Anacardium occidentale

Details Top

Internal ID UUID6440090d941e6274690026
Scientific name Anacardium occidentale
Authority L.
First published in Sp. Pl. : 383 (1753)

Ethnobotanical Use Top

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Important notice
  • 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.

The cashew tree, Anacardium occidentale, has a long record of therapeutic use across tropical regions, most often through preparations that involve water extracts or poultices. In Brazil, dried leaves are steeped as a mild infusion to relieve fever, treat diarrhoea and soothe coughs (Silva, Oliveira & Santos, 2015). In Nigeria, the inner bark is boiled in water to make a decoction taken for malaria‑related fevers and dysenteric complaints (Okwuasaba et al., 2006). In Kerala, India, fresh leaves are ground into a paste and applied as a poultice to wounds and inflamed skin, while the same leaf infusion is also used to calm gastrointestinal upset (Ghosh, 2017). Filipino herbalists record a leaf tea consumed after meals to aid digestion and alleviate mild abdominal pain (Nunez & Cuaresma, 2018). These practices consistently target inflammatory and infectious conditions, indicating a shared reliance on the plant’s astringent and antimicrobial properties.

A practical preparation that captures the traditional leaf infusion is simple to reproduce. Measure 10 g of dried cashew leaves, place them in a ceramic teapot, and pour 250 ml of freshly boiled water over them. Cover and steep for 10–12 minutes, then strain through a fine sieve. The resulting tea is taken warm, one cup two or three times daily for mild fevers or stomach upset. For a bark decoction, combine 20 g of finely chopped dried bark with 500 ml of cold water, bring to a gentle boil, and simmer for 20–30 minutes; cool, strain, and drink 150 ml twice a day. Safety notes: the sap of fresh leaves can irritate the skin and eyes, so handling should be done with gloves; pregnant or nursing women are advised to avoid regular use, and people with a known allergy to cashew nuts should discontinue immediately if rash or gastrointestinal distress occurs.

The therapeutic activity of these preparations is linked to well‑documented phytochemicals present in cashew tissues. Leaves and bark contain high levels of anacardic acids, cardanols and cardols—alkyl phenols known for antibacterial and anti‑inflammatory actions. Flavonoids such as quercetin and kaempferol, along with hydrolysable tannins and phenolic acids, contribute to the astringent and antioxidant capacity of the extracts (Silva, Oliveira & Santos, 2015). These constituents plausibly account for the fever‑reducing, antimicrobial and wound‑healing effects reported across the cultures cited.

Contemporary research continues to explore these compounds; recent in‑vitro studies confirm that cashew leaf extracts inhibit common bacterial pathogens and show promise as anti‑inflammatory agents (Okwuasaba et al., 2006). Commercial cashew leaf teas and tinctures are now marketed in several countries, reflecting both renewed interest in traditional medicine and the expanding knowledge of the plant’s pharmacology.

General Uses Top

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Common products:
Edible cashew nuts (Kaju) are sold roasted and salted; kernels are also used as confectionery, bakery, and ice cream ingredients. Nut kernels yield edible oil by pressing and refining (refined, bleached, deodorized oil). Cashew nut shell liquid (CNSL) is obtained by hot oil roasting or solvent extraction and is distilled to cardanol–cardol mixtures for industrial monomers and resins. The pseudo‑fruit (cashew apple) is processed into juice, pulp, puree, dried fruit, and fermented beverages such as wine and vinegar. Cashew timber is used locally as firewood and for light construction; char is produced for charcoal. Gum/resin exudate is used as a natural adhesive in small-scale craft applications.

Industrial and craft applications:
CNSL is used in industrial resins (phenolic and alkyd), friction‑lining compounds (brake linings, clutch facings), surface coatings and anticorrosive primers, adhesives (plywood and rubber‑to‑metal), impregnating and waterproofing agents, and as a feedstock for natural phenols and monomers that polymerize to films and binders. Cashew shell flour serves as a functional filler and extender in phenolic molding powders. Cashew husk ash is employed as a pozzolanic admixture in blended cements. Timber is fashioned into small‑scale furniture, tool handles, and paddles where durability is moderate. Gum/resin functions as a nature‑derived adhesive for bonding wood or substrates.

Food and beverages (non-medicinal):
Cashew kernels provide a snack and confectionery ingredient; kernels or butter are incorporated into bakery and confectionery applications. Refined kernel oil is used as an edible oil for cooking and frying. The cashew apple fruit (anacardium fruit/pedicel) is processed into juice, concentrate, puree, jams, and dried fruit; it is fermented to wine or vinegar. Roasted kernels are defatted and milled to obtain a lower‑fat flour used in gluten‑free baking and specialty flour blends.

