Scientific name	Authority	First published in
Jasminum vulgatius	Lam.	Fl. Franç. 2: 306 (1779)
Jasminum affine	Royle	Edwards's Bot. Reg. 31: t. 26. 1845
Jasminum officinale var. piliferum	P.Y.Pai	Acta Bot. Yunnan. 1: 155 (1979)
Jasminum officinale var. tibeticum	C.Y.Wu	Acta Bot. Yunnan. 1: 155 (1979)
Jasminum officinale var. argenteovariegatum	Weston	Bot. Univ. 1: 132. 1770
Jasminum officinale var. aureovariegatum	Weston	Bot. Univ. 1: 132. 1770
Jasminum officinale var. acutum	Stokes	Bot. Comm. 1: 20. 1830
Jasminum officinale var. pumilum	Stokes	Bot. Comm. 1: 21. 1830
Jasminum officinale var. tenuifolium	Stokes	Bot. Comm. 1: 21. 1830
Jasminum officinale var. bosphoricum	K.Koch	Linnaea 23: 594. 1850
Jasminum officinale var. affine	(Royle ex Lindl.) G.Nicholson	Ill. Dict. Gard. 2: 208 1885
Jasminum officinale f. affine	(Royle ex Lindl.) Rehder	Bibl. Cult. Trees 577 1949
Jasminum officinale var. aureum	Bean	Trees & Shrubs Brit. Isles 1: 661. 1914
Jasminum officinale f. aureovariegatum	(Weston) Rehder	Bibl. Cult. Trees 577 1949
Jasminum viminale	Salisb.	Prodr. Stirp. Chap. Allerton : 12 (1796)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	common jasmine
Arabic	قين
Arabic	سيس
Arabic	سجلاط
Arabic	ياسمين بلدي
Arabic	ياسمين شامي
Azerbaijani	dərman jasmini
azb	آغ جاسمین
Bulgarian	бял жасмин
Catalan	gessamí
Catalan	llessamí
Catalan	gessamí blanc
Welsh	jasmin yr haf
German	echter jasmin
Persian	یاس سفید
Finnish	rohtojasmiini
frr	echt jasmiin
Galician	xasmín
Hungarian	közönséges jázmin
Indonesian	melati gambir
Korean	자스미눔 오피시날레
ks	چَمبہٕ
Malayalam	ജാസ്മീനം ഒഫിസിനേൽ
Marathi	सायली
Polish	jaśmin lekarski
Punjab	یاسمین
Pashto	سپين یاسمين
Russian	Жасмин белый
sc	gesminu
Tamil	மௌவல்
Turkish	hakiki yasemin
Vietnamese	nhài thường
Chinese	耶悉茗
Chinese	素馨子
Chinese	素方花
Chinese	大花素馨花

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Algeria

Asia-temperate click to expand
- Caucasus
  - Transcaucasus
- China
  - China South-central
  - Tibet
- Middle Asia
  - Tadzhikistan
- Western Asia
  - Afghanistan
  - Iran
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
  - East Himalaya
  - Nepal
  - Pakistan
  - West Himalaya

Europe click to expand
- Northern Europe
  - Great Britain
- Southeastern Europe
  - Bulgaria
  - Italy
  - Romania
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - France
  - Portugal

Southern America click to expand
- Caribbean
  - Cuba
  - Dominican Republic
  - Haiti
  - Leeward Islands
  - Puerto Rico
  - Venezuelan Antilles

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000813314
UNII	X3314B4SYD
USDA Plants	JAOF
Tropicos	23000192
INPN	104041
Flora of Italy	3969
KEW	urn:lsid:ipni.org:names:609672-1
The Plant List	kew-351433
Missouri Botanical Garden	282951
PFAF	Jasminum officinale
Open Tree Of Life	78874
Observations.org	136385
NCBI Taxonomy	126433
NBN Atlas	NBNSYS0000033956
Nature Serve	2.139700
IPNI	609672-1
iNaturalist	164233
GBIF	3172261
Freebase	/m/05t0hfh
EPPO	IASOF
EOL	487209
USDA GRIN	20668
Wikipedia	Jasminum_officinale
CMAUP	NPO13180

