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Nepeta suavis

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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 UUID643fe46202d5a182260158
Scientific name Nepeta suavis
Authority Stapf
First published in Bull. Misc. Inform. Kew 1896: 19 (1896)

Description Top

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Synonyms Top

Scientific name Authority First published in
Afridia nepetiformis Duthie J. Bombay Nat. Hist. Soc. 11: 696 (1898)
Afridia suavis K.Schum. Just's Bot. Jahresber. 27(1): 535 (1901)

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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-0000251380
Tropicos 50311781
KEW urn:lsid:ipni.org:names:452761-1
The Plant List kew-135002
Open Tree Of Life 6082837
IPNI 452761-1
GBIF 5609616

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
Nepetolide: A New Diterpene from Nepeta suavis Javid Hussain, Farman Ullah, Hidayat Hussain, Tasleem Hussain, M. Raza Shah Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNB-2008-0518
Nepetadiol, a new triterpenediol from Nepeta suavis F. U. Khan, J. Hussain, I. U. Khan, R. Ullah, I. Ali, Z. Muhammad, H. Hussain, M. R. Shah Springer Science and Business Media LLC 07-Jun-2011
doi:10.1007/S10600-011-9890-8

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 / Triterpenoids
(3S,5S,8R,9R,10R,13R,14R,16R,17R)-4,4,8,10,13-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,7,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,16-diol 162983992 Click to see CC(CCC=C(C)C)C1C(CC2C1(CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)O 444.70 unknown https://doi.org/10.1007/S10600-011-9890-8
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1515/ZNB-2008-0518
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1515/ZNB-2008-0518
> 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/10.1515/ZNB-2008-0518
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/10.1515/ZNB-2008-0518
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/10.1515/ZNB-2008-0518
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/10.1515/ZNB-2008-0518
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,4S,5S,8R,9S,10R,12R)-9-[2-(furan-3-yl)ethyl]-5-hydroxy-9,10,12-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 162916213 Click to see CC1CC2C3(C(C1(C)CCC4=COC=C4)CCC(C3C(=O)O2)O)C 332.40 unknown https://doi.org/10.1515/ZNB-2008-0518
9-[2-(Furan-3-yl)ethyl]-5-hydroxy-9,10,12-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 162916212 Click to see CC1CC2C3(C(C1(C)CCC4=COC=C4)CCC(C3C(=O)O2)O)C 332.40 unknown https://doi.org/10.1515/ZNB-2008-0518

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