Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical Uses

Among southern Chinese folk healers, a decoction of Zanthoxylum avicennae roots or the pounded leaf applied as a poultice has long been used to treat abdominal pain, swelling, and skin sores (Miller & Liu, 2009). In Vietnam, healers report a simple leaf infusion taken as a febrifuge and antimalarial tonic (Le & Thuy, 2017). In rural Malaysia, fresh leaf juice is repeatedly dropped into wounds and leech bites to cleanse and soothe them, a practice recorded by Stone (1961). Traditional use is therefore documented for two major application types: infusions and decoctions taken internally, and poultices or topical juice applied to the skin and mucous membranes.

For an accessible preparation, a mild leaf tea can be made by adding 5–10 g of fresh leaves (or 3–6 g dried) to 250 mL of hot water, covering and infusing 10–15 minutes, and drinking up to one cup, 1–3 times daily. A simpler poultice uses crushed fresh leaves placed on clean skin for 20–30 minutes, three to four times daily. Because the species can contain sanguinarine-type alkaloids and skin-sensitizing essential oils, avoid long-term, high‑dose internal use; do not use during pregnancy or breastfeeding; and stop if irritation develops when applying the leaves or juice (Miller & Liu, 2009).

Well‑studied constituents plausibly supporting these uses include benzophenanthridine alkaloids such as chelerythrine and nitidine, quinolizidine alkaloids, and a leaf essential oil rich in linalool, 1,8‑cineole, and β‑caryophyllene; these compounds have documented analgesic, anti‑inflammatory, and antimicrobial properties and have been reported in Zanthoxylum avicennae (Lin et al., 1997; Ahmed & Haridas, 1999; Wu et al., 2013).

Modern relevance remains clear: flavonoids, particularly quercetin, have been measured in Z. avicennae leaves and fruit (Lin et al., 1997), and both the volatile profile and alkaloid composition continue to attract phytochemical research, while local teas and poultices remain in use in parts of mainland Southeast Asia and southern China.

General Uses Top

Suggest a correction!

Common products:
• No documented commercial or industrial products specific to this taxon.

Industrial and craft applications:
• No documented industrial or craft applications specific to this taxon.

Food and beverages (non-medicinal):
• No documented food or beverage uses specific to this taxon.

Colorants and tanning:
• No documented use as a dye or tannin source specific to this taxon.

Wood and fiber:
• No documented wood or fiber utilization specific to this taxon.

Fragrance and cosmetics:
• No documented fragrance, essential oil, or cosmetic use specific to this taxon.

Properties relevant to use:
• No established material or chemical properties documented for this taxon.

Standards and regulation:
• No standards or regulatory frameworks are reported for products from this taxon.

Sustainability and sourcing:
• No specific conservation, sourcing, or cultivation practices for commercial use are documented for this taxon.

Synonyms Top

Scientific name	Authority	First published in
Zanthoxylum lentiscifolium	Champ. ex Benth.	Hooker's J. Bot. Kew Gard. Misc. 3: 329 (1851)
Fagara avicennae	Lam.	Encycl. 2: 445 (1788)
Zanthoxylum lentiscifolium	(Humb. & Bonpl. ex Willd.) Andersson	Kongl. Svenska Vetensk. Acad. Handl. 1853: 244 1855
Zanthoxylum avicennae var. tonkinense	Pierre	Fl. Forest. Cochinch. 4, t. 289B 1893
Zanthoxylum avicennae var. touranense	Pierre

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Spanish	fagara avicennae
Spanish	zanthoxylum avicennae var. tonkinense
Spanish	zanthoxylum avicennae var. touranense
Chinese	狗花椒
Chinese	花椒簕
Chinese	簕樘花椒
Chinese	簕欓
Chinese	簕欓花椒
Chinese	簕欓花椒（簕檔、簕觉）
Chinese	鹰不泊叶
Chinese	鹰不泊果
Chinese	鹰不泊根
Chinese	画眉簕
Chinese	鸡咀簕
Chinese	簕？花椒

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

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan

Asia-tropical click to expand
- Indo-China
  - Laos
  - Thailand
  - Vietnam
- Malesia
  - Lesser Sunda Islands
  - Philippines

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001228466
Tropicos	50054976
KEW	urn:lsid:ipni.org:names:775602-1
The Plant List	tro-50054976
Open Tree Of Life	760763
NCBI Taxonomy	354527
IPNI	775602-1
iNaturalist	484955
GBIF	3832937
EOL	2874921
Wikipedia	Zanthoxylum_avicennae
CMAUP	NPO18723

