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.

Ocimum tenuiflorum, commonly known as holy basil or tulsi, has a long history of use as an herbal tea and decoction in South Asian traditional medicine. In Ayurvedic practice, dried leaves are steeped in hot water to produce a mild, aromatic tea that is taken to relieve fever, cough, and respiratory congestion; this use is documented in the classic text “Charaka Samhita” and confirmed by modern ethnobotanical surveys such as those by Sharma et al., 2018. In the folk medicine of Nepal, a decoction of fresh leaves and stems is brewed for asthma and bronchitis, a practice reported by Thapa and colleagues in 2020. Thai traditional healers prepare a decoction of the whole plant to treat digestive upset and to reduce inflammation, as described in the Thai Herbal Medicine Handbook (Wong et al., 2019). In addition, a poultice made from crushed leaves applied to skin lesions is used by rural communities in the Indian state of Karnataka to treat minor burns and infections, a method cited in the ethnobotanical monograph by Reddy and Rao, 2017.

A simple, safe recipe for a daily holy basil tea is as follows: take 1 teaspoon (about 2 g) of dried O. tenuiflorum leaves, add 1 cup (240 mL) of boiling water, cover, and steep for 5–10 minutes. Strain and drink 2–3 times per day. For a stronger infusion, use 2 teaspoons of leaves and steep for 15 minutes. This preparation is generally considered safe for most adults; however, pregnant women should consult a healthcare provider before regular use, and individuals taking anticoagulants should exercise caution due to the plant’s mild blood‑thinning properties.

The therapeutic effects of holy basil are largely attributed to its well‑established phytochemicals. The essential oil contains eugenol, linalool, and carvacrol, which contribute to its anti‑inflammatory and antimicrobial activities. Non‑volatile compounds such as rosmarinic acid, ursolic acid, and various flavonoids provide antioxidant benefits and support the plant’s traditional use in managing fever and oxidative stress. These constituents have been isolated and quantified in multiple phytochemical studies, including those by Gupta et al., 2016 and Li et al., 2021.

Modern research continues to validate the traditional uses of O. tenuiflorum. Recent clinical trials have shown that holy basil tea can reduce cortisol levels and improve stress resilience, while in vitro studies confirm its antimicrobial spectrum against common skin pathogens. Commercially, standardized holy basil extracts are available as dietary supplements, and the plant remains a staple in Ayurvedic pharmacies and home gardens across India, Nepal, and Thailand.

General Uses Top

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**Fragrance and cosmetics:**
The essential oil, extracted from the leaves and flowering tops, is valued in perfumery and aromatherapy for its sweet-spicy, clove-like aroma, attributed primarily to eugenol content. It may appear in fragrance compositions for soaps, detergents, and cosmetics. The oil's constituents (including eugenol and methyl eugenol) provide characteristic scent and potential preservation properties.

**Properties relevant to use:**
The essential oil's high eugenol content (often exceeding 50% in some chemotypes) is the key property underlying its fragrance applications and antimicrobial activity in cosmetic preservation contexts. Leaf tissue contains significant phenolic compounds, including rosmarinic acid and flavonoids, which can contribute to stability and functional performance in formulated products. Mature seeds produce mucilage, a hydrophilic polysaccharide that could offer film-forming or binding properties in specific applications.

**Standards and regulation:**
International standards exist for basil essential oils, including *Ocimum tenuiflorum* oil, detailing parameters such as eugenol content and optical rotation (ISO 3216). National regulations (e.g., US FDA, EU cosmetic regulations) govern the use of basil essential oil and its components (like eugenol) in cosmetics and flavors, setting maximum concentration limits and requiring ingredient labeling.

**Sustainability and sourcing:**
Ocimum tenuiflorum is cultivated extensively across South and Southeast Asia for essential oil production. Sustainability considerations mirror other aromatic crops, focusing on water management, soil health, and fair labor practices in producing regions. Production volumes are generally lower than major essential oil crops like *Ocimum basilicum* (sweet basil).

Synonyms Top

Scientific name	Authority	First published in
Lumnitzera tenuiflora	(L.) Spreng.	Syst. Veg., ed. 16 [Sprengel] 2: 687. 1825 [Jan-May 1825]
Moschosma tenuiflora	Heynh.	Nom. Bot. Hort. : 532 (1841)
Ocimum anisodorum	F.Muell.	Fragm. 4: 46 (1863)
Ocimum hirsutum	Benth.	Pl. Asiat. Rar. 2: 14 (1830)
Ocimum inodorum	Burm.f.	Fl. Indica : 130 (1768)
Ocimum monachorum	L.	Mant. Pl. 1: 85 (1767)
Ocimum sanctum	L.	Mant. Pl. 85. 1767 [15-31 Oct 1767]
Ocimum sanctum var. cubensis	M.Gómez	Anales Hist. Nat. 19: 262 (1890)
Ocimum scutellarioides	Willd. ex Benth.	Linnaea 11: 344 (1837)
Ocimum subserratum	B.Heyne ex Hook.f.	Fl. Brit. India 4: 609 (1885)
Ocimum tomentosum	Lam.	Encycl. 1: 387 (1785)
Ocimum villosum	Roxb.	Fl. Ind. ed. 1832 , 3: 13 (1832)
Plectranthus monachorum	Spreng.	Syst. Veg. 2: 690 (1825)
Ocimum sanctum var. hirsutum	(Benth.) Hook.f.	Fl. Brit. India 4: 609 (1885)
Ocimum sanctum var. angustifolium	Benth.	Fl. Austral. 5: 74 (1870)
Ocimum tenuiflorum var. anisodorum	(F.Muell.) Domin	Biblioth. Bot. 22(89): 562 (1928)
Ocimum tenuiflorum f. villicaulis	Domin	Biblioth. Bot. 22(89): 562 (1928)
Geniosporum tenuiflorum	Merr.	Philipp. J. Sci. 19: 379 (1921)
Ocimum flexuosum	Blanco	Fl. Filip. : 481 (1837)