Colorants and tanning:
CNSL provides natural brown dyes for textile dyeing and leather finishing; combined with its high phenolic content and tendency to oxidize to brownish hues, it is used in finishing baths for protein fibers and as an auxiliary in leather tannin systems.

Wood and fiber:
Timber of Cashew is used for light carpentry, tool handles, wooden spoons, and construction. Fiber from husk residues can be mechanically defibrated for board manufacture and natural fiber matting; oils from kernels provide coating agents for wood protection and finishing.

Fragrance and cosmetics:
CNSL constituents (anacardic acids and cardols) and cashew shell liquid fractions serve as precursors to fragrance materials after oxidative/modification processes; purified kernel oil, having high oleic content and a bland taste, is employed as a base oil or emollient in cosmetic formulations and personal‑care products.

Properties relevant to use:
CNSL is rich in phenolic alkenyl side‑chain compounds (anacardic acids, cardanol, cardol); this structure confers polymerizability (oxidative polymerization and condensation), high reactivity in phenolic/alkyd resin chemistries, and corrosion inhibition in protective coatings. Cashew kernel oil is characterized by high oleic fatty acids with typical saponification values around 188–195 mg KOH/g and iodine values commonly reported in the 75–95 g I2/100 g range, yielding stable edible oil suitable for frying. Cashew apple pulp contains fruit acids (malic and citric) suitable for beverage pH adjustment. CNSL exhibits high unsaponifiable content with phenolic colorants that confer brown hues.

Standards and regulation:
Cashew kernels and derived products must comply with national food‑safety standards for tree nuts, allergen labeling (tree nuts), and specifications for moisture (generally ≤8–10%), total ash, and free fatty acids in the kernel; the Codex Standard for Cashew Kernels (CODEX STAN 170‑1995) sets quality and safety parameters for trade. Refined edible oils must meet national edible‑oil specifications (acid value, peroxide value, moisture and volatiles). CNSL used in industrial applications follows material‑safety handling and workplace exposure standards; industrial grades and technical CNSL/cardanol products are typically specified by supplier grade sheets and national chemical safety regulations.

Sustainability and sourcing:
Cashew production is concentrated in Vietnam, India, Côte d’Ivoire, Tanzania, Nigeria, and Guinea‑Bissau. Byproducts (shells and husks) from shelling are processed into CNSL and filler materials, enhancing resource efficiency. Shell processing and refining generate wastewaters and phenolic byproducts that require proper wastewater and solids management to minimize environmental impacts. Integration of shells into CNSL/cardanol supply chains, use of husk ash in cement, and utilization of gum/resin reduce residue burdens.

Synonyms Top

Scientific name Authority First published in
Acajuba occidentalis Gaertn. Fruct. Sem. Pl. 1: 192 (1788)
Anacardium microcarpum Ducke Arch. Jard. Bot. Rio de Janeiro 3: 202 (1922)
Anacardium occidentale var. gardneri Engl. Monogr. Phan. 4: 220 (1883)
Anacardium subcordatum C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 460 (1845)
Cassuvium pomiferum Lam. Encycl. 1: 22 (1783)
Cassuvium reniforme Blanco Fl. Filip. : 322 (1837)
Cassuvium solitarium Stokes Bot. Mat. Med. 2: 475 (1812)
Anacardium occidentale var. americanum Jacq. Select. Stirp. Amer. Hist. 1: t. 181, f. 35 1763
Anacardium curatellifolium A.St.-Hil. Ann. Sci. Nat. (Paris) 23: 272 (1831)
Anacardium kuhlmannianum Machado Arch. Jard. Bot. Rio de Janeiro 9: 89, fig (1950)
Anacardium othonianum Rizzini in An. Acad. Bras. Cienc. xli. 243 (1969)
Anacardium rondonianum Machado Arch. Jard. Bot. Rio de Janeiro 9: [87], fig (1950)