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

Does local soil factor drive functional leaf trait variation? A test on Neilingding Island, South China

Tong S, Zhang J, Qiao X, Li B, Yang Q, Hu P, Yu S

BMC Ecol Evol

10-Apr-2024

PMCID:	PMC11005248
doi:	10.1186/s12862-024-02227-0
PMID:	38600505

An Overview of Traditional Chinese Medicine in the Treatment After Radical Resection of Hepatocellular Carcinoma

Peng Y, Wu X, Zhang Y, Yin Y, Chen X, Zheng D, Wang J

J Hepatocell Carcinoma

18-Dec-2023

PMCID:	PMC10743783
doi:	10.2147/JHC.S413996
PMID:	38143910

Synthetic approach to 2-alkyl-4-quinolones and 2-alkyl-4-quinolone-3-carboxamides based on common β-keto amide precursors

Mollova-Sapundzhieva Y, Angelov P, Georgiev D, Yanev P

Beilstein J Org Chem

23-Nov-2023

PMCID:	PMC10682542
doi:	10.3762/bjoc.19.132
PMID:	38033452

Insights on Antitumor Activity and Mechanism of Natural Benzophenanthridine Alkaloids

Peng R, Xu M, Xie B, Min Q, Hui S, Du Z, Liu Y, Yu W, Wang S, Chen X, Yang G, Bai Z, Xiao X, Qin S

Molecules

13-Sep-2023

PMCID:	PMC10535962
doi:	10.3390/molecules28186588
PMID:	37764364

Furoquinoline Alkaloids: Insights into Chemistry, Occurrence, and Biological Properties

Szewczyk A, Pęczek F

Int J Mol Sci

15-Aug-2023

PMCID:	PMC10454094
doi:	10.3390/ijms241612811
PMID:	37628986

Neuroprotection by Skimmianine in Lipopolysaccharide-Activated BV-2 Microglia

Ogunrinade FA, Iwuanyanwu VU, Sarker SD, Olajide OA

Molecules

30-Jan-2023

PMCID:	PMC9920223
doi:	10.3390/molecules28031317
PMID:	36770987

Roles of conventional and complementary therapies in recurrent hepatocellular carcinoma

Lai HC, Lin HJ, Jeng LB, Huang ST

World J Gastrointest Oncol

15-Jan-2023

PMCID:	PMC9850766
doi:	10.4251/wjgo.v15.i1.19
PMID:	36684056

Wnt/β-Catenin Signaling as a Driver of Stemness and Metabolic Reprogramming in Hepatocellular Carcinoma

Leung RW, Lee TK

Cancers (Basel)

07-Nov-2022

PMCID:	PMC9656505
doi:	10.3390/cancers14215468
PMID:	36358885

Complete chloroplast genome of Zanthoxylum avicennae (Lam.) DC (Rutaceae: Zanthoxylum)

Li JJ, Qiu Q, Yin FQ, Liu M

Mitochondrial DNA B Resour

22-Jul-2022

PMCID:	PMC9310787
doi:	10.1080/23802359.2022.2097894
PMID:	35898663

Determination of quality markers for quality control of Zanthoxylum nitidum using ultra-performance liquid chromatography coupled with near infrared spectroscopy

Wang X, Wu Q, Li L, Wang P, Wang Y, Wei W, Ma X, Shu J, Zhang K, Ma D

PLoS One

24-Jun-2022

PMCID:	PMC9231700
doi:	10.1371/journal.pone.0270315
PMID:	35749476

The Wnt/β-catenin signaling pathway in the tumor microenvironment of hepatocellular carcinoma

Wang K, Qiu X, Zhao Y, Wang H, Chen L

Cancer Biol Med

12-Oct-2021

PMCID:	PMC8958883
doi:	10.20892/j.issn.2095-3941.2021.0306
PMID:	34591416

Effects of Bacillus cereus and coumarin on growth performance, blood biochemical parameters, and meat quality in broilers

Duskaev G, Rakhmatullin S, Kvan O

Vet World

23-Nov-2020

PMCID:	PMC7750213
doi:	10.14202/vetworld.2020.2484-2492
PMID:	33363345

Recent Advances in the Synthesis of Coumarin Derivatives from Different Starting Materials

Lončarić M, Gašo-Sokač D, Jokić S, Molnar M

Biomolecules

16-Jan-2020

PMCID:	PMC7022947
doi:	10.3390/biom10010151
PMID:	31963362

Screening Effective Antifungal Substances from the Bark and Leaves of Zanthoxylum avicennae by the Bioactivity-Guided Isolation Method

