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Hypoestes serpens

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64402179cf1ac595907012
Scientific name Hypoestes serpens
Authority R.Br.
First published in Prodr. Fl. Nov. Holland. : 474 (1810)

Description Top

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Synonyms Top

Scientific name Authority First published in
Calophanes mauritianus T.Anderson J. Proc. Linn. Soc., Bot. 7: 23, nomen. 1863 [1864 publ. 1863]
Dyschoriste mauritiana Kuntze Revis. Gen. Pl. 2: 486 (1891)
Hypoestes alsine Nees Prodr. 11: 502 (1847)
Hypoestes calaminthoides Baker J. Linn. Soc., Bot. 20: 222 (1883)
Hypoestes adscendens Nees Prodr. 11: 502 (1847)
Justicia serpens Vahl Symb. Bot. 2: 2 (1791)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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

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Database ID/link to page
World Flora Online wfo-0000728655
Tropicos 102893
KEW urn:lsid:ipni.org:names:49996-1
The Plant List kew-2859477
Open Tree Of Life 6076829
IPNI 49996-1
iNaturalist 475666
GBIF 3776764
EOL 23326718
CMAUP NPO24284

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
Antifungal isopimaranes from Hypoestes serpens. Rasoamiaranjanahary L, Guilet D, Marston A, Randimbivololona F, Hostettmann K Phytochemistry 01-Sep-2003
doi:10.1016/S0031-9422(03)00154-7
PMID:12943772
Antifungal diterpenes from Hypoestes serpens (Acanthaceae). Rasoamiaranjanahary L, Marston A, Guilet D, Schenk K, Randimbivololona F, Hostettmann K Phytochemistry 01-Feb-2003
doi:10.1016/S0031-9422(02)00551-4
PMID:12620345
A new diterpene from Hypoestes serpens. Andriamihaja B, Martin MT, Rasoanaivo P, Frappier F J Nat Prod 01-Feb-2001
doi:10.1021/NP0001474
PMID:11430004

