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Maackia hupehensis

Maackia hupehensis - 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 UUID643fdbbf4aa37858105954
Scientific name Maackia hupehensis
Authority Takeda
First published in C.S.Sargent, Pl. Wilson.2: 98 (1914)

Description Top

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Synonyms Top

Scientific name Authority First published in
Maackia chinensis Takeda Notes Roy. Bot. Gard. Edinburgh8: 103 (1913)
Maackia floribunda var. chinensis (Takeda) Hatus. J. Jap. Bot.12: 875 (1936)

Common names Top

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Language Common/alternative name
Hungarian kínai sárgafa
Chinese 马鞍树
Chinese 臭槐
Chinese 山槐
Chinese 槐树
Chinese 一种维管植物

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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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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000197219
Tropicos 13062979
KEW urn:lsid:ipni.org:names:505352-1
The Plant List ild-43762
Open Tree Of Life 224609
NCBI Taxonomy 449085
IUCN Red List 152840066
IPNI 505352-1
iNaturalist 525693
GBIF 5360283
EOL 648257
USDA GRIN 410874

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
Bioactive Lipodepsipeptides Produced by Bacteria and Fungi Evidente A Int J Mol Sci 15-Oct-2022
PMCID:PMC9659194
doi:10.3390/ijms232012342
PMID:36293201
Evolutionary response to the Qinghai-Tibetan Plateau uplift: phylogeny and biogeography of Ammopiptanthus and tribe Thermopsideae (Fabaceae) Shi W, Liu PL, Duan L, Pan BR, Su ZH PeerJ 31-Jul-2017
PMCID:PMC5541923
doi:10.7717/peerj.3607
PMID:28785518
Plants as highly diverse sources of construction wood, handicrafts and fibre in the Heihe valley (Qinling Mountains, Shaanxi, China): the importance of minor forest products Kang J, Kang Y, Feng J, Liu M, Ji X, Li D, Stawarczyk K, Łuczaj Ł J Ethnobiol Ethnomed 30-Jun-2017
PMCID:PMC5493080
doi:10.1186/s13002-017-0165-8
PMID:28666450
Endophytic fungi: a reservoir of antibacterials Deshmukh SK, Verekar SA, Bhave SV Front Microbiol 08-Jan-2015
PMCID:PMC4288058
doi:10.3389/fmicb.2014.00715
PMID:25620957
Lupin Alkaloids from Chinese Maackia Hupehensis. Yong-Hong WANG, Jia-Shi LI, Hajime KUBO, Kimio HIGASHIYAMA, Hideaki KOMIYA, Shigeru OHMIYA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.47.1308
(+)-Hupeol, a Possible Non-basic Metabolite of the Lupine Alkaloid (−)-Cytisine in Chinese Maackia hupehensis† Yong-hong Wang, Hajime Kubo, Kimio Higashiyama, Hideaki Komiya, Jia-Shi Li, Shigeru Ohmiya Royal Society of Chemistry (RSC) 26-Jul-2002
doi:10.1039/A708797G

