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Streptocarpus dunnii

Streptocarpus dunnii - 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 UUID64404684ac04e295794409
Scientific name Streptocarpus dunnii
Authority Mast.
First published in Gard. Chron. , n.s., 25: 625 (1886)

Description Top

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Synonyms Top

Scientific name Authority First published in
Streptocarpus armitagei Baker f. & S.Moore J. Bot. 39: 262 (1901)

Common names Top

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Language Common/alternative name
Chinese 邓氏海角苣苔
Chinese 邓氏苣苔

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001064712
Tropicos 14000910
KEW urn:lsid:ipni.org:names:382903-1
The Plant List tro-14000910
Open Tree Of Life 840772
NCBI Taxonomy 121487
IPNI 382903-1
iNaturalist 489705
GBIF 5591270
EOL 5650339

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
Augmentation of NAD+ by Dunnione Ameliorates Imiquimod-Induced Psoriasis-Like Dermatitis in Mice Lee SH, Kim HJ, Oh GS, Lee SB, Khadka D, Cao W, Choe SK, Shim H, Kim CD, Kwak TH, So HS J Inflamm Res 13-Aug-2022
PMCID:PMC9386739
doi:10.2147/JIR.S372543
PMID:35991005
Convergent evolution of plant specialized 1,4-naphthoquinones: metabolism, trafficking, and resistance to their allelopathic effects Meyer GW, Bahamon Naranjo MA, Widhalm JR J Exp Bot 01-Dec-2020
PMCID:PMC7853596
doi:10.1093/jxb/eraa462
PMID:33258472
Antimalarial Properties of Dunnione Derivatives as NQO2 Substrates Chhour M, Aubouy A, Bourgeade-Delmas S, Pério P, Ternet-Fontebasso H, Haidara M, Ferry G, Nepveu F, Boutin JA, Reybier K Molecules 15-Oct-2019
PMCID:PMC6832513
doi:10.3390/molecules24203697
PMID:31618826
Pharmacological stimulation of NQO1 decreases NADPH levels and ameliorates acute pancreatitis in mice Shen A, Kim HJ, Oh GS, Lee SB, Lee S, Pandit A, Khadka D, Sharma S, Kim SY, Choe SK, Yang SH, Cho EY, Shim H, Park R, Kwak TH, So HS Cell Death Dis 18-Dec-2018
PMCID:PMC6315021
doi:10.1038/s41419-018-1252-z
PMID:30584237
A Dunnione Compound MB12662 Improves Cisplatin-Induced Tissue Injury and Emesis Park D, Jo IG, Jang JY, Kwak TH, Yoo SK, Jeon JH, Choi EK, Joo SS, Kim O, Kim YB Biomol Ther (Seoul) 01-Sep-2015
PMCID:PMC4556205
doi:10.4062/biomolther.2015.034
PMID:26336585
Inhibitory effects of a β-dunnione compound MB12662 on gastric secretion and ulcers Jo IG, Park D, Kyung J, Kim D, Cai J, Kim J, Kwak TH, Yoo SK, Jeong HS, Kim YB Lab Anim Res 27-Sep-2013
PMCID:PMC3791353
doi:10.5625/lar.2013.29.3.178
PMID:24106514
Pair-flowered cymes in the Lamiales: structure, distribution and origin Weber A Ann Bot 24-Jul-2013
PMCID:PMC3828946
doi:10.1093/aob/mct156
PMID:23884395
Enantiomeric Natural Products: Occurrence and Biogenesis Finefield JM, Sherman DH, Kreitman M, Williams RM Angew Chem Int Ed Engl 03-May-2012
PMCID:PMC3498912
doi:10.1002/anie.201107204
PMID:22555867
Structures of unusually prenylated naphthoquinones of Streptocarpus dunnii and its cell cultures. Kenichiro Inoue, Shinichi Ueda, Hidekazu Nayeshiro, Hiroyuki Inouye Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.30.2265
Isolation, structure elucidation, and cytotoxic evaluation of furanonaphthoquinones from in vitro plantlets and cultures of Streptocarpus dunnii. Sheridan H, Nestor C, O'Driscoll L, Hook I J Nat Prod 28-Jan-2011
doi:10.1021/NP100358A
PMID:21174407
Inhibition of LFA-1 mediated T-cell motility by naphthoquinones. Sheridan H, Hook I, Nestor C, Coppins J, Ehrhardt C, Frankish N Planta Med 01-Sep-2008
doi:10.1055/S-2008-1081303
PMID:18666044
Quinones of streptocarpus dunnii Kenichiro Inoue, Shinichi Ueda, Hidekazu Nayeshiro, Hiroyuki Inouyet Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)86973-3