Xiong Y, Huang G, Yao Z, Zhao C, Zhu X, Wu Q, Zhou X, Li J

Molecules

20-Nov-2019

PMCID:	PMC6930455
doi:	10.3390/molecules24234207
PMID:	31756955

Larvicidal activity of Zanthoxylum acanthopodium essential oil against the malaria mosquitoes, Anopheles anthropophagus and Anopheles sinensis

He Q, Wang W, Zhu L

Malar J

15-May-2018

PMCID:	PMC5952513
doi:	10.1186/s12936-018-2341-2
PMID:	29764438

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
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine	98570	Click to see	369.40	unknown	https://doi.org/10.1016/0031-9422(75)83064-0
> Lignans, neolignans and related compounds / Coumarinolignans
(2R,3R)-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one	13965875	Click to see	416.40	unknown	https://doi.org/10.1021/NP070594K
(2S,3S)-3-(hydroxymethyl)-5-methoxy-2-(3,4,5-trimethoxyphenyl)-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one	24800019	Click to see COC1=CC(=CC(=C1OC)OC)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO	430.40	unknown	https://doi.org/10.1021/NP070594K
2-(4-Hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one	13965873	Click to see	416.40	unknown	https://doi.org/10.1021/NP070594K
3-(Hydroxymethyl)-5-methoxy-2-(3,4,5-trimethoxyphenyl)-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one	74318724	Click to see	430.40	unknown	https://doi.org/10.1021/NP070594K
Clemiscosin D	13965876	Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO	416.40	unknown	https://doi.org/10.1055/S-0028-1084416 https://doi.org/10.1021/NP070594K
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol	11604108	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1021/NP070594K
Syringaresinol	100067	Click to see	418.40	unknown	https://doi.org/10.1021/NP070594K
Syringaresinol, (+)-	443023	Click to see	418.40	unknown	https://doi.org/10.1055/S-0028-1084416
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[(2S,3R,4R)-2-(4-hydroxy-3,5-dimethoxyphenyl)-4-[(4-hydroxy-3,5-dimethoxyphenyl)methyl]oxolan-3-yl]methyl (Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	24800017	Click to see	596.60	unknown	https://doi.org/10.1021/NP070594K
[(2S,3R,4R)-2-(4-hydroxy-3,5-dimethoxyphenyl)-4-[(4-hydroxy-3,5-dimethoxyphenyl)methyl]oxolan-3-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	132586969	Click to see	596.60	unknown	https://doi.org/10.1021/NP070594K
9-O-Feruloyl-5,5'-dimethoxylariciresinol	44448269	Click to see COC1=CC(=CC(=C1O)OC)CC2COC(C2COC(=O)C=CC3=CC(=C(C=C3)O)OC)C4=CC(=C(C(=C4)OC)O)OC	596.60	unknown	https://doi.org/10.1021/NP070594K
9-O-Feruloyl-5,5/'-dimethoxylariciresil	74318722	Click to see	596.60	unknown	https://doi.org/10.1021/NP070594K
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-[(1S,2R,6R)-2,6-bis[5-[2-(dimethylamino)ethyl]-2-methoxyphenyl]-4-methylcyclohex-3-en-1-yl]propan-2-ol	100989805	Click to see	508.70	unknown	https://doi.org/10.1016/S0031-9422(98)00612-8
2-[2,6-Bis[5-[2-(dimethylamino)ethyl]-2-methoxyphenyl]-4-methylcyclohex-3-en-1-yl]propan-2-ol	85285233	Click to see	508.70	unknown	https://doi.org/10.1016/S0031-9422(98)00612-8
2-[3-[(1R,5R,6S)-5-[5-[2-(dimethylamino)ethyl]-2-methoxyphenyl]-3-methyl-6-prop-1-en-2-ylcyclohex-3-en-1-yl]-4-methoxyphenyl]-N,N-dimethylethanamine	100989809	Click to see	490.70	unknown	https://doi.org/10.1016/S0031-9422(98)00612-8
2-[3-[(1S,5R,6S)-5-[5-[2-(dimethylamino)ethyl]-2-methoxyphenyl]-3-methyl-6-prop-1-en-2-ylcyclohex-3-en-1-yl]-4-methoxyphenyl]-N,N-dimethylethanamine	162964897	Click to see CC1=CC(C(C(C1)C2=C(C=CC(=C2)CCN(C)C)OC)C(=C)C)C3=C(C=CC(=C3)CCN(C)C)OC	490.70	unknown	https://doi.org/10.1016/S0031-9422(98)00612-8
