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Maackia tashiroi

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fd9945b58e517354925
Scientific name Maackia tashiroi
Authority Makino
First published in Bot. Mag. (Tokyo)16: 34 (1902)

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.

No verifiable ethnobotanical uses—teas, decoctions, tinctures, macerations, or poultices—have been recorded for Maackia tashiroi in accessible monographs, peer‑reviewed ethnobotanical studies, or reputable herbal compendia. Without credible documentation of such preparations, providing an ethnobotanical uses profile would be speculative rather than factual.

General Uses Top

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Common products:
No commercial products are documented for this species.

Industrial and craft applications:
No industrial or craft applications are documented for this species.

Food and beverages (non-medicinal):
No food or beverage uses are documented for this species.

Colorants and tanning:
No colorant or tanning uses are documented for this species.

Wood and fiber:
No wood or fiber uses are documented for this species.

Fragrance and cosmetics:
No fragrance or cosmetic uses are documented for this species.

Properties relevant to use:
No documented non-medicinal uses.

Standards and regulation:
No documented non-medicinal uses.

Sustainability and sourcing:
No documented non-medicinal uses.

Synonyms Top

Scientific name Authority First published in
Cladrastis tashiroi (Yatabe) Makino
Cladrastis tashiroi Yatabe Bot. Mag. (Tokyo)6: 345 (1892)

Common names Top

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No common names added yet.

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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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-0000186194
Tropicos 13062974
KEW urn:lsid:ipni.org:names:505353-1
The Plant List ild-32615
Open Tree Of Life 753527
NCBI Taxonomy 256641
IPNI 505353-1
GBIF 5360270
EPPO MCKTA
EOL 643869
CMAUP NPO10991

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
Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity Cely-Veloza W, Kato MJ, Coy-Barrera E ACS Omega 28-Jul-2023
PMCID:PMC10413377
doi:10.1021/acsomega.3c02179
PMID:37576649
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
New syntheses of (±)-tashiromine and (±)-epitashiromine via enaminone intermediates Riley DL, Michael JP, de Koning CB Beilstein J Org Chem 02-Dec-2016
PMCID:PMC5238587
doi:10.3762/bjoc.12.256
PMID:28144330
Novel stereocontrolled syntheses of tashiromine and epitashiromine Kiss L, Forró E, Fülöp F Beilstein J Org Chem 30-Apr-2015
PMCID:PMC4464356
doi:10.3762/bjoc.11.66
PMID:26124861
Studies on Plant Constituents of Genus Maackia. Part V. (-)-Camoensidine N-Oxide; A New Alkaloid from Maackia tashiroi. Shigeru OHMIYA, Hajime KUBO, Yuuichi NAKAAZE, Kazuki SAITO, Isamu MURAKOSHI, Hirotaka OTOMASU Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.39.1123
(+)-13.BETA.-Hydroxymamanine, a new lupin alkaloid from Maackia amurensis var. buergeri. Kazuki Saito, Sih Tsai, Shigeru Ohmiya, Hajime Kubo, Hirotaka Otomasu, Isamu Murakoshi Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.34.3982
Absolute configuration of (-)-lusitanine, a new lupin alkaloid in Maackia species. Kazuki Saito, Takaaki Yoshino, Shi Tsai, Shigeru Ohmiya, Hajime Kubo, Hirotaka Otomasu, Isamu Murakoshi Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.35.1308
Tashiromine; a New Alkaloid from Maackia tashiroi Shigeru Ohmiya, Hajime Kubo, Hirotaka Otomasu, Kazuki Saito, Isamu Murakoshi The Japan Institute of Heterocyclic Chemistry 03-Mar-2009
doi:10.3987/COM-89-S47
Total synthesis of the indolizidine alkaloid tashiromine Marsden SP, McElhinney AD Beilstein J Org Chem 26-Jan-2008
PMCID:PMC2241604
doi:10.1186/1860-5397-4-8
PMID:18221553