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 / Anthracenes / Anthraquinones
1-Hydroxy-2-methylanthraquinone 160817 Click to see CC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 238.24 unknown https://doi.org/10.1016/S0031-9422(00)86973-3
https://doi.org/10.1248/CPB.30.2265
https://doi.org/10.1055/S-2008-1081303
https://doi.org/10.1021/NP100358A
Digiferruginol 32209 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)CO)O 254.24 unknown https://doi.org/10.1016/S0031-9422(00)86973-3
https://doi.org/10.1248/CPB.30.2265
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,9R,10R,13R,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 163005518 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C 398.70 unknown https://doi.org/10.1248/CPB.30.2265
> Organoheterocyclic compounds / Naphthofurans
(2R,3aR,9bS)-2,3,3-trimethyl-3a,9b-dihydro-2H-benzo[g][1]benzofuran-4,5-dione 163048128 Click to see CC1C(C2C(O1)C3=CC=CC=C3C(=O)C2=O)(C)C 244.28 unknown https://doi.org/10.1021/NP100358A
(2R)-7-hydroxy-2,3,3-trimethyl-2H-benzo[g][1]benzofuran-4,5-dione 162952270 Click to see CC1C(C2=C(O1)C3=C(C=C(C=C3)O)C(=O)C2=O)(C)C 258.27 unknown https://doi.org/10.1248/CPB.30.2265
(2R)-7-methoxy-2,3,3-trimethyl-2H-benzo[f][1]benzofuran-4,9-dione 102484290 Click to see CC1C(C2=C(O1)C(=O)C3=C(C2=O)C=CC(=C3)OC)(C)C 272.29 unknown https://doi.org/10.1021/NP100358A
(2S)-2,3,3-trimethyl-2H-benzo[f][1]benzofuran-4,9-dione 92151541 Click to see CC1C(C2=C(O1)C(=O)C3=CC=CC=C3C2=O)(C)C 242.27 unknown https://doi.org/10.1021/NP100358A
https://doi.org/10.1248/CPB.30.2265
(2S)-6-hydroxy-2,3,3-trimethyl-2H-benzo[g][1]benzofuran-4,5-dione 163023013 Click to see CC1C(C2=C(O1)C3=C(C(=CC=C3)O)C(=O)C2=O)(C)C 258.27 unknown https://doi.org/10.1248/CPB.30.2265
(3R)-6-hydroxy-7-methoxy-alpha-dunnione, (-)- 53325375 Click to see CC1C(C2=C(O1)C(=O)C3=CC(=C(C=C3C2=O)O)OC)(C)C 288.29 unknown https://doi.org/10.1021/NP100358A
(3R)-7-hydroxy-alpha-dunnione 11436816 Click to see CC1C(C2=C(O1)C(=O)C3=C(C2=O)C=CC(=C3)O)(C)C 258.27 unknown https://doi.org/10.1021/NP100358A
(3R)-Alpha-Dunnione 51354251 Click to see CC1C(C2=C(O1)C(=O)C3=CC=CC=C3C2=O)(C)C 242.27 unknown https://doi.org/10.1021/NP100358A
(3R)-Dunnione, (rel)- 53322969 Click to see CC1C(C2=C(O1)C3=CC=CC=C3C(=O)C2=O)(C)C 242.27 unknown https://doi.org/10.1248/CPB.30.2265
https://doi.org/10.1016/S0031-9422(00)86973-3
https://doi.org/10.1021/NP100358A
2,3,3-trimethyl-3a,9b-dihydro-2H-benzo[g][1]benzofuran-4,5-dione 142624056 Click to see CC1C(C2C(O1)C3=CC=CC=C3C(=O)C2=O)(C)C 244.28 unknown https://doi.org/10.1021/NP100358A
3,3-Dimethyl-2-methylidenebenzo[g][1]benzofuran-4,5-dione 11564963 Click to see CC1(C(=C)OC2=C1C(=O)C(=O)C3=CC=CC=C32)C 240.25 unknown https://doi.org/10.1248/CPB.30.2265
https://doi.org/10.1016/S0031-9422(00)86973-3
6-hydroxy-7-methoxy-2,3,3-trimethyl-2H-benzo[f][1]benzofuran-4,9-dione 75597485 Click to see CC1C(C2=C(O1)C(=O)C3=CC(=C(C=C3C2=O)O)OC)(C)C 288.29 unknown https://doi.org/10.1021/NP100358A
7-hydroxy-2,3,3-trimethyl-2H-benzo[f][1]benzofuran-4,9-dione 72961166 Click to see CC1C(C2=C(O1)C(=O)C3=C(C2=O)C=CC(=C3)O)(C)C 258.27 unknown https://doi.org/10.1021/NP100358A
7-Hydroxy-alpha-dunnione 101781364 Click to see CC1C(C2=C(O1)C(=O)C3=C(C2=O)C=CC(=C3)O)(C)C 258.27 unknown https://doi.org/10.1055/S-2008-1081303
7-methoxy-2,3,3-trimethyl-2H-benzo[f][1]benzofuran-4,9-dione 75597484 Click to see CC1C(C2=C(O1)C(=O)C3=C(C2=O)C=CC(=C3)OC)(C)C 272.29 unknown https://doi.org/10.1021/NP100358A
dl-alpha-Dunnione 262098 Click to see CC1C(C2=C(O1)C(=O)C3=CC=CC=C3C2=O)(C)C 242.27 unknown https://doi.org/10.1248/CPB.30.2265
https://doi.org/10.1055/S-2008-1081303
https://doi.org/10.1021/NP100358A
Dunnione 262097 Click to see CC1C(C2=C(O1)C3=CC=CC=C3C(=O)C2=O)(C)C 242.27 unknown https://doi.org/10.1248/CPB.30.2265
https://doi.org/10.1016/S0031-9422(00)86973-3
https://doi.org/10.1021/NP100358A
Naphtho(1,2-b)furan-4,5-dione, 2,3-dihydro-6-hydroxy-2,3,3-trimethyl- 176518 Click to see CC1C(C2=C(O1)C3=C(C(=CC=C3)O)C(=O)C2=O)(C)C 258.27 unknown https://doi.org/10.1248/CPB.30.2265
Naptho(1,2-b)furan-4,5-dione, 2,3-dihydro-7-hydroxy-2,3,3-trimethyl- 184063 Click to see CC1C(C2=C(O1)C3=C(C=C(C=C3)O)C(=O)C2=O)(C)C 258.27 unknown https://doi.org/10.1248/CPB.30.2265

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