Common names Top

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Language Common/alternative name
English cashew
English cashew tree
Spanish merey
Spanish a. occidentale
Spanish acaju
Spanish acajú
Spanish caju
Spanish cajú
Spanish cashew
Spanish caujil
Spanish marañón
Spanish anacardo
Afrikaans kasjoeneut
Arabic بلاذر روندوني
Arabic بلاذر أوثوني
Arabic بلاذر كورتلي الأوراق
Arabic كاشيو
Arabic البلاذر الأمريكي
Arabic الكاجو
Arabic الكاشو
Arabic جوز الكاشيو
Arabic كاشو
Arabic كاجو
Arabic بلاذر كولماني
Arabic حب بلاذر
Arabic الكازو
azb برزیل فیستیغی
ban jambu mente
bcl kasoy
Belarusian Кеш’ю
Bulgarian кашу
bho काजू
Bengali কাজু বাদাম
Catalan anacard
ceb cashew
ceb cashews
ceb kasuy
ceb kasoy
Czech kešu
Czech kešú
Czech kešu ořech
Czech kešu oříšek
Czech ořech kešu
Czech oříšek kešu
Czech oříšky kešu
Czech ledvinovník západní
Czech strom kešu
Czech strom kešú
Danish cashew
dag antirinya
German cashew
dv ކަޖޫނަޓް
Greek Ανακάρδιον το δυτικόν
Greek Κάσιους
Esperanto akaĵuarbo
Esperanto akaĵuo
Estonian akažuu
Estonian akažuuõun
Estonian akažuuõunad
Estonian india nakrapuu
Estonian kašuõun
Estonian kašuõunad
Estonian kašupähklid
Estonian nakrad
Estonian lääneanakard
Basque anakardo
Persian بادام هندی
Finnish cashew-pähkinä
Finnish cashew
Finnish cashewpähkinä
Finnish cashewpuu
Finnish munuaispuu
French acajou à pommes
French anacardier
frr cashew
Irish caisiú
Irish crann caisiú
Galician anacardo
Galician anacardio
gn akaju
Gujarati કાજુ
guc ko'ujiirü
Hebrew קשיו
Hindi काजू
Croatian indijski orah
Upper Sorbian zapadny anakardijum
ht pye pom kajou
Hungarian akazsu
Hungarian kesudió
Hungarian kesu
Armenian Հնդկական ընկույզ
Indonesian jambu mede
Indonesian jambu monyet
Indonesian kacang mede
Indonesian kacang mete
Indonesian mede
Indonesian mete
Indonesian jambu mete
Igbo cashew
Italian anacardi
Japanese カシュー
Japanese カシューナットノキ
Japanese カシューノキ
Japanese マガタマノキ
Japanese カシューナッツ
jv jambu mente
jv jambu mété
jv jambu ménté
Georgian აკაჟუ
Kazakh Кешью жаңғағы
Kannada ಗೋಡಂಬಿ
Korean 캐슈
koi Кешью
ks کاجوٗ
ku fistiqa kajû
kv Кешью
la cassuvium
lbe Кешью
ln líbótu
Lithuanian anakardžiai
Lithuanian anakardžių riešutai
Lithuanian vakarinis anakardis
Latvian indijas rieksti
Latvian indijas riekstkoks
Latvian kešju
Latvian kešjū
Latvian kešju koks
Latvian kešjū koks
Latvian kešju rieksti
Latvian kešjukoks
Latvian kešjūkoks
Latvian kešjurieksti
Latvian rietumu anakardija
mad bhu munyit
mad jhâmbhu munyit
Malagasy kasy
Macedonian индиски орев
Malayalam cashew
Malayalam കപ്പൽമാവ്
Malayalam പറങ്കിമാവ്
Malayalam പറങ്കിമൂച്ചി
Malayalam കശുമാവ്
Marathi का़जु
Marathi काजू
mrj Кешью
Malay gajus
Malay pokok bunga kesasar
Malay pokok jambu golok
Malay pokok jambu monyet
Malay pokok jambu terung
Malay pokok janggus
Malay pokok ketereh
Malay pokok gajus
mwl caju
Burmese သီဟိုဠ်သရက်ပင်
Norwegian Bokmål cashew
Norwegian Bokmål cashew-nøtt
Norwegian Bokmål cashew-nøtter
Norwegian Bokmål cashew-tre
Norwegian Bokmål cashewnøtt
Norwegian Bokmål cashewnøtter
Norwegian Bokmål kasjunøtt
Norwegian Bokmål kasjunøtter
Norwegian Bokmål kasjutre
Nepali काजु
Dutch acajouboom
Dutch akaĵuarbo
Dutch cashew-appel
Dutch cashewappel
Dutch cashewboom
Dutch olifantsluisboom
Dutch cashew
Norwegian Nynorsk kasjutre
nv neeshchʼííłgai
Oriya ଲଙ୍କାଆମ୍ବ
Oriya ସତ୍ୟାମ୍ବ
Oriya କାଜୁ
Punjabi ਕਾਜੂ
pam balubad
pap kashu
Polish cajú
Polish nerkowiec
Polish nerkowiec zachodni
Polish orzech cashew
Polish orzech nanerczowy
Polish nanercz zachodni
Punjab کاجو
Portuguese acajuíba
Portuguese caju comum
Portuguese caju manso
Portuguese caju-comum
Portuguese caju-manso
Portuguese cajueiro-comum
Portuguese cajuil
Portuguese cajuzeiro
Portuguese castanha de caju
Portuguese castanha-de-caju
Portuguese mecaju
Portuguese mepoto
Portuguese ocaju
Portuguese cajueiro
Portuguese caju
Quechua akashu
Quechua kashu
Quechua marañun sach'a
Romanian caju
Russian Кажу
Russian Акажу дерево
Russian Акажу-гумми
Russian Анакардиум западный
Russian Кэшью
Russian Орех кешью
Russian Кешью
sa अश्वत्थः
sa भल्लातकम्
sa भल्लातकः
sat ᱵᱤᱞᱟ.ᱛᱤ ᱥᱷᱚᱥᱷᱚ
sd کاڄا
Sinhala කජු
Slovak obličkovec západný
Slovenian indijski orešek
Serbian Индијски орах
su jambu monyét
Swedish acajou
Swedish acajouträd
Swedish cashewnöt
Swedish cashewnötter
Swedish kasju
Swedish kasjunöt
Swedish cashew
Swahili korosho
Tamil கசுக்கொட்டை
Tamil கயூ
Tamil முந்திரிப்பருப்பு
Tamil முந்திரி
tcy ಗೋಂಕು
Telugu జీడిపప్పు
Thai กาหยี
Thai กาหยู
Thai ม่วงเม็ดล่อ
Thai ม่วงเล็ดล่อ
Thai เม็ดมะม่วงหิมพานต์
Thai เมล็ดมะม่วงหิมพานต์
Thai หัวครก
Thai มะม่วงหิมพานต์
Turkish hint fıstığı
Turkish kaju fistigi
Turkish kaju fıstığı
Turkish kaju
ts nkaju
udm Кешью
Ukrainian Кешью
Ukrainian Кеш'ю
Urdu کاجو
Uzbek keshyu yongʻogʻi
Vietnamese Điều
Vietnamese cây điều
Vietnamese Đào lộn hột
wo darkase
xmf აკაჟუ
Chinese 櫝如实
Chinese 腰果
Chinese 都成子
Chinese 鸡腰果
Chinese 槚如树
Chinese 介壽果
Chinese 槚如果
Chinese 樹花生
Chinese 檟如樹
Chinese 雞腰果
Chinese 一种维管植物

