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Internal ID UUID64400bcb76298089491469
Scientific name Atriplex muricata
Authority Humb. & Bonpl. ex Willd.
First published in Sp. Pl., ed. 4 , 4: 959 (1806)

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Synonyms Top

Scientific name Authority First published in
Atriplex cristata var. parvifolia (Kunth) Kuntze Revis. Gen. Pl. 3(2): 266 (1898)
Atriplex glomerata S.Watson ex Standl. N. Amer. Fl. 21(1): 54. 1916 [27 Nov 1916]
Atriplex kunthiana (Moq.) D.Dietr. Syn. Pl. 5: 536 (1852)
Atriplex microphylla D.Dietr. Syn. Pl. 5: 536 (1852)
Atriplex parviflora Steud. Nomencl. Bot. , ed. 2, 1: 169 (1840)
Atriplex parvifolia Kunth Nov. Gen. Sp. 2: 192 (1817)
Atriplex pentandra subsp. muricata (Humb. & Bonpl. ex Willd.) H.M.Hall & Clem. Phylogen. Meth. : 295 (1923)
Obione kunthiana Moq. Chenop. Monogr. Enum. : 72 (1840)
Obione parvifolia (Kunth) Moq. Chenop. Monogr. Enum. : 73 (1840)

Common names Top

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Language Common/alternative name
German obione muricata (humb. & bonpl. ex willd.) moq.

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southwest

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000556316
USDA Plants ATMU3
Tropicos 7202512
KEW urn:lsid:ipni.org:names:163993-1
The Plant List kew-2665529
Open Tree Of Life 6037862
IPNI 163993-1
iNaturalist 287744
GBIF 3757113
CMAUP NPO9144

