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Abutilon pakistanicum

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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 UUID6440065d31ed9227278137
Scientific name Abutilon pakistanicum
Authority Jafri & Ali
First published in Fl. Karachi : 220 (1966)

Description Top

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Synonyms Top

Scientific name Authority First published in
Abutilon cornutum (Humb. & Bonpl. ex Willd.) Sweet Hort. Brit. , ed. 2: 65 (1830)
Abutilon cornutum Dalzell ex T.Cooke Fl. Bombay 98.
Sida cornuta Humb. & Bonpl. ex Willd. Enum. Pl. [Willdenow] 724. 1809

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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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-0000512159
Tropicos 19602697
KEW urn:lsid:ipni.org:names:323558-2
The Plant List kew-2610854
Open Tree Of Life 6116927
IPNI 323558-2
GBIF 3936891
EOL 2884890

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
New Glycosidic Constituents of <i>Abutilon pakistanicum</i> Bakhat Ali, Itrat Fatima, Abdul Malik, Zaheer Ahmed Wiley 11-Nov-2010
doi:10.1002/HLCA.201000075
Flavonoidal C-Glycosides from Abutilon pakistanicum Zaheer Ahmed, Munawar Hussain, Durey Nayab Zahra, Abdul Malik, Asam Ejaz, Hina Siddiqui, Muhammad Iqbal Choudhary The Japan Institute of Heterocyclic Chemistry 16-Feb-2009
doi:10.3987/COM-07-11184
A New Pentacyclic Triterpene from Abutilon pakistanicum Zaheer Ahmed, Syed Najam-ul-Hussain Kazmi, Abdul Malik American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50071A032

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 / Tigliane and ingenane diterpenoids
[(1R,2R,6S,10R,11R,13S,14R,15R)-13-acetyloxy-8-formyl-1-hydroxy-4,12,12,15-tetramethyl-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] 2-(methylamino)benzoate 162901456 Click to see CC1C(C2(C(C2(C)C)C3C1(C4C=C(C(=O)C4CC(=C3)C=O)C)O)OC(=O)C)OC(=O)C5=CC=CC=C5NC 521.60 unknown https://doi.org/10.1021/NP50071A032
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(6aR,6bR,8aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol 145706026 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1021/NP50071A032
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1021/NP50071A032
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1021/NP50071A032
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/10.1021/NP50071A032
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
6,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 24860198 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=CC(=C(C=C3O2)O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.3987/COM-07-11184
6,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]chromen-4-one 24860199 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=CC(=C(C=C3O2)O)O)C4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.3987/COM-07-11184
6,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 74336038 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=CC(=C(C=C3O2)O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.3987/COM-07-11184
6,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]chromen-4-one 74336039 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=CC(=C(C=C3O2)O)O)C4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.3987/COM-07-11184
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
[(2S,3R,4R,5S)-3,4-dihydroxy-5-[4-(5,6,7-trihydroxy-4-oxochromen-2-yl)phenoxy]oxolan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 102258261 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(O2)OC3=CC=C(C=C3)C4=CC(=O)C5=C(O4)C=C(C(=C5O)O)O)O)O)O 564.50 unknown https://doi.org/10.1002/HLCA.201000075
[3,4-Dihydroxy-5-[4-(5,6,7-trihydroxy-4-oxochromen-2-yl)phenoxy]oxolan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 162894065 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(O2)OC3=CC=C(C=C3)C4=CC(=O)C5=C(O4)C=C(C(=C5O)O)O)O)O)O 564.50 unknown https://doi.org/10.1002/HLCA.201000075
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(1S,2S,4S,5S,6R,10S)-10-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-methoxyoxan-2-yl]oxy-5-hydroxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-2-yl]methyl 3,4-dimethoxybenzoate 102258263 Click to see COC1C(C(C(OC1OC2C3C(C=CO2)C(C4C3(O4)COC(=O)C5=CC(=C(C=C5)OC)OC)O)CO)O)O 540.50 unknown https://doi.org/10.1002/HLCA.201000075
[(1S,2S,4S,5S,6R,10S)-5-hydroxy-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-2-yl]methyl 3,4-dimethoxybenzoate 102258262 Click to see COC1=C(C=C(C=C1)C(=O)OCC23C4C(C=COC4OC5C(C(C(C(O5)CO)O)O)O)C(C2O3)O)OC 526.50 unknown https://doi.org/10.1002/HLCA.201000075
[10-[4,5-Dihydroxy-6-(hydroxymethyl)-3-methoxyoxan-2-yl]oxy-5-hydroxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-2-yl]methyl 3,4-dimethoxybenzoate 163085168 Click to see COC1C(C(C(OC1OC2C3C(C=CO2)C(C4C3(O4)COC(=O)C5=CC(=C(C=C5)OC)OC)O)CO)O)O 540.50 unknown https://doi.org/10.1002/HLCA.201000075
[5-Hydroxy-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-2-yl]methyl 3,4-dimethoxybenzoate 163049405 Click to see COC1=C(C=C(C=C1)C(=O)OCC23C4C(C=COC4OC5C(C(C(C(O5)CO)O)O)O)C(C2O3)O)OC 526.50 unknown https://doi.org/10.1002/HLCA.201000075

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