Phytochemical Profile Top

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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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Benzyl salicylate 8363 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2O 228.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S,2R,4aS,4bS,5R,8aS)-2-ethenyl-2,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9-octahydro-1H-phenanthrene-1,5-diol 10946660 Click to see CC1(CCC(C2(C1CC=C3C2CCC(C3O)(C)C=C)C)O)C 304.50 unknown https://doi.org/10.1016/S0031-9422(03)00154-7
(2R,4bS,8aS,10S)-10-hydroxy-2,4b,8,8-tetramethyl-2-vinyl-3,4,5,6,7,8a,9,10-octahydrophenanthren-1-one 10380213 Click to see CC1(CCCC2(C1CC(C3=C2CCC(C3=O)(C)C=C)O)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(03)00154-7
(4aS,4bS,7R,8S,10aS)-7-ethenyl-8-hydroxy-1,1,4a,7-tetramethyl-2,3,4b,5,6,8,10,10a-octahydrophenanthren-4-one 10266929 Click to see CC1(CCC(=O)C2(C1CC=C3C2CCC(C3O)(C)C=C)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(03)00154-7
2-Ethenyl-10-hydroxy-2,4b,8,8-tetramethyl-3,4,5,6,7,8a,9,10-octahydrophenanthren-1-one 22298414 Click to see CC1(CCCC2(C1CC(C3=C2CCC(C3=O)(C)C=C)O)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(03)00154-7
2-ethenyl-2,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9-octahydro-1H-phenanthrene-1,5-diol 85341382 Click to see CC1(CCC(C2(C1CC=C3C2CCC(C3O)(C)C=C)C)O)C 304.50 unknown https://doi.org/10.1016/S0031-9422(03)00154-7
7-Ethenyl-8-hydroxy-1,1,4a,7-tetramethyl-2,3,4b,5,6,8,10,10a-octahydrophenanthren-4-one 163057075 Click to see CC1(CCC(=O)C2(C1CC=C3C2CCC(C3O)(C)C=C)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(03)00154-7
7-Ethenyl-9-hydroxy-1,1,4a,7-tetramethyl-2,3,4b,5,6,9,10,10a-octahydrophenanthren-4-one 22297703 Click to see CC1(CCC(=O)C2(C1CC(C3=CC(CCC32)(C)C=C)O)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(03)00154-7
7beta-Hydroxyisopimara-8(14),15-dien-1-one 637317 Click to see CC1(CCC(=O)C2(C1CC(C3=CC(CCC32)(C)C=C)O)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(03)00154-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Dolabellane and neodolabellane diterpenoids
(3aR,5E,9E,12aS)-3a,6-dimethyl-1-propan-2-yl-4,7,8,11,12,12a-hexahydro-3H-cyclopenta[11]annulene-10-carboxylic acid 162967367 Click to see CC1=CCC2(CC=C(C2CCC(=CCC1)C(=O)O)C(C)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(02)00551-4
(3aR,5E,9Z,12aS)-1-isopropyl-3a,6-dimethyl-4,7,8,11,12,12a-hexahydro-3H-cyclopenta[11]annulene-10-carboxylic acid 5316958 Click to see CC1=CCC2(CC=C(C2CCC(=CCC1)C(=O)O)C(C)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(02)00551-4
(3aR,5Z,9E,12aS)-3a,6-dimethyl-1-propan-2-yl-4,7,8,11,12,12a-hexahydro-3H-cyclopenta[11]annulene-10-carboxylic acid 101229719 Click to see CC1=CCC2(CC=C(C2CCC(=CCC1)C(=O)O)C(C)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(02)00551-4
3a,6-dimethyl-1-propan-2-yl-4,7,8,11,12,12a-hexahydro-3H-cyclopenta[11]annulene-10-carboxylic acid 637233 Click to see CC1=CCC2(CC=C(C2CCC(=CCC1)C(=O)O)C(C)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(02)00551-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Fusicoccane diterpenoids
1,4-Dimethyl-8-methylidene-12-propan-2-yltricyclo[9.3.0.03,7]tetradecane-4,12-diol 78384935 Click to see CC(C)C1(CCC2(C1CCC(=C)C3CCC(C3C2)(C)O)C)O 306.50 unknown https://doi.org/10.1016/S0031-9422(02)00551-4
Fusicoserpenol A 5317434 Click to see CC(C)C1(CCC2(C1CCC(=C)C3CCC(C3C2)(C)O)C)O 306.50 unknown https://doi.org/10.1016/S0031-9422(02)00551-4
methyl (1R,7S,11R)-1,4-dimethyl-5,14-dioxo-12-propan-2-yltricyclo[9.3.0.03,7]tetradeca-3,8,12-triene-8-carboxylate 162941044 Click to see CC1=C2CC3(C(CC=C(C2CC1=O)C(=O)OC)C(=CC3=O)C(C)C)C 342.40 unknown https://doi.org/10.1021/NP0001474
Methyl 1,4-dimethyl-5,14-dioxo-12-propan-2-yltricyclo[9.3.0.03,7]tetradeca-3,8,12-triene-8-carboxylate 85146443 Click to see CC1=C2CC3(C(CC=C(C2CC1=O)C(=O)OC)C(=CC3=O)C(C)C)C 342.40 unknown https://doi.org/10.1021/NP0001474
Serpendione 10450072 Click to see CC1=C2CC3(C(CC=C(C2CC1=O)C(=O)OC)C(=CC3=O)C(C)C)C 342.40 unknown https://doi.org/10.1021/NP0001474
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2'-Hydroxyflavone 161860 Click to see C1=CC=C(C(=C1)C2=CC(=O)C3=CC=CC=C3O2)O 238.24 unknown via CMAUP database
5-Hydroxyflavone 68112 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=CC=C3O2)O 238.24 unknown via CMAUP database
Flavone 10680 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=CC=CC=C3O2 222.24 unknown via CMAUP database
Primetin 11055 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=CC(=C3O2)O)O 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5-Dihydroxyflavone 5393151 Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=CC=C3O2)O)O 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Clitorin 11592917 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / Monohydroxyflavonoids
4'-Hydroxyflavone 229016 Click to see C1=CC=C2C(=C1)C(=O)C=C(O2)C3=CC=C(C=C3)O 238.24 unknown via CMAUP database

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