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

Corythauma ayyari (Insecta, Heteroptera, Tingidae) depends on its host plant to spread in Europe

Durand M, Guilbert E

PLoS One

26-Mar-2024

PMCID:	PMC10965059
doi:	10.1371/journal.pone.0295102
PMID:	38530816

Dynamic Analysis of Chlorophyll a Fluorescence in Response to Time-Variant Excitations during Strong Actinic Illumination and Application in Probing Plant Water Loss

Chen J, Guo Y, Tan J

Plant Phenomics

16-Feb-2024

PMCID:	PMC10870241
doi:	10.34133/plantphenomics.0151
PMID:	38370572

Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species

Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E

Antibiotics (Basel)

07-Feb-2024

PMCID:	PMC10885947
doi:	10.3390/antibiotics13020163
PMID:	38391549

Alternative Crops for the European Tobacco Industry: A Systematic Review

Mavroeidis A, Stavropoulos P, Papadopoulos G, Tsela A, Roussis I, Kakabouki I

Plants (Basel)

15-Jan-2024

PMCID:	PMC10818552
doi:	10.3390/plants13020236
PMID:	38256796

Assessing deep convolutional neural network models and their comparative performance for automated medicinal plant identification from leaf images

Dey B, Ferdous J, Ahmed R, Hossain J

Heliyon

13-Dec-2023

PMCID:	PMC10767391
doi:	10.1016/j.heliyon.2023.e23655
PMID:	38187334

Pest categorisation of Pochazia shantungensis

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A

EFSA J

31-Oct-2023

PMCID:	PMC10617311
doi:	10.2903/j.efsa.2023.8320
PMID:	37915980

The significance of essential oils and their antifungal properties in the food industry: A systematic review

Abdi-Moghadam Z, Mazaheri Y, Rezagholizade-shirvan A, Mahmoudzadeh M, Sarafraz M, Mohtashami M, Shokri S, Ghasemi A, Nickfar F, Darroudi M, Hossieni H, Hadian Z, Shamloo E, Rezaei Z

Heliyon

29-Oct-2023

PMCID:	PMC10637975
doi:	10.1016/j.heliyon.2023.e21386
PMID:	37954273

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

In-vitro antibacterial, antioxidant and anti-inflammatory and In-silico ADMET, molecular docking study on Hardwickia binata phytocompunds with potential inhibitor of skin cancer protein

Manimegalai P, Selvam K, Prakash P, Kirubakaran D, Shivakumar MS, SenthilNathan S

In Silico Pharmacol

23-Sep-2023

PMCID:	PMC10517914
doi:	10.1007/s40203-023-00163-3
PMID:	37750071

Integrative management of anaplastic astrocytoma through a combination of Ayurveda and conventional care: A case report

Gautama PA, Subramanian N, Varma RG, Gangadharan GG

J Ayurveda Integr Med

11-Jul-2023

PMCID:	PMC10692369
doi:	10.1016/j.jaim.2023.100748
PMID:	37442646

Phytochemicals as Antimicrobials: Prospecting Himalayan Medicinal Plants as Source of Alternate Medicine to Combat Antimicrobial Resistance

Ashraf MV, Pant S, Khan MA, Shah AA, Siddiqui S, Jeridi M, Alhamdi HW, Ahmad S

Pharmaceuticals (Basel)

15-Jun-2023

PMCID:	PMC10302623
doi:	10.3390/ph16060881
PMID:	37375828

A review of nanomaterials from synthetic and natural molecules for prospective breast cancer nanotherapy

