(1R,13R,15S)-5,7-Dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-trien-15-ol 13855654 Click to see C1CC23CCN(C2CC1O)CC4=CC5=C(C=C34)OCO5 273.33 unknown via CMAUP database
Ambelline 25092366 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown via CMAUP database
Augustine 157561 Click to see COC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C6C1O6 301.34 unknown via CMAUP database
Buphanisin 12302149 Click to see COC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 285.34 unknown via CMAUP database
Flexinine 398936 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C6C5O6)O)OCO4 287.31 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
Galantamine 9651 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown via CMAUP database
Galanthaminone 10356588 Click to see CN1CCC23C=CC(=O)CC2OC4=C(C=CC(=C34)C1)OC 285.34 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
Hippeastrine 441594 Click to see CN1CCC2=CC(C3C(C21)C4=CC5=C(C=C4C(=O)O3)OCO5)O 315.32 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown via CMAUP database
> Alkaloids and derivatives / Harmala alkaloids
5-Bromo-8-methoxy-1-methyl-beta-carboline 42638980 Click to see CC1=NC=CC2=C1NC3=C(C=CC(=C23)Br)OC 291.14 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Erioflorin acetate 5281443 Click to see CC1=CC2C(C(CC3(C(O3)CC1OC(=O)C)C)OC(=O)C(=C)C)C(=C)C(=O)O2 390.40 unknown via CMAUP database
Ovatifolin 5281492 Click to see CC1=CC2C(C(CC(=CCC1)COC(=O)C)O)C(=C)C(=O)O2 306.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Bipyridines and oligopyridines
pterocellin E 24770105 Click to see CC(C)CC1=NC=CC2=C1N3C=C(C(=O)C(=C3C2=O)C4=C5C(=O)C6=C(N5C=C(C4=O)OC)C(=NC=C6)CC(C)C)OC 566.60 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives
pterocellin C 24770104 Click to see CC(C)CC1=NC=CC2=C1N3C=C(C(=O)C(=C3C2=O)CCCCC(=O)C)OC 382.50 unknown via CMAUP database
pterocellin D 24770102 Click to see CC(C)CC1=NC=CC2=C1N3C=C(C(=O)C(=C3C2=O)C(C)C)OC 326.40 unknown via CMAUP database
pterocellin F 24770103 Click to see CC(C)CC1=NC=CC2=C1N3C=C(C(=O)C(=C3C2=O)CC4=C5C(=O)C6=C(N5C=C(C4=O)OC)C(=NC=C6)CC(C)C)OC 580.60 unknown via CMAUP database
Pyrido[4,3-b]indolizine-5,7-dione, 8-methoxy-1-(2-methylpropyl)- 9971118 Click to see CC(C)CC1=NC=CC2=C1N3C=C(C(=O)C=C3C2=O)OC 284.31 unknown via CMAUP database
Pyrido[4,3-b]indolizine-5,7-dione, 8-methoxy-1-(phenylmethyl)- 10426008 Click to see COC1=CN2C(=CC1=O)C(=O)C3=C2C(=NC=C3)CC4=CC=CC=C4 318.30 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1|A,2|A)-crinan-1,2-diol 399199 Click to see C1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C(C1O)O 289.33 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(1R,12R)-16-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-17-ol 155518405 Click to see COC1=C(C2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5)O 314.29 unknown https://doi.org/10.1021/NP058070C
(1R,12R)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-15-ol 44575281 Click to see C1C2C(C3=C(O1)C=CC(=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown https://doi.org/10.1021/NP058070C
(1R,6R,13R)-6-(2-hydroxypropan-2-yl)-7,11,20-trioxapentacyclo[11.7.0.02,10.04,8.014,19]icosa-2(10),3,8,14(19),15,17-hexaen-17-ol 162907383 Click to see CC(C)(C1CC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC(=C5)O)O 340.40 unknown https://doi.org/10.1021/NP058070C
(1S,13R)-7,11,17,19,23-pentaoxahexacyclo[11.10.0.02,10.04,8.014,22.016,20]tricosa-2(10),3,5,8,14,16(20),21-heptaene 13885695 Click to see C1C2C(C3=C(O1)C=C4C(=C3)C=CO4)OC5=CC6=C(C=C25)OCO6 308.30 unknown https://doi.org/10.1021/NP50051A002
(1S,13S)-7,11,17,19,23-pentaoxahexacyclo[11.10.0.02,10.04,8.014,22.016,20]tricosa-2(10),3,5,8,14,16(20),21-heptaene 3003960 Click to see C1C2C(C3=C(O1)C=C4C(=C3)C=CO4)OC5=CC6=C(C=C25)OCO6 308.30 unknown https://doi.org/10.1021/NP058070C
(2R,10R,18S)-17,17-dimethyl-3,12,16-trioxapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(13),4(9),5,7,14,20-hexaene-6,18-diol 163073385 Click to see CC1(C(CC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC(=C5)O)O)C 340.40 unknown https://doi.org/10.1021/NP058070C
17,17-Dimethyl-3,12,16-trioxapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(13),4(9),5,7,14,20-hexaene-6,18-diol 73050258 Click to see CC1(C(CC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC(=C5)O)O)C 340.40 unknown https://doi.org/10.1021/NP058070C
4-Hydroxypterocarpin 24042196 Click to see COC1=C(C2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5)O 314.29 unknown https://doi.org/10.1021/NP058070C