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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
(+)-Elwesine 70697964 Click to see C1CC23CCN(C2CC1O)CC4=CC5=C(C=C34)OCO5 273.33 unknown via CMAUP database
(+)-epi-Vittatine 12304132 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
(11S,13beta,19S)-1,2-Didehydrocrinan-3alpha,11-diol 5282088 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown via CMAUP database
(1R,13S,15R,18R)-9,15-dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 92211489 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown via CMAUP database
(1S,13R,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 42579248 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
11-Epicrinamine 5281172 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
11-O-Methylcrinamine 101493050 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)OC 315.40 unknown via CMAUP database
3-O-Acetylhamayne 443671 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown via CMAUP database
Crinamin 73620 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
Crinine 398937 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
Hamayne 443670 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown via CMAUP database
Powellin 443669 Click to see COC1=C2CN3CCC4(C3CC(C=C4)O)C2=CC5=C1OCO5 301.34 unknown via CMAUP database
Vittatine 443693 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
[(1S,12S,14R)-4-acetyl-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-14-yl] acetate 21826143 Click to see CC(=O)N1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)OC(=O)C 357.40 unknown via CMAUP database
Epinorgalanthamine 443721 Click to see COC1=C2C3=C(CNCCC34C=CC(CC4O2)O)C=C1 273.33 unknown via CMAUP database
Galantamine 9651 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown via CMAUP database
Norgalanthamine 9838394 Click to see COC1=C2C3=C(CNCCC34C=CC(CC4O2)O)C=C1 273.33 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
(1S,17S,18S,19R)-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraene-17,18-diol 7060909 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown via CMAUP database
[(1S,17S,18S,19S)-17-hydroxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraen-18-yl] hexadecanoate 54764247 Click to see CCCCCCCCCCCCCCCC(=O)OC1C(C=C2CCN3C2C1C4=CC5=C(C=C4C3)OCO5)O 525.70 unknown via CMAUP database
Lycorine O1,O2-di-(beta-D-glucopyranoside) 101529183 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5OC6C(C(C(C(O6)CO)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)OCO4 611.60 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
Crinasiadine 442850 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC=C4NC3=O 239.23 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 / Protoberberine alkaloids and derivatives
16,19-Dimethoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(21),2,4(8),9,13,15,17,19-octaene 25051817 Click to see COC1=C2C=C3C4=CC5=C(C=C4CC[N+]3=CC2=C(C=C1)OC)OCO5 336.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethylparaben 8434 Click to see CCOC(=O)C1=CC=C(C=C1)O 166.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Aminobenzaldehyde 11158 Click to see C1=CC(=CC=C1C=O)N 121.14 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(-)-8-Demethylmaritidine 443683 Click to see COC1=C(C=C2CN3CCC4(C3CC(C=C4)O)C2=C1)O 273.33 unknown via CMAUP database
(4aS,10bR)-Noroxomaritidine 11184826 Click to see COC1=C(C=C2CN3CCC4(C3CC(=O)C=C4)C2=C1)O 271.31 unknown via CMAUP database
1-Epideacetylbowdensine 443673 Click to see COC1=C2CN3CCC4(C3CCC(C4O)O)C2=CC5=C1OCO5 319.40 unknown via CMAUP database
1-Epijosephinine 70697961 Click to see CC(=O)OC1CCC2C3(C1O)CCN2CC4=CC5=C(C=C34)OCO5 331.40 unknown via CMAUP database
1-O-Acetylbulbisine 70698017 Click to see CC(=O)OC1C(CCC2C13CCN2CC4=C(C5=C(C=C34)OCO5)OC)O 361.40 unknown via CMAUP database
2-O-Acetylbulbisine 56928078 Click to see CC(=O)OC1CCC2C3(C1O)CCN2CC4=C(C5=C(C=C34)OCO5)OC 361.40 unknown via CMAUP database
2-O-Acetylcrinamabine 70697942 Click to see CC(=O)OC1CCC2(C3(C1O)CCN2CC4=CC5=C(C=C34)OCO5)O 347.40 unknown via CMAUP database
3-O-Acetyl-8-O-demethylmaritidine 52937473 Click to see CC(=O)OC1CC2C3(CCN2CC4=CC(=C(C=C43)OC)O)C=C1 315.40 unknown via CMAUP database
4a-Dehydroxycrinamabine 398935 Click to see C1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C(C1O)O 289.33 unknown via CMAUP database
7-Methoxycrinamabine 70698020 Click to see COC1=C2CN3CCC4(C2=CC5=C1OCO5)C3(CCC(C4O)O)O 335.40 unknown via CMAUP database
7H-Pyrrolo(3,2,1-de)phenanthridin-7-one, 10-hydroxy-9-methoxy- 5488695 Click to see COC1=C(C=C2C3=CC=CC4=C3N(C=C4)C(=O)C2=C1)O 265.26 unknown via CMAUP database
9-Methoxy-10-hydroxy-4aalpha,6-dihydro-5alpha,10balpha-ethanophenanthridine-3(4H)-one 11140214 Click to see COC1=C(C2=C(CN3CCC24C3CC(=O)C=C4)C=C1)O 271.31 unknown via CMAUP database
CID 3738100 3738100 Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)[O-])OCO4 265.26 unknown via CMAUP database
Crinamabine 15378991 Click to see C1CC2(C3(CCN2CC4=CC5=C(C=C43)OCO5)C(C1O)O)O 305.32 unknown via CMAUP database
Hippacine 10015025 Click to see C1=CC2=C3C(=C1)C4=CC(=C(C=C4C(=O)N3C=C2)O)O 251.24 unknown via CMAUP database
Hippadine 100605 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5 263.25 unknown via CMAUP database
Maritinamine 11818191 Click to see COC1=C(C=C2CN3CCC4(C3CC(CC4)O)C2=C1)O 275.34 unknown via CMAUP database
Pratorimine 181937 Click to see COC1=C(C=C2C(=C1)C3=CC=CC4=C3N(C2=O)C=C4)O 265.26 unknown via CMAUP database
Siculine 11208052 Click to see COC1=C(C=C2CN3CCC4(C3CC(C=C4)O)C2=C1)O 273.33 unknown via CMAUP database
Ungeremine 159646 Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)O)OCO4 266.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-Caffeoyltyramine 9994897 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC(=C(C=C2)O)O)O 299.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Paprazine 5372945 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
(S)-2-(3-Hydroxy-4-methoxyphenyl)chroman-7-ol 44257179 Click to see COC1=C(C=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O)O 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4'-Hydroxy-7-methoxyflavan 185609 Click to see COC1=CC2=C(CCC(O2)C3=CC=C(C=C3)O)C=C1 256.30 unknown via CMAUP database

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