Kumar P, Mangla B, Javed S, Ahsan W, Musyuni P, Sivadasan D, Alqahtani SS, Aggarwal G

Front Pharmacol

19-May-2023

PMCID:	PMC10237355
doi:	10.3389/fphar.2023.1149554
PMID:	37274111

Development and Characterization of Methyl-Anthranilate-Loaded Silver Nanoparticles: A Phytocosmetic Sunscreen Gel for UV Protection

Ghazwani M, Hani U, Alqarni MH, Alam A

Pharmaceutics

08-May-2023

PMCID:	PMC10221274
doi:	10.3390/pharmaceutics15051434
PMID:	37242676

Comparison of the Polyamine Content of Five Spring Flowers with Wheat Germ as a Rich Anti-aging Polyamine Source for Preparation of Nutraceutical Products

Mohajeri M, Ayatollahi SA, Goli M, Mokhtari S, Khandan M, Nasiri A, Kobarfard F

Iran J Pharm Res

25-Apr-2023

PMCID:	PMC10728854
doi:	10.5812/ijpr-134938
PMID:	38116557

Specialized metabolites from plants as a source of new multi-target antiviral drugs: a systematic review

Ponticelli M, Bellone ML, Parisi V, Iannuzzi A, Braca A, de Tommasi N, Russo D, Sileo A, Quaranta P, Freer G, Pistello M, Milella L

Phytochem Rev

12-Mar-2023

PMCID:	PMC10008214
doi:	10.1007/s11101-023-09855-2
PMID:	37359711

Phytochemical Profile Top

Add a new one!