6-(2-Hydroxypropan-2-yl)-7,11,20-trioxapentacyclo[11.7.0.02,10.04,8.014,19]icosa-2(10),3,8,14(19),15,17-hexaen-17-ol 73004322 Click to see CC(C)(C1CC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC(=C5)O)O 340.40 unknown https://doi.org/10.1021/NP058070C
Neodulin 100179 Click to see C1C2C(C3=C(O1)C=C4C(=C3)C=CO4)OC5=CC6=C(C=C25)OCO6 308.30 unknown https://doi.org/10.1021/NP058070C
rautandiol A 11674519 Click to see CC1(C(CC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC(=C5)O)O)C 340.40 unknown https://doi.org/10.1021/NP058070C
rautandiol B 11551842 Click to see CC(C)(C1CC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC(=C5)O)O 340.40 unknown https://doi.org/10.1021/NP058070C
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Dehydroneotenone 100751 Click to see COC1=CC2=C(C=C1C3=COC4=C(C3=O)C=C5C=COC5=C4)OCO2 336.30 unknown https://doi.org/10.1021/NP058070C
https://doi.org/10.1021/NP50051A002
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-3-enes / Isoflav-3-enones
Pachyrrhizin 101277 Click to see COC1=CC2=C(C=C1C3=CC4=C(C=C5C(=C4)C=CO5)OC3=O)OCO2 336.30 unknown https://doi.org/10.1021/NP50051A002
https://doi.org/10.1021/NP058070C
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
12-Hydroxyerosone 44575274 Click to see COC1=C(C=C2C(=C1)CCC3C2(C(=O)C4=C(O3)C=C5C(=C4)C=CO5)O)OC 366.40 unknown https://doi.org/10.1021/NP058070C
13-Hydroxy-16,17-dimethoxy-2,6-dioxapentacyclo[11.8.0.03,11.05,9.014,19]henicosa-3(11),4,7,9,14,16,18-heptaen-12-one 75048861 Click to see COC1=C(C=C2C(=C1)CCC3C2(C(=O)C4=C(O3)C=C5C(=C4)C=CO5)O)OC 366.40 unknown https://doi.org/10.1021/NP058070C
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
(1R,6R,13R)-13-hydroxy-16,17-dimethoxy-6-prop-1-en-2-yl-2,7-dioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one 11851283 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4CCC5=CC(=C(C=C5C4(C3=O)O)OC)OC 408.40 unknown https://doi.org/10.1021/NP058070C
(2R,6aS,12aS)-1,2,6,6a,12,12a-Hexahydro-2-isopropenyl-8,9-dimethoxychromeno[3,4-b] furo(2,3-h)chromen-6-one 24794374 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4CCC5=CC(=C(C=C5C4C3=O)OC)OC 392.40 unknown https://doi.org/10.1021/NP058070C
13-Hydroxy-16,17-dimethoxy-6-prop-1-en-2-yl-2,7-dioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one 73126439 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4CCC5=CC(=C(C=C5C4(C3=O)O)OC)OC 408.40 unknown https://doi.org/10.1021/NP058070C
16,17-Dimethoxy-6-prop-1-en-2-yl-2,7-dioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one 74316742 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4CCC5=CC(=C(C=C5C4C3=O)OC)OC 392.40 unknown https://doi.org/10.1021/NP058070C
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 2-O-methylated isoflavonoids
(6R)-6-(6-methoxy-1,3-benzodioxol-5-yl)-6,7-dihydrofuro[3,2-g]chromen-5-one 92169662 Click to see COC1=CC2=C(C=C1C3COC4=C(C3=O)C=C5C=COC5=C4)OCO2 338.30 unknown https://doi.org/10.1021/NP50051A002
Neotenone 73603 Click to see COC1=CC2=C(C=C1C3COC4=C(C3=O)C=C5C=COC5=C4)OCO2 338.30 unknown https://doi.org/10.1021/NP50051A002
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Isoelliptol 44575275 Click to see COC1=CC(=C(C=C1C2=COC3=C(C2=O)C=C4C=COC4=C3)OC)OC 352.30 unknown https://doi.org/10.1021/NP058070C
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(13R)-5,7,11,14,18-pentaoxahexacyclo[11.11.0.02,10.04,8.015,23.017,21]tetracosa-2,4(8),9,15(23),16,19,21-heptaen-24-one 163194463 Click to see C1C2C(C3=CC4=C(C=C3O1)OCO4)C(=O)C5=C(O2)C=C6C(=C5)C=CO6 336.30 unknown https://doi.org/10.1021/NP50051A002
(1R,13R)-5,7,11,14,18-pentaoxahexacyclo[11.11.0.02,10.04,8.015,23.017,21]tetracosa-2,4(8),9,15(23),16,19,21-heptaen-24-one 21676231 Click to see C1C2C(C3=CC4=C(C=C3O1)OCO4)C(=O)C5=C(O2)C=C6C(=C5)C=CO6 336.30 unknown https://doi.org/10.1021/NP50051A002
(1S,13R)-1-hydroxy-5,7,11,14,18-pentaoxahexacyclo[11.11.0.02,10.04,8.015,23.017,21]tetracosa-2,4(8),9,15(23),16,19,21-heptaen-24-one 154495953 Click to see C1C2C(C3=CC4=C(C=C3O1)OCO4)(C(=O)C5=C(O2)C=C6C(=C5)C=CO6)O 352.30 unknown https://doi.org/10.1021/NP50051A002
Dolineone 5316959 Click to see C1C2C(C3=CC4=C(C=C3O1)OCO4)C(=O)C5=C(O2)C=C6C(=C5)C=CO6 336.30 unknown https://doi.org/10.1021/NP50051A002
Rotenolone 68184 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC 410.40 unknown https://doi.org/10.1021/NP50051A002
Rotenone 6758 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1021/NP058070C

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