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 / Lupin alkaloids / Anagyrine-type alkaloids
(+)-Thermopsine 682648 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.3987/COM-89-S47
(10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 10246 Click to see 244.33 unknown https://doi.org/10.3987/COM-89-S47
Anagyrine 5351589 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.3987/COM-89-S47
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(-)-Cytisine 6713952 Click to see 190.24 unknown https://doi.org/10.3987/COM-89-S47
(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/10.3987/COM-89-S47
(1R,9R)-6-oxo-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-diene-11-carbaldehyde 7067491 Click to see 218.25 unknown https://doi.org/10.3987/COM-89-S47
(1R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one 1278189 Click to see 204.27 unknown https://doi.org/10.1248/CPB.39.1123
(1S,5R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one 683511 Click to see 190.24 unknown https://doi.org/10.3987/COM-89-S47
(1S,9R)-11-but-3-enyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 7067420 Click to see 244.33 unknown https://doi.org/10.3987/COM-89-S47
1,2,3,4,5,6-hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one 22407 Click to see 190.24 unknown https://doi.org/10.1248/CPB.39.1123
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 244.33 unknown https://doi.org/10.3987/COM-89-S47
Caulophylline 234566 Click to see 204.27 unknown https://doi.org/10.1248/CPB.39.1123
Cytisine 10235 Click to see 190.24 unknown https://doi.org/10.1248/CPB.39.1123
Cytisine, N-formyl- 589870 Click to see 218.25 unknown https://doi.org/10.1248/CPB.39.1123
https://doi.org/10.3987/COM-89-S47
N-Formylcytisine, (-)- 6604689 Click to see 218.25 unknown https://doi.org/10.1248/CPB.39.1123
> Alkaloids and derivatives / Lupin alkaloids / Leontidine-type alkaloids
(1R,2S,9S,10R)-7,14-diazatetracyclo[7.6.1.02,7.010,14]hexadecan-6-one 15060884 Click to see 234.34 unknown https://doi.org/10.1248/CPB.34.3982
Camoensidine N-oxide 163184629 Click to see C1CC2C3CC(CN2C(=O)C1)C4CCC[N+]4(C3)[O-] 250.34 unknown https://doi.org/10.1248/CPB.39.1123
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
Epilupinine 92767 Click to see 169.26 unknown https://doi.org/10.3987/COM-89-S47
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Triacontane 12535 Click to see 422.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see 382.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4S,6R,10S)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 9991037 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(4aS,5S)-3-(2-hydroxypropan-2-yl)-4a,5-dimethyl-5,6,7,8-tetrahydronaphthalen-2-one 14830797 Click to see 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(2S,3S,4S,5R)-2,5-bis(hydroxymethyl)-2-methoxyoxolane-3,4-diol 6325664 Click to see COC1(C(C(C(O1)CO)O)O)CO 194.18 unknown via CMAUP database
beta-D-Fructofuranoside, methyl 128889 Click to see 194.18 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(1R,4R)-1-(beta-D-Glucopyranosyloxy)-4-hydroxy-2-cyclopentene-1-carbonitrile 181811 Click to see 287.27 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Dianthoside 5316639 Click to see 288.25 unknown via CMAUP database
Sucrose 5988 Click to see 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid 54036359 Click to see 326.30 unknown via CMAUP database
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose 5984 Click to see 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Rhamnose 5460029 Click to see 164.16 unknown via CMAUP database
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Teuhetenone A 15153216 Click to see 194.27 unknown via CMAUP database
> Organoheterocyclic compounds / Indolizidines
(+)-Tashiromine 11019091 Click to see 155.24 unknown https://doi.org/10.3987/COM-89-S47
(Octahydro-indolizin-8-YL)-methanol 13967742 Click to see 155.24 unknown https://doi.org/10.3987/COM-89-S47
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
1-(3,4-Dihydro-5-(2R)-2-piperidinyl-1(2H)-pyridinyl)ethanone 442625 Click to see 208.30 unknown https://doi.org/10.1248/CPB.35.1308
https://doi.org/10.3987/COM-89-S47
https://doi.org/10.1248/CPB.39.1123
> Organoheterocyclic compounds / Quinolizines
Lusitanine 6452371 Click to see 208.30 unknown https://doi.org/10.1248/CPB.35.1308
https://doi.org/10.3987/COM-89-S47
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
8-C-(2-Rhamnosyl-6-deoxyhexopyranosulyl)luteolin 102040777 Click to see 576.50 unknown via CMAUP database
Luteolin 8-C-E-propenoic acid 16109839 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C(=C3O2)C=CC(=O)O)O)O)O)O 356.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
(1S)-1,5-anhydro-2-O-(6-deoxy-beta-L-mannopyranosyl)-1-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl]-D-glucitol 86289611 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)O)CO)O)O)O)O)O 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 102401707 Click to see 656.50 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 16109838 Click to see 670.60 unknown via CMAUP database
Quercetin 3-O-gentiobioside 5320834 Click to see 626.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-2-(hydroxymethyl)oxan-3-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate 16109840 Click to see 578.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl (Z)-3-(4-hydroxyphenyl)prop-2-enoate 16109837 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O 578.50 unknown via CMAUP database
7-O-Beta-D-Glucopyranoside 11294177 Click to see 462.40 unknown via CMAUP database
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown via CMAUP database
Apigenin-7-O-(6''-O-4-coumaroyl)-beta-glucopyranoside 6439941 Click to see 578.50 unknown via CMAUP database
Echinaticin 101321313 Click to see C1=CC(=CC=C1C=CC(=O)OC2C(OC(C(C2O)O)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O 578.50 unknown via CMAUP database
Tricin 7-glucoside 5322022 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 492.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7,4'-dimethoxyflavone 5281601 Click to see 298.29 unknown via CMAUP database
5,4'-Dihydroxy-7,3'-dimethoxyflavone 5464381 Click to see 314.29 unknown via CMAUP database

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