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 / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol	10393	Click to see C1=CC(=CC=C1CCO)O	138.16	unknown	https://doi.org/10.1248/CPB.47.1582
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Olivil	5273570	Click to see COC1=C(C=CC(=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)OC)O)O	376.40	unknown	https://doi.org/10.1248/CPB.47.1582
5-(4-Hydroxy-3-methoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-4-(hydroxymethyl)oxolan-3-ol	586733	Click to see COC1=C(C=CC(=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)OC)O)O	376.40	unknown	https://doi.org/10.1248/CPB.47.1582
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(3S)-3beta,6beta,9beta-Trimethyl-4beta-(angeloyloxy)-6,7alpha-dihydroxy-9-(methoxymethyl)-2,3,3abeta,5,6,7,9,9balpha-octahydro-4H-cyclohepta[2,1-b:3,4-c']difuran-2-one	102321417	Click to see CC=C(C)C(=O)OC1CC(C2=C(C3C1C(C(=O)O3)C)C(OC2O)(C)COC)(C)O	410.50	unknown	via CMAUP database
[(3S,3aR,4S,6S,9bS)-6-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate	101672241	Click to see CC=C(C)C(=O)OC1CC(C2=CCC(=C2C3C1C(C(=O)O3)C)C)(C)O	346.40	unknown	via CMAUP database
[(3S,3aR,4S,6S,9bS)-6-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate	101078309	Click to see CC=C(C)C(=O)OC1CC(C2=CCC(=C2C3C1C(C(=O)O3)C)C)(C)O	346.40	unknown	via CMAUP database
[(3S,3aR,4S,6S,9R,9bS)-6,9-dihydroxy-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate	15922700	Click to see CC=C(C)C(=O)OC1CC(C2=C(C3C1C(C(=O)O3)C)C(CC2=O)(C)O)(C)O	378.40	unknown	via CMAUP database
[(3S,3aR,4S,6S,9R,9bS)-6,9-dihydroxy-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate	101143220	Click to see CC=C(C)C(=O)OC1CC(C2=C(C3C1C(C(=O)O3)C)C(CC2=O)(C)O)(C)O	378.40	unknown	via CMAUP database
8alpha-Angeloyl-2alpha,4alpha,10beta-trihydroxy-6betaH,7alphaH-1(5)-guaien-12,6alpha-olide	643640	Click to see CC=C(C)C(=O)OC1CC(C2=C(C3C1C(C(=O)O3)C)C(CC2O)(C)O)(C)O	380.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives / Jasmonic acids
2-[(1R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl]acetate	25245750	Click to see CCC=CCC1C(CCC1=O)CC(=O)[O-]	209.26	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(2S)-2-(3,8-dimethylazulen-5-yl)propanoic acid	3083593	Click to see CC1=C2C=CC(=C2C=C(C=C1)C(C)C(=O)O)C	228.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(5Z)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylic acid	89887620	Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)O)CC(=O)OCCC3=CC(=C(C=C3)O)O	526.50	unknown	https://doi.org/10.1248/CPB.47.1582
(Z)-methyl 4-(2-(3,4-dihydroxyphenethoxy)-2-oxoethyl)-3-ethylidene-2-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-3,4-dihydro-2H-pyran-5-carboxylate	134688908	Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O	540.50	unknown	https://doi.org/10.1248/CPB.47.1582
methyl (4S,5E,6S)-4-[2-[(2S)-2-(3,4-dihydroxyphenyl)-2-methoxyethoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate	10840796	Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC(C3=CC(=C(C=C3)O)O)OC	570.50	unknown	https://doi.org/10.1248/CPB.47.1582
methyl (4S,5E,6S)-5-ethylidene-4-(2-methoxy-2-oxoethyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate	10788149	Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OC	418.40	unknown	https://doi.org/10.1248/CPB.47.1582
methyl (5Z)-5-ethylidene-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate	14136858	Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC=C(C=C3)O	524.50	unknown	https://doi.org/10.1248/CPB.47.1582
methyl 5-ethylidene-4-(2-methoxy-2-oxoethyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate	72726525	Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OC	418.40	unknown	https://doi.org/10.1248/CPB.47.1582
Oleoside dimethyl ester	14038300	Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OC	418.40	unknown	https://doi.org/10.1248/CPB.47.1582
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3R,3aS,7R,10E,11aS)-7-hydroxy-3,10-dimethyl-6-methylidene-3,3a,4,5,7,8,9,11a-octahydrocyclodeca[b]furan-2-one	13821246	Click to see CC1C2CCC(=C)C(CCC(=CC2OC1=O)C)O	250.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3R)-3abeta,4,5,5a,6,7,8,9,9abeta,9balpha-Decahydro-3alpha,5aalpha,9-trimethyl-6alpha,9beta-dihydroxynaphtho[1,2-b]furan-2(3H)-one	14110909	Click to see CC1C2CCC3(C(CCC(C3C2OC1=O)(C)O)O)C	268.35	unknown	via CMAUP database
Dihydrosantamarin	13895713	Click to see CC1C2CCC3(C(CC=C(C3C2OC1=O)C)O)C	250.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Costunolide derivative	54607887	Click to see CC1C2CCC(=CCC(C(=CC2OC1=O)C)O)C	250.33	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine	247	Click to see C[N+](C)(C)CC(=O)[O-]	117.15	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
(2S)-pyrrolidin-1-ium-2-carboxylate	6971047	Click to see C1CC([NH2+]C1)C(=O)[O-]	115.13	unknown	via CMAUP database
