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Jasminum lanceolarium

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644049c4c46da211360358
Scientific name Jasminum lanceolarium
Authority Roxb.
First published in Hort. Bengal. 3 (1814), nomen; Fl. Ind., ed. Carey & Wall., i. 97 (1820);Fl.Ind.,ed. Carey, i. 98 (1832).

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Jasminum lanceolarium var. puberulum Hemsl. J. Linn. Soc., Bot. 26(173): 78 1889
Jasminum lanceolarium f. unifoliolatum Hand.-Mazz. Symb. Sin. 7(4): 1012 1936

Common names Top

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Language Common/alternative name
Tamil அசாமிய தேநீர் மல்லி
Chinese 破骨风
Chinese 北清香藤
Chinese 披針葉茉莉花
Chinese 清香藤
Chinese 光清香藤
Chinese 川清茉莉

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001087401
Tropicos 23000953
The Plant List tro-23000953
Open Tree Of Life 1070451
NCBI Taxonomy 310427
IPNI 609574-1
iNaturalist 553467
GBIF 3683761
USDA GRIN 405181

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China Lu Z, Chen H, Lin C, Ou G, Li J, Xu W J Ethnobiol Ethnomed 21-Jun-2022
PMCID:PMC9210605
doi:10.1186/s13002-022-00544-6
PMID:35729593
Multifloroside Suppressing Proliferation and Colony Formation, Inducing S Cell Cycle Arrest, ROS Production, and Increasing MMP in Human Epidermoid Carcinoma Cell Lines A431 Zhang X, Li Y, Feng Z, Zhang Y, Gong Y, Song H, Ding X, Yan Y Molecules 18-Dec-2019
PMCID:PMC6983163
doi:10.3390/molecules25010007
PMID:31861384
Prioritizing fodder species based on traditional knowledge: a case study of mithun (Bos frontalis) in Dulongjiang area, Yunnan Province, Southwest China Geng Y, Hu G, Ranjitkar S, Wang Y, Bu D, Pei S, Ou X, Lu Y, Ma X, Xu J J Ethnobiol Ethnomed 04-May-2017
PMCID:PMC5418811
doi:10.1186/s13002-017-0153-z
PMID:28472968
A Newly Identified Passive Hyperaccumulator Eucalyptus grandis × E. urophylla under Manganese Stress Xie Q, Li Z, Yang L, Lv J, Jobe TO, Wang Q PLoS One 01-Sep-2015
PMCID:PMC4556624
doi:10.1371/journal.pone.0136606
PMID:26327118
Plant-derived triterpenoids and analogues as antitumor and anti-HIV agents Kuo RY, Qian K, Morris-Natschke SL, Lee KH Nat Prod Rep 13-Aug-2009
PMCID:PMC3773821
doi:10.1039/b810774m
PMID:19779642
Two new flavanone glycosides of Jasminum lanceolarium and their anti-oxidant activities. Sun JM, Yang JS, Zhang H Chem Pharm Bull (Tokyo) 01-Mar-2007
doi:10.1248/CPB.55.474
PMID:17329896
Four New Secoiridoid Glucosides from <i>Jasminum </i><i>urophyllum</i> Ya-Ching Shen, Pei-Wen Hsieh American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP960719D

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
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3S,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496911 Click to see 742.70 unknown https://doi.org/10.1248/CPB.55.474
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(4S,5E,6S)-5-[2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxyethylidene]-4-(2-methoxy-2-oxoethyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylic acid 162848865 Click to see COC(=O)CC1C(=COC(C1=CCOC(=O)C=CC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)C(=O)O 582.50 unknown https://doi.org/10.1021/NP960719D
(4S,5E,6S)-5-[2-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxyethylidene]-4-(2-methoxy-2-oxoethyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylic acid 163072529 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC=C2C(C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CC(=O)OC)O 596.50 unknown https://doi.org/10.1021/NP960719D
(4S,5E,6S)-5-[2-[(Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxyethylidene]-4-(2-methoxy-2-oxoethyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylic acid 102065495 Click to see 596.50 unknown https://doi.org/10.1021/NP960719D
(4S,5E,6S)-5-[2-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyethylidene]-4-(2-methoxy-2-oxoethyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylic acid 102065496 Click to see COC(=O)CC1C(=COC(C1=CCOC(=O)C=CC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C(=O)O 566.50 unknown https://doi.org/10.1021/NP960719D
Jaslanceoside B, >=95% (LC/MS-ELSD) 98277439 Click to see COC(=O)CC1C(=COC(C1=CCOC(=O)C=CC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C(=O)O 566.50 unknown https://doi.org/10.1021/NP960719D
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-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-carbaldehyde 124407318 Click to see 440.70 unknown https://doi.org/10.1248/CPB.55.474
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1248/CPB.55.474
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1248/CPB.55.474
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 154497544 Click to see 372.40 unknown https://doi.org/10.1248/CPB.55.474
Syringin 5316860 Click to see 372.40 unknown https://doi.org/10.1248/CPB.55.474

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