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Internal ID UUID643fd99a3d425191352700
Scientific name Thermopsis alterniflora
Authority Regel & Schmalh.
First published in Izv. Imp. Obshch. Lyubit. Estestv. Moskovsk. Univ.34(2): 18 (1882)

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Synonyms Top

Scientific name Authority First published in
Thermopsis rigida Vassilcz. Sovetsk. Bot.1936(3): 47 (1936)

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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000186300
Tropicos 13033613
KEW urn:lsid:ipni.org:names:521155-1
The Plant List ild-32737
Open Tree Of Life 3928780
Observations.org 122916
IPNI 521155-1
GBIF 5360219
EOL 643920
Elurikkus 527841
USDA GRIN 36512

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)!
Title Authors Publication Released IDs
Flavonoids of Thermopsis alterniflora N. Sh. Kattaev, G. K. Nikonov Springer Science and Business Media LLC 09-Jul-2008
doi:10.1007/BF00570657
Spectrophotometric determination of flavones and isoflavones inThermopsis alterniflora L. D. Kotenko, A. U. Mamatkhanov, M. T. Turakhozhaev Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630203
Flavonoids of Thermopsis alterniflora M. P. Yuldashev, �. Kh. Batirov, A. D. Vdovin, V. M. Malikov, M. R. Yagudaev Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00597707
Chromatopolarographic determination of the amount of cytisine in Thermopsis alterniflora E. K. Dobronravova, T. T. Shakirov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568499
A study of the alkaloids of Thermopsis alterniflora R. A. Shaimardanov, S. Iskandarov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568689
Dimethamine — A new bimolecular alkaloid from Thermopsis alterniflora S. Iskandarov, V. I. Vinogradova, R. A. Shaimardanov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565303
Flavonoids of Thermopsis alterniflora N. Sh. Kattaev, G. K. Nikonov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564317

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
(+)-Thermopsine 682648 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1007/BF00565303
https://doi.org/10.1007/BF00568689
(1R,9R,10S,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 101622983 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1007/BF00565303
(1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 6920824 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1007/BF00565303
7,14-Methano-4H,6H-dipyrido[1,2-a:1',2'-E][1,5]diazocin-4-one, 7,7a,8,9,10,11,13,14-octahydro-, [7R-(7alpha,7aalpha,14alpha)]- 91746595 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1007/BF00568499
Thermopsine 92768 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1007/BF00568689
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(+)-Cytisine 683511 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1007/BF00565303
(1R,9R,10R)-11-methyl-10-prop-2-enyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 102247462 Click to see CN1CC2CC(C1CC=C)CN3C2=CC=CC3=O 244.33 unknown https://doi.org/10.1007/BF00568689
(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/10.1007/BF00565303
(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 CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1007/BF00568689
(1S,9R)-11-methyl-5-[(1S,4R,9R)-11-methyl-6-oxo-7,11-diazatricyclo[7.3.1.02,7]tridec-2-en-4-yl]-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 162875717 Click to see CN1CC2CC(C1)C3=CC(CC(=O)N3C2)C4=CC=C5C6CC(CN(C6)C)CN5C4=O 408.50 unknown https://doi.org/10.1007/BF00565303
1,5-Methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one, 1,2,3,4,5,6-hexahydro-3-methyl-4-(2-propenyl)- 157031 Click to see CN1CC2CC(C1CC=C)CN3C2=CC=CC3=O 244.33 unknown https://doi.org/10.1007/BF00568499
https://doi.org/10.1007/BF00568689
11-Methyl-5-(11-methyl-6-oxo-7,11-diazatricyclo[7.3.1.02,7]tridec-2-en-4-yl)-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 162875716 Click to see CN1CC2CC(C1)C3=CC(CC(=O)N3C2)C4=CC=C5C6CC(CN(C6)C)CN5C4=O 408.50 unknown https://doi.org/10.1007/BF00565303
Citizin 22407 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1007/BF00568689
Cytisinicline 10235 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1007/BF00568689
N-Methylcytisine 234566 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1007/BF00568689
Pharmakon1600-01504027 6708720 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1007/BF00568499
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Sparteine 7014 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1007/BF00568499
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Tertiary amines / Tertiary alkylarylamines / Dialkylarylamines
Methapyrilene 4098 Click to see CN(C)CCN(CC1=CC=CS1)C2=CC=CC=N2 261.39 unknown https://doi.org/10.1007/BF00564317
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin 65084 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1007/BF00564317
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00630203
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl (E)-but-2-enoate 94855606 Click to see CC=CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)OC)O)O)O)O 530.50 unknown https://doi.org/10.1007/BF00597707
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl (E)-but-2-enoate 13872455 Click to see CC=CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)OC)O)O)O)O 530.50 unknown https://doi.org/10.1007/BF00597707
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl (E)-but-2-enoate 14334939 Click to see CC=CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O 500.40 unknown https://doi.org/10.1007/BF00597707
[3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl but-2-enoate 73188638 Click to see CC=CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)OC)O)O)O)O 530.50 unknown https://doi.org/10.1007/BF00597707
[3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl but-2-enoate 72730074 Click to see CC=CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O 500.40 unknown https://doi.org/10.1007/BF00597707
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00597707
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00597707
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1007/BF00570657
https://doi.org/10.1007/BF00564317
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1007/BF00564317
Teralin 14077813 Click to see COC1=C(C=CC(=C1)O)C2=COC3=C(C2=O)C=CC(=C3)O 284.26 unknown https://doi.org/10.1007/BF00570657
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
(3S)-5-hydroxy-3-(4-hydroxyphenyl)-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 162958775 Click to see C1C(C(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)CO)O)O)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1007/BF00564317
3-(4-Methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 3733033 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1007/BF00597707
5,7,4'-Trihydroxyisoflavanone 7-O-glucoside 21941294 Click to see C1C(C(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)CO)O)O)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1007/BF00564317
CID 14334937 14334937 Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O 444.40 unknown https://doi.org/10.1007/BF00597707
Genistin 5281377 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1007/BF00564317
Genistoside 5284639 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1007/BF00564317
Ononin 442813 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1007/BF00597707
Rothindin 3085261 Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O 444.40 unknown https://doi.org/10.1007/BF00597707
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1007/BF00630203
https://doi.org/10.1007/BF00597707

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