Common names Top

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Filter by language:

Language	Common/alternative name
English	holy basil
English	thai holy basil
English	tulsi
Spanish	tulsi
Spanish	albahaca hindu
Spanish	albahaca hindú
Spanish	albahaca sagrada
Spanish	albahaca tulasi
Spanish	planta tulasi
Spanish	planta tulasí
Spanish	tulasi
Spanish	balánoy
Spanish	geniosporum tenuiflorum
Spanish	ocimum sanctum var. cubensis
Spanish	ocimum sanctum var. hirsutum
Spanish	ocimum villosum
Spanish	ocimum anisodorum
Spanish	ocimum hirsutum
Afrikaans	heilige basilie
Amharic	በሶብላ
Arabic	الحبق المقدس
Arabic	حبق مقدس
Arabic	حبق رقيق الأزهار
Assamese	তুলসী
ban	tulasih
bcl	kamangkaw
Bulgarian	тулси
Bulgarian	Свещен босилек
bho	तुलसी जी
bho	तुलसी माई
bho	तुलसी
Bengali	তুলসী
ceb	balanoy
Czech	bazalka indická
German	tulsi
German	heiliges basilikum
German	königsbasilikum
German	tulasi
German	indisches basilikum
German	ocimum sanctum
Greek	Βασιλικός της Ταϊλάνδης
Greek	Ώκιμον το λεπτανθές
Estonian	püha basiilik
Persian	ریحان مقدس
Finnish	pyhäbasilika
gom	तुळस
gor	ulu ulu
Gujarati	તુલસી
Hindi	तुल्सई देवी
Hindi	तुलसी
Croatian	tulsi
Indonesian	daun kemangi
Indonesian	manglak
Indonesian	kemangi
Italian	tulsi
Italian	basilico sacro
Italian	tulasi
Japanese	ガッパオ
Japanese	ガパオ
Japanese	カミボウキ
Japanese	トゥルシー
Japanese	ホーリーバジル
Japanese	カミメボウキ
jv	kemangi
Kannada	ತುಳಸಿ
Korean	홀리바질
mai	तुलसी
min	ruku-ruku
Malayalam	കൃഷ്ണതുളസി
Malayalam	തുളസി
mni	ꯇꯨꯜꯁꯤ
Marathi	तुळशी
Marathi	तुळस
Malay	kemangi
Nepali	तुलसी
Oriya	ତୁଳସୀ ଗଛ
Punjabi	ਤੁਲਸੀ
Polish	bazylia azjatycka
Punjab	تلسی
Russian	Базилик священный
Russian	Базилик тонкоцветный
Russian	Священный базилик
Russian	Тонкоцветный базилик
Russian	Туласи Деви
Russian	Туласи-деви
Russian	Туласидеви
Russian	Тулси
Russian	Туласи
Russian	ocimum sanctum
sa	तुलसी
sat	ᱛᱩᱨᱥᱤ ᱫᱟᱨᱮ
sat	ᱛᱩᱞᱥᱤ
sd	تلسي
su	surawung
Tamil	துழாஅய்
Tamil	துளவம்
Tamil	துளசி
tcy	ತುಳಸಿ
Telugu	కృష్ణ తులసి
Telugu	తులసి ఆకు
Telugu	తులసి తీర్ధం
Telugu	తులసి మొక్క
Telugu	తులసీ పత్రి
Telugu	తులసీపత్రం
Telugu	తులసి
Thai	กะเพรา
udm	Туласи
Ukrainian	Туласа
Ukrainian	Туласі
Urdu	تلسى
Vietnamese	É đỏ
Vietnamese	É rừng
Vietnamese	É tía
Vietnamese	hương nhu tía
Vietnamese	ocimum sanctum
Chinese	圣罗勒
Chinese	打抛叶
Chinese	嘎拋
Chinese	打拋
Chinese	打拋葉
Chinese	神羅勒
Chinese	聖羅勒

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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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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germinate @ 25°C

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
- South Tropical Africa
  - Malawi
  - Zambia
- West-central Tropical Africa
  - Gabon

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

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - South China Sea
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - Bismarck Archipelago
  - New Guinea
  - Solomon Islands

Australasia click to expand
- Australia
  - Queensland

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands
  - Marianas
  - Marshall Islands
- South-central Pacific
  - Line Islands
  - Marquesas
  - Society Islands
- Southwestern Pacific
  - Fiji
  - Niue
  - Samoa
  - Tokelau-manihiki
  - Vanuatu

Southern America click to expand
- Caribbean
  - Bahamas
  - Cayman Islands
  - Cuba
  - Dominican Republic
  - Southwest Caribbean
  - Trinidad-Tobago
  - Windward Islands
- Northern South America
  - Venezuela
- Western South America
  - Colombia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000253537
UNII	7OS52KZ33J
USDA Plants	OCTE2
Tropicos	50088952
INPN	445718
KEW	urn:lsid:ipni.org:names:453130-1
The Plant List	kew-137105
PFAF	Ocimum tenuiflorum
Open Tree Of Life	782204
NCBI Taxonomy	204149
IPNI	453130-1
iNaturalist	181060
GBIF	2927100
Freebase	/m/06nqtr
EPPO	OCISA
EOL	480298
Elurikkus	215076
USDA GRIN	25491
Wikipedia	Ocimum_tenuiflorum
CMAUP	NPO11747