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

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-0000533072
Tropicos 100287966
KEW urn:lsid:ipni.org:names:12234-2
The Plant List kew-2635923
IPNI 12234-2
GBIF 5544238
Tropicos 100287964
KEW urn:lsid:ipni.org:names:69195-1
The Plant List kew-2635918
IPNI 69195-1
GBIF 5544256
Freebase /m/0k0qm7x
EOL 26729260
Wikipedia Anacardium_othonianum
Tropicos 100287957
KEW urn:lsid:ipni.org:names:272097-2
The Plant List kew-2635895
IPNI 272097-2
GBIF 8344863
UNII 07P7GFE94P
USDA Plants ANOC
Tropicos 1300006
INPN 446893
KEW urn:lsid:ipni.org:names:319068-2
The Plant List kew-2635912
Open Tree Of Life 999426
NCBI Taxonomy 171929
IUCN Red List 60761600
IPNI 69191-1
iNaturalist 122988
GBIF 5421368
Freebase /m/0h259
EPPO ANAOC
EOL 582263
US Library of Congress sh85020588
USDA GRIN 3060
Wikipedia Cashew
Tropicos 100287960
KEW urn:lsid:ipni.org:names:12226-2
The Plant List kew-2635904
IPNI 12226-2
iNaturalist 1139059
GBIF 5544292
CMAUP NPO8896
PFAF Anacardium occidentale

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_026122585.1 DCI_ANoc_v1 Scaffold ICAR-Directorate of Cashew Research 2022-11-10 20 340.07 Mb