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 / Lupin alkaloids / Anagyrine-type alkaloids
Epibaptifoline 91747695 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1039/A708797G
https://doi.org/10.1248/CPB.47.1308
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(-)-Cytisine 22407 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1248/CPB.47.1308
(1R,5S)-3-(3-Oxo-butyl)-1,2,3,4,5,6-hexahydro-1,5-methano-pyrido[1,2-a][1,5]diazocin-8-one 44398032 Click to see CC(=O)CCN1CC2CC(C1)C3=CC=CC(=O)N3C2 260.33 unknown https://doi.org/10.1248/CPB.47.1308
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 1747617 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1248/CPB.47.1308
https://doi.org/10.1039/A708797G
(1R,9S)-11-[(2-oxopyrrolidin-1-yl)methyl]-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 10637026 Click to see C1CC(=O)N(C1)CN2CC3CC(C2)C4=CC=CC(=O)N4C3 287.36 unknown https://doi.org/10.1248/CPB.47.1308
(1S,5R)-3,4,5,6-tetrahydro-1H-1,5-methanopyrido[1,2-a][1,5]diazocin-8(2H)-one 6713952 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1248/CPB.47.1308
https://doi.org/10.1039/A708797G
1,5-Methano-8H-pyrido[1,2-a][1,5]diazocin-8-one, 3-(3-butenyl)-1,2,3,4,5,6-hexahydro-, (1R)- 547355 Click to see C=CCCN1CC2CC(C1)C3=CC=CC(=O)N3C2 244.33 unknown https://doi.org/10.1039/A708797G
https://doi.org/10.1248/CPB.47.1308
11-(3-Oxobutyl)-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 56674705 Click to see CC(=O)CCN1CC2CC(C1)C3=CC=CC(=O)N3C2 260.33 unknown https://doi.org/10.1248/CPB.47.1308
11-[(2-Oxopyrrolidin-1-yl)methyl]-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 73201089 Click to see C1CC(=O)N(C1)CN2CC3CC(C2)C4=CC=CC(=O)N4C3 287.36 unknown https://doi.org/10.1248/CPB.47.1308
Caulophylline 670971 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1248/CPB.47.1308
Cytisine, N-formyl- 589870 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown https://doi.org/10.1039/A708797G
https://doi.org/10.1248/CPB.47.1308
Cytisinicline 10235 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1248/CPB.47.1308
N-[(6-oxo-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-11-yl)methyl]acetamide 73201090 Click to see CC(=O)NCN1CC2CC(C1)C3=CC=CC(=O)N3C2 261.32 unknown https://doi.org/10.1248/CPB.47.1308
N-[[(1R,9S)-6-oxo-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-11-yl]methyl]acetamide 10801388 Click to see CC(=O)NCN1CC2CC(C1)C3=CC=CC(=O)N3C2 261.32 unknown https://doi.org/10.1248/CPB.47.1308
N-Formylcytisine 179619 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown https://doi.org/10.1248/CPB.47.1308
N-Methylcytisine 234566 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1248/CPB.47.1308
Rhombifoline 92795 Click to see C=CCCN1CC2CC(C1)C3=CC=CC(=O)N3C2 244.33 unknown https://doi.org/10.1248/CPB.47.1308
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
1-Epilupinine 92767 Click to see C1CCN2CCCC(C2C1)CO 169.26 unknown https://doi.org/10.1039/A708797G
https://doi.org/10.1248/CPB.47.1308
Lupinine 91461 Click to see C1CCN2CCCC(C2C1)CO 169.26 unknown https://doi.org/10.1248/CPB.47.1308
Octahydro-2H-quinolizin-1-ylmethanol 297272 Click to see C1CCN2CCCC(C2C1)CO 169.26 unknown https://doi.org/10.1248/CPB.47.1308
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Pyridinones
(1S,9R,10R)-10-hydroxy-11-oxa-7-azatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 163104393 Click to see C1C2CN3C(=O)C=CC=C3C1COC2O 207.23 unknown https://doi.org/10.1039/A708797G
(1S,9R)-10-hydroxy-11-oxa-7-azatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 10889080 Click to see C1C2CN3C(=O)C=CC=C3C1COC2O 207.23 unknown https://doi.org/10.1039/A708797G
https://doi.org/10.1248/CPB.47.1308
> Organoheterocyclic compounds / Quinolizines
Lusitanine 6452371 Click to see CC(=O)NC=C1CCCN2C1CCCC2 208.30 unknown https://doi.org/10.1248/CPB.47.1308
https://doi.org/10.1039/A708797G
N-(2,3,4,6,7,8,9,9a-octahydroquinolizin-1-ylidenemethyl)acetamide 78410938 Click to see CC(=O)NC=C1CCCN2C1CCCC2 208.30 unknown https://doi.org/10.1248/CPB.47.1308

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