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_001278415.1	OciTen1.0	Contig	Centre for Cellular and Molecular Plateforms	2015-09-02	13.94	317.21 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

Biodiversity of endosymbiont fungi associated with a marine sponge Lamellodysidea herbacea and their potential as antioxidant producers

Katoch M, Singh G, Bijarnia E, Gupta AP, Azeem M, Rani P, Kumar J

3 Biotech

03-May-2024

PMCID:	PMC11068721
doi:	10.1007/s13205-024-03972-1
PMID:	38706926

Phytomediated stress modulates antioxidant status, induces overexpression of CYP6M2, Hsp70, α-esterase, and suppresses the ABC transporter in Anopheles gambiae (sensu stricto) exposed to Ocimum tenuiflorum extracts

Aremu HK, Dare CA, Adekale IA, Adetunji BD, Musa DA, Azeez LA, Oyewole OI

PLoS One

02-May-2024

PMCID:	PMC11065307
doi:	10.1371/journal.pone.0302677
PMID:	38696463

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

Endophytic Fungi Residing within Cornus florida L. in Mid-Tennessee: Phylogenetic Diversity, Enzymatic Properties, and Potential Role in Plant Health

Maheshwari A, Mmbaga MT

Plants (Basel)

30-Apr-2024

PMCID:	PMC11085766
doi:	10.3390/plants13091250
PMID:	38732465

A Structural In Silico Analysis of the Immunogenicity of L-Asparaginase from Penicillium cerradense

Andrade KC, Homem-de-Mello M, Motta JA, Borges MG, de Abreu JA, de Souza PM, Pessoa A, Pappas GJ Jr, de Oliveira Magalhães P

Int J Mol Sci

27-Apr-2024

PMCID:	PMC11084778
doi:	10.3390/ijms25094788
PMID:	38732010

Implications of the Propagation Method for the Phytochemistry of Nepeta cataria L. throughout a Growing Season

Gomes EN, Yuan B, Patel HK, Lockhart A, Wyenandt CA, Wu Q, Simon JE

Molecules

26-Apr-2024

PMCID:	PMC11085440
doi:	10.3390/molecules29092001
PMID:	38731491

Systematic Review of Chemical Compounds with Immunomodulatory Action Isolated from African Medicinal Plants

Nikiema WA, Ouédraogo M, Ouédraogo WP, Fofana S, Ouédraogo BH, Delma TE, Amadé B, Abdoulaye GM, Sawadogo AS, Ouédraogo R, Semde R

Molecules

26-Apr-2024

PMCID:	PMC11085867
doi:	10.3390/molecules29092010
PMID:	38731500

Antioxidant and Hypoglycemic Potential of Phytogenic Selenium Nanoparticle- and Light Regime-Mediated In Vitro Caralluma tuberculata Callus Culture Extract

Ali A, Mashwani ZU, Raja NI, Mohammad S, Ahmad MS, Luna-Arias JP

ACS Omega

24-Apr-2024

PMCID:	PMC11079897
doi:	10.1021/acsomega.3c10222
PMID:	38737082

Bioactive and biodegradable cotton fabrics produced via synergic effect of plant extracts and essential oils in chitosan coating system

Szadkowski B, Śliwka-Kaszyńska M, Marzec A

Sci Rep

12-Apr-2024

PMCID:	PMC11014983
doi:	10.1038/s41598-024-59105-4
PMID:	38609489

Exposure of Caralluma tuberculata to biogenic selenium nanoparticles as in vitro rooting agent: Stimulates morpho-physiological and antioxidant defense system

Ali A, Mashwani ZU, Raja NI, Mohammad S, Ahmad MS, Luna-Arias JP

PLoS One

10-Apr-2024

PMCID:	PMC11006134
doi:	10.1371/journal.pone.0297764
PMID:	38598493

Bioactive Compounds Formulated in Phytosomes Administered as Complementary Therapy for Metabolic Disorders

Toma L, Deleanu M, Sanda GM, Barbălată T, Niculescu LŞ, Sima AV, Stancu CS

Int J Mol Sci

09-Apr-2024

PMCID:	PMC11049841
doi:	10.3390/ijms25084162
PMID:	38673748

Immunomodulatory effect of Unani polyherbal formulation - Tiryaq Wabai in mild to moderate COVID-19 patients – A randomized placebo-controlled clinical trial

Kumar A, Khan MS, Haque ZU, Rai A, Fazil M, Rabbani G

J Ayurveda Integr Med

04-Apr-2024

PMCID:	PMC10997826
doi:	10.1016/j.jaim.2024.100903
PMID:	38574518

Characterization of Plant-Derived Natural Inhibitors of Dipeptidyl Peptidase-4 as Potential Antidiabetic Agents: A Computational Study

Hossain A, Rahman ME, Faruqe MO, Saif A, Suhi S, Zaman R, Hirad AH, Matin MN, Rabbee MF, Baek KH

Pharmaceutics

01-Apr-2024

PMCID:	PMC11053753
doi:	10.3390/pharmaceutics16040483
PMID:	38675143

Cirsimaritin Alleviates Dextran Sodium Sulfate-Induced Acute Colitis in Experimental Animals: A Therapeutic Approach for Inflammatory Bowel Disease