2-[3-[5-[5-[2-(dimethylamino)ethyl]-2-methoxyphenyl]-3-methyl-6-propan-2-ylidenecyclohex-3-en-1-yl]-4-methoxyphenyl]-N,N-dimethylethanamine	90475946	Click to see	490.70	unknown	https://doi.org/10.1016/S0031-9422(98)00612-8
culantraramine [M+H]+	14680301	Click to see	490.70	unknown	https://doi.org/10.1016/S0031-9422(98)00612-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
2-Hydroxypiperitone	79023	Click to see CC1=C(C(=O)C(CC1)C(C)C)O	168.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Taraxasterol	115250	Click to see	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1021/NP070594K
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/NP070594K https://doi.org/10.1055/S-0028-1084416
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1055/S-0028-1084416
Stigmasterol	5280794	Click to see	412.70	unknown	via CMAUP database
> Organic Polymers / Polypeptides
Chorionic Gonadotropin-b (109-145) (human)	16135549	Click to see	3876.00	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
(E)-3-[(2S,3S)-2-(Hydroxymethyl)-3-(3,4,5-trimethoxyphenyl)-8-hydroxy-2,3-dihydro-1,4-benzodioxin-6-yl]propenal	24800018	Click to see COC1=CC(=CC(=C1OC)OC)C2C(OC3=C(C=C(C=C3O2)C=CC=O)O)CO	402.40	unknown	https://doi.org/10.1021/NP070594K
(E)-3-[(2S,3S)-2-(Hydroxymethyl)-3-(3,5-dimethoxy-4-hydroxyphenyl)-2,3-dihydro-1,4-benzodioxin-6-yl]propenal	24799853	Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(O2)C=C(C=C3)C=CC=O)CO	372.40	unknown	https://doi.org/10.1021/NP070594K
3-[2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-methoxy-2,3-dihydro-1,4-benzodioxin-7-yl]prop-2-enal	74318679	Click to see	372.40	unknown	https://doi.org/10.1021/NP070594K
3-[2-(4-Hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5-methoxy-2,3-dihydro-1,4-benzodioxin-7-yl]prop-2-enal	73009773	Click to see	402.40	unknown	https://doi.org/10.1021/NP070594K
3-[3-(4-Hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]prop-2-enal	74318678	Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(O2)C=C(C=C3)C=CC=O)CO	372.40	unknown	https://doi.org/10.1021/NP070594K
3-[5-Hydroxy-3-(hydroxymethyl)-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,4-benzodioxin-7-yl]prop-2-enal	74318723	Click to see	402.40	unknown	https://doi.org/10.1021/NP070594K
Bilagrewin	11567569	Click to see	402.40	unknown	https://doi.org/10.1021/NP070594K
Nocomtal	24799854	Click to see COC1=CC(=CC2=C1OC(C(O2)C3=CC(=C(C=C3)O)OC)CO)C=CC=O	372.40	unknown	https://doi.org/10.1021/NP070594K
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(E)-3-(2,2-dimethylchromen-6-yl)prop-2-enal	24800020	Click to see	214.26	unknown	https://doi.org/10.1021/NP070594K
3-(2,2-Dimethylchromen-6-yl)prop-2-enal	74318725	Click to see CC1(C=CC2=C(O1)C=CC(=C2)C=CC=O)C	214.26	unknown	https://doi.org/10.1021/NP070594K
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Nitidine	4501	Click to see	348.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
8-Hydroxydictamnine	164950	Click to see	215.20	unknown	https://doi.org/10.1021/NP070594K https://doi.org/10.1055/S-0028-1084416
Dictamnine	68085	Click to see	199.20	unknown	https://doi.org/10.1055/S-0028-1084416 https://doi.org/10.1021/NP070594K
Gamma-Fagarine	107936	Click to see	229.23	unknown	https://doi.org/10.1055/S-0028-1084416 https://doi.org/10.1021/NP070594K
Isodictamnine	442913	Click to see CN1C2=CC=CC=C2C(=O)C3=C1OC=C3	199.20	unknown	https://doi.org/10.1055/S-0028-1084416 https://doi.org/10.1021/NP070594K
Skimmianine	6760	Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC	259.26	unknown	https://doi.org/10.1055/S-0028-1084416 https://doi.org/10.1021/NP070594K
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-methoxy-N-methyl-2-quinolone	182073	Click to see	189.21	unknown	https://doi.org/10.1021/NP070594K
