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Internal ID UUID644024187ef28010473374
Scientific name Vellozia declinans
Authority Goethart & Henrard
First published in Blumea 2: 369 (1937)

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Synonyms Top

Scientific name Authority First published in
Vellozia leptopetala Goeth. & Henrard Blumea 2: 374 (1937)
Vellozia epidendroides var. divaricata L.B.Sm. Contr. U.S. Natl. Herb. 35: 289. 1962
Vellozia confusa L.B.Sm. & Ayensu Smithsonian Contr. Bot. 30: 88 1976

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0000751669
Tropicos 33600106
KEW urn:lsid:ipni.org:names:262808-2
The Plant List kew-291199
Open Tree Of Life 3968435
NCBI Taxonomy 1289396
IPNI 262808-2
GBIF 2863683
EOL 1083428

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed CentralĀ®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Pimarane and cleistanthane diterpenes from velloziaceae: absolute configuration and biomimetic conversion A.C. Pinto, M.l. Patitucci, R.S. Da Silva, P.P.S. Queiroz, A. Kelecom Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)91585-6
Two diterpenes with a cleistanthane skeleton from Vellozia declinans Angelo C. Pinto, Ligia M.M. Valente, Moacir G. Pizzolatti Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98271-2
Diterpenoids from Vellozia declinans Angelo C. Pinto, Rosangela De A. Epifanio, Moacir G. Pizzolatti Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80451-J

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 / Phenanthrenes and derivatives / Phenanthrols
6,6,14-Trimethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadeca-1,7,9(17),13,15-pentaene 86257793 Click to see CC1=C2CCOC3=C2C(=C4CCCC(C4=C3)(C)C)C=C1 266.40 unknown https://doi.org/10.1016/0031-9422(92)80451-J
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aR,10aR)-8-ethyl-4a-(hydroxymethyl)-1,1,7-trimethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 163189125 Click to see CCC1=C(C=CC2=C1C(=O)CC3C2(CCCC3(C)C)CO)C 300.40 unknown https://doi.org/10.1016/S0031-9422(00)98271-2
(4aR,10aS)-8-ethyl-1,1,7-trimethyl-9-oxo-3,4,10,10a-tetrahydro-2H-phenanthrene-4a-carbaldehyde 101637190 Click to see CCC1=C(C=CC2=C1C(=O)CC3C2(CCCC3(C)C)C=O)C 298.40 unknown https://doi.org/10.1016/S0031-9422(00)98271-2
(4aS,10aS)-8-ethyl-1,1,4a,7-tetramethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 14287359 Click to see CCC1=C(C=CC2=C1C(=O)CC3C2(CCCC3(C)C)C)C 284.40 unknown https://doi.org/10.1016/0031-9422(92)80451-J
https://doi.org/10.1016/S0040-4020(01)91585-6
(4aS,9S,10aS)-8-ethyl-1,1,4a,7-tetramethyl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol 101637191 Click to see CCC1=C(C=CC2=C1C(CC3C2(CCCC3(C)C)C)O)C 286.50 unknown https://doi.org/10.1016/0031-9422(92)80451-J
8-Ethyl-1,1,4a,7-tetramethyl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol 162892456 Click to see CCC1=C(C=CC2=C1C(CC3C2(CCCC3(C)C)C)O)C 286.50 unknown https://doi.org/10.1016/0031-9422(92)80451-J
8-ethyl-1,1,7-trimethyl-9-oxo-3,4,10,10a-tetrahydro-2H-phenanthrene-4a-carbaldehyde 163010947 Click to see CCC1=C(C=CC2=C1C(=O)CC3C2(CCCC3(C)C)C=O)C 298.40 unknown https://doi.org/10.1016/S0031-9422(00)98271-2
8-ethyl-4a-(hydroxymethyl)-1,1,7-trimethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 163098901 Click to see CCC1=C(C=CC2=C1C(=O)CC3C2(CCCC3(C)C)CO)C 300.40 unknown https://doi.org/10.1016/S0031-9422(00)98271-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,4R,9R,10S,13S,14R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-ene-2,14-diol 101615188 Click to see CC1(CCCC2(C1CC(C34C2C=CC(C3)C(C4)(C)O)O)C)C 304.50 unknown https://doi.org/10.1016/S0040-4020(01)91585-6
https://doi.org/10.1016/0031-9422(92)80451-J
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 14191460 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
20-Hydroxylupan-3-one 14191461 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(92)80451-J
> Organoheterocyclic compounds / Naphthopyrans
(1R,10S,12R,14S)-5,13,13-trimethyl-9,18-dioxapentacyclo[8.6.2.12,6.01,12.010,19]nonadeca-2(19),3,5-trien-14-ol 162851736 Click to see CC1=C2CCOC34C2=C(C=C1)C5(CCC(C(C5C3)(C)C)O)CO4 314.40 unknown https://doi.org/10.1016/0031-9422(92)80451-J
5,13,13-Trimethyl-9,18-dioxapentacyclo[8.6.2.12,6.01,12.010,19]nonadeca-2(19),3,5-trien-14-ol 162851735 Click to see CC1=C2CCOC34C2=C(C=C1)C5(CCC(C(C5C3)(C)C)O)CO4 314.40 unknown https://doi.org/10.1016/0031-9422(92)80451-J
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
(1R,10S,12R)-5,13,13-trimethyl-9,18-dioxapentacyclo[8.6.2.12,6.01,12.010,19]nonadeca-2(19),3,5,15-tetraen-14-one 14191470 Click to see CC1=C2CCOC34C2=C(C=C1)C5(CO3)C=CC(=O)C(C5C4)(C)C 310.40 unknown https://doi.org/10.1016/0031-9422(92)80451-J
5,13,13-Trimethyl-9,18-dioxapentacyclo[8.6.2.12,6.01,12.010,19]nonadeca-2(19),3,5,15-tetraen-14-one 14191469 Click to see CC1=C2CCOC34C2=C(C=C1)C5(CO3)C=CC(=O)C(C5C4)(C)C 310.40 unknown https://doi.org/10.1016/0031-9422(92)80451-J

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