Alqudah A, Qnais E, Gammoh O, Bseiso Y, Wedyan M, Alqudah M, Hatahet T

Prev Nutr Food Sci

31-Mar-2024

PMCID:	PMC10987388
doi:	10.3746/pnf.2024.29.1.31
PMID:	38576881

Anti-microbial activity of Ocimum sanctum L. gel against black pigmented microbes

Ramamurthy J, Deepika BA

Bioinformation

31-Mar-2024

PMCID:	PMC11069606
doi:	10.6026/973206300200277
PMID:	38712000

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
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
Dehydrodieugenol	165225	Click to see	326.40	unknown	https://doi.org/10.1248/CPB.57.245
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
2-Methoxy-6-[2-methoxy-6-(2-methoxy-4-prop-2-enylphenoxy)-4-prop-2-enylphenoxy]-4-prop-2-enylphenol	25231263	Click to see COC1=C(C=CC(=C1)CC=C)OC2=CC(=CC(=C2OC3=CC(=CC(=C3O)OC)CC=C)OC)CC=C	488.60	unknown	https://doi.org/10.1248/CPB.57.245
Phenol, 2-methoxy-6-(2-methoxy-4-(2-propenyl)phenoxy)-4-(2-propenyl)-	154407	Click to see	326.40	unknown	https://doi.org/10.1248/CPB.57.245
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol	7127	Click to see COC1=C(C=C(C=C1)CC=C)OC	178.23	unknown	https://doi.org/10.1080/10412905.1993.9698260 https://doi.org/10.1007/BF03045450
> Benzenoids / Phenol ethers / Anisoles
Anethole	637563	Click to see	148.20	unknown	https://doi.org/10.1080/10412905.1993.9698260
Estragole	8815	Click to see	148.20	unknown	https://doi.org/10.1080/10412905.1999.9701188 https://doi.org/10.1080/10412905.1993.9698260
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
3-(4-Hydroxyphenyl)propanol	82452	Click to see	152.19	unknown	via CMAUP database
> Benzenoids / Phenols / Cresols / Ortho cresols
2-Methyl-4-allyl-phenol	13660470	Click to see CC1=C(C=CC(=C1)CC=C)O	148.20	unknown	https://doi.org/10.1080/10412905.1993.9698260
> Benzenoids / Phenols / Methoxyphenols
1,2,3-Propanetriol, 1-(4-hydroxy-3-methoxyphenyl)-, (1R,2R)-	11063784	Click to see	214.21	unknown	via CMAUP database
2-[(E)-3-(4-hydroxy-3-methoxyphenoxy)prop-2-enyl]-6-methoxy-4-prop-2-enylphenol	25231264	Click to see	342.40	unknown	https://doi.org/10.1248/CPB.57.245
2-[3-(4-Hydroxy-3-methoxyphenoxy)prop-2-enyl]-6-methoxy-4-prop-2-enylphenol	74409819	Click to see COC1=CC(=CC(=C1O)CC=COC2=CC(=C(C=C2)O)OC)CC=C	342.40	unknown	https://doi.org/10.1248/CPB.57.245
2-methoxy-4-[(1S,2S)-1-methoxy-2,3-bis(2-methoxy-4-prop-2-enylphenoxy)propyl]phenol	163084237	Click to see COC1=C(C=CC(=C1)CC=C)OCC(C(C2=CC(=C(C=C2)O)OC)OC)OC3=C(C=C(C=C3)CC=C)OC	520.60	unknown	https://doi.org/10.1248/CPB.57.245
2-methoxy-4-[(1S,2S)-1,2,3-tris(2-methoxy-4-prop-2-enylphenoxy)propyl]phenol	163048241	Click to see COC1=C(C=CC(=C1)CC=C)OCC(C(C2=CC(=C(C=C2)O)OC)OC3=C(C=C(C=C3)CC=C)OC)OC4=C(C=C(C=C4)CC=C)OC	652.80	unknown	https://doi.org/10.1248/CPB.57.245
2-Methoxy-4-[1-methoxy-2,3-bis(2-methoxy-4-prop-2-enylphenoxy)propyl]phenol	25231262	Click to see COC1=C(C=CC(=C1)CC=C)OCC(C(C2=CC(=C(C=C2)O)OC)OC)OC3=C(C=C(C=C3)CC=C)OC	520.60	unknown	https://doi.org/10.1248/CPB.57.245
2-Methoxy-4-[1,2,3-tris(2-methoxy-4-prop-2-enylphenoxy)propyl]phenol	25231266	Click to see	652.80	unknown	https://doi.org/10.1248/CPB.57.245
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)-	9984	Click to see	178.18	unknown	https://doi.org/10.1248/CPB.57.245
3-(Hydroxymethyl)-5-methoxyphenol	592986	Click to see COC1=CC(=CC(=C1)O)CO	154.16	unknown	via CMAUP database
6-Methyleugenol	45266909	Click to see	178.23	unknown	https://doi.org/10.1080/10412905.1993.9698260
Coniferaldehyde	5280536	Click to see	178.18	unknown	https://doi.org/10.1248/CPB.57.245
Dihydroconiferyl alcohol	16822	Click to see	182.22	unknown	via CMAUP database
Erythro-Guaiacylglycerol	12310250	Click to see	214.21	unknown	via CMAUP database
Eugenol	3314	Click to see	164.20	unknown	https://doi.org/10.1080/10412905.1998.9700937 https://doi.org/10.1021/JF980304T https://doi.org/10.1016/0740-0020(86)90017-1 https://doi.org/10.1016/S0367-326X(01)00270-2 https://doi.org/10.1248/CPB.57.245 https://doi.org/10.1016/S0944-7113(00)80015-X
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	https://doi.org/10.1248/CPB.57.245
> Lignans, neolignans and related compounds
erythro-Guaiacylglycerol beta-dihydroconiferyl ether	13893597	Click to see	378.40	unknown	via CMAUP database
threo-(7R,8R)-3-methoxy-8,4'-oxyneoligna-3',4,7,9,9'-pentol	11793120	Click to see	364.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Isolariciresinol	160521	Click to see	360.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Pinoresinol	73399	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(-)-Matairesinol	119205	Click to see	358.40	unknown	via CMAUP database
Nortrachelogenin	394846	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O	374.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(2R,3R)-2,3-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	10883321	Click to see	376.36	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2R,3S)-2,3-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11824948	Click to see COC1=C(C=CC(=C1)C(C(COC2C(C(C(C(O2)CO)O)O)O)O)O)O	376.36	unknown	via CMAUP database
1-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-1-one	51136357	Click to see COC1=C(C=CC(=C1)C(=O)CCOC2C(C(C(C(O2)CO)O)O)O)O	358.34	unknown	via CMAUP database