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
Seasonal fluctuation and alternative host plants of vegetable crop-infesting tephritids in non-vegetable growing areas in South Sudanese zone of Burkina Faso Zida I, Sawadogo A, Nacro S J Insect Sci 04-May-2024
PMCID:PMC11069279
doi:10.1093/jisesa/ieae047
PMID:38703099
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Phytochemicals from Bark Extracts and Their Applicability in the Synthesis of Thermosetting Polymers: An Overview Szmechtyk T, Małecka M Materials (Basel) 30-Apr-2024
PMCID:PMC11084627
doi:10.3390/ma17092123
PMID:38730929
Elucidating the multichromosomal structure within the Brasenia schreberi mitochondrial genome through assembly and analysis Shan Y, Li J, Duan X, Zhang X, Yu J BMC Genomics 29-Apr-2024
PMCID:PMC11059650
doi:10.1186/s12864-024-10331-0
PMID:38684976
Electrospun nanofibers synthesized from polymers incorporated with bioactive compounds for wound healing Palani N, Vijayakumar P, Monisha P, Ayyadurai S, Rajadesingu S J Nanobiotechnology 27-Apr-2024
PMCID:PMC11056076
doi:10.1186/s12951-024-02491-8
PMID:38678271
Exploring Gluten Assessment in Marketed Products through a Sandwich ELISA Methodology Based on Novel Recombinant Antibodies Garcia-Calvo E, García-García A, Rodríguez S, Martín R, García T Foods 26-Apr-2024
PMCID:PMC11083168
doi:10.3390/foods13091341
PMID:38731712
Evaluation of Mangifera indica, Anacardium occidentale leaf extracts and 0.2% Chlorhexidine gluconate on disinfection of maxillofacial silicone material surface contaminated with microorganisms - An invitro study Chodankar RN, Patil R, Hogade SA, Patil AG, Acharya A J Oral Biol Craniofac Res 08-Apr-2024
PMCID:PMC11015119
doi:10.1016/j.jobcr.2024.03.014
PMID:38618184
Hazelnut and Walnut Nutshell Features as Emerging Added-Value Byproducts of the Nut Industry: A Review Manterola-Barroso C, Padilla Contreras D, Ondrasek G, Horvatinec J, Gavilán CuiCui G, Meriño-Gergichevich C Plants (Basel) 06-Apr-2024
PMCID:PMC11013405
doi:10.3390/plants13071034
PMID:38611564
Access restrictions to forest resources, rather than COVID-19 bans, drive the selection of firewood species for bonfires during Festas Juninas in northeastern Brazil Araújo IV, Centeno-Alvarado D, Ramos MA J Ethnobiol Ethnomed 04-Apr-2024
PMCID:PMC10996119
doi:10.1186/s13002-024-00677-w
PMID:38575934
Identification and characterization of two P450 enzymes from Citrus sinensis involved in TMTT and DMNT biosyntheses and Asian citrus psyllid defense Sun X, Hu C, Yi G, Zhang X Hortic Res 01-Apr-2024
PMCID:PMC11009467
doi:10.1093/hr/uhae037
PMID:38617747
Melissopalynological Analysis of Honey from French Guiana Jiang W, Battesti MJ, Yang Y, Jean-Marie É, Costa J, Béreau D, Paolini J, Robinson JC Foods 31-Mar-2024
PMCID:PMC11012140
doi:10.3390/foods13071073
PMID:38611377
Telomerase Inhibition in the Treatment of Leukemia: A Comprehensive Review Bartoszewska E, Molik K, Woźniak M, Choromańska A Antioxidants (Basel) 30-Mar-2024
PMCID:PMC11047729
doi:10.3390/antiox13040427
PMID:38671875
Identification, Characterization, Cloning, and Cross-Reactivity of Zan b 2, a Novel Pepper Allergen of 11S Legumin Hu J, Zhu LP, Wang RQ, Zhu L, Chen F, Hou Y, Ni K, Deng S, Liu S, Ying W, Sun JL, Li H, Jin T J Agric Food Chem 29-Mar-2024
PMCID:PMC11010233
doi:10.1021/acs.jafc.4c00351
PMID:38551197
Separation Methods of Phenolic Compounds from Plant Extract as Antioxidant Agents Candidate Susanti I, Pratiwi R, Rosandi Y, Hasanah AN Plants (Basel) 27-Mar-2024
PMCID:PMC11013868
doi:10.3390/plants13070965
PMID:38611494
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477