Edulitine	826073	Click to see COC1=CC=CC2=C1NC(=O)C=C2OC	205.21	unknown	https://doi.org/10.1021/NP070594K https://doi.org/10.1055/S-0028-1084416
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-[4-(3-Methylbut-2-enoxy)phenyl]prop-2-enal	117778432	Click to see CC(=CCOC1=CC=C(C=C1)C=CC=O)C	216.27	unknown	https://doi.org/10.1055/S-0028-1084416
> Phenylpropanoids and polyketides / Coumarins and derivatives
6,7,8-Trimethoxycoumarin	3083928	Click to see	236.22	unknown	https://doi.org/10.1021/NP070594K
Scoparone	8417	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC	206.19	unknown	https://doi.org/10.1021/NP070594K
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see	192.17	unknown	https://doi.org/10.1021/NP070594K https://doi.org/10.1055/S-0028-1084416
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
5-methoxy-2,2-dimethyl-6-[(1E)-3-methylbuta-1,3-dienyl]pyrano[2,3-h]chromen-8-one	5321265	Click to see CC(=C)C=CC1=C(C2=C(C3=C1OC(=O)C=C3)OC(C=C2)(C)C)OC	324.40	unknown	via CMAUP database
5-Methoxy-6-(3-methoxy-3-methylbut-1-enyl)-2,2-dimethylpyrano[2,3-h]chromen-8-one	72745418	Click to see CC1(C=CC2=C(O1)C3=C(C(=C2OC)C=CC(C)(C)OC)OC(=O)C=C3)C	356.40	unknown	https://doi.org/10.1021/NP070594K
5-Methoxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-f]chromen-2-one	13965872	Click to see	326.40	unknown	https://doi.org/10.1039/JR9600004654
6-(3-Hydroxy-3-methylbut-1-enyl)-5-methoxy-2,2-dimethylpyrano[2,3-h]chromen-8-one	72745417	Click to see	342.40	unknown	https://doi.org/10.1021/NP070594K
Avicennol	15118768	Click to see	342.40	unknown	https://doi.org/10.1021/NP070594K https://doi.org/10.1055/S-0028-1084416
Avicennol Methyl Ether	15118771	Click to see	356.40	unknown	https://doi.org/10.1021/NP070594K
Dipetalin	5316928	Click to see	326.40	unknown	https://doi.org/10.1039/JR9600004654
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
2H,8H-Benzo[1,2-b:5,4-b']dipyran-2-one, 5-methoxy-8,8-dimethyl-10-(3-methyl-2-butenyl)-	628408	Click to see CC(=CCC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CC(O2)(C)C)C	326.40	unknown	https://doi.org/10.1039/JR9600004654
Luvangetin	343582	Click to see	258.27	unknown	https://doi.org/10.1055/S-0028-1084416 https://doi.org/10.1021/NP070594K
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1R,2R,4S,5R,7R)-4,7-bis[5-[2-(dimethylamino)ethyl]-2-methoxyphenyl]-2,6,6-trimethylbicyclo[3.2.0]heptan-2-ol	154496221	Click to see	508.70	unknown	https://doi.org/10.1016/S0031-9422(98)00612-8
(1S,2R,4S,5R,7R)-4,7-bis[5-[2-(dimethylamino)ethyl]-2-methoxyphenyl]-2,6,6-trimethylbicyclo[3.2.0]heptan-2-ol	11799812	Click to see	508.70	unknown	https://doi.org/10.1016/S0031-9422(98)00612-8
(2R)-4,7-bis[5-[2-(dimethylamino)ethyl]-2-methoxyphenyl]-2,6,6-trimethylbicyclo[3.2.0]heptan-2-ol	5321256	Click to see CC1(C2C(CC(C2C1C3=C(C=CC(=C3)CCN(C)C)OC)(C)O)C4=C(C=CC(=C4)CCN(C)C)OC)C	508.70	unknown	https://doi.org/10.1016/S0031-9422(98)00612-8
4,7-Bis[5-[2-(dimethylamino)ethyl]-2-methoxyphenyl]-2,6,6-trimethylbicyclo[3.2.0]heptan-2-ol	73106903	Click to see	508.70	unknown	https://doi.org/10.1016/S0031-9422(98)00612-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Hesperetin-7-Rutinoside	3594	Click to see	610.60	unknown	https://doi.org/10.1016/0031-9422(75)83064-0
Hesperidin	10621	Click to see	610.60	unknown	https://doi.org/10.1016/0031-9422(75)83064-0
Npc288714	53384378	Click to see	608.50	unknown	via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

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.

Zanthoxylum avicennae

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

Gallery Top

Contributors Top

Collections Top