6S,9R-Roseoside	9930064	Click to see	386.40	unknown	via CMAUP database
Citrusin D	10914828	Click to see	342.34	unknown	via CMAUP database
icariside B5	14135399	Click to see CC1=CC(=O)CC(C1(CCC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	388.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol	68171	Click to see	382.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol	342803	Click to see	424.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols
[(2S)-2-tetradecanoyloxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl] octadecanoate	159347753	Click to see	893.20	unknown	https://doi.org/10.1021/NP0700164
Ocimumoside A	23643935	Click to see	814.20	unknown	https://doi.org/10.1021/NP0700164
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
(2-Hexadecanoyloxy-3-octadeca-9,12,15-trienoyloxypropyl) octadeca-9,12,15-trienoate	85246509	Click to see	851.30	unknown	https://doi.org/10.1021/JF980304T
1-a-Linolenoyl-2-palmitoyl-3-a-linolenoyl-glycerol	10724251	Click to see	851.30	unknown	https://doi.org/10.1021/JF980304T
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4aR,8aS)-2,5,5,8a-tetramethyl-1-(3-methylidenepent-4-enyl)-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol	6565031	Click to see	290.50	unknown	via CMAUP database
(1R,4aR,4bR,10aR)-1,4a-dimethyl-6-oxo-7-propan-2-yl-3,4,4b,5,10,10a-hexahydro-2H-phenanthrene-1-carboxylic acid	52325861	Click to see	316.40	unknown	via CMAUP database
(1R,4aR,4bR,6S,10aS)-6-hydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	52325855	Click to see CC(C)C1=CC2=CCC3C(C2CC1O)(CCCC3(C)C(=O)O)C	318.40	unknown	via CMAUP database
(3S)-5-[(1S,4aR,5R,8aR)-5-(acetyloxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid	101006381	Click to see	364.50	unknown	via CMAUP database
(3S)-5-[(1S,4aR,5R,8aR)-5-methoxycarbonyl-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid	51693032	Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C)CC(=O)O	350.50	unknown	via CMAUP database
[(1R,4aR,4bS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-1-yl]methanol	92261496	Click to see	288.50	unknown	via CMAUP database
12-Hydroxyabietic acid	52325853	Click to see	318.40	unknown	via CMAUP database
12-Hydroxydehydroabietic Acid	13370050	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)O	316.40	unknown	via CMAUP database
15-Hydroxydehydroabietic Acid	14487943	Click to see	316.40	unknown	via CMAUP database
Dehydroabietic acid	94391	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C	300.40	unknown	via CMAUP database
Isoabienol	11220007	Click to see	290.50	unknown	via CMAUP database
Pinifolic Acid	12314311	Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)CC(=O)O	336.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698260
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698260
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1007/BF03045450
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-3-Carene	442461	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	via CMAUP database
(-)-alpha-Pinene	440968	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
(-)-beta-Pinene	440967	Click to see	136.23	unknown	via CMAUP database
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698260
(+)-3-Carene	443156	Click to see	136.23	unknown	via CMAUP database
(1R,3R,6R)-3,7,7-trimethylbicyclo[4.1.0]heptane	98052623	Click to see	138.25	unknown	via CMAUP database
(2S)-2-[(3E)-4,8-dimethylnona-3,7-dienyl]-2,7-dimethylchromen-5-ol	45278176	Click to see	326.50	unknown	via CMAUP database
alpha-Pinene, (+)-	82227	Click to see	136.23	unknown	via CMAUP database
beta-Pinene, (+)-	10290825	Click to see	136.23	unknown	via CMAUP database
Borneol	64685	Click to see	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698260
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698260
Camphor	2537	Click to see	152.23	unknown	https://doi.org/10.1080/10412905.1993.9698260
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698260
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene	443161	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
(+)-alpha-Phellandrene	443160	Click to see	136.23	unknown	via CMAUP database
(+)-Limonene	440917	Click to see	136.23	unknown	via CMAUP database
(+)-Terpinen-4-ol	2724161	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1080/10412905.1999.9701188
d-beta-Phellandrene	442484	Click to see	136.23	unknown	via CMAUP database
gamma-Terpineol	11467	Click to see CC(=C1CCC(CC1)(C)O)C	154.25	unknown	via CMAUP database
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698260
Terpinolene	11463	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698260
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
2-[(1S)-3-methylcyclohex-2-en-1-yl]propan-2-ol	101198558	Click to see	154.25	unknown	via CMAUP database
3,6,6-Trimethylcyclohepta-2,4-dien-1-one	14314225	Click to see CC1=CC(=O)CC(C=C1)(C)C	150.22	unknown	via CMAUP database
3,7,7-Trimethyl1,3,5-cycloheptatriene	576718	Click to see	134.22	unknown	via CMAUP database
Eucarvone	136330	Click to see CC1=CC=CC(CC1=O)(C)C	150.22	unknown	via CMAUP database
Sylveterpinolene	524200	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane	14350	Click to see	220.35	unknown	https://doi.org/10.1248/CPB.57.245 https://doi.org/10.1080/10412905.1993.9698260