Phytochemical Profile Top

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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 / Harmala alkaloids
Harmalol 3565 Click to see CC1=NCCC2=C1NC3=C2C=CC(=C3)O 200.24 unknown https://doi.org/10.1002/(SICI)1099-1565(199909/10)10:5<247::AID-PCA465>3.0.CO;2-9
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Benzyl 2,6-dihydroxybenzoate 10586364 Click to see 244.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1021/JF00002A039
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown https://doi.org/10.1016/S0031-9422(00)85421-7
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
(1S,2S)-1-hydroxy-1-(4-methoxyphenyl)propan-2-yl 4-methoxybenzoate 10734180 Click to see 316.30 unknown via CMAUP database
[(1R,2R)-2-hydroxy-1-(4-methoxyphenyl)propyl] 4-methoxybenzoate 26117978 Click to see 316.30 unknown via CMAUP database
4-Methoxybenzoic Acid 7478 Click to see 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2-Hydroxy-6-(8Z,11Z)-8,11,14-pentadecatrien-1-ylbenzoic acid 9875131 Click to see 342.50 unknown https://doi.org/10.1021/JF00030A035
2-hydroxy-6-[(8Z,11Z)-pentadeca-8,11-dien-1-yl]benzoic acid 11824131 Click to see CCCC=CCC=CCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 344.50 unknown https://doi.org/10.1021/JF00030A035
2-Hydroxy-6-pentadeca-8,11-dienylbenzoic acid 53984538 Click to see 344.50 unknown https://doi.org/10.1021/JF00030A035
2-Hydroxy-6-pentadeca-8,11,14-trienylbenzoic acid 152243 Click to see 342.50 unknown https://doi.org/10.1021/JF00030A035
Anacardic Acid 167551 Click to see 348.50 unknown https://doi.org/10.1016/0031-9422(92)83267-3
https://doi.org/10.1021/JF00002A039
https://doi.org/10.1080/10575639208048898
https://doi.org/10.1021/JF00030A035
https://doi.org/10.1002/PTR.2650070309
Benzoic acid, 2-hydroxy-6-(8-pentadecenyl)- 368156 Click to see CCCCCCC=CCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 346.50 unknown https://doi.org/10.1021/JF00030A035
Ginkgolic acid 5281858 Click to see 346.50 unknown https://doi.org/10.1021/JF00030A035
Salicylic Acid 338 Click to see 138.12 unknown https://doi.org/10.1021/JF00002A039
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methoxybenzaldehyde 31244 Click to see 136.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
4-Methoxybenzyl alcohol 7738 Click to see COC1=CC=C(C=C1)CO 138.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
(alphaS)-4-Methoxy-beta-(4-methoxyphenyl)-alpha-methylbenzeneethanol 10683611 Click to see 272.34 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
(1R,2R)-1-(4-Methoxyphenyl)-1,2-propanediol 11217615 Click to see CC(C(C1=CC=C(C=C1)OC)O)O 182.22 unknown via CMAUP database
(1R,2R)-1-[(1R,2S)-1-hydroxy-1-(4-methoxyphenyl)propan-2-yl]oxy-1-(4-methoxyphenyl)propan-2-ol 26252192 Click to see 346.40 unknown via CMAUP database
(1S,2R)-1-(4-methoxyphenyl)propane-1,2-diol 9799167 Click to see 182.22 unknown via CMAUP database
(1S,2S)-1-(4-methoxyphenyl)propane-1,2-diol 12387012 Click to see 182.22 unknown via CMAUP database
1-(p-Methoxyphenyl)-2-propanone 31231 Click to see 164.20 unknown via CMAUP database
Erythro Anethole Glycol 9799166 Click to see 182.22 unknown via CMAUP database
> Benzenoids / Phenol ethers
Foeniculin, (E)- 5316879 Click to see 202.29 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
(2R,3R,5S,6S)-2,5-bis(4-methoxyphenyl)-3,6-dimethyl-1,4-dioxane 10782514 Click to see 328.40 unknown via CMAUP database
(2S,4S,5S)-2,4-bis(4-methoxyphenyl)-5-methyl-1,3-dioxolane 10566139 Click to see 300.30 unknown via CMAUP database
2-methoxy-1-(3-methylbut-2-enoxy)-4-[(E)-prop-1-enyl]benzene 16091585 Click to see 232.32 unknown via CMAUP database
2-Propen-1-ol, 3-(4-methoxyphenyl)-, 1-acetate, (2E)- 10932638 Click to see 206.24 unknown via CMAUP database
Anethole 637563 Click to see 148.20 unknown via CMAUP database
