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Internal ID UUID644036bf74db0099879600
Scientific name Croton hovarum
Authority Leandri
First published in Ann. Mus. Colon. Marseille , sér. 5, 7(1): 40 (1939)

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Synonyms Top

Scientific name Authority First published in
Croton ivohibensis Leandri Ann. Mus. Colon. Marseille , sér. 5, 7(1): 37 (1939)
Croton rubricapitirupis Leandri Adansonia , n.s., 13: 173 (1973)
Croton cassinoides var. alaotrensis Radcl.-Sm. Gen. Croton Madag. Comoro : 10 (2016)
Croton anisatus var. hirsutus Radcl.-Sm. Gen. Croton Madag. Comoro : 14 (2016)
Croton greveanus var. ambositrensis Leandri ex Radcl.-Sm. Gen. Croton Madag. Comoro : 39 (2016)
Croton ivohibensis var. lepidotus Radcl.-Sm. Gen. Croton Madag. Comoro : 149 (2016)
Croton hovarum var. lepidotus Radcl.-Sm. Gen. Croton Madag. Comoro : 179 (2016)
Croton hovarum var. subglaber Radcl.-Sm. Gen. Croton Madag. Comoro : 179 (2016)

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Distribution (via POWO/KEW) Top

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000931269
Tropicos 12805299
KEW urn:lsid:ipni.org:names:342693-1
The Plant List kew-50150
Open Tree Of Life 3913929
IUCN Red List 137507512
IPNI 342693-1
GBIF 3058277
EOL 1147095

Genomes (via NCBI) Top

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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
Clerodane diterpenes and other constituents of Croton hovarum Hans C. Krebs, Harisolo Ramiarantsoa Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00624-9
Clerodane diterpenes of Croton hovarum Hans C. Krebs, Harisolo Ramiarantsoa Elsevier BV 30-Apr-2003
doi:10.1016/S0031-9422(96)00815-1

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(1R,2R,4aR,5R,6R,8aS)-1-[2-(furan-3-yl)-2-oxoethyl]-5,6-dihydroxy-2,4a,5-trimethyl-3,4,6,7,8,8a-hexahydro-2H-naphthalene-1-carbaldehyde 15276130 Click to see CC1CCC2(C(C1(CC(=O)C3=COC=C3)C=O)CCC(C2(C)O)O)C 348.40 unknown https://doi.org/10.1016/0031-9422(95)00624-9
(1R,2R,4aR,5R,8aS)-1-[2-(furan-3-yl)-2-oxoethyl]-2,4a,5-trimethyl-6-oxo-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carbaldehyde 162844021 Click to see CC1CCC2(C(C(=O)CCC2C1(CC(=O)C3=COC=C3)C=O)C)C 330.40 unknown https://doi.org/10.1016/S0031-9422(96)00815-1
1-[2-(furan-3-yl)-2-oxoethyl]-2,4a,5-trimethyl-6-oxo-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carbaldehyde 162844020 Click to see CC1CCC2(C(C(=O)CCC2C1(CC(=O)C3=COC=C3)C=O)C)C 330.40 unknown https://doi.org/10.1016/S0031-9422(96)00815-1
1-[2-(furan-3-yl)-2-oxoethyl]-5,6-dihydroxy-2,4a,5-trimethyl-3,4,6,7,8,8a-hexahydro-2H-naphthalene-1-carbaldehyde 162868594 Click to see CC1CCC2(C(C1(CC(=O)C3=COC=C3)C=O)CCC(C2(C)O)O)C 348.40 unknown https://doi.org/10.1016/0031-9422(95)00624-9
2-(5,6-dihydroxy-1,2,4a,5-tetramethyl-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl)-1-(furan-3-yl)ethanone 14109744 Click to see CC1CCC2(C(C1(C)CC(=O)C3=COC=C3)CCC(C2(C)O)O)C 334.40 unknown https://doi.org/10.1016/S0031-9422(96)00815-1
https://doi.org/10.1016/0031-9422(95)00624-9
2-[(1S,2R,4aR,5R,6R,8aR)-5,6-dihydroxy-1,2,4a,5-tetramethyl-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-1-(furan-3-yl)ethanone 14109746 Click to see CC1CCC2(C(C1(C)CC(=O)C3=COC=C3)CCC(C2(C)O)O)C 334.40 unknown https://doi.org/10.1016/S0031-9422(96)00815-1
https://doi.org/10.1016/0031-9422(95)00624-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(95)00624-9
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(95)00624-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(96)00815-1

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