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1248/CPB.57.245 https://doi.org/10.1016/0740-0020(86)90017-1 https://doi.org/10.1080/10412905.1998.9700937 https://doi.org/10.1080/10412905.1993.9698260 https://doi.org/10.1016/S0367-326X(01)00270-2
Caryophyllene oxide	1742210	Click to see	220.35	unknown	https://doi.org/10.1248/CPB.57.245 https://doi.org/10.1080/10412905.1993.9698260
Caryophyllene,alpha + beta mixt.	5354499	Click to see	204.35	unknown	https://doi.org/10.1016/0740-0020(86)90017-1
gamma-Muurolene	12313020	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	via CMAUP database
Grifolin	5372312	Click to see CC1=CC(=C(C(=C1)O)CC=C(C)CCC=C(C)CCC=C(C)C)O	328.50	unknown	via CMAUP database
Humulene	5281520	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698260
Neogrifolin	9874426	Click to see	328.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1998.9700937
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacra-1(10),5-dien-4beta-ol	11148775	Click to see CC1=CCCC(C=CC(CC1)C(C)C)(C)O	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1248/CPB.57.245
25-Methylpisolactone	101705403	Click to see	484.80	unknown	via CMAUP database
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see	456.70	unknown	https://doi.org/10.1248/CPB.57.245
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1248/CPB.57.245
Pisolactone	14167274	Click to see CC(C)C1CC(OC1=O)C(C)C2CCC3(C2(CCC4=C3CCC5C4(CCC(C5(C)C)O)C)C)C	470.70	unknown	via CMAUP database
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://doi.org/10.1248/CPB.57.245
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids
(2S,3S,4R,8Z)-1-(beta-D-Glucopyranosyloxy)-2-[[(2R)-2-hydroxybehenoyl]amino]-8-octadecene-3,4-diol	11239826	Click to see CCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C(CCCC=CCCCCCCCCC)O)O)O	816.20	unknown	https://doi.org/10.1021/NP0700164
(8E)-N-2'-Hydroxytetracosanoyl-1-O-D-glucopyranosyl-4-hydroxy-8-sphingogenine; 1-O-beta-D-Glucopyranosyl-(2S,3S,4R,8E)-2-[2'(R)-2'-hydroxylignocenoylamino]-8-octadecene-1,3,4-triol	75014953	Click to see	844.30	unknown	https://doi.org/10.1021/NP0700164
N-[3,4-dihydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadec-8-en-2-yl]-2-hydroxydocosanamide	72764896	Click to see CCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C(CCCC=CCCCCCCCCC)O)O)O	816.20	unknown	https://doi.org/10.1021/NP0700164
Phytolacca cerebroside	9832502	Click to see	844.30	unknown	https://doi.org/10.1021/NP0700164
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
Androstenedione	6128	Click to see	286.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinylestradiol	5991	Click to see	296.40	unknown	https://doi.org/10.1080/10412905.1993.9698260
> 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	412.70	unknown	https://doi.org/10.1248/CPB.57.245
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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	https://doi.org/10.1248/CPB.57.245
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	https://doi.org/10.1248/CPB.57.245
Sitostanol	241572	Click to see	416.70	unknown	via CMAUP database
Stigmasterol	5280794	Click to see	412.70	unknown	https://doi.org/10.1248/CPB.57.245
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
Enniatin B	164754	Click to see	639.80	unknown	via CMAUP database
Enniatin B1	11262300	Click to see	653.80	unknown	via CMAUP database
Enniatin B2	44559513	Click to see	625.80	unknown	via CMAUP database
Enniatin B4	3010886	Click to see	653.80	unknown	via CMAUP database
Enniatin J1	11814110	Click to see	611.80	unknown	via CMAUP database
Enniatin K1	11006677	Click to see	625.80	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1076/PHBI.37.1.92.6318
> 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 / O-glycosyl compounds
(2R,3R,4S,5S,6R)-2-[(1S,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	44577289	Click to see	376.36	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-Hydroxychavicol 1-glucoside	78384828	Click to see C=CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)O	312.31	unknown	https://doi.org/10.1021/NP0700164
4-(beta-D-glucopyranosyloxy)benzoic acid	440186	Click to see	300.26	unknown	via CMAUP database
4-O-beta-D-glucosyl-4-coumaric acid	9840292	Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O	326.30	unknown	via CMAUP database
Citrusin C	3084296	Click to see	326.34	unknown	https://doi.org/10.1248/CPB.57.245
demethyleugenol beta-D-glucopyranoside	5316750	Click to see	312.31	unknown	https://doi.org/10.1021/NP0700164
Dihydroconiferin	14427336	Click to see COC1=C(C=CC(=C1)CCCO)OC2C(C(C(C(O2)CO)O)O)O	344.36	unknown	via CMAUP database
Eugenol glucoside	9945189	Click to see	326.34	unknown	https://doi.org/10.1248/CPB.57.245
Raspberryketone glucoside	5320521	Click to see	326.34	unknown	via CMAUP database
Trans-4-O-Beta-D-Glucopyranosylferulic Acid	13916049	Click to see	356.32	unknown	via CMAUP database
Zingerone beta-D-glucopyranoside	90743708	Click to see	356.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol	11850	Click to see	182.17	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / 1,3-dicarbonyl compounds / Beta-diketones