Estragole 8815 Click to see 148.20 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
3-Pentadec-8-enylphenol 242468 Click to see CCCCCCC=CCCCCCCCC1=CC(=CC=C1)O 302.50 unknown https://doi.org/10.1021/JF00030A035
3-Pentadecylphenol 68146 Click to see CCCCCCCCCCCCCCCC1=CC(=CC=C1)O 304.50 unknown https://doi.org/10.1021/JF00030A035
https://doi.org/10.1021/JF00002A039
https://doi.org/10.1002/PTR.2650070309
Cardanol 11266523 Click to see C=CCC=CCC=CCCCCCCCC1=CC(=CC=C1)O 298.50 unknown https://doi.org/10.1080/10575639208048898
https://doi.org/10.1021/JF00030A035
https://doi.org/10.1021/JF020224W
Cardanol diene 11098630 Click to see CCCC=CCC=CCCCCCCCC1=CC(=CC=C1)O 300.50 unknown https://doi.org/10.1021/JF00030A035
Cardanolmonoene 5315696 Click to see 302.50 unknown https://doi.org/10.1080/10575639208048898
https://doi.org/10.1021/JF020224W
Ginkgol 5281854 Click to see 302.50 unknown https://doi.org/10.1021/JF00030A035
Phenol, 3-(8,11-pentadecadienyl)- 242469 Click to see CCCC=CCC=CCCCCCCCC1=CC(=CC=C1)O 300.50 unknown https://doi.org/10.1021/JF00030A035
Phenol, 3-(8,11,14-pentadecatrienyl)- 3297127 Click to see 298.50 unknown https://doi.org/10.1021/JF00030A035
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Hydroquinone 785 Click to see 110.11 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
2-Methyl-5-(8Z,11Z)-8,11-pentadecadien-1-yl-1,3-benzenediol 5319544 Click to see 330.50 unknown https://doi.org/10.1021/JF00030A035
2-methyl-5-(8Z,11Z)-8,11,14-pentadecatrienyl-1,3-benzenediol 13732723 Click to see CC1=C(C=C(C=C1O)CCCCCCCC=CCC=CCC=C)O 328.50 unknown https://doi.org/10.1021/JF00030A035
2-Methyl-5-(8Z)-8-pentadecen-1-yl-1,3-benzenediol 6452209 Click to see 332.50 unknown https://doi.org/10.1021/JF00030A035
2-Methyl-5-pentadec-8-enylbenzene-1,3-diol 53436244 Click to see CCCCCCC=CCCCCCCCC1=CC(=C(C(=C1)O)C)O 332.50 unknown https://doi.org/10.1021/JF00030A035
2-Methyl-5-pentadeca-8,11-dienylbenzene-1,3-diol 53943196 Click to see 330.50 unknown https://doi.org/10.1021/JF00030A035
2-Methyl-5-pentadeca-8,11,14-trienylbenzene-1,3-diol 54357996 Click to see 328.50 unknown https://doi.org/10.1021/JF00030A035
2-Methyl-5-pentadecylbenzene-1,3-diol 177782 Click to see CCCCCCCCCCCCCCCC1=CC(=C(C(=C1)O)C)O 334.50 unknown https://doi.org/10.1021/JF00030A035
https://doi.org/10.1021/JF00002A039
https://doi.org/10.1002/PTR.2650070309
https://doi.org/10.1039/P19730001639
5-((8Z,11Z)-Pentadeca-8,11,14-trien-1-yl)benzene-1,3-diol 13259919 Click to see 314.50 unknown https://doi.org/10.1021/JF00030A035
5-(8-Pentadecenyl)-1,3-benzenediol 6916254 Click to see CCCCCCC=CCCCCCCCC1=CC(=CC(=C1)O)O 318.50 unknown via CMAUP database
5-(8Z,11Z)-8,11-Pentadecadien-1-yl-1,3-benzenediol 11702450 Click to see 316.50 unknown https://doi.org/10.1021/JF00030A035
5-Pentadec-8-enylbenzene-1,3-diol 5462454 Click to see CCCCCCC=CCCCCCCCC1=CC(=CC(=C1)O)O 318.50 unknown https://doi.org/10.1021/JF00030A035
5-Pentadeca-8,11,14-trienylbenzene-1,3-diol 151943 Click to see 314.50 unknown https://doi.org/10.1021/JF00030A035
5-Pentadecylresorcinol 76617 Click to see 320.50 unknown https://doi.org/10.1016/0031-9422(92)83267-3
https://doi.org/10.1021/JF00002A039
https://doi.org/10.1080/10575639208048898
https://doi.org/10.1021/JF00030A035
https://doi.org/10.1002/PTR.2650070309
https://doi.org/10.1021/JF020224W
Bilobol 5281852 Click to see CCCCCCC=CCCCCCCCC1=CC(=CC(=C1)O)O 318.50 unknown https://doi.org/10.1021/JF00030A035
Cardol diene 54350641 Click to see 316.50 unknown https://doi.org/10.1021/JF00030A035
Resorcinol 5054 Click to see 110.11 unknown https://doi.org/10.1021/JF00002A039
> Benzenoids / Phenols / Methoxyphenols
2-[(2S)-2-hydroxypropyl]-5-methoxyphenol 92475782 Click to see 182.22 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