Betonicine	164642	Click to see C[N+]1(CC(CC1C(=O)[O-])O)C	159.18	unknown	via CMAUP database
Stachydrine	115244	Click to see C[N+]1(CCCC1C(=O)[O-])C	143.18	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline	305	Click to see C[N+](C)(C)CCO	104.17	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(E)-jasmone	1549019	Click to see CCC=CCC1=C(CCC1=O)C	164.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Cycloheptafurans
[(2S,5S,6R,7S,9S)-9-hydroxy-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.02,6]trideca-1(13),10-dien-7-yl] (E)-2-methylbut-2-enoate	102008485	Click to see CC=C(C)C(=O)OC1CC(C2=COC(=C2C3C1C(C(=O)O3)C)C)(C)O	348.40	unknown	via CMAUP database
[(2S,5S,6R,7S,9S)-9-hydroxy-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.02,6]trideca-1(13),10-dien-7-yl] acetate	15127111	Click to see CC1C2C(CC(C3=COC(=C3C2OC1=O)C)(C)O)OC(=O)C	308.33	unknown	via CMAUP database
2-Butenoic acid, 2-methyl-, (3S,3aR,4S,6S,9bS)-2,3,3a,5,6,9b-hexahydro-6-hydroxy-3,6,9-trimethyl-2-oxo-4H-cyclohepta(2,1-b:3,4-c')difuran-4-yl ester, (2Z)-	102008484	Click to see CC=C(C)C(=O)OC1CC(C2=COC(=C2C3C1C(C(=O)O3)C)C)(C)O	348.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
[(3R,3aR,4S,9aS,9bR)-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] acetate	102014217	Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC(=O)C	304.34	unknown	via CMAUP database
[(3S,3aR,4S,9aR,9bS)-9a-hydroxy-3,6,9-trimethyl-2,7-dioxo-3a,4,5,9b-tetrahydro-3H-azuleno[4,5-b]furan-4-yl] acetate	76764466	Click to see CC1C2C(CC(=C3C(=O)C=C(C3(C2OC1=O)O)C)C)OC(=O)C	320.30	unknown	via CMAUP database
14-Deoxylactucin	156302	Click to see CC1=C2C(C3C(C(C1)O)C(=C)C(=O)O3)C(=CC2=O)C	260.28	unknown	via CMAUP database
Austricin	6713966	Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)O	262.30	unknown	via CMAUP database
Dehydroleucodine	73440	Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)C	244.28	unknown	via CMAUP database
Hydroxyachillin	10038339	Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)O	262.30	unknown	via CMAUP database
Matricarin	3083923	Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC(=O)C	304.34	unknown	via CMAUP database
Matricin	92265	Click to see CC1C2C(CC(=C3C=CC(C3C2OC1=O)(C)O)C)OC(=O)C	306.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2R,3R,4R,5R,6R)-4-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-5-hydroxy-2-[[(1S,2S,4S,5S,6S,10S)-2-(hydroxymethyl)-10-[(2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-5-yl]oxy]-6-methyloxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	162821200	Click to see CC1C(C(C(C(O1)OC2C3C=COC(C3C4(C2O4)CO)OC5C(C(C(C(O5)CO)O)O)O)OC(=O)C=CC6=CC=C(C=C6)O)OC(=O)C=CC7=CC(=C(C=C7)O)O)O	816.80	unknown	https://doi.org/10.1248/CPB.47.1582
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetagetin-6,7-3',4'-tetramethyl Ether	5316832	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)OC	374.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Isoschaftoside	3084995	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	564.50	unknown	via CMAUP database
Schaftoside	442658	Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O	564.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Luteolin 7-glucuronide	5280601	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Kaempferol-3-O-rutinoside	5318767	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)O)O)O)O)O)O	594.50	unknown	via CMAUP database
Rutin	5280805	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)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
6-Hydroxyluteolin 7-glucoside	185766	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	464.40	unknown	via CMAUP database
Apigetrin	5280704	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	via CMAUP database
Isorhoifolin	9851181	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O	578.50	unknown	via CMAUP database
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin	5281612	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Centaureidin	5315773	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O	360.30	unknown	via CMAUP database
Pectolinarigenin	5320438	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O	314.29	unknown	via CMAUP database
Santin	5281695	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC	344.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-3,6,7,4'-tetramethoxyflavone	5318355	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC	358.30	unknown	via CMAUP database
Artemetin	5320351	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC	388.40	unknown	via CMAUP database
Eupatorin	97214	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O	344.30	unknown	via CMAUP database

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Jasminum officinale

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top