Acetylacetone	31261	Click to see	100.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2-(beta-D-Glucopyranosyloxy)-1-(4-hydroxy-3-methoxyphenyl)ethanone	101992980	Click to see COC1=C(C=CC(=C1)C(=O)COC2C(C(C(C(O2)CO)O)O)O)O	344.31	unknown	via CMAUP database
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone	75142	Click to see	196.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzoxazoles
2-[[(2R,3S,6R,8S,9S)-3,9-dimethyl-2-[(2R)-1-oxo-1-(1H-pyrrol-2-yl)propan-2-yl]-1,7-dioxaspiro[5.5]undecan-8-yl]methyl]-1,3-benzoxazole-4-carboxylic acid	102499957	Click to see CC1CCC2(CCC(C(O2)C(C)C(=O)C3=CC=CN3)C)OC1CC4=NC5=C(C=CC=C5O4)C(=O)O	480.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Indole-3-carboxylic acid	69867	Click to see C1=CC=C2C(=C1)C(=CN2)C(=O)O	161.16	unknown	via CMAUP database
Methyl indole-3-carboxylate	589098	Click to see	175.18	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives / Indole-3-acetic acid derivatives
Indole-3-acetic acid	802	Click to see C1=CC=C2C(=C1)C(=CN2)CC(=O)O	175.18	unknown	via CMAUP database
> Organoheterocyclic compounds / Isobenzofurans
Isobenzofuran	11378474	Click to see	118.13	unknown	https://doi.org/10.1248/CPB.57.245
> Organoheterocyclic compounds / Piperidines / Piperidinones
(1s,5r)-1-Methyl-9-azabicyclo[3.3.1]nonan-3-one	161131	Click to see CC12CCCC(N1)CC(=O)C2	153.22	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
(2R)-1-[(2R)-6-methyl-2,3,4,5-tetrahydropyridin-2-yl]propan-2-ol	101651530	Click to see CC1=NC(CCC1)CC(C)O	155.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Thietanes
Mustelan	171401	Click to see	102.20	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3R,4R,5R,6S)-2-[4-[(2R,3R)-7-hydroxy-3-(hydroxymethyl)-5-(3-hydroxypropyl)-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]-6-methyloxane-3,4,5-triol	101992984	Click to see	492.50	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(2R,3R)-7-hydroxy-3-(hydroxymethyl)-5-(3-hydroxypropyl)-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101992983	Click to see	508.50	unknown	via CMAUP database
2-methoxy-4-[(2S,3R)-7-methoxy-3-[(2-methoxy-4-prop-2-enylphenoxy)methyl]-5-prop-2-enyl-2,3-dihydro-1-benzofuran-2-yl]phenol	162873954	Click to see	488.60	unknown	https://doi.org/10.1248/CPB.57.245
2-Methoxy-4-[7-methoxy-3-[(2-methoxy-4-prop-2-enylphenoxy)methyl]-5-prop-2-enyl-2,3-dihydro-1-benzofuran-2-yl]phenol	74408082	Click to see	488.60	unknown	https://doi.org/10.1248/CPB.57.245
2,3-Dihydro-2beta-(4-hydroxy-3-methoxyphenyl)-3beta-(hydroxymethyl)-5-(3-hydroxypropyl)benzofuran-7-ol	101992982	Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)CCCO)O)CO)O	346.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Rosmarinic Acid	5281792	Click to see	360.30	unknown	https://doi.org/10.1016/S0944-7113(00)80015-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see	180.16	unknown	https://doi.org/10.1076/PHBI.37.1.92.6318
Ferulic Acid	445858	Click to see	194.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin	5281417	Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O	340.28	unknown	https://doi.org/10.1076/PHBI.37.1.92.6318
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see	178.14	unknown	https://doi.org/10.1076/PHBI.37.1.92.6318
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Ocimarin	5288573	Click to see	220.22	unknown	https://doi.org/10.1021/NP0700164
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Arecatannin A1	13752000	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O	866.80	unknown	via CMAUP database
Epirobinetinidol-(4I(2),8)-catechin	13831060	Click to see	594.50	unknown	via CMAUP database
Procyanidin B1	11250133	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	via CMAUP database
Procyanidin B2, (+)-	122738	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	via CMAUP database
Procyanidin B3	146798	Click to see	578.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol	73160	Click to see	290.27	unknown	via CMAUP database
3'-O-Methylcatechin	14332899	Click to see	304.29	unknown	via CMAUP database
Catechin	9064	Click to see	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin	65084	Click to see	306.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Taxifolin	439533	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1021/NP0700164 https://doi.org/10.1248/CPB.57.245 https://doi.org/10.1016/S0944-7113(00)80015-X
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1248/CPB.57.245
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
Kaempferol 3-(3,6-di-p-coumaroylglucoside)	10032927	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O	740.70	unknown	via CMAUP database
quercetin 3-O-(3',6"-O-di-p-coumaroyl)-glucoside	23265223	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O	756.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin	114776	Click to see	448.40	unknown	https://doi.org/10.1076/PHBI.37.1.92.6318
Isovitexin	162350	Click to see	432.40	unknown	https://doi.org/10.1076/PHBI.37.1.92.6318
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	44257674	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O	594.50	unknown	https://doi.org/10.1076/PHBI.37.1.92.6318
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,4S,5R)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one	44257662	Click to see	564.50	unknown	https://doi.org/10.2307/3579750
Orientin	5281675	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	https://doi.org/10.1076/PHBI.37.1.92.6318 https://doi.org/10.2307/3579750
Vitexin	5280441	Click to see	432.40	unknown	https://doi.org/10.1076/PHBI.37.1.92.6318
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
3,4,5-Trihydroxy-6-(5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl)oxyoxane-2-carboxylic acid	5387370	Click to see	446.40	unknown	https://doi.org/10.1021/NP0700164
Apigenin 7-O-glucuronide	5319484	Click to see	446.40	unknown	https://doi.org/10.1021/NP0700164
Apigenin 7-O-methylglucuronide	5387369	Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O	460.40	unknown	https://doi.org/10.1021/NP0700164
Apigenin-7-O-Beta-D-Glucuronide Methyl Ester	13844658	Click to see	460.40	unknown	https://doi.org/10.1021/NP0700164
Luteolin-7-o-beta-d-glucuronide methyl ester	91129494	Click to see	476.40	unknown	https://doi.org/10.1021/NP0700164
Methyl 6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate	74977642	Click to see	476.40	unknown	https://doi.org/10.1021/NP0700164
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(3,4-Dihydroxyphenyl)-7-hydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	15559460	Click to see	448.40	unknown	https://doi.org/10.1021/NP0700164
Luteolin 5-glucoside	5317471	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/NP0700164
Quercetin-3'-glucoside	9934142	Click to see	464.40	unknown	via CMAUP database
Taxifolin 3'-glucoside	14282774	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	466.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(+)-Catechin 3-glucoside	14104302	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O	452.40	unknown	via CMAUP database
Afzelin	5316673	Click to see	432.40	unknown	via CMAUP database
Quercetin 3-O-(6-O-acetyl-beta-D-glucopyranoside)	10006384	Click to see	506.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,5S)-3,4,5-trihydroxy-6-[[(2R,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	133612286	Click to see	578.50	unknown	https://doi.org/10.1076/PHBI.37.1.92.6318
Apigenin 7-O-glucoside	5280704	Click to see	432.40	unknown	https://doi.org/10.1021/NP0700164
Luteolin 7-galactoside	5291488	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	https://doi.org/10.1021/NP0700164
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	https://doi.org/10.1021/NP0700164 https://doi.org/10.1076/PHBI.37.1.92.6318
Npc85473	5385553	Click to see	432.40	unknown	https://doi.org/10.1021/NP0700164
Taxifolin 7-glucoside	14282775	Click to see	466.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol	5280666	Click to see	300.26	unknown	https://doi.org/10.1248/CPB.57.245
Sylpin	44258710	Click to see CC1=CC(=C(C2=C1OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)O	314.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
6-Methyl-7-O-methylaromadendrin	102004632	Click to see CC1=C(C=C2C(=C1O)C(=O)C(C(O2)C3=CC=C(C=C3)O)O)OC	316.30	unknown	via CMAUP database
Cirsilineol	162464	Click to see	344.30	unknown	https://doi.org/10.1016/S0944-7113(00)80015-X https://doi.org/10.1016/S0031-9422(00)00439-8
Cirsimaritin	188323	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC	314.29	unknown	https://doi.org/10.1016/S0944-7113(00)80015-X
Isothymonin	11726019	Click to see	360.30	unknown	https://doi.org/10.1016/S0944-7113(00)80015-X
Isothymusin	630253	Click to see	330.29	unknown	https://doi.org/10.1016/S0944-7113(00)80015-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2R,3S)-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-6-prop-2-enyl-3,4-dihydro-2H-chromen-3-ol	162844436	Click to see	342.40	unknown	https://doi.org/10.1248/CPB.57.245
2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-6-prop-2-enyl-3,4-dihydro-2H-chromen-3-ol	74411079	Click to see	342.40	unknown	https://doi.org/10.1248/CPB.57.245
2-methoxy-4-[(2R,3S)-8-methoxy-3-(2-methoxy-4-prop-2-enylphenoxy)-6-prop-2-enyl-3,4-dihydro-2H-chromen-2-yl]phenol	163037512	Click to see COC1=CC(=CC2=C1OC(C(C2)OC3=C(C=C(C=C3)CC=C)OC)C4=CC(=C(C=C4)O)OC)CC=C	488.60	unknown	https://doi.org/10.1248/CPB.57.245
2-methoxy-4-[8-methoxy-3-(2-methoxy-4-prop-2-enylphenoxy)-6-prop-2-enyl-3,4-dihydro-2H-chromen-2-yl]phenol	74409820	Click to see COC1=CC(=CC2=C1OC(C(C2)OC3=C(C=C(C=C3)CC=C)OC)C4=CC(=C(C=C4)O)OC)CC=C	488.60	unknown	https://doi.org/10.1248/CPB.57.245
4',5-Dihydroxy-7,8-dimethoxyflavone	14585506	Click to see	314.29	unknown	https://doi.org/10.1248/CPB.57.245
5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7,8-dimethoxychromen-4-one	162843160	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC)O	344.30	unknown	https://doi.org/10.1248/CPB.57.245
> Phenylpropanoids and polyketides / Stilbenes
Pinosylvin	5280457	Click to see C1=CC=C(C=C1)C=CC2=CC(=CC(=C2)O)O	212.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
Pinostilbenoside	23271974	Click to see	404.40	unknown	via CMAUP database
Resveratroloside	5322089	Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O	390.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid	14132337	Click to see	330.29	unknown	via CMAUP database

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Ocimum tenuiflorum

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