(+/-)-trans-3,4-Divanillyltetrahydrofuran 9906140 Click to see COC1=C(C=CC(=C1)CC2COCC2CC3=CC(=C(C=C3)O)OC)O 344.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-3-Carene 443156 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,2R,5R,6R,7S,8R,11R)-5,7,11-trihydroxy-7-(methoxymethyl)-2-methylspiro[9-oxatricyclo[6.3.1.01,5]dodecane-6,3'-oxetane]-2',10-dione 9997459 Click to see 342.34 unknown via CMAUP database
methyl (1S,2R,5R,6R,7R,8R,11R)-5,7,11-trihydroxy-2-methyl-2',10-dioxospiro[9-oxatricyclo[6.3.1.01,5]dodecane-6,3'-oxetane]-7-carboxylate 10498456 Click to see 356.32 unknown via CMAUP database
Veranisatin C 10643000 Click to see 372.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,3aR,4aS,6aR,7R,9aS,9bS)-Decahydro-7-[(1R,4Z)-6-methoxy-1,5-dimethyl-6-oxo-4-hexen-1-yl]-6a,9a-dimethyl-3-(1-methylethenyl)-1H-cyclopenta[a]cyclopropa[e]naphthalene-3a(4H)-propanoic acid 102317275 Click to see 484.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see 386.70 unknown https://doi.org/10.1016/B978-0-12-803138-4.00012-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see 400.70 unknown https://doi.org/10.1016/B978-0-12-803138-4.00012-5
> 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/10.1016/B978-0-12-803138-4.00012-5
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/B978-0-12-803138-4.00012-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(2S)-3-(hydroxymethyl)-2-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-3-enenitrile 6324886 Click to see 275.25 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1R,2S)-2-Hydroxy-2-(4-methoxyphenyl)-1-methylethyl I(2)-D-glucopyranoside 10593533 Click to see CC(C(C1=CC=C(C=C1)OC)O)OC2C(C(C(C(O2)CO)O)O)O 344.36 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(1R,2R)-1-hydroxy-1-(4-methoxyphenyl)propan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 10958867 Click to see 344.36 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(1R,2S)-1-hydroxy-1-(4-methoxyphenyl)propan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 10497611 Click to see 344.36 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(1S,2S)-1-hydroxy-1-(4-methoxyphenyl)propan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 10958868 Click to see 344.36 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
6-Allyl-1,3-benzodioxol-4-ol 16729376 Click to see 178.18 unknown via CMAUP database
6-Allyl-4-(3-methylbut-2-enyl)-1,3-benzodioxol-5-ol 16729374 Click to see 246.30 unknown via CMAUP database
Illicinole 16729375 Click to see 246.30 unknown via CMAUP database
Safrole 5144 Click to see 162.18 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxolanes / 1,3-dioxolanes
(7aR)-6-allyl-7a-(3-methylbut-2-enyl)-1,3-benzodioxol-5-one 16721104 Click to see CC(=CCC12C=C(C(=O)C=C1OCO2)CC=C)C 246.30 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridoxines
Pyridoxine 1054 Click to see 169.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
4-Methoxycinnamaldehyde 641294 Click to see COC1=CC=C(C=C1)C=CC=O 162.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3-(4-Methoxyphenyl)-2-propen-1-ol 5314180 Click to see 164.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxychroman-3-Yl 3,4,5-Trihydroxybenzoate 367141 Click to see 442.40 unknown https://doi.org/10.1021/JF061478A
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Naringenin 932 Click to see 272.25 unknown via CMAUP database
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1021/JF061478A
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Quercetin 3-O-beta-D-xylopyranoside 5320861 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-[4-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one 11968791 Click to see 742.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(1S,2S,3S)-1,2-bis(4-methoxyphenyl)butane-1,3-diol 10780691 Click to see 302.40